HERITAGE REHABILITATION CENTER

21414 S. VERMONT AVENUE, TORRANCE, CA 90502 (310) 320-8714
For profit - Limited Liability company 161 Beds CHARIS TRUST DTD 12/22/16 Data: November 2025
Trust Grade
23/100
#821 of 1155 in CA
Last Inspection: June 2025

Inspected within the last 6 months. Data reflects current conditions.

Overview

Heritage Rehabilitation Center has a Trust Grade of F, indicating significant concerns and poor quality of care. Ranking #821 out of 1155 facilities in California places it in the bottom half, and it is #191 out of 369 in Los Angeles County, meaning only a few local options are worse. The facility's situation is worsening, with issues increasing from 16 in 2024 to 23 in 2025. Staffing is a relative strength with a 4/5 star rating and a turnover rate of 26%, which is better than the state average. However, there are serious concerns, including a failure to monitor a resident's critical condition, which resulted in their death, and another resident experienced a significant fall risk due to inadequate safety measures, highlighting the facility's struggles with resident care and safety.

Trust Score
F
23/100
In California
#821/1155
Bottom 29%
Safety Record
High Risk
Review needed
Inspections
Getting Worse
16 → 23 violations
Staff Stability
✓ Good
26% annual turnover. Excellent stability, 22 points below California's 48% average. Staff who stay learn residents' needs.
Penalties
✓ Good
$38,687 in fines. Lower than most California facilities. Relatively clean record.
Skilled Nurses
○ Average
Each resident gets 38 minutes of Registered Nurse (RN) attention daily — about average for California. RNs are the most trained staff who monitor for health changes.
Violations
⚠ Watch
58 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★☆☆☆
2.0
Overall Rating
★★★★☆
4.0
Staff Levels
★★★★★
5.0
Care Quality
★☆☆☆☆
1.0
Inspection Score
Stable
2024: 16 issues
2025: 23 issues

The Good

  • 4-Star Staffing Rating · Above-average nurse staffing levels
  • 5-Star Quality Measures · Strong clinical quality outcomes
  • Low Staff Turnover (26%) · Staff stability means consistent care
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover is low (26%)

    22 points below California average of 48%

Facility shows strength in staffing levels, quality measures, staff retention, fire safety.

The Bad

2-Star Overall Rating

Below California average (3.1)

Below average - review inspection findings carefully

Federal Fines: $38,687

Above median ($33,413)

Moderate penalties - review what triggered them

Chain: CHARIS TRUST DTD 12/22/16

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 58 deficiencies on record

5 actual harm
Jul 2025 1 deficiency
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0628 (Tag F0628)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a written copy of the bed hold notice was created and provid...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a written copy of the bed hold notice was created and provided to one of three sampled resident's (Residents 1) responsible party (RP) within 24 hours of transferring Resident 1 to a General Acute Care Hospital (GACH).This deficient practice resulted in the incomplete status of Resident 1 bed hold availability and no documented notice provided to RP.Findings:During a review of Resident 1's admission Record, the admission Record indicated Resident 1 was initially admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including Huntington's disease (nerve cells in parts of the brain that gradually break down and die), major depressive disorder (a mood disorder that causes a persistent feeling of sadness and loss of interest), and dementia (a progressive state of decline in mental abilities). During a review of Resident 1's Minimum Data Set (MDS- a resident assessment tool) dated 9/13/2024, the MDS indicated Resident 1's cognition (ability to think, understand, learn, and remember) was severely impaired. The MDS indicated Resident 1 was dependent (helper does all the work) with Activities of Daily Living (ADLs- activities such as bathing, dressing, and toileting a person performs daily). During a review of Resident 1's progress noted dated 9/13/2025 and timed at 12:05 a.m., the progress note indicated Resident 1 was transferred to GACH for further assessment.During a review of Resident 1's Medical Record, the Medical Record indicated no documented evidence that a written Bed Hold notice, or Transfer Agreement form was created. During a concurrent interview and record review on 7/25/2025 at 4:03 p.m., with Licensed Vocational Nurse (LVN) 1, LVN 1 stated Resident 1 was transferred to GACH on 9/13/2024. LVN 1 stated upon transfer of a resident, a bed hold notice form and a notice of transfer form is to be completed immediately. During an interview on 7/25/2025 at 4:23 p.m., with the Medical Records Supervisor (MRS), the MRS stated there was no bed hold notice form or transfer form for Resident 1's transfer to GACH on 9/13/2024. The MRS stated with any transfer out of the facility, these forms need to be completed because the bed hold agreement is an agreement with Medi-Cal and, so the resident and/or resident representative is aware of the bed hold policy and their rights. During an interview on 7/25/2025 at 4:34 p.m., with the Director of Nursing (DON), the DON stated the nurse's are responsible for ensuring the bed hold notice and transfer forms are completed. The DON stated the bed hold notification is important to be completed to ensure the resident or resident representative is aware of the possibility their bed will be given away after seven days. The DON stated it is important these forms are completed and sent to the Ombudsman, so they are aware and to ensure the transfer was appropriate. During a review of the facility's policy and procedure (P&P) titled, Bed-Holds and Returns, undated, the P&P indicated, Prior to transfers and therapeutic leaves, residents or resident representatives will be informed in writing of the bed-hold and return policy.
Jun 2025 21 deficiencies 2 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Quality of Care (Tag F0684)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to provide the necessary care and treatment for four of six sampled re...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to provide the necessary care and treatment for four of six sampled residents (Resident 19, 14. 61 and 39). The facility failed to: 1. Ensure Licensed Vocational Nurse (LVN) 8, LVN 9 and Registered Nurse (RNS) 4 assessed and monitored Resident 19 when the resident had a change in condition (COC- a sudden, clinically important deviation from a patient's baseline in physical, cognitive [ability to think, and understand] behavioral, or functional status which without immediate intervention, may result in complications or death) manifested by shivering and shaking on 6/8/2025 at 11:10 p.m., and every two hours thereafter. 2. Ensure LVN 8 informed LVN 9 of Resident 19's shivering and shaking on 6/8/2025 at 11:10 p.m. during change of shift handoff. These failures resulted in Resident 19 found unresponsive on 6/9/2025, at 4:14 a.m., pronounced dead on 6/9/2025 at 5:03 a.m. after cardiopulmonary resuscitation (CPR- an emergency procedure used to restart a person's heart and breathing by giving strong, rapid pushes to the chest to keep blood moving through the body) efforts. 3. Ensure Resident 14 was provided with medications for constipation ( a condition in which stool becomes hard, dry , difficult to pass, and bowel movements become infrequent) when Resident 14 had no bowel movement ( the movement of feces through bowel and out of anus) for three days. This failure had the potential to put Resident 14 at risk for fecal impaction ( hardened stool that is stuck in the rectum) that could lead to bowl obstruction ( partial or complete blockage of small or large intestine which is life threatening). 4.a.Ensure licensed staff document a change in condition each time Resident 61's nasogastric tube (NG tube- a thin flexible tube inserted through the nose, down the throat, and into the stomach) was pulled out by Resident 61. b. Ensure an order was obtained prior to reinserting Resident 61's NG tube. Document the location of the NG tube placement for Resident 61. These failures had the potential to cause delay in provision of necessary care and treatment to Resident 61 and complications of prolonged used of NG tube. 5. Ensure Resident 39's physician was notified that Resident 39 was taking clopidogrel (a medication used to prevent blood clots with a side effect of bleeding), after the resident sustained a fall. This failure prevented the physician from being able to make informed decisions regarding the care and treatment of Resident 39. Findings: 1. During a review of Resident 19's admission Record, the admission Record indicated Resident 19 was initially admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including congestive heart failure (CHF-a heart disorder which causes the heart to not pump the blood efficiently, sometimes resulting in leg swelling), diabetes mellitus (DM- a disorder characterized by difficulty in blood sugar control and poor wound healing), cardiomyopathy ( a long term condition that affects the heart muscle making it harder to pump blood), Covid -19 (highly contagious respiratory disease caused by Coronavirus which is transmitted thru coughing, talking , sneezing and touching contaminated surfaces ), and end stage renal disease (ESRD- irreversible kidney failure) with dependence on renal hemodialysis (procedure to remove waste products and excess fluids from the blood when kidneys stop working properly). The admission Record indicated the resident was discharged to a funeral home on 6/9/2025 at 10:25 a.m. During a review of Resident 19's Minimum Data Set (MDS-resident assessment tool) dated 5/15/2025, the MDS indicated Resident 19 had moderately impaired cognitive skills (ability to think, understand, learn, and remember) and was dependent on staff (helper does all the effort to complete the activity) with bathing, dressing, toilet transfer (ability to get on and off a toilet or a commode) and toileting hygiene. During a review of Resident 19's Weights and Vital Signs (VS- basic functions of the body such as temperature, blood pressure (a pressure of the blood against the artery walls when the heart beats), pulse and respiratory rate [breathing] rate), the Weights and Vital Signs Summary indicated the following: 1. On 6/8/2025, at 5:57 p.m. Resident 19's blood pressure (bp reading was 130/72 millimeters of mercury (mmHg-unit of blood pressure measure) 2. On 6/8/2025, at 10:59 a.m. Resident 19's heart rate (HR- number of times the heart beats per minute; reference range is between 60 to 100 beats per minute) was 65 beats per minute, respiratory rate (RR-number of breaths a person takes per minute; reference range is between 12 to 18 breaths per minute) was 18 RR per minute, temperature was 97.5 degrees Fahrenheit (°F- unit of measurement; reference range between 97 degrees F to 99 degrees F), and oxygen saturation (O2 Sat- concentration of oxygen in the blood; reference range between 95 percent to 100 percent) was 97 percent (%) on room air (no supplemental oxygen used). During a review of Resident 19's Transfer/Discharge summary, dated [DATE] and timed at 8:09 a.m., the Transfer/Discharge Summary indicated on 6/9/2025, at 4:30 a.m. , the charge nurse was summoned due to Resident 19 not responding and not breathing. The Transfer/Discharge Summary indicated Registered Nurse (RNS) 4 responded to the summon right away. The Transfer/Discharge Summary indicated chest compressions ( applying pressure on someone's chest in order to help blood flow through the heart in an emergency situation) were started, oxygen was delivered to Resident 19 via Ambu bag (a portable, hand held device used to provide respiratory support to patients in emergency situation), and 911( number that is called in order to contact the emergency services) was called. The Transfer /Discharge Summary indicated paramedics (highly trained healthcare professionals who provide emergency medical care) arrived on 6/9/2025 at 4:35 a.m. and continued cardiopulmonary resuscitation (CPR- an emergency procedure used to restart a person's heart and breathing by giving strong, rapid pushes to the chest to keep blood moving through the body) on Resident 19. The Transfer/Discharge Summary indicated paramedics' team leader pronounced Resident 19 expired on 6/9/2025 at 5:03 a.m. During a review of Resident 19's Emergency Medical Services (EMS-a system that respond to emergencies in need of highly skilled prehospital clinicians) Incident Information dated 6/9/2025, at 4:35 a.m., the EMS Incident Form indicated EMS team was notified on 6/9/2025 at 4:35 a.m. of Resident 19's cardiac arrest ( heart malfunctions and stops beating on its own caused by an electrical problem in the heart). The EMS Incident Information indicated a team was dispatched to the facility and arrived at 4:40 a.m. The EMS Incident Information indicated facility staff stated to the EMS team that Resident 19 was last seen on 6/9/2025, at 4:15 a.m. sleeping and breathing. The EMS Incident Form indicated Resident 19 was in asystole ( when heart's electrical system fails entirely causing the heart to stop pumping and is also known as flat line) upon assessment and throughout the entirety of the resuscitative effort provided to the resident. The EMS Incident Information indicated the time of death of Resident 19 was 5:03 a.m. on 6/9/2025. During a review of Resident 19's Medication Administration (MAR) dated 5/18/2025, the MAR indicated an order for Humulin (Insulin NPH- intermediate acting insulin to treat DM that reaches the blood stream in about 2 to 4 hours) suspension 100 unit/milliliter (ml-unit of measurement) inject 10 unit subcutaneously (applied under the skin ) in the evening for DM with food. During a review of Resident 19's Care Plan titled, Potential for hyperglycemia (condition in which the level of sugar in the blood) /hypoglycemia (low blood sugar). related to DM, initiated on 5/31/2024 and revised on 5/20/2025, the Care Plan indicated Resident 19 had an episode of hyperglycemia and hypoglycemia The Care Plan indicated the goal for Resident 19 was to be asymptomatic ( not showing symptoms) of hyperglycemia and hypoglycemia daily for three months. The Care Plan indicated the interventions included to notify the physician of the resident's change in condition and to monitor, document, and report to the physician as needed any signs and symptoms of hypoglycemia such as sweating, tremor ( shaking movements in one or more parts of the body), increased heart rate, pallor (skin paleness), nervousness, confusion, slurred speech and lack of coordination. During a telephone interview on 6/12/2025 at 10:49 a.m., with Certified Nursing Assistant (CNA) 8, CNA 8 stated on 6/8/2025, at 11:10 p.m. he noticed Resident 19 was shaking and shivering. CNA 8 stated he gave him (Resident 19) a blanket. CNA 8 stated he told Licensed Vocational Nurse (LVN) 8 about Resident 19's shaking and shivering and that Resident 19 did not look good because his upper body was shaking. CNA 8 stated LVN 8 took Resident 19's temperature and told CNA 8 that Resident 19 was okay, and that Resident 19 had been shaking and shivering because had taken a shower. CNA 8 stated on 6/9/2025, from12:00 a.m. to 12:30 a.m. Resident 19 was awake, and was no longer shaking, appeared awake but was staring at the ceiling. CNA 8 stated he asked Resident 19 at that time if he was okay, and the Resident 19 stated he was okay. CNA 8 stated on 6/8/2025, after 12:30 a.m. he got busy with other residents and did not see Resident 19 until 4:14 a.m. on 6/9/2025. CNA 8 stated on 6/9/2025, at 4:14 a.m. he entered Resident 19's room and turned on the lights upon entrance., CNA 8 stated he did not hear Resident 19 talking but he (CNA 8) did not look at Resident 19 as he was to changing Resident 19's roommate. CNA 8 stated after he almost finished changing Resident 19's roommate incontinent pad (diaper), he looked at Resident 19 and saw Resident 19 not moving, his chest did not rise or fall and looked dead. CNA 8 stated he notified LVN 9 immediately. LVN 9 called RNS 4 and called Code Blue (announcement in the facility that someone is experiencing a life-threatening medical emergency). CNA 8 stated LVN 8 and LVN 9 did not tell him to monitor or check on Resident 19 after he had an episode of shaking and shivering on 6/8/2025 at 11:10 p.m. During a concurrent interview and record review on 6/12/2025, at 7:19 a.m. and subsequent telephone interview on 6/12/2025, at 10:14 a.m. with LVN 9, Resident 19's electronic medical records (EHR) was reviewed. LVN 9 stated he did not see Resident 19 after 11:30 p.m. on 6/8/2025 when Resident 19 had episode of shaking and shivering because he was busy with another resident (unknown) who was restless, confused and was trying to get out of bed. LVN 9 stated most of his time on 6/9/2025 was spent with that resident (unknown) . LVN 9 stated he saw Resident 19 awake, resting comfortably at 11:30 p.m. on 6/8/2025 but did not talk to the resident. LVN 9 stated the last time he saw Resident 19 was on 6/8/2025 at 11:30 p.m. LVN 9 stated LVN, RN, or CNA should conduct rounding (in general) every two hours. LVN 9 stated he received report from LVN 8 from outgoing 7 p.m.- 11 pm shift but LVN 8 did not mention any change in Resident 19's condition such as shaking and shivering and reported Resident 19 was okay. LVN 9 stated he notified RNS 4 that he was busy with another resident (unknown) on 6/9/2025. LVN 9 stated RNS 4 did not come to see him (LVN 9) or see Resident 19. LVN 9 stated on 6/9/2025, at 4:30 a.m., CNA 8 notified him that Resident 19 was not breathing, and code blue was announced. LVN 9 stated they initiated CPR and EMS arrived on 6/9/2025 at 4:35 a.m. and took over the CPR During a telephone interview on 6/12/2025, at 11:39 a.m. with LVN 8, LVN 8 stated on 6/8/2025, at around 11:00 p.m., CNA 8 notified LVN 8 that Resident 19 was shivering and shaking. LVN 8 stated he provided an extra blanket and took Resident 19's temperature. LVN 8 stated he took the temperature, and it was normal but did not remember what the temperature was when Resident 19 was shivering and shaking. LVN 8 stated he did not document the temperature on Resident 19's health record. LVN 8 stated Resident 19's shivering and shaking considered a change in the resident's condition because it probably was indicating the resident had a fever or hypoglycemia (low blood sugar). LVN 8 stated he did not do a change of condition because he had done his intervention already by checking Resident 19's temperature and providing Resident 19 with a blanket. LVN 8 stated he did not inform Resident 19's physician about the shivering and shaking and did not check Resident 19's other vital signs including blood pressure, pulse rate, respiratory rate, oxygen saturation, and blood sugar. LVN 8 stated he should have checked the Resident 19's vital signs, notified the physician to address the change in condition , initiate a COC, monitor Resident 19 frequently (at least every two hours) and checked his blood sugar when Resident 19 was shivering and shaking as Resident 19 had a history of hypoglycemia (low blood sugar) and was receiving insulin (medication to treat DM). LVN 8 stated Resident 19 had a change in condition due to low blood sugar last month (May). LVN 8 stated he administered NPH Insulin (intermediate acting insulin to treat DM that reaches the blood stream in about 2 to 4 hours) on 6/8/2025 at 6:00 p.m., LVN 8 stated NPH insulin could lower the blood sugar within 4 to 5 hours of administration. LVN 8 stated failure to monitor Resident 19 after the resident was having symptoms of shaking and shivering could have contributed to Resident 19's death. LVN 8 stated he should have checked Resident 19's vital signs, notify the physician who could have ordered a transfer to the hospital for further evaluation, monitor the resident by conducting a COC to ensure Resident 19's condition would not worsen. LVN 8 stated he should have informed LVN 9 and RNS 4 regarding Resident 19's shaking and shivering to keep an eye on Resident 19 on 6/8/2025. During an interview on 6/12/2025, at 8:29 a.m., with RNS 4, RNS 4 stated on 6/8/2025, at 10:30 p.m. Resident 19 was asleep. RNS 4 stated she did not go to Resident 19's room until the resident was found pulseless and not breathing on 6/9/2025 at 4:30 a.m. RNS 4 stated on 6/9/2025, at 4:30 a.m. Resident 19 was pulseless and they were unable to check his vital signs. RNS 4 stated they initiated CPR on Resident 19 and another staff called 911. During an interview on 6/12/2025, at 3:19 p.m. with RNS 2, RNS 2 stated when Resident 19 had shaking and shivering on 6/8/2025 at 11:10 p.m., Resident 19 should have been monitored closely as it was considered a COC. RNS 2 stated a COC should be performed when the condition of a resident deviated from his baseline (an initial measurement of a condition that is taken at an early time point and used for comparison over time to look for changes in condition) . RNS 2 stated doing COC was important to ensure monitoring of the change of condition was performed, assessment and evaluation of the resident's condition done, and the physician informed to obtain physician orders for treatment. During an interview on 6/12/2025, at 4:49 p.m. with the Director of Nursing (DON), the DON stated facility staff should checked resident every two hours. The DON stated Resident 19's symptoms of shaking and shivering were considered a change of condition. The DON stated LVN 8 should have done a COC, checked the full set of vital signs, not just the temperature, including blood sugar because Resident 19 received 10 units of NPH insulin on 6/8/2025 at 4:38 p.m., and 2 units of sliding scale Regular insulin at 9:32 p.m. The DON stated LVN 8 should have informed LVN 9 and RNS 4 when Resident 19's had episode of shivering and shaking on 6/8/2025 at 11:10 p.m., during handoff. The DON stated COC was a monitoring tool and not having vital signs documented meant VS were not done. The DON stated the licensed nurse should have done a COC, took a full set of vital signs, rechecked resident's blood sugar, notified the physician, assessed and monitored Resident 19 when he had shivering and shaking. The DON stated Resident 19 should have been monitored and assessed and could have transferred to general acute care hospital (GACH) in a timely manner. The DON stated Resident 19 expired on 6/9/2025, at 5:03 a.m. 3. During a review of Resident 14's admission Record, the admission Record indicated Resident 14 was initially admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including constipation, repeated falls, urinary tract infection (UTI- an infection in the bladder/urinary tract), polyp of the colon (mall clump of cells that forms in the lining of the colon), and major depressive disorder( serious mental illness characterized by persistent sadness, loss of interest in activities, and significant impairment in daily functioning). During a review of Resident 14's MDS dated [DATE], the MDS indicated Resident 14 had an intact cognition and required partial/moderate assistance (helper does less than half the effort) with toilet transfer( ability to get on and off a toilet commode), bed mobility, and bathing. The MDS indicated Resident 14 was always incontinent ( having no or insufficient voluntary control ) of stool. During a review of Resident 14's Activities of Daily Living (ADL- activities such as bathing, dressing and toileting a person performs daily) Task for bowel and bladder elimination, the ADL Task indicated Resident 14 did not have a bowel movement (BM-process of emptying the bowels of solid or semisolid feces) on 6/1/2025, 6/2/2025, 6/3/2025 and on 6/7/2025, 6/8/2025, 6/9/2025. During a review of Resident 14's Care Plan titled, Potential Alteration in Bowel Elimination related to Constipation, initiated on 4/26/2025. the Care Plan indicated the goal for Resident 14 to have bowel movement regularly for the next three months. The Care Plan indicated the interventions included monitoring for bowel movement, for amount, consistency and frequency, review medication that cause constipation, and administer medication as ordered. During a review of Resident 14's Physician's Order Summary Report , the Physician's Order Summary Report, dated 5/5/2025 indicated an order of Sertraline (medication used to treat depression) 25 milligrams (mg-. unit of measurement) one tablet at bedtime for depression. During a review of Resident 14's Physician's Order Summary Report, the Physician's Order Summary Report dated 5/5/2025 indicated a physician's order to monitor side effects of anti-depressant (medication used to treat depression) medication such as constipation. During a review of Resident 14's Physician's Order Summary Report, the Physician's Order Summary Report dated 5/23/2025 indicated an order of Bisacodyl ( used to treat constipation) 10 mg Suppository, to insert one suppository rectally ( given via rectum) as needed for constipation if no BM in 24 hours. During a review of Resident 14's Physician's Order Summary Report, the Physician's Order Summary Report indicated an order for 70 percent (%- quantify the amount or concentration of the medicine) Sorbitol solution (used to treat occasional episodes of constipation) 30 milliliter (ml- unit of measurement) every 6 hours as needed for constipation. During an interview on 6/9/2025, at 11:03 a.m. with Resident 14, Resident 14 complained of constipation and stated she did not have a bowel movement for a while. Resident 14 stated she kept telling the staff about her concern (constipation). During an interview on 6/10/2025, at 12:06 p.m. with Certified Nursing Assistant (CNA 5), CNA5 stated if the resident (in general) has no bowel movement for three days, the CNA notifies the charge nurse CNA 5 stated she did not check Resident 14 if the resident had BM for the past few days (6/7/2025, 6/8/2025, 6/9/2025). CNA 5 stated she should have checked if Resident 14 had a bowel movement for the past few days (6/7/2025, 6/8/2025, 6/9/2025). CNA 5 stated Resident 14 would get constipated with the risk to go to the hospital. During a concurrent interview and record review on 6/10/2025 at 3:22 p.m., with LVN 11, Resident 14's MAR and ADL Task for Bowel and Bladder Elimination were reviewed. LVN 11 stated Resident 14 had no bowel movement on 5/28/2025, 5/29/2025, 5/30/2025 and on 6/7/2025, 6/8/2025, 6/9/2025, and 6/10/2025. LVN 11 verified through MAR review that Resident 14 did not receive any as needed (prn) medications for constipation on the days Resident 14 had no BM for 3 days. LVN 11 stated the licensed nurse should have assessed Resident 14 for abdominal pain, asked the resident if she had a bowel movement monitored BM frequency, and administered prn medications for constipation. LVN 11 stated Resident 14 could be at risk for bowel obstruction (occurs when something blocks the normal passage of digested food, and fluids), sepsis ( serious condition in which the body responds improperly to an infection) or infection that could lead to death if constipation was not addressed. During an interview on 6/12/2025, at 3:08 p.m. with RN Supervisor (RNS 2), RNS 2 stated Resident 14 could be at risk for fecal impaction ( a large lump of dry, hard stool that stays stuck in the rectum), bowel obstruction, abdominal discomfort, nausea, vomiting and could increase Resident 14 risk for hospitalization if constipation was not addressed. RNS 2 stated the licensed nurse should have monitored Resident 14's BM frequency and on if there was no BM on the third day, the licensed nurse should have administered the prn medication for constipation as ordered. During an interview on 6/12/2025, at 4:43 p.m. with the DON, the DON stated the LVN (in general) should have monitored Resident 14's BM frequency, informed the physician and administered prn medication for constipation on the third day if the resident had no bowel movement. The DON stated if Resident 14's constipation was not addressed the resident appetite would be affected by the resident would have an abdominal discomfort and vomiting, and possible bowel obstruction. 4. During a review of Resident 61's admission Record, the admission Record indicated Resident 61 was admitted to the facility on [DATE] with diagnoses including dementia ( a progressive state of decline in mental abilities) and dysphagia (difficulty swallowing). During a review of Resident 61's MDS dated [DATE], the MDS indicated Resident 61's cognition was severely impaired and was dependent for toileting, showering, dressing, personal hygiene, and rolling to either side in bed. During a review of Resident 61's Order Summary Report, the Order Summary Report indicated there were a total of seven orders (5/9/2024, 8/12/2024, 10/27/2024, 11/19/2024, 1/11/2025, 4/24/2025, and 5/25/2025) placed for chest X-rays (pictures of the inside of your body) for NG tube placement. During a review of Resident 61's Order Summary Report, the Order Summary Report indicated an order was placed 1/11/2025 and 4/24/2025 for a chest X-ray for NG tube placement with no order to re-insert the NG tube. During a review of Resident 61's COC dated 1/11/2025, timed 10:30 a.m., the COC indicated Resident 61 pulled out her NG tube. No COC for 4/24/2025 for when Resident 61 pulled out her NG tube. During a review of Resident 61's Care Plan title Potential for injury related to pulling out NG tube, the Care Plan indicated there were no revisions made to the care plan after Resident 61 pulled her NG tube out on 5/9/2024, 8/12/2024, 10/27/2024, 11/19/2024, 1/11/2025, 4/24/2025 and 5/25/2025. During an interview on 6/11/2025 at 9:19 a.m., with Certified Nurse Assistant (CNA) 9, CNA 9 stated Resident 61 has mitten restraints (prevents someone from grabbing something) because she tends to pull out her NG tube. During a concurrent interview and record review on 6/12/2025 at 8:29 a.m., the Licensed Vocational Nurse (LVN) 9, LVN 9 stated Resident 61 pulls her NG tube out at least every three months. LVN 9 stated there should be an order for NG tube re-insertion, a COC documented, and documentation indicating when and which nostril the NG tube was placed. LVN 9 validated there were no orders to re-insert Resident 61's NG tube on 1/11/2025 and 4/24/2025. LVN 9 validated there were no COC documented on 4/24/2025. LVN 9 validated there were no documentation when and where the NG tube was re-inserted on 5/9/2024, 8/12/2024, 10/27/2024, 11/19/2024, 1/11/2025, 4/24/2025, and 5/25/2025. LVN 9 stated there should be a progress note indicating which nostril the NG tube was placed. During an interview on 6/12/2025 at 10:10 a.m., with the Registered Nurse Supervisor (RNS) 2, RNS 2 stated when Resident 61 pulls out her NG tube, there should be an order to re-insert the NG tube, a COC documented, and documentation of which nostril the NG tube was placed. RNS stated it was important to document which nostril the NG tube was placed to better monitor for complications of the affected nostril and to ensure they rotate sites of where the NG tube was placed. During an interview on 6/13/2025 at 9:24 a.m., with the Director of Nursing (DON), the DON stated Resident 61 had removed her NG tube several times and each time there should be an order to re-insert, a COC documented, and documentation of re-insertion and which nostril the NG tube was re-inserted and if not, this was to be considered inaccurate documentation. During a review of the facility's policy and procedure (P&P) titled Nasogastric Tube Insertion and Care, undated, the P&P indicated, Verify that there is a physician's order for insertion of the nasogastric tube. The person performing this procedure should record the following information in the resident's medical records: the date and time the procedure was performed, the size and length of the nasogastric tube, and verification of tube placement. During a review of the facility's P&P titled, Charting and Documentation, undated, the P&P indicated, The following documentation is to be documented in the resident medical record: treatments or services performed, changes in the residents condition, events, incidents, or accidents involving the resident and progress toward or changes in the care plan goals and objectives. 5. During a review of Resident 39's admission Record, the admission Record indicated Resident 39 was admitted to the facility on [DATE] with the diagnoses including malignant neoplasm of prostate (prostate cancer) and cerebral vascular accident (CVA - a stroke, loss of blood flow to a part of the brain). During a review of Resident 39's Medication Administration Record (MAR) for 11/ 2024, the MAR indicated Resident 39 was receiving clopidogrel 75 milligrams (mg- unit of measurement) daily to prevent a stroke During a review of Resident 39's care plan, titled Resident was at risk for bleeding/bruising/skin tear/hematuria (blood in the urine) /melena (blood in the stool) secondary to clopidogrel, the Care Plan interventions included to monitor Resident 39 for bruises or bleeding episodes. The care plan interventions also indicated the physician should be notified accordingly for unusual observation related to clopidogrel. During a review of Resident's 39's Change of Condition Evaluation (COC- a tool used by health care professionals when communicating about critical changes in residents' status) dated 11/9/2024, the COC indicated Resident 39 fell from the wheelchair to the ground. The COC did not indicate Licensed Vocational Nurse (LVN) 10 reported the resident was on clopidogrel to the on-call physician. During an interview on 6/12/2025 at 2:27 p.m., with LVN 10, LVN 10 stated they should have notified Resident 39's physician that Resident 39 was on clopidogrel because of the potential risk for bleeding. LVN 10 stated the physician would have ordered labs and an x-ray (create images of the inside of the body) immediately to see if Resident 55 was bleeding internally had they been notified. LVN 10 stated it was important to notify the doctor of antiplatelets (medications used to prevent blood clots) when a resident falls because of the risk for internal bleeding. During an interview on 6/12/2025 at 1:59 p.m., with Registered Nurse Supervisor (RNS) 3, RNS 3 stated, If a resident falls and the physician just orders to monitor the resident when they are on antiplatelet therapy, the nurse was responsible to take the initiative and notify the physician to recommend an x-ray and evaluation. This resident (Resident 39) should have at least had an x-ray done for possible internal bleeding. During an interview on 6/12/2025 at 5:13 p.m., with the Director of Nursing (DON), the DON stated that notifying the physician of a resident being on blood thinners or antiplatelets after they fall will determine the physician's course of actions and what they would order; it was part of the facility's protocol to accurately report to the doctor. During a review of facility's policy and procedure (P&P)titled, Change in a Resident's Condition, undated, the P&P indicated the facility will promptly notify resident's attending physician and representatives of changes in the resident's medical/ mental condition. The P&P indicated the Nurse Supervisor/Charge Nurse will record in the resident's medical record information relative to changes in the resident's medical condition. During a review of facility's Job Description of a Charge Nurse undated, the Job Description of a Charge Nurse indicated the charge nurse will accurately assess, document, and report the resident's symptoms, reactions, progress to the attending physician ,nursing supervisor , DON, Administrator and other participating in care and treatment of the resident. The Job Description of a Charge Nurse indicated the charge nurse will promptly notify the attending physician and responsible party, family of change in resident's condition and in accordance with the facility's policies and procedures.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Accident Prevention (Tag F0689)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure residents, who were identified at risk for fall...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure residents, who were identified at risk for falls, did not fall and sustain injury for two of three sampled residents (Resident 50 and Resident 89). The facility failed to: 1. Ensure Resident 50's talking device (recordable voice alarm with a personalized message that plays when an alarm is triggered) was turned on as one of the interventions of fall risk prevention program for Resident 50. 2. Ensure the licensed nurses evaluated the effectiveness of interventions of Resident 50's care plan titled, At risk for falls, difficulty maintaining sitting/standing balance, history of falls/multiple falls initiated on 12/25/2024, after the resident's fall on 4/19/2025, to develop new interventions to prevent the resident's fall on 5/22/2025 with injuries. 3. Ensure staff followed the facility's policy and procedure (P&P) titled, Safety and Supervision of Residents, undated, which indicated, The care team will target interventions that will reduce individual risks related to hazards in the environment including adequate supervision and assistive devices (equipment that can help you perform tasks and activities). 4. Ensure Resident 89, who required supervision at all times, was supervised while smoking on 2/27/2025 at 1:45 p.m., in accordance with the facility's policy and procedure (P&P) titled, Smoking Policy-Residents (undated). 5. Ensure Restorative Nursing assistant (RNA) 1 did not leave Resident 89 unsupervised on 2/27/2025 at 1:45 p.m., when RNA 1 wheeled Resident 89 to designated smoking area in front of the facility. 6. Ensure staff followed Resident 89's Care Plan, titled Resident 89 is at risk for injury related to smoking, dated 9/11/2023, by not leaving Resident 89 unsupervised while smoking. 7. Ensure the spray bottle containing clear liquid was labeled to identify ingredients inside the bottle, affecting one of four medication carts (Medication Cart B2). These failures resulted in: A. Resident 50 falling from a bed to the floor on 5/22/2025 around 7:25 a.m., sustaining a right inferior (lower) pubic ramus (a bone in the pelvis, specifically a thin, flat part of the pubic bone) fracture (broken bone) right superior (above) pubic ramus (a break in the upper part of the pubic bone on the right side of the pelvis) fracture, right sacral (tail bone) fracture, and bilateral rib fractures which required hospitalization in a general acute care hospital (GACH) for evaluation and treatment. B. Resident 89 falling from a wheelchair and sustaining a nose fracture small cut on a forehead that was bleeding, bruised ( skin is not broken but is discolored) and swollen. Resident 89 sustained abrasions (superficial wound caused by scraping away of the skin's outer layer) to the forehead and left knee. Resident 89 was transferred to GACH on 2/27/2025 at 3:42 p.m., for further evaluation and treatment of swelling to both eyes. C. Had the potential to result in accidental exposure to or ingestion of isopropyl alcohol. Findings: A. During a review of Resident 50's admission Record, the admission Record indicated Resident 50 was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including dementia (a progressive state of decline in mental abilities), osteoporosis (weak and brittle bones due to a lack of calcium [mineral needed for healthy bones] and Vitamin D {nutrients needed to keep bones healthy}), fractures of left and right humerus (the long bone of the upper arm), repeated falls, and lack of coordination. During a review of Resident 50's Change in Condition (COC- a sudden clinically important deviation from a patient's baseline in physical, cognitive, behavioral, or functional condition) Form dated 12/22/2024 and timed at 2:16 p.m., the COC Form indicated Resident 50 informed the charge nurse (unknown) that she fell in the bathroom the day before (12/21/2024) after getting up unassisted. The COC Form indicated Resident 50 stated she lost her footing, fell on the ground, but was able to get up and went back to her bed on her own without calling for assistance. The COC Form indicated Resident 50 had a hematoma (a solid swelling of clotted blood within the tissues) to her right side of the head. The COC Form indicated Resident 50 was on toileting every two hours and as needed, frequent visual checks and talking device in place and working. During a review of Resident 50's Care Plan titled, At risk for falls, difficulty maintaining sitting/standing balance, history of falls/multiple falls initiated on 12/25/2024, the Care Plan goal for Resident 50 was to have decrease in significant injury as a result from falls and to minimize the risk for falls in the next three months. The Care Plan interventions included to apply and check the talking device while in bed and or wheelchair to remind and redirect Resident 50 to call for assistance and to have frequent visual checks. During a review of Resident 50's Interdisciplinary Team (IDT team members from different departments working together with a common purpose to set goals and make decisions that ensure residents receive the best care) Note dated 1/9/2025 timed at 11:14 a.m., the IDT Note indicated on 12/22/2024 around 7:15 a.m., Licensed Vocational Nurse (LVN) 12 observed Resident 50 with a hematoma to the right side of her head. IDT Note indicated Resident 50 stated she fell in the bathroom on 12/21/2024. Resident 50 stated she went to the bathroom unassisted and when she was returning back to bed, she lost her footing, bumped herself ( unknown where) and ended up on the floor. Resident 50 stated she got up and went back to bed. The IDT Note indicated Resident 50 was on fall management program which consist of a talking device to remind and redirect Resident 50 to call for assistance, and a perimeter mattress (type of mattress designed with raised edges or bolsters to prevent falls and provide a safer sleep environment) for extra support. The IDT Note indicated Resident 50 was able to silence or turned off her talking device because she wanted to go to the bathroom by herself. During a review of Resident 50's COC dated 4/19/2025 and timed at 6:30 a.m., the COC indicated Resident 50 was found sitting on the bathroom floor after getting out of bed unassisted and suddenly feeling weak. During a review of Resident 50's IDT Note dated 4/28/2025 timed at 10:25 a.m., the IDT note indicated Resident 50 had an incident on 4/19/2025 around 6 a.m., when Resident 50 was observed sitting on the floor outside the bathroom. The IDT note indicated Resident 50 was assessed with no injury. The IDT note indicated Resident 50 was currently on a toileting schedule and has a talking device to remind and redirect Resident 50 to call for assistance. The IDT note indicated Resident 50 was observed by staff that she can manipulate the talking device. During a review of Resident 50's Minimum Data Set ( MDS-resident assessment tool) dated 5/22/2025, the MDS indicated Resident 50 had moderately impaired cognitive skills (ability to think, understand, learn, and remember) for daily decision making and was dependent (helper does all the effort) with toileting hygiene, showering and bathing. During a review of Resident 50's Physician's Order Summary Report, the Physician's Order Summary Report indicated an order to apply and check talking device while in bed and or wheelchair to remind and redirect the resident to call for assistance. During a review of Resident 50's COC dated 5/22/2025 and timed at 7:25 a.m., the COC indicated Resident 50 had an unwitnessed fall and was found lying on the floor. During a review of the facility's Investigation Report, (undated), the Investigation report indicated at the time of the incident (on 5/22/2025), Resident 50's talking device was noted to be disconnected. During a review of Resident 50's COC dated 5/22/2025 and timed at 2:58 p.m., the COC indicated Resident 50 had an open area to her right eyebrow. Registered Nurse Supervisor (RNS) called 911 and Resident 50 was transferred to GACH on 5/22/2025 (unknown time). During a review of Resident 50's GACH's Consultation Notes report dated 5/23/2025, the Consultation Note report indicated Per the facility, Resident 50's bed alarm (talking device) did not alarm, and she got out of bed by herself and fell. The Consultation Note report indicated Resident 50 had a computed tomography scan (CT- a medical imaging procedure that uses x-rays to create detailed, cross-sectional images of the body's internal structures) of the abdomen and pelvis on 5/22/2025. The CT scan indicated Resident 50 had a right inferior pubic ramus fracture, a right superior pubic ramus fracture, a right sacral fracture, and multiple bilateral rib fractures. During a concurrent observation and interview on 6/10/2025 at 8:22 a.m., Resident 50 was observed with a right eye bruise. Resident 50 stated she fell the other day (unable to state exact date). During an interview on 6/11/2025 at 1:46 p.m., with Certified Nurse Assistant (CNA) 1, CNA 1 stated Resident 50 had a fall on 5/22/2025 and sustained a fracture. CNA 1 stated Resident 50 was confused and forgot to use her call light. During a concurrent interview and record review on 6/12/2025 at 8:55 a.m., with Licensed Vocational Nurse (LVN) 9, LVN 9 stated Resident 50 was a high fall risk. LVN 9 stated Resident 50's room was close to the nurse's station. LVN 9 stated after each fall, the care plan should be revised to evaluate the effectiveness of interventions to prevent future falls from occurring. Reviewed Resident 50's Care Plan, LVN 9 stated Resident 50's care plan was not revised following her fall on 4/19/2025 and it should have been done because additional interventions could have prevented the resident's fall on 5/22/2025 which resulted in multiple fractures. LVN 9 stated Resident 50's fall was preventable if she had been monitored more closely and had a bedside commode (portable toilet) at her bedside as she gets up without assistance to use the bathroom. During a concurrent interview and record review on 6/12/2025 at 10:10 a.m., with Registered Nurse Supervisor (RNS) 2, Resident 50's Care plan was reviewed. RNS 2 stated Resident 50 was a high risk for fall and recently had a fall on 5/22/2025. RNS 2 stated after a resident falls, the care plan should be revised to add new interventions. RNS 2 stated after Resident 50's fall on 4/19/2025, the care plan was not reviewed and revised. RNS 2 stated it was important to revise the care plan after a fall because the interventions in place were not effective, therefore, a new intervention could be added to prevent future falls. During an interview on 6/13/2025 at 9:24 a.m., with the Director of Nursing (DON), the DON stated a care plan was a guide that outlines the plan of care for the resident. The DON stated the care plan includes goals and interventions and should be revised when interventions were not effective. The DON stated Resident 50's care plan should have been revised after each fall so new interventions could be added to prevent future falls. During an interview on 6/13/2025 at 10:16 a.m., with the Quality Assurance Licensed Vocational Nurse (QA LVN), the QA LVN stated Resident 50 tends to disconnect the talking device. During a review of the facility's P&P titled, Safety and Supervision of Residents undated, the P&P indicated, Resident safety and supervision and assistance to prevent accidents are facility-wide priorities. Implementing interventions to reduce accident risks and hazards shall include the following: ensuring that interventions are implemented and documenting interventions. During a review of the facility's P&P titled, Care Plans, Comprehensive Person-Centered undated, the P&P indicated, Assessments of residents are ongoing, and care plans are revised as information about the residents and residents' conditions change. C.During a concurrent observation and interview on 6/10/2025 at 9:20 a.m. during medication pass with the Licensed Vocational Nurse (LVN) 1, LVN 1 used a few sprays from an unlabeled spray bottle containing clear liquid to sanitize his hands. LVN 1 stated the spray bottle contained hand sanitizer and they transferred the liquid from the original large container into the smaller spray bottle that was in use at medication cart. LVN 1 showed a large bottle labeled with 70 percent (%) isopropyl alcohol stating that the contents of the unlabeled spray bottle were the same as the large container. During an interview on 6/12/2025 at 12:51 p.m. with the Director of Nursing (DON), the DON stated it was important that the unlabeled spray bottle with clear liquid was labeled to identify its ingredients inside, which was isopropyl alcohol, to prevent any accidental ingestion by facility residents. During a concurrent observation and interview on 6/12/2025 at 12:13 p.m. with the Quality Assurance Licensed Vocational Nurse (QA LVN), observed Medication Cart B2 contained an unlabeled spray bottle. QA LVN stated the facility started receiving the large isopropyl alcohol containers recently and so they had to transfer the liquid into a smaller spray bottle to be stored on medication carts. QA LVN stated it was important to label the small spray bottle to identify that it contained 70% isopropyl alcohol, to maintain safety of facility's staff and residents. QA LVN stated it would be a risk for residents if they just grabbed it and ingested by accident. During a review of the facility's policy and procedure (P&P) titled, Safety and Supervision of Residents, undated, the P&P indicated, Our facility strives to make the environment as free from accident hazards as possible. Resident safety and supervision and assistance to prevent accidents are facility-wide priorities. The P&P indicated, Employees shall be trained on potential accident hazards and demonstrate competency on how to identify and report accident hazards and try to prevent avoidable accidents. B. During a review of Resident 89's admission Record, the admission Record indicated, Resident 89 was originally admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including repeated falls, nicotine (the additive drug found in tobacco products) dependency, bone density disorder (the bones are weak and more likely to break than normal), osteoarthritis (a degenerative joint disease, in which the tissues in the joint breakdown over time), and muscle wasting (the weakening, shrinking, and loss of muscle tissue). During a review of Resident 89's Care Plan, titled Resident 89 is at risk for injury related to smoking, dated 9/11/2023, the Care Plan indicated the interventions included not to leave Resident 89 alone while smoking, and provide supervision when resident is smoking. During a review of Resident 89's Physician's Order Summary, dated 11/28/2024, the Physician's Order Summary indicated Resident 89 had an order for fall precautions (measures taken to reduce the risk of falling and the likelihood of serious injury if a fall does occur). During a review of Resident 89's Smoking Safety Evaluation, dated 2/13/2025, the Smoking Safety Evaluation indicated, Resident 89 required supervision to smoke safely. During a review of Resident 89's Fall Risk Evaluation, dated 2/13/2025, the Fall Risk Evaluation indicated Resident 89 was at risk for fall. The Fall Risk Evaluation indicated Resident 89 was chairbound (confined to a chair, typically due to illness, injury, or disability) and had a balance problem while standing and walking. During a review of Resident 89's COC Evaluation dated 2/27/2025 timed at 2:27 p.m., the COC indicated that on 2/27/2025 around 2:05 p.m., Resident 89 was found on the ground in front of the facility (designated smoking area). The COC indicated Resident 89 sustained a bump on the forehead with open area. The COC indicated Resident 89 stated that she dropped her cigarettes and wanted to pick it up. The COC indicated Resident 89's physician was informed and ordered to transfer Resident 89 to GACH. During a review of Resident 89's Physician's Order Summary, dated 2/27/2025, the Physician's Order Summary indicated an order to transfer Resident 89 to GACH for further evaluation of the bump on the head after falling. During a record review of Resident 89's GACH's Emergency Department (ED) Notes, dated 2/27/2025, the ED Notes indicated Resident 89 had a bilateral nasal (nose) bone fracture with, moderate soft tissue swelling over the left periorbital (around the eye) and nasal region. The ED Noted indicated a Computerized Topography (CT -medical imaging that create detailed images of the body) of the head was done and CT scan result was bilateral (both) nasal bone fracture with moderate soft tissue swelling over the left periorbital and nasal region. The ED Notes indicated Resident 89 had an abrasion (superficial wound caused by scraping the skin) to the left forehead and mild laceration (a wound where the skin and underlying tissues are torn or cut) which was repaired with Steri-Strips (thin sticky adhesive bandages used to close small, shallow wounds or surgical incisions, often as an alternative to stiches or staples) During a review of Resident 89's Physician's Order Summary, dated 2/27/2025, the Physician's Order Summary indicated to apply Betadine (solution used to treat or prevent skin infection in minor cuts, or scrapes) to the left forehead abrasion topically (to the skin) in the morning. The Physician's Order Summary indicated the following order: 1. Monitor Resident 89's forehead bump with Steri-Strips for increase discoloration, bleeding, drainage, increase swelling, discharges, pain, and signs and symptoms of infection. 2. Cleanse forehead bump with Normal Saline (salt solution used for cleansing wounds), pat dry, apply Steri-Strips, and cover with gauze dressing. 3. Monitor Resident 89's right periorbital purplish discoloration for presence of increase discoloration, open area, bleeding, drainage, increase swelling, discharges, pain, signs and symptoms of infection every shift. 4. Apply Vitamin A&D external ointment (skin protectant and can aid in the healing of minor cuts, cuts, scrapes) to Resident 89's left knee abrasion daily. During a review of Resident 89's Physician's Order Summary, dated 2/28/2025, the Physician's Order Summary indicated an order to monitor Resident 89 nose discoloration and left periorbital area for increase of purplish discoloration, open area, bleeding, drainage, increase swelling, discharges, pain, signs and symptoms of infection every shift. The Physician's Order Summary indicated an order for ice compress to the forehead and facial affected area for 10 to 20 minutes to reduce swelling three times a day. During a review of Resident 89's Minimum Data Set (MDS-resident assessment tool), dated 5/15/2025, the MDS indicated, Resident 89 was dependent on nursing staff for toileting, dressing, and transferring. The MDS indicated Resident 89 needed partial to moderate assistance from nursing staff with walking, standing and sitting. During a review of Resident 89's Physician's Progress Note dated 6/4/2025, the Physician's Progress Note indicated, Resident 89 was able to express needs and make healthcare decisions. During an interview on 6/11/2025 at 2:52 p.m., with Restorative Nursing Assistant (RNA) 1, RNA 1 stated on 2/27/2025 at 1:45 p.m., RNA 1 wheeled Resident 89 to the designated smoking area in front of the facility. RNA 1 stated she stayed for 10 minutes and supervised Resident 89 while the resident was smoking. RNA 1 stated Resident 89 wanted to stay longer in the designated smoking area to get some fresh air. RNA 1 stated she left Resident 89 alone at the designated smoking area and went back inside the facility to assist another resident with RNA services. RNA 1 stated she asked the Receptionist (RCPT) to call her when Resident 89 was ready to come back inside the facility. RNA 1 stated she heard RCPT responded okay. RNA 1 stated she heard from another staff that Resident 89 fell from his wheelchair while trying to pick up a cigarette from the ground. RNA 1 stated Resident 89 was on the ground and was bleeding from the forehead. RNA 1 stated other staff helped her (RNA 1) to put Resident 89 back on the wheelchair and wheeled Resident 89 back to the facility. RNA 1 stated that she should have not left Resident 89 unsupervised while smoking in the designated smoking area for safety and prevent Resident 89 from falling. RNA 1 stated facility did not have an assigned staff to supervise the smoking area. RNA 1 stated a certified nursing assistant (CNA) assigned to the resident was responsible for supervising the resident while the resident smokes. During an interview on 6/12/2025 at 1:52 p.m., with RCPT, RCPT stated there have been instances when facility staff were supervising residents' while smoking in the designated smoking area and will step out for few minutes and return right away. RCPT stated she does not recall RNA 1 telling her to call her when Resident 89 was ready to come back inside the facility. RCPT stated she saw Resident 89 at the designated smoking area before the fall. RCPT stated she stepped away from the receptionist desk and heard about Resident 89 fall. RCPT stated she no longer supervised residents outside the designated smoking area because she was not at the receptionist's desk continuously. During an interview on 6/12/2025 at 4:04 p.m., with the Director of Nursing (DON), the DON stated if a resident requires supervision during scheduled smoking time, the facility staff should always be at the designated smoking area to supervise residents for safety and prevent fall. The DON stated Resident 89 needed supervision for safety when smoking in the designated smoking area. During a review of the facility's P&P titled, Safety and Supervision of Residents, undated, the P&P indicated the facility strives to make the environment as free from hazards as possible. Resident safety and supervision and assistance to prevent accidents are facility-wide priorities. During a review of the facility's P&P titled, Smoking Policy-Residents, undated, the P&P indicated any resident with restricted smoking privileges requiring monitoring shall have the direct supervision of a staff member, family member, visitor or volunteer worker at all times while smoking.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to accurately assess and code the Minimum Data Set (MDS,...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to accurately assess and code the Minimum Data Set (MDS, resident assessment tool) assessments for one of six sampled residents (Resident 32) by failing to ensure Section GG 0115A was coded accurately to indicate functional limitations in range of motion (limited ability to move a joint that interferes with daily functioning, including activities of daily living, or places the resident at risk of injury) of Resident 32's both arms. This deficient practice had the potential to result in delayed or missed identification of joint range of motion (ROM, full movement potential of a joint) changes, inaccurate care planning, and inadequate provision of services and treatments for Resident 32. Findings: During a review of Resident 32's admission Record, the admission indicated Resident 32 was originally admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including osteoarthritis (loss of protective cartilage that cushions the ends of your bones) of the left shoulder and the left hand and contracture (loss of motion of a joint associated with stiffness and joint deformity) of an unspecified joint (where two bones meet). During a review of Resident 32's MDS, dated [DATE], the MDS indicated Resident 32 was cognitively (ability to think, understand, learn, and remember) intact. The MDS indicated Resident 32 required partial/moderate assistance for eating, oral hygiene, and upper body dressing, substantial/maximal assistance for rolling to both sides and transfers, and was dependent for toilet hygiene, lower body dressing, personal hygiene, and bathing. Section GG 0115A of the MDS for functional limitations in ROM was coded zero which indicated Resident 32 had no ROM limitations in both arms. During a review of Resident 32's Joint Mobility Evaluation (JME, a brief assessment of a resident's ROM in both arms and both legs), dated 6/27/2024, the JME indicated Resident 32 had minimal (26 - 50 percent [%]) ROM limitations in both shoulders and severe (76-100%) ROM limitations in both hands/fingers. During a review of Resident 32's MDS, dated [DATE], the MDS indicated Resident 32 was cognitively intact. The MDS indicated Resident 32 required partial/moderate assistance for eating, oral hygiene, and upper body dressing, substantial/maximal assistance for rolling to both sides and transfers, and was dependent for toilet hygiene, lower body dressing, personal hygiene, and bathing. Section GG 0115A of the MDS for functional limitations in ROM was coded zero which indicated Resident 32 had no ROM limitations in both arms. During a review of Resident 32's JME, dated 9/27/2024, the JME indicated Resident 32 had minimal ROM limitations in both shoulders and severe ROM limitations in both hands/fingers. During an observation and interview on 6/10/25 at 9:58 a.m., in Resident 32's room, Resident 32 was lying in bed. Resident 32's both elbows were bent, and both hands were in a fisted position with thin gauze material in the palms of both hands. The fingers of the left hand were hyperextended (the extension of a body part beyond it's normal limits) in the middle joints and bent at the fingertips. The fingers of the right hand were bent into a fisted position with the pointer finger hyperextended at the middle joint and bent at the fingertip. Resident 32 was unable to raise both arms to shoulder height and was unable to open both hands. During a concurrent interview and record review on 6/12/2025 at 3:25 p.m., the Minimum Data Set Nurse 1 (MDSN 1) and Minimum Data Set Nurse 2 (MDS 2) stated the MDS was an assessment tool completed upon admission, quarterly, and upon a significant change of condition to identify the needs of the residents in the facility. MDSN 1 and MDSN 2 stated the facility monitored for changes in joint ROM by the MDS (section GG0115) and JMEs performed by the Rehab Department. MDSN 1 and MDSN 2 stated Section GG 0115A indicated if a resident had functional ROM limitations in both arms. MDSN 1 and MDSN 2 stated they typically had a licensed therapist from Rehab assist in assessing a resident's ROM, observed a resident actively move his or her arms and legs to perform activities of daily living (ADLs, basic activities such as eating, dressing, and toileting) and compared the results to the JME when coding Section GG 0115. MDSN 1 and MDSN 2 reviewed Resident 32's MDS assessments, dated 6/27/2024 and 9/27/2024, and confirmed Section GG 0115A of both MDS assessments were coded a zero which mean Resident 32 had no ROM limitations in both arms. MDSN 1 and MDSN 2 reviewed Resident 32's JMEs, dated 6/27/2024 and 9/27/2024, and confirmed the JMEs indicated Resident 32 had minimal ROM limitations in both shoulders and severe ROM limitations in both hands. MDSN 1 and MDSN 2 confirmed Section GG 0115A on MDS assessments, dated 6/27/2024 and 9/27/2024, were coded incorrectly and should have been coded two since Resident 32 had ROM limitations in both arms. MDSN 1 and MDSN 2 stated it was important the MDS was coded accurately to ensure the facility provided the appropriate care, services, exercises, and equipment the residents needed. During an interview on 6/12/2025 at 5:13 pm, the Director of Nursing (DON), the DON stated it was important the MDS was coded accurately to ensure the facility was able to assess if the care provided was appropriate for the resident's needs. The DON stated incorrect coding of the MDS could potentially result in an inaccurate assessment of the resident which could negatively impact the care and services he or she received. During a review of the facility's Policy and Procedures (P&P) titled, Resident Assessments, revised 10/2023, the P&P indicated The resident assessment coordinator was responsible for ensuring the interdisciplinary team conducted timely and appropriate resident assessments. The P&P indicated all persons who completed any portion of the MDS resident assessment form must sign the document attesting to the accuracy of such information.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to review and revise the comprehensive care plan for two of four sampl...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to review and revise the comprehensive care plan for two of four sampled residents (Resident 50 and 61) by failing to: 1.Revise and update Resident 50's care plan after a fall on 4/19/2025. 2.Revise and update Resident 61's care plan after Resident 61 pulled out her nasogastric tube (NG tube- a thin flexible tube inserted through the nose, down the throat, and into the stomach) and conduct an Interdisciplinary Team (IDT) conference. These failures resulted in Resident 50 falling on 5/22/2025 and Resident 61 pulling out her NG tube multiple times. Findings: 1. During a review of Resident 50's admission Record, the admission Record indicated Resident 50 was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including dementia (a progressive state of decline in mental abilities), osteoporosis (weak and brittle bones due to a lack of calcium and Vitamin D), fractures of left and right humerus (the long bone of the upper arm), repeated falls, and lack of coordination. During a review of Resident 50's Minimum Data Set (MDS-resident assessment tool) dated 5/22/2025, the MDS indicated Resident 50 had moderately impaired cognitive skills (ability to think, understand, learn, and remember) for daily decision making and was dependent (helper does all the effort) with toileting hygiene, showering and bathing. During a review of Resident 50's Change in Condition (COC- a sudden clinically important deviation from a patient's baseline in physical, cognitive, behavioral, or functional condition) dated 4/19/2025 and timed at 6:30 a.m., the COC indicated Resident 50 was found sitting on the bathroom floor after getting out of bed unassisted and suddenly feeling weak. During a review of Resident 50's Interdisciplinary Team (IDT team members from different departments working together with a common purpose to set goals and make decisions that ensure residents receive the best care) Note dated 4/28/2025 timed at 10:25 a.m., the IDT note indicated Resident 50 had an incident on 4/19/2025 around 6 a.m., when Resident 50 was observed sitting on the floor outside the bathroom. The IDT note indicated Resident 50 was assessed with no injury. The IDT note indicated Resident 50 was currently on a toileting schedule and has a talking device to remind and redirect Resident 50 to call for assistance. The IDT note indicated Resident 50 was observed by staff that she can manipulate the talking device. During a review of Resident 50's Care Plan titled, At risk for falls, difficulty maintaining sitting/standing balance, history of falls/multiple falls initiated on 12/25/2024, the Care Plan goal for Resident 50 was to have decrease in significant injury as a result from falls and to minimize the risk for falls in the next three months. The Care Plan interventions included call light within reach and respond in a timely manner, care items within reach, check for wetness, keep resident clean and dry at all times, frequent visual checks, bed in low position, schedule toileting every two hours and as needed, and supervise/assist resident with bedside care. During a review of Resident 50's Care Plan titled, At risk for falls, difficulty maintaining sitting/standing balance, history of falls/multiple falls initiated on 12/25/2024, the Care Plan did not indicate any revision on Resident 50's fall risk interventions and safety precautions after Resident 50 had a fall on 4/19/2025. During a review of Resident 50's COC dated 5/22/2025 and timed at 7:25 a.m., the COC indicated Resident 50 had an unwitnessed fall and was found lying on the floor. 2. During a review of Resident 61's admission Record, the admission Record indicated Resident 61 was admitted to the facility on [DATE] with diagnoses including dementia ( a progressive state of decline in mental abilities) and dysphagia (difficulty swallowing). During a review of Resident 61's MDS dated [DATE], the MDS indicated Resident 61's cognition was severely impaired and was dependent for toileting, showering, dressing, personal hygiene, and rolling to either side in bed. During a concurrent interview and record review on 6/12/2025 at 8:55 a.m., with Licensed Vocational Nurse (LVN) 9, LVN 9 stated Resident 61 has pulled out her NG tube several times. LVN 9 validated that the care plan was not updated after each time Resident 61 pulled out her NG tube on 8/12/2024 and 4/24/2025. LVN 9 stated the care plan should be revised after each time Resident 61 pulls out her NG tube being it increases her risk of aspiration (when the feeding formula or stomach contents go into the lungs instead of the digestive system). LVN 9 stated revising the care plan was important to do to possibly lessen the number of times Resident 61 pulls out her NG tube and increase monitoring for Resident 61. During a concurrent interview and record review on 6/12/2025 at 10:10 a.m., with Registered Nurse Supervisor (RNS) 2, RNS 2 validated Resident 61's care plan was not revised after she pulled her NG tube out on 8/12/2024 and 4/24/2025. RNS 2 stated the care plan should be updated after each time Resident 61 pulls out her NG tube so additional interventions could be added to prevent Resident 61 from pulling out her NG tube in the future. During a subsequent concurrent interview and record review on 6/12/2025 at 8:55 a.m., with LVN 9, LVN 9 stated Resident 50 was a high fall risk and that was the reason why Resident 50's room was closer to the nurse's station. LVN 9 stated after a fall, the care plan should be revised to prevent future falls from occurring. LVN 9 validated Resident 50's care plan dated 12/25/2025 was not revised following her fall on 4/19/2025 and it should have been done because additional interventions could have prevented the most recent fall on 5/22/2025 which resulted in fractures (broken bone). LVN 9 stated Resident 50's fall on 5/22/2025 was preventable if she had been monitored more closely and had a bedside commode (portable toilet) at her bedside being she gets up without assistance to use the bathroom. During a subsequent concurrent interview and record review on 6/12/2025 at 12:24 p.m., with RNS 2, RNS 2 stated Resident 50 was a high fall risk and recently had a fall on 5/22/2025. RNS 2 stated after Resident 50's fall on 4/19/2025 Resident 50's care plan should be revised to add new interventions to prevent future falls. RNS 2 validated Resident 50's care plan was not revised and should have been. RNS 2 stated its important to revise the care plan after a fall because the interventions in place were not effective, therefore new interventions will be added to prevent future falls. During an interview on 6/13/2025 at 9:24 a.m., with the Director of Nursing (DON), the DON stated a care plan is a guide and outlines the plan of care for the resident. The DON stated the care plan includes goals and interventions and should be revised when not effective. The DON stated Resident 50's care plan should have been revised after each fall so new interventions could be added to prevent future falls as well as for Resident 61 when she pulls out her NG tube. During a review of the facility's P&P titled, Care Plans, Comprehensive Person-Centered undated, the P&P indicated, Assessments of residents are ongoing, and care plans are revised as information about the residents and residents' conditions change.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure that facility staff did not administer Residen...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure that facility staff did not administer Resident 120's benzonatate (a medication used to treat cough) capsules via gastrostomy tube ([G-tube] a soft tube surgically placed directly into the stomach for administration of medication and nutrition), for one of six sampled residents. This deficient practice failed to provide medication in accordance with professional standards of practice and had the potential to result in adverse effects and untreated cough for Resident 120. Findings: During a review of Resident 120's admission Record dated 6/10/2025, the admission Record indicated Resident 120 was admitted to facility on 5/22/2025 with diagnoses including but not limited to dysphagia (difficulty swallowing), aphasia (a disorder that makes it difficult to speak) following cerebral infarction (loss of blood flow to a part of the brain), pneumonia (an infection/inflammation in the lungs) due to methicillin susceptible staphylococcus aureus (a type of bacteria) and pneumonitis (inflammation of the lung tissue) due to inhalation of food and vomit. During a review of Resident 120's History and Physical (H&P), dated 5/23/2025, the H&P indicated, Resident 120 did not have the capacity to understand and make decisions. During a review of Resident 120's Minimum Data Set (MDS - resident assessment tool), dated 5/26/2025, the MDS indicated Resident 120 was unable to complete assessment for cognition (ability to think, understand, learn, and remember). The MDS indicated Resident 120 needed maximal assistance from the facility staff for Activities of Daily Living (ADLs) such as oral hygiene, upper and lower body dressing, putting on/taking off footwear, dependent on staff for toileting, showering and personal hygiene. The MDS indicated there was no assessment for the level of assistance needed for eating due to medical condition or safety concerns. During an observation on 6/10/2025 at 1:48 p.m. in Resident 120's room, Licensed Vocational Nurse (LVN) 3 prepared ipratropium inhalation solution (a medication used to relieve difficulty in breathing) 0.02% for administration via nebulizer as needed for cough. Resident 120, who was non-verbal, indicated refusal of the medication by nodding her head when informed by LVN 3 about the medication and its purpose. During an interview on 6/10/2025 at 1:48 p.m. in Resident 120's room, a family member expressed concern that as needed cough medications were not administered unless Resident 120 specifically requested them. The family member could not recall the names of the medications but believed there was another as needed medication besides the ipratropium inhalation solution that helped with the cough. During a concurrent interview and record review on 6/10/2025 at 2:22 p.m. with LVN 3, the medication card for Resident 120's benzonatate 100 mg and the Medication Administration Record (MAR) for June 2025 were reviewed. The medication card indicated, Benzonatate 100 mg, take 1 capsule via G-tube every 12 hours as needed for cough. The MAR indicated, benzonatate 100 mg capsules were administered as needed on 6/1/2025, 6/2/2025 and 6/9/2025. LVN 3 stated Resident 120 wanted the ipratropium inhalation solution for cough, but then she refused to take the medication. LVN 3 stated Resident 120 was on G-tube feedings, and had a physician order for benzonatate capsule 100 mg via G-tube every 12 hours as needed for cough. During a review of Resident 120's Order Summary Report dated 6/11/2025, the order summary report indicated, but not limited to the following physician order: Tessalon [NAME] (generic name - benzonatate) oral capsule 100 milligrams ([mg] a unit of measurement for mass), give 1 capsule via G-tube every 12 hours as needed for cough, order date 5/30/2025, start date 5/30/2025 Geri-Tussin ([generic name - guaifenesin] a medication used to treat cough) oral liquid 100 mg/5 milliliters ([mL] a unit of measurement for volume), give 10 mL by mouth every 12 hours for cough for 1 week, order date 6/4/2025, start date 6/4/2025, end date 6/11/2025 Geri-Tussin oral liquid 100 mg/5 mL, give 10 mL by mouth every 6 hours as needed for cough for 2 weeks, order date 6/4/2025, start date 6/11/2025, end date 6/25/2025 Geri-Tussin oral liquid 100 mg/5 mL, give 10 mL via g-tube every 12 hours for cough until 6/11/2025 20:59 (10:59 p.m.) total 1 week (started on 6/4/2025), order date 6/10/2025, start date 6/10/2025, end date 6/11/2025 Geri-Tussin oral liquid 100 mg/5 mL, give 10 mL via g-tube every 6 hours as needed for cough for 2 weeks, order date 6/10/2025, start date 6/11/2025, end date 6/25/2025 Ipratropium bromide inhalation solution 0.02%, 1 vial inhale orally via nebulizer (a device that converts liquid medication into a mist that can be inhaled into the lungs to treat breathing difficulty) every 6 hours as needed for cough, order date 6/8/2025, start date 6/8/2025 During an interview on 6/10/2025 at 4:03 p.m. with LVN 3, LVN 3 stated the facility was instructed by the pharmacy (PH 1) to puncture benzonatate capsule, remove the medication fluid and pour it in the g-tube with water as instructed per physician order. LVN 3 stated she did not have a reference or literature to indicate this method of use for benzonatate capsule and stated she would ask PH 1 to provide that information. During a phone interview on 6/10/2025 at 5:15 p.m. with Registered Pharmacist (RPH 1), RPH 1 stated that they instructed facility staff to squeeze/aspirate the benzonatate capsule to extract the medication from the capsule and then pour and administer via g-tube directly, followed by a water flush as directed by physician order. RPH 1 mentioned that there were no specific references or literature available regarding the use of benzonatate capsules via g-tube but noted that both RPH 1 and other pharmacists had observed this method being used. RPH 1 stated that according to hospital records, pharmacists' experience, and doctor's orders, administering benzonatate capsules via g-tube was deemed acceptable because the benefits of treating cough outweighed the potential risk of mucosal membrane irritation. During a phone interview again on 6/11/2025 at 10:24 a.m. with RPH 1, RPH 1 stated for an example, in cases of drug- drug interactions we still give medications, similarly, although there were no studies regarding the use of benzonatate capsule via g-tube, but it has been used safely in that manner. RPH 1 stated although the mechanism of action indicated a localized effect, benzonatate capsule would still be absorbed via gastrointestinal tract and have peripheral (effects outside of brain and spinal cord), and central (effects within brain and spinal cord) effect. RPH 1 then stated he recommended to the Director of Nursing (DON) and the physician in the morning to try guaifenesin liquid via g-tube for Resident 120 first before trying benzonatate capsule via g-tube. During an interview on 6/12/2025 at 1:03 p.m. with the DON, the DON stated for a resident with g-tube, the staff should have selected a liquid formulation to be administered via g-tube. the DON stated benzonatate capsule could cause burning sensation in the mouth if given by removing the liquid from the capsule. The DON stated there was a risk for benzonatate capsule to not be properly aspirated for the dose needed. The DON stated it would not be possible to ensure its safety and efficacy for Resident 120. The DON stated facility staff should check medication card, drug handbook or call pharmacy to determine if the medication was on the do not crush list. During a review of the facility's Tessalon [NAME] and capsule's package insert, dated 12/2015, the document indicated, Swallow Tessalon capsules and [NAME] whole. Do not break, chew, dissolve, cut, or crush Tessalon capsules and [NAME]. Release of Tessalon from the capsule in the mouth can produce a temporary local anesthesia of the oral mucosa and choking could occur. During a review of the facility's Policy and Procedure (P&P) titled, Administering Medications, undated, the P&P indicated, Medications shall be administered in a safe and timely manner, and as prescribed. The individual administering medications must check the label three times to verify the right medication , right time and right method of administration before giving the medication. During a review of the facility's P&P titled, Administering Medications through an Enteral Tube, undated, the P&P indicated, 1. Request liquid forms of medications from the pharmacy, if possible. 2. Do not crush or split medications for administration through an enteral tube unless first checking with the pharmacy or facility approved 'Do not Crush Medication List.' 3. Do not crush the contents of an opened capsule. Do not administer oily medications through an enteral tube.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

Based on observation, interviews and record reviews, the facility failed to provide the necessary treatment and services to minimize the risk of development of pressure injuries (PIs, areas of damaged...

Read full inspector narrative →
Based on observation, interviews and record reviews, the facility failed to provide the necessary treatment and services to minimize the risk of development of pressure injuries (PIs, areas of damaged skin caused by staying in one position for too long) for one of three sampled residents (Resident 115) by failing to: a.Ensure the low air loss mattress (LALM - a pressure relieving mattress filled with air) remains inflated. This deficient practice had the potential for Resident 115 to develop new pressure injury and skin wounds to worsen. Findings: During a review of Resident 115's admission Record, the admission Record indicated the facility admitted Resident 115 on 4/21/2025 with diagnoses of muscle wasting and atrophy ( partial or complete wasting away of the body ), not elsewhere classified, multiple sites, pressure-induces deep tissue damage of sacral region ( pressure ulcer of lower back and spine), pressure-induces deep tissue damage of the left heel, pressure-induces deep tissue damage of the right heel and essential primary hypertension ( high blood pressure). During a review of Resident 115's Minimum Data Set (MDS, a care assessment and screening tool), dated 4/24/2025, the MDS indicated Resident 115 cognition was intact and required substantial/maximal assistance (helper does more than half the effort) for showering, supervision or touching assistance ( helper provides verbal cues and/ or touching /steadying and/or contact guard assistance as resident completes activity) with eating, oral hygiene and personal hygiene. During a review of Resident 115's Order Summary Report (OSR) dated 4/22/2025, the OSR indicated that Resident 115 was prescribed a LALM for wound management. During a review of Resident 115's care plan titled, At Decubitus Risk to Further Develop Pressure Ulcer indicated the nursing intervention for low air loss mattress. During an observation on 6/9/2025, at 10:45 a.m., Resident 115 was observed in bed with the LALM deflated. The resident stated that the bed was hard. During a concurrent observation and interview on 6/9/ 2025, at 3:05 p.m., with the Registered Nurse 4 (RN 4), RN 4 stated that the bed used by Resident 115 is designed to help prevent pressure ulcers. RN 4 explained that it is the Certified Nursing Assistant's (CNA) responsibility to inform the charge nurse if the air mattress is not inflated. It is also the nursing staff's duty, along with the treatment nurse, to ensure that the bed is properly set up and inflated. The Licensed Vocational Nurse (LVN) emphasized the importance of keeping the resident's bed inflated at all times to prevent further deterioration of the wounds. During an observation and interview on 6/9/2025 at 3:15 p.m., Treatment Nurse 1 (TN 1) mentioned he visited resident 115 an hour earlier but did not check the mattress patency. TN 1 noted that Resident 115 has pressure wounds, which could worsen without the mattress. He emphasized that the resident needs the LALM on. During an interview on 6/13/2025 at 10:20 a.m. with the Director of Nursing, it was stated that an LALM is a preventive measure to prevent skin breakdown. The responsibility to ensure it is functioning lies with the TN and the LVN. If it is not working, it can hinder its purpose and potentially worsen the wound. During a review of the facility's policies and procedures (P&P) titled Support Service Guidelines undated, the P&P indicated the purpose of this procedure is to provide guidelines for the assessment of appropriate pressure reducing and relieving devices for residents at risk for skin breakdown. 1.Any individual at risk for developing pressure ulcers should be placed on a redistribution support surface, such as a foam, gel, static air, alternating air or air- loss or gel when lying in bed.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0688 (Tag F0688)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to improve and/or prevent a decline in range of motion (...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to improve and/or prevent a decline in range of motion (ROM, full movement potential of a joint) for one of six sampled residents (Resident 39) by failing to provide Resident 39 with active assistive range of motion (AAROM, movement at a given joint with a person's own effort and assistance from an external force or another person) exercises to the left ankle per Restorative Nursing Aide (RNA, nursing aide program that helps residents maintain their function and joint mobility) physician's orders and in accordance with Physical Therapy (PT, profession aimed in the restoration, maintenance, and promotion of optimal physical function) recommendations. This deficient practice had the potential to cause Resident 39 to have a decline in ROM leading to contracture (loss of motion of a joint) development and have a decline in physical functioning and mobility (ability to move). Findings: During a review of Resident 39's admission Record, the admission Record indicated Resident 39 was originally admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including malignant neoplasm of the prostate (cancerous tumor of the prostate gland), contracture of an unspeficied joint (where two bones meet), and muscle wasting (thinning or loss of muscle tissue). During a review of Resident 39's PT Evaluation and Plan of Treatment (PT Eval), dated 1/14/2025, the PT Eval indicated Resident 39 had impaired strength in both hips, knees, and ankles. During a review of Resident 39's PT Discharge summary, dated [DATE], the PT Discharge Summary indicated discharge recommendations for a Restorative Nursing Aide (nursing aide program that help residents maintain any progress made after therapy intervention to maintain their function) program for PROM exercises and stretching to Resident 39's both legs. During a review of Resident 39's Minimum Data Set (MDS, resident assessment tool), dated 3/18/2025, the MDS indicated Resident 39 was cognitively (ability to think, understand, learn, and remember) intact. The MDS indicated Resident 39 required supervision or touching assistance for eating, substantial/maximal assistance for upper body dressing, and was dependent for oral hygiene, toileting hygiene, bathing, lower body dressing, personal hygiene, rolling, and transfers. The MDS indicated Resident 39 had functional ROM limitations (limited ability to move a joint that interferes with daily functioning, including activities of daily living, or places the resident at risk of injury) in one leg (hip, ankle, knee, foot). During a review of Resident 39's Order Summary Report, the Order Summary Report indicated a physician's order for RNA to provide AAROM exercises to Resident 39's left leg, three times a week. During an observation on 6/10/2025 at 9:27 am, in Resident 39's room, Resident 39 was lying in bed. Resident 39's right leg was straight with a slight bend in the knee and the toes pointing downwards. Resident 39's left leg was bent and outwardly rotated with the knee fully bent and the toes slightly pointing downwards. Resident 39 tried to straighten the left knee and left ankle but could not and stated he needed assistance to move the leg because it was so painful. During an observation of Resident 39's RNA session on 6/11/2025 at 8:56 am, in Resident 39's room, Resident 39 was lying in bed. Restorative Nursing Aide 1 (RNA 1) assisted Resident 39 with ROM exercises to both shoulders, elbows, wrists, and hands. RNA 1 assisted Resident 39 with ROM exercises to the left hip and left knee. RNA 1 did not assist Resident 39 with left ankle ROM exercises. After completing left hip and left knee ROM exercises, RNA 1 applied a splint to Resident 39's left knee and proceeded to assist Resident 39 with ROM exercises to the right hip, knee, and ankle. During an interview on 6/11/2025 at 9:07 am, RNA 1 stated she did not provide ROM exercises to Resident 39's left ankle but should have. RNA 1 confirmed there was an RNA order for RNA to provide AAROM to Resident's left leg which meant assisting with ROM exercises to the entire leg, including the left hip, knee, and ankle. RNA 1 stated Resident 39 required assistance with ROM exercises to both legs due to weakness, particularly the left leg. RNA 1 stated it was important to assist Resident 39 with left ankle ROM because the left ankle was stiff, and he was unable to move the ankle on his own. RNA 1 stated it was important to provide ROM exercises as ordered to prevent joint stiffness. During an interview on 6/12/2025 at 2:49 pm, the Director of Rehabilitation (DOR), the DOR stated the purpose of RNA services was to maintain and improve a resident's functional level and ROM. The DOR stated the Rehab department determined the types of exercises RNAs were to perform when creating an RNA program. The DOR stated if an RNA order was written for ROM exercises to the left leg, it was expected the RNA provide ROM to the entire leg, including the hip, knee, and ankles. The DOR stated if RNA did not provide RNA services as ordered, it could potentially result in Resident 39's decline in ROM, functional mobility, activities of daily living (ADLs, basic activities such as eating, dressing, toileting), and quality of life. During an interview on 6/12/2025 at 5:13 pm, the Director of Nursing (DON), the DON stated the purpose of the RNA program was to ensure the residents in the facility attained and maintained their highest level of function, ADLs, and mobility. The DON stated if residents did not receive RNA services as ordered, it could potentially result in a decline in ROM, mobility, and ADLs. During a review of the facility's Policy and Procedure (P&P), titled Resident Mobility and ROM, revised 7/2017, the P&P indicated residents would not experience an avoidable reduction in ROM and residents with limited ROM would receive treatment and services to increase and/or prevent a further decrease in ROM.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Incontinence Care (Tag F0690)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to ensure two sampled residents (Resident 78 and Resident 95) were prov...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to ensure two sampled residents (Resident 78 and Resident 95) were provided with a bowel and bladder retraining and/or toileting program ( aims to help individuals regain control over their bowel and bladder functions through a structured approach), to regain normal bowel and bladder function as much as possible and received appropriate treatment and services to restore continence. This failure had a potential risk for Resident 78 and Resident 95 to lose their ability to regain control of bowel and bladder function, which could result in loss of dignity. Findings: 1. During a record review of Resident 78's admission Record, the admission Record indicated Resident 78 was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including mild protein-calorie malnutrition (a mild deficiency in the intake of both protein and calories, resulting in adequate nutrition), nausea with vomiting, and muscle wasting. During a review of Resident 78's History and Physical (H&P), the H&P indicated, Resident 78 was able to express needs, communicate, follow commands and talk in full sentences. During a review of Resident 78's Minimum Data Set (MDS-a resident assessment tool), dated 4/15/2025, the MDS indicated Resident 78 was dependent on nursing staff with transferring. The MDS indicated Resident 78 needed substantial to maximal assistance with toileting, showering, dressing, sitting and standing. The MDS indicated Resident 78 needed setup or clean-up assistance from nursing staff with eating and oral hygiene. 2. During a record review of Resident 95's admission Record, the admission Record indicated Resident 95 was admitted to the facility on [DATE] with diagnoses including chronic cystitis (repeat occurrence of bladder inflammation, often caused by bacterial infections), urinary tract infection (a bacterial infection of the urinary system) and diverticulosis (a condition where small, bulging pouches (diverticula) develop in the lining of the digestive tract). During a review of Resident 95's Care Plan, titled, Resident is incontinent in bowel and bladder functions, dated 1/6/2025, the Care Plan indicated to provide incontinent care as needed. During a review of Resident 95 Order Summary, dated 1/25/2025, the Order Summary indicated Resident 95 had an order for cranberry extract 250 milligram (mg) give two tablets by mouth once a day to prevent urinary tract infections. During a review of Resident 95's MDS dated [DATE], the MDS indicated, Resident 95 had the ability to express ideas, wants and understand others. The MDS indicated Resident 95 was dependent on nursing staff with toileting, showering and dressing. The MDS indicated Resident 95 was not in a toileting program for urinary incontinence. The MDS indicated Resident 95 was always incontinent with urine and bowel. The MDS indicated Resident 95 was not currently in a toileting program to manage the resident's bowel incontinence. During a review of Resident 95's Weekly Summary Nurse Progress Note, dated 6/3/2025, the Weekly Summary Nurse Progress Note indicated Resident 95 was always incontinent of urine. The Weekly Summary Nurse Progress Note indicated Resident 95 was always incontinent with the bowel. The Weekly Summary Nurse Progress Note indicated Resident 95 was not in a bowel and bladder management program. During an interview on 6/9/2025 at 11:41 a.m., with Resident 95, Resident 95 stated she was not incontinent and was embarrassed when she was admitted to the facility and was told she had to wear diapers. During an interview on 6/10/2025 at 10:53 a.m., with Certified Nursing Assistant (CNA) 12, CNA 12 stated Resident 95 was incontinent to urine and bowel. CNA 12 stated Resident 95 wears diapers. CNA 12 stated Resident 95 requires minimal assistance and has never assisted Resident 95 to the bathroom. During a concurrent interview and record review on 6/10/2025 at 12:06 p.m., with Licensed Vocational Nurse (LVN) 2, Resident 95's Bowel and Bladder Evaluation, dated 3/25/2025 was reviewed. The Bowel and Bladder Evaluation indicated Resident 95 was incontinent with bowel and bladder. The Bowel and Bladder Evaluation indicated Resident 95 was able to call for assistance when she needed toileting and or changing. The Bowel and Bladder Evaluation indicated will continue to check and change Resident 95's diaper. LVN 2 stated Resident 95 was continent because she was aware of when she must use the bathroom. LVN 2 stated Resident 95 will have feeling of embarrassment if told she was incontinent and use a diaper. During a concurrent interview and record review 6/10/2025 at 11:51 a.m., with LVN 2, Resident 78's Bowel and Bladder Evaluation, dated 4/15/2025 was reviewed. The Bowel and Bladder Evaluation indicated Resident 78 had frequent incontinence of both bowel and bladder functions. The Bowel and Bladder Evaluation indicated Resident 78 was able to use a urinal and say if he needs to go to the bathroom or needs to be changed. LVN 2 stated Resident 78 was not incontinent and was able to use the urinal. During an interview on 06/12/2025 at 8:24 a.m., with Registered Nurse Supervisor (RNS), RNS 2 stated Resident 78 was admitted to the facility for management of left knee prosthesis ( an artificial body part, such as a leg) . RNS 2 stated Resident 78 needed assistance with toileting and uses a urinal. RNS 2 stated Resident 78 loses control of his bowel and bladder function because he was unable to get assistance to the bathroom. RNS 2 stated Resident 78 was able to feel the urge to urinate and defecate. RNS 2 stated Resident 78 should be on a bowel and bladder training program. RNS 2 stated she does not know why Resident was not on a bowel bladder program. RNS 2 stated Resident 78 could have a decline in bladder and bowel function, skin break down if left in adult diapers too long. RNS 2 stated Resident 78's dignity will be affected. During an interview on 6/12/2025 at 8:52 a.m., with Registered Nurse Supervisor, (RNS) 2, RNS 2 stated Resident 95 was not in a bowel or bladder program. RNS 2 stated facility needs a better bowel and bladder management program with accurate documentation. RNS 2 stated facility need to have proper assessments to provide care and management when a problem with bowel and bladder was identified. During an interview on 6/12/2025 at 2:35 p.m., with the Minimum Data Set Nurse (MDSN), the MDSN 1 stated on the MDS she coded Resident 78 as incontinent because he cannot hold his urine or stool long enough to be assisted to bathroom by the certified nursing assistants. MDSN 1 stated the certified nursing assistants told MDSN that Resident 78 cannot hold his urine. MDSN 1 stated Resident 78 was not in any bladder or bowel program. MDSN 1 stated Resident 78 dignity can be affected. During an interview on 6/12/2025 at 3:37 p.m., with the Director of Nursing (DON), the DON stated Resident 78 and Resident 95 will not be able to have the correct care provided and dignity will be affected if they were told to use diapers when they are able to feel the urge and call for assistance to go to the bathroom. During a review of the facility's policy and procedure (P&P), titled Urinary Continence and Incontinence-Assessment and Management, undated, the P&P indicated, .The physician and staff will provide appropriate services and treatment to help residents restore or improve bladder function and prevent urinary tract infections to the extent possible. During a review of the facility's P&P, titled Bowel Elimination, the P&P indicated, Purpose: Ensure resident bowel function will be restored as much as possible and provide toileting program.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation interview, and record review the facility failed to ensure one of one sampled resident (Resident 62) was pr...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation interview, and record review the facility failed to ensure one of one sampled resident (Resident 62) was provided with water at the bedside. This failure had the potential to put Resident 62 at risk for dehydration (occurs when your body loses more fluids than it takes in, leading to an insufficient amount of water for normal function.) Findings: During a review of Resident 62's admission Record, the admission Record indicated Resident 62 was originally admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including to constipation (digestive issue where bowel movements become less frequent, and stools become difficult to pass) diabetes mellitus (DM-a disorder characterized by difficulty in blood sugar control and poor wound healing), nausea with vomiting gastro-esophageal reflux (a condition in which acidic gastric fluid flows backward into the esophagus, resulting in heartburn.) During a review of Resident 62's Minimum Data Set (MDS - a resident assessment tool), dated 5/28/2025, the MDS indicated, Resident 62 had the ability to express ideas and wants. The MDS indicated Resident 65 needed set up or clean-up assistance from nursing staff with eating. The MDS indicated Resident 62 needed partial to moderate assistance with oral hygiene, personal hygiene and dressing. During a review of Resident 62's Care Plan, titled, Potential alteration in bowel elimination related to constipation, dated 2/19/2022, the Care Plan interventions indicated to offer and give resident adequate fluids. During a review of Resident 62's Nutritional Review/Progress Notes, dated 5/28/2025, the Nutritional Review/Progress Notes indicated, .Resident 62 remains at risk to weight changes and dehydration . During a concurrent observation and interview on 6/09/2025 at 12:01 p.m., with Resident 62 in Resident 62's room, observed Resident 62's dry mouth and lips and no pitcher of water at bedside. Resident 62 stated he did not have water since yesterday evening. During an interview on 6/09/2025 at 12:04 p.m., with Certified Nursing Assistant (CNA) 6, CNA 6, stated a hydration nurse and certified nursing assistants go to each resident rooms and refills each residents' pitcher with water starting at 7 a.m. CNA 6 stated resident with no fluid restrictions should always have water at the bedside. During an interview on 6/10/25 at 3:42 p.m., with Certified Nursing Assistant (CNA) 10, CNA 10 stated the hydration nurse passes water and snacks to the residents at 9 a.m., 2 p.m., 7 p.m., and as needed. CNA 10 stated the hydration nurses were responsible for refilling the residents' pitchers with water if they notice the resident was without water. CNA 10 stated Resident 62 will become dehydrated, thirsty, skin and lips will be dry if the resident was not given water. During an interview on 6/11/2025 at 9:16 a.m., with Licensed Vocational Nurse (LVN) 4, LVN 4 stated a designated person goes to every resident's room and changes their water and offers ice or to refill the residents' pitcher of water. LVN 4 stated this was done, once a day in the morning around 9 a.m. LVN 4 stated the facility has multiple hydration nurses and they are expected to provide residents with water at the bedside. LVN 4 stated residents need to be given water to prevent the resident from experiencing constipation, dry lips, dry skin, and poor skin elasticity. During an interview on 6/12/2025 at 9:59 a.m., with Registered Nurse Supervisor (RNS) 2, RNS 2 stated the hydration nurse do rounds and offer residents snacks, water and juice and refill the resident's pitcher of water. RNS 2 stated Resident 62 does not have any water restriction. RNS 2 stated Resident 62 resident should always have water at the bedside if not on a water restriction. RNS 2 stated Resident 62 will have dehydration, dry skin, and poor skin turgor and can become thirsty, weak, and sunken eyes if not provided with water at all times. During an interview on 6/12/2025 at 4:13 p.m., with the Director of Nursing (DON), the DON stated the nurses are to provide residents with drinking water for adequate hydration. The DON stated the residents can be dehydrated, have dry skin and dry mouth if adequate hydration id not maintained. During a review of the facility's policy and procedures (P&P), titled Resident Hydration and Prevention of Dehydration, undated, the P&P indicated, This facility will strive to provide adequate hydration and to prevent and treat dehydration. During a review of the facility's policy and procedures (P&P), titled Hydration Nurse, undated, the P&P indicated, The primary purpose of your job position is to provide each of your assigned residents with routine daily hydration care and services in accordance with the resident's assessment and care plan, and as may be directed by your supervisors.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to maintain a medication error rate of less than 5% (per...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to maintain a medication error rate of less than 5% (percent) during medication pass for two of six sampled residents (Residents 30 and 47) by failing to: 1. Ensure administration of metformin (a medication used to treat high blood glucose) within one hour of its scheduled time of administration as per facility's policy and procedure (P&P) titled, Administering Medications, undated, affecting one of six sampled residents during medication administration (Resident 30). 2. Ensure Resident 47's aspirin [a medication used to prevent heart attack (flow of blood and oxygen is blocked) and stroke (loss of blood flow to a part of the brain)] chewable tablet was administered as a chewable according to manufacturer formulation specifications instead of being swallowed without chewing, on 6/10/2025, affecting one of six sampled residents during medication administration (Resident 47). These deficient practices of medication administration error rate of 8% exceeded the five (5) percent threshold. Findings: 1. During a review of Resident 30's admission Record (a document containing demographic and diagnostic information), dated 6/11/2025, the admission record indicated, Resident 30 was admitted to facility on 1/21/2021 with diagnosis including, but not limited to, Type 2 Diabetes Mellitus (DM - a disorder characterized by difficulty in blood sugar control and poor wound healing) without complications. During a review of Resident 30's Minimum Data Set ([MDS], a resident assessment tool) dated 5/2/2025, the MDS indicated, Resident 30's cognition (mental action or process of acquiring knowledge and understanding through thought and the senses). The MDS indicated Resident 30 needed setup or clean-up assistance from the facility staff for performing activities of daily living (ADLs - routine tasks/activities such as bathing, dressing and toileting a person performs daily to care for themselves) such as eating and oral hygiene, supervision assistance for personal hygiene, moderate assistance for toileting hygiene, upper and lower body dressing, putting on/taking off footwear, and dependent on facility staff for showering. During an observation on 6/10/2025 at 10:02 a.m. with Licensed Vocational Nurse (LVN) 2, LVN 2 prepared the following nine medications to be administered to Resident 30. 1. One tablet of aspirin enteric coated 81 milligrams ([mg] a unit of measurement for mass) 2. One tablet of metformin 500 mg 3. One tablet of vitamin C (ascorbic acid - a vitamin used to treat low level of vitamin C) 4. One capsule of docusate sodium (a medication used to treat constipation) 250 mg 5. One tablet of famotidine (a medication used to treat acid reflux) 20 mg 6. One tablet of Januvia [(generic name - sitagliptin) a medication used to treat high blood glucose) 50 mg 7. One tablet of lisinopril (a medication used to treat high blood pressure) 5 mg 8. One tablet of metoprolol succinate (a medication used to treat high blood pressure) extended release (ER) 25 mg 9. One tablet of sodium chloride (a supplement used to balance sodium levels) 1 gram ([gm] a unit of measurement for mass) During a medication reconciliation review on 6/10/2025 at 12:21 p.m., Resident 30's Order Summary Report, dated 6/11/2025, was reviewed for metformin's order details. The order summary report included the following physician order scheduled to be administered daily at 8:00 a.m.: Metformin hydrochloride (HCl) tablet 500 mg, give 1 tablet by mouth two times a day for DM with meals, order date 12/6/2023, start date 12/6/2023. During a concurrent interview and record review on 6/11/2025 at 11:59 a.m. with Registered Nurse Supervisor (RNS) 2, the order details and medication administration details for Resident 30's metformin 500 mg in the electronic health record (EHR) were reviewed. RNS 2 noted that Resident 30's metformin 500 mg was administered more than one hour after its scheduled time, categorizing it as late administration. RNS 2 explained that LVN 2 was supposed to administer the medication on 6/10/2025 by 9:00 a.m., with the original scheduled time being 8:00 a.m., but it was administered at 10:00 a.m. RNS 2 mentioned there could be a risk for abnormal blood glucose levels for Resident 30 due to this delay. During a review of Resident 30's administration history for metformin 500 mg, dated 5/31/2025 to 6/10/2025, the document indicated metformin 500 mg was not administered within one hour of scheduled time of 8:00 am for five times. During an interview on June 12, 2025, at 1:03 p.m. with the Director of Nursing (DON), it was stated that facility staff are permitted to administer medication within one hour before or after the scheduled time. The DON emphasized the importance of adhering to the 'specific time code' as it reflects the physician's required schedule for administration. For instance, if the specific administration time is 8 a.m., the medication should be given by 9 a.m. Medications administered after 10 a.m. or at 10:22 a.m. would be considered late. The DON explained that late administration and not giving the medication with meals could lead to risks such as gastric irritation and hyperglycemia. 2. During a review of Resident 47's admission record, dated 6/10/2025, the admission record indicated, Resident 47 was originally admitted to the facility on [DATE] with diagnoses including, but not limited to, atherosclerosis of aorta (a build-up of fat and cholesterol in the largest artery in the body increasing the risk for blood clots, heart attack [blockage of blood flow to the heart] and stroke) and malignant neoplasm (cancer) of unspecified site of left female breast. During a review of Resident 47's MDS, dated [DATE], the MDS indicated, Resident 47's cognition was intact. The MDS indicated Resident 47 needed setup or clean-up assistance from the facility staff for eating, oral hygiene and personal hygiene, maximal assistance for upper body dressing and dependent for toileting hygiene, showering, lower body dressing and putting on/taking off footwear. During a medication pass observation on 6/10/2025 from 8:39 a.m. to 9:01 a.m. with LVN 1, LVN 1 prepared and administered the following five medications to Resident 47, one of which included one tablet of aspirin 81 mg chewable tablet. LVN 1 did not instruct Resident 47 to chew aspirin before swallowing and the resident was observed swallowing all medications including aspirin chewable tablet. 1. One tablet of aspirin 81 mg chewable tablet 2. One tablet of docusate sodium 100 mg 3. One tablet of letrozole (a hazardous medication used to treat cancer) 2.5 mg 4. One tablet of losartan-hydrochlorothiazide (a combination of two medications used to treat high blood pressure) 100-25 mg 5. One capsule of fish oil (a supplement used to lower cholesterol) 1000 mg During a review of Resident 47's Order Summary Report, dated 05/30/2025, the document indicated following physician orders: Aspirin Tablet Chewable 81 mg, give 1 tablet by mouth one time a day for anti-platelet agent to prevent stroke and heart attack with breakfast, order date: 5/30/2024, start date: 5/31/2024. During a review of Resident 47's order summary report, dated 6/11/2025, the document indicated the aspirin order was changed as following: Aspirin enteric coated (EC) adult low dose oral tablet delayed release 81 mg, give 1 tablet by mouth in the morning for anti-platelet agent to prevent stroke and heart attack with breakfast, order date 6/10/2025, start date 6/11/2025. During an interview on 6/10/25, at 9:01 a.m., LVN 1 stated that they did not instruct Resident 47 to chew aspirin, and the resident swallowed it along with her other medications. LVN 1 noted that chewing an aspirin chewable tablet could result in a faster onset of action to prevent stroke if chewed before swallowing. During an interview on 6/11/2025 at 12:17 p.m. with Registered Nurse 2 (RNS 2), RNS 2 stated that Resident 47 should have been instructed to take the chewable aspirin tablet by chewing and swallowing it, in accordance with the manufacturer's guidelines. RNS 2 explained that if the aspirin is not taken as specified by the manufacturer, there could be a risk of poor absorption, rendering it less effective in preventing blood clots or stroke. During an interview on 6/12/2025 at 12:55 p.m. with the DON, DON stated the resident should have chewed the chewable aspirin tablet before swallowing. DON stated the medication effect might be slower than intended which would delay the effect of blood clotting and prevent stroke. DON stated facility staff should have verified the order with physician if the chewable aspirin order did not indicate chew and swallow the tablet. During a review of manufacturer labeling of the facility administered aspirin chewable tablet, the document indicated, Chew or crush tablets completely before swallowing, do not swallow tablets whole. During a review of the facility's P&P, titled Administering Medications, undated, the P&P indicated, Medications may not be prepared in advance and must be administered within one (1) hour of their prescribed time, unless otherwise specified (for example, before and after meal orders). The P&P indicated, Medications shall be administered in a safe and timely manner, and as prescribed. The individual administering medications must check the label three times to verify the right medication , right time and right method of administration before giving the medication.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure residents were free from significant medication errors for one (Resident 30) of six sampled residents during medicatio...

Read full inspector narrative →
Based on observation, interview, and record review, the facility failed to ensure residents were free from significant medication errors for one (Resident 30) of six sampled residents during medication administration, by failing to administer Resident 30's metformin (a medication used to treat high blood glucose) within one hour of its scheduled time of administration as per facility's policy and procedure (P&P) titled, Administering Medications, undated. This deficient practice failed to provide medication in accordance with the physician's orders or professional standards of practice and had the potential to result in hyperglycemia (high blood glucose) for Resident 30. Findings: During a review of Resident 30's admission Record (a document containing demographic and diagnostic information), dated 6/11/2025, the admission record indicated, Resident 30 was admitted to facility on 1/21/2021 with diagnosis including, but not limited to, Type 2 Diabetes Mellitus (DM - a disorder characterized by difficulty in blood sugar control and poor wound healing) without complications. During a review of Resident 30's Minimum Data Set ([MDS], a resident assessment tool) dated 5/2/2025, the MDS indicated, Resident 30's cognition (mental action or process of acquiring knowledge and understanding through thought and the senses). The MDS indicated Resident 30 needed setup or clean-up assistance from the facility staff for performing activities of daily living (ADLs - routine tasks/activities such as bathing, dressing and toileting a person performs daily to care for themselves) such as eating and oral hygiene, supervision assistance for personal hygiene, moderate assistance for toileting hygiene, upper and lower body dressing, putting on/taking off footwear, and dependent on facility staff for showering. During an observation on 6/10/2025 at 10:02 a.m. with Licensed Vocational Nurse (LVN) 2, LVN 2 prepared nine medications to be administered to Resident 30. During a medication reconciliation review on 6/10/2025 at 12:21 p.m., Resident 30's Order Summary Report (a document containing a summary of all active physician orders), dated 6/11/2025, metformin's order details were reviewed. The order summary report indicated, but not limited to the following physician order scheduled to be administered daily at 8:00 a.m.: Metformin hydrochloride (HCl) tablet 500 milligrams ([mg] - a unit of measurement for mass), give 1 tablet by mouth two times a day for DM with meals, order date 12/6/2023, start date 12/6/2023. During a concurrent interview and record review on 6/11/2025 at 11:59 a.m. with Registered Nurse Supervisor (RNS) 2, Resident 30's order details and medication administration details in electronic health record (EHR) for metformin 500 mg were reviewed. RNS 1 stated Resident 30's metformin 500 mg was administered more than one hour after its scheduled administration time, so it would be considered a late administration. RNS 1 stated LVN 2 should have administered the medication on 6/10/2025 by 9:00 a.m. because it was scheduled to be administered on 6/10/2025 at 8:00 a.m., but it was administered by LVN 2 at 10:00 a.m. RNS 1 stated there would be a risk for abnormal blood glucose levels for Resident 30. During a review of Resident 30's administration history for metformin 500 mg, dated 5/31/2025 to 6/10/2025, the document indicated metformin 500 mg was not administered within one hour of scheduled time of 8:00 am for five times, listed as below. 6/10/2025: administered at 10:22 a.m. during medication pass observation 6/9/2025: documented as administered at 9:42 a.m. 6/5/2025: documented as administered at 4:12 p.m. 6/3/2025: documented as administered at 11:14 p.m. 6/2/2025: documented as administered at 12:05 p.m. During an interview on 6/12/2025 at 1:03 p.m. with the Director of Nursing (DON), DON stated the facility staff was allowed to give a medication one hour before or one hour after the scheduled time of administration. DON stated it was important to follow the 'specific time code' because that would be the physician's required scheduled time of administration. DON stated if the specific time for administration was 8 a.m. then facility staff should have given the medication by 9 a.m. DON stated if the medication was given after 10 a.m. or at 10:22 a.m., it would be considered late administration. DON stated the medication if given late and not given with meals, there was a risk for gastric irritation and hyperglycemia. During a review of the facility's P&P, titled Administering Medications, undated, the P&P indicated, Medications may not be prepared in advance and must be administered within one (1) hour of their prescribed time, unless otherwise specified (for example, before and after meal orders). The P&P indicated, Medications shall be administered in a safe and timely manner, and as prescribed. The individual administering medications must check the label three times to verify the right medication , right time and right method of administration before giving the medication.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Medical Records (Tag F0842)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** During a review of Resident 19's admission Record, the admission Record indicated Resident 19 was initially admitted to the faci...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** During a review of Resident 19's admission Record, the admission Record indicated Resident 19 was initially admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including congestive heart failure (CHF-a heart disorder which causes the heart to not pump the blood efficiently, sometimes resulting in leg swelling), diabetes mellitus (DM- a disorder characterized by difficulty in blood sugar control and poor wound healing), cardiomyopathy ( a long term condition that affects the heart muscle making it harder to pump blood), Covid -19 (highly contagious respiratory disease caused by Coronavirus which is transmitted thru coughing, talking , sneezing and touching contaminated surfaces ), and end stage renal disease (ESRD- irreversible kidney failure) with dependence on renal hemodialysis (procedure to remove waste products and excess fluids from the blood when kidneys stop working properly). The admission Record indicated the resident was discharged to a funeral home on 6/9/2025 at 10:25 a.m. During a review of Resident 19's Minimum Data Set (MDS-resident assessment tool) dated 5/15/2025, the MDS indicated Resident 19 had moderately impaired cognitive skills (ability to think, understand, learn, and remember) and was dependent on staff (helper does all the effort to complete the activity) with bathing, dressing, toilet transfer (ability to get on and off a toilet or a commode) and toileting hygiene. During a review of Resident 19's Emergency Medical Services (EMS-a system that respond to emergencies in need of highly skilled prehospital clinicians) Incident Information dated 6/9/2025, at 4:35 a.m., the EMS Incident Form indicated EMS team was notified on 6/9/2025 at 4:35 a.m. of Resident 19's cardiac arrest ( heart malfunctions and stops beating on its own caused by an electrical problem in the heart). The EMS Incident Information indicated a team was dispatched to the facility and arrived at 4:40 a.m. The EMS Incident Information indicated facility staff stated to the EMS team that Resident 19 was last seen on 6/9/2025, at 4:15 a.m. sleeping and breathing. The EMS Incident Form indicated Resident 19 was in asystole ( when heart's electrical system fails entirely causing the heart to stop pumping and is also known as flat line) upon assessment and throughout the entirety of the resuscitative effort provided to the resident. The EMS Incident Information indicated the time of death of Resident 19 was 5:03 a.m. on 6/9/2025. During a record review of Resident 19's Medication Administration Record (MAR) dated 6/9/2025 indicated resident 19 received the following medications. 1.Aspirin ( blood thinning medicine)81 milligrams (mgs.- unit of measurement) signed and administered at 9:00 a.m. 2.Docusate Sodium ( medicine used as a stool softener)oral capsule 100 mgs. 1 capsule by mouth signed and administered at 9:00 a.m. 3.Nephro ( a specialized nutritional shake designed specifically for people on dialysis)4 ounces (oz- unit of measurement) signed and administered at 9:00 a.m. 4.Calcium Acetate ( medicine to lower high phosphorus level in the blood in people with kidney disease)oral 667 mgs. 2 tablets signed by mouth and administered at 9:00 a.m. 5.Diet percentage (the amount of food the resident had eaten) was 100 percent for breakfast signed by Licensed Vocational Nurse (LVN 6). 6.Prostat ( concentrated liquid protein)sugar free liquid 30 milliliters (ml- unit of measurement) signed and administered at 9:00 a.m. 7.Capsaicin ( medication used to relieve minor muscle or joint pain) external cream 0.025 percent (% - unit of strength or concentration) apply to neck topically (apply to the skin) signed and administered at 9:00 a.m. 8.Insulin NPH (an intermediate -acting insulin providing a longer duration of action)28 units ( u- unit of measurement) subcutaneously ( injection given in the layer of fat just below the skin) in the morning for diabetes with food and blood sugar taken was 220 mgs/dl ( milligrams per deciliter - unit of measurement) signed and administered at 7:30 a.m. During a concurrent interview and record review on 6/12/2025, at 7:19 a.m. with LVN 9, Resident 19's MAR dated 6/9/2025 were reviewed. LVN 9 confirmed Resident 19's medications were documented on 6/9/2025 at 7:30 a.m., 9:00 a.m. and blood sugar was taken on 6/9/2025 at 7:30 a.m. LVN 9 stated documenting inaccurately could have a potential for medication error. During an interview and record review on 6/12/2025, at 9:08 a.m. with LVN 6, reviewed Resident 19's MAR dated 6/9/2025. LVN 6 stated she signed the medications for 9:00 a.m. and blood sugar reading on 6/9/2025 at 7:30 a.m. on 6/9/2025. LVN 6 stated when a licensed nurse was administering medicines and obtaining blood sugar, the licensed nurse should check the resident's armband (wristband that will ensure positive patient identification and time saving communication of sensitive data in a healthcare environment) for the name, date of birth and picture of the resident in the electronic health record to ensure it was the correct resident. LVN 6 stated she did not administer the medication to Resident 19 and admitted she made a mistake in documenting. LVN 6 stated she should not have signed the MAR of Resident 19 because if the medications were signed in the MAR, it indicated that she had administered them to the resident which could lead to medication error. LVN 6 stated she was overwhelmed on 6/9/2025 and was aware Resident 19 expired in the early morning. During an interview on 6/12/2025 ,at 8:29 a.m. with Registered Nurse Supervisor (RNS 4), RNS 4 stated LVN 6 should have practiced and performed right patient, right dose, right time and right frequency before administering medications to all the residents to prevent committing medication error. During an interview on 6/12/2025, at 4:46 p.m. with the Director of Nursing (DON), the DON stated LVN 6 not documenting accurately in Resident 19's MAR had the potential for committing medication error during medication administration. During a review of facility's policy and procedure (P&P) titled, Administering Medications, undated, the P&P indicated the licensed nurse administering the medication must check the label 3 times to verify the right medication, right dosage, right time and right method of administration before giving medications. Based on observation, interview, and record review, the facility failed to ensure two of six sampled residents (Resident 115 and 19) had accurate documentation on the physician's orders and Medication Administration Record (MAR) by failing to: 1.Ensure Resident 115's physician orders indicated the specific type of splint (rigid material or apparatus used to support and immobilize a broken bone or impaired joint) Resident 115 had to wear on the right leg at all times. 2.Ensure Resident 115's physician's order for a CAM boot splint (othopedic device used to immobilize or protect the foot and ankle after an injury or surgery) to the right leg was discontinued when the splint was discontinued by the physician. These deficient practices resulted in staff confusion and had the potential to negatively impact the provision of necessary care and services, cause miscommunication among staff, and cause a decline in range of motion (ROM, full movement potential of a joint), mobility, and overall function. 3. Ensure Licensed Vocational Nurse (LVN 6) did not document on Resident 19's Medication Administration Record that medications were given on 6/9/2025 at 9 a.m. Resident 19 had expired on 6/9/2025 at 5:03 a.m. This deficient practice had the potential to put other residents at risk for medication error. Findings: During a review of Resident 115's admission Record, the admission Record indicated Resident 115 was admitted to the facility on [DATE] with diagnoses including a fracture (broken bone) of the lateral malleolus (bony prominence on the outer side of the ankle) of the right fibula (one of the two bones of the lower part of the leg) and ataxic gait (uncoordinated walking pattern). During a review of Resident 115's Minimum Data Set (MDS, a resident assessment tool), dated 4/24/2025, the MDS indicated Resident 115 was cognitively (ability to think, understand, learn, and remember) intact. The MDS indicated Resident 115 required supervision/touching assistance for eating and oral hygiene, partial/moderate assistance for upper body dressing, substantial/maximal assistance for bathing, and was dependent in toilet hygiene, lower body dressing, rolling, and transfers. The MDS indicated Resident 115 had functional ROM limitations (limited ability to move a joint that interferes with daily functioning, including activities of daily living, or places the resident at risk of injury) in one leg. During a review of Resident 115's Order Summary Report, the Order Summary Report indicated a physician's order, dated 4/21/2025, for keep leg immobilizer (device used to reduce or eliminate movement of a body part) at right leg in place at all times. During a review of Resident 115's Physical Therapy (PT, profession aimed in the restoration, maintenance, and promotion of optimal physical function) Evaluation, dated 5/14/2025, the PT Evaluation indicated Resident 115 was able to put as much weight as tolerated through the right leg while wearing a CAM boot which was to be worn at all times. During a review of Resident 115's Nursing Progress Note, dated 5/27/2025, the Nursing Progress Note indicated Resident 115 returned from an orthopedic ( refers to the medical specialty focused on the musculoskeletal system) appointment with a new physician's order to discontinue the (right leg) boot. During a concurrent observation and interview on 6/10/2025 at 10:23 pm, in Resident 115's room, Resident 115 was sitting in wheelchair with no splints on the right leg. Resident 115 stated she used to have a boot on the right leg because she broke her ankle. Resident 115 stated she no longer wore the boot because it was heavy and hard to move around when wearing it. During an observation of Resident 115's Restorative Nursing Aide (nursing aide program that help residents maintain any progress made after therapy intervention to maintain their function) session on 6/11/2025 at 11:01 am, in Resident 115's room, Resident 115 was sitting in a wheelchair with a platform walker (type of walking assistive device with forearm supports to provide extra support during walking) positioned in front of her body and no splint on the right leg. Resident 115's family member was at the bedside. Restorative Nursing Aide 1 (RNA 1) and Restorative Nursing Aide 2 (RNA 2) assisted Resident 115 into a standing position three times using the platform walker. Resident 115 stated she had pain in both legs when standing and refused to participate in further sit to stand transfers. During an interview on 6/11/2025 at 11:21 pm, RNA 2 stated Resident 115 used to have a boot on the right foot at all times but did not know if, why, or when it was discontinued. RNA 2 stated she did not know if Resident 115 had any other splints or immobilizers for the right leg other than the boot. RNA 2 stated she assumed Resident 115's boot was discontinued since she stopped wearing it. During a concurrent interview and record review on 6/11/2025 at 11:43 am, Licensed Vocational Nurse 8 (LVN 8) stated the charge nurse was responsible for updating the physician's order when a resident returned from a consultation appointment. LVN 8 reviewed Resident 115's physician's order, dated 4/21/2025, and confirmed Resident 115 had a physician's order for Resident 115 to wear an immobilizer on the right leg at all times. LVN 8 reviewed Resident 115's Nursing Progress Notes, dated 5/27/2025, and confirmed Resident 115 returned from an orthopedic appointment with a new physician's order to discontinue the boot. LVN 8 stated he was unsure if the boot mentioned in the Nursing Progress Note was different from the immobilizer on the physician's order. LVN 8 stated he did not know what type of splint and/or which joint (where two bones meet) of the leg Resident 115 was supposed to wear the boot and/or immobilizer on since the physician's order did not specify the type of immobilizer or splint to be worn. LVN 8 stated he was confused and had to investigate if Resident 115 had any other immobilizers other than the boot on the right foot. During a follow up interview on 6/11/2025 at 3:33 pm, LVN 8 stated he spoke with the Director of Rehabilitation (DOR) who confirmed Resident 115 previously wore a CAM boot, which was a type of splint, at all times but no longer needed it since it was discontinued by the physician after her follow up orthopedic appointment. LVN 8 stated the nurse who received the physician's order to discontinue the boot should have discontinued the physician's order but did not. LVN 8 stated the physician's order should have specified the type of splint Resident 115 should have been wearing at all times to avoid confusion and ensure staff were implementing the appropriate precautions. LVN 8 stated it was important documentation, including physician's orders were clear and accurate to prevent confusion and to ensure staff provided the appropriate care for the residents. During an interview on 6/12/2025 at 5:13 pm, the Director of Nursing (DON) stated it was important documentation, including physician's orders related to splints were current, specific, and accurate to ensure staff provided the appropriate care for residents in the facility. The DON stated splint orders must include the specific type of splint a resident has to wear to avoid confusion and inaccurate provision of services. The DON stated if a splint was discontinued by the physician, the splint order must also be discontinued in the electronic health record. The DON stated if staff immobilized a resident by splinting a body part when the resident did not require immobilization, it could have a negative impact of the resident's care, limit his or her ability to move, and limit his or her abilities to participate and improve in functional activities such as mobility and activities of daily living (basic activities such as eating, dressing, toileting). During a review of the facility's undated job description titled Charge Nurse, the job description indicated one of the specific responsibilities of the charge nurse included accurately interpreting and implementing physician orders. During a review of the facility's undated policy and procedure (P&P) titled Orthotic Devices, the P&P indicated an orthotic or splint was used to promote healing, prevent complications and to maintain function and comfort. The P&P indicated the details about the specific orthotic device, date ordered, and any modification made should be documented. During a review of the facility's undated P&P titled Charting and Documentation, the P&P indicated all services provided to the resident, or any changes in the resident's medical or mental condition, shall be documented in the resident's medical record.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure Certified Nursing Assistant (CNA 5) wear prope...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure Certified Nursing Assistant (CNA 5) wear proper personal protective equipment (PPE-clothing and equipment that is worn or used to provide protection against hazardous substances and/or environments) and practice hand hygiene for one of two sampled resident ( Resident 119) who had Covid 19 ( highly contagious respiratory disease) before entering the room. This failure had the potential to transmit and spread infection among residents ,visitors and staff. Findings: During a review of Resident 119's admission Record, the admission Record indicated Resident 119 was initially admitted to the facility on [DATE] and was readmitted on [DATE] with diagnoses including hemiplegia (paralysis of one side of the body) and hemiparesis (weakness of one side of the body) affecting the left non-dominant side following a stroke[occurs when a blood vessel that carries oxygen and nutrients to the brain is blocked by a clot or bursts]), Covid 19 ,bradycardia ( heart rate is very slow and heart cannot pump enough to the body) and presence of cardiac pacemaker (a small, electronic device that helps regulate a slow or irregular heartbeat). During a review of Resident 119's Minimum Data Set (MDS-a resident assessment tool) dated 5/27/2025, the MDS indicated Resident 119 had severely impaired cognitive (ability to think, understand, learn, and remember) skills. The MDS indicated Resident 119 was dependent(helper does all the effort) on staff with eating, bathing, dressing, oral hygiene, toileting hygiene and bed mobility. During an observation in Resident 119's room, CNA 5 who was wearing a N95 mask (a respiratory protective device designed to achieve a very close facial fit and very efficient filtration of airborne particles) entered Resident 119's room without hand hygiene and not wearing a protective gown and face shield. Observed CNA5 provided and covered Resident 119 who was lying in bed and carried a transparent plastic bag outside the room. During an interview on 6/9/2025, at10:56 a.m. and subsequent interview on 6/10/2025, at 11:51 a.m. with CNA 5, CNA 5 stated she wore only N 95 mask and did not practice hand hygiene when she entered Resident 119's room. CNA 5 stated she should have practiced hand hygiene, worn gloves, gown, N95 mask and face shield before entering Resident 119's room because it could spread the disease to other residents, staff and visitors. During an interview on 6/9/2025, at 10:38 a.m. with Infection Preventionist Nurse (IPN), IPN stated all staff should practice hand hygiene and wear a gown, N95 mask, gloves and face shield before entering a resident who had Covid 19 to prevent spread of infection. IPN stated that CNA 5 should have worn the proper PPE used for residents who had Covid 19 and practiced hand hygiene before entering Resident 119's room. During an interview on 6/12/2025, at 2:13 p.m. with RN Supervisor (RNS 2 ) , RNS 2 stated, the staff should practice hand hygiene, wear PPE consisting of gown, gloves, mask and face shield every time the staff enter the room of residents who had Covid 19 to prevent spread of Covid 19 to residents and staff. RNS 2 stated residents who had Covid 19 were on droplet (a set of infection control measures used to prevent the spread of diseases that are transmitted through respiratory droplets produced by an infected person when they cough, sneeze, talk or sing) and contact precautions( infection control measures used in healthcare settings to prevent the spread of infection transmitted by direct or indirect contact with a patient or their environment). During a review of facility's policy and procedure (P&P) titled, Isolation-Categories of Transmission-Based Precautions, revised 9/2023, the P&P indicated Contact Precautions are implemented for residents known or suspected to be infected with microorganisms that can be transmitted by direct contact with the resident or indirect contact with the environmental surfaces or resident-care items in the resident's environment. The P & P indicated staff and visitors should wear gloves and a disposable gown before entering the resident's room. The P&P indicated droplet precautions are implemented for an individual documented or suspected to have an infection transmitted by droplets and masks, gloves, gown and face shields are worn when entering the room.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0558 (Tag F0558)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the nursing staff failed to: 1.Ensure that the call light device was within ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the nursing staff failed to: 1.Ensure that the call light device was within easy reach for Resident 42 and Resident 45. 2.Provide a communication board (a visual aid often featuring pictures, symbols, or words to help individuals with aphasia express themselves and understand others when verbal communication is difficult) for Resident 120, who is aphasic. These deficient practices had the potential to result in a delay of care and the residents needs not being met. Findings: a.During a review of Resident 42's admission Record, the admission Record indicated Resident 42 was initially admitted to the facility on [DATE] and last admitted on [DATE] with a diagnosis including ataxic gait ( an abnormal walking pattern ), repeated falls, and depression , unspecified ( a condition of persistent sadness and loss of intertest in activities). During a review of Resident 42's History and Physical (H&P), dated 3/25/2025, the H&P indicated, Resident 42 does not have the capacity (ability) to understand and make decisions. During a review of Resident 42's Minimum Data Set (MDS, a resident assessment tool) dated 3/28/2025, it was noted that Resident 42 requires substantial to maximum assistance (helper lifts or holds trunk or limbs and provides more than half the effort) with lying to sitting on the side of the bed, sitting to standing, and toilet transfers. Due to medical conditions, Resident 42 has not attempted walking 10 feet. During a record review of Resident 42's care plan dated 3/25/2025, it was noted that Resident 42 is at risk for falls due to difficulty maintaining sitting/standing balance and a history of multiple falls. The care plan includes an intervention to ensure the call light is within reach and that staff respond in a timely manner. During an observation on 6/9/2025 at 10:45 a.m., Resident 42 was in bed with the call light found on the right side of the bed, hanging on the floor. During an observation and interview at 11:00 a.m. with Certified Nursing Assistant 7 (CNA 7), CNA 7 stated that Resident 42 is blind and knows how to locate their call light. The CNA emphasized that the call light should always be within the resident's reach to ensure their safety and meet any potential needs. During an interview on 6/9/2025 at 12:20 p.m., with the Registered Nurse 4 (RN 4) , RN 4 stated we make rounds every two hours and while rounding we make sure the call light is in reach. RN 4 stated it is important to make sure call light is in reach to avoid accidents. RN 4 stated especially for a resident who has a visual impairment it should be within reach. b. During a review of Resident 45's admission Record, the admission Record indicated, Resident 45 was initially admitted to the facility on [DATE] and last readmitted on [DATE] with diagnoses including chronic kidney disease stage 2 ( mild kidney damage) of pulmonary hypertension ( blood pressure in the lungs is abnormally high) , hyperlipidemia ( elevated levels of fat in the blood) and a need for assistance with personal care. During a review of Resident 45's MDS dated [DATE], the MDS indicated Resident 45 cognition (mental action or process of acquiring knowledge and understanding through thought, experience, and the senses) was moderately impaired. Resident 45 requires set -up or clean- up assistance (helper sets up or clean up; resident completes activity) with eating, oral hygiene and dependent ( resident does none of the effort to complete the activity or the assistance of 2 or more helpers is required for the resident to complete the activity) with upper and lower body dressing and toilet hygiene. During a review of Resident 45's care plan dated 4/14/2025 the care plan indicated Resident 45 requires assistance with ADL's ( activities of daily living- basic tasks an individual perform to maintain their personal hygiene, care and independence) self -care and mobility secondary to recent decline in functional ability. The care plan intervention indicated to encourage resident to use call light for assistance. During an observation on 6/9/2025 at 10:23 a.m., Resident 45 requested assistance with retrieving the call light. The call light was located on the left side of the bed, hanging. Licensed Vocational Nurse 12 (LVN 12) arrived, picked up the call light from the side of the bed, and handed it to the resident. LVN 12 mentioned that it is important to ensure the call light is within the resident's reach to prevent falls. c. During a review of Resident 120's admission Record, the admission Record indicated, Resident 120 was initially admitted to the facility on [DATE] with diagnoses including hemiplegia (paralysis of one side of the body) and hemiparesis ( weakness affecting one side of the body) following cerebral infarction ( when blood flow to part of the brain is blocked leading to tissue damage and death) and aphasia ( difficulty speaking). During a review of Resident 120's H&P dated 5/23/2025, the H&P indicated, Resident 120 does not have the capacity to understand and make decisions. During a review of Resident 120's MDS dated [DATE], the MDS indicated Resident 120 requires substantial/maximum assistance with upper and lower body dressing ,oral hygiene. Resident 120 is dependent ( resident does none of the effort to complete an activity) with upper and lower body dressing . During a review of Resident 120's care plan there was no care plan addressing Resident 120's aphasia. During an observation and interview on 6/10/2025 at 3:46 p.m., Resident 120's family member stated that Resident 120 did not have a communication board and has never been provided with one to assist in communicating with the staff. During an interview on at 6/10/2025 at 11:00 a.m., with Certified Nurse Assistant 3 (CNA 3), CNA 3 states Resident 120 does not have a communication board, and she does not know what one looks like. During an interview on 6/10/2025 at 2:23 p.m., with the Licensed Vocational Nurse 8 (LVN 8) , LVN 8 stated he was the one who placed a communication board in resident 120's room on 6/10/2025 because there was none. LVN 1 stated it is important there is a communication board available for Resident 120 so we can help her with her basic needs. During an interview on 6/13/2025 at 10:10 a.m., with Director of Nursing (DON), DON stated call lights should be in reach for easy access so residents can get the help that is needed. DON stated when working with a resident who has trouble communicating, they should have a communication board , DON stated the resident's self-esteem can be lowered, and they can be at risk for injury. During a review of the facility's P&P titled Answering the Call light undated, the P&P indicated the purpose of this procedure is to respond to the resident's requests and needs : 1.When a resident is in bed or confined to a chair be sure the call light is within easy reach of the residents. During a review of the facility's P&P titled Heritage Rehabilitation Center undated, the P&P indicated caring for someone with aphasia requires patience, understanding, and communication strategies that go beyond spoken words. Focusing on a quiet, well- lit environment, utilizing nonverbal cues , and providing clear , simple communication can significantly improve the experience for both the individual with aphasia and their caregivers. Use Alternative Communication Systems: Consider using visual aids like pictures , diagrams, or writing , and explore technology like smart phones or tablets with communication apps.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0697 (Tag F0697)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to ensure the resident, who had unrelieved pain on his shoulder, neck, ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to ensure the resident, who had unrelieved pain on his shoulder, neck, and legs, was provided with effective pain management (the process of alleviating the resident's pain to a level that is acceptable to the resident and is based on his or her clinical condition and established treatment goal) for one of one sampled resident (Resident 55). The facility failed to: 1. Ensure Lidocaine patch (topical [applied to the surface of the body] pain relievers that work by numbing the skin) and Aspercrem (topical pain relief designed to relieve minor aches and pains associated with conditions like arthritis and backaches) were offered and given to Resident 55 in 4/2025, 5/2025 and 6/2025, as ordered by the physician. 2. Ensure Resident 55's pain level rated 8 out of 10 on a pain rating scale (pain screening tool using numerical value to assess the level of pain ranging from 0 to 10 where (0) No Pain, (1-3) Mild Pain, (4-6) Moderate Pain, and (7-10) Severe Pain) on 6/9/2025 at 12:11 p.m., to his left shoulder and left leg pain was managed and the resident's physician informed. 3. Ensure facility held an Interdisciplinary Team (IDT- team members from different departments working together with a common purpose to set goals and make decisions that ensure residents receive the best care) meeting with Resident 55 and family member to discuss Resident 55's refusal of pain medication and addressed pain management. 4. Ensure facility staff notified the facility's Medical Director when Resident 55's physician refused to order stronger pain medication than Tylenol (pain medication) 325 milligram (mg-unit of measurement) two tablets by mouth every four hours as needed for moderate pain. These deficient practices had the potential for Resident 55 to experience unrelieved pain to his shoulder, neck and legs, continue to refuse activities of daily living, and Restorative Nursing Assistant (RNA- nursing aide program that helps residents to maintain their function and joint mobility) services. Findings: During a review of Resident 55's admission Record, the admission Record indicated Resident 55 was originally admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including gout (a type of inflammatory arthritis that causes pain and swelling in the joints), back pain, peripheral vascular disease ( circulatory condition in which narrowed blood vessels reduce blood flow to the limbs), history of falls, and transient ischemic attack (a brief episode of neurological dysfunction caused by a temporary interruption of blood flow to the brain). During a review of Resident 55's Care Plan titled Resident 55 with episodes of refusal of pain medication, dated 9/29/2021, the Care Plan indicated the goal for Resident 55 was to take his medications on time and as ordered daily for three months. The Care Plan interventions indicated to explain the importance of taking the medication and the negative consequences of not taking the medications to Resident 55, explain the medication ordered, frequency, dosage, and indications. Inform Resident 55's of resident's continued refusal of taking medication. During a review of Resident 55's Physician's Orders, dated 3/23/2023, the Physician's Orders indicated Resident 55 had an order for Lidocaine patch 4.0 percent (%) apply to right neck and right shoulder topically as needed for pain management. During a review of Resident 55's Physicians' Order dated 6/9/2024, the Physicians' Order indicated and order to monitor for pain intensity using pain rating scale every shift. During a review of Resident 55's Physician's Orders, dated 10/27/2024, the Physician's Orders indicated Resident 55 had an order for Aspercreme heat gel 10% apply to left arm, hand, and leg topically as needed for pain daily. During a review of Resident 55's Medication Administration Record (MAR) for the months of 4/2025, 5/2025 and 6/2025, the MAR indicated Lidocaine patch and Aspercreme was not given to Resident 55. During a review of Resident 55's Physician's Order dated 5/19/2025, the Physician's Order indicated an order to monitor Resident 55's frequency of pain every shift. During a review of Resident 55's Minimum Data Set (MDS- a resident assessment tool), dated 5/23/2025, the MDS indicated, Resident 55 was able to express ideas and wants and had the ability to understand others. The MDS indicated, Resident 55 was dependent (helper does all the effort) on nursing staff with toileting, showering, dressing, and transferring. The MDS indicated, Resident 55 needed partial to moderate assistance (helper does less than half of the effort) from nursing staff with oral hygiene, personal hygiene, lying down, sitting and rolling from left to right. The MDS indicated for one to three days, Resident 55 rejected care that was necessary to achieve the resident's goals for health and well-being. The MDS indicated Resident 55 had no pain in the last five days. During a review of Resident 55's IDT Note, dated 5/27/2025, the IDT Conference Note indicated, Resident 55 continues to refuse participation in group activities despite encouragement. The IDT Conference Note indicated Resident 55 had episodes of refusal of the RNA program. During an interview on 6/9/2025 at 12:11 p.m., with Resident 55, Resident 55 stated he had a pain on his left shoulder and left leg which he rated 8 of 10 pain on a pain rating scale and was getting worse. Resident 55 stated he had been offered Tylenol for pain. Resident 55 stated he refused to take the Tylenol because it was not relieving his pain. Resident 55 stated he does not ask for pain medication anymore he lays in bed grinding his teeth to not deal with his left shoulder and left leg pain. During a concurrent interview and record review on 6/11/2025 at 9:00 a.m., with Licensed Vocational Nurse (LVN) 4, Resident 55's Nurses Progress Notes, dated 5/28/2025 were reviewed. The Nurses Progress Notes indicated, Resident 55 was asking for Tylenol with Codeine (pain medication that belongs to narcotics) instead of regular Tylenol. The Nurses Progress Notes indicated Resident 55's family member asked for Tramadol (also known as a narcotic pain medication) for Resident 55. The Nurses Progress Notes indicated, Resident 55 refused nursing care and often refused activities of daily living due to pain. The Nurses Progress Notes indicated, Resident 55 request for Tylenol with Codeine and Tramadol was denied by the doctor. LVN 4 stated Resident 55 had an order for Tylenol, Lidocaine patch, and Aspercreme for left arm pain. LVN 4 stated there was no documentation of why the request for Tylenol with Codeine and Tramadol was denied. The LVN 4 stated she forgot to document Resident 55's pain level on 5/28/2025. LVN 4 stated Resident 55 becomes agitated and does not want to participate in activities and personal care because the pain was not managed. LVN 4 stated she heard Resident 55 stated to licensed staff to get him out of the facility and that he wants to go home whenever he had pain to the shoulder, neck and legs. During an interview on 6/12/2025 at 11:39 a.m., with Certified Nursing Assistant (CNA) 6, CNA 6 stated Resident 55 does not like to participate to any activities and personal care like bed baths. CNA 6 stated Resident 55 expressed to CNA 6, he does not want to be touched due to pain on Resident 55's neck, shoulder, arms and legs on 5/28/2025. CNA 6 stated she reported to the charge nurse Resident 55 did not want a bed bath, and the charge nurse talked to him and offered pain medication. During a concurrent interview and record review on 6/12/2025 at 12:08 p.m., with Restorative Nurse Assistant (specialized CNAs who focus on rehabilitative care to help residents regain or maintain their functional abilities) (RNA) 1, Resident 55's Documentation Survey Report dated 5/2025 and 6/2025, were reviewed. The Documentation Survey Report indicated documentation of Resident Refused (Rr) and Not Applicable (Na) Resident 55's RNA services for the following days: 5/5/2025-resident refused 5/8/2025-resident refused 5/12/2025-resident refused 5/13/2025-resident refused 5/14/2025-resident refused 5/16/2025-resident refused 5/28/2025-resident refused 6/3/2025-not applicable 6/6/2025-not applicable 6/9/2025-not applicable RNA 1 stated Resident 55 refuses RNA and only gets out of bed to go to the bathroom. RNA 1 stated Rr means the resident refused and Na means the resident was not able to tolerate RNA due to pain or weakness. RNA 1 stated she reported to the charge nurse (unknown) Resident 55 refusal to participate in RNA services due to pain. During a concurrent interview and record review on 6/12/2025 at 12:40 p.m., with Licensed Vocational Nurse (LVN) 2, Resident 55's Care Plans dated 9/29/2021, 5/19/2023 and 6/13/2024 were reviewed. The Care Plans indicated on 9/29/2021 Resident 55 refused to take pain medication. The Care Plan indicated on 5/19/2023 Resident 55 refused to shower, refused to be cleaned and refused to be changed. The Care Plan indicated on 6/13/2024 Resident 55 had episodes of refusing RNA program. LVN 2 stated on 6/12/2025 Resident 55 had pain and was refusing to bathe and refusing acetaminophen for pain. LVN 2 stated there was no documentation of Resident 55's pain level on 6/12/2025. Reviewed Progress Notes on 6/11/2025 and there was a documentation Resident 55's pain level was 8/10 to the shoulders, legs and neck. During a concurrent interview and record review on 6/12/2025 at 2:16 p.m., with Registered Nurse Supervisor (RNS) 2, Resident 55 Nurses Progress Notes, dated 5/28/2025 were reviewed. The Nurses Progress Notes indicated, Resident 55 was requesting Tylenol with Codeine, Resident 55 doctor made aware, and request denied. RNS 2 Resident 55 has gout, right shoulder pain and neck pain. RNS 2 stated Resident 55's pain should have been reassessed when Resident 55 complained of pain level 8/10 to his shoulders, legs and neck. RNS 2 stated Resident 55 should have had a diagnostic test to rule out the cause of his pain and a referral for pain consultation. RNS 2 stated Resident 55's pain affects his participation with activities of daily living, unable to participate in RNA services, refused to get out of bed, and refuse to participate in facility's activities. During an interview on 6/12/2025 at 3:42 p.m., with the Director of Nursing (DON), the DON stated it was not acceptable for Resident 55 to have constant pain and was not managed accordingly. The DON stated Resident 55 continues to refuse Tylenol. The DON stated Resident 55 does not want to get out of bed and refuses activities of daily living. During a review of the facility's policy and procedure (P&P), titled Pain Assessment and Management, undated, the P&P indicated, The purposes of this procedure are to help staff identify pain in the resident and develop interventions that are consistent with the resident's goals and needs and that address the underlying causes of pain. The pain management program is based on a facility-wide commitment to resident comfort. Pain management is defined as the process of alleviating the resident's pain to a level that is acceptable to the resident and is based on his or her clinical condition and established treatment goal. During a review of the facility's P&P, titled Care Plans, Comprehensive Person-Centered, undated, the P&P indicated, A comprehensive, person-centered care plan that includes objectives and timetables to meet the resident's physical, psychosocial and functional needs is developed and implemented for each resident.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Pharmacy Services (Tag F0755)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1. Administer metformin ( a medication for treating ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1. Administer metformin ( a medication for treating high blood glucose), within one hour of its scheduled administration time according to the facility's undated policy and procedure titled Administering Medications. This affects one of the six sampled residents during medication administration (Resident 30). 2a. Ensure Resident 47's aspirin [a medication used to prevent heart attack (flow of blood and oxygen is blocked) and stroke (loss of blood flow to a part of the brain)] chewable tablet was administered as a chewable according to manufacturer formulation specifications instead of being swallowed without chewing, on 6/10/2025, affecting one of six sampled residents during medication administration (Resident 47). 2b. Wear gloves during the administration and handling of Letrozole (a hazardous medication used to treat cancer) for Resident 47 as per facility's P&P titled, Handling of Hazardous Drugs in Healthcare Setting, undated, affecting one of six sampled residents during medication administration (Resident 47). 3. Ensure disposal of discarded medications in an irretrievable, safe and secure manner, as per facility's P&P titled, Discarding and Destroying Medications, undated and Discontinued Medications, undated, affecting three of four inspected medication carts (Station B1 Medication Cart, Station B2 Medication Cart and Station A Medication Cart). These deficient practices failed to provide medications in accordance with the physician's orders or professional standards of practice and had the potential to result in adverse events such as stroke and hyperglycemia (high blood glucose) for Residents 30 and 47, pose an occupational health hazard for facility staff and residents, and increased risk for misuse, drug loss, accidental exposure and/or potential diversion of prescription medications. Findings: 1. During a review of Resident 30's admission Record (a document containing demographic and diagnostic information), dated 6/11/2025, the admission record indicated, Resident 30 was admitted to facility on 1/21/2021 with diagnosis including, but not limited to, Type 2 Diabetes Mellitus (DM - a disorder characterized by difficulty in blood sugar control and poor wound healing) without complications. During a review of Resident 30's Minimum Data Set ([MDS], a resident assessment tool) dated 5/2/2025, the MDS indicated, Resident 30's cognition (mental action or process of acquiring knowledge and understanding through thought and the senses). The MDS indicated Resident 30 needed setup or clean-up assistance from the facility staff for performing activities of daily living (ADLs - routine tasks/activities such as bathing, dressing and toileting a person performs daily to care for themselves) such as eating and oral hygiene, supervision assistance for personal hygiene, moderate assistance for toileting hygiene, upper and lower body dressing, putting on/taking off footwear, and dependent on facility staff for showering. During an observation on 6/10/2025 at 10:02 a.m. with Licensed Vocational Nurse (LVN) 2, LVN 2 prepared nine medications to be administered to Resident 30. During a medication reconciliation review on 6/10/2025 at 12:21 p.m., Resident 30's Order Summary Report (a document containing a summary of all active physician orders), dated 6/11/2025, metformin's order details were reviewed. The order summary report indicated, but not limited to the following physician order scheduled to be administered daily at 8:00 a.m.: Metformin hydrochloride (HCl) tablet 500 milligrams ([mg] - a unit of measurement for mass), give 1 tablet by mouth two times a day for DM with meals, order date 12/6/2023, start date 12/6/2023. During an interview and record review on 6/11/2025 at 11:59 a.m. with Registered Nurse Supervisor (RNS) 2, it was noted that Resident 30's metformin 500 mg was administered more than an hour late. RNS 1 explained that LVN 2 should have given the medication by 9:00 a.m. on 6/10/2025, but it was administered at 10:00 a.m. This delay could pose a risk for abnormal blood glucose levels for Resident 30. During a review of Resident 30's administration history for metformin 500 mg, dated 5/31/2025 to 6/10/2025, the document indicated metformin 500 mg was not administered within one hour of scheduled time of 8:00 am for five times. During an interview on 6/12/2025 at 1:03 p.m. with the Director of Nursing (DON), DON stated the facility staff was allowed to give a medication one hour before or one hour after the scheduled time of administration. DON stated it was important to follow the 'specific time code' because that would be the physician's required scheduled time of administration. DON stated if the specific time for administration was 8 a.m. then facility staff should have given the medication by 9 a.m. DON stated if the medication was given after 10 a.m. or at 10:22 a.m., it would be considered late administration. DON stated the medication if given late and not given with meals, there was a risk for gastric irritation and hyperglycemia. 2a and 2b. During a review of Resident 47's admission record, dated 6/10/2025, the admission record indicated, Resident 47 was originally admitted to the facility on [DATE] with diagnoses including, but not limited to, atherosclerosis of aorta (a build-up of fat and cholesterol in the largest artery in the body increasing the risk for blood clots, heart attack [blockage of blood flow to the heart] and stroke) and malignant neoplasm (cancer) of unspecified site of left female breast. During a review of Resident 47's MDS, dated [DATE], the MDS indicated, Resident 47's cognition was intact. The MDS indicated Resident 47 needed setup or clean-up assistance from the facility staff for eating, oral hygiene and personal hygiene, maximal assistance for upper body dressing and dependent for toileting hygiene, showering, lower body dressing and putting on/taking off footwear. During a medication pass observation on 6/10/2025 from 8:39 a.m. to 9:01 a.m. with LVN 1, LVN 1 prepared and administered Resident 47's medications that included one tablet of aspirin 81 mg chewable tablet and one tablet of letrozole 2.5 mg. LVN 1 did not wear gloves while handling letrozole tablet that belonged to a hazardous category of medications. LVN 1 did not instruct Resident 47 to chew aspirin before swallowing and the resident was observed swallowing all medications including aspirin chewable tablet. During a review of Resident 47's Order Summary Report, dated 05/30/2025, the document indicated following physician orders: Aspirin Tablet Chewable 81 mg, give 1 tablet by mouth one time a day for anti-platelet agent to prevent stroke and heart attack with breakfast, order date: 5/30/2024, start date: 5/31/2024. Letrozole tablet 2.5 mg, give 1 tablet by mouth one time a day for breast cancer, order date 11/10/2021, start date 11/11/2021. During a review of Resident 47's order summary report, dated 6/11/2025, the document indicated the aspirin order was changed as following: Aspirin enteric coated (EC) adult low dose oral tablet delayed release 81 mg, give 1 tablet by mouth in the morning for anti-platelet agent to prevent stroke and heart attack with breakfast, order date 6/10/2025, start date 6/11/2025. During an interview on 6/10/2025 at 9:01 a.m. with LVN 1, LVN 1 stated he did not instruct Resident 47 to chew aspirin and resident swallowed it along with her other medications. LVN 1 stated aspirin chewable tablet would have a faster onset of action to prevent stroke if it was chewed before swallowing. During an interview on 6/11/2025 at 11:31 a.m., LVN 5 mentioned that she typically wore gloves before administering Resident 47's letrozole, as the medication card indicated it was hazardous. LVN 5 explained that letrozole could be toxic upon direct contact with bare hands. During an interview on 6/11/2025 at 12:17 p.m. with RNS 2, RNS 2 stated Resident 47 should have been instructed to take aspirin chewable tablet as a chew and swallow based on manufacturer requirements. RNS 2 stated if aspirin was not taken per manufacturer requirements, there would be a risk of poor absorption and may not be effective to prevent blood clots or stroke. During an interview on 6/12/2025 at 12:55 p.m. with the DON, DON stated the resident should have chewed the chewable aspirin tablet before swallowing. DON stated the medication effect might be slower than intended which would delay the effect of blood clotting and to prevent stroke. DON stated facility staff should have verified the order with physician if the chewable aspirin order did not indicate chew and swallow the tablet. During an interview on 6/12/2025 at 1:30 p.m. with the DON, DON stated letrozole belonged to hazardous category which was a cancer medication. DON stated the facility nurse should have worn gloves throughout the process of preparing and administering letrozole or any other hazardous medication to residents because of their risk of skin irritation and reproductive risk for females. DON stated the facility staff should provide gloves to the resident if they were going to make any contact with letrozole tablet. During a review of manufacturer labeling of the facility administered aspirin chewable tablet, the document indicated, Chew or crush tablets completely before swallowing, do not swallow tablets whole. During a review of the facility's P&P, titled Administering Medications, undated, the P&P indicated, Medications may not be prepared in advance and must be administered within one (1) hour of their prescribed time, unless otherwise specified (for example, before and after meal orders). The P&P indicated, Medications shall be administered in a safe and timely manner, and as prescribed. The individual administering medications must check the label three times to verify the right medication , right time and right method of administration before giving the medication. During a review of the facility's P&P titled, Handling of Hazardous Drugs in Healthcare Setting, undated, the P&P indicated, When handling hazardous drugs during medication administration, healthcare workers should prioritize safety and follow established protocols. This includes: 1. Personal Protective Equipment (PPE) - a. Wear gloves when handling the drug, b. Dispose of PPE properly after each use, following facility protocols. The facility's active list of hazardous medications included letrozole. 3a. During a concurrent observation and interview on 6/11/2025 at 1:24 p.m. with LVN 5 of Station B2 Medication Cart, the medication cart contained two red containers filled with a lot of medications, with open lids in the bottom drawer. The two red containers indicated, 'biohazard', along with handwritten word 'pills' on one container and 'liquid meds' on another container. LVN 5 stated the tablets, capsules or pills in the red containers could be loose pills and medications refused by facility residents. LVN 5 stated when the resident refused a medication, LVN would discard it in the red bin, and made a note in resident's chart that medication was refused. LVN 5 stated, if she needed to dispose of narcotic (a term used for controlled medications [medications that the use and possession of are controlled by the federal government]) medications, she would call another licensed nurse as a cosigner, sign in the book, crush the medication, throw in the red bin, would put water in the crushed powder and then discarded and destroyed. LVN 5 stated, she did not see any problem with this method of destruction of medications. LVN 5 stated the red bin contained a lot of medications but could not say for sure if it had controlled medications. LVN 5 stated, you probably can retrieve the medications from the red bin if you have long fingers. LVN 5 stated the medications in the red bin were accessible and were not discarded in an irretrievable manner. LVN 5 stated, it is hard for me to say that there is a risk for diversion because it has not happened, because only licensed nurses have access to the cart. 3b. During a concurrent observation and interview on 6/11/2025 at 2:04 p.m. with LVN 6 of Station B1 Medication Cart, the medication cart contained one red container filled with a lot of medications, with an open lid in the bottom drawer. The red container indicated, 'biohazard', along with handwritten word 'crushed pills.' LVN 6 stated the red bin contained medications that were refused or if dropped on the floor. LVN 6 stated the medications in the red bin were noncontrolled prescription medications and supplements. LVN 6 stated she thought there were probably three months of more medications. LVN 6 first stated if it was a controlled medication to be wasted, they would need two nurses to sign in the book, and controlled medication would be crushed and wasted in the red bin for controlled and noncontrolled medications. LVN 6 then corrected herself and stated the red bin would get controlled and noncontrolled medications, but controlled were medications were very rare, less than once a month. LVN 6 stated it was not good to have those medications sitting there in the medication cart, waiting to be discarded because that could have increased the risk for misuse and diversion. 3c. During a concurrent observation and interview on 6/11/2025 at 4:58 p.m. with LVN 7 of Station A Medication Cart, the medication cart contained three red containers, one of which was filled with lot of loose tablets and capsules, another one was filled with tablets and capsules mixed with some type of liquid, and one more container that was empty, all with open lids in the bottom drawer. The red containers indicated, 'biohazard' along with handwritten word 'pills' on one of the containers. LVN 7 stated the red bin contained refused medications and those that were to treat high blood pressure (BP), where the medication would need to be discarded in the red bin if resident's BP was outside of the prescribed parameters. LVN 7 stated she would pour water in the red bin so that the medications when discarded into the red bin would be irretrievable and could not be misused or abused. LVN 7 stated there were no controlled medications in the red bin, because controlled medications were handed over to the DON for disposal. LVN 7 stated there was a risk of spilling the medications and liquid in the medication cart, which could make unsafe and unsanitary conditions for medication storage in the medication cart. During an interview on 6/12/2025 at 12:26 p.m. with the DON, DON stated facility staff should not be destroying controlled medications on the floor. DON stated the facility staff should maintain a pill packet for controlled medication that needed disposal, document and sign in the book with two nurses' signatures and then should be brought to the DON for its destruction later with a pharmacist. DON stated the medication carts should not have the red biohazard bins or loose tablets discarded in red bins stored in medication carts. DON stated there was a risk that someone could retrieve the loose tablets or capsules from the red container and cause an accidental exposure or misuse. DON stated it was not sanitary to look at the red containers with liquid along with capsules and tablets. During a review of the facility's P&P titled, Discarding and Destroying Medications, undated, the P&P indicated, Medications will be disposed of in accordance with federal, state and local regulations governing management of non-hazardous pharmaceuticals, hazardous waste and controlled substances. The P&P indicated, all unused controlled substances shall be retained in a securely locked area with restricted access until disposed of. Non-controlled and Schedule V (non-hazardous) controlled substances will be disposed of in accordance with state . non-hazardous medications. The P&P indicated, Destruction of a controlled substance must render it non-retrievable, meaning that cannot be illegally diverted. During a review of the facility's P&P titled, Discontinued Medications, undated, the P&P indicated, Discontinued medications must be destroyed in accordance with established policies.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1. Maintain a clean and safe environment for medicat...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1. Maintain a clean and safe environment for medication storage by removing unsealed red biohazard containers filled with discarded medications in tablets, capsules and liquid form from three of the four inspected carts (Station B1, Station B2, and Station A). 2.Ensure that Resident 30 does not self-administer medications without facility supervision by safeguarding his medications during the medication pass, affecting one of six residents (Resident 30). 3. Ensure Resident 40's Humulin N ([generic name - insulin human isophane NPH] a type of insulin [a hormone that removes excess sugar from the blood, can be produced by the body or given artificially via medication] used to treat high blood sugar) was labeled with an open date and Resident 76's Breyna ([generic name - budesonide with formoterol] a medication delivered in the form of inhalation spray through a device used to treat breathing problems) were labeled in accordance with the manufacturer specifications and per facility's policy and procedure (P&P) titled, Labeling of Medication Containers, undated and Storage of Medications, undated, affecting two of four medication cards inspected (Station C Medication Cart and Station A Medication Cart). These deficient practices resulted in an unclean, unsecure and unsanitary environment for medication storage in medication carts and resident rooms, self-administration of medications without supervision, and had the potential to result in medication errors and/or choking, administering medications that had become expired, ineffective, or toxic due to improper labeling and/or storage, possibly leading to adverse health consequences such as shortness of breath, abnormal blood glucose levels and hospitalization for Residents 30, 40 and 76. Findings: 1a. During a concurrent observation and interview on [DATE] at 1:24 p.m. with Licensed Vocational Nurse (LVN) 5 of Station B2 Medication Cart, the medication cart contained two red containers filled with a lot of medications, with open lids in the bottom drawer. The two red containers indicated, biohazard, along with handwritten word 'pills' on one container and 'liquid meds' on another container. LVN 5 stated the tablets, capsules or pills in the red containers could be loose pills and medications refused by facility residents. LVN 5 stated that when the resident refused medication, LVN would discard it in the red bin, and made a note in resident's chart that medication was refused. LVN 5 stated, if she needed to dispose of narcotic (a term used for controlled medications [medications that the use and possession of are controlled by the federal government]) medications, she would call another licensed nurse as a cosigner, sign in the book, crush the medication, throw in the red bin, would put water in the crushed powder and then discarded or destroyed. LVN 5 stated, she did not see any problem with this method of destruction of medications. LVN 5 stated the red bin contained a lot of medications but could not be sure if it had controlled medications. LVN 5 stated, you probably can retrieve the medications from the red bin if you have long fingers. LVN 5 stated the medications in the red bin were accessible and were not discarded in an irretrievable manner. LVN 5 stated, it is hard for me to say that there is a risk for diversion because it has not happened, because only licensed nurses have access to the cart. 1b. During a concurrent observation and interview on [DATE] at 2:04 p.m. with LVN 6 of Station B1 Medication Cart, the medication cart contained one red container filled with a lot of medications, with an open lid in the bottom drawer. The red container indicated, biohazard', along with handwritten word 'crushed pills.' LVN 6 stated the red bin contained medications that were refused or if they dropped on the floor. LVN 6 stated the medications in the red bin were noncontrolled prescription medications and supplements. LVN 6 stated the red biohazard bin might contain three months' worth of medications. LVN 6 first stated if it was a controlled medication that needed to be wasted, they would need two nurses to sign in the book, and controlled medication would be crushed and wasted in the red bin for controlled and noncontrolled medications. LVN 6 then corrected herself and stated the red bin would get controlled and noncontrolled medications, but controlled were medications were very rare, less than once a month. LVN 6 stated it was not good to have those medications sitting there in the medication cart, waiting to be discarded because that increased the risk for medication misuse and diversion. 1c. During a concurrent observation and interview on [DATE] at 4:58 p.m. with LVN 7 of Station A Medication Cart, the medication cart contained three red containers, one of which was filled with loose tablets and capsules, another one was filled with tablets and capsules mixed with some type of liquid, and another container was empty. All three containers were stored with their lids open in the bottom drawer. The red containers indicated, biohazard' along with handwritten word 'pills' on one of the containers. LVN 7 stated the red bin contained refused medications and those that were to treat high blood pressure (BP), where the medication would need to be discarded in the red bin if resident's BP was outside of the prescribed parameters. LVN 7 stated she would pour water in the red bin so that the medications when discarded into the red bin would be irretrievable and could not be misused or abused. LVN 7 stated there were no controlled medications in the red bin, because controlled medications were handed over to the DON for disposal. LVN 7 stated there was a risk of spilling the medications and liquid in the medication cart, which could cause unsafe and unsanitary conditions for medication storage in the medication cart. During an interview on [DATE] at 12:26 p.m. with the Director of Nursing (DON), DON stated the medication carts should not have the red biohazard bins or loose tablets discarded in red bins stored in medication carts. DON stated there was a risk that someone could retrieve the loose tablets or capsules from the red container and cause accidental exposure or drug misuse. DON stated it was not sanitary to look at the red containers with liquid along with capsules and tablets. During a review of the facility's P&P titled, Storage of Medications, undated, the P&P indicated, The facility shall store all drugs and biologicals in a safe, secure, and orderly manner. The nursing staff shall be responsible for maintaining medication store AND preparation areas in a clean, safe, and sanitary manner. 2. During a concurrent observation and interview on [DATE] at 10:02 a.m. with Licensed Vocational Nurse (LVN) 2, LVN 2 prepared the following nine medications to be administered to Resident 30. 1. One tablet of aspirin [a medication used to prevent heart attack (flow of blood and oxygen is blocked) and stroke (loss of blood flow to a part of the brain)] enteric coated 81 milligrams ([mg] a unit of measurement for mass) 2. One tablet of metformin (a medication used to treat high blood glucose) 500 mg 3. One tablet of vitamin C (ascorbic acid - a vitamin used to treat low level of vitamin C) 4. One capsule of docusate sodium (a medication used to treat constipation) 250 mg 5. One tablet of famotidine (a medication used to treat acid reflux) 20 mg 6. One tablet of Januvia [(generic name - sitagliptin) a medication used to treat high blood glucose) 50 mg 7. One tablet of lisinopril (a medication used to treat high blood pressure) 5 mg 8. One tablet of metoprolol succinate (a medication used to treat high blood pressure) extended release (ER) 25 mg 9. One tablet of sodium chloride (a supplement used to balance sodium levels) 1 gram ([gm] a unit of measurement for mass) LVN 2 placed a tray with two medicine cups on Resident 30's bedside table, one containing lisinopril and metoprolol succinate, and another cup with all the other medications. LVN 2 turned away to retrieve gloves, during which time Resident 30 ingested all the medications except for the lisinopril and metoprolol succinate. Upon returning, LVN 2 observed that Resident 30 had taken some of the medications unsupervised. LVN 2 remarked, No, no, no, let me take your blood pressure before you continue with your medications. When Resident 30 was about to take the lisinopril and metoprolol succinate, LVN 2 stated, It is okay; you did not take the blood pressure medications yet. Let me take your blood pressure first. During an interview on [DATE] at 11:59 a.m. with the Registered Nurse Supervisor (RNS) 2, RNS 2 stated that facility staff should not leave medications unattended with the resident. RNS 2 mentioned that facility staff should watch the residents take their medications to ensure they do not fail to take them or hide them. Additionally, it is important for facility staff to observe residents while they are swallowing medications to monitor for any side effects or difficulty swallowing, thus preventing the risk of choking. During an interview on [DATE] at 1:25 p.m., the Director of Nursing (DON) emphasized that staff should follow the pour, pass, sign method. Staff must ensure residents take their medications and do not hide them. The nurse should check the resident's blood pressure before preparing the medication. Additionally, staff must observe residents taking their medications to verify proper administration. During a review of the facility's P&P titled, Administering Medications, undated, the P&P indicated, Medications shall be administered in a safe and timely manner, and as prescribed. 3a. During a concurrent inspection and interview on [DATE] at 12:47 p.m. with LVN 4 of the Station C Medication Cart, the following medication was not labeled with an open date as required by manufacturer's specifications and per P&P titled, Labeling of Medications and Storage of Medications: One opened Humulin N 100 units / 10 milliliters ([mL] a unit of measurement for volume) vial for Resident 40 with no open date. According to the manufacturer's product labeling, unopened vial(s) should be stored under refrigeration at 2-degree Celsius ([°C] a unit of temperature) to 8°C (36-degree Fahrenheit [(°F) is a unit of temperature] to 46°F) and open or in-use bottle may be stored at room temperature below 30°C (86°F) for 31 days and must be discarded thereafter. LVN 4 stated the Humulin N should have had an open date because it was important and a requirement for the facility to be able to determine the 28-day expiration date for insulin. LVN 4 stated Resident 40 might not get the full benefit of the insulin, could cause hyperglycemia or abnormal blood glucose levels, possibly leading to hypoglycemic shock and altered consciousness, hospitalization and coma. During an interview on [DATE] at 1:40 p.m., the Director of Nursing (DON) indicated that facility staff should label the insulin vial with an open date upon opening. This practice ensures that staff are aware of the 28-day usage period for insulin. Without labeling, the expiration date would be unclear, potentially impacting the efficacy and safety of the insulin for controlling blood sugar in residents. 3b. During a concurrent inspection and interview on [DATE] at 4:58 p.m. with LVN 7 of the Station A Medication Cart, the following medication was not labeled with an open date as required by manufacturer's specifications and per P&P titled, Labeling of Medications and Storage of Medications: One package of Breyna 160 microgram ([mcg] a unit of measure for mass) - 4.5 mcg (a combination of budesonide and formoterol) inhalation aerosol for Resident 76 with no open date. According to the manufacturer's product labeling, Breyna inhaler should be discarded when the labeled number of inhalations have been used or within 3 months after removal from the foil pouch. LVN 7 stated she should have discarded the medication within 30 days based on facility's policy. LVN 7 stated that medication might not be safe or effective for Resident 76 and might not help with breathing difficulty. LVN 7 stated resident could have shortness of breath lead to hospitalization. During an interview on [DATE] at 1:45 p.m. with DON, DON stated the facility nurse should have placed an open date on the Breyna inhaler, because if it was continued to be used after 3 months, there was a potential risk for ineffectiveness and safety. DON stated the facility policy addressed this as part of the labeling the containers with an open date for single-use and multiple-use containers. DON stated the medication might not be effective for its intended use to manage asthma or Chronic Obstructive Pulmonary Disease ([COPD] a condition that causes difficulty breathing). During a review of the facility's P&P titled, Labeling of Medication Containers, undated, the P&P indicated, All medications maintained in the facility shall be properly labeled in accordance with current state and federal regulations. The P&P indicated, Labels for individual drug containers shall include all necessary information, such as: a. The resident's name , h. The expiration date when applicable use.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0790 (Tag F0790)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to provide necessary dental services for four of four samp...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to provide necessary dental services for four of four sampled residents (Resident 78,105, 6 and 10). This failure had the potential to lead to weight loss, inability to chew effectively, or infection of the mouth. Findings: During a record review of Resident 78's admission Record, the admission Record indicated Resident 78 was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including mild protein-calorie malnutrition (a mild deficiency in the intake of both protein and calories, resulting in adequate nutrition), nausea with vomiting, and muscle wasting. During a review of Resident 78's History and Physical (H&P), the H&P indicated, Resident 78 he was able to express needs, communicate, follow commands and talk in full sentences. During a review of Resident 78's Minimum Data Set (MDS-a resident assessment tool), the MDS indicated, Resident 78 was dependent on nursing staff with transferring. The MDS indicated Resident 78 needed substantial to maximal assistance with toileting, showering, dressing, sitting and standing. The MDS indicated Resident 78 needed setup or clean-up assistance from nursing staff with eating and oral hygiene. During a review of Resident 78's Order Summary, dated 8/26/2024, the Order Summary indicated, Resident 78 had an order for a dental consultation for a pulled tooth. During a review of Resident 78's Change of Condition ([COC] a sudden, clinically important deviation from a patient's baseline in physical, cognitive (ability to think, understand, learn, and remember) behavioral, or functional status which without immediate intervention, may result in complications or death ) Evaluation, dated 11/4/2024, the Change of Condition Evaluation indicated, Resident 78 had right upper and right lower teeth pain. The Change of Condition Evaluation indicated Resident 78 received a written order from the doctor to have a dental follow-up due to teeth pain. The Change of Condition Evaluation indicated the order was noted and carried out. During a review of Resident 78's Social Services Director Note, dated 3/25/2025, the Social Services Director Note indicated, Resident 78 asked about the next dental visit. The Social Services Director Note indicated Resident 78 stated, I think I'm supposed to be getting dentures. The Social Services Director Note indicated Resident 78 was informed of a dental clearance for teeth extractions, signed by the doctor and the clearance was sent to the dentist. During a review of Resident 78's Onsite Mobile Dental report, dated 4/29/2025, the Onsite Mobile Dental report indicated Resident 78 was recommended new dentures. The Onsite Mobile Dental report indicated dental impressions (a model or cast for dentures) in three weeks. During a review of Resident 78's Onsite Mobile Dental report, dated 5/14/2025, the Onsite Mobile Dental report indicated Resident 78 needs dental impressions the last week of May 2025. During an interview on 6/9/2025 at 11:00 a.m., with Resident 78, Resident 78 stated, he had his teeth removed six weeks ago and needs dentures. Resident 78 stated he has problems with chewing. During an interview on 6/10/25 at 2:42 p.m., with Social Service Director (SSD), the SSD stated, Resident 78 had teeth extractions done on 4/29/2025 and needed dental impressions within three weeks. SSD stated Resident 78 had been wanting new dentures. The SSD stated she did not follow up on the Onsite Mobile Dental for Resident 78 to have dental impressions for new dentures. During an interview on 6/12/2025 at 3:41 p.m., with the Director of Nursing, the DON stated the Onsite Mobile Dental report for Resident 78 to have dental impressions should have been followed up by the SSD. The DON stated not having dentures affects eating and chewing and Resident 78 has a potential for weight loss. During a review of the facility's policy and procedure (P&P), titled Social Service Policy & Procedure Ancillary Services, undated, the P&P indicated .Social Services will coordinate efforts with the ancillary service provides on recommended follow up, such as ordering glasses, hearing aids, or dentures until the need is met . During a record review of Resident 6's admission Record, the admission Record indicated Resident 6 was initially admitted to the facility on [DATE] and was readmitted on [DATE] with diagnosis including diabetes mellitus (DM- a disorder characterized by difficulty in blood sugar control and poor wound healing) ), dementia ( a progressive state of decline in mental abilities), schizoaffective disorder( a mental illness that can affect thoughts, mood, and behavior) and candidal stomatitis (infection in the mouth caused by a fungus leading to inflammation and redness). During a review of Resident 6's Minimum Data Set (MDS- a resident assessment tool ) dated 3/26/2025, the MDS indicated Resident 6 had moderately impaired cognitive skills ( person had problems remembering things, concentrating, making and solving decisions) and required partial/ moderate assistance (helper does less than the effort) with oral hygiene, bed mobility, and upper body dressing( ability to dress and undress below the waist). During a review of Resident 6's Onsite Mobile Dental Note dated 1/15/2025 , the Onsite Mobile Dental Note indicated Resident 6's upper and lower dentures were okay. During a concurrent observation and interview on 6/9/2025, at 4:33 p.m. with Resident 6 , Resident 6 was edentulous ( complete loss of natural teeth). Resident 6 stated her upper and lower dentures do not fit her and told several unnamed staff about her dentures. During a concurrent interview and record review on 6/10/2025, at 2:12 p.m. and subsequent interview on 6/11/2025, at 9:22 a.m. with Social Services Director (SSD), Resident 6's Dental Notes dated 1/15/2025 was reviewed. SSD stated the last dental evaluation or check up was dated 1/15/ 2025 which indicated Resident 6's dentures were okay. SSD stated the facility does not follow up for any concerns regarding dental needs of a resident. SSD stated social services perform their assessments every 3 months to know if a resident had a concern with their vision or dental. SSD stated she will add Resident 6 to the list of residents that will be seen by a dentist to evaluate her dentures. During a review of Resident 10's admission Record, the admission Record indicated Resident 10 was initially admitted to the facility on [DATE] and was readmitted on [DATE] with diagnoses including DM, bilateral sensorineural hearing loss (trouble hearing in both ears due to the damage in the inner ear or auditory nerve), repeated falls, spinal stenosis (happens when the space inside the backbone is too small causing pressure on the spinal cord and nerves that travel through the spine) and need for assistance with personal care. During a review of Resident 10's MDS dated [DATE],the MDS indicated Resident 10 had moderately impaired cognitive skills and was dependent ( helper does all the effort) on the staff with bathing, dressing, toileting hygiene, transfer in and out of a tub or shower. During a review of Resident 10's Onsite Mobile Dental Note dated 5/10/2025, the Onsite Mobile Dental Note indicated Resident 10 had periodontal x-rays ( dental imaging that focuses on the bone supporting the teeth) and resident's dentures were adjusted. During a concurrent observation and interview on 6/10/2025, at 9:49 a.m. with Resident 10, Resident 10 stated her dentures would not hold and cannot use them when she eats. Observed Resident 10 not wearing dentures and meal tray ticket indicated Resident 10's diet was Fortified (certain nutrients were added to the food to improve nutritional value) no added salt(NAS) CCHO (controlled carbohydrate - designed to manage blood sugar levels by providing consistent amount of carbohydrate throughout the day) diet in regular texture (normal or expected feel of a food item when eaten), thin /regular liquid consistency with meals. During an interview on 6/12/2025, at 1:50 p.m. with Certified Nursing Assistant (CNA11), CNA 11 stated Resident 10 had dentures, but she would still cut the food into small pieces to help Resident 10. CNA 11 stated Resident 10 will have difficulty in chewing her food, cause her to choke on her food if her dentures did not fit well. During an interview on 6/11/2025, at 8:59 a.m. with SSD , SSD stated Resident 10 received new dentures and was delivered on 2/11/2025. SSD stated the family member (FM) requested to get Resident 10's dentures adjusted and none of the staff notified her about the upper and lower dentures not fitting on the resident. SSD stated Resident 10 would not be able to chew her food well and might not be able to get proper nutrition due to ill-fitting dentures. During an interview on 6/12/2025, at 4:41 p.m. with the Director of Nursing (DON) , the DON stated residents whose dentures were not fitting well would not be able to eat properly which could affect their chewing leading to weight loss. During a review of facility's policy and procedure (P&P), titled Social Service Department Role and Function, undated, the P&P indicated The facility will provide medically related social services to all residents in an effort to help them achieve and maintain their highest practicable level of physical, mental and psychosocial functioning. During a review of Resident 105's admission Record, the admission Record indicated Resident 105 was admitted to the facility on [DATE] with diagnoses including dysphagia (difficulty swallowing) and schizophrenia (a mental illness that is characterized by disturbances in thought). During a review of Resident 105's Minimum Data Set (MDS- a resident assessment tool) dated 5/6/2025, the MDS indicated Resident 105's cognition (ability to think, understand, learn, and remember) was intact and required moderate assistance (helper does less than half the effort) with toileting, showering, and dressing. During a concurrent observation and interview on 6/9/2025 at 11:09 a.m., with Resident 105, Resident 105 was observed to have chipped and discolored teeth. Resident 105 stated he has not seen a dentist since he was admitted to the facility (11/4/2024) but would like to. Resident 105 stated he was aware his teeth look bad which affects his appearance, and he was concerned he will lose his teeth if he does not see a dentist. During a concurrent interview and record review on 6/10/2025 at 12:11 p.m., with Licensed Vocational Nurse (LVN) 1, LVN 1 stated there are no orders for Resident 105 to be seen by a dentist and there was no orders that he was seen by a dentist here at the facility in the past. LVN 1 stated Resident 105 should be seen by a dentist because his teeth does not look good, and it could lead to infection. LVN 1 stated its important to maintain good oral hygiene because Resident 105 could potentially cause the resident to not feel good if his teeth do not look good and he could potentially lose his teeth. During an interview on 6/10/2025 at 2:46 p.m., with the Social Services Director (SSD) 1, the SSD 1 stated Resident 105 was not seen by a dentist, he was missed and was unsure as to why. SSD 1 stated Resident 105 should have been seen because not seeing the dentist could cause his teeth to fall out, affect his dignity, cause pain, or lead to an infection. During an interview on 6/13/2025 at 9:24 a.m., with the Director of Nursing (DON), the DON stated the nursing staff were responsible for assessing the residents teeth and if there were any concerns, the nursing staff will inform the SSD to make dental appointments. The DON stated good oral hygiene was important to maintain, because it can prevent bacteria from building up which can lead to an infection and can also affect their eating abilities. The DON stated Resident 105 not having dental services could potentially cause Resident 105 to have low self-esteem. During a review of the facility's policy and procedure (P&P) titled, Social Service Department Role and Function undated, the P&P indicated, It is the policy of this facility to provide medically related social services to all residents, in an effort to help them achieve and maintain their highest practicable level of physical, mental, and psychological functioning. During a review of the facility's P&P titled, Ancillary Services undated, the P&P indicated, It is the policy of this facility to obtain dental, optometry, ophthalmology, podiatry, audiology, and psychological/psychiatric services for residents who present with or request a need for these ancillary services. All residents will be assessed for ancillary needs upon admission and reassessed quarterly and as needed. All residents will have access to ancillary services.
CONCERN (F)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected most or all residents

Based on observation and interview, the facility failed to store, handle and maintain food/food supplies with professional standard for food service safety for 125 residents who eat in the kitchen whe...

Read full inspector narrative →
Based on observation and interview, the facility failed to store, handle and maintain food/food supplies with professional standard for food service safety for 125 residents who eat in the kitchen when : 1.Staff failed to wear a hair net while in the kitchen. 2. Food stored in the refrigerator had no label and open date. 3.The counter mounted can opener had a black tarry substance present. 4.One large dented can of jack pot brand 6 pounds 11 ounce of pineapple on the shelf. 5.Floor underneath the triple sink with small white particle and thick black tarry film. These failures had the potential to result in pathogen (germ) exposure to residents and placed residents at risk for developing foodborne illness (food poisoning) with symptoms including upset stomach, stomach cramps, nausea, vomiting, diarrhea and fever and can lead to other serious medical complications and hospitalization. During a concurrent observation and interview on 6/9/2025 at 8:19 a.m., with Dietary Staff Supervisor (DSS) in the kitchen, Dietary Aide (DA) 2 walked into the kitchen without wearing a hair net. DSS told the DA 2 to put on a hairnet. DA 2 put on a hairnet and stated DA 2 forgot to put one on. During an observation of the reach in refrigerator the DSS removed a container of prunes from the refrigerator and stated she will throw them away because the prunes had no open date label. During an interview at 6/12/2025 at 4:11 p.m., with the Director of Nursing (DON), the DON stated anybody who enters the kitchen needs to wear a hairnet to prevent food from falling into the food. The DON stated if the food was not labeled and dated we can not determine when the food was opened or prepared and we must dispose it. The DON stated this is an infection control issue. During a review of the facility's policy and procedures (P&P), titled Dress Code, dated 2023, the P&P indicated, Proper Dress: .Hat for hair, if hair is short, which completely cover hair. Hair net for hair, if hair is long (over the ears or longer) . During a review of the facility's policy and procedures (P&P), titled Labeling and Dating of Food, dated 2023, the P&P indicated, All food items in the storeroom, refrigerator, and freezer need to be labeled and dated. During an initial observation and interview on 6/9/2025 at 8:16 a.m., with the Dietary Supervisor (DS), there was one large can of pineapple on a shelf with the canned foods. DS stated she did not know there was a dent on the can. DS then removed the can and placed it where it can be returned. During an observation and interview on 6/9/2025 at 8:10 a.m.with the Dietary Aide (DA), observed countertop can opener with thick black tarry substance on the base of the can opener. The DA stated she did not know what the tarry substance was, and the staff usually clean the can opener after use. DA stated the can opener was used last night 6/8/2025. DA stated this can be harmful to the residents if the dirty can opener was used as this can contaminate the food . During a record review of the assignment for cleaning of the floors a signature was missing for the date of 6/9/2025, DSD stated if it was not signed it was not done. During an observation and interview on 6/9/2025 at 8:34 a.m., with the DS, DS stated she did not know what the black tarry substance was on the can opener. DS stated the can opener had to have been used last night 6/9/2025. In the corner underneath the 3 basins sink there were little white particles and black hard substance stuck to the floor and the plastic mat was sticky. DS stated the staff cannot get under the sink to clean the floors. DS stated it was important to get rid of the dented cans because the quality of the product of the cans and the product can have a chemical reaction and harm the resident , she stated it was best not to use the dented can, to be on the safe side. During a review of the facility's Policy and Procedure (P&P) titled, Food Storage-Dented Cans: dated 2023, the P&P indicated Food in unlabeled, rusty, leaking, broken containers or cans with side seam dents , rim dents, or swell shall not be retained or used by the facility. All dented cans ( defined as side seam or rim dents ) and rusty cans are to be separated from remaining stock and placed in a specified labeled area for return to purveyor for refund. All leaking cans are to be disposed of immediately. During a review of the facility's Policy and Procedure (P&P) titled, Can Opener and Base : dated 2023, the P&P indicated Proper sanitation and maintenance of the can opener and base is important to sanitary food preparation. Metal shavings and shredded can result from a dull cutting blade or worn-out cogwheel .The can opener must be thoroughly cleaned each work shift and, when necessary , more frequently.
CONCERN (F)

Potential for Harm - no one hurt, but risky conditions existed

QAPI Program (Tag F0867)

Could have caused harm · This affected most or all residents

Based on interview and record review, the facility's Quality Assessment and Assurance Committee (QAA) failed to implement corrective action from the last re-certification survey in regard to the facil...

Read full inspector narrative →
Based on interview and record review, the facility's Quality Assessment and Assurance Committee (QAA) failed to implement corrective action from the last re-certification survey in regard to the facility repeated deficient practices. Findings: During a review of the facility's Statement of Deficiencies for the 2024 Recertification survey indicated the following repeat deficiencies: Nutrition/Hydration, pain management, food procurement, store/prepare/serve-sanitary, QAPI QAA improvement, reasonable accommodation of needs /preferences, development/ implement comprehensive care plan, Infection prevention & control, quality of care, pharmaceutical services, drug regimen review, labeling and storage of drugs. During a concurrent interview and record review on 06/13/25 at 10:41 a.m., with the Director of Nursing (DON), Administrator (ADM) and Quality Assurance (QA) nurse, reviewed QAPI reports on falls. QA nurse confirmed that these deficiencies were identified and went up and down, but facility was working on them. Per reports goals of QAPI reports as follows: 1.To decrease the number of repeated falls by 10 percent (%) for three months, and no major injury for 3 months. 2. Decrease number of falls events occurring in the evening by 5 % for 3 months. The evaluation reports were as follows: January fall rate 13% Goal not met February fall rate 16% Goal not met March fall rate 9% Goal met April fall rate 10% Goal not met May all rate 14% Goal not met The ADM stated the facility will work on identified repeated deficiencies. The ADM also reports that they were finding different way to improve , by having extra staff , talk with family members , having their Quarterly meeting and as needed if there was any emergency so that they would be able to meet their goals. During a review of the facility's undated policy and procedure (P&P) titled, Quality Assurance and Performance Improvement, (QAPI) indicated that the responsibilities of the QAPI committee are to: a. Collects and analyze performance indicator data and other information: b. Identify, evaluate, monitor and improve facility system processes that support the delivery of care and services c. Identify and help resolve negative outcomes and/ or care quality problems identified during the QAPI process. d. Utilizes the root cause analysis to help identify where identified problems points to underlying systematic problems e. Help departments, consultants and ancillary services implement systems to correct potential and actual issues in quality of care.
CONCERN (F)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0925 (Tag F0925)

Could have caused harm · This affected most or all residents

Based on observation and interview the facility failed to provide an effective pest control by: a. Preventing an infestation of tiny flies (Drain Flies) in the kitchen. This deficient practice had the...

Read full inspector narrative →
Based on observation and interview the facility failed to provide an effective pest control by: a. Preventing an infestation of tiny flies (Drain Flies) in the kitchen. This deficient practice had the potential to affect the residents by causing disease for the 127 residents who eat food in the kitchen. Findings: During an initial observation in the kitchen on 6/9/2025 at 8:16 a.m. with the Dietary Supervisor (DS), two small flies were seen flying over a mat placed in front of the triple sink. Additionally, there were small white particles and a black tarry substance observed on the floor under the sink. The mat was noted to be sticky. DS mentioned that staff are unable to clean under the sink. During a second kitchen inspection on 6/10/2025 at 9:15 a.m., multiple tiny flies flew from the mat in front of the three sinks. The area around the drain under the mat was moist. During a record review of the Orkin Service Report (OSR) dated 5/21/2025 at 8:09 a.m., a technician checked the kitchen for any pest activity and treated as needed. During a review of the records for the floor cleaning assignment, a signature was missing for the date of 6/9/2025. The DS stated that if it is not signed, it is considered not done. During an interview on 6/10/2025 at 12:34 p.m., DS mentioned that the floors and underneath the sink should be cleaned daily. DS noted that water accumulation and dirt on the floor can harbor microorganisms. Additionally, DS stated that flies in the kitchen carry germs, which can potentially cause illness among residents. During a review of the facility's Policy and Procedure (P&P) titled, Sanitation: dated 2023, the P&P indicates, on a monthly basis, a pest control company will inspect and service the Food & Nutrition Services Department. If at any time additional servicing is needed, the pest control is notified.
May 2025 1 deficiency
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0553 (Tag F0553)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure two of five sampled residents (Resident 1 and 2) participate...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure two of five sampled residents (Resident 1 and 2) participated in care plan meetings to discuss her care and discharge goals. This deficient practice had the potential to violate Resident 1 and 2's right to be an active participant in her care. Findings: a. During a review of Resident 1's admission record (Face Sheet), the Face Sheet indicated Resident 1 was initially admitted to the facility on [DATE] and was readmitted on [DATE] with diagnoses including hemiplegia (total paralysis of the arm, leg, and trunk on the same side of the body) and hemiparesis (one sided muscle weakness) following cerebral infarction (blood flow to a part of the brain is blocked that leads to tissue death) affecting right dominant side and aphasia. During a review of Resident 1's History and Physical (H&P) dated 4/5/2025, the H&P indicated Resident 1 has limited decision-making capacity. During a review of Resident 1's Minimum Data Set ([MDS] a resident assessment tool) dated 4/14/2025, the MDS indicated Resident 1's cognitive skills (the mental action or process of acquiring knowledge and understanding through thought, experience, and senses) were mildly impaired. The MDS indicated Resident 1 was dependent on chair/bed-to-chair transfer, toilet transfer, toileting hygiene, bathing, putting on shoes, lower body (below waist) dressing, and required moderate assistance (provide less than half the effort) for eating, oral hygiene, personal hygiene, and upper body (above waist) dressing. During an interview on 5/6/2025 at 2:44p.m. at Social Service Assistant (SSA), SSA stated the family decided to take her home on 5/5/2025 SSA stated the doctor tried explaining it to FM 1, but stated she wasn't understanding and indicated if Resident 1 continued to make progress during rehabilitation, they can continue billing the insurance, but if not, they cannot continue to bill the insurance as it would be considered fraudulent SSA stated IDT meeting discusses how the resident is doing and the Social Service (SS), nursing, activities, and dietary attend the meeting. SSA stated she would document when a resident had an IDT meeting, but indicated there were no IDT meetings done for Resident 1 as they did not want to appoint one person to be in charge. SSA stated IDT meetings are important when families are not decisive and would like all the residents to have one to eliminate any confusion. During an interview on 5/6/2025 at 3:38p.m. with FM 1, FM 1 stated GACH told her sister that Resident 1 was supposed to get four to six weeks of rehabilitation service at the facility. FM 1 stated when she spoke to the doctor from the facility, she informed her Resident 1 was not progressing. FM 1 stated her understanding that Resident 1 had four to six weeks at the facility, but it has only been there for three weeks and four days. FM 1 stated since the doctor from GACH said four to six weeks, the plan was to have Resident 1 stay for six weeks and bring her home. FM 1 stated the tone the doctor used was disrespectful, she was tapping on her screen, very contentious. FM 1 stated they felt like the doctor would not treat Resident 1 with dignity and respect that she deserves. FM 1 stated she does not know regarding the first IDT meeting as it was not offered and was mentioned to her, but it could have been mentioned to her other family members that live within the vicinity. b. During a review of Resident 2's Face Sheet, the Face Sheet indicated Resident 2 was admitted to the facility on [DATE] with diagnoses including muscle wasting, spinal stenosis (condition occurs when the space in the backbone narrows), and radiculopathy (nerve root in the spine is compressed or irritated). During a review of Resident 2's H&P dated 4/22/2025, the H&P indicated Resident 2 does not have the capacity to understand and make decisions. During a review of Resident 2's MDS dated [DATE] the MDS indicated Resident 2's cognitive skills were mildly impaired. The MDS indicated Resident 2 was dependent in toileting hygiene, lower body dressing, putting on footwear, required maximal assistance (provides more than half the effort) for chair/bed-to-chair transfer, toilet transfer, bathing, and required supervision for eating, oral hygiene, upper body dressing, and personal hygiene. The MDS indicated Resident 1 utilized a walker and a wheelchair. During an interview on 5/6/2025 at 3:23p.m. with SSA, SSA stated she does not recall doing an IDT meeting for Resident 2 and does not see any IDT meeting documentation. SSA stated she should have had an IDT meeting and realistically, all residents should have one. During an interview on 5/6/2025 at 3:10p.m. with Director of Nursing (DON), DON stated IDT meeting is composed of several different department heads to discuss care issues, concerns, or speak with the resident or family with plans or any ongoing concerns. DON stated they need to have IDT meetings for each resident in the facility and at minimum would do it quarterly or as needed if there are any concerns that have been identified. DON stated IDT meeting is done upon admission within 14 days. DON stated if the family prefers to have the IDT meeting earlier, they will accommodate as needed. DON stated discharge planning is discussed between IDT meetings and options are given. DON stated for custodial care (non-medical assistance provided to individuals who require help with daily activities due to physical, mental, or cognitive limitations) IDT meetings are done quarterly, however for residents who require skilled needs are here for a short period of time, so they do IDT meetings within the first 14 days with an active discussion about how the residents will be discharged . DON stated if there are no IDT meetings, the plan of care would not be as cohesive as they want it to be, questions or concerns would not be addressed in a timely manner, and expectations about care would not be discussed. During a review of the facility's Policy and Procedure (P&P) titled, Interdisciplinary Team Participation, undated, the P&P indicated it is the policy of this facility to have the Social Service Department participate in the Interdisciplinary team. According to CFR §483.20(k)(2), Interdisciplinary means that professional disciplines, as appropriate, will work together to provide the greatest benefit to the resident. Social Service staff. participate in all IDT functions, including but not limited to: 1) MOS 3.0 Assessment 2) Care Planning 3) Behavior Management 4) Weight Variance, if requested 5) Restraint Review 6) All-Staff in-service education 7) Rehab Meeting, if requested 8) Discharge Planning meetings 9) Bioethics 10) Quality Assurance/Utilization Review During a review of the facility's P&P titled, Resident Rights, undated, the P&P indicated residents are entitled to exercise their rights and privileges to the fullest extent possible. During a review of the facility's P&P titled, SOCIAL SERVICE DEPARTMENT ROLE & FUNCTION/Medically-related Social Services, undated, the P&P indicated life in a skilled nursing facility, even for a short stay, can present psychosocial challenges which can impact a resident's ability to attain and maintain his or her highest level of psychosocial functioning. Social Service staff support residents in a variety of ways to prevent and minimize psychosocial decline and empower residents. Social Service interventions will be documented in the resident's care plan, with accompanying documentation in the Social Service progress notes in the medical record
Oct 2024 1 deficiency
MINOR (B) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Minor Issue - procedural, no safety impact

Deficiency F0912 (Tag F0912)

Minor procedural issue · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to provide 80 square feet of space per resident in multip...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to provide 80 square feet of space per resident in multiple resident bedrooms (29 and 30). This failure to provide adequate space had the possibility for negatively affecting the residents' quality of life, safety, and plan of care. Findings: During an observation on 10/22/2024 at 3:05 p.m. and interview with the Maintenance Supervisor (MS), MS completed the measurements of the following rooms: a. Resident room [ROOM NUMBER] and 30 measured 77.66 square feet (sq ft). MS stated the required room size for three of residents living in each of these room was 240 sq ft. During an observation on 10/22/2024 at 3:05 p.m., the residents' quality of life, care needs and safety were not adversely affected by the room size. Residents residing in rooms [ROOM NUMBERS] did not complain of the room space. During an interview with the Administrator on 10/22/2024 at 3:48 p.m., a room waiver for room [ROOM NUMBER] and room [ROOM NUMBER] has not been submitted by the facility for 2023 or 2024.
Aug 2024 1 deficiency
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure Certified Nursing Assistant 1 (CNA 1) followed ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure Certified Nursing Assistant 1 (CNA 1) followed proper hand hygiene for contact isolation (the use of personal protective equipment [PPE - gown, mask, and gloves] for patients with diseases [illness or sickness characterized by specific signs or symptoms] caused by bacteria [germs] and viruses [a type of germ which causes disease] that are spread through direct and indirect contact) for Clostridioides difficile ([C. diff] a bacteria that causes diarrhea [the passage of three or more loos or liquid stools in one day or more frequent passage than is normal for the individual] and inflammation [the body ' s immune system ' s (body ' s protection against germs) response to an irritant] in the large intestine) for one of three sampled residents (Resident 2) when CNA 1 did not wash her hands with soap and water after providing direct care to Resident 2. This deficient practice has the potential to spread contagious bacteria and spores such as C.diff to other residents. Findings: During a review of Resident 2 ' s admission Record (Face Sheet), the Face Sheet indicated Resident 2 was admitted to the facility on [DATE] with diagnoses including enterocolitis (inflammation in the intestines) due to C.diff. During a review of Resident 2 ' s Minimum Data Set ([MDS] a standardized assessment and care screening tool) dated 7/1/2024, the MDS indicated Resident 2 ' s cognition (the mental action or process of acquiring knowledge and understanding through thought, experience, and the senses) was severely impaired and Resident 2 was dependent (helper does all the effort) on facility staff for completion of activities of daily living ([ADLs] eating, personal hygiene, and transfers). During a review of Resident 2 ' s Order Summary Report (Physician ' s Order), dated 8/13/2024, the Physician ' s Order indicated Resident 2 required contact isolation for C.diff. During a review of the Isolation Sign (a sign placed outside of a patient ' s room indicting what type of precaution they are on, and which PPE should be used upon entering the room) outside of Resident 2 ' s room, the Isolation Sign indicated Resident 2 was on Contact and Spore (a cell which certain bacteria produce to defend itself) Precautions. The Isolation Sign indicated facility staff and visitors should be cleaning hands with soap and water upon exiting the room. During an observation on 8/26/2024 at 12:29 p.m. outside of Resident 2 ' s room, CNA 1 was observed removing her gown and gloves, applied hand sanitizer to both of her hands, then proceeded to walk down the hallway to get Resident 2 some blankets. CNA 1 did not wash her hands with soap and water upon exiting Resident 2 ' s room. During an interview on 8/26/2024 at 12:29 p.m., CNA 1 stated she knew Resident 2 was on contact isolation for C.diff and only used hand sanitizer upon exiting Resident 2 ' s room but should have washed her hands with soap and water. CNA 2 stated all staff should wash their hands upon exiting Resident 2 ' s room to prevent the spread of germs to residents and staff. During an interview on 8/26/2024 at 2:43 p.m., the Director of Nursing (DON) stated C.diff cannot be killed by hand sanitizer alone, staff should be washing their hands with soap and water after providing care to residents in contact isolation for C.diff. The DON stated if staff do not preform the correct hand hygiene, there is a risk of transferring germs and bacteria to residents and staff. During a review of facility ' s policy and procedure (P/P) titled Handwashing/Hand Hygiene undated, the P/P indicated when there is likely exposure to spores (i.e., C-diff) all employees must wash their hands for 30-60 seconds with soap and water as alcohol-based hand rubs are inactive against the effective removal of spores.
Jun 2024 13 deficiencies 2 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0692 (Tag F0692)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, and record review, the facility failed to prevent the resident's unplanned severe weight loss (a weight loss...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, and record review, the facility failed to prevent the resident's unplanned severe weight loss (a weight loss greater than 5 % in one month, greater that 7.5% in three months and greater than 10 % in 6 months) of nine (9) pounds ([lbs.] 9.57 percent [%] in one month for one of two sampled residents (Resident 129). The facility failed to: 1. Ensure the Registered Dietician's ([RD] a health professional who has a special training in diet and nutrition) recommendation to increase Resident 129's enteral (form of nutrition that is delivered into the digestive system as liquid) feeding from 250 milliliter ([ml] unit of measurement) four times per day to 250 ml five times per day totaling 1500 calories ([kCal] energy people get from the food and drink they consume, and the energy they use in physical activity) were followed and provided. 2.Ensure staff monitored Resident 129's weight and reported the resident's five pounds weigh loss to Resident 129's physician and RD in accordance with the care plan titled Risk for Malnutrition (lack of significant nutrients [substance used in the body to function] leading to physical decline). 3. Ensure the facility's staff informed the RD when Resident 129 had a 9.57 % weight loss from 4/29/2024 through 6/1/2024 for RD to evaluate and make necessary recommendations on Resident 129's enteral feeding formula to provide Resident 129 with a sufficient amount of calories and nutrients to prevent Resident 129's severe weight loss of 9.57 % in 34 days in accordance with the facility's policy and procedure (P&P) titled, Nutrition (Impaired/Unplanned Weight Loss-Clinical Protocol. 4. Ensure licensed staff followed facility's P&P titled, Weight Assessment and Intervention and immediately notified the Dietician in writing of Resident 129's weight loss of 5% or more since the last weight assessment on 4/29/2024. 5. Ensure the RD completed Resident 129's full nutritional assessment upon admission to the facility on 4/27/2024 and monitor Resident 129's weight and caloric intake, who was receiving tube feeding nutrition, and makes appropriate recommendations for intervention to enhance tolerance and nutritional adequacy of tube feedings per facility's P & P. These deficient practiced resulted in Resident 129's severe weight loss of 9.57 % in 34 days and placed Resident 129 at risk for malnutrition, dehydration (dangerous loss of body fluid caused by illness, sweating, or inadequate intake), skin break down, having feelings of depression and hopelessness. Findings: During a review of Resident 129's admission Record, indicated Resident 129 was admitted to the facility on [DATE], with diagnoses including amyotrophic lateral sclerosis ( a nervous system disease that affects nerve cells in the brain and spinal cord), dysphagia (difficulty of swallowing), gastrostomy tube ([GT] a soft tube surgically inserted directly into the stomach to administer medication, fluids and nutrition), deep tissue injury ([DTI] purple or maroon localized area of discolored intact skin or blood-filled blister due to damage of underlying soft tissue from pressure) to a sacral (tailbone) area, and muscle wasting (loss of muscle tissue). During a review of Resident 129's History and Physical (H&P), dated 4/28/2024, the H&P indicated, Resident 129 did not have decision making capacity. During a review of Resident 129's Minimum Data Set ([MDS], a standardized assessment and care screening tool]) dated 5/1/2024, the MDS indicated Resident 129 was dependent (helper does all of the effort) on staff with oral hygiene, toileting hygiene, and personal hygiene. The MDS indicated Resident 129 height was five feet (unit of measurement) and three inches (unit of measurement) and weighed 94 pounds ([lbs.] unit of weight). The MDS indicated Resident 129 was receiving nutrition via GT. During a review of Resident 129's Weights and Vitals Summary from 4/29/2024 to 6/1/2024, the Weights and Vitals Summary indicated the following resident's weekly weight: 1. On 4/29/2024 - 94 pounds. 2. On 5/5/2024- 93.4 pounds. 3. On 5/12/2024- 87 pounds (7.0 pounds [7.45%] weight loss). 4. On 5/19/2024- 87.4 pounds (6.6 pounds [7.02%] weight loss). 5. On 5/26/2024- 85.4 pounds (8.6 pounds [9.15 %] weight loss). 6. On 6/1/2024- 85 pounds (9.0 pounds [9.57 %] weight loss). During an interview on 6/12/2024 at 10:30 a.m., the License Vocational Nurse (LVN 5) stated when Resident 129 had a weight loss of nine (9) pounds from 4/29/2024 to 6/1/2024, a change of condition (COC) documentation should have been done, Resident 129's physician and RD should have been informed and an Interdisciplinary team ([IDT]- group of healthcare professional s working together to plan the care needed for each residents) meeting should be held immediately in order to address the resident's weight loss and recommend interventions to prevent further resident's weight loss. LVN 5 stated Resident 129 was getting weighed weekly due to a weight loss. LVN 5 stated she did not report Resident 129's severe weight loss of 9 pounds (9.57 %) to RD and the physician. LVN 5 stated severe weight loss should be reported immediately to Resident 129's physician and RD because Resident 129 could lose more weight that can lead to hospitalization due to malnutrition. During a review of Resident 129's care plan titled, Risk for Malnutrition, dated 4/28/2024 indicated a goal for Resident 129 was not to have significant weight loss of five lbs. in one month (5 % in one month, 7.5 % in 3 months, 10 % in 6 months). The care plan interventions included to monitor the resident's weight and report five lbs. weight loss to the physician and RD promptly and notify the physician of significant weight change and refer to dietician. During a review of Resident 129's Care Plan titled GT feeding, dated 4/28/2024 indicated a goal for Resident 129 was to maintain adequate nutrition and hydration (fluid intake) status and to have a stable weight with no signs and symptoms of malnutrition or dehydration. During a review of RD's Nutrition/Dietary Progress Note dated 4/28/2024 and timed at 6:55 p.m., the Nutrition/Dietary Progress Note indicated Resident 129 was receiving 250 ml of enteral feeding with formula Fibersource 1.2 four times daily. Resident 129 body mass index ([BMI] measure body weight to height and whether a resident has a healthy weight) was 17.9 (BMI between 18.5 and 24.9 -underweight, BMI healthy range -between 25 and 29.9, and BMI between 30 and 39.9- overweight). The RD's Nutrition/Dietary Progress Note indicated RD's recommendation to change GT enteral feeding formula to 250 ml five times a day to provide Resident 129 with 1250 ml (1500 kcal) daily. The RD's Nutrition/Dietary Progress Note indicated the RD's full assessment of Resident 129 nutritional needs will follow. During a review of Resident 129's Nutritional Review Screening, dated 4/29/2024 completed by Dietary Supervisor (DS) indicated based on Resident 129's usual body weight (UBW) of 115 lbs. the resident's estimated daily need for calories were 1495-1709 kcal. The Nutritional Review Screening indicated recommendation including change enteral feeding to 250 ml five times daily to provide 1250 ml equal to 1500 kcal, 67 grams of protein, 1512 ml of free water (fluids with no salt content), and Multivitamins (dietary supplement containing all or most of the vitamins) with Minerals. During a review of Resident 129's Medication Administration Record (MAR) dated 5/2024, the MAR indicated the Enteral Feeding Order for Fibersource HN 1.2 four times a day as follows: 250 ml (Breakfast), 500 ml (Lunch), 250 ml (Dinner), 250 ml (Bedtime). During a review of Resident 129's Physician Order Summary dated 5/2024, indicated Enteral Feeding Order for Fibersource HN 1.2 four times a day as follows: 250 ml (Breakfast), 500 ml (Lunch), 250 ml (Dinner), 250 ml (Bedtime). During a review of Resident 129's MAR for the month 5/2024 indicated Resident 129 only received 250 ml of Fibersource for lunch instead of 500 ml as ordered: 1. From 5/3/2024 to 5/13/2024 (10 days) - Fibersource 250 ml. 2. On 5/14/2024- Fibersource 300 ml. 3. From 5/18/2024 to 5/20/2024 (there days)- Fibersource 250 ml. 4. On 5/27/2024- Fibersource 250 ml. During a concurrent interview and record review on 6/12/2024 at 11:05 a.m., the Director of Nursing (DON) stated residents (in general) with weight loss will trigger for weekly weight variance review (report generated to determine how much weight a resident has lost and recommendations to prevent further weight loss) and a weekly weight variance meeting to discuss the plan of care for a residents (in general). The DON stated Resident 129 was triggered for a weight variance weekly review meetings because the resident was at high risk for weight loss. The DON stated weekly weight variance meeting allows the facility to monitor Resident 129's weight and allows the facility to ensure that implemented interventions were successful. The DON stated weekly weight variance meeting also allows to evaluate if other interventions could be implemented to prevent further weight loss. The DON stated the weekly weight variance meetings were documented on the Progress Notes by nursing and the RD. After a review of Resident 129's Nurses Progress Notes and RD Progress Notes the DON stated, there was no documentation from nursing and the RD for the weekly variance meetings to address the resident's weight loss. The DON stated, if there was no documentation it means it was not done. After the DON reviewed Resident 129's Initial Nutritional Assessment, the DON confirmed the last documentation from the RD was the initial mini nutritional assessment (nutrition screening and assessment tool that can identify residents who are malnourished or at risk of malnutrition) done on 4/29/2024. The DON stated 9.57 % weight loss was considered a severe weight loss and required weekly monitoring by the facility. The DON stated the RD should have monitor Resident 129 to ensure the resident did not lose additional weight. The DON stated the staff communicates with the RD via text message regarding the weekly weight variance meetings. The DON stated it was the licensed nurses responsibility to ensure Resident 129's weight loss was communicated to the resident's physician and RD in order to prevent negative outcomes such as severe weight loss and dehydration. The DON stated when residents (in general) do not receive adequate nutrition they could have negative effects such as skin break down and malnutrition. During a concurrent interview and record review on 6/12/2024 at 1:30 p.m. with RD, the RD stated she was responsible for nutritional assessments of residents on admission and quarterly assessment which includes evaluating and addressing residents' (in general) high risk for weight loss. RD stated residents (in general) who were on GT feedings should be weighed weekly and a weekly variance meeting should be held to discuss interventions to prevent weight loss. The RD stated she does not attend the weight variance meeting; the licensed staff communicates with her via text message about any weight loss and other concerns discussed during the weight variance meeting. The RD stated she follows up with residents (in general) that have weight loss weekly. The RD stated she has done Resident 129's mini nutritional assessment on 4/29/2024 and a full assessment of Resident 129 nutritional status and needs should have been done as well. The RD confirmed that Resident 129's full assessment had not been done since the resident's admission to the facility on 4/27/2024. After RD reviewed her weekly progress notes, for Resident 129, she stated there was no weekly documentation for Resident 129's weight loss. Resident 129's Nutrition/Dietary Progress, dated 4/28/2024, indicated recommendation to change GT feeding to 250 ml five times daily to provide 1250 ml equivalent of 1500 kcal. with full assessment to follow. Reviewed Resident 129's MAR date 5/2024, the MAR indicated Enteral Feed Order four times a day Fibersource HN 1.2 250 ml (Breakfast), 500 ml (Lunch), 250 ml (Dinner), 250 ml (Bedtime). The RD stated Resident 129's enteral feeding order for 250 ml four times a day was not providing enough calories to Resident 129 and confirmed the facility's staff did not follow with her recommendation to increase the feeding to 250 ml five times a day. The RD stated Resident 129 did not receive the estimated needs of 1511 to 1727 kcal a day. The RD stated 9.57 % weight loss in 34 days was considered a severe weight loss and the facility's staff should have reported it immediately to Resident 129's physician and her. The RD stated Resident 129 could have become malnourished which would cause further skin breakdown from not receiving enough calories and protein per day. During a concurrent interview and record review on 6/12/2024 at 2:09 p.m., with LVN 1, LVN 1 stated during weekly weight variance meetings residents (in general) weight loss was discussed. LVN 1 stated any recommendations from the weekly weight variance meetings were communicated to the RD via text message and documented on the Nurses Progress Notes. LVN 1 reviewed Resident 129's Nurses Progress Notes and stated there was no documentation RD was notified about Resident 129's severe weight loss. LVN 1 confirmed that there was no documentation for Resident 129's weekly weight variance meeting and it was not held since Resident 129's admission on [DATE]. LVN 1 stated if it was not documented it means it was not done. LVN 1 stated 9.57 % weight loss in 34 days was considered a severe and had the potential to cause a negative outcome for Resident 129's health. During an interview on 6/12/2024 at 2:23 p.m., the Dietary Supervisor (DS) stated she attends the weekly weight variance meetings. The DS stated she communicates with RD on Mondays regarding the weekly weight variance meeting. The DS stated there was no weight variance meeting held for Resident 129's severe weight loss of 9.57 % in 34 days from 4/27/2024 to 6/1/2024. The DS stated it was important to monitor Resident 129's weight to ensure that the interventions were effective in order to prevent further weight loss. The DS stated Resident 129's severe weight loss put the resident at risk for dehydration, malnutrition, skin breakdown and hospitalization. The DS stated nursing staff document the weekly weight variance meetings in a resident's (in general) Progress Notes. The DS stated 9.57% of weight loss in 34 days was considered a severe weight loss. During a review of the facility's P&P titled, Weight Assessment and Intervention dated 9/2008, indicated, Any weight change of 5% or more since the last weight assessment will be retaken the next day for confirmation. If the weight is verified, nursing will immediately notify the Dietician in writing. Verbal notification must be confirmed in writing. The Dietician will review the unit weight record by the 15th of the month for follow individual weight trends over time. During a review of the facility's P&P titled, Enteral Nutrition, dated 11/2018, the P&P indicated, The dietician with input from the provider and nurses: estimate calorie, protein, nutrients, and fluid needs. Determine whether the resident's current intake is adequate to meet his or her nutritional needs. The dietician monitors residents who are receiving enteral nutrition and makes appropriate recommendations for intervention to enhance tolerance and nutritional adequacy of enteral feedings. During a review of the facility's P&P titled, Nutritional Assessment, [undated], indicated, The Dietician, in conjunction with the nursing staff and healthcare practitioners, will conduct a nutritional assessment for each resident upon admission and as indicated by a change in condition that place the resident at risk for impaired nutrition. During a review of the facility's P&P titled, Nutrition Impaired/Unplanned Weight Loss-Clinical Protocol, [undated], indicated, The Physician and staff will closely monitor residents who have been identified as having impaired nutrition or risk factors for developing impaired nutrition. Such monitoring may include evaluating the care plan to determine if the interventions are being implement and whether they are effective in attaining the established nutritional and weight goals.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0697 (Tag F0697)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure the resident, who had a Stage 4 pressure ulcer ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure the resident, who had a Stage 4 pressure ulcer (wound that penetrate all layers of skin exposing muscles, tendons [tissue that unites a muscle with a bone] cartilage {tissue that lines a joints}, and bones caused by prolonged pressure on the skin) to sacrum (tailbone area), did not experience unnecessary pain and suffering during pressure ulcer treatment and repositioning for one of five sampled residents (Resident 73). The facility failed to: 1. Ensure the Registered Nurse (RN 6) provided Resident 73 with effective pain relieve when Resident 73 loudly screamed and moaned during the sacral pressure ulcer treatment. 2. Evaluate the pain relieve effectiveness of Tylenol (pain medication) 325 milligrams ([mg]-a unit of measurement) two tablets given to Resident 73's as ordered prior to pressure ulcer treatment before the start of pressure ulcer treatment. 3. Notify Resident 73's physician (MD 1) of Resident 73's pain management with Tylenol was unsuccessful when Resident 73 continue to moan and scream during the pressure ulcer treatment on 6/10/2024 and 6/13/2024. 4. Ensure RN 6 identified frequency, location, quality, onset, and manner of pain when Resident 73's experienced pain, in accordance with the resident's Care Plan titled, Potential for altered comfort which maybe evidenced by grimacing or moaning related to a Stage 4 pressure ulcer to the sacral area, bilateral knee osteoarthritis (degenerative joint disease) and pancreatic mass (tumor that forms in the cells of pancreas) dated 4/20/2023. These failures resulted in Resident 73's to experience severe, unrelieved, and uncontrolled pain manifested by loud screaming and moaning during pressure ulcer treatment and personal care on 6/10/2024 and 6/13/2024. Findings: During an observation and concurrent interview on 6/10/2024, at 10:09 a.m., Resident 73 was observed screaming, groaning, and moaning with facial grimaces (facial expression usually suggesting pain or disgust). Concurrently, during an interview, Resident 73 nodded the head Yes and grimaced when asked if she was having pain. During an interview on 6/10/2024, at 10:09 a.m. with Resident 62 (Resident 73's roommate) Resident 62 stated Resident 73 was constantly groaning and moaning especially when staff was cleaning or doing personal care. Resident 62 stated staff members were aware of Resident 73's moaning and screaming. During an observation of RN 6 preparation for Resident 73's sacral pressure ulcer treatment on 6/10/2024, at 10:30 a.m., in Resident 73's room, Resident 73's physician (MD 1) entered the resident 's room and informed RN 6 he (MD 1) will put an order for Norco (narcotic [used to treat moderate to severe pain] pain medication) to administer prior to pressure ulcer treatment as Resident 73 was observed moaning and screaming. RN 6 replied to MD 1 that Resident 73 does not need Norco as Resident 73 will receive Lidocaine spray (anesthetic topical [applied to the skin] spray) prior to the pressure ulcer treatment. During an observation Resident 73's pressure ulcer treatment on 6/10/2024, at 10:32 a.m., Resident 73 was observed screaming and moaning when RN 6 positioned Resident 73 on her back with head of the bed in a flat position. RN 6 left Resident 73's room and ask another staff member to assist during pressure ulcer treatment. RN 6 came back with the Director of Staff Development (DSD). RN 6 and DSD turned Resident 73 to her right side. Resident 73 continuously moaned and screamed. RN 6 was observed to spray Resident 73's sacral Stage 4 pressure ulcer surrounding area with Lidocaine spray before the start of treatment. Resident 73 screamed and moaned louder when RN 6 cleaned the reddened surrounding area of Stage 4 sacral pressure ulcer with Hibiclens (liquid antibacterial cleanser) and applied Collagen powder (wound dressing that is applied topically) to the pressure ulcer. RN 6 completed the pressure ulcer treatment despite Resident 73's moaning and screaming. During a review of Resident 73's admission Record, the admission Record indicated Resident 73 was originally admitted to the facility on [DATE] and was readmitted on [DATE] with diagnoses including unspecified dementia (loss of cognitive functioning such as thinking, remembering, and reasoning to such an extent that it interferes with a person's daily life and activities), osteoarthritis of both knee (degenerative joint disease), a Stage 4 pressure ulcer to the sacral region, and attention/ concentration deficit. During a review of Resident 73's History and Physical (H& P) dated 5/9/2024, indicated Resident 73 was not able to express needs, communicate, not to follow commands and talked in full sentences. Resident 73 had no decisions making capacity. During a review of Resident 73's Minimum Data Set ([MDS] standardized assessment and care screening tool) dated 5/1/2024, indicated Resident 73 was dependent on staff for bed mobility, moving from sitting on side of bed to lying flat on bed, toileting hygiene, bathing, dressing, personal hygiene, and oral hygiene. The MDS indicated Resident 73 had a Stage 4 pressure ulcer on the sacrum (sacral area). During a review of Resident 73's Physician's Order dated 6/10/2024, the Physician's Order indicated the order for Lidocaine spray to apply to the resident's sacral area topically every day for pain management during sacral pressure ulcer treatment. During a review of Resident 73's Physician Order dated 4/20/2024, the Physician order indicated to cleanse sacral wound with Hibiclens, pat dry, apply Collagen powder to the pressure ulcer base then apply Hydrofera Blue (special dressing type) then cover with Allevyn (dressing) every day (7 a.m.to 3 p.m.) Monday, Wednesday, and Friday. During an interview on 6/10/2024, at 10:45 a.m., and subsequent interview on 6/10/2024, at 11:22 am., with RN 6, RN 6 stated the Lidocaine spray was the only medicine he used to help with Resident 73's pain during pressure ulcer treatment. During a concurrent interview and record review on 6/12/2024 at 9:36 a.m., with DSD, the DSD stated for residents, who are not able to verbalize pain, the facility was using the facial pain scale tool (a picture with of different facial expressions referencing different pain level to help a resident effectively communicate the severity of their physical pain) to assess pain level. The DSD stated Resident 73 screamed loudly when RN 6 cleansed Resident 73's pressure ulcer with Hibiclens and when the Collagen powder was applied to the resident's Stage 4 sacral pressure ulcer. The DSD stated when Resident 73 screamed loudly during the pressure ulcer treatment, RN 6 should have stopped the treatment, assessed Resident 73 pain level, including the non-verbal cues like facial grimacing, notified the physician, and provide Resident 73 pain medication. The DSD reviewed Resident 73's Medication Administration Record (MAR) and stated Resident 73 received Tylenol 325 mg two tablets on 6/10/2024, at 10:07 a.m., prior to pressure ulcer treatment for pain level 3 out of 10 on a pain scale rating from zero to ten (pain screening tool using numerical value to assess the level of pain ranging from 0 to 3-mild pain, from 4 to 6- moderate pain, and from 7 to 9-severe pain, and 10- the worse pain possible). The DSD stated based on Resident 73 screaming and moaning during sacral pressure ulcer treatment Tylenol given at 10:07 a.m. was not effective to alleviate Resident 73's pain. The DSD stated Resident 73 experienced excruciating (extremely painful, causing intense suffering) pain and discomfort during the pressure ulcer treatment which was unnecessary pain. The DSD stated RN 6 should have asked the physician for a stronger pain medication after the resident screamed during sacral pressure ulcer treatment on 6/10/2024. During an interview on 6/12/2024, at 3:31 p.m., with Treatment Nurse (TN 1), the TN 1 stated she coordinated Resident 73's pressure ulcer treatment with the charge nurse in order to give pain medication to the resident before pressure ulcer treatment. TN 1 stated for residents, who could not verbalize pain and its severity, the staff used non-verbal indication of pain like screaming, moaning, or crying, and facial grimace. TN 1 stated Resident 73 screamed and moaned during pressure ulcer treatment, and it was an indication the resident was in excruciating pain. TN 1 stated Lidocaine spray was used topically and only applied on the skin and would not be enough to help with the pain during treatment. TN 1 stated if the resident screamed and moaned during pressure ulcer treatment RN 6 should have stopped the treatment, call the physician because the Lidocaine spray was not effective in managing Resident 73's pain. TN 1 stated Resident 73 should be assessed for pain before and during pressure ulcer treatment. TN 1 stated Resident 73's unrelieved pain could affect her health and comfort if her pain was not managed effectively. During an interview and record review on 6/12/2024 at 4:08 p.m., RN 6 stated when Resident 73 screamed from pain during the pressure ulcer treatment, he should stopped the treatment and notified the Resident 73's MD 1. RN 6 stated on 6/10/2024, MD 1 came to the resident's room and told him (RN 6) about ordering Norco for pain because of the moaning and crying, and confirmed he told MD 1 Resident 73 did not need Norco because the Lidocaine spray was being applied to the pressure ulcer. RN 6 stated Resident 73's family did not want the resident to have any strong pain medication. RN 6 confirmed thru record review of Interdisciplinary Team Meeting ([IDT]-a healthcare team members and resident / family representative collaborate, solve problems, plan, and coordinate care of the resident) Notes and Care Plan there was no documentation of Resident 73's family not wanting strong pain medication to be given to Resident 73 during pressure ulcer treatment. RN 6 stated Resident 73 was suffering from pain during a sacral pressure ulcer treatment manifested by the resident's screaming and moaning. RN 6 stated Resident 73 continued to suffer from pain because her pain was not addressed and managed during the pressure ulcer treatment on 6/10/2024. RN 6 stated Tylenol's pain relieve effectiveness was not evaluated prior to begin the treatment. During an observation on 6/13/2024, at 10:54 a.m., with TN 1 and Certified Nursing Assistant (CNA 5) in Resident 73's room, Resident 73 was observed starting moaning during repositioning. Resident 73 observed moaned louder as the TN 1 started to clean the surrounding skin area of the sacral pressure ulcer and applying the Collagen powder on the pressure ulcer. TN 1 observed to pause the pressure ulcer treatment and started reassuring the resident and massaging the resident's skin. TN 1 was observed to resume the treatment when Resident 73 stopped moaning. During an interview on 6/13/2024, at 12:45 p.m. the TN 1 stated Resident 73 moaned during pressure ulcer treatment due to pain. TN 1 stated the resident had dementia and it was hard to tell when the resident was in pain, but the presence of pain should still be addressed by staff by using the resident's facial clues, grimacing, moaning and jerky movement during treatment. During an interview on 6/13/2024, 2:04 p.m., CNA 5 stated every time she would clean and change Resident 73 after a bowel movement, the resident would moan and cry. CNA 5 stated Resident 73 would also moan during pressure ulcer treatment. During a review of Resident 73's Care Plan titled Potential for altered comfort evidenced by grimacing or moaning related to a Stage 4 pressure ulcer to the sacrum, bilateral knee osteoarthritis and pancreatic mass (tumor that forms in the cells of pancreas), dated 4/20/2023, the goal for Resident 73 was to be comfortable. The Care Plan's interventions included to identify frequency, location, quality, onset, and manner of expressed pain and administer medication as ordered. During a review of Resident 73's Care Plan titled, Resident has a Stage 4 sacral pressure ulcer on admission, initiated on 10/30/2023 indicated one of the interventions was to assess pain and discomfort at site of the altered skin area. During a concurrent interview and record review of Resident 73's Physician Order on 6/13/2024, at 3:31 p.m. with Director of Nursing (DON), the DON confirmed the physician order for Tylenol 325 mg two tablets for pain relief did not include the pain parameters, however, Resident 73 had an order to monitor the intensity of pain using numerical pain rating scale. The DON stated pain level was not assessed properly and Resident 73's pain was not managed effectively during pressure ulcer treatment. The DON stated Resident 73 should be assessed for pain during and after pressure ulcer treatment. The DON stated if the resident was experiencing pain by screaming and moaning, the pressure ulcer treatment should be stop, the staff should have assessed the resident for pain, addressed the pain if pain was present, called Resident 73's physician to notify about the presence of pain. The DON stated Resident 73 had experienced undue suffering which could have been prevented if the resident was assessed properly for pain management. During a review of facility's policy and procedure (P&P) titled Pain Assessment and Management, undated, the P&P indicated to observe the resident during rest and movement for physiologic and behavioral (non-verbal) signs of pain. The P& P indicated possible behavioral signs of pain are verbal expressions such as groaning, crying, screaming, facial expressions such as grimacing, frowning, behavior such as resisting care, irritability, or depression. The P&P indicated to review resident's treatment record to identify any situations or interventions where an increase in the resident's pain may be anticipated such as treatment like wound care or dressing changes. During a review of facility's P&P titled Pressure Ulcer Treatment, undated, the P&P indicated to review the resident's care plan to assess for any special needs of the resident. The P&P indicated for residents who had a Stage 4 Pressure Injury one of the guidelines was to manage pain during wound care. According to a review the article titled The Symptoms of Pain with Pressure Ulcer: A Review of the Literature, dated 5/2008 on website for Wound Care Leading Management and Prevention, pain is an issue in persons with pressure ulcers, measuring and managing pain will become more important for effective care with an aging population at risk for pressure ulcer development. https://www.hmpgloballearningnetwork.com/site/wmp/content/the-symptom-pain-with-pressure-ulcers-a-review-literature
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0584)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide a comfortable room temperature on one of five...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide a comfortable room temperature on one of five sampled residents (Resident 25). This deficient practice had the potential to place Resident 25 at risk for disturbed sleep and can negatively impact resident's comfort and health. Findings: During a review of Resident 25's admission Record, indicated the Resident 25 was initially admitted on [DATE] and was readmitted on [DATE] to the facility with diagnoses including presence of cardiac pacemaker( small electrical device implanted in the chest to treat abnormal heart rhythms), end stage renal disease (a medical condition in which a person's kidneys cease functioning on a permanent basis) , cardiomyopathy( heart muscles became stretched, weakened and unable to pump blood or function well) and diabetes( high blood sugar). During a review of Resident 25's Minimum Data Set ([MDS] standardized assessment and care screening tool) dated 4/25/2024, the MDS indicated Resident 25 had an intact cognition ((ability to think, understand, learn, and remember) and required partial /moderate assistance (helper does less than half the effort) with bed mobility and transferring from to and from a bed to chair. During a concurrent observation and interview on 6/11/2024, at 9:05 a.m., in Resident 25's room, Resident 25 was lying in bed covered with three blankets and a towel covering her head. Observed an electric fan located in Resident 25's roommate's bed. Resident 25 stated the facility put the air conditioner so high that she could not sleep at night and had to use four blankets to keep her warm. Resident 25 stated she had told an unnamed nurse and unnamed certified nursing assistant (CNA) and they had told her they are going to fix the room temperature. Resident 25 stated it was useless to talk about being cold especially during the night where the staff would just give her all the blankets they could find in the facility because nobody had helped her. Resident 25 stated she felt like she was going to get sick and had lost sleep because the room temperature was too cold for her. During an interview on 6/11/2024, at 4:28 p.m. with CNA 7, CNA 7 stated she gave Resident 25 because Resident 25 was complaining her room was cold. CNA 7 stated she did not notify anyone about Resident 25's complaint of being cold in her room. CNA7 stated the resident would remain cold and uncomfortable if her concern will not be addressed. During a telephone interview on 6/12/2024, at 9:22 a.m., with CNA 6, CNA 6 stated whenever she would go to Resident 25's room, the resident would ask to turn off the air conditioner because she was cold. CNA 6 stated Resident 25's roommate preferred the room to be cold and liked the electric fan turn on in her room at times. CNA 6 stated she offered blankets and towel for the head to Resident 25 when she was complaining of being cold. CNA 6 stated she did not notify the charge nurse because Resident 25's roommate liked her room cold. CNA 6 stated Resident 25's roommate would sometimes turn on the electric fan at night and liked the room temperature cold because of her asthma (condition in which the airways narrow and swell causing extra mucus production) and fibromyalgia (long term condition that involves widespread body pain and tiredness). CNA 6 stated she should have reported Resident 25's complaint about the room temperature being cold to the charge nurse. CNA 6 stated Resident 25 could get sick and might catch a cold (viral infection) if her concern was not properly addressed. During an interview on 6/12/2024, at 2:28 p.m., with Maintenance Director (MD), MD stated the air conditioning was centralized and he usually received a call from the staff if something needs to be repaired in the facility. The MD stated he only received a call from the staff on 6/11/2024 evening to check the thermostat because Resident 25's complaint of being cold in her room. MD stated Resident 25's roommate complained the room was hot and wanted the room to be cold but Resident 25 liked her room warm. MD stated he checked residents' room temperature everyday and had to maintain a temperature of 70 to 74 degrees Fahrenheit ([°F] unit of measurement). MD stated he did not keep a temperature log or document temperatures of the room. MD stated checking the temperatures of residents' room temperature was important to ensure the residents are comfortable. MD stated Resident 25 might not be able to sleep well if her room was cold. During an interview on 6/12/2024, at 2:43 p.m., with Social Service Director (SSD), SSD stated she spoke to Resident 25 yesterday evening after Licensed Vocational Nurse (LVN 8) told her about Resident 25's complaint of being cold in her room. SSD stated Resident 25 would not feel comfortable and might lose sleep if the temperature of the room is too cold for her. During an interview on 6/13/2024, at 3:31 p.m., with the Director of Nursing (DON), the DON stated she was not informed of Resident 25's complaint of being cold in her room. The DON stated cold room would cause discomfort to the resident. During a review of facility's policy and procedure(P&P) titled Homelike Environment revised 2/2021, indicated the facility's staff and management will maximize the characteristics of the facility that will reflect a personalized and homelike setting including a comfortable and safe temperature to the residents. The P&P indicated the staff will provide person-centered care that emphasizes the resident's comfort, and personal needs or preferences.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0604 (Tag F0604)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure one of one sampled resident (Resident 73) was ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure one of one sampled resident (Resident 73) was free of unnecessary physical restraints (any object or device that an individual cannot remove easily which restricts freedom of movement) by failing to: 1.Ensure on-going assessment and reevaluation of physical restraints' continuous use were conducted and documented. 2. Follow policy and procedure (P&P) regarding the use of restraints. These deficient practices had the potential to place Resident 73 at risk for unnecessary prolonged use of physical restraints, impaired blood circulation, skin injuries and contracture (permanent tightening of muscles that causes tissues and joints to become stiff and short). Findings: During a review of Resident 73's admission Record , indicated the Resident 73 was originally admitted to the facility on [DATE] and was readmitted on [DATE] with diagnoses including unspecified dementia (loss of cognitive functioning such as thinking, remembering, and reasoning to such an extent that it interferes with a person's daily life and activities) without behavioral disturbance, bilateral primary osteoarthritis of knee((degenerative joint disease both knees), pressure ulcer of sacral region stage 4,and attention/ concentration deficit. During a review of Resident 73's History and Physical (H&P) dated 5/9/2024, the H&P indicated Resident 73 was not able to express needs, communicate nor follow commands and talked in full sentences. The H& P indicated the resident did not have a capacity to make decisions. During a review of Resident 73's Minimum Data Set ([MDS] a standardized assessment and care screening tool) dated 5/1/2024, the MDS indicated Resident 73 was dependent on staff with bed mobility, moving from sitting on side of bed to lying flat on bed, toileting hygiene, bathing, dressing, personal hygiene, and oral hygiene. The MDS indicated the resident was not on any form of restraints. During a review of Resident 73's Physician Order Summary Report dated 2/25/2024, indicated a physician's telephone order of applying hand mittens to bilateral (both) hands every shift for prevention of pulling out nasogastric tube([NGT] thin, soft tube that goes in through the nose, down the throat, and into the stomach used to give medicines, liquids, and liquid food). During a review of Resident 73's Physician Order Summary Report dated 11/7/2023, indicated to remove hand mittens and inspect skin integrity for any redness, swelling or open area every shift and to change hand mittens as needed if soiled. During a review of Resident 73's Care Plan titled Bilateral hand mittens for tendency of pulling out NGT initiated 11/6/2023 with goal of Resident 73 will not develop any complication related to the use of bilateral hand mittens. The Care Plan interventions including assessment for possible discontinuance of bilateral hand mittens. During an observation on 6/10/2024, at 10:09 a.m., in Resident 73's room, Resident 73 was lying in bed turned to the right side, moaning, and groaning with bilateral hand mittens on and NGT on the left nares (nostril). During a subsequent interview on 6/12/2024, at 11:45 a.m., and on 6/12/2024, at 3:02 p.m. with Certified Nursing Assistant (CNA 5), CNA 5 stated she did not know what the name of the device on her (Resident 73) both hands but whenever she takes care of Resident 73, she would change both mittens, check the skin, and make sure they were not tight. CNA5 stated the mittens could cause poor circulation if they are not checked and too tight. During a concurrent interview and record review on 6/12/2024 at 10:45 a.m., with Registered Nurse (RN) 2 stated Resident 73 had bilateral hand mittens which was a form of restraint and were used to prevent removal of NGT. Reviewed Resident 73's electronic health record (EHR) RN 2 stated there was no documentation about assessment and monitoring of the usage of bilateral hand mittens. During a concurrent interview and record review on 6/12/2024, at 11:04 a.m., with Assistant Director of Nursing (ADON), ADON confirmed there was no documentation restraints were reassessed and evaluated for continued use. The ADON confirmed the physician order of bilateral hand mittens was ordered on 2/25/2024, and the order had no end date. ADON validated thru record review Resident 73's Interdisciplinary Team Meeting ([IDT] group of professional and direct care staff that have primary responsibility for the development of a plan for the care of a resident) Notes dated 2/6/2024 and 4/30/2024 did not address the restraint's use. ADON stated the CNAs could remove the bilateral hand mittens with the supervision of a licensed nurse. ADON stated licensed nurses were responsible for monitoring, removal, and assessment of restraints. ADON stated the resident could be a high risk for skin breakdown, and impairment of circulation due to restricted movement if the resident was not being monitored and reassess for the use of the bilateral hand mittens. During an interview on 6/13/2024, at 2:45 p.m., with RN 1, RN 1 stated the facility monitor and assess the restraints every 2hours by assessing skin integrity, circulation, and presence of contractures. RN1 stated Resident 73 might end up with contracture, impaired circulation, blood clots due to immobility if not monitored or reassessed with the usage of bilateral hand mittens. During a review of Resident 73's Medication Administration Record (MAR) for the month of June 2024, MAR indicated to remove hand mittens and inspect for any redness, swelling or open area every shift. The MAR indicated removal of hand mittens are performed every shift. The MAR indicated only a check (check symbol meant it was administered) and initials of licensed nurse. During a concurrent interview and record review on 6/13/2024, at 3:31 p.m. with Director of Nursing (DON), the DON stated the facility evaluates resident if there was a medical necessity on using restraints, and consent was obtained if resident required restraints. The DON stated restraint order included indication, monitoring and duration on how long restraints will be used on the resident. The DON stated the facility conducted quarterly restraint assessment, and care plan was initiated. DON confirmed the last quarterly restraint assessment was done last January 2024. The DON stated not monitoring and assessing continued use of hand mittens on Resident 73 could place resident at risk for skin breakdown, decreased functional use of both hands and the facility would not know if resident had developed contracture. During a review of facility's policy and procedure (P&P) titled Use of Restraints revised April 2017, the P&P indicated Restraints shall only be used upon the written order of a physician and the order should include the specific reason for the restraint, how the restraint will be used to benefit the medical symptom, the type of restraint and the period of time for the use of restraint. The P&P indicated a resident placed in a restraint will be observed at least every thirty minutes by nursing personnel and documentation of the use of restraints included length of effectiveness of the restraint time, observation, range of motion and repositioning. The P&P indicated restrained individuals will be reviewed regularly at least quarterly to determine whether they are candidates for restraint reduction or total restraint elimination.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0645 (Tag F0645)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to complete a preadmission screening and annual resident...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to complete a preadmission screening and annual resident review (PASARR) I accurately for one of one sampled resident (Resident 50) who has a diagnosis of major depressive disorder (affects how you feel, think, and behave that can lead to a variety of emotional and physical problems). This deficient practice had the potential to result in inappropriate placement and delay of needed services for Resident 50. Findings: During a review of Resident 50's admission Record, Resident 50 was admitted to the facility on [DATE] with a diagnosis of major depressive disorder. During a review of Resident 50's Minimum Data Set (MDS- a standardized assessment and care screening tool), dated 4/5/2024, indicated Resident 50 was assessed in needing maximal assistance for all activities of daily living (ADL). During a review of Resident 50's Physician Order Summary Report, Resident 50 was prescribed Quetiapine Fumarate (medication used to treat certain mental/mood disorders) for psychosis (a collection of symptoms that affect the mind, where there has been some loss of contact with reality) manifested by hostility (emotionally charged aggressive behavior) and agitation (unable to relax and be still). During a review of the PASARR I, dated 4/24/2024, the PASARR I indicated a negative level I screen. The PASARR I indicated Resident 50 has a serious mental disorder (conditions that affect your thinking, feeling, mood, and behavior). During an interview on 6/13/2024 at 10:14 a.m., with the medical records director (MRD), the MRD stated she was responsible for overseeing the PASARR and ensuring it was done correctly. MRD stated Resident 50 has a negative PASARR I because she has dementia (impaired ability to remember, think, or make decisions that interferes with doing everyday activities) and that was what she was taught. During an interview on 6/13/2024 at 3:20 p.m., with the Director of Nursing (DON), the DON stated that if a resident has a mental disorder and was prescribed medications for the mental disorder, the PSARR I should reflect as positive. The DON stated the PASARR I should have been corrected and was missed by us. The DON stated any resident with a mental disorder should be evaluated accurately so they could be treated and cared for correctly. During a review of the facility's policy and procedure (P&P) titled, admission Criteria, revised January 2024, the P&P indicated If the Level I screen indicates that the individual may meet the criteria for a mental disorders (MD), intellectual disabilities (ID- when limitations in your mental abilities affect intelligence, learning, and everyday life skills), or related disorders (RD), he or she is referred to the states PASARR representative for the Level II (evaluation and determination) screening process.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure the label of a bubble pack (unit-dose card that packages doses of medication within small, clear, or light-resistant p...

Read full inspector narrative →
Based on observation, interview, and record review, the facility failed to ensure the label of a bubble pack (unit-dose card that packages doses of medication within small, clear, or light-resistant plastic bubbles) reflected the current dosage, and/or a change in dosage, for one (1) of 30 sampled residents (Resident 239). This deficient practice had the potential for medication error. Findings: During an observation on 6/12/2024 at 2:55 p.m. at the nursing station A medication cart, the Licensed Vocational Nurse (LVN 5) presented a bubble pack belonged to Resident 239. The pharmacy label on the bubble read: hydrocodone-acetaminophen (potent narcotic for the treatment of pain) 10-325 milligrams ([mg] unit to measure mass), take one tablet by mouth every eight hours for pain management. During a review of Resident 239's physician orders indicated Norco 10-325 mg, give 1 tablet by mouth every 6 hours as needed (PRN) for moderate to severe pain (pain level 6-10), ordered on 6/7/2024 at 12:13 p.m. During an interview on 6/12/2024 at 3:03 p.m., the Director of Nursing (DON) stated Resident 239's routine order of Norco had been discontinued and replaced by a PRN order. The DON stated when there was a change of dosage and the remainder tablets can be used, the nurse should contact the pharmacy and obtain a change of dose sticker to be placed on the bubble pack. -+ During a review of the facility's policy and procedures (P&P) titled Guidelines for Medication Administration (undated) indicated, . If a discrepancy exists, . consult the appropriate resource(s) such as the pharmacist . If label directions are incorrect, the medication nurse is responsible for affixing a direction change sticker. If the Medication Administration Record and the medication labeling do not match, the medication nurse should investigate the discrepancy .
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0558 (Tag F0558)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility staff failed to ensure call light was within reach for two of f...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility staff failed to ensure call light was within reach for two of four sampled residents (Resident 3 and Resident 22). This deficient practice had the potential for Resident 3 and 22 not to receive necessary assistance when needed, and experienced loss of self-esteem. Findings: During a review of Resident 3's admission Order, the admission Record indicated Resident 3 was admitted to the facility on [DATE] and re-admitted on [DATE], with diagnoses including paraplegia (paralysis that affects your legs, but not your arms), and unspecified epilepsy (disorder in which nerve cell activity in the brain is disturbed, causing seizures [involuntary muscle movements]) During a review of Resident 3's Minimum Data Sheet (MDS- a comprehensive assessment and care planning tool) dated 5/10/2024 indicated Resident 3 had moderate cognitive impairment (ability to learn, understand, and make decisions) and requires maximum assistance for toileting hygiene, shower/bathe self, upper body dressing, lower body dressing, putting on/taking off footwear and personal hygiene. During a review of Resident 3's care plan revised on 8/14/2020, indicated Resident 3 was high risk for falls and has history of fall, seizure, and episodes of removing seatbelt. The Care Plan interventions including call light must be within reach and respond to call light in a timely manner. During a review of Resident 22's admission Order, the admission Record indicated Resident 22 was admitted to the facility on [DATE] with diagnoses including diabetes mellitus (high blood sugar), essential hypertension (high blood pressure) and unspecified dementia (a loss of thinking, remembering, and reasoning skills). During a review of Resident 22's MDS dated [DATE] indicated Resident 22 had severe cognitive impairment and requires assistance for all activities of daily living (ADL'S). During a review of Resident 22's care plan revised on 8/17/2020, i8ndicated Resident 22 was at risk for falls/risk for injury related to noncompliance. The Care Plan indicated interventions including call light must be within reach and respond to call light in a timely manner. During an observation on 6/10/2024 at 10:48 a.m.,11:45 a.m.12:47 p.m., and 2:10 p.m. observed Resident 3 call light hanging at the side of the bed and not within reach. During an observation on 6/11/2024 at 9:05 a.m.,10:03 a.m., and 11:01 a.m., observed Resident 22's call light was on the floor and not within reach. During an interview on 6/11/2024 at 2:50 p.m., the Director of Staff Development (DSD) stated if resident cannot reach the call light to ask for help, it will frustrate them and affect their psychosocial wellbeing and may feel like less important and unwanted. During an interview on 6/11/2024 at 2:57 p.m., Certified Nursing Assistant (CNA 2) stated call light should be within reach to prevent fall and injury and Resident 3 and 22's needs will be provided in a timely manner. During an interview on 6/13/2024 at 8:54 a.m., Licensed Vocational Nurse (LVN 4) stated if residents' call light was not within reach, Resident 3 and 22 will not be able to call for help when needed and had the potential to affect their psychosocial wellbeing and delayed the care needed. During a record review of the facility's policy and procedure (P&P) titled Answering the Call Light (undated) indicated, The purpose of this procedure was to respond to the resident's requests and needs. When the resident is in bed or confined to a chair be sure the call light is within easy reach of the resident. Some residents may not be able to use their call light. Be sure you check these residents frequently. Report all defective call lights to the Nurse Supervisor promptly. Answer the resident's call as soon as possible. Be courteous in answering the resident's call.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** c.During a review of Resident 9's admission Record, indicated Resident 9 was re-admitted to the facility on [DATE] with diagnose...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** c.During a review of Resident 9's admission Record, indicated Resident 9 was re-admitted to the facility on [DATE] with diagnoses including atrial fibrillation (an irregular and often very rapid heart rhythm) and congestive heart failure (CHF- heart does not pump blood as efficiently as it should). During a review of Resident 9's Minimum Data Set (MDS- a standardized assessment and care screening tool), dated 5/26/2024, indicated Resident 9 was assessed in needing maximal assistance with bathing and dressing. During a review of Resident 9's Physician Order's, the Physician Order's indicated Resident 9 order for Coumadin for atrial fibrillation. During a review of Resident 9's care plan, the care plan indicated Resident 9 has the potential for bleeding gums, bruises on arms or legs, petechiae (tiny spots of bleeding under the skin), nosebleeds, melena (black stools that comes from bleeding in your stomach), hematuria (blood in urine), and hematemesis (vomiting of blood) secondary to Coumadin therapy. During an interview on 6/12/24 at 1:40 p.m., Licensed Vocational Nurse (LVN) 6 stated that there was no documentation that Resident 9 was being assessed for sign and symptoms of bleeding and bruising. LVN 6 stated there should be assessment for signs and symptoms of bleeding as Resident 9 was on Coumadin therapy. During a review of Resident 103's admission Record, Resident 103 was readmitted to the facility on [DATE] with diagnoses including of atrial fibrillation and cerebral infarction (stroke- loss of blood flow to part of the brain causing tissue damage). During a review of Resident 103's MDS, dated [DATE], indicated Resident 103 was assessed in needing maximal assistance with bathing, dressing, and transferring. During a review of Resident 103's Physician Orders, the Physician Order's indicated Resident 103 order for Coumadin for atrial fibrillation. During a review of Resident 103's care plan, the care plan indicated Resident 103 was at risk for ecchymosis (bruising), bleeding, epistaxis (nose bleeds), hematuria, gum bleeding, and bleeding from other sources secondary to Coumadin therapy. During an interview on 6/12/24 at 1:55 p.m., with the Registered Nurse Supervisor (RNS) 2, RNS 2 stated Resident's 9 and 103 were taking Coumadin and confirmed there was no documentation that the residents were being monitored for the side effects and complications of Coumadin therapy as indicated in the care plan. RNS 2 stated they should be following the care plan for Resident's 9 and 103 to prevent complications of Coumadin therapy such as internal bleeding or death. During an interview on 6/13/24 at 3:34 p.m., with the Director of Nursing (DON), the DON stated Resident 103 has been on Coumadin since May of 2023. The DON stated there was no documentation that Resident 103 was being monitored for side effects and complications of Coumadin therapy as indicated in the care plan. The DON stated not following the care plan for Coumadin therapy could potentially lead to blood loss and death. During a review of the facility's undated policy and procedure (P/P) titled, Care Plan - Comprehensive, the P/P indicated comprehensive care plans are developed and maintained for each resident that identified the highest level of functioning the resident may be expected to attain. The P/P indicated the comprehensive care plan was developed for each resident and included measurable objectives and timetables to meet the resident's medical, nursing, mental and psychological needs. The P/P indicated each resident's comprehensive care plan was designed to .identify the professional services that are responsible for each element of care, aid in preventing or reducing declines in the resident's functional status and/or functional levels, enhance the optimal functioning of the resident by focusing on a rehabilitative program, and reflect currently recognized standards of practice for problem areas and conditions. Based on observation, interview, and record review, the facility failed to develop and/or implement an individualized person-centered plan of care with measurable objectives, timeframe, and interventions to meet the residents' needs for four of eight sampled residents (Residents 66 and 73, 9 and 103) by failing to: a. Develop a care plan for Restorative Nursing Aide (RNA, nursing aide program that helps residents maintain their function and joint mobility) services for Resident 66. b. Develop a care plan for RNA services for Resident 73 These deficient practices had the potential to negatively affect the delivery of necessary care and services for Residents 66 and 73. c.Follow the care plan interventions for Resident 9 and 103 who were at risk for bleeding while on Coumadin (blood thinner) therapy. This deficient practice had the potential to result in complications from the use of Coumadin such as bruising and bleeding. Findings: a. During a review of Resident 66's admission Record indicated Resident 66 was admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including muscle wasting and atrophy (decrease in size or wasting away of a body part of tissue) and ataxic gait (uncoordinated manner of walking). During a review of Resident 66's Minimum Data Set (MDS, a standardized assessment and care-screening tool), dated 4/26/2024, the MDS indicated Resident 66 had severe cognitive (ability to think, understand, learn, and remember) impairment. The MDS indicated Resident 66 was dependent in eating, hygiene, toileting, bathing, and transfers (moving from one surface to another). The MDS indicated Resident 66 had functional limitations in range of motion (limited ability to move a joint that interferes with daily functioning, including activities of daily living, or places the resident at risk of injury) in one leg (hip, knee, ankle, foot). During a review of Resident 66's Physician's Orders, dated 5/3/2024, the Physician's Orders indicated for Resident 66 to receive RNA services for passive range of motion (PROM, movement at a given joint with full assistance from another person) exercises to the left arm and PROM exercises to the right arm, seven times a week. During a review of Resident 66's Physician's Orders, dated 5/6/2024, the Physician's Orders indicated for Resident 66 to receive RNA services for PROM exercises to the left leg and PROM exercises to the right leg, every day, seven times a week. During a review of Resident 66's comprehensive care plan, the care plan did not indicate a care plan for RNA services. During an observation and interview on 6/11/2024 at 4:26 p.m., Resident 66 was lying in bed with the head of the bed elevated. Resident 66 was unable to raise both arms to shoulder level, fully straighten both elbows, and make full fists with both hands. Resident 66's both legs were resting on a pillow with the toes on both feet pointing downwards. Resident 66 stated she was unable to bend and straighten both ankles and both knees. During an interview and record review on 6/13/2024 at 10:37 a.m., the Minimum Data Set Nurse 1 (MDS 1) and Minimum Data Set Nurse 2 (MDS 2) stated the purpose of a comprehensive care plan was to provide an individualized plan of care to meet the specific needs of the residents. MDS 1 and MDS 2 reviewed Resident 66's electronic medical record and confirmed Resident 66 was receiving RNA services for PROM to both arms and both legs. MDS 1 and MDS 2 reviewed resident 66's comprehensive care plan and confirmed Resident 66 did not have a care plan for RNA services. MDS 1 and MDS 2 stated Resident 66 should have had a care plan for RNA services since Resident 66 was receiving RNA services to maintain her level of function and range of motion (ROM, full movement potential of a joint). MDS 1 and MDS 2 stated it was important for care plans to be developed, implemented, and accurate to ensure the appropriate care was provided to each individual resident. MDS 1 and MDS 2 stated the residents may not receive the treatment and services they required if it was not care planned. b. During a review of Resident 73's admission Record indicated Resident 73 admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including osteoarthritis (loss of protective cartilage that cushions the ends of your bones) of both knees and chronic kidney disease (gradual loss of kidney function). During a review of Resident 73's MDS, dated [DATE], the MDS indicated Resident 73 had severe cognitive impairment. The MDS indicated Resident 73 was dependent in eating, hygiene, toileting, bathing, and bed mobility. The MDS indicated Resident 73 had functional limitations in range of motion in one arm (shoulder, elbow, wrist, hand). During a review of Resident 73's Physician's Orders, dated 10/31/2023, the Physician's Orders indicated for Resident 73 to receive RNA services for PROM exercises to the left leg, PROM exercises to the right leg, PROM exercises to the left arm, and PROM exercises to the right arm, every day, seven times a week. During a review of Resident 73's comprehensive care plan, the care plan did not indicate a care plan for RNA services. During an observation on 6/12/2024 at 9:47 a.m., Resident 73 was sleeping with the head turned to the right. The right elbow was bent upwards, and the right hand was in fist with a white, mesh mitt on top of it. During an interview and record review on 6/13/2024 at 10:37 a.m., the Minimum Data Set Nurse 1 (MDS 1) and Minimum Data Set Nurse 2 (MDS 2) stated the purpose of a comprehensive care plan was to provide an individualized plan of care to meet the specific needs of the residents. MDS 1 and MDS 2 reviewed Resident 73's electronic medical record and confirmed Resident 73 was receiving RNA services for PROM to both arms and both legs. MDS 1 and MDS 2 reviewed resident 73's comprehensive care plan and confirmed Resident 73 did not have a care plan for RNA services. MDS 1 and MDS 2 stated Resident 73 should have had a care plan for RNA services since Resident 73 was receiving RNA services to maintain his level of function and range of motion (ROM, full movement potential of a joint). MDS 1 and MDS 2 stated it was important for care plans to be developed, implemented, and accurate to ensure the appropriate care was provided to each individual resident. MDS 1 and MDS 2 stated the residents may not receive the treatment and services they required if it was not care planned. During an interview on 6/13/2024 at 1:55 p.m., the Director of Nursing (DON) stated the comprehensive care plan was a communication tool used to identify and address the care needs of the residents. The DON stated it was important for care plans to be up to date and accurate to ensure the current care needs of the resident were accurately and appropriately addressed.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0688 (Tag F0688)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide treatments and services to five of eight samp...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide treatments and services to five of eight sampled residents (Residents 23, 66, 84, 117, and 43) to prevent and/or limit a decline in joint (where two bones meet) range of motion ([ROM] full movement potential of a joint) and mobility (ability to move). a. For Resident 23, the facility failed to provide Restorative Nursing Aide ([RNA] nursing aide program that helps residents maintain their function and joint mobility) ROM exercises to Resident 23's both legs and assist with arm bicycle (stationary piece of equipment using a cycling motion for the arms to provide a cardiovascular and strength workout exercises, seven (7) times a week as ordered. b. For Resident 66, the facility failed to provide RNA ROM exercises to both arms and both legs, 7 times a week as ordered. c.For Resident 84, the facility failed to provide RNA services for: 1.ROM exercises to the left arm, 7 times a week as ordered. 2.Right arm strengthening exercises on the arm bicycle, 7 times a week as ordered. 3.Ambulation (walking) exercises, three (3) times a week as ordered. 4.Sit to stand exercises, 3 times a week as ordered. 5.Gentle passive stretching of the left ankle, 7 times a week as ordered. 6.Application of a left-hand splint (rigid material or apparatus used to support and immobilize a broken bone or impaired joint), 3 times a week as ordered. d.For Resident 117, the facility failed to provide RNA ROM exercises to the right arm, the right leg, ambulation exercises, and arm bicycle exercises, seven times a week as ordered. e. For Resident 43, the facility failed to provide RNA exercises on 6/11/2024. These deficient practices had the potential to cause residents 23, 66, 84, 117 and, 43 to have a decline in mobility, lead to further contractures (loss of motion of a joint) and have a decline in physical functioning such as the ability to eat, dress, and walk. Findings: a. During a concurrent observation and interview on 6/12/2024 at 9:22 a.m., in Resident 23's room, with Resident 23, observed Resident 23 was lying in bed. Resident 23 was able to bend both elbows and make a fist with both hands. Resident 23's both legs resting on a pillow with both knees slightly bent and the toes on both feet were pointing downwards. Resident 25 bent both knees and hips slightly and was unable to bring the toes of both feet upwards. Resident 23 stated RNA staff did not visit regularly and assisted with exercises about 3 times a week if she was lucky. During a review of Resident 23's admission Record, the admission Record indicated Resident 23 was admitted to the facility on [DATE] and re-admitted the resident on 3/14/2014 with diagnoses including right sided hemiplegia (weakness to one side of the body) and hemiparesis (inability to move one side of the body) following a cerebral infarction (stroke, blockage of the flow of blood brain, causing or resulting in brain tissue death), paraplegia (paralysis or weakness of the legs and lower body, typically caused by spinal injury or disease), and contractures of both ankles and both feet. During a review of Resident 23's Minimum Data Set ([MDS], a standardized assessment and care screening tool), dated 4/19/2024, the MDS indicated Resident 23 had moderate cognitive (ability to think, understand, learn, and remember) impairment. The MDS indicated Resident 23 required set-up assistance for eating and was dependent for oral hygiene, toileting, bathing, dressing, personal hygiene, bed mobility, and transfers (moving from one surface to another). The MDS indicated Resident 23 had functional limitations in ROM (limited ability to move a joint that interferes with daily functioning, including activities of daily living, or places the resident at risk of injury) of both legs (hip, knee, ankle, foot). During a review of Resident 23's Physician Order Summary Report, the Order Summary Report dated 10/8/2014 indicated a physician order, for the RNA to assist Resident 23 with arm cycle exercises, seven times a week. During a review of Resident 23's Physician Order Summary Report, dated 6/22/2024 indicated a physician order, for RNA to provide active assistive ROM (AAROM, movement at a given joint with a person's own effort and assistance from an external force or another person) to the left leg with gentle passive (requiring total assistance from another person or equipment) stretch at the end of knee flexion (knee in a bent position), seven times a week. During a review of Resident 23's Physician Order Summary Report, dated 6/22/2024 indicated a physician order, for RNA to provide AAROM exercises to the right leg with gentle passive stretch at the end of knee flexion, seven times a week. During a review of Resident 23's May RNA Documentation Survey Report, indicated for RNA to assist Resident 23 with arm bicycle exercises, seven times a week as tolerated. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/31/2024. During a review of Resident 23's May RNA Documentation Survey Report, indicated for RNA to provide AAROM exercises to Resident 23's left leg, seven times a week as tolerated. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/31/2024. During a review of Resident 23's May RNA Documentation Survey Report, indicated for RNA to provide AAROM exercises to Resident 23's right leg, seven times a week as tolerated. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/31/2024. During a review of Resident 23's June RNA Documentation Survey Report, indicated for RNA to assist Resident 23 with arm bicycle exercises, seven times a week as tolerated. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, and 6/10/2024. During a review of Resident 23's June RNA Documentation Survey Report, indicated for RNA to provide AAROM exercises to Resident 23's right leg, seven times a week as tolerated. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, and 6/10/2024. During a review of Resident 23's June RNA Documentation Survey Report, indicated for RNA to provide AAROM exercises to Resident 23's left leg, seven times a week as tolerated. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, and 6/10/2024. b. During a concurrent observation and interview on 6/11/2024 at 4:26 p.m., with Resident 66 in Resident 66's room, observed Resident 66 lying in bed with the head of the bed elevated. Resident 66 was unable to raise both arms to shoulder level, fully straighten both elbows, and make full fists with both hands. Resident 66's both legs were resting on a pillow with the toes on both feet pointing downwards. Resident 66 stated she was unable to bend and straighten both ankles and both knees. During a review of Resident 66's admission Record, the admission Record indicated Resident 66 was admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including muscle wasting and atrophy (decrease in size or wasting away of a body part of tissue) and ataxic gait (uncoordinated manner of walking). During a review of Resident 66's MDS, dated [DATE], the MDS indicated Resident 66 had severe cognitive impairment. The MDS indicated Resident 66 was dependent in eating, hygiene, toileting, bathing, and transfers. The MDS indicated Resident 66 had functional limitations in ROM of one leg (hip, knee, ankle, foot). During a review of Resident 66's Physician Order Summary Report, dated 5/3/2024, indicated for RNA to provide passive range of motion (PROM, movement at a given joint with full assistance from another person) exercises to Resident 66's left arm, seven times a week. During a review of Resident 66's Physician Order Summary Report dated 5/3/2024, indicated for RNA to provide PROM exercises to Resident 66's right arm, seven times a week. During a review of Resident 66's Physician Order Summary Report dated 5/6/2024, indicated for RNA to provide PROM exercises to Resident 66's left leg, seven times a week. During a review of Resident 66's Physician Order Summary Report, dated 5/6/2024, indicated for RNA to provide PROM exercises to Resident 66's right leg, seven times a week. During a review of Resident 66's May RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 66's left arm, seven times a week. The squares on the Survey Report were blank on the following days: 5/5/2024 to 5/9/2024, 5/11/2024 to 5/14/2024, 5/16/2024, 5/21/2024, 5/23/2024 to 5/25/2024, and 5/27/2024 to 5/30/2024. During a review of Resident 66's May RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 66's right arm, seven times a week. The squares on the Survey Report were blank on the following days: 5/5/2024 to 5/9/2024, 5/11/2024 to 5/14/2024, 5/16/2024, 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/25/2024, and 5/27/2024 to 5/30/2024. During a review of Resident 66's May RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 66's left leg, seven times a week. The squares on the Survey Report were blank on the following days: 5/6/2024 to 5/9/2024, 5/11/2024 to 5/14/2024, 5/16/2024, 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/25/2024, and 5/27/2024 to 5/30/2024. During a review of Resident 66's May RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 66's right leg, seven times a week. The squares on the Survey Report were blank on the following days: 5/6/2024 to 5/9/2024, 5/11/2024 to 5/14/2024, 5/16/2024, 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/25/2024, and 5/27/2024 to 5/30/2024. c. During a concurrent observation and interview on 6/11/2024 at 3:33 p.m., with Resident 84 in Resident 84's room, observed Resident 84 lying in bed with a hand splint was sitting on the table next to Resident 84's bed. Resident 84's left arm was positioned with the elbow bent at a 90-degree angle, the wrist straight, the fingers of the hand were bent, and the thumb was resting on top of the pointer finger (finger next to the thumb). Resident 84's toes of both feet were pointing downwards. Resident 84 was unable to actively move the left hip and left knee. Resident 84 stated RNA staff assisted with exercises of both arms and both legs, walking, standing, and placement of the splint on the left hand but did not come every day. During a review of Resident 84's admission Record, the admission Record indicated Resident 84 was admitted to the facility on [DATE] with diagnoses including muscle wasting and atrophy and ataxia (decreased muscle control). During a review of Resident 84's MDS, dated [DATE], the MDS indicated Resident 84 was cognitively intact. The MDS indicated Resident 84 required set-up assistance for eating and oral hygiene, substantial/maximal assistance for upper body dressing, partial/moderate assistance for rolling to both sides and personal hygiene, and dependent in toileting, bathing, lower body dressing, and transfers. The MDS indicated Resident 84 had functional limitations in ROM in one arm (shoulder, elbow, wrist, hand) and one leg (hip, knee, ankle, foot). During a review of Resident 84's Physician Order Summary Report, dated 2/14/2022, indicated for RNA to provide PROM exercises to Resident 84's left arm in all planes and gentle passive stretching of the left elbow, wrist, fingers, and shoulder, seven times a week. During a review of Resident 84's Physician Order Summary Report, dated 2/14/2022, indicated for RNA to provide strengthening exercises to Resident 84's right arm using an arm bicycle, for 15 minutes, seven times a week. During a review of Resident 84's Physician Order Summary Report, dated 12/1/2023, indicated for RNA to provide Resident 84 with walking exercises, three times a week. During a review of Resident 84's Physician Order Summary Report, dated 12/1/2023, indicated for RNA to assist Resident 84 with sit to stand exercises, three times a week. During a review of Resident 84's Physician Order Summary Report, dated 12/1/2023, indicated for RNA to provide gentle passive stretching of Resident 84's left ankle, seven times a week. During a review of Resident 84's Physician Order Summary Report dated 7/18/2023, indicated for RNA to apply a resting hand splint (medical device that supports the hand, wrist, and fingers) to Resident 84's left hand for a maximum of four hours daily, seven times a week. During a review of Resident 84's May RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 84's left arm in all planes and gentle passive stretching of the left elbow, wrist, fingers, and shoulder, seven times a week. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/16/2024, 5/19/2024, 5/21/2024 to 5/31/2024. During a review of Resident 84's May RNA Documentation Survey Report, indicated for RNA to provide strengthening exercises to Resident 84's right arm using an arm bicycle, for 15 minutes, seven times a week. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/16/2024, 5/19/2024, 5/21/2024 to 5/31/2024. During a review of Resident 84's May RNA Documentation Survey Report, indicated for RNA to provide Resident 84 with walking exercises, three times a week. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/16/2024, 5/19/2024, 5/21/2024 to 5/31/2024. During a review of Resident 84's May RNA Documentation Survey Report, indicated for RNA to assist Resident 84 with sit to stand exercises, three times a week. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/16/2024, 5/19/2024, 5/21/2024 to 5/31/2024. During a review of Resident 84's May RNA Documentation Survey Report, indicated for RNA to provide gentle passive stretching of Resident 84's left ankle, seven times a week. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/16/2024, 5/19/2024, 5/21/2024 to 5/31/2024. During a review of Resident 84's May RNA Documentation Survey Report, indicated for RNA to apply a resting hand splint to Resident 84's left hand for a maximum of four hours daily, seven times a week. The squares on the Survey Report were blank on the following days: 5/2/2024, 5/3/2024, 5/5/2024 to 5/9/2024, 5/11/2024 to 5/16/2024, 5/19/2024, 5/21/2024 to 5/31/2024. During a review of Resident 84's June RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 84's left arm in all planes and gentle passive stretching of the left elbow, wrist, fingers, and shoulder, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, 6/10/2024, and 6/11/2024. During a review of Resident 84's June RNA Documentation Survey Report, indicated for RNA to provide strengthening exercises to Resident 84's right arm using an arm bicycle, for 15 minutes, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, 6/10/2024, and 6/11/2024. During a review of Resident 84's June RNA Documentation Survey Report, indicated for RNA to provide Resident 84 with walking exercises, three times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, 6/10/2024, and 6/11/2024. During a review of Resident 84's June RNA Documentation Survey Report, indicated for RNA to assist Resident 84 with sit to stand exercises, three times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, 6/10/2024, and 6/11/2024. During a review of Resident 84's June RNA Documentation Survey Report, indicated for RNA to provide gentle passive stretching of Resident 84's left ankle, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, 6/10/2024, and 6/11/2024. During a review of Resident 84's June RNA Documentation Survey Report, indicated for RNA to apply a resting hand splint to Resident 84's left hand for a maximum of four hours daily, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/8/2024, and 6/10/2024. d. During a concurrent observation and interview on 6/11/2024 at 9:51 a.m., with Resident 117 in Resident 117's room, observed Resident 117 was lying in bed. Resident 117 made a partial fist with the right hand and was unable to move his right wrist, elbow, and shoulder. Resident 117 was unable to actively move his right leg and stated he needs help walking. Resident 117 stated staff did not assist with walking and exercises for his arms and legs every day. During a review of Resident 117's admission Record, the admission Record indicated Resident 117 was admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including right-sided hemiplegia and hemiparesis following an intracranial hemorrhage (bleeding of the brain), dysarthria (motor speech disorder in which the muscles used to produce speech are damaged or weak), and muscle wasting and atrophy. During a review of Resident 117's MDS, dated [DATE], the MDS indicated Resident 117 was cognitively intact. The MDS indicated Resident 117 was dependent in eating, hygiene, toileting, bathing, and transfers. The MDS indicated Resident 117 had functional limitations in ROM in one arm (shoulder, elbow, wrist, hand) and one leg (hip, knee, ankle, foot). During a review of Resident 117's Physician Order Summary Report, dated 4/20/2024, indicated for RNA to provide PROM exercises to Resident 117's right leg, seven times a week. During a review of Resident 117's Physician Order Summary Report, dated 4/20/2024, indicated for RNA to provide PROM exercises to Resident 117's right arm, seven times a week. During a review of Resident 117's Physician Order Summary Report, dated 5/28/2024, indicated for RNA to provide exercises to Resident 117's both arms using an arm bicycle, seven times a week. During a review of Resident 117's Physician Order Summary Report, dated 5/29/2024 indicated for RNA to provide Resident 117 with walking exercises wearing an ankle foot orthosis (AFO, brace to hold the foot and ankle in the correct position) and using a hemi-walker (assistive device that allows a person to lean on one side while walking for support), seven times a week. During a review of Resident 117's May RNA Documentation Survey Report indicated for RNA to provide PROM exercises to Resident 117's right leg, seven times a week. The squares on the Survey Report were blank on the following days: 5/2/2024 to 5/9/2024, 5/11/2024 to 5/17/2024, 5/19/2024, and 5/21/2024 to 5/31/2024. During a review of Resident 117's May RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 117's right arm, seven times a week. The squares on the Survey Report were blank on the following days: 5/2/2024 to 5/9/2024, 5/11/2024 to 5/17/2024, 5/19/2024, and 5/21/2024 to 5/31/2024. During a review of Resident 117's May RNA Documentation Survey Report, indicated for RNA to provide Resident 117 with walking exercises wearing an AFO and using a hemi-walker, 7 times a week. The squares on the Survey Report were blank on the following days: 5/29/2024, 5/30/2024, and 5/31/2024. During a review of Resident 117's May RNA Documentation Survey Report, indicated for RNA to provide exercises to Resident 117's both arms using an arm bicycle, seven times a week. The squares on the Survey Report were blank on the following days: 5/6/2024 to 5/9/2024, 5/11/2024 to 5/14/2024, 5/16/2024, 5/17/2024, 5/19/2024, 5/21/2024, 5/23/2024 to 5/25/2024, and 5/27/2024 to 5/30/2024. During a review of Resident 117's June RNA Documentation Survey Report, indicated for RNA to provide PROM exercises to Resident 117's right leg, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/10/2024. During a review of Resident 117's June RNA Documentation Survey Report, the Survey Report indicated for RNA to provide PROM exercises to Resident 117's right arm, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/10/2024. During a review of Resident 117's June RNA Documentation Survey Report, indicated for RNA to provide Resident 117 with walking exercises wearing an AFO and using a hemi-walker, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/10/2024. During a review of Resident 117's June RNA Documentation Survey Report, indicated for RNA to provide exercises to Resident 117's both arms using an arm bicycle, seven times a week. The squares on the Survey Report were blank on the following days: 6/1/2024, 6/3/2024 to 6/10/2024. During a concurrent interview and record review on 6/13/2024 at 10:54 a.m., the Director of Staff Development (DSD) reviewed the RNA May 2024 and June 2024 Documentation Survey Reports and physician's orders for Residents 23, 66, 84, and 117. The DSD confirmed Residents 23, 66, and 117 had physician orders for RNA to provide RNA services seven times a week. The DSD confirmed Resident 84 had physician's orders for RNA to provide RNA services three times a week and seven times a week. The DSD stated a blank square on the RNA Survey Report indicated the resident was not seen for RNA treatment that day. The DSD confirmed Resident 23 missed 25 RNA sessions for AAROM exercises of both legs and arm bicycle exercises for the month of May. The DSD confirmed Resident 23 missed eight (8) RNA sessions for AAROM exercises for both legs and arm bicycle exercises for the month of June. The DSD confirmed Resident 66 missed 19 RNA sessions for left arm PROM exercises and 20 RNA sessions for PROM of the right arm and both legs for the month of May. The DSD confirmed Resident 84 missed 8 RNA sessions for walking exercises and sit to stand exercises for the month of May. The DSD confirmed Resident 84 missed 25 RNA sessions for left ankle ROM exercises, application of a left-hand splint, PROM of the left arm, and strengthening exercises on the arm bike for the month of May. The DSD confirmed Resident 84 missed three RNA sessions for walking exercises and sit to stand exercises for the month of June. The DSD confirmed Resident 84 missed nine (9) RNA sessions for left ankle ROM exercises, application of a left-hand splint, PROM of the left arm, and strengthening exercises on the arm bike for the month of June. The DSD confirmed Resident 117 missed 27 RNA sessions for PROM exercises of the right leg and right arm for the month of May. The DSD confirmed Resident 117 missed three RNA sessions for walking exercises and arm bike exercises for the month of May. The DSD confirmed Resident 117 missed nine RNA sessions for PROM exercises of the right leg, PROM exercises of the right leg, walking exercises, and arm bike exercises for the month of June. The DSD stated Residents 23, 66, 84, and 117 did not receive RNA treatments as ordered by the physician due to insufficient RNA staffing in the months of May and June 2024. The DSD stated it was important for RNA to provide services as prescribed by the physician because missed treatments could place residents at risk for a functional decline and contractures. During an interview on 6/13/2024 at 1:55 p.m., the Director of Nursing (DON) stated the purpose of the RNA program was to maintain and/or improve a resident's current level of function and prevent declines in ROM and functional mobility. The DON stated missed RNA treatments could potentially cause a resident to experience a decline in overall function and mobility. e. During a review of Resident 43's admission Order, the admission Record indicated Resident 43 was admitted to the facility on [DATE] and re-admitted on [DATE], with diagnoses including chronic obstructive pulmonary disease ([COPD] a lung condition that cause breathing difficulties), hypertensive heart disease with heart failure (heart muscle is unable to pump enough blood to meet the body's needs for blood and oxygen), and bilateral primary osteoarthritis of knee (a degenerative joint disease that affects both knees, causing pain, stiffness, swelling, and decreased mobility). During a review of Resident 43's Minimum Data Sheet (MDS a comprehensive assessment and care screening tool) dated 4/12/2024 indicated Resident 43 had no cognitive impairment (ability to learn, understand, and make decisions) and dependent assistance for toileting hygiene, shower/bathe self, lower body dressing, putting on/taking off footwear and personal hygiene. During a review of Resident 43's care plan revised on 10/12/2023, Resident 43 had potential for impaired physical mobility related to limited movement due to hemiplegia (refers to a severe or complete loss of strength and hemiparesis (refers toa relatively mild loss of strength), osteoarthritis and COPD and one of the interventions is to provide RNA program for both upper and lower arm bike exercises daily times seven days a week as tolerated, provide both lower extremities active range of motion (AROM movement at a given joint) exercises daily seven times a week as tolerated. During a concurrent interview and record review on 6/12/2024 at 10:03 a.m., with RNA 3, reviewed RNA Documentation Survey Report dated 6/11/2024 which indicated the squares on the Survey Report was signed by RNA 3 and recorded that RNA exercises was given to Resident 43. RNA 3 stated she did not provide RNA exercises to Resident 43 on 6/11/2024 but documented in the RNA Documentation Survey Report that RNA exercises was provided on 6/11/2024. RNA 3 stated if range of motion exercises were not given according to the order, it had the potential to cause decline in Resident 43's physical functioning. During a review of the facility's undated policy and procedure (P&P), titled Rehabilitative Nursing Care, the P&P indicated rehabilitative nursing care was provided for each resident admitted and was designed to assist each resident to achieve and maintain an optimal level of self-care and independence. The P&P indicated RNA was performed daily for those residents who required such services and included assisting residents use their prosthetic devices, assisting resident to carry out prescribed therapy exercises, and assisting resident with ROM exercises. During a record review of the facility's P&P titled Range of Motion Exercises (undated), indicated: The purpose of this procedure was to exercise the resident's joints and muscles. The following information should be recorded in the resident's medical record: 1. The date and time that the exercises were performed. 2. The name and title of the individual(s) who performed the procedure. 3. The type of ROM exercise given. 4. Whether the exercise was active or passive. 5. How long the exercise was conducted. 6. If and how the resident participated in the procedure or any changes in the resident's ability to participate in the procedure. 7. Any problems or complaints made by the resident related to the procedure. 8. If the resident refused the treatment, the reason(s) why and the intervention taken. 9. The signature and title of the person recording the data. CROSS REFERENCE TO F725
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0725 (Tag F0725)

Could have caused harm · This affected multiple residents

Based on interview and record review, the facility failed to provide adequate and sufficient nursing staff to provide care for residents requiring Restorative Nursing Aide (RNA, nursing aide program t...

Read full inspector narrative →
Based on interview and record review, the facility failed to provide adequate and sufficient nursing staff to provide care for residents requiring Restorative Nursing Aide (RNA, nursing aide program that helps residents maintain their function and joint mobility) services. This deficient practice had the potential for 95 residents with physician's orders for RNA to experience a decline in range of motion (ROM, full movement potential of a joint) and mobility (ability to move). Findings: During a review of the Order Listing Report of RNA orders for 6/2024 indicated 95 residents had physician's orders for RNA to provide either assistance with sit-to-stand transfers, ROM exercises to the arms, ROM exercises to the legs, application of splints (material used to restrict, protect, or immobilize a part of the body to support function, assist and / or increase range of motion), ambulation (walking), stair climbing exercises, or exercises on the arm bicycle (stationary piece of equipment using a cycling motion for the arms to provide a cardiovascular and strength workout). During a review of the facility's Nursing Staffing Assignment and Sign in Sheets for the month of May 2024 indicated the following total number of RNAs present for the day (7 a.m. to 3 p.m. shift and 6:30 a.m. to 3 p.m. shift): Wednesday, 5/1/2024: Four (4) RNAs Thursday, 5/2/2024: Three (3) RNAs Friday, 5/3/2024: 4 RNAs Saturday, 5/4/2024: Two (2) RNAs Sunday, 5/5/2024: 2 RNAs Monday, 5/6/2024: 3 RNAs Tuesday, 5/7/2024: 4 RNAs Wednesday, 5/8/2024: 3 RNAs Thursday, 5/9/2024: 3 RNAs Friday, 5/10/2024: 3 RNAs Saturday, 5/11/2024: 3 RNAs Sunday, 5/12/2024: 2 RNAs Monday, 5/13/2024: 3 RNAs Tuesday, 5/14/2024: 3 RNAs Wednesday, 5/15/2024: 4 RNAs Thursday, 5/16/2024: 3 RNAs Friday, 5/17/2024: 4 RNAs Saturday, 5/18/2024: 2 RNAs Sunday, 5/19/2024: 2 RNAs Monday, 5/20/2024: 4 RNAs Tuesday, 5/21/2024: 4 RNAs Wednesday, 5/22/2024: 2 RNAs Thursday, 5/23/2024: 4 RNA Friday, 5/24/2024: 4 RNAs Saturday, 5/25/2024: 3 RNAs Sunday, 5/26/2024: 2 RNA Monday, 5/27/2024: 4 RNA Tuesday, 5/28/2024: 3 RNAs Wednesday, 5/29/2024: 3 RNAs Thursday, 5/30/2024: Five (5) RNAs Friday, 5/31/2024: 4 RNAs During a review of the facility's Nursing Staffing Assignment and Sign in Sheets for the month of June 2024 indicated the following total number of RNAs present for the day (7 a.m. to 3 p.m. shift and 6:30 a.m. to 3 p.m. shift): Saturday, 6/1/2024: 4 RNAs Sunday, 6/2/2024: 3 RNAs Monday, 6/3/2024: 4 RNAs Tuesday, 6/4/2024: 2 RNAs Wednesday, 6/5/2024: 2 RNAs Thursday, 6/6/2024: 3 RNAs Friday, 6/7/2024: 4 RNAs Saturday, 6/8/2024: 3 RNAs Sunday, 6/9/2024: 3 RNAs Monday, 6/10/2024: 3 RNAs Tuesday, 6/11/2024: 3 RNAs During an interview on 6/11/2024 at 11:12 a.m., Restorative Nursing Aide 1 (RNA 1) stated she tried to provide RNA services to about 15 to 20 residents per day. RNA 1 stated RNA services included assisting residents with exercises, ROM, ambulation, feeding assistance, stationary bike exercises, application of splints, assisting Certified Nursing Assistants (CNA) with daily care, mechanical lift transfers (a mechanical piece of equipment that allows a person to be transferred from one surface to another), and weights (performed upon admission, daily, weekly, and monthly). RNA 1 stated many residents in the facility would not be seen for RNA treatment due to lack of staffing. During an interview 6/11/2024 at 3:16 p.m., RNA 4 stated the RNAs were unable to provide RNA services to all the residents on their daily schedule as ordered due to lack of time and staffing. RNA 4 stated the RNAs in the facility had a lot of tasks assigned to them daily and were often asked to assist the other CNAs with their daily care in addition to their current workload. RNA 4 stated if an RNA called out sick or got re-assigned for the day as a CNA, the RNA who was covering their shift would have double or triple their daily workload. RNA 4 stated the facility needed more RNAs to ensure all residents on the RNA program were seen as scheduled. During an interview on 6/13/2024 at 8:50 a.m., Restorative Nursing Aide 3 (RNA 3) stated the RNA staff were unable to provide services to all the residents who had RNA orders due to short staffing, particularly on weekends. RNA 3 stated she was re-assigned to perform CNA duties about one time a week and was asked to assist the other CNAs with their tasks daily in addition to her current daily workload. RNA 3 stated if an RNA was re-assigned as a CNA for the day or called out sick, the RNA who was covering for the day would have double or triple the workload and would be unable to provide RNA services to the residents as ordered. During a concurrent interview and record review on 6/13/2024 at 1:02 p.m., the Director of Staff Development (DSD) reviewed the Nursing Staffing Assignment and Sign in Sheets for the months of May 2024 and June 2024. The DSD stated the facility required a minimum of 4 RNAs on the floor daily to ensure all residents with RNA orders received RNA services as ordered. The DSD confirmed the RNA program was insufficiently staffed for the months of May 2024 and June 2024 - particularly on the weekends. The DSD stated many residents who required RNA services per physician's order were not receiving RNA services due to lack of RNA staff. The DSD stated there was potential for residents to experience a decline in function if RNA was not being provided as ordered. During an interview on 6/13/2024 at 1:55 p.m., the DON stated the purpose of the RNA program was to maintain and/or improve a resident's current level of function and prevent declines in ROM and functional mobility. The DON stated missed RNA treatments could potentially cause a resident to experience a decline in overall function and mobility. During a review of the facility's undated Policy and Procedure (P&P), titled Staffing, the P&P indicated the facility provided adequate staffing on each shift to ensure the resident's needs and services were met. CROSS REFERENCE TO F688
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Pharmacy Services (Tag F0755)

Could have caused harm · This affected multiple residents

Based on observations, interviews, and record review, the facility failed to: 1.Ensure to keep a separate log of uses from the emergency medication supplies. 2.Ensure the licensed nurses would documen...

Read full inspector narrative →
Based on observations, interviews, and record review, the facility failed to: 1.Ensure to keep a separate log of uses from the emergency medication supplies. 2.Ensure the licensed nurses would document inventory count (cycle count) of narcotics (medication used to moderate to severe pain) stored in the Cubex (an automated dispensing cabinet with a computer-controlled system that stores and dispense medications) at change of shift. Twenty-four of 124 shifts did not have nurses' signatures, and the existing signatures of the remaining 100 shifts had identical signatures for the performing and witnessing nurses. 3.Ensure there were administration record of narcotic medications for three (3) of 30 sampled residents (Residents 5, 43, 239). 4.Ensure the facility's consent policy is outdated and did not match with current regulations. These deficient practices had the potential for loss of accountability, medication errors, issues in residents' rights, and/or diversions or theft of medications. Findings: 1. During a concurrent observation, interview, and record review on 6/11/2024 at 11:43a.m., with Assistant Director of Nursing (ADON) in the medication storage room at the nursing station A, there was an Emergency Kit ([EKIT] an emergency drug supply) logbook. Reviewed the logbook and the Emergency Drug Supply Log Sheet with the ADON, the ADON stated licensed nurses document medication taken from the EKIT and the Cubex on the Emergency Drug Supply Log Sheet. During a review of the Cubex pharmacy transactions on 5/30/2024 indicated, there was a tablet of alprazolam (used to treat anxiety) 0.25 milligrams ([mg] a unit to measure mass) issued for Resident 5 on 5/30/2024 at 3:59 p.m. During a review of Resident 5's physician orders indicated an order dated 5/30/2024 at 2:28 p.m. for alprazolam 0.25 mg, give 1 tablet by mouth every eight (8) hours as needed for anxiety. During an interview on 6/11/2024 at 11:45 p.m., ADON stated this issuance of alprazolam was not recorded in the Emergency Drug Supply Log Sheet. During a review of the facility's policy and procedures (P&P), (undated), indicated . Cubex .Emergency STAT orders may be retrieved pursuant to the order of a prescriber for emergency or immediate administration to a resident of the facility . The CUBEX System keeps a complete and accurate record of all users accessing the cabinet . During a review of the facility's P&P, Emergency Equipment, Supplies and Medications (E-KIT) (undated), indicated . Separated records of use shall be maintained for drugs administered from the supply. Such records shall include the name and dose of the drug administered, name of the patient, the date and time of administration and the signature of the person administering the dose . 2. During an interview on 6/11/2024 at 11:45 p.m., with ADON stated the registered nurse (RN) of the incoming shift would perform the Cubex cycle count (a method of checks and balances by which the facility confirms physical inventory counts match their inventory records) with the outgoing RN of every shift. During a concurrent interview and record review on 6/11/2024 12:01 p.m. with RN 2 reviewed Cubex controlled substance count with shift change sheet, RN 2 stated she performed the cycle count of Cubex this morning with the outgoing RN, however, she stated she forgot to sign in the shift count sheet. During a review of the cycle count sheet, there are two columns, tilted Nurse 1 and Nurse 2, under each shift. A further review of the cycle count records indicated there were 24 of 124 total shifts did not have nurses' signatures between 5/1/24 to 6/11/2024 morning; 100 of the 124 shifts had identical signatures for both incoming and outgoing nurses. During an interview on 6/11/2024 at 12:11 p.m., the Director of Nursing (DON) stated two RNs perform the Cubex cycle count at each shift and there were three shifts per day. DON referred to the cycle count sheet and stated one of the columns would be signed by the outgoing nurse, the other column by the incoming nurse. DON confirmed the signatures of both columns looked identical for the shifts that had signatures, and there were multiple shifts without signatures. DON stated the RNs did not sign the sheet correctly. Also, DON stated some forgot to sign as they completed the count. During an interview on 6/11/2024 at 4 p.m., the DON stated she could not locate the Cubex cycle count policy. 3. During a review of Resident 5's physician orders indicated an order dated 5/30/2024 at 2:28 p.m., for alprazolam 0.25 mg, give 1 tablet by mouth every 8 hours as needed for anxiety. During a review of the Cubex transactions on 5/30/2024 indicated, there was a tablet of alprazolam 0.25 mg issued for Resident 5 on 5/30/2024 at 3:59 PM. During an interview on 6/12/2024 at 11:20 a.m., reviewed Resident 5's electronic medication administration record (eMAR) of May 2024. The DON stated the administering nurse did not record the administration of Resident 5's alprazolam on 5/30/2024. During an observation on 6/12/2024 at 2:22 p.m. at the medication cart labeled Station B1 (7-3 shift (morning shift), 3-11 shift (afternoon shift), the licensed vocation nurse (LVN 7) presented a bubble pack (form of tamper-evident packaging of medication) of hydrocodone-acetaminophen (potent narcotic for the treatment of pain) 5-325 mg for Resident 43. During a review of Resident 43's physician order of hydrocodone-acetaminophen 5-325 mg (dated 5/30/2024 at 6:44 PM) indicated to give 1 tablet by mouth every 6 hours as needed for severe pain. During a review of the Narcotic and Hypnotic Record for Resident 43's hydrocodone-acetaminophen 5-325 mg indicated there were three doses issued in June 2024: one dose on 6/1/2024 at 9:13 AM, 6/8/2024 at 2 p.m., and one dose on 6/11/2024 at 2:19 p.m. During a concurrent interview and record review on 6/12/2024 at 2:35 p.m. with the DON, reviewed Resident 43's eMAR. The DON stated there was no documentation in MAR for two of three doses shown on narcotic record; the doses on 6/8/2024 at 2 p.m., and on 6/11/24 at 2:19 p.m., did not have a matching administration record in the resident's eMAR. During an observation on 6/12/2024 at 2:55 p.m. at the nursing station A medication cart, the licensed vocational nurse (LVN 5) presented a bubble pack of Norco 10/325 mg for Resident 239. During a review of Resident 239's physician order of Norco 10-325 mg dated 6/7/2024 at 12:13 p.m. indicated to give 1 tablet by mouth every 8 hours as needed for moderate to severe pain. During a review of the Narcotic and Hypnotic Record for Resident 239's Norco 10-325 mg indicated there was one dose issued on 6/1/2024 at 9:13 a.m. Norco narcotic record 6/12/24 at 6 AM. During a concurrent interview and record review on 6/12/2024 at 3:03 p.m., with the DON, reviewed Resident 239's eMAR. The DON stated there was no documentation in the eMAR for the following doses as indicated on the Narcotic Record: 6/7/2024 at 6 a.m., and 6/12/2024 at 6 a.m. The DON stated the administering nurses did not document the administrations of these two doses. During a review of the facility's P&P titled Oral Medication Administration (undated) indicated, . Return to the Medication Cart and document medication administration with initials in appropriate spaces on the MAR. 4. During an interview on 6/12/2024 at 9:54 a.m., the ADON stated the prescriber obtained informed consents for residents' psychotropic uses; when facility got the order, nurses contact resident and/or family member to inform them of such order and verify if they had given consent to receive the psychotropic medications. During a review of the facility's P&P, Consent Requirements For Psychotherapeutic Medications (undated), indicated . There is no requirement to obtain a new consent when a dosage change is made . The facility and nurses are neither responsible to determine that all risks are enumerated and disclosed .The facility is not responsible for obtaining a signature . During an interview on 6/12/2024 at 10:10 a.m., ADON acknowledged the facility P &P did not match the current regulatory requirements. During a telephone interview on 6/12/2024 at 3:27 p.m. the facility consultant pharmacist stated the facility was aware of the outdated consent policy and they were in the process of updating the policy.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

QAPI Program (Tag F0867)

Could have caused harm · This affected multiple residents

Based on interview and record review, the facility's Quality Assessment and Assurance ([QAA] a group which develops and implements appropriate plans of action to correct identified quality deficiencie...

Read full inspector narrative →
Based on interview and record review, the facility's Quality Assessment and Assurance ([QAA] a group which develops and implements appropriate plans of action to correct identified quality deficiencies) committee and Quality Assurance Performance Improvement ([QAPI] a group who takes a systemic, interdisciplinary, comprehensive, and data driven approach to maintaining and improving safety and quality in nursing homes while involving residents and families) committee failed to: 1. Ensure on-going assessment and reevaluation of physical restraints' continuous use were conducted. 2. Identify, assess, and implement interventions on residents with severe weight loss. 3. Identify, assess, and implement interventions on residents with pain during wound care treatment. 4. Ensure Restorative Nurse Aide services were implemented to residents as ordered. These deficient practices placed the residents at risk for not receiving the quality-of-care treatment necessary to adequately meet their highest practicable well-being and placed the residents. Findings: During an interview with the Administrator, Quality Assurance Nurse and the Director of Nursing (DON) on 6/13/2024 at 3:09 p.m., the DON stated not being able to identify systemic issues identified even before the survey. The QA Nurse and the DON, both stated QAA was supposed to identify systemic issues and address it. The Administrator acknowledged the facility had opportunities for improvement of all mentioned deficient practices. During a record review of the facility's policy and procedure (P&P) titled Quality Assurance and Performance Improvement (QAPI) Program revised 3/2020, the policy indicated This facility shall develop, implement, and maintain an ongoing, facility-wide, data-driven QAPI program that is focused on indicators of the outcomes of care and quality of life for our residents. To provide a means to measure current and potential indicators for outcomes of care and quality of life. To provide a means to establish and implement performance improvement projects to correct identified negative or problematic indicators. To reinforce and build upon effective systems and processes related to the delivery of quality car and services. To establish systems through which to monitor and evaluate corrective actions.
CONCERN (F)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected most or all residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to maintain and observe infection control practices by f...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to maintain and observe infection control practices by failing to: 1. Ensure Certified Nursing Assistant (CNA) 1 and 2, performed hand hygiene in between residents when passing lunch trays. 2. Ensure Restorative Nursing Aide 1 (RNA 1) use the appropriate cleaning agent to effectively clean and disinfect a cloth gait belt (safety device worn around the waist that can be used help safely transfer a person from one surface to another or while walking) after completing RNA walking exercises with Resident 96. These deficient practices had the potential to result in cross contamination (physical movement or transfer of harmful bacteria from one person, object, or place to another) and place residents at risk for the spread of infection. 3.Ensure Resident 3's nephrostomy tube (a drainage tube placed into the kidney to drain urine directly from the kidney) drainage should be below the level of the kidneys. This deficient practice had the potential for backflow of urine that can lead to infection. Findings: 1.During an observation on 6/13/2024 at 12:40 p.m., in the hallway, Certified Nursing Assistant (CNA) 1 and 2, were observed not performing hand hygiene while passing meal trays to the residents. During an interview on 6/13/2024 at 12:50 p.m., with CNA 1, CNA 1 stated she did not perform hand hygiene between residents while passing out their lunch trays. CNA 1 stated she should be performing hand hygiene when passing trays to prevent the spread of infection. During an interview on 6/13/2024 at 12:50 p.m., with CNA 2, CNA 2 stated she was rushing when passing out the lunch trays and forgot to perform hand hygiene. CNA 2 stated she should have performed hand hygiene because it was important in the prevention of spreading germs and infection to the residents. During an interview on 6/13/2024 at 1:04 p.m., with the Infection Prevention Nurse (IP), the IP Nurse stated the staff should be performing hand hygiene when passing lunch trays to prevent the spread of infection which could potentially cause the residents to get sick. During a record review of the facility's policy and procedure (P&P), titled Handwashing/Hand Hygiene, revised August 2019, indicated, All personnel shall follow the handwashing/hand hygiene procedures to help prevent the spread of infections to other personnel, residents, and visitor. 2. During a review of Resident 96's admission Record indicated Resident 96 was admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses including spinal stenosis (condition that occurs when the spaces in the spine narrow and put pressure on the spinal cord and nerve roots), metabolic encephalopathy (brain dysfunction caused by a chemical imbalance in the blood), and high white blood cell (part of the body responsible for protecting the body from infection) count. During an observation and interview on 6/11/2024 at 9:21 a.m., with RNA 1 in the hallway, RNA 1 was observed completing walking exercises with Resident 96. Resident 96 was walking down the hallway using a walker (type of mobility aid with wide base of support) and had a cloth gait belt around the waist. RNA 1 assisted Resident 96 to walk down the hall into an activity room and assisted Resident 96 onto a bicycle machine for further exercises. Once Resident 96 was seated on the bicycle machine, RNA 1 removed the cloth gait belt from Resident 96's waist, walked to the dining room, and sprayed the cloth gait belt on both sides with liquid in a clear spray bottle labeled 70% isopropyl alcohol. RNA 1 stated cloth gait belts were made of fabric and used either 70% isopropyl alcohol or bleach wipes to disinfect cloth gait belts in between resident use. RNA 1 stated it was important to properly clean and disinfect cloth gait belts before and after resident use to prevent the spread of infection. During an interview on 6/11/2024 at 11:46 a.m., the Administrator (ADM) stated the 70% isopropyl spray could be used as a disinfectant for many surfaces throughout the facility but was unsure if it was the appropriate cleaning agent to be used to disinfect porous (having small spaces or holes through which liquid or air may pass) materials such as fabric. During an interview and record review on 6/12/2024 at 11:14 a.m., the Infection Preventionist nurse (IP) stated cloth gait belts were cleaned and disinfected using either the 70% isopropyl alcohol spray or the bleach germicidal wipes (disinfecting wipes) before and after resident use. The IP stated cloth gait belts were made of fabric, a porous material. The IP reviewed the manufacturer instructions for both the 70% isopropyl alcohol and the bleach germicidal wipes. The IP confirmed manufacturer instructions for the isopropyl alcohol spray indicated the alcohol spray could only be used on the skin for minor cuts or burns or on hard, non-porous surfaces and was ineffective on porous materials such as fabric. The IP confirmed the bleach germicidal wipes were to be used on non-porous, hard surfaces only and could not be used on fabric per manufacturer's instructions. The IP stated the isopropyl alcohol spray and bleach germicidal wipes were ineffective cleaning agents because cloth gait belts were made of porous materials. The IP stated the only way to properly clean and disinfect cloth gait belts was to launder them after each resident use. The IP stated it was important to clean and disinfect shared equipment properly to prevent the spread of infection and avoid cross contamination. During an interview on 6/13/2024 at 1:55 p.m., the Director of Nursing (DON) stated shared resident equipment such as gait belts must be cleaned and disinfected in between resident use. The DON stated it was important shared resident equipment was cleaned and disinfected appropriately and according to manufacturer's guidelines to prevent the spread of infection. During a review of the facility's undated policy and procedure (P&P), titled, Infection Control, the P&P indicated staff were to select equipment that could be easily cleaned and disinfected. The P&P indicated, do not use fabric-based equipment (e.g., chairs, stuffed toys, furry toys, transfer belts) if it will likely be contaminated with body fluids. During a review of the facility's P&P, revised 10/2018, titled, Cleaning and Disinfection of Resident-Care Items and Equipment, indicated Resident care equipment, including reusable items and durable medical equipment will be cleaned and disinfected according to current Centers for Disease Control and Prevention (CDC) recommendations for disinfection and the Occupational Safety and Health Administration (OSHA) Bloodborne Pathogens Standard. The P&P further indicated reusable resident care equipment will be decontaminated and/or sterilized between residents according to manufacturer's instructions. 3. During a review of Resident 3's admission Order, the admission Record indicated Resident 3 was admitted to the facility on [DATE] and re-admitted on [DATE], with diagnoses including paraplegia (paralysis that affects your legs, but not your arms), and unspecified epilepsy (disorder in which nerve cell activity in the brain is disturbed, causing seizures [involuntary muscle movements]) During a review of Resident 3's Minimum Data Sheet (MDS- a comprehensive assessment and care planning tool) dated 5/10/2024 indicated Resident 3 had moderate cognitive impairment (ability to learn, understand, and make decisions) and requires maximum assistance for toileting hygiene, shower/bathe self, upper body dressing, lower body dressing, putting on/taking off footwear and personal hygiene. During an observation on 06/10/2024 at 10:48 a.m.,11:45 a.m., 12:47 p.m., and 2:10 p.m., observed Resident 3 nephrostomy tube bag on top of the bed next to the resident parallel to his body. During an interview on 6/11/2024 at 2:50 p.m., the Director of Staff Development (DSD) stated nephrostomy tube drainage must be below the Resident 3's kidney to prevent reflux (flow backwards) of the urine to prevent infection. During an interview on 6/13/2024 at 8:54 a.m., the Licensed Vocational Nurse (LVN 4) stated when nephrostomy tube bag was in the same level of the kidney urine does not flow by gravity and can create urine backflow and might lead to infection. During a review of facility's P&P titled Nephrostomy Tube, Care of(undated), indicated Drainage should be below the level of the kidneys.
Apr 2024 1 deficiency
CONCERN (E) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to: 1. Ensure two of two clean linen carts did not have unnecessary items such as a box of gloves, trash bags, assignment sheets...

Read full inspector narrative →
Based on observation, interview, and record review, the facility failed to: 1. Ensure two of two clean linen carts did not have unnecessary items such as a box of gloves, trash bags, assignment sheets, and container of perfumed body fragrance noted inside of the clean linen carts. 2. Ensure a box of clean gloves did not have soiled gloves inside for one of three resident rooms. These deficient practices had the potential to result in cross contamination (process by which germs are unintentionally transferred from one object to another) and the spread of infections in the facility. Findings: During a concurrent observation and interview, on 4/2/2024, at 9:20 a.m., with Certified Nurse Assistant 2 (CNA 2), in the hallway, CNA 2 was observed to have trash bags, and an assignment sheet laying on top of clean linens inside of the clean linen cart. CNA 2 stated the gloves, trash bags, and assignment sheet were inside of the linen cart because there was no other place to put them. CNA 2 stated leaving the box of gloves, trash bags, and the assignment sheets inside of the linen cart can contaminate clean linen and spread infection to other residents. During a concurrent observation and interview on 4/2/2024, at 9:30 a.m., with CNA 1, in the hallway, CNA 1 was observed to have a pink bottle of body spray lying in between three (3) clean bath towels and four (4) clean sheets in the clean linen cart. CNA 1 stated the pink container of body spray should not be lying inside of the linen cart because of cross contamination that could spread infection to other residents. During a concurrent observation and interview on 4/2/2024, at 4:20 p.m., with CNA 3, in Resident 2's room, CNA 3 was observed grabbing two gloves from a box of gloves that had soiled gloves with brown substance. CNA 3 stated the soiled gloves should not be in the box of clean gloves because it can cause infection to another resident. During an interview on 4/3/2024, at 11:56 a.m., with the Infection Preventionist ([IP] a healthcare worker who specializes in preventing infection and to keep infection from spreading), the IP stated, staff were not allowed to have any personal items like body spray, trash bags, or any items in the clean linen cart. The IP stated soiled gloves should not be in the clean box of gloves because of cross contamination and risk of spreading infection to residents in the facility. During a review of the facility's policy and procedure titled, Standard Precautions, dated, 10/2018, the policy stated, linen carts should be free from unnecessary items that might contaminate the clean linen inside the cart. The policy indicated gloves were removed promptly after use, before touching non contaminated items and environmental surfaces, and before going to another resident. The policy indicated Resident - care equipment soiled with blood, body fluids, secretions, and excretions were handled in a manner that prevents skin and mucous membrane exposure, contamination of clothing, and transfer of microorganisms (germs) to other residents and environments.
Nov 2023 1 deficiency
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Safe Transfer (Tag F0626)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure one of five sampled residents (Resident 1), who was transfer...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure one of five sampled residents (Resident 1), who was transferred from the facility to a General Acute Care Hospital (GACH) for evaluation and treatment following a change of condition (COC) that Resident 1 experienced on [DATE], was readmitted to the facility after the seven-day bed hold expired, Resident 1 was cleared by the GACH to return to the facility and there were multiple female beds available. This deficient practice resulted in Resident 1's unnecessary stay in a GACH after the Resident 1 was cleared by the GACH to return to the facility. This had the potential for Resident 1's continuity of care to be interrupted and inconsistently provided. Findings: During a review of Resident 1's admission Record (Face sheet), the Face Sheet indicated Resident 1 was initially admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses that included spinal stenosis of the lumbar region (a condition of narrowing of the spinal canal compressing the nerves that result in pain and numbness), pressure ulcers (an injury that breaks down the skin and underlying tissue) to Resident 1's right buttock, and her right and left heels, and diabetes mellitus ([DM] a chronic condition associated with abnormally high levels of sugar in the blood). During a review of Resident 1's Minimum Data Set ([MDS] a standardized assessment and care screening tool), dated [DATE], the MDS indicated Resident 1 was able to make independent decisions that were reasonable and consistent. The MDS indicated Resident 1 required an extensive two-person physical assist to complete her activities of daily living ([ADL] residents' daily self-care activities such as bed mobility, toilet use and personal hygiene), she had an indwelling urinary catheter (a catheter placed in the bladder to drain urine from the bladder into a bag outside of the body), a colostomy (an opening in the belly that is made during a surgery procedure to allow waste to leave the body) and three Stage 4 pressure ulcers (a deep wound that may impact the muscle, tendons, ligaments and bone) that were present upon admission to the facility. During a review of Resident 1's Situational Background Assessment Recommendation ([SBAR] a form of communication between members of a health care team) Communication Form and Progress Note dated [DATE], the SBAR indicated Resident 1 was transferred to a GACH on [DATE] because of Resident 1's altered level of consciousness ([ALOC] a change in a person's state of awareness [ability to relate to self and the environment] and arousal [alertness]) and hyperglycemia (high blood glucose [sugar]) with a blood sugar (b/s) level of 514 milligrams ([mg] a unit of measurement/deciliter ([dl] a unit of measurement), with a normal b/s range of 70 mg/dl to 100 mg/dl. During a review of Resident 1's Order Summary (Physician's Order) dated [DATE], the Physician's Order indicated to transfer Resident 1 to a GACH due to altered mental status ([AMS] a changed level of awareness or mental state that falls short of unconsciousness, with a seven-day bed hold. During a review of GACH 2's Face Sheet, the Face Sheet indicated Resident 1 was admitted to GACH 2 on [DATE]. During a review of GACH 2's History and Physical (H&P), the H&P indicated Resident 1 was admitted to GACH 2 from GACH 1 on [DATE]. During a review of the facility's Daily Room List, the Daily Room List indicated the facility had 25 available female on [DATE] and [DATE], 23 available female beds on [DATE], and 20 available female beds on [DATE], [DATE] and 11/6 2023. During a telephone interview on [DATE] at 9:42 a.m., Resident 1's Emergency Contact (EC) stated, the facility did not inform her of the facility's intention to discharge Resident 1 from the facility. The EC stated the [NAME] Officer informed her Resident 1 had a large unpaid bill and the facility was no longer equipped to care for Resident 1. During a telephone interview on [DATE] at 1:51 p.m., the Case Manager (CM) from the GACH stated she called the facility on [DATE] at 3:17 p.m., after faxing Resident 1's clinical inquiry to the facility and spoke to the facility's admission Personnel (AP) and the facility's Director of Nursing (DON) to report Resident 1 was ready for discharge back to the facility. The CM stated the DON said something about staffing issues and Resident 1 needed a higher level of care due to her wound and they were unable to provide care to her anymore. The CM stated she referred Resident 1's case to their Social Worker (SW) and the SW reported to her (CM) that Resident 1 had not paid her copayment/share of cost at the facility. During an interview on [DATE] at 2:03 p.m., the DON stated she and the Administrator (ADM) decided they would not readmit Resident 1 to the facility because the facility was not able to accommodate Resident 1's wound care needs and procedures. During an interview on [DATE] at 3:07 p.m., the Admissions Personnel (AP) stated she received a call from the CM at the GACH on [DATE] indicating Resident 1 was ready to return to the facility, however, because of Resident 1's acuity (the severity of a resident's illness and the level of attention or service the resident will need from professional staff) which included Resident 1's pressure sores to her heels, therapy would be unsafe for Resident 1 so the facility was unable to readmit Resident 1. During an interview on [DATE] at 10:56 a.m., the Administrator (ADM) stated the facility will not readmit Resident 1 due to the resident's high acuity. During a telephone interview on [DATE] at 11:10 a.m., Resident 1's Physician stated, Resident 1's current health status is the same as it was when Resident 1 was initially admitted to the facility ([DATE]) and the facility staff provided care to Resident 1from her admission to her discharge ([DATE]). During a review of the facility's Policy and Procedure (P/P) titled, Bed Holds and Readmission, dated 5/2011, the P/P indicated that a resident who was away from the facility past seven days due to hospitalization or other medical treatment, will be readmitted to the first available bed in a semi- private room, if the resident needs the care provided by the facility and wished to be readmitted . During a review of the facility's undated P/P, titled, Notice of a Transfer and/or Discharge the P/P indicated the resident, and his/her representative will be given a thirty (30) day notice of an impending transfer or discharge from the facility when the transfer or discharge is necessary for the resident's welfare and when the resident's needs cannot be met in the facility and if the resident has failed after reasonable and appropriate notice, to pay for (or to have paid under Medicare or Medicaid) a stay in the facility.
Oct 2023 1 deficiency 1 Harm
SERIOUS (G) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Actual Harm - a resident was hurt due to facility failures

Accident Prevention (Tag F0689)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, and record review, the facility failed to ensure a resident was placed securely in the sling (part of a lift...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, and record review, the facility failed to ensure a resident was placed securely in the sling (part of a lift system placed under and around patients who have mobility issues to assist them to be lifted and transferred safely from a bed, wheelchair, toilet, or shower) for a mechanical lift (a device used to ensure the safe transfer of patients from one location to another), prior to being transferred from a bed to a wheelchair, for one of three sampled residents (Resident 1). This deficient practice resulted in Resident 1 falling from the mechanical lift onto his bed and sustaining a fracture (partial or complete break in the bone) of his clavicle (the collar bone) and his rib (chest bone). Resident 1 was transferred to a General Acute Care Hospital (GACH) for evaluation, treatment, and a Computed Tomography scan ([CT scan] a diagnostic imaging procedure that uses a combination of x-rays and computer technology to produce images of the inside of the body) of his head. Findings: During a review of Resident 1's admission Record (Face sheet), the Face Sheet indicated, Resident 1 was initially admitted to the facility on [DATE] and re-admitted on [DATE]. The Face Sheet indicated, Resident 1 had diagnoses of hemiplegia (paralysis on one side of the body) and hemiparesis (weakness or inability to move on one side of the body) following a cerebral infarction (a stroke) affecting the left dominant side of Resident 1's body, epileptic seizures (a disorder of the brain causing uncontrolled electrical activity in the brain, which may produce a physical convulsion, thought disturbances, or a combination of symptoms and a nontraumatic intracranial hemorrhage (bleeding into the brain in the absence of trauma or surgery). During a review of Resident 1's Minimum Data Set ([MDS] a standardized assessment and care screening tool), dated 3/29/2023, the MDS indicated, Resident 1's cognition (thinking, attention, language, learning, memory, and perception) was intact. The MDS indicated, Resident 1 required extensive one-person physical assist for bed mobility. Resident 1 was totally dependent and required a two-person physical assist for transfers and toilet use. During a review of Resident 1's Care Plan, dated 4/5/2022, the Care Plan indicated Resident 1 had an activity of daily living ([ADL] activities related to personal care) self-care performance deficit related to hemiplegia and hemiparesis. The goals indicated, Resident 1 would improve his functional abilities with less support from staff while maintaining comfort and safety. The Care Plan interventions indicated, Resident 1 required assistance and may use a mechanical lift for transfers. During a review of Resident 1's Nursing Progress Notes, dated 6/13/2023, timed at 5:15 p.m., the Progress Notes indicated, at approximately 12:30 p.m., Resident 1 was found on the floor with his head on the lap of Certified Nurse Assistant (CNA) 1. The Progress Notes indicated CNA 1 reported that Resident 1 had an assisted fall while being transferred from his bed to his wheelchair using a mechanical lift. The Progress Notes indicated Resident 1 had a bump on his left forehead and Resident 1 reported he hit his head but stated he did not remember where he hit his head. The Progress Notes indicated Resident 1's physician was called, and an order was obtained to transfer Resident 1 to a GACH for further evaluation and a CT scan of Resident 1's head. During a review of Resident 1's Situation, Background, Assessment, & Recommendation ([SBAR] a form of communication between members of a health care team) dated 6/13/2023 and timed at 1:14 p.m., the SBAR indicated, Resident 1's left upper extremity was sensitive to touch, he was unable to move, and he had a left forehead bump with discoloration and slight bleeding at the site that was sensitive to touch. During a review of Resident 1's Physician Orders, dated 6/13/2023, the Physician's Orders indicated, to transfer Resident 1 to a GACH emergency room (ER) for further evaluation after Resident 1 fell and sustained a head injury. During a review of Resident 1's Nursing Progress notes, dated 6/13/2023, at 6:29 p.m., the Nursing Progress notes indicated, Resident 1was picked up by an ambulance and transported to the GACH. During a review of the GACH's CT report of Resident 1's chest dated 6/13/2023, and timed at 8:01 p.m., the CT indicated, Resident 1 had a nondisplaced (a fracture in which the bone cracks or breaks but retains its proper alignment) left sixth posterior (direction toward the back of the body) rib fracture. During a review of the GACH's X-ray of Resident 1's left shoulder, dated 6/13/2023, and timed at 9:56 p.m., the X-ray indicated, Resident 1 had an anterior (front) subluxation (dislocation) of the left humeral head (shoulder) and a nondisplaced fracture of the distal (away from the trunk of the body) left clavicle (collar bone). During a review of the GACH's Emergency Department (ED) Physician Notes, dated 6/13/2023 and timed at 10:36 p.m., the ED notes indicated, Resident 1 had a shoulder reduction (the process of returning the shoulder to its normal position following a shoulder dislocation) and Resident 1's left shoulder was placed in a sling (a device that keeps the arm against the body and prevents too much movement). During an observation on 10/24/2023, at 12:38 p.m., CNA 1 prepared to transfer Resident 2 using a mechanical lift. CNA 1 quickly attached each hook on the mechanical lift to the sling that was under Resident 2. CNA 1 got assistance from another CNA (CNA 2) but CNA 1 nor CNA 2 did not check to ensure all hooks were safely connected and secured to the mechanical lift prior to transferring Resident 2 from his bed. During an interview on 10/24/2023, at 1:09 p.m., CNA 1 stated, there should be two people assisting while using a mechanical lift at all times. CNA 1 stated, regarding the fall incident on 6/13/2023, she looked for assistance to transfer Resident 1, but everyone was busy, and Resident 1 told her to hurry up because his family was visiting so she transferred Resident 1 using the mechanical lift alone without assistance from another staff member. CNA 1 stated, she put the sling under Resident 1's body and placed the hooks from the mechanical lift into the sling's openings. Resident 1 held onto the bar on the mechanical lift with his right hand while she lifted him using the mechanical lift. CNA 1 stated, one of the hooks on the upper left side of the sling came off and Resident 1 fell on top of the upper left side of his bed. CNA 1 stated Resident 1's legs were still in the sling and hanging from the mechanical lift and he was at an angle diagonally across his bed. CNA 1 stated she lowered the mechanical lift and Resident 1 fell onto the bed with his body slightly raised in the air while still attached to the sling that was still attached to the mechanical lift. Resident 1's right foot was hanging off the bed touching the ground and his left leg was on the bed. CNA 1 stated Resident 1 was holding onto her and would not let her go. Resident 1 was too heavy, and she had to lower Resident 1 onto the floor. CNA 1 stated she used the mechanical lift alone, because everyone was busy, and she felt confident enough to transfer Resident 1 on her own. CNA 1 stated it was important to use two people to assist when using the mechanical lift to keep the resident safe. CNA 1 stated she was instructed during in-services that two people were to always be present and assist when using a mechanical lift. During an interview on 10/24/2023, at 2:50 p.m., LVN 1 stated, CNA 1 reported to her that Resident 1 fell, she (LVN 1) went to Resident 1's room where she saw Resident 1 on the floor next to his bed. LVN 1 stated she assessed Resident 1 and noted a bump on the left side of Resident 1's head. During an interview on 10/24/2023, at 3:01 p.m., Registered Nurse Supervisor (RNS) 1 stated, two people were needed to transfer a patient using a mechanical lift. RNS 1 stated, CNA 1 reported that she was transferring Resident 1 from his bed to his wheelchair when Resident 1 slipped from the mechanical lift. RNS 1 stated when she entered Resident 1's room, CNA 1 was holding Resident 1's head in her lap and CNA 1 told her that she (CNA 1) caught Resident 1 when Resident 1 slipped from the mechanical lift. RNS 1 stated she assessed Resident 1 and found a bump on Resident 1's left forehead During an interview on 10/24/2023, at 3:37 p.m., the Director of Staff Development (DSD) stated, if a resident could only use one side of his body, then two people should assist when using a mechanical lift. The DSD stated Resident 1 required two people to transfer him using a mechanical lift because Resident 1 had left sided weakness and Resident 1's right side might not be strong enough to hold onto the mechanical lift. The DSD stated this injury was avoidable if the policy and procedure had been followed. The DSD stated, staff should make sure the sling is safely secured on the hooks of the mechanical lift, the second person provides a second check for safety and supports the upper back of the resident during the transfer. The DSD stated if everyone was busy, CNA 1 should have waited until someone came to assist before transferring Resident 1 by herself. During an interview on 10/25/2023, at 4:39 p.m., Director of Nursing (DON) 2 stated, it was reported to her that Resident 1 slipped from a mechanical lift, complained of chest pain, and was transferred to a GACH for a CT scan. DON 2 stated the hooks of the mechanical lift that go into the sling should have been checked to make sure the hooks were secured properly, and CNA 1 must have missed a step when using the mechanical lift. DON 2 stated the importance of using two people and checking that the hooks were secured properly was to prevent an accident such as a fall from the mechanical lift. During a review of the facility's Policy and Procedure (P/P), Lifting Machine, using a Portable revised 4/2007, the P/P indicated the portable lift can be used by one nursing assistant if the resident can participate in the lifting procedures. If not, two nursing assistants will be required to perform the procedure.
Nov 2022 1 deficiency
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to ensure one of three sampled resident (Resident 1) was not left soile...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to ensure one of three sampled resident (Resident 1) was not left soiled with feces or urine for an extended period and skin integrity was maintained. This deficient practice resulted in Resident 1 developing moisture associated skin damage ([MASD] erosion of the skin caused by prolonged exposure to moisture and its contents, including urine, and stool) which had the potential risk to develop into a pressure ulcers (injury to skin and underlying tissue resulting from prolonged pressure on the skin) ) and other related skin infections. During a review of Resident 1 ' s admission Record ( face sheet ) , the face sheet indicated, Resident 1 was admitted to the facility on [DATE] with diagnoses of but not limited to impingement syndrome of the left shoulder (a condition in which the tendons of the rotator cuff of the shoulder are pinched as they pass between the top of the upper arm and tip of the shoulder), hemiplegia (paralysis on one side of the body), type 2 diabetes mellitus ( (a condition in which the body fails to metabolize (process) glucose (sugar) correctly ), overflow incontinence (involuntary release of urine from an overfull urinary bladder), and diarrhea ( loose stool). During a review of Resident 1 ' s History and Physical (H&P), dated 7/22/2022, the H&P indicated, Resident 1 had the mental capacity to understand and make decisions. During a review of Resident 1 ' s progress notes dated 7/21/2022 to 8/29/2022, the progress notes indicated Resident 1 was incontinent (unable to control urination and bowel movement) and had 98 bowel movements. During a review of Resident 1 ' s Minimum Data Set ( (MDS - a comprehensive assessment and care screening tool), dated 7/27/2022, the MDS indicated, Resident 1 required extensive assistance with toilet use, mobility, transferring, locomotion on the unit, dressing, eating, toilet use and personal hygiene. During a review of Resident 1 ' s progress notes dated 8/17/2022, 8/18/2022, 8/19/2022, and 8/27/2022, the progress notes indicated Resident 1 was receiving ongoing treatment for MASD. During a review of Resident 1 ' s Skin and wound evaluation Form dated 8/26/22, the Skin and wound evaluation form indicated, Resident 1 acquired MASD on the perianal area while in the facility. During a review of Resident 1 ' s Skin Evaluation dated 8/27/2022, the Skin Evaluation, indicated Resident 1 required incontinence management, a moisture barrier, moisture control, and a turning and repositioning program. During a telephone interview on 11/9/2022 at 11:22 a.m. with Resident 1, Resident 1 stated she went to the facility because she had major surgeries on her left shoulder, Resident 1 stated her right side was weak due to a stroke and she could not walk, dress, shower and toilet without assistance. Resident 1 stated while a resident in the facility she laid in feces and had to wait at least half an hour to an hour before someone came to assist her. Resident 1 stated she has bed sores that developed in the facility. During an interview on 11/22/2022 at 10 :45 a.m. with Certified Nurse Assistant (CNA) 1, CNA 1 stated, Resident 1 would complain about waiting for a diaper change. CNA 1 stated the maximum Resident 1 would have to wait to be cleaned up from urine or feces was no more than twenty minutes because she would be assisting another resident and had already cleaned Resident 1 multiple times. During an interview on 11/22/22 at 11:02 a.m. with Licensed Vocational Nurse (LVN) 1, LVN 1 stated, Resident 1 had frequent diarrhea and would complain about waiting to be cleaned from the diarrhea, LVN 1 stated Resident 1 waited 10 minutes to be cleaned and would explain to Resident 1 that the CNA assigned to Resident 1 was assisting other residents. LVN 1 stated she understands the risk of skin issues developing if residents are left soiled in feces. LVN 1 stated she did not think waiting ten minutes in feces was a long time due to staff having other residents to attend to. During a concurrent interview and record review, on 11/22/22 at 11:33 a.m. with Registered Nurse (RN) 1, reviewed Resident 1 ' s treatment nurse notes indicated Resident 1 had MASD. RN 1 stated MASD was due to a resident being wet for long periods of time and not turning or repositioning the resident. RN 1 stated Resident 1 had issues with diarrhea and developed MASD while a resident at the facility. RN 1 stated five to twenty minutes was too long for a resident to have to wait to be cleaned when soiled with feces or urine, because the resident could develop bed sores the resident needs to be cleaned right away. During an interview on 11/22/2022 at 12:05 p.m. with the Director of Nursing (DON), the DON stated it was unacceptable for resident to wait for 20 minutes and left soiled and not changed in a timely manner. The DON stated it was all about the residents ' dignity. DON stated the facility was Resident 1 ' s home, and Resident 1 needs must be addressed by staff. The DON stated residents should not have to wait for their assigned nurse to be assisted. The DON stated staff should be doing rounding every two hours and thirty minutes before the shift ends to check the residents for toileting needs and call lights. During a review of the facility ' s policy and procedure (P&P) titled, Pressure Ulcer Risk Assessment, undated, the P&P indicated, Pressure ulcers are often made worse by continual pressure, heat, moisture, irritating substances on the resident's skin (i.e., perspiration, feces, urine, wound discharge, soap residue, etc.), decline in nutrition and hydration status, acute illness and/or decline in the resident's physical and/or mental condition. Once a pressure ulcer develops, it can be extremely difficult to heal. Routinely assess and document the condition of the resident's skin per facility wound and skin care program for any signs and symptoms of irritation or breakdown. Immediately report any signs of a developing pressure ulcer to the supervisor. Skin will be assessed upon admission for the presence of ulcer or any skin impairments, and for developing pressure ulcers on a weekly basis or more frequently if indicated.
Jul 2021 16 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0584)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure personal property was kept safe from loss or t...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure personal property was kept safe from loss or theft for one out of one (1) sampled residents (Resident 53). This deficient practice resulted in Resident 53 losing her diamond ring, which upset the resident, and had the potential to result in further loss of personal belongings. Findings: During a review of Resident 53's admission Record, dated July 15, 2021, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including osteoarthritis (breakdown of cartilage in joints), type 2 diabetes mellitus, end stage renal disease (ESRD - permanent kidney function loss), dependence on renal dialysis (procedure to remove waste products from the blood when the kidneys no longer function), and major depressive disorder. During a review of Resident 53's Resident's Clothing and Possessions, dated September 7, 2019, indicated the resident only had one gown and one silver chain for keys documented as her personal belongings. During a review of Resident 53's Resident's Clothing and Possessions, dated July 9, 2021, indicated the resident had one glasses, one upper denture, one white watch, and two yellow gold rings documented as her personal belongings. During a review of the facility's Theft/Loss Report Control Log, dated June 2021, indicated Resident 53 was missing a ring and that her family had reported the incident to law enforcement. During a concurrent observation and interview, on July 7, 2021, at 3:24 p.m., in room [ROOM NUMBER], with Resident 53, the resident was observed wearing a gold ring with a row of [NAME] diamonds varying in sizes. Resident 53 stated she has things stolen from her all the time such as shoes and a diamond ring. The resident stated her diamond ring was stolen off her finger about two weeks ago and that the facility is aware of it but has not done anything about it and expressed she believed the facility was not going to do anything. During an interview, on July 9, 2021, at 11:30 a.m., with Certified Nurse Assistant (CNA) 14, CNA 14 stated Resident 53 likes to wear jewelry and leaves for her dialysis appointments with her jewelry. CNA 14 stated charge nurses keep residents' jewelry in the medication carts for safekeeping, but some residents who are alert like to keep their personal belongings with themselves. CNA 14 stated CNAs complete inventory lists upon a resident's admission to the facility or when a resident leaves and returns. CNA 14 stated CNAs have another CNA or charge nurse verify items because residents may have valuable items, further stating it is important to complete inventory lists to document residents' belongings. CNA 14 stated if a resident loses items but the inventory list is not complete, the resident can blame staff. CNA 14 stated the facility is responsible for residents' belongings and it's not nice to lose things. During a concurrent observation, interview, and record review, on July 9, 2021, at 2:49 p.m., in room [ROOM NUMBER], with CNA 14, CNA 14 stated CNAs document residents' belongings upon admission and when new items are brought to the facility on the inventory sheet. If belongings are not documented on the inventory list, it means the resident did not have it. CNA 14 observed Resident 53 and stated the resident was wearing a watch, a yellow gold diamond ring, and another yellow ring on her pinky with stones. CNA 14 stated staff do not need to remove residents' jewelry when going out for any appointments, including for dialysis. CNA 14 reviewed Resident 53's Resident's Clothing and Possessions, dated September 7, 2019, and stated this was the only inventory list in the resident's medical chart. CNA 14 stated not all of Resident 53's jewelry is documented in her inventory list and should be updated to reflect her current belongings. CNA 14 stated it was not right that the resident's belongings were not fully documented and that whomever was caring for the resident should have updated the inventory list. CNA 14 stated inventory lists need to be completed because residents' belongings could become lost, someone could have taken it, or a resident could have misplaced it because some residents are forgetful. CNA 14 stated Resident 53 is sometimes forgetful. CNA 14 stated she was going to update the resident's inventory list and will document all her belongings, such as the resident's dentures, rings, and clothing. CNA 14 stated Resident 53 had not mention anything about missing belongings to her, but that she had recently heard of the resident's allegation of someone stealing her ring. During an interview, on July 14, 2021, at 1:48 p.m., with CNA 1, CNA 1 stated CNAs fill out the inventory lists when a resident is newly admitted and the form is given to the nurse supervisor. CNA 1 stated the nurse supervisor or social worker updates inventory lists if residents have new belongings. CNA 1 stated jewelry is supposed to kept in the medicine carts, and if a resident needs or wants it, the charge nurses give it to the CNA to give to the resident. When jewelry is taken off, the CNA gives it back to the charge nurse to put away. CNA 1 stated if a resident has four necklaces, then it should be reflected on the inventory list. However, CNA 1 stated no description is written. CNA 1 stated some resident keep their belongings to themselves - if a resident is alert, the resident will let the CNA know what items they want to wear. CNA 1 stated the facility provides a lock and key for alert resident who want to keep their belongings with them. CNA 1 stated residents are allowed to wear their jewelry to their appointments and can decide how they want to dress. CNA 1 stated staff cannot remove a resident's jewelry or belongings without their permission. CNA 1 stated if a resident reports something as missing, it is reported to the nurse supervisor who will then discuss the issue with the resident. CNA 1 stated Resident 53 had lost her wedding ring, which the nurse supervisor and social worker discussed with the resident, and police came the next day to speak with the resident and CNAs. CNA 1 stated Resident 53 is alert, can do her own makeup and puts on her jewelry by herself. During an interview, on July 15, 2021, at 8:47 a.m., with Licensed Vocational Nurse (LVN) 9, LVN 9 stated all of a resident's belongings should be documented on their inventory list because the facility is responsible for whatever belongings the resident or their family brings into the facility. LVN 9 stated if items are not documented, the facility is still liable. LVN 9 stated she had heard Resident 53 lost her engagement or wedding ring a couple months ago, and that the resident had claimed it as lost or stolen. LVN 9 stated Resident 53 has a lock and key for her nightstand and that only the resident has the key, which she wears around her neck. LVN 9 stated she was not sure who provided the resident with the lock and key, but stated the facility placed the bolts for the lock. During an interview, on July 15, 2021, at 8:59 a.m., with Quality Assurance (QA), QA stated she had heard during a morning meeting that Resident 53 had recently lost her wedding ring, but was not sure when it occurred. QA stated she attended a meeting with Resident 53 and her husband to discuss the missing ring because the resident thought a staff member took it. QA stated staff was not able to find the resident's ring. QA stated Resident 53 has a locked table to store her belongings because she had claimed a missing ring about three years ago. QA stated the SSD investigates claims of lost belongings and stated the DSD and Administrator (ADM) spoke with Resident 53 and her husband regarding her missing ring, but was not sure what the outcome was. During an interview, on July 15, 2021, at 9:23 a.m., with the Social Services Director (SSD), the SSD stated she is responsible for following up on grievances and lost belongings. The SSD stated when an item is reported as missing, she discusses the matter with the resident and asks where it was last seen, tries to locate the missing item, such as clothing or dentures, throughout the facility including the laundry area and kitchen. The SSD stated if the missing item is found, it is returned to the resident; if not found, replacement is offered. The SSD stated Resident 53 had reported a lost ring in June 2021, but was off work at the time and was informed when she returned to work three days after the incident. The SSD stated SSA 1 and SSA 2 from the social services department completed the report and looked for the ring even though other staff had already looked for it. The SSD stated a meeting was held with Resident 53 and her husband to discuss how to resolve the issue and offered replacement or reimbursement, to which the resident and husband asked the facility to continue looking for the ring and stated they would let the facility know if they want reimbursement. The SSD stated as current, the ring has not been found, nor has the resident or husband said anything else regarding the issue. During an interview, on July 15, 2021, at 9:33 a.m., with Social Services Assistant (SSA) 2, SSA 2 stated inventory lists are completed by the SSD and SSA 1, but was not sure when they complete the forms. SSA 2 then stated she would find out and left the room. At 9:37 a.m., SSA 2 returned and stated inventory lists are completed by the CNAs upon new admissions. If any belongings need to be added to inventory lists after admission, they can be added by the nursing staff or the SSD. SSA 2 stated she herself does not fill out the inventory lists; her responsibilities include updating communication boards and arranging transportation services. SSA 2 stated items should be documented on the inventory list and written down specifically, such as the amount, color, and type. SSA 2 stated the residents' family and whomever completes the inventory lists signs the form. SSA 2 stated if an item is not written on the resident's inventory list, it means it did not belong to the resident. SSA 2 stated inventory lists should reflect everything a resident considers part of their belongings. SSA 2 stated if something is lost, it is reported to the Director of Staff Development (DSD) who creates a theft and loss report, then conducts interviews with nursing staff and the resident. SSA 2 stated the resident's family is called for the cost of missing belongings or is sometimes asked to buy the item themselves and present the facility with a receipt to reimburse with money. SSA 2 stated missing items are verified with the resident and checked on their inventory list. SSA 2 stated all staff are responsible for residents' belongings. If an item is reported as missing but is not on the inventory list, the facility calls family to ask if the resident did have the item but does not offer reimbursement because it was not documented; the inventory list verifies each item that belongs to a resident. SSA 2 stated inventory lists are updated whenever family brings in belongings as soon as it is brought into the facility. SSA 2 stated Resident 53 had reported a missing ring to a CNA who then informed the DSD who further reported to social services. SSA 2 stated she, SSA 1, and the DSD interviewed Resident 53 and CNA 6, who was assigned to care for the resident that morning. During a concurrent interview and record review, on July 15, 2021, at 10:00 a.m., of the facility's Theft and Loss Report, dated June 16, 2021, with SSA 2, the document indicated Resident 53 reported a one carat diamond ring as missing. SSA 2 stated the resident had a prior claim of her ring missing (a previous year, but was unable to recall when exactly), and stated it was the same ring as recently reported missing. The facility had asked the Resident 53's husband to keep her belongings but he refused and was documented. SSA 2 stated the SSD was aware of the ring because she had found it when it was first reported missing and was documented on the resident's inventory list. SSA 2 stated the facility sometimes offers reimbursement for items not documented on the inventory list in an effort to make residents happy. SSA 2 stated the facility offered the resident and her husband reimbursement for the missing ring but has not heard back from the husband. SSA 2 reviewed Resident 53's Resident's Clothing and Possessions, dated September 7, 2019, and stated there was no ring documented. SSA 2 stated Resident 53 has many personal belongings in her room and also reviewed the residents Resident's Clothing and Possessions, dated July 9, 2021, and stated all of Resident 53's personal items in her room should have been documented. SSA 2 stated the nurses need to verify the resident's belongings in her room and document the items on the inventory list with social services. During an interview, on July 15, 2021, at 10:48 a.m., with the ADM, the ADM stated there are no audits done on inventory lists; if anything new is brought into the facility, it should be added to the resident's inventory list. A review of the facility's policy and procedure (P&P), entitled Theft & Loss, dated June 2019, indicated the following: All newly admitted residents are assisted to complete an inventory of personal items, signed by the resident (or representative) and at least one staff member. Items added later will be signed and dated by same . Facility will report to the local law enforcement agency within 36 hours when the administrator of the facility has reason to believe patient property with a then-current value of one hundred dollars ($100) or more has been stolen.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Assessments (Tag F0636)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, and record review, the facility failed to ensure the Minimum Data Set ([MDS] a standardized assessment and ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, and record review, the facility failed to ensure the Minimum Data Set ([MDS] a standardized assessment and care screening tool) assessment accurately reflected the discharge status of 1 out of 3 sampled residents (108). Resident 108 who was discharge to the community and the MDS indicated she was discharged to the General Acute Care Hospital (GACH). This deficient practice had the potential to put Resident 1 at risk of not receiving optimal care for a safety discharge. Findings: During a record review, the Face Sheet, indicated Resident 108 was admitted on [DATE]. Diagnosis included left leg fracture (broken bone) and diabetes mellitus (abnormal blood sugar). During a record review the Skilled Nursing Facility Discharge Instructions dated 5/28/21 and timed 10:59 p.m., indicated Resident 109 was discharge home. During a record review the Progress note dated 5/28/21 and timed 11:24 p.m., indicated Resident 109 and the responsible party received discharge instructions prior to being discharge home. During a record review the MDS dated [DATE], indicated Resident 109 was discharge to the GACH. During a concurrent interview and record review on 7/14/21 at 8:38 a.m., MDS Nurse 2 stated Resident 109 was discharge home and the MDS dated [DATE] indicated Resident 109 was discharge to the GACH and that was wrong. MDS Nurse 2 stated the discharge assessment was important to be accurate to ensure Resident 109 received the proper discharge follow up and received a safety discharge. The Center for Medicare and Medicaid ([CMS] part of the department of health and human services) MDS guidance titled The Long-Term Care Facility Resident Assessment Instrument 3.0 User's Manual dated 10/19, indicated residents should be the primary source of information for resident assessment items. The manual indicated the intent of the MDS section A was to obtain key information to uniquely identify each resident, the home in which they resided, and the reasons for assessment. The MDS manual indicated to review the Resident's medical records including the discharge orders for documentation of discharge location.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to ensure one out of two residents (Resident 87) who rece...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to ensure one out of two residents (Resident 87) who received oxygen (a gas used by a person to increase the amount of oxygen the lungs receive and deliver to the blood) had the nasal cannula (device used to deliver oxygen) properly place consistent with professional standards of practice. Resident 87 who was a total care and was dependent on the staff to ensure he received oxygen. The deficient practice had the potential to cause Resident 87 to not receive the needed oxygen to maintain physiological function. Findings: During a record review for Resident 87, the admission record indicated Resident 87 was originally admitted on [DATE] and readmitted on [DATE]. Diagnoses included epilepsy (seizure activity that causes a burst of uncontrolled electrical activity between brain cells that causes temporary abnormalities in muscle tone or movements such as stiffness, twitching or limpness, behaviors, sensations or states of awareness), functional quadriplegia (complete inability to move due to severe disability or frailty caused by another medical condition without physical injury or damage to the spinal cord), and cerebrovascular disease (occurs if the flow of oxygen-rich blood to a portion of the brain is blocked. Without oxygen, brain cells start to die after a few minutes) During a record review for Resident 87, the care plan oxygen therapy shortness of breath dated 1/11/19, indicated Resident 87 intervention included receiving breathing treatment as ordered, and oxygen as needed. During a record review for resident 87, the progress notes titled Physicians' History and Physical dated 1/9/21, indicated Resident 89 required total care was non-verbal and was usually able to open eyes. During a record review for Resident 87, the Minimum Data Set ([MDS] a standardized assessment and care screening tool) dated 5/26/21, indicated Resident 87 was never or rarely understood and rarely or never understood others. The MDS indicated resident 87 was total dependent and required two-person assistance with bed mobility, transfer, dressing, and toilet use. During a record review for Resident 87, the Order Summary Report dated 7/8/21, indicated Resident 87 had orders to receive oxygen at three liters for a minute via a nasal cannula continuously every shift. During an observation and concurrent interview on 7/12/21, at 8:18 a.m., Resident 87 was on the bed with the nasal cannula above his nose, oxygen tank was running at 4 liters per a minute. Certified Nurse Assistant (CAN 15) confirmed Resident 87 did not have the nasal cannula into his nose and stated she would put the nasal cannula back into Resident 87's nose. During a concurrent observation and interview on 7/15/21, at 7:40 a.m., Resident 87 was on the bed, the oxygen tank read the oxygen was delivered at three liters per minute (lpm) and the nasal cannula was on Resident 87's chest. Licensed Vocational Nurse (LVN 9) was notified Resident 87 required assistance. LVN 9 came into Resident 87 room and stated Resident 87 received continues oxygen therapy. LVN 9 place the nasal cannula into Resident's 87 nose and adjusted the elastic band bellow Resident 87 chin. LVN 9 stated Resident 87 need to have the oxygen or he would not receive the needed oxygen his brain needed. LVN 9 stated Resident 87 did not have the capacity to move the nasal cannula as he was contracted (a condition of shortening and hardening of muscles, tendons, or other tissue, often leading to deformity and rigidity of joints). LVN 9 stated when Resident 87 was changed the staff may have forgot to adjust the nasal cannula elastic band that secured the nasal cannula in place for Resident 87. LVN 9 stated the nasal cannula elastic band was loose and was supposed to be secured to prevent the nasal cannula from moving. The facility's undated policy titled Oxygen Administration undated, indicated to verify the physician's orders for the facility's protocol for oxygen administration and review the resident's care plan to assess for any special needs of the resident. The policy indicated oxygen therapy was administered by way of an oxygen mask, nasal cannula, and/or nasal catheter, the oxygen mask was a device that fitted over the resident's nose and mouth and was placed by an elastic band placed around the resident's head. The policy stated the nasal cannula was a tube that was placed approximately one-half inch into the residents' nose that was held in place approximately one half inch into the resident's nose and was held in place by an elastic band placed around the resident's head
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0675 (Tag F0675)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to monitor a certified nursing assistants (CNA 6) positi...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to monitor a certified nursing assistants (CNA 6) positions while feeding one of 27 residents, Resident 82. This failed practice had the potential to cause the resident to eat faster, have difficulty swallowing, and diminish the resident's dignity. Findings: During a concurrent observation and interview on 7/14/2021 at 7:43 in Resident 87's room, Resident 82 was observed lying in bed and CNA 6 was standing over the bedside table and feeding Resident 82. Surveyor further observed a beige folding chair in the corner. CNA 6 stated Resident 82 ate 75% of her breakfast, and standing over the resident while feeding her may make her feel uncomfortable. During a review of Resident 82's admission record (AR) indicated Resident 82 was re-admitted on [DATE] with diagnosis of Dementia (is a general term for loss of memory, language, problem-solving and other thinking abilities that are severe enough to interfere with daily life), gastro-esophageal reflux disease without esophagitis (is a chronic disease that occurs when stomach acid or bile flows into the food pipe and irritates the lining), and other lack of coordination. During a review of Resident 82's minimum data set (MDS-an assessment and care planning tool) dated 6/12/2021, indicated Resident 82 had clear speech, limited ability to making concrete request, and responds adequately to simple, direct communication only. The MDS further assessed Resident 82 requiring extensive assistance with dressing, toilet use, and personal hygiene. During a review of Resident 82's care plan, dated 6/10/2021, indicated Resident 82 has decline in memory, concentration, orientation, language and judgement related to Dementia with Parkinson's disease. Nursing interventions included to be at his/her eye level, call the resident by name, and ask how you can help. A review of the facility policy titled Assistance with Meals, revised August 2009, indicated residents shall receive assistance with meals in a manner that meets the individual needs of each resident. Residents who cannot feed themselves will be feed with attention to safety, comfort and dignity, for example not standing over residents while assisting with meals; keeping interaction with other staff to a minimum while assisting residents with meals; avoiding the use of labels when referring to residents (e.g., feeders).
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Quality of Care (Tag F0684)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure three out of three (3) sampled residents (Resi...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure three out of three (3) sampled residents (Residents 93 and 25) received treatment and care in accordance with professional standards of practice to meet the residents' physical, mental, and psychosocial needs as evidenced by: 1. For Resident 93, nursing staff failed to notify the physician of, create an SBAR (abbreviation for Situation, Background, Assessment, Recommendation - a communication tool) for, and update the resident's care plan to reflect the resident's complaint of burning with urination; 2. For Resident 5, who had a recent history of seizure a burst of uncontrolled electrical activity between brain cells (also called neurons or nerve cells) that causes temporary abnormalities in muscle tone or movements (stiffness, twitching or limpness), behaviors, sensations or states of awareness), the facility failed to ensure Resident 5 receive proper seizure precaution the deficient practice had the potential to cause Resident 5 to suffer an injury such as a fall from a seizure activity. These deficient practices had the potential to negatively affect Resident 286, 67, and 51's physical, mental, and psychosocial needs. Findings: a. During a review of Resident 93's admission Record, dated July 14, 2021, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including muscle wasting and atrophy, systemic lupus erythema (autoimmune disease in which the immune system attacks its own tissues), fibromyalgia (widespread muscle pain and tenderness), lack of coordination, history of falling, retention of urine, and urinary tract infections (infection in any part of the urinary system - kidneys, bladder, or urethra). During a review of Resident 93's Care Plan, revised on May 20, 2021, indicated the resident had episodes of burning sensation with urination on April 21, 2021 and May 20, 2021 with interventions including assessing and asking the resident if she experiences painful urination. During a review of Resident 93's Care Plan, dated November 17, 2020, indicated the resident had the potential to develop urinary tract infection (UTI) with interventions to Report to MD [physician] for any of those mentioned sign and symptoms but does not specify what signs and symptoms to monitor. During an interview, on July 7, 2021, at 10:06 a.m., with Resident 93, the resident stated she was admitted to the facility in October 2020 and has had eight to nine UTIs since. Resident 93 stated she once had to wait two hours to have her disposable brief changed that was soiled with a lot of feces, and that she started wearing disposable briefs three months ago. The resident stated staff had even put towels in between her legs which baffled her. During an interview, on July 8, 2021, at 8:19 a.m., with Resident 93, the resident stated staff put a towel in between her legs a long time ago when she was first admitted and had lots of urine she could not control. Resident 93 stated this happened twice but has not happened since November 2020. The resident stated she had just returned to the facility from the hospital recently to treat her UTI a few days ago. During a concurrent observation and interview, on July 9, 2021, at 11:08 a.m., with Certified Nurse Assistant (CNA) 11, CNA 11 was observed coming out of room [ROOM NUMBER]. CNA 11 stated she had just assisted Resident 93 with cleaning her face and back, and provided perineal (private parts) care. CNA 11 stated the resident is incontinent (uncontrolled) of bladder and bowel and used to have a foley catheter (a thin sterile tube that is inserted into the urethra to drain urine from the bladder) but not anymore. CNA 11 stated Resident 93 informed her today that it hurts when she urinates and was having difficulty urinating starting this morning. CNA 11 stated she was going to tell the charge nurse about the resident's painful urination with burning sensation because it be indicative of UTI. During an interview, on July 9, 2021, at 1:15 a.m., with Resident 93, the resident stated it burns when she urinates and that it feels like hot water. Resident 93 stated she informed a nurse about the painful urination. The resident further stated she does not want to urinate because of the burning sensation. Resident 93 stated she had informed another nurse she believed her UTI was not gone and that she needed to be retested. The resident stated her foley catheter was removed a few days ago and believed it hurt to urinate because maybe her body needed to get used to the catheter being removed. Resident 93 stated she usually knows when she needs to urinate but now cannot feel the sensation so her urine just flows out. The resident stated the burning sensation with urination started at approximately 6:30 a.m. this morning, then urinated around 9:30 a.m. and told a nurse that she was experiencing burning with urination. Resident 93 stated she had told another nurse about the burning with urination about thirty minutes ago. During an interview, on July 9, 2021, at 1:29 p.m., with Licensed Vocational Nurse (LVN) 10, LVN 10 stated Resident 93 has a history of several UTIs, urinary retention, and was treated for Extended Spectrum Beta-Lactamases (ESBL - enzymes produced by certain bacteria that may be resistant to antibiotics) two weeks ago. LVN 10 stated it had been reported to her that Resident 93 had burning sensation with urination and that the physician was notified, the resident was being monitored, and nurses were waiting for physician's order if needed. During a concurrent interview and record review, on July 13, 2021, at 11:03 a.m., with LVN 3, LVN 3 stated Resident 93 had a recent diagnosis of UTI. A review of Resident 93's electronic health record (EHR) indicated the resident was admitted to the facility on [DATE] with a history of UTI. LVN 3 stated Resident 93 has chronic UTI and was referred to a urologist but she cancelled multiple times because of other health concerns. Upon further review of Resident 93's EHR, LVN 3 stated there was no SBAR (abbreviation for Situation, Background, Assessment, Recommendation - a communication tool) documented for July 9, 2021. LVN 3 stated she had worked over the weekend but was not aware Resident 93 had complained of burning sensation with urination; LVN 3 stated she did not receive report regarding this issue from the residents, CNAs, or licensed nurses. LVN 3 stated there were no new orders for Resident 93. LVN 3 stated if a resident complains of burning upon urination, nurses need to contact the physician and document an SBAR note, perform 72 hour monitoring of the resident, and note whether the physician places any new orders or not. LVN 3 stated nurses can expect an order for a urine specimen collection to complete a urinalysis (urine test used to detect disorders or illness). During a concurrent interview and record review, on July 14, 2021, at 9:38 a.m., of Resident 93's EHR, with LVN 9, LVN 9 stated if a resident has a change of condition (COC), the physician must be notified, suggested orders documented in the resident's EHR, and family informed. LVN 9 stated care plans and SBAR note should be done right away for any change of condition. If a COC happened during the morning shift, then it should be endorse to the evening shift because the following shift is responsible for following up. The person notified of the COC is responsible for creating a care plan. If missed, the next shift follows up to complete it. LVN 9 stated burning with urination should be care planned because the physician usually orders a urinalysis to see what is going on with the resident, such as if there are any ongoing infections. If there is no care plan, then nurses cannot do monitoring of the resident because it is an intervention to apply to the resident and determine if it is effective or not. A review of the progress note, dated July 9, 2021, documented by LVN 10, indicated the Resident 93 was on monitoring after her foley catheter removal. LVN 9 stated the last documentation regarding Resident 93 experiencing pain with urination was on May 23, 2021. LVN 9 stated there were no notes regarding burning sensation with urination for the resident in SBAR, but it should have been documented in SBAR or a progress note. LVN 9 stated if a COC is not documented or care planned right away, it can harm the resident because no one would know what is going on with the resident's health status. LVN 9 reviewed Resident 93's care plan and stated there was no care plan for burning with urination for the month of July 2021. During an interview, on July 15, 2021, at 9:18 a.m., with LVN 10, LVN 10 stated she was informed about Resident 93 experiencing burning sensation with urination by the nurse on the previous shift when it first occurred, and that the nurse had contacted the physician. LVN 10 stated the resident was being monitored for urinary retention but that there was no monitoring for the burning sensation with urination, and that she should have caught it by the end of her shift. LVN 10 stated she should have verified that Resident 93's care plan was updated to reflect her complaint of burning with urination. A review of the facility's policy and procedure (P&P), entitled Change in a Resident's Condition or Status, not dated, indicated the facility shall notify the resident's physician of changes in the resident's medical/mental condition and/or status within twenty-four hours. This P&P also indicated the nurse supervisor or charge nurse will record in the resident's medical record information relative to changes in the resident's medical/mental condition or status. This P&P further indicated a significant change of condition is a decline or improvement in the resident's status that requires interdisciplinary review and/or revision to the care plan. A review of the facility's P&P, entitled Urinary Tract Infections/Bacteriuria, not dated, indicated nurses should observe, document, and report signs and symptoms in detail. b. During a review of the admission Record, indicated Resident 5 was originally admitted on [DATE] and readmitted on [DATE]. Diagnosis included diabetes mellitus (abnormal blood sugar), ESRD, dementia (memory loss), and dysphagia (difficulty swallowing). During a Record review for Resident 5, the care plan seizure disorder dated 6/10/21, indicated a goal to prevent traumatic injuries. The care plan interventions included keep the environment free of safety hazards and reduce unsafe activities. During a record review for Resident 5, the Progress Note dated 5/25/21, and timed 2 p.m., indicated the hemodialysis center notified the facility about Resident 5 transfer to the general acute care hospital (GACH) due to a seizure. During a record review for Resident 5, the Progress Notes titled Physician's History & Physical dated 6/18/21, and timed 4:39 p.m., indicated Resident 5 was profoundly demented, did not speak, was confused, forgetful, required total care, did not have the capacity to understand and be understood, and had a history of seizure disorder. During a Record review for Resident 5 the Order Summary Report dated 7/8/21, indicated Resident 5 had an order for levetiracetam solution 100 milligrams ([mg] unit of measurement)/ milliliter ([ml] unit of measurement) 2.5 ml two times a day for seizure. During a record review for Resident 5, the Minimum Data Set ([MDS a standardized assessment and care screening tool) dated 7/29/21, indicated Resident 5 was rarely or never understood and sometimes was able to understand others. The MDS indicated Resident 5 required one-person extensive assistance with bed mobility, dressing, toilet use, and personal hygiene. During a concurrent observation and interview on 7/8/21, at 7:51 a.m., in Resident 5's room, Resident 5 had two half side rails up, not padded and the bed was elevated at the level of the waist. CAN 7 came into Resident 5's room and confirmed Resident 5 bed rails were up, did not have any covers, and the bed was elevated. CAN 5 lower the bed for Resident 5 and stated Resident 5 was a fall risk and the bed should be in the lowest position to prevent Resident 5 from having a hard fall. During a concurrent interview and record review on 7/12/21, at 10:09 a.m., licensed Vocational Nurse (LVN 9) stated the progress note dated 5/25/21, indicated Resident 5 had a seizure at the hemodialysis center and was send to the General Acute Care Center (GACH). LVN 9 stated Resident 5 was on seizure safety precautions such as a clutter free environment, side rails up and padded to decrease the risk of Resident 5 hitting her head and prevent an injury. During an interview on 7/13/21, at 12:49 p.m., the director of nursing (DON) stated seizure precaution was very important and was important to ensure the staff knew what to do and what to monitor the resident during a seizure. The DON stated seizure prevention included padding the residents side rails and monitoring the seizure medication level to prevent residents from having an injury. The DON stated he did not know why the seizure precautions such as padded side rails had been implemented today for residents with seizures. The DON the seizure precautions should have been implemented but during the COVID-19 outbreak residents were moved to different rooms and the facility did not followed up on the seizure precaution. A review of the facility's undated policy titled Seizures management undated indicated a purpose to provide guidelines to safely manage the resident who was having a seizure. The policy indicated steps in the procedure of a seizure included taking measures to prevent the resident from falling out of bed. The facility's policy titled Seizures and Epilepsy- Clinical Protocol undated, indicated seizure assessment and recognition included identifying individuals who had a seizure and received seizure medication. The policy indicated the staff would monitor the progress of an individual with a new seizure or seizure disorder and would modify interventions accordingly. During a review of the admission Record, indicated Resident 5 was originally admitted on [DATE] and readmitted on [DATE]. Diagnosis included diabetes mellitus (abnormal blood sugar), ESRD, dementia (memory loss), and dysphagia (difficulty swallowing). During a Record review for Resident 5, the care plan seizure disorder dated 6/10/21, indicated a goal to prevent traumatic injuries. The care plan interventions included monitor labs as ordered. During a record review for Resident 5, the Progress Note dated 5/25/21, and timed 2 p.m., indicated the hemodialysis center notified the facility about Resident 5 transfer to the general acute care hospital (GACH) due to a seizure During a record review for Resident 5, the physician telephone order dated 6/1/21 and times 10:03 p.m., indicated an order to draw levetiracetam level in two weeks (6/15/21) one time only. During a record review for Resident 5, the Progress Notes titled Physician's History & Physical dated 6/18/21, and timed 4:39 p.m., indicated Resident 5 was profoundly demented, did not speak, was confused, forgetful, required total care, did not have the capacity to understand and be understood, and had a history of seizure disorder. During a Record review for Resident 5 the Order Summary Report dated 7/8/21, indicated Resident 5 had an order for levetiracetam solution 100 milligrams ([mg] unit of measurement)/ milliliter ([ml] unit of measurement) 2.5 ml two times a day for seizure. During a record review for Resident 5, the Minimum Data Set ([MDS a standardized assessment and care screening tool) dated 7/29/21, indicated Resident 5 was rarely or never understood and sometimes was able to understand others. The MDS indicated Resident 5 required one-person extensive assistance with bed mobility, dressing, toilet use, and personal hygiene. During a concurrent interview and record review on 7/12/21, at 10:09 a.m., LVN 9 stated Resident 5 was receiving levetiracetam and the laboratory result for the levetiracetam level on 6/1/21 was 73.5 which was high. LVN 9 stated the physician was notified and new orders to check the levetiracetam levels on 6/15/21 were received. LVN 9 stated the orders were not carried out because Resident 5 was discharge to the General Acute Care Hospital (GACH). LVN 9 checked the GACH records for Resident 5 and could not find any laboratory results for levetiracetam. LVN 9 stated the levetiracetam levels were not checked for Resident 5 after she returned from the hospital. LVN 9 stated the facility should have checked the levetiracetam level for Resident 5 to ensure the medication was functioning properly and preventing Resident 5 from having seizures. During an interview on 7/13/21, at 12:49 p.m., the director of nursing (DON) stated seizure precaution was very important and was important to ensure the staff knew what to do and what to monitor residents with seizures. The DON stated seizure prevention included padding the residents side rails and monitoring the seizure medication level to prevent residents from having an injury. The DON the seizure precautions should have been implemented for seizure residents. A review of the facility's policy titled Seizures and Epilepsy- Clinical Protocol undated, indicated seizure assessment and recognition included assessing and documenting/reporting whether the resident has a known seizure disorder or history of actual seizure activity and last blood level of any anticonvulsants being given. The policy indicated seizure treatment and management included the physician identification and order of appropriate treatment. The policy indicated seizure management included the physician order of antiepileptic medication blood levels periodically and results interpreted appropriately.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to follow up with the facility's Registered Dietician (RD) recommendat...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to follow up with the facility's Registered Dietician (RD) recommendations for weight loss for one of 21 residents (Resident 69) who had 23 percent (%) significant weight loss in one month. This deficient practice had the potential to cause Resident 69 to experience dehydration, loss of caloric intake, and more serious complications that may lead to immediate death. Findings: During a review of Resident 69's admission Record (Face sheet), the admission Record indicated Resident 69 was initially admitted to the facility on [DATE]. Resident 69's diagnoses included malignant neoplasm of the ileum (small intestinal cancer), type 2 diabetes mellitus with other specified complications (inability to metabolize glucose in the body causing elevated blood sugar levels), and anemia (low blood count). During a review of Resident 69's Minimum Data Set (MDS), a standardized assessment and care-screening tool, dated 4/21/21, the MDS indicated Resident 69 had cognitive (ability to make decisions, understand, learn) impairment for daily decision-making. The MDS indicated Resident 69 required extensive assistance for activities of daily living ([ADLs] daily self-care activities such as dressing, toileting and personal hygiene) During a review of Resident 69's Care Plan titled, Potential for weight loss related to weight loss risk factors, poor PO (by mouth) intake, cancer, malnutrition, muscle wasting, anemia, and compromised function of gastrointestinal, dated 2/19/21, the care plan indicated the staff's interventions included to refer to the dietician for nutritional assessment, dietary supplements as ordered Prostat Sugar Free (SF) 30 milliliters (ML) TID (three times a day). During a review of Resident 69's History and Physical (H/P), dated 5/25/21, the H/P indicated Resident 69 did not have the capacity to understand and make decisions. During a review of Resident 69's Weight Record, the weight record indicated the following weights: On 4/2021 -150.1 pounds On 6/2021 -127.2 pounds, On 7/2021 -115 pounds, with a 12.2 pound significant (10%) weight loss in one (1) month, and a 38.8 pound significant (23%) weight loss in three (3) months. During a review of Resident 69's Nurses Progress Note dated 7/8/21, the Nurses Progress Note indicated the RD recommended adding fortified foods (foods that have nutrients added to them that do not naturally occur in the food) to the resident's diet and SF Prostat 30 ml TID. The Nurses Progress Note indicated the goal was for the resident to eat as desired. During a review of Resident 69's dietary intake percentage dated 5/2021, 6/2021, 7/2021, the dietary intake percentage indicated maximum intake PO of 20 - 50 % during breakfast, lunch, and dinner. During a concurrent interview and record review on 7/08/21 at 1:28 PM, with Licensed Vocational Nurse 8 (LVN 8), LVN 8 stated Resident 69 had an increasingly loss of weight since March 2021 to present. LVN 8 verified the RD recommended Prostat 30 ml TID. During an interview on 7/12/21 at 2:09 PM with LVN 8 and Quality Assurance (QA) nurse, LVN 8 and QA Nurse stated Resident 69 had a gastrostomy ([GT] tube surgically inserted into the stomach for nutrition, hydration, and medication) for abdominal compression, an abdominal mass and the GT was not for enteral (tube) feeding. LVN 8 and QA Nurse stated Resident 69 was losing weight because she was not eating, and the resident was placed on hospice (care that focuses on comfort at the end of life) and they did report any changes to the hospice nurse. LVN 8 and QA Nurse stated the hospice visits once a week and when there was change of condition. LVN 8 and QA Nurse stated on 7/8/21, the RD reviewed Resident 69's weights and noted the increased weight loss of 23% in three months and recommended Prostat 30 ml TID, but we have not followed up to notify the hospice agency. LVN 8 and QA Nurse verified the RD's recommendation was not noted in Resident 69's order. During an interview on 7/12/21 at 2:09 PM with the RD, the RD stated an order was recommended for Prostat 30 ml on 7/8/21 because the RD did not like to see resident's losing weight. The RD stated she did not know the order was not followed up. The RD stated she just called and spoke to the hospice nurse and they approved resident to receive Prostat, and Resident 69's family was also in agreement for the resident to receive Prostat since the resident tolerates oral fluid. During an interview on 7/13/21 at 11:11 AM with the Director of Nurses (DON), the DON stated Resident 69 had been under hospice care since April 2021. The DON stated when the RD gave a recommendation, the Assistant DON (ADON) was supposed to receive a copy of the recommendation because she was part of weight lost program and the floor nurses. The DON stated the charge nurse was supposed to call and notify Resident 69's physician within 72 hours of the recommendation. The DON stated he did not know about the order/ recommendation from the RD, and therefore did not follow up on it. During an interview on 7/13/21 at 11:27 AM with the ADON, the ADON stated when the RD made recommendations, the charge nurse received the recommendation and it takes 72 hours to get it from the provider, and if the physician did not follow up the ADON has to follow up. The ADON stated she did not know about Resident 69's order until 7/12/21. The ADON called the hospice doctor after discovery of the recommendation and the physician okayed the order for Prostat. During a concurrent interview and review of Resident 69's Medication Administration Record (MAR) on 7/14/21 at 10:31 AM, the MAR indicated an order for Prostat 30 ml TID with a start date on 7/12/21. The MAR indicated Prostat was not administered to Resident 69. LVN 3 stated she had not given Resident 69 the supplement because she did not check the orders. LVN 3 stated she did not know Resident 69 had a new order and no one endorsed the new order to her. LVN 3 stated she was supposed to check the resident's orders prior to medication administration but was not checking. During a review of a care plan meeting note on 7/14/21 at 1:27 PM, the note indicated the RD, Dietary Services Supervisor (DSS), ADON, and the Hospice Registered Nurse (RN) met to go over Resident 69's plan of care related to significant weight loss and overall nutritional decline. Hospice RN requested an updated order summary list. Per Hospice RN, the physician approved the RD's recommendation for Prostat 30 ml TID for additional caloric supplement. The note indicated the Hospice RN stated Resident 69's family were updated on a regular basis and understood the resident was expected to have continuous nutritional decline and weight loss due to multiple refusal of meals. Hospice Physician and Resident 69's family were agreeable to dietary supplements. Goals were to keep Resident 69 comfortable through supportive care. During a review of the facility's undated policy and procedure (P/P) titled, Nutritional Assessment, the P/P indicated the following: 1. The Dietician, in conjunction with the nursing staff and healthcare practitioners, will conduct a nutritional assessment for each resident upon admission and as indicated by a change in condition that places the resident at risk for impaired nutrition. 2. The nutritional assessment will be conducted by the multidisciplinary team and shall identify at least the following components: a. Usual body weight b. Current height and weight c. A description of the resident's usual intake and appetite d. A history of reduced appetite or progressive weight loss or gain prior to admission. 3. Once current conditions and risk factors for impaired nutrition are assessed and analyzed, individual care plans will be developed that address or minimize to the extent possible the resident's risks for nutritional complications. Such interventions will be developed within the context of the resident's prognosis and personal preferences. 4. The dietician then makes recommendations based on the clinical assessments and resident's preferences. These recommendations are given to the nursing staff who must get approval from the physician/practitioner before initiating any of the dietary recommendations. 5. Licensed nurses will document the response of the physician/practitioner and whether they are agreeable to the Dietician's recommendations. The practitioner has 72 hours to respond to the Dietician's recommendations. 6. Licensed nurses must return the completed Dietary recommendations report to the Assistant Director of Nursing (ADON) within 72 hours. The ADON will audit the Dietary recommendations to ensure that they have been carried out or documentation for the physician's declination is properly recorded.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1. Label one Oxycontin (a medication used to treat p...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1. Label one Oxycontin (a medication used to treat pain) package, in accordance with federal, state requirements, and current professional principals, affecting one of four observed residents (Resident 81) for medication administration. 2. Store one insulin (medication used to regulate blood sugar levels) vial for Resident 80, and one ophthalmic (medication used for the eye) bottle for Resident 44 in accordance with the manufacturer's requirements in one of two inspected medication carts (Medication Cart Station A). These deficient practices increased the risk that Residents 44, 80 and 81, could have received medication that had become ineffective or toxic due to improper storage or labeling, without identification and instruction of use due to lack of proper labeling, possibly leading to accidental use, resulting in health complications, hospitalization or death. Findings: During a review of Resident 81's Order Summary Report, printed on [DATE], the Order Summary Report indicated Resident 81 was admitted to the facility on [DATE] with diagnosis that included pain in the knee. The Order Summary Report indicated Resident 81 was prescribed Oxycontin ER 20 milligram ([mg] unit of mass) tablet by mouth two times a day for pain management related to pain in the knee starting [DATE]. During a review of Resident 81's Medication Administration Record ([MAR]- a record of medications administered to a resident) for the month of [DATE], the MAR indicated Resident 81 was administered Oxycontin two times a day (9:00 AM and 9:00 PM) from [DATE] to [DATE] by two different licensed nursing staff. During an observation on [DATE] at 10:30 AM, Licensed Vocational Nurse 6 (LVN 6) was observed preparing an Oxycontin 20 mg extended release (slow releasing medication) tablet for Resident 81. The Oxycontin tablets were inside the manufacturers package, and the package was not affixed with a pharmacy prepared label. According to federal, state and professional standards, any medication dispensed by the pharmacy must have a pharmacy label affixed to the medication. The label must contain the prescription number, date it was prepared, resident's name, medication name, dose, direction of use, expiration date of the medication, ordering physician name, and the name of the pharmacy dispensing. During a concurrent observation and interview on [DATE] at 11:01 AM with LVN 6, LVN 6 stated the Oxycontin package did not have a pharmacy label on it, and the facility policy was to have each resident's medication package labeled with the name of the resident, name of the medication and the directions on how to take the medication, by the dispensing pharmacy. LVN 6 stated the medication belonged to Resident 81. LVN 6 took out her sharpie and wrote the residents name on one side of the box. LVN 6 stated it was likely the pharmacy sent two Oxycontin packages attached to each other and one of the packages had the pharmacy label affixed. LVN 6 stated she would request for a refill with appropriate labeling from the dispensing pharmacy. During an interview on [DATE] at 12:21 PM with the Director of Nursing (DON), the DON stated each resident's medication must contain a label from the dispensing pharmacy that included the name of the resident, the name and dose of the medication, the directions on how to take the medication, the date the medication was filled by the pharmacy and the expiration date. The DON stated that if a medication package contained no label, the facility's process was to not accept the medication and that nursing staff should call the dispensing pharmacy for relabeling. The DON stated not having resident medications properly labeled was a safety concern. The DON stated that the labeling was to ensure each resident received the correct medication, and the nurses have the correct instructions on how to administer the medication safely. During an observation of Medication Cart Station A on [DATE] at 1:17 PM, the following medications were found stored in a manner contrary to their respective manufacturer's requirements, or not labeled with an open date as required by their respective manufacturer's specifications: 1. One unopened vial of Levemir (a brand name for a type of insulin) insulin for Resident 80 was found stored at room temperature and not labeled with a date on which storage at room temperature began. According to the manufacturer's product labeling, unopened Levemir insulin vial should be stored in the refrigerator between 36 and 46 degrees Fahrenheit (F) and used or discarded within 42 days of opening or once they've been stored at room temperature. 2. One unopened latanoprost (an ophthalmic [relating to the eye] medication used to treat high pressure in the eye) for Resident 44 was found stored at room temperature and not labeled with a date on which storage at room temperature began. According to the manufacturer's product labeling, unopened latanoprost bottles should be stored in the refrigerator between 36 and 46 degrees and used or discarded within 6 weeks of opening or once stored at room temperature. During an interview on [DATE] at 1:53 PM with LVN 5, LVN 5 stated the Levemir insulin vial for Resident 80 was not stored properly, and that it should have been refrigerated. LVN 5 stated the Levemir was considered expired and would not be affective. LVN 5 stated if this insulin was used accidentally for residents it can have adverse reactions (harmful, unwanted effects of medications) such as clammy skin, dizziness, weakness, high or low blood sugar levels, the blood sugars to go high or down, leading to coma (a state of deep unconsciousness caused by injury or illness), hospitalization and possibly death. LVN 5 also stated the latanoprost ophthalmic bottle for Resident 44 was not stored properly, and that it should have been refrigerated. LVN 5 stated the latanoprost bottle was considered expired and would not be affective. LVN 5 stated if the latanoprost was used accidentally for residents it can have adverse reactions, their eye condition can get worse, leading to more eye nerve damage and eventually cause blindness. LVN 5 stated he would not use the expired Levemir and latanoprost, and dispose of them, and reorder new ones from the pharmacy. During an interview on [DATE] at 12:53 PM with the DON stated medications would lose their efficacy if they are not stored properly. The DON stated that improperly stored insulin was expired and would cause high or low blood sugars in residents and endanger their health, possibly leading to coma, hospitalization, or death. The DON stated that ophthalmic medications would also lose their efficacy if not stored properly and were considered expired. The DON stated if these expired eye medications were used, they could cause the residents discomfort in the eye, and potentially lead to eye nerve damage and blindness. The DON stated the facility failed to store the medications properly according to manufacturer guidelines and facility policies. During a telephone interview on [DATE] at 1:12 PM with the dispensing pharmacy's Director of Pharmacy (DOP), the DOP stated no medication should leave the pharmacy without a label. The DOP stated the pharmacy had four check stations to ensure all medication dispensing requirements were met. The DOP stated that not having medications labeled was a serious concern for theft within the dispensing pharmacy, and a serious safety concern if administered to the wrong residents. During a telephone interview on [DATE] at 2:34 PM with the DOP, the DOP stated the dispensing pharmacy failed to label the manufacturer package of the Oxycontin dispensed for Resident 81. The DOP stated the dispensing records indicated the Oxycontin for Resident 81 was dispensed as one manufacturer package containing twenty tablets, and a separate package containing eight tablets, both placed in a Ziploc bag that was labeled with the pharmacy label. The DOP stated that both the pharmacy technician and pharmacist failed to ensure the dispensed package contained a label and have now began a new process for labeling multi-package medication orders. During a review of the facility's policy and procedure (P/P) titled, Labeling of Medication Containers, dated [DATE], the P/P indicated, all medications maintained in the facility shall be properly labeled in accordance with current state and federal regulations. The P/P stated any medication packaging or containers that are inadequately or improperly labeled shall be returned to the issuing pharmacy. Labels for individual drug containers shall include all necessary information, such as: The resident's name; The prescribing physicians name; The name, .of the issuing pharmacy; The name, strength, and quantity of the drug; The prescription number; The date the medication was dispensed; Appropriate accessory and cautionary statements; The expiration date ; and Directions for use. During a review of the facility's P/P titled, Storage of Medications, dated [DATE], indicated the facility shall store all drugs and biologicals in a safe, secure and orderly manner. Drug containers that have missing, incomplete, improper, or incorrect labels shall be returned to the pharmacy for proper labeling before storing. The facility shall not use discontinued, outdated or deteriorated drugs or biologicals. Medications requiring refrigeration must be stored in a refrigerator. During a review of the facility's P/P titled, Administering Medications, dated [DATE], indicated the individual administering the medication must check the label to verify the right resident, right medication, right dosage, right time and right method (route) of administration before giving the medication. The P/P indicated expiration/beyond use date on the medication label must be checked prior to administering. When opening a multi-dose container, the date opened shall be recorded on the container. Medication in multidose vials may be used (until the manufacturer's expiration date/for the length of time allowed by state law/according to facility policy for thirty days). During a review of the facility's undated document titled, Insulin Overview, the Insulin Overview indicated Levemir expiration date is 42 days. During a review of facility's undated document titled, EXPIRATION DATES, the document indicated insulins (all brands) expire in 28 days refrigerated or unrefrigerated, Xalatan eye drops expire in 6 weeks and to keep in refrigerator before initial opening then ok at room temperature, and all other open ophthalmics and injectables are good for 6 months after opening.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Laboratory Services (Tag F0770)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure two of two (2) sampled residents (Residents 7 ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure two of two (2) sampled residents (Residents 7 and 32) received laboratory blood draws/tests as ordered by the physician. This deficient practice had the potential to delay necessary care and services. Findings: During a review of Resident 7's admission Record (a document that provides patient information at-a-glance), dated July 15, 2021, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including epilepsy (seizure disorder - sudden, uncontrolled electrical activity in the brain that causes temporary abnormalities in muscle tone or movements, behaviors, sensations, or states of awareness), muscle wasting and atrophy, dementia (a decline in memory, language, problem-solving and other thinking skills that affect a person's ability to perform everyday activities), and quadriplegia (paralysis of all four limbs). During a review of Resident 7's Physician Order Summary, dated July 15, 2021, indicated the resident's physician ordered phenytoin level (a blood test indicating seizure management) monthly starting on November 26, 2017. This document also indicated the resident was prescribed Levetiracetam (a medication used to treat seizures) five milliliters via gastrostomy tube (g-tube - a surgically placed tube inserted through the abdomen that delivers nutrition and/or medication directly to the stomach) two times a day for seizure disorder starting on January 14, 2019. Resident 7 also had physician order for Phenytoin (a medication used to treat seizures) 100 milligrams via g-tube two times a day for seizure disorder starting on April 2, 2021. During a review of the facility's Consultant Pharmacist's Medication Regimen Review, dated May 8, 2021, indicated the Consultant Pharmacist (CP) had a recommendation To comply with CMS [Centers for Medicare and Medicaid Services] regulations which require monitoring of drug-related lab work, please ask the MD [physician] if we can obtain an order for the following lab work for monitoring purposes: Recheck Dilantin [for seizure monitoring] to determine if the level from 4/2021 has stabilized on the new dosing regimen. This document also indicated the physician recommended Dilantin and valproic acid (for seizure monitoring) levels drawn every three months. During a review of Resident 32's admission Record, dated July 13, 221, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including Parkinson's disease (a progressive nervous system disorder that affects movement), muscle wasting and atrophy, ataxic gait (difficulty walking), heart failure (a condition in which the heart cannot pump enough blood to meet the body's needs), type 2 diabetes mellitus (chronic condition that affects how the body processes sugar), acute kidney failure (condition in which the kidneys lose the ability to filter waste products from blood), dysphagia (difficulty swallowing), hypertension (high blood pressure), and major depressive disorder (mental health disorder characterized by persistently depressed mood or loss of interest in activities, causing significant impairment in daily life). During a review of Resident 32's Physician Order Summary, dated July 2, 2021, indicated the resident's physician ordered thyroid stimulating hormone (TSH - affects metabolism) and lipid (fat) panel every six months starting on February 3, 2021. This document also indicated the physician ordered weight change monitoring monthly and increased total cholesterol and triglycerides (fats) every six months, both starting on February 2, 2021. During a concurrent interview and record review, on July 13, 2021, at 1:17 p.m., with Registered Nurse (RN) 1, RN 1 reviewed Resident 32's electronic health record (EHR) for lab results and stated there were no TSH or lipid panel levels done for the resident. RN 1 reviewed the physician order for TSH and lipid panel blood draws and stated they should have been drawn the next day after the order was placed, then initiated to have the blood draws every six months. RN 1 stated it is important to complete blood draw orders to compare results and determine how the resident is doing. RN 1 stated TSH levels are done to check the thyroid in the case a resident is not eating well. RN 1 stated since the labs were not completed, Resident 32 needed follow up with the physician to obtain a stat order to draw the lab now. During a concurrent interview and record review, on July 14, 2021, at 1:57 p.m., with the Director of Staff Development (DSD), the DSD reviewed Resident 32's EHR and stated the physician ordered TSH and lipid panel blood draw on February 2, 2021. The DSD also reviewed the resident's Lab Results Report from February 15, 2021 to June 21, 2021 and stated there were no TSH or lipid panel blood draws done for Resident 32. The DSD stated the TSH and lipid panel blood draw should have been completed the day after the order was placed and six months after because the resident is receiving medication that needs to be monitored and to ensure nothing else medically is going on with the resident. The DSD stated missed labs can put a resident in danger. Regarding Resident 7, the DSD stated the resident is on seizure precautions, which entails ensuring medications are given properly, labs are drawn, and monitoring the resident for medication effectiveness and seizure activity. The DSD stated Dilantin levels should be checked for residents taking Dilantin and Levetiracetam, and drawn depending on physician's orders. The DSD reviewed Resident 7's Lab Results Report and confirmed there was no Dilantin or valproic acid level for the month of May 2021 or afterwards. Resident 7's Lab Results Report indicated the resident had Dilantin levels higher than the therapeutic range (10 - 20 mcg/mL); 22.9 on March 23, 2021 and 21.3 on March 30, 2021. The DSD stated if labs are not completed, there is no way to know the resident's level which could lead to seizures. During a concurrent interview and record review, on July 15, 2021, at 4:00 p.m., with the Director of Nursing (DON), the DON stated the CP comes to the facility once a month and reviews a list of active residents in the facility and their medications for recommendations. Afterwards, the CP's recommendations are emailed to him and Licensed Vocational Nurse (LVN) 9, who is responsible for referring the CP's recommendations to the physician and documenting their response. The DON reviewed the facility's Consultant Pharmacist's Medication Regimen Review, dated May 8, 2021, for Resident 7 and stated the physician ordered Dilantin and valproic acid levels to be drawn every three months. The DON also reviewed Resident 7's laboratory results and physician orders in the resident's EHR and stated there were no orders input for the Dilantin and valproic acid after the physician's recommendation; the last Dilantin level was drawn on April 5, 2021. The DON stated the physician's recommendation needed to be clarified because it was unclear when to start the order - whether from the last time it was drawn or three months from the recommendation. The DON stated these missed labs affect the resident because it is important to monitor if Dilantin levels are within the therapeutic range, further stating if low, can cause seizures. During a concurrent interview and record review, on July 15, 2021, at 8:39 a.m., with LVN 9, LVN 9 stated the CP's drug regimen review recommendations are emailed to the DON and a copy is provided to her. Then when the physician comes to the facility, she gives them the recommendations where they write their orders. Once completed, she carries out the order by inputting it into the EHR and returns the recommendations to the DON who ensures that the recommendations have been carried out. A review of the facility's undated policy and procedure (P&P), entitled Drug Regimen Review, not dated, indicated the facility is to follow up on the consultant pharmacist's recommendations in a timely manner. This P&P further indicated the facility is responsible for documenting the follow through of each monthly consultant pharmacist report and that the Director of Nursing (DON) is responsible for ensuring proper follow-through.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to implement the care plans for two 6 out of 27 sampled re...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to implement the care plans for two 6 out of 27 sampled residents (5, 32, 53, 69, and 95) to eliminate or decrease the risks by: a. Resident 5 and 95, who were receiving hemodialysis ([HD] a treatment that does some of the things done by healthy kidneys. It is needed when your own kidneys can no longer take care of your body's needs) the facility failed to ensure Resident 5 and 95 had a HD emergency kit in their room. b. Resident 32, 53, and 93 who were a fall risk, the facility failed to ensure Resident 32, 53, and 93 had a fall wrist band. C. Resident 69 who had a weight loss, the facility failed to ensure Resident 69 received Prostat (a supplement) to manage weight loss. The deficient practice result in Resident 5, 32, 53, 69, and 95 not receiving individualized care which had the potential to result in Resident 5, 32, 53, 69, and 95 to suffer an accident such as a fall, major bleeding, and decline of function. Findings A1. During a concurrent observation and interview on 7/7/21, at 9:23 a.m., Resident 95 stated she had not seen a HD emergency kit in her room. During an interview and concurrent record review on 7/8/21, at 8:04 a.m., LVN 7 checked Resident 95 room and stated that was not a HD emergency kit in the room. LVN 7 stated Resident 95 should have had the emergency HD kit in the room to stop the bleeding from the HD site. LVN 7 stated Resident 95 could bleed to death if HD site had a problem and would be hard to control the bleeding. During an interview on 7/13/21, at 7:45 a.m., the Director of Staff Development (DSD) stated the reason for a care plan was to provide care specific to the resident to ensure the resident received the needed care. The DSD stated the care plan should be revised immediately when there was a new order or a change in the resident's condition. During a review of the admission Record, indicated Resident 95 was admitted on [DATE]. Diagnosis included diabetes mellitus (abnormal blood sugar), end stage renal disease ([ESRD] the stage of renal impairment that appears irreversible and permanent and requires a regular course of dialysis or kidney transplantation to maintain life). During a record review for Resident 95, the History Physical dated 6/14/21, indicated Resident 97 had the capacity of understand and be understood During a Record review for Resident 95, the Care plan potential for complications of ESRD dated 6/12/21, indicated a goal to prevent complications related to HD. The care plan interventions included HD emergency e-kit at the bedside. During a Record review for Resident 5 the Order Summary Report dated 7/8/21, indicated Resident 5 had an order for a HD bleeding E-kit in the room every shift. During a record review for Resident 95, the Minimum Data Set ([MDS a standardized assessment and care screening tool) dated 7/14/21, indicated Resident 95 had the ability to understand and be understood. The MDS indicated Resident 95 required one-person extensive assistance with bed mobility, transfer, dressing, and toilet use. The facility's policy titled Care of Hemodialysis Resident undated, indicated the resident with HD treatment would have a care plan according to their specific needs, based upon the HD treatment and type of access. The facility's policy titled Comprehensive Care Plans undated, indicated the facility developed an individualized care plan that included measurable objectives and timetables to meet the resident's medical, nursing, mental, and psychological needs. The policy indicated the care plan was designed to incorporate identified problem areas, incorporate risk factors associated with identified problems, aid in preventing or reducing decline , comprehensive care plan would be periodically reviewed and revised by the interdisciplinary team after the onset of a new problem, change of condition, to address changes in behavior and care, and as appropriate or necessary. A2. During an observation on 7/7/21, at 10:30 a.m., in Resident 5's room no visible HD emergency kit. During an observation and interview on 7/8/21, at 7:51 a.m., In resident 5's room, CAN 7 stated that was no HD emergency kit in Resident 5' s room. CAN 7 stated she had never seen a HD emergency kit. During an interview on 7/13/21, at 7:45 a.m., the Director of Staff Development (DSD) stated the reason for the care plan was to provide care specific to the resident to ensure the resident received the needed care. The DSD stated the care plan should be revised immediately when there was a new order or a change in the resident's condition During a review of the admission Record, indicated Resident 5 was originally admitted on [DATE] and readmitted on [DATE]. Diagnosis included diabetes mellitus (abnormal blood sugar), ESRD, dementia (memory loss), and dysphagia (difficulty swallowing). During a Record review for Resident 5, the Care plan needs for HD dated 9/24/20, indicated a goal to prevent complications related to HD. The care plan interventions included HD emergency kit at the bedside. During a record review for Resident 5, the History Physical dated 6/18/21, indicated Resident 5 was profoundly demented, did not speak, was confused, forgetful and required total care did did not have the capacity to understand and be understood During a Record review for Resident 5 the Order Summary Report dated 7/8/21, indicated Resident 5 had an order for a HD emergency kit in the room every shift. During a record review for Resident 5, the Minimum Data Set ([MDS a standardized assessment and care screening tool) dated 7/29/21, indicated Resident 5 was rarely or never understood and sometimes was able to understand others. The MDS indicated Resident 5 required one-person extensive assistance with bed mobility, dressing, toilet use, and personal hygiene. The facility's policy titled Care of Hemodialysis Resident undated, indicated the resident with HD treatment would have a care plan according to their specific needs, based upon the HD treatment and type of access. The facility's policy titled Comprehensive Care Plans undated, indicated the facility developed an individualized care plan that included measurable objectives and timetables to meet the resident's medical, nursing, mental, and psychological needs. The policy indicated the care plan was designed to incorporate identified problem areas, incorporate risk factors associated with identified problems, aid in preventing or reducing decline , comprehensive care plan would be periodically reviewed and revised by the interdisciplinary team after the onset of a new problem, change of condition, to address changes in behavior and care, and as appropriate or necessary b. During a review of Resident 64's admission Record (Face sheet) indicated the resident was initially admitted to the facility on [DATE] with diagnosis including malignant neoplasm of ileum(small intestinal cancer), type 2 diabetes mellitus with other specified complications (inability to metabolize glucose in the body causing elevated blood sugar levels), anemia (low blood count). c. During a review of Resident 69's Minimum Data Set (MDS), a standardized assessment and care screening tool, dated 4/21/21, indicated the resident had cognitive (ability to make decisions, understand, learn) impairment, with daily decision making. The MDS assessment indicated the resident required extensive assistance for activities of daily living ({ADLs}) such as bed mobility, transfer, locomotion on unit and off unit, dressing, toilet, and personal hygiene. During a review of Resident 69's Care Plan dated 2/19/21 indicated Resident 69, for potential for weight loss related to weight loss risk factors, poor PO intake, cancer, malnutrition, muscle wasting, anemia, and compromised function of gastrointestinal. Care plan interventions indicated all interventions will align with the family's preference for intensity of care. Refer to dietician for nutritional assessment. Dietary supplements as ordered Prostat Sugar Free (SF) 30ML TID (Three times a day). During a review of Resident 69's History and Physical dated 5/25/21, indicated Resident 64 do not have the capacity to understand and make decisions. During a review of a document titled weight record indicated weight 4/2021 -150.1#, 6/2021 -127.2#, 7/2021 -115#, with 12.2# significant (10%) weight loss x1 month, and 38.8# significant (23%) weight loss x 3months. Duirng a review of Nurses progress note dated 7/8/21, indicated RD recommended adding fortified to the diet and sugar free (SF) Prostat 30ml TID. Goal is for resident to eat as desired. duirng a review of dietary intake percentage dated 5/2021, 6/2021, 7/2021, indicated maximum intake PO of 20 - 50 % during breakfast, lunch, and dinner. On 7/08/21 at 01:28 P.M., during interviews and record review Licensed Vocational Nurse (LVN 8) stated resident had increasingly loss of weight since March to present. On record review, the facility RD recommended prostat 30 ml TID for resident. On 7/12/21 at 2:09 P.M., during interview LVN 8, and QA nurse stated resident has GT for abdominal compression, she has abdominal mass and not for enteral feeding. Resident is losing weight because she's not eating. Resident is on hospice care and we report any changes to hospice nurse. The hospice visits once a week and when there is change of condition. On 7/8/21 the RD reviewed residents' weight and noted the increased weight loss of 23% in three months and recommended prostat 30ml TID, but we have not followed up to notify the hospice care, the recommendation is not noted in the resident's order. On 7/12/21 at 2:09P.M., during an interview RD stated order was recommended for Prostat 30ml on 7/8/21 because I do not like to see resident's losing weight, but I did not know that it was not followed up. I just called and spoke to the hospice nurse and they approved resident to receive prostat, and family of resident is also in agreement for resident to receive prostat since resident tolerates oral fluid. On 7/13/21 at 11:11 A.M., during an interview DON stated Resident on Hospice since April 2021. When RD give recommendation the ADON was supposed to get a copy because she is part of weight lost program and the floor nurses. The charge nurse was supposed to call the Doctor. the doctor was supposed to be notified within 72hrs of the recommendation. DON stated he did not know about the order/ recommendation from the RD, and therefore did not follow up on it. On 7/13/21 at 11:27 A.M., during an interview ADON stated when the RD makes recommendation charge nurse receives and it takes 72 hours to get it from the provider, and if the physician did not follow up the ADON has to follow up. I did not know about the order until 7/12/21. we called the hospice doctor after discovery of the recommendation and the physician okayed the order for Prostat. On 7/14/21 at 10:31 A.M., during an observation and record review resident had order for Prostat 30ml TID started 7/12/21. MAR indicated resident was not receiving the order. during interview LVN 3, stated I have not been given resident the supplement because I did not check on the orders. I did not know resident had a new order. No one endorsed it to me. Resident only receives PRN orders for pain management. I am supposed to check resident's orders prior to medication administration but I was not checking. I have prostat in the medication cart. It is a house supply. On 7/14/21 at 01:27 P.M., during an record Review: RD, DSS and ADON with hospice, RN from CV Hospice to go over plan of care related to significant weight loss and overall nutritional decline. Hospice RN requested updated order summary list. Per hospice RN, MD approved of RD recommendation for ProStat 30ml TID for additional caloric supplement. Hospice nurse states that family are updated on a regular basis and understand that the resident is expected to have continuous nutritional decline and weight loss due to multiple refusal of meals. Hospice MD and family are agreeable to dietary supplements. Goals are to keep the resident comfortable through supportive care. A review of undated Facility's Policy and Procedure titled Care Plans-Comprehensive indicated the following: 1. Each resident's comprehensive care plan is designed to: a. Incorporate identified problem areas. b. Incorporate risk factors associated with identified problems c. Build on the resident's strengths d. Reflect treatment goals, timetables, and objectives in measurable outcomes. e. Identify the professional services that are responsible for each element of care.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and review facility failed to revise the care plan for 4 out of 4 residents (20, 5, 87, 95) to ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and review facility failed to revise the care plan for 4 out of 4 residents (20, 5, 87, 95) to reflect the individualized professional standards of care. This deficiency has the potential to harm by negating plans and care specific to the individual's needs. Findings: a) During a review of the Charge Nurse (LVN/RN) job description, dated 2003, the document indicates that the charge nurse is to, Cooperate with other resident services when coordinating nursing services to ensure that the resident's total regimen of care is maintained. The job description also indicates, Transcribe physician's orders to resident charts, cardex, medication cards, treatment/care plans, as required. During a review of the Nurse Supervisor (RN) job description, dated 2003, the document indicates to, Assist in developing methods for coordinating nursing services with other resident services to ensure the continuity of the residents' total regimen of care. The job description also indicates, Review nurses' notes to ensure that they are informative and descriptive of the nursing care being provided, that they reflect the resident's response to the care, and that such care is provided in accordance with the resident's wishes. During a review of the Director of Nursing (DON) job description, dated 2003, the document indicates, Develop a written plan of care (preliminary and comprehensive) for each resident that identifies the problems/needs of the resident, indicates the care to be given, goals to be accomplished, and which professional service is responsible for each element of care. During a review of Resident 20's admission Face Sheet, the document indicates that Resident 20's most recent admission was on 2/29/2020 with diagnoses of Left Ventricular Failure (a failure to pump oxygen-rich blood from the lungs to the top left chamber of the heart down through the left bottom chamber of the heart that causes shortness of breath and fatigue), epilepsy (a brain disorder that presents itself as convulsions and unconsciousness from an abnormal electrical conduction) and a history of falls. During a review of Resident 20's Order Summary Report, dated 7/2/2021, the document indicates an order for seizure precautions dated 2/29/2020, an order to schedule a neurology consult to evaluate seizure and dementia, and an order to schedule an EEG. During a review of Resident 20's MDS dated [DATE], the document indicates Resident 20 has clear speech, usually is understood, and usually understands others During an interview on 7/8/2021 at 3:56 pm, LVN 5 (started 4/1/21) stated that the process of revising the care plan is a requirement of the nurse and the charge nurse. LVN 5 stated that they are currently the Charge Nurse. LVN 5 stated the process of revising a care plan starts with a physician order or an assessment of a need by the nurse or a member of the IDT. LVN stated that they are expected as the Charge Nurse to reflect new or revised orders on the care plan by entering the information and dating the revised intervention. During a concurrent observation, interview and review on 7/8/2021 at 4:00 pm of Resident 20's medical record, LVN 5 stated the care plan does not reflect the order for seizure precautions on 2/29/2020. LVN 5 stated that the order for an EEG (A test to monitor electrical conduction of the brain) was not in the care plan and should be there reflecting the date of the scheduled EEG. When asked what could happen should there not be a care plan for Resident 20, LVN 5 stated that the resident could possibly be harmed should the staff miss the interventions. When asked if seizure precautions had been put on Resident 20's care plan, LVN 5 stated that it had not but that there was mention of epilepsy within the care plan for Self Care Performance Deficit (initiated 10/13/2017) as well as on the care plan for High Risk For Altered Nutrition. On observation of Resident 20's bed, LVN 5 stated that Resident 20 did not have any seizure pads and should have if they are on seizure precautions. LVN 5 stated that Resident 20 also has a care plan for the medication Levetiracetam (an anticonvulsant), initiated on 3/8/2016, and the interventions for the medication require the nurse to: monitor the resident for Change of Condition (specifically in mental status/consciousness), initiated 3/8/2016, notify MD and family members, initiated 3/8/2016, reduce unsafe activities, initiated 3/8/2016, stay with the resident during seizure activity, initiated 3/8/2016, administer Levetiracetam tablet 1000 mg one tab two times a day as ordered and care plan intervention initiated on 3/8/2016, bilateral padded side rails for seizure precaution (initiated 1/31/2020). b. During a record review for Resident 87, the admission record indicated Resident 87 was originally admitted on [DATE] and readmitted on [DATE]. Diagnoses included epilepsy (seizure activity that causes a burst of uncontrolled electrical activity between brain cells that causes temporary abnormalities in muscle tone or movements such as stiffness, twitching or limpness, behaviors, sensations or states of awareness), functional quadriplegia (complete inability to move due to severe disability or frailty caused by another medical condition without physical injury or damage to the spinal cord), and cerebrovascular disease (occurs if the flow of oxygen-rich blood to a portion of the brain is blocked. Without oxygen, brain cells start to die after a few minutes) During a record review for Resident 87, the care plan oxygen (odorless gas that is present in the air and necessary to maintain life) therapy shortness of breath dated 1/11/19, indicated Resident 87 intervention included would receive breathing treatment as ordered and oxygen as needed. During a record review for Resident 87, the Minimum Data Set ([MDS] a standardized assessment and care screening tool) dated 5/26/21, indicated Resident 87 was never or rarely understood and rarely or never understood others. The MDS indicated resident 87 was total dependent and required two-person assistance with bed mobility, transfer, dressing, and toilet use. During a record review for Resident 87, the Order Summary Report dated 7/8/21, indicated Resident 87 had orders to receive oxygen at three liters for a minute (lpm) via a nasal cannula (an oxygen delivery device attached to the head with 2 prongs inserted in the nose) continuously every shift. During an observation and concurrent interview on 7/12/21, at 8:18 a.m., Resident 8 was on the bed with the nasal cannula above his nose, oxygen tank (a container with oxygen inside) indicated the oxygen deliver was 4 lpm. Certified Nurse Assistant (CAN 15) stated she would put the nasal cannula back into Resident 87's nose. During an interview on 7/13/21, at 7:45 a.m., the Director of Staff Development (DSD) stated the reason for the care plan was to provide care specific to the resident to ensure the resident received the needed care. The DSD stated the care plan should be revised immediately when there was a new order or a change in the resident's condition During a concurrent interview and record review on 7/15/21, at 10:02 a.m., Licensed Vocational Nurse (LVN 9) stated Resident 87 had an order to receive oxygen therapy at 3 lpm, continuously, and via a nasal cannula. LVN 9 stated Resident 87 care plan was not revised and the care plan indicated Resident 87 received oxygen therapy as needed. LVN 9 stated the care plan was supposed to be revised when the facility received the order for continuous oxygen on 1/11/19. LVN 9 stated the care plan had interventions of the treatments the staff provided to the residents and the care plan for Resident 87 was not customized to his care needs. The facility's policy titled Comprehensive Care Plans undated, indicated the facility developed an individualized care plan that included measurable objectives and timetables to meet the resident's medical, nursing, mental, and psychological needs. The policy indicated the care plan was designed to incorporate identified problem areas, incorporate risk factors associated with identified problems, aid in preventing or reducing decline , comprehensive care plan would be periodically reviewed and revised by the interdisciplinary team after the onset of a new problem, change of condition, to address changes in behavior and care, and as appropriate or necessary The facility's policy titled Oxygen Administration undated, indicated to verify the physician's orders for the facility's protocol for oxygen administration and review the resident's care plan to assess for any special needs of the resident. The policy indicated oxygen therapy was administered by way of an oxygen mask, nasal cannula, and/or nasal
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Accident Prevention (Tag F0689)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and review, the facility failed to respond promptly to a bed alarm and provide a hazard-free env...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and review, the facility failed to respond promptly to a bed alarm and provide a hazard-free environment for 4 out of 4 sampled residents (61, 87, 20, 157). These deficient practices had the potential to cause falls and injuries to Residents 61, 87, 20, 157 and other residents in the facility. Findings: 1) During a review of Resident 61's admission Face Sheet dated indicated Resident 61 was admitted to the facility on [DATE] with diagnoses including epilepsy (a brain disorder that causes unconsciousness and fainting ), paraplegia (an inability to move and feel the lower legs and lower body ), and history of COVID-19 (a serious, life-threatening and highly contagious disease causing difficulty breathing). During a review of Resident 61's Minimum Data Set ([MDS] a care planning and assessment tool) dated 10/1/2020, indicated Resident 61 had a clear speech, was usually understood ,and able to understand others. During a review of Resident 61's Order Summary Report dated 7/2/21, indicated Dilantin Suspension (an anti-convulsant) 125 mg/5 ml, give 10 ml by mouth at bedtime every Saturday and Sunday, and give 8 ml by mouth every Monday through Friday. The Order Summary Report also indicated padded side rails for seizure precautions every shift, monitor for signs and symptoms Dilantin toxicity (high levels of medication, that can cause uncoordinated movements, slurred speech, confusion and nausea), every shift. During a review of Resident 61's Care Plan for seizure activity dated 4/20/2020, indicated to keep the environment free of hazards and reduce unsafe activities. During an observation of Resident 61's room on 7/9/21 at 08:15 am, a Certified Nurisng Assistant 7 (CNA ) stated Resident 61's right sided bed rail was padded on the outer part of the rail and not the inner portion like it should. CNA 7 stated the pad was on the outside of the right upper rail to protect the bed and wall. CNA 7 also stated staff did not know the pad had to be on the inside to protect Resident 61 instead of protecting the bed from the wall. When asked what would happen if Resident 61 had a seizure, CNA 7 stated the resident would hit the head on the rail. During an observation, interview and record review on 7/13/212 at 08:55 Licensed Vocational Nurse (LVN 4) stated Resident 61's physician orders dated 7/2/21, indicated seizure prcautions. LVN 4 also stated Resident 61's bedrails were padded on the outside instead of the inside of the bed and did not protected the resident in event of a seizure. LVN 4 added the staff had to ensure Resident 61's bed rails were padded, the environment kept clutter free to prevent him from hitting his head against the rail. 2) During a review of Resident 87's admission Face Sheet, indicated Resident 87 was initially admitted to the faxcility on 4/26/2017 and re-admitted on [DATE]. Resident 87's diagnoses included cerebrovascular disease ([CVA] a group of conditions that affect the blood flow and blood vessels of the brain) , epilepsy and Parkinson's disease (a disorder that affects movement and causes one to shake). During a review of Resident 87's MDS dated [DATE], indicated Resident 87 was unable to understand and be understood by others. The MDS also indicated the resident depended on staff for activities of daily living (ADLs), including washing, dressing, and feeding. During a review of Resident 87's Order Summary Report dated 7/9/2021, indicated the resident was to to be on seizure precautions, and was to be monitored every shift for any seizure activities. During a review of Resident 87's Care Plan dated 5/21/2021, indicated the resident had seizure activities, was on anticonvulsant (seizure medication). The care plan however did not indicated the resident's rails should be padded. During a concurrent observation and interview on 7/9/21 at 08:40 am LVN 4 and CNA 7 validated that Resident 87 did not have any seizure pads on the right and left upper rails of the bed. When asked what could happen if Resident 87 should they have a seizure while in bed, LVN 4 stated the resident could be injured. 3) During a review of Resident 20's admission Face Sheet, dated 7/14/2021, indicated Resident 20 was admitted to the facility on [DATE] with diagnoses including left ventricular failure (a condition that occurs when the heart does not beat like it should causing shortness of breath and fatigue), epilepsy and a history of falls. During a review of Resident 20's Order Summary Report dated 7/2/2021, indicated Resident 20 would be monitored for seizure activities and would be on seizure precautions. During a review of Resident 20's MDS dated [DATE], indicated Resident 20 could understand and be understood by others. During a review of Resident 20's Care Plan dated 1/31/2020 indicated the resident was on seizure precautions such as keeping the environment hazard free, reducing unsafe activities, and bilateral padded side rails on the bed. During a concurrent observation and interview on 7/8/2021 at 04:00 p.m., LVN 5 stated Resident 20 did not have any seizure pads on the bedrails. LVN 5 also stated Resident 20 was supposed to have seizure precautions because the resident had a diagnosis of epilepsy and physician orders indicating to place Resident 20 on seizure precautions. According to LVN 5, Resident 20 was supposed to have bilateral padded side rails for seizure precaution because without them, the resident could be injured during a seizure. 4) During a concurrent observation and interview on 7/7/21 at 10:00 a.m., Resident 157 activated her bed alarm and when no staff came to her aid, she ambulated 2 feet to sit in her wheelchair without any assistance. While her alarm was on, a Restorative Nursing Assistant 1 (RNA 1) walked past Resident 157's room and up the hallway for 1 minute before responding to the bed alarm. The resident stated most often staff do not respond to her call light on time. According to Resident 157 the bed alarm usually got staff's attention faster than the call light. During an interview on 7/13/2021 at 7:57 a.m., RNA 1 stated he should have responded to Resident 157's call light promptly because if staff fail to respond in a timely manner, it might cause the resident to fall and injure her hip or head. During an interview on 7/13/2021 at 12:20 p.m., the Director of staff Development (DSD), stated certified nursing assistants receive report of residents with high fall risk in huddle (staff meeting), and were supposed to respond to the talking devices (bed alarm) as soon as possible. During a review of Resident 157 admission record indicated Resident 157 was admitted to the facility on [DATE] with diagnoses including a personal history of traumatic fracture (breakage of bones due to an accident, fall or other kind of force), presence of right artificial hip joint, and a history of falling. During a review of Resident 157's MDS dated [DATE] indicated Resident 157 was able to understand and be understood by others. The MDS also indicated Resident 157 required extensive assistance walking in the room, toilet use, and personal hygiene. During a review of Resident 157's Fall Risk Assessment, dated 6/18/2021, indicated Resident 157 had a fall risk score of 20 (A score of 10 and above indicated high fall risk). It also indicated contributing factors for high fall risk were intermittent confusion, 1 to 2 falls in the past 3 months, and climbing out of bed, or getting out of bed or chair unassisted. During a review of Resident 157's care plan dated 6/18/2021 indicated Resident 157 was at risk for falls related to a history of multiple falls. The nursing interventions included placing the resident's call light within reach and responding to it in a timely manner, checking Resident 157 for wetness, keeping her clean and dry at all times, and supervising/assisting the resident with activities of daily living (ADLs), toileting, and transferring if appropriate. During a review of the facility's undated policy and procedure titled, Managing Fall Risk, indicated the purpose of the policy was to identify residents at risk for falls, initiate interventions to prevent falls and reduce the risk of injury related to falls. It also indicated fall management protocol included placing a yellow star on the room, name label and resident ambulation equipment, placing residents' ambulation equipment, call lights, and telephones within reach, providing residents with well-lit and clutter free environment, monitoring residents every 2 hours or as needed. A review of the facility's undated policy titled Fall Prevention- Potential Interventions indicated bed wheels should have the brakes on, wheels locked and beds in low positions. During a review of the facility's policy titled Accidents and Incidents - Investigating and Reporting, dated April 2013, indicated the staff will documenting date, time, place, the nature of the accident, witnesses of the accident, the person or person's injured and their condition. It also indicated the satff would notificatify residents' family and physician, of the disposition of the injured person, follow-up information, as well as corrective actions. A review of the facility's undated policy titled Seizure Management indicated safety measures for a resident when a seizure occured would include avoiding falls, avoiding leaving the resident alone, not placing objects in the resident's mouth, and preventing injury at any time during and after the seizure.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0698 (Tag F0698)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to have a Hemodialysis ([HD] process of purifying the bl...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to have a Hemodialysis ([HD] process of purifying the blood of a person whose kidneys are not working normally) emergency kit (E-kit) available at the bedside for two of three residents (Residents 5 and 95) who were receiving Hemodialysis treatment. The deficient practice had the potential to result in Residents 5 and 95 not receiving lifesaving interventions for HD emergencies such as severe bleeding. Finding: a. During an interview on 7/7/21 at 9:23 a.m. with Resident 95, Resident 95 stated she had not seen a HD kit in her room. During an interview and concurrent record review on 7/8/21 at 8:04 a.m. with Licensed Vocational Nurse 7 (LVN 7), LVN 7 checked Resident 95's room and stated there was not a HD E-kit in the resident's room. LVN 7 stated Resident 95 should have an E-kit in the room to stop the bleeding from the HD site. LVN 7 stated Resident 95 could bleed to death if the HD site bled and was not controlled. During a review of Resident 95's admission Record, the admission Record indicated Resident 95 was admitted to the facility on [DATE]. Resident 95's diagnoses included diabetes mellitus (abnormal blood sugar), and end stage renal disease ([ESRD] the stage of renal impairment that appears irreversible and permanent and requires a regular course of dialysis or kidney transplantation to maintain life). During a review of Resident 95's History and Physical (H/P) dated 6/14/21, the H/P indicated Resident 97 had the capacity of understand and be understood During a review of Resident 95's care plan titled, Potential for complications of ESRD, dated 6/12/21, the care plan indicated the goal was to prevent Resident 95 from complications related to HD. The care plan interventions included to provide a HD E-kit at the bedside. During a review of Resident 95's Order Summary Report dated 7/8/21, the Order Summary Report indicated Resident 95 had an order for a HD emergency E-kit in the room every shift. During a review of Resident 95's Minimum Data Set (MDS), a standardized assessment and care-screening tool, dated 7/14/21, the MDS indicated Resident 95 had the ability to understand and be understood. The MDS indicated Resident 95 required a one-person extensive assistance with bed mobility, transfer, dressing, and toilet use. b. During an observation on 7/7/21 at 10:30 a.m., Resident 5's room did not have a visible HD E-kit. During a concurrent observation and interview on 7/8/21 at 7:51 a.m., in Resident 5's room, with Certified Nursing Assistant 7 (CNA 7), CNA 7 stated there was no HD E-kit in Resident 5' s room. CNA 7 stated she did not know of, or was trained on HD E-kits. During a review of Resident 5's admission Record, the admission Record indicated Resident 5 was originally admitted to the facility on [DATE], and readmitted on [DATE]. Resident 5's diagnosis included diabetes mellitus, ESRD, dementia (memory loss), and dysphagia (difficulty swallowing). During a review of Resident 5's care plan titled, Needs for HD, dated 9/24/20, the care plan indicated a goal was to prevent complications related to HD. The care plan interventions included to provide a HD E-kit at the bedside. During a review of Resident 5's H/P, dated 6/18/21, the H/P indicated Resident 5 was profoundly demented, did not speak, was confused, forgetful and required total care. The H/P indicated Resident 5 did not have the capacity to understand and be understood. During a review of Resident 5's Order Summary Report dated 7/8/21, the Order Summary Report indicated Resident 5 had an order for a HD bleeding E-kit in the room every shift. During a review of Resident 5's MDS, dated [DATE], the MDS indicated Resident 5 was rarely or never understood and sometimes was able to understand others. The MDS indicated Resident 5 required one-person extensive assistance with bed mobility, dressing, toilet use, and personal hygiene. During a review of the facility's undated policy and procedure (P/P) titled, Care of Hemodialysis Resident, the P/P indicated the resident with HD treatment would have a care plan according to their specific needs, based upon the HD treatment and type of access.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0726 (Tag F0726)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to ensure licensed and unlicensed staff, in accordance with the nursing standards of practice, were able to identify residents r...

Read full inspector narrative →
Based on observation, interview, and record review, the facility failed to ensure licensed and unlicensed staff, in accordance with the nursing standards of practice, were able to identify residents requiring seizure (burst of uncontrolled electrical activity between brain cells that causes temporary abnormalities in muscle tone or movements [stiffness, twitching or limpness], behaviors, sensations or states of awareness) precautions, monitored residents at risk for seizures, and demonstrated the ability to care for residents during and after a seizure. This deficient practice had the potential to place residents at risk for seizures to result in serious harm or inadequate care and services. Findings: During a review of the Competency Evaluations dated 2001, the Competency Evaluations indicated the Certified Nurse Aides (CNA) must pass a skills check to determine competency upon hire, and this includes, but is not limited to: transferring and positioning, vital signs, intake and output, weighing residents, skin care, feeding techniques, bed making, and body mechanics. The Competency Evaluations indicated the licensed nurses must pass a written and demonstration skills check to determine competency upon hire and this includes, but is not limited to: medication administration, intravenous medications and fluids, abuse detection and reporting, care of the resident with dementia, proper body mechanics, prevention of injury, and resident safety awareness, and proper documentation. The document indicated there would be annual re-evaluations of skills, and that educational in-services would occur as needed, depending of the needs. During a review of the job description for the Certified Nursing Assistant (CNA), dated 2003, the job description indicated the CNA should follow established safety precautions in the performance of all duties, report all safety violations, use only equipment they have been trained in, use only the equipment and supplies necessary to do the job, to inform the charge nurse of the equipment and supply needs, and inform the charge nurse of any changes in the resident's condition so that appropriate information can be entered on the resident's care plan. During a review of the undated job description for the Restorative Nursing Assistant (RNA), the document indicated the RNA reports and charts significant changes in resident's condition or motivational level. The RNA job description indicated they attend all required meetings and in-services. The RNA qualifications indicated in the job description stated the RNA should have the ability to apply commonsense understanding to carry out instructions in written, oral, or diagram form, the ability to deal with problems involving several concrete variables in standardized situations, and the ability to read and interpret documents such as safety rules and procedure manuals. During a review of the Charge Nurse (Licensed Vocational Nurse [LVN]/Registered Nurse [RN]) job description dated 2003, the job description indicated they are to ensure that all nursing personnel comply with the written policies and procedures established by the facility, ensure all nursing service personnel are in compliance with their respective job descriptions, participate in the development, implementation and maintenance of the procedures for reporting hazardous conditions or equipment, ensure adequate equipment is maintained on the unit at all times to meet the needs of the residents, review care plans daily to ensure that appropriate care is being rendered, and ensure that the CNA's are aware of the resident care plans. During a review of the Nursing Supervisor (RN) job description, dated 2003, the job description indicated the Nursing Supervisor (RN) participated in developing, maintaining, and updating written policies and procedures that govern the day-to-day functions of the nursing service department, ensure that the Nursing Service Procedures Manual was current and reflected the day-to-day nursing procedures performed in the facility, ensure that all nursing service personnel comply with the procedures, ensure that all nursing service personnel were in compliance with their job descriptions, ensure that direct nursing care be provided by a licensed nurse, a certified nursing assistant, and/or nurse aide trainee qualified to perform the procedure, consult with the resident, his/her family, and the resident's physician in planning the resident's care, treatment, rehabilitation, as necessary, ensure that all resident care rooms, treatment areas, are maintained in a clean, safe, and sanitary manner, and ensure that an adequate supply level of equipment was maintained on the premises at all times to meet the needs of the residents. During a review of the (undated) Director of Staff Development (DSD) job description, the job description indicated the DSD coordinated and conducted an effective ongoing in-service plan for all employees, reinforced nursing education and training to meet annual 24-hour requirement for all nursing assistants, provides and coordinates annual in-services for all facility employees in accordance with State and Federal regulations and Facility Policy, sets up the orientation program for all employees, coordinates theoretical and clinical orientation for all new employees, and meets with personnel as appropriate to assist in identifying and correcting all problem areas and/or improvement of services. During a review of the Director of Nursing Services (DON) job description, dated 2003, the job description indicated the DON ensure that direct nursing care be provided by a licensed nurse, a CNA, and/or a nurse aide trainee qualified to perform the procedure, develop and participate in the planning, conducting, and scheduling of timely in-service training classes that provide instructions on how to do a job, and ensure a well-educated nursing service department, and assist support services in developing, implementing, and conducting in-service training programs that relate to the nursing service department, and attend and participate in continuing educational programs designed to keep the DON abreast of changes in the profession. The document indicated the DON was to ensure all resident care rooms, treatment areas, are maintained in a clean, safe, and sanitary manner, monitor nursing service personnel to ensure they are following established safety regulations in the use of equipment and supplies, and develop, implement, and maintain a procedure for reporting hazardous conditions or equipment. During an interview on 7/8/21 at 3:40 PM with CNA 10, CNA 10 stated staff observe the residents to know what their needs are for the day and asked the charge nurse if the resident was non-verbal. CNA 10 stated if a resident was at risk for a fall, there was a star on the name plaque outside the room on the wall near the door, and the resident wore a yellow wrist band. CNA 10 stated for those residents who are at risk for seizures, the charge nurse would inform the cna's so the cna's can keep checking on residents. CNA 10 stated they make sure to put the bed height down and just keep monitoring them. CNA 10 stated if they have a seizure they call the charge nurse right away. During a concurrent interview and review on 7/8/2021 at 3:46 PM with RNA 2, RNA 2 stated she was assigned to Rooms 9, 10, 12, 14B, 15, 16B, 17B, and 21A. RNA 2 stated the RNA's worked as both CNAs and as RNA's. RNA 2 stated they inquire if they have any residents who were newly admitted and then ask the charge nurse about the resident. RNA 2 stated they received an in-service on seizures. RNA 2 stated she did not have a resident who was at-risk for a seizure. RNA 2 stated the nurse should tell them if they have a resident with seizures. RNA 2 stated they do not know about preventing or putting anything in the room for a resident who was at-risk for seizures. Upon review of the medical records for the residents assigned to RNA 2, RNA 2 stated they were not aware that two residents in her assignment were at risk for seizures and in need of seizure precautions. During an interview on 7/8/2021 at 3:56 PM with LVN 5, LVN 5 stated if a resident was in a wheelchair, they put the resident on the floor, turned them on their side, put something in their mouth so they did not bite their tongue, and made sure they did not have clothing that was tight so the seizing resident did not choke. LVN 5 stated they placed the resident in a side-lying recovery position and made sure that no hazardous things were on the floor, and they monitored the resident until they recovered. LVN 5 stated if the resident continued to seize, they called the RN supervisor. LVN 5 stated they put a spoon in the resident's mouth depending on how long the seizure was. LVN 5 stated the staff make sure the resident was not having a seizure by monitoring, taking vital signs, or if the resident at risk for a seizure goes to activities, they tell the activities staff that the resident was at-risk. LVN 5 stated that they also make sure to give them their medication on time. LVN 5 stated that after the CNA was done with doing bath care, they make sure the bed rail was up and bed height was down. LVN 5 stated the CNA told her their residents do not have padded rails because the pads are hard to find. LVN 5 stated that they have not completed their education for seizures. LVN 5 stated they think some should have their rails padded for their safety. LVN 5 stated that with pads placed properly on the rail, if the resident moves [during a seizure] they won't fall. LVN 5 stated that they can get hurt during a seizure but it depends on where the resident was. LVN 5 stated the resident might have bleeding inside, bump on the head, and discoloration. LVN 5 stated they wouldn't let that happen to the resident. LVN 5 stated they have only one resident that was at risk for seizures. During an interview on 7/9/21 at 11:53 am with the Director of Staff Developer (DSD), the DSD initially stated that they do not regularly teach the staff about seizures, what seizure precautions are, or what to do if a resident has a seizure. The DSD stated they have padded side rails and CNA's are aware if the residents are having a Change of Condition that they are to report it to the charge nurse. The DSD then stated that they have not ever given an in-service to the staff on seizures in the six years that they have been in the DSD position. The DSD stated they are responsible for training the CNAs and RNA's upon hire and then annually. During a concurrent observation and interview on 7/9/21 at 12:24 PM with LVN 4, LVN 4 stated she had only witnessed two residents have a seizure in the last five years. LVN 4 stated she was unsure which residents were on seizure precautions. When asked what would they do if a resident had a seizure and how would they know what it looked like, LVN 4 stated the resident would suddenly be unresponsive or would start shaking. LVN 4 stated the staff would want to time the seizure, lay the resident flat in the bed or on the floor, make sure the resident did not get hurt during the seizure and then call the doctor. When asked why would they lay the resident flat, LVN 4 stated she did not know. When asked what could happen if a resident had a seizure and the staff was unaware of the necessary precautions for a resident with a seizure, LVN 4 stated they could have difficulty breathing. LVN 4 stated three residents were currently on seizure precautions. All three residents were observed laying in their bed with two upper side rails up without padded rails, as verified by LVN 4. During a concurrent observation and interview on 7/13/21 at 8:35 am with CNA 7, CNA 7 stated seizure precautions included the head of the bed elevated at 90 degrees and the bed level in a position that the resident did not fall out of bed. During a concurrent interview and review on 7/13/21 at 12:50 PM with the DON, the DON stated they were responsible for the staffing and training of the licensed nurses. The DON stated they provide staff in-services on a regular basis. The DON stated the in-services they provided to the licensed nurses in 2021 did not include seizure precautions. The DON stated the care plan was an intervention specific to the resident's needs and were updated any time there was a new order for the resident or a Change of Condition for the resident on that day - that was done immediately to provide proper care to the resident. The DON stated if the care plan indicated seizure precaution then they put pads on the side rails, the licensed nurses gave medication properly, labs were done to monitor levels of the medications, and they monitor for signs and symptoms of the resident shaking, eyes rolling, and/or twitching. The DON stated they have a monthly meeting in which they discuss skills and validated checklists. The DON stated that they will implement the care as soon as possible for seizures, stating that the licensed nurses are taught to monitor the seizure medication levels, prevent injuries during the seizure such as falls and injury from hitting the metal side rails (place pads). The DON stated that part of the prevention from injury during a seizure they teach the licensed nurses to insert on the side of the mouth a tongue depressor that is wrapped in gauze if the resident looks like they are biting their tongue or lip. When asked what could happen if the gauze comes undone in the resident's mouth, the DON stated that the gauze that was in the resident's mouth had the potential to obstruct the resident's airway and cause injury. When asked what could happen if the tongue depressor breaks off and splinters in the resident's mouth, the DON stated that the tongue depressor had the potential to obstruct the airway and cause injury. The DON stated other prevention measures included padding the side rails of the resident's bed and was the DON, ADON, DSD and the Charge Nurses responsibility to follow up and make sure the pads are on the rails. During a review of the facility's undated policy and procedure (P/P) titled, Seizure Management, the P/P indicated the staff will obtain equipment and supplies including suction equipment and artificial airway to help manage an active seizure. The P/P indicated the steps in the procedure during an active seizure including: not to place an object in the resident's mouth. The P/P indicated there are some seizures that occur without convulsions, and may manifest through confusion, an aura, hallucinations, difficulty speaking or understanding, dizziness, loss of consciousness, loss of balance and coordination, sudden numbness, tingling or weakness, or sudden headache. Under the Steps in the Procedure, it indicated that, If staff suspect a seizure, they will: 1. Have at least one person stay with the resident, while having another staff member get needed equipment and notify a Registered Nurse (RN) or Licensed Vocation Nurse (LVN). 2. If convulsions are tonic/clonic (grand mal), monitor the airway and take steps as needed to maintain an open airway. 3. If the resident is having a seizure while standing, try to guide the resident to the floor and protect his/her head. 4. If the resident is having a seizure while in bed, take measures to prevent the resident from falling out of bed and do not leave the resident unattended. 5. As much as possible, remove loose objects near the resident. 6. If possible, turn the resident on his/her side. 7. Tilt the head forward (i.e. chin towards the chest) 8. Loosen clothing 9. Do not attempt to place objects in the resident's mouth. 10. Do not attempt to restrain the resident 11. Note the time and duration of the seizure activity. The P/P indicated the physician and staff will identify those who have had a seizure or epilepsy and those on antiepileptic medications for any reason. The P/P indicated those individuals who are identified, the staff and physician should periodically document the absence of seizures as well as any recurrences.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Pharmacy Services (Tag F0755)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to ensure to dispose of controlled ([C], medications that have the potential for abuse and may also lead to physical or psycholo...

Read full inspector narrative →
Based on observation, interview, and record review, the facility failed to ensure to dispose of controlled ([C], medications that have the potential for abuse and may also lead to physical or psychological dependence) and non-controlled (NC) medications in a manner that is not retrievable, in the one inspected pharmaceutical waste bin (bucket used for disposing medication) inside the Director of Nursing (DON's) office. As a result, control and accountability of C and NC medications awaiting final disposition (process of returning and/or destroying unused medications) did not follow the facility policy and procedures. This deficient practice increased the opportunity for C and NC medication diversion (the transfer of medications from a lawful to an unlawful channel of distribution or use), and increased the risk that residents and staff in the facility could have accidental administration and exposure to harmful medications, possibly leading to physical and psychosocial harm and hospitalization. Findings: During a concurrent observation and interview on 7/7/21 at 3:30 PM with the Director of Nursing (DON), in the DON's office, the pharmaceutical waste bin was observed to contain a mixture of unopened and unused medications in their original manufacturer packaging, as well as intact (not damaged or impaired in any way) and unused medication tablets and capsules out of their manufacturer packaging. The DON stated the pharmaceutical waste bin contained both C and NC medications that were disposed of by pouring small amount of water in the bin. The DON stated the C and NC medications in the bin remained in a form that can potentially be re-used. The DON stated if the medications are not destroyed properly in a manner that is not retrievable for re-use, then there can be the potential of accidental misuse and diversion. During a review of the facility's undated policy and procedure (P/P) titled, Disposal of Non-Controlled Drugs, the P/P indicated when non-controlled drugs expire, are discontinued, or the resident expires or is discharged they will be given to the director of nursing or a charge nurse employed by the facility in compliance with applicable regulations by the Department of Health such as Title 22 and the Medical Waste Management Act (MWMA). During a review of the facility's undated P/P titled, Disposal of Controlled Drugs, the P/P indicated when controlled drugs expire, are discontinued, or the resident expires or is discharged they will be given to the director of nursing or a registered nurse employed by the facility and appointed for disposal in compliance with applicable regulations by the Department of Health such as Title 22 and the Medical Waste Management Act (MWMA). The P/P indicated controlled drugs shall be made unusable e.g. by adding household bleach.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure its medication error rate was less than five p...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure its medication error rate was less than five percent (%) due to two errors observed out of 26 total opportunities (error rate of 7.69 %). The medication errors were as follows: 1. Resident 606 received a form of calcium carbonate with vitamin D (a combination medication used to promote bone health, treat low blood calcium levels, and protect against osteoporosis [a condition where the bones become fragile and brittle from low calcium and vitamin D levels]) that was different than the one ordered by his attending physician. 2. Resident 610 received a form of multivitamin (a medication used as a dietary supplement to provide essential vitamins, minerals, and other nutritional elements) that was different than the one ordered by his attending physician. These deficient practices of failing to administer medication in accordance with the attending physician's orders increased the risk that Residents 606 and 610 could have experienced adverse effects (unwanted, uncomfortable, or dangerous effects that a medication may have) related to their medication therapy. This increased the potential that Residents 606 and 607 may have experienced a negative impact to their health and well-being. Findings: During an observation on 7/7/21 at 8:58 AM of Medication Cart Station A, Licensed Vocational Nurse 1 (LVN 1) was observed administering calcium carbonate with vitamin D 600 milligram ([mg] - a unit of measure of mass) / 400 international units ([IU] - unit of measure of mass) to Resident 606. Resident 606 was observed swallowing the medication whole with water. During a review of Resident 606's Order Summary Report (a report that includes a list of the residents current medications) dated 7/2/21, the Order Summary Report indicated Resident 606 was admitted to the facility on [DATE] with diagnoses including disorder of bone density (disease characterized by low amount and volume of bone tissue) and age-related osteoporosis with current fracture (crack or break) of the right femur (thigh bone). The Order Summary Report indicated Resident 606 was prescribed calcium carbonate with vitamin D 600 mg / 800 IU tablet by mouth twice daily, starting 6/25/21. The order summary report indicated the medication should have 600 mg of calcium with 800 IU of vitamin D. The clinical record contained no documentation that the resident should be given a form of calcium with vitamin D that contained 400 IU of vitamin D. During an observation on 7/7/21 at 10:05 AM of Medication Cart Station A, LVN 1 was observed administering a multivitamin with minerals tablet to Resident 607. Resident 607 was observed swallowing the medication whole with water. During a review of Resident 610's Order Summary Report for dated 7/2/21, the Order Summary Report indicated Resident 610 was admitted to the facility on [DATE] and prescribed multivitamin tablet by mouth once daily, starting 6/30/21. The Order Summary Report indicated the medication should be the multivitamin form, and not with minerals. The clinical record contained no documentation Resident 610 should be given a form of multivitamin that contained minerals. During an interview on 7/7/21 at 11:45 AM with LVN 1, LVN 1 stated the medications administered to residents should match the exact physician orders. LVN 1 stated she administered calcium with vitamin D 600 mg / 400 IU to Resident 606. LVN 1 stated she failed to administer calcium with vitamin D 600 mg / 800 IU to Resident 606, as prescribed by the physician. LVN 1 stated that as a result, Resident 606 received vitamin D that was 400 IU less than what was prescribed by the physician, which may cause Resident 606's bones to become fragile and break. LVN 1 stated she administered multivitamin with minerals to Resident 610. LVN 1 stated she failed to administer the correct form of multivitamin to Resident 610, as prescribed by the physician. LVN 1 stated giving additional minerals to residents can cause buildup in their body and may be harmful to their health if they are unable to absorb and process the medication properly. LVN 1 stated she would notify the physicians for administering the wrong form of medications to Residents 606 and 610 and obtain additional orders as necessary. During an interview on 7/9/21 at 1:33 PM with the Director of Nursing (DON), the DON stated medications administered must match the physician orders exactly per the facility's policy and follow the five rights of medication administration (1. Right patient, 2. Right drug, 3. Right dose, 4. Right route, 5. Right time.). The DON stated LVN 1 failed to administer the correct calcium with vitamin D medication to Resident 606 and the correct multivitamin medication to Resident 610. The DON stated LVN 1 contacted the physicians to inform of the medication error and obtain new orders as needed. The DON stated giving wrong mediations to residents can potentially harm their health. During a review of the facility's undated policy and procedure (P/P) titled, Medication Administration - General Guidelines, the P/P indicated medications are administered as prescribed in accordance with good nursing principles and practices and only by persons legally authorized to do so. The P/P indicated medications are administered in accordance with written orders of the attending physician.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Medical Records (Tag F0842)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure nursing staff accurately calculated and docume...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure nursing staff accurately calculated and documented the total weekly intake and output (of fluids) for four out of four (4) sampled residents (Residents 7, 32, 53, and 76). This deficient practice resulted in inaccurate documentation of the residents' total weekly intake and output, and had the potential to place the residents at risk for inaccurate evaluation of the residents' progression or regression of the delivery of care services. Findings: During a review of Resident 7's admission Record (a document that provides patient information at-a-glance), dated July 15, 2021, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including epilepsy (seizure disorder - sudden, uncontrolled electrical activity in the brain that causes temporary abnormalities in muscle tone or movements, behaviors, sensations, or states of awareness), muscle wasting and atrophy, dementia (a decline in memory, language, problem-solving and other thinking skills that affect a person's ability to perform everyday activities), and quadriplegia (paralysis of all four limbs). During a review of Resident 7's Medication Administration Record (MAR), dated July 2021, indicated the documented total weekly intake and output for the month were less than the documented 24-hour intake and output. During a review of Resident 32's admission Record, dated July 13, 221, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including Parkinson's disease (a progressive nervous system disorder that affects movement), muscle wasting and atrophy, ataxic gait (difficulty walking), heart failure (a condition in which the heart cannot pump enough blood to meet the body's needs), type 2 diabetes mellitus (chronic condition that affects how the body processes sugar), acute kidney failure (condition in which the kidneys lose the ability to filter waste products from blood), dysphagia (difficulty swallowing), hypertension (high blood pressure), and major depressive disorder (mental health disorder characterized by persistently depressed mood or loss of interest in activities, causing significant impairment in daily life). During a review of Resident 32's Medication Administration Record (MAR), dated July 2021, indicated the documented total weekly intake and output for the month were less than the documented 24-hour intake and output. During a review of Resident 53's admission Record, dated July 15, 2021, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including osteoarthritis (breakdown of cartilage in joints), type 2 diabetes mellitus, end stage renal disease (ESRD - permanent kidney function loss), dependence on renal dialysis (procedure to remove waste products from the blood when the kidneys no longer function), and major depressive disorder. During a review of Resident 53's Medication Administration Record (MAR), dated July 2021, indicated the documented total weekly intake and output for the month were less than the documented 24-hour intake and output. During a review of Resident 76's admission Record, dated July 15, 2021, indicated the resident was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses including ataxic gait, history of falling, dysphagia, dementia, type 2 diabetes mellitus, chronic kidney disease, anemia (low red blood cells), and major depressive disorder. During an interview, on July 13, 2021, at 4:05 p.m., with Licensed Vocational Nurse (LVN) 8, LVN 8 stated night shift licensed nurses calculate fluid intake and output for the whole day for residents with orders for 24-hour intake and output monitoring. LVN 8 stated nurses can see all documented intake and output from other shifts in the facility's electronic documentation system to add all the results. LVN 8 stated fluid intake is calculated by glass or pitcher - one glass of water equates to 60 milliliters (mL), two glasses equates to 120mL. LVN 8 stated nurses track the number of glasses a resident drinks by checking their water pitcher but could not remember how much liquid it holds. LVN 8 stated nurses check the water pitcher to calculate how much fluid was given at the end of each shift, including water given during medication pass, staring from the beginning of the shift. LVN 8 stated nurses also include gastrostomy tube (g-tube - a surgically inserted tube into the stomach to deliver nutrients or medications) feedings, medications, and flushes. LVN 8 stated the last in-service on how to calculate intake and output was less than a year ago, provided by the Director of Nursing (DON). During a review of Resident 76's Medication Administration Record (MAR), dated July 2021, indicated the documented total weekly intake and output for the month were less than the documented 24-hour intake and output. During an interview, on July 13, 2021, at 4:47 p.m., with the Director of Staff Development (DSD), the DSD stated nurses measure residents' fluid intake and output by using a urinal or hat for continent (able to control bladder/bowel) residents, or with a graduate when emptying a foley catheter bag for incontinent (unable to control bladder/bowel) residents. The DSD stated it is important to obtain accurate input and output to monitor residents on fluid restriction, such as those on dialysis (procedure to filter blood for those with kidney failure). The DSD stated she could not remember the minimum output per hour. During an interview, on July 14, 2021, at 10:39 a.m., with the DSD, the DSD stated night shift nurses calculate the intake and output for both 24-hour and weekly intake and output. The DSD stated the 24-hour intake and output is calculated by adding the documented amounts for all three shifts of the day. The DSD stated the weekly intake and output is calculated by adding up the amounts documented for each day to get the full amount for the week. The DSD stated the DON ensures licensed nurses are performing the task and that medical records does audits daily. During a concurrent interview and record review, on July 14, 2021, at 11:14 a.m., with the DON, the DON stated strict intake and output monitoring requires the use of an indwelling foley catheter (a thin, sterile tube inserted into the urethra to collect urine from the bladder) to obtain the most accurate urine output, or a bladder scanner to check the residual amount for those with urinary retention. The DON stated intake is recorded by documenting the amount of fluid a resident receives, further stating g-tube feedings, flushes, liquid medications are measurable. The DON stated licensed nurses on night shift calculate 24-hour output by adding the amounts documented from each shift for the day, and is documented in the residents' medication administration record (MAR). The DON stated weekly output is based on the 24-hour totals from Monday through Sunday, and is recorded every Sunday by night shift. The DON stated weekly output is calculated starting with the result for Monday during the day shift. The DON reviewed Resident 7's MAR, dated July 2021, and stated the total weekly intake and output results were not calculated correctly because the amounts were lower than the 24-hour intake and output results, and should have been higher if calculated correctly. The DON stated he could not remember the last time he provided an in-service on calculating intake and output because of the pandemic, but would do an in-service for each shift today and tomorrow. During an interview, on July 14, 2021, at 1:12 p.m., with Certified Nurse Assistant (CNA) 17, CNA 17 stated nurses measure output using a urinal for males or a hat for females. CNA 17 stated it is important to obtain accurate intake and output readings to monitor if residents are voiding (urinating). CNA 17 stated if a resident is not voiding, they may be dehydrated or may not be drinking enough fluids. CNA 17 stated the DSD, Quality Assurance, or Assistant DON usually provides in-services. CNA 17 stated CNAs give intake and output amounts to the charge nurse at the end of the shift so they can document the amounts. During a concurrent interview and record review, on July 14, 2021, at 1:35 p.m., with LVN 2, LVN 2 stated charge nurses are responsible for documenting residents' intake and output, which is provided to them by the CNAs. LVN 2 showed the facility's intake and output log and stated the CNAs use the form to record measurements. However, for July 13, 2021, it was observed there was only one log for the night shift and none for the day or evening shifts. LVN 2 stated there is supposed to be a log for every shift and was not sure why logs were missing. LVN 2 stated some CNAs use the form and other write their own notes on paper. LVN 2 stated documentation of accurate intake and output is important to know if a resident is not drinking enough water, or is drinking too much, because some are on fluid restriction, such as congestive heart failure (CHF - a condition in which the heart cannot pump enough blood to meet the body's needs) or other health conditions that require monitoring. A review of the facility's policy and procedure (P&P), entitled Output, Measuring and Recording, not dated, indicated the amount (in mLs) of liquid consumed should be recorded in the resident's medical record.
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • 26% annual turnover. Excellent stability, 22 points below California's 48% average. Staff who stay learn residents' needs.
Concerns
  • • Multiple safety concerns identified: 5 harm violation(s), $38,687 in fines, Payment denial on record. Review inspection reports carefully.
  • • 58 deficiencies on record, including 5 serious (caused harm) violations. Ask about corrective actions taken.
  • • $38,687 in fines. Higher than 94% of California facilities, suggesting repeated compliance issues.
  • • Grade F (23/100). Below average facility with significant concerns.
Bottom line: Trust Score of 23/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Heritage Rehabilitation Center's CMS Rating?

CMS assigns HERITAGE REHABILITATION CENTER an overall rating of 2 out of 5 stars, which is considered below average nationally. Within California, this rating places the facility higher than 0% of the state's 100 nursing homes. A rating at this level reflects concerns identified through health inspections, staffing assessments, or quality measures that families should carefully consider.

How is Heritage Rehabilitation Center Staffed?

CMS rates HERITAGE REHABILITATION CENTER's staffing level at 4 out of 5 stars, which is above average compared to other nursing homes. Staff turnover is 26%, compared to the California average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Heritage Rehabilitation Center?

State health inspectors documented 58 deficiencies at HERITAGE REHABILITATION CENTER during 2021 to 2025. These included: 5 that caused actual resident harm, 52 with potential for harm, and 1 minor or isolated issues. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Heritage Rehabilitation Center?

HERITAGE REHABILITATION CENTER is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility is operated by CHARIS TRUST DTD 12/22/16, a chain that manages multiple nursing homes. With 161 certified beds and approximately 129 residents (about 80% occupancy), it is a mid-sized facility located in TORRANCE, California.

How Does Heritage Rehabilitation Center Compare to Other California Nursing Homes?

Compared to the 100 nursing homes in California, HERITAGE REHABILITATION CENTER's overall rating (2 stars) is below the state average of 3.1, staff turnover (26%) is significantly lower than the state average of 46%, and health inspection rating (1 stars) is much below the national benchmark.

What Should Families Ask When Visiting Heritage Rehabilitation Center?

Based on this facility's data, families visiting should ask: "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" "Can I speak with family members of current residents about their experience?"

Is Heritage Rehabilitation Center Safe?

Based on CMS inspection data, HERITAGE REHABILITATION CENTER has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 2-star overall rating and ranks #100 of 100 nursing homes in California. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Heritage Rehabilitation Center Stick Around?

Staff at HERITAGE REHABILITATION CENTER tend to stick around. With a turnover rate of 26%, the facility is 20 percentage points below the California average of 46%. Low turnover is a positive sign. It means caregivers have time to learn each resident's needs, medications, and personal preferences. Consistent staff also notice subtle changes in a resident's condition more quickly. Registered Nurse turnover is also low at 28%, meaning experienced RNs are available to handle complex medical needs.

Was Heritage Rehabilitation Center Ever Fined?

HERITAGE REHABILITATION CENTER has been fined $38,687 across 3 penalty actions. The California average is $33,466. While any fine indicates a compliance issue, fines under $50,000 are relatively common and typically reflect isolated problems that were subsequently corrected. Families should ask what specific issues led to these fines and confirm they've been resolved.

Is Heritage Rehabilitation Center on Any Federal Watch List?

HERITAGE REHABILITATION CENTER is not on any federal watch list. The most significant is the Special Focus Facility (SFF) program, which identifies the bottom 1% of nursing homes nationally based on persistent, serious quality problems. Not being on this list means the facility has avoided the pattern of deficiencies that triggers enhanced federal oversight. This is a positive indicator, though families should still review the facility's inspection history directly.