FITCHBURG REHABILITATION AND NURSING CENTER

94 SUMMER STREET, FITCHBURG, MA 01420 (978) 343-3530
For profit - Limited Liability company 87 Beds EPHRAM LAHASKY Data: November 2025
Trust Grade
10/100
#286 of 338 in MA
Last Inspection: March 2025

Within standard 12-15 month inspection cycle. Federal law requires annual inspections.

Overview

Fitchburg Rehabilitation and Nursing Center has received a Trust Grade of F, indicating significant concerns about the quality of care being provided. With a state rank of #286 out of 338 facilities in Massachusetts, they are in the bottom half of nursing homes, and #44 out of 50 in Worcester County means there are only a few local options that are better. While the facility is showing some improvement, reducing issues from 21 in 2024 to 14 in 2025, there are still serious staffing and care deficiencies that need to be addressed. Staffing is rated below average at 2 out of 5 stars, but turnover is better than average at 37%, suggesting some consistency in staffing, although RN coverage is only average. The facility has incurred $43,719 in fines, which is concerning and indicates ongoing compliance issues, and specific incidents include failures to notify doctors of critical lab results for two residents, resulting in serious health complications. Overall, while there are some strengths, the significant issues and low ratings suggest families should proceed with caution when considering this facility.

Trust Score
F
10/100
In Massachusetts
#286/338
Bottom 16%
Safety Record
High Risk
Review needed
Inspections
Getting Better
21 → 14 violations
Staff Stability
○ Average
37% turnover. Near Massachusetts's 48% average. Typical for the industry.
Penalties
✓ Good
$43,719 in fines. Lower than most Massachusetts facilities. Relatively clean record.
Skilled Nurses
⚠ Watch
Each resident gets only 28 minutes of Registered Nurse (RN) attention daily — below average for Massachusetts. Fewer RN minutes means fewer trained eyes watching for problems.
Violations
⚠ Watch
42 deficiencies on record. Higher than average. Multiple issues found across inspections.
★☆☆☆☆
1.0
Overall Rating
★★☆☆☆
2.0
Staff Levels
★★☆☆☆
2.0
Care Quality
★☆☆☆☆
1.0
Inspection Score
Stable
2024: 21 issues
2025: 14 issues

The Good

  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover below average (37%)

    11 points below Massachusetts average of 48%

Facility shows strength in fire safety.

The Bad

1-Star Overall Rating

Below Massachusetts average (2.9)

Significant quality concerns identified by CMS

Staff Turnover: 37%

Near Massachusetts avg (46%)

Typical for the industry

Federal Fines: $43,719

Above median ($33,413)

Moderate penalties - review what triggered them

Chain: EPHRAM LAHASKY

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 42 deficiencies on record

5 actual harm
Mar 2025 11 deficiencies 2 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0658 (Tag F0658)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #29 was admitted to the facility in February 2023 with diagnoses including achondroplasia and hydronephrosis. Review...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #29 was admitted to the facility in February 2023 with diagnoses including achondroplasia and hydronephrosis. Review of the Minimum Data Set (MDS) asssessment dated 12/4/24, indicated Resident #29 is cognitively intact as evidenced by a score of 14 out of a possible 15 on the Brief Interview for Mental Status exam. The MDS also indicated Resident #29 requires assistance for bathing, dressing and toileting. Review of Resident #29's physicians orders indicated: Sodium Chloride Oral Tablet 1 GM (Sodium Chloride) Give 1 tablet by mouth three times a day for Hyponatremia Repeat BMP every week until sodium level normalizes and adjust salt tablet, 10/18/24. Additional review of Resident #29's physicians orders indicated: November 2024: labs were not obtained the weeks of 11/10/24, 11/17/24 and 11/24/24. December 2024: no labs were obtained. January 2025: no labs were obtained. February 2025: labs were not obtained the weeks of 2/2/25, 2/9/25, and 2/16/25. During an interview on 3/7/25 at 11:25 A.M., the Assistant Director of Nursing (ADON) said staff should implement physicians orders. The ADON said that if the nursing staff had questions related to Resident #29's ordered weekly labs, they should have called the physician for clarification. 3. Resident #1 was admitted to the facility in February 2023 with diagnoses including peripheral vascular disease and lymphedema. Review of Resident #1's Minimum Data Set (MDS) assessment dated [DATE] indicated the Resident scored a 15 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam indicating he/she was cognitively intact. The MDS further indicated the Resident had wounds. On 3/4/25 at 8:13 A.M., the surveyor observed Resident #1 lying in his/her bed. The air mattress was set at 10/380 lbs (pounds). On 3/6/25 at 7:59 A.M., the surveyor observed Resident #1 lying in his/her bed the air mattress was set at 10/380 lbs (pounds). On 3/6/25 at 11:00 A.M., the surveyor observed Resident #1 lying in his/her bed the air mattress was set at 10/380 lbs (pounds). Review of the medical record indicated the following physician order dated 4/18/24: - Low air loss mattress check settings and functions every shift - settings at 10/350 Lbs - every shift for preventative skin check proper function. Review of the current Treatment Administration Record (TAR) indicated the nurses had signed off that the air mattress was set at 10/350 Lbs. During an interview on 3/6/25 at 11:07 A.M., Nurse #6 said the physician order should match the air mattress setting and that nurses are responsible for ensuring the air mattress is checked for correct setting and proper functioning. During an interview on 3/7/25 at 11:10 A.M., the Assistant Director of Nursing (ADON) said the physician orders should match Resident #1's actual mattress pressure. Based on observation, record review and interview, the facility failed to meet professional standards of practice for three Residents (44, #29, and #1) out of a total of 20 sampled residents. Specifically, 1. For Resident #44, the facility failed to: a.) adequately assess, monitor, and implement a physician order for fluid restrictions (limiting the amount of fluid a person takes in) from August 2024 to March 2025. Subsequently, Resident #44 was hospitalized in February 2025, and admitted to ICU (intensive care unit) with diagnosis of acute hypoxic respiratory failure, acute renal failure and septic shock., b.) failed to follow up on physician recommendations for new prosthetic leg, and c.) failed to implement a physician order for bilateral shoulder X-ray. 2. For Resident #29, the facility failed to obtain labs as ordered by the physician. 3. For Resident #1, the facility failed to ensure the air mattress was set per the physician order. Findings include: 1. Resident #44 was admitted to the facility in August 2024 with diagnoses that include, chronic kidney disease stage 4 severe, retention of urine, type 2 diabetes mellitus, and congestive heart failure (CHF). Review of the most recent Minimum Data Set (MDS) assessment, dated 2/17/25, indicated that Resident #44 was cognitively intact as evidenced by a Brief Interview for Mental Status score of 15 out of 15. Further review of the MDS indicated Resident #44 requires substantial/maximal assistance for self-care and mobility, has functional limitation in range of motion to lower the extremity and has an impairment on one side requiring the use of an orthotic/ prosthetic. a. Review of Resident #44's active physicians orders indicated: No Concentrated Sweets diet- Regular texture, Thin consistency, 1500 ml/day fluid restriction 1500 ml (milliliters) Total in 24 hrs (hours): Nursing 660ml/24hr, (240 ml on 7-3, 240ml on 3-11, 180 ml on 11-7) Dietary 840ml/24 hrs) 360ml @ breakfast, 240ml lunch, 240 ml @ Dinner). Dated 8/27/24. Review of Resident #44's MAR and TAR failed to indicate monitoring of fluids and did not contain any information related to fluid restrictions. Review of Resident #44's nutrition care plan indicated: - Resident is nutritionally at risk r/t (related to) CHF, diabetes, anemia, COPD, poor dentition. Dated as revised 8/28/24. Interventions included: - Record and monitor intakes. - Continue diet as ordered. Review of Resident #44's current dietary slip failed to indicate fluid restrictions. Review of Resident #44's Kardex, (a form indicating level of care needs) failed to indicate the Resident was on fluid restrictions. Review of the nursing progress note dated 8/30/24, indicated: fluid restrictions maintained. Review of the Nutritional Risk Evaluation dated 1/13/25 indicated: Nutritional Plan: Identified at-risk for weight loss and dehydration - Yes. - Resident is on 1500ml F/R (fluid restriction). Resident had been admitted to Hospital for acute on chronic CHF and acute on chronic Renal failure. Resident had diuretics for excess water. Note that he/she is on diuretic and may experience wt.(weight) fluctuations via fluid shifts. He/she knows his nutritional expectations while on a diabetic diet with F/R. Will continue to monitor ongoing trends and adjust needs accordingly. Review of the nursing progress note dated 1/31/25 indicated: This RN was notified by this patients significant other that he/she would like this patient to be sent out to hospital. When RN asked why, he/she stated that he/she thinks he/she has pneumonia. I went to assess the patient.BP slightly low, 90/56, o2 90% on RA (room air), pulse 54. Afebrile. Patient agreeable to send out to hospital. EMS was called and patient was transferred out. Review of Resident #44's medical record indicated the following Nursing progress note dated 2/11/25, Per discharge paperwork the Resident was found to be covid positive, was admitted to ICU (intensive care unit) for management of acute hypoxic respiratory failure, acute renal failure and septic shock. Review of the hospital discharge paperwork dated 2/11/25, indicated that Resident #44 was admitted to the hospital and diagnosed with acute renal failure superimposed on stage 4 chronic kidney disease, acute hypoxic respiratory failure, hypokalemia (low potassium level), hyponatremia (low sodium level), community acquired PNA (pneumonia), and sepsis. - Disease course complicated by worsening kidney function. - AKI (acute kidney injury), hyponatremia, urinary retention. During an interview on 3/6/25 at 9:48 A.M., Certified Nursing Assistant (CNA)#6 said Resident #44 is not on fluid restrictions and said the Resident can have anything he/she wants to drink to stay hydrated. During an interview on 3/7/25 at 11:02 A.M., the assistant Director of Nurses (ADON) said Resident #44 has an order for fluid restrictions and said staff should be following the orders as written. The ADON said the care plan should indicate fluid restrictions and the order should be on the Medication Administration Record (MAR) or on the Treatment Administration Record (TAR) to track fluids. The ADON said the dietary slip should indicate the Resident is on fluid restrictions. During an interview on 3/10/25 at 10:17 A.M., Nurse Practitioner (NP) #1 said Resident #44 is very fragile and needs close monitoring due to his/her medical conditions and requires close monitoring of fluid restrictions. NP #1 said fluid restrictions should have been completed as ordered with ongoing monitoring of the fluid restrictions daily. NP #1 said staff should be following fluid restrictions as ordered especially after the recent hospitalization. b. During an observation on 3/4/25 at 9:45 A.M., Resident #44 was sitting in bed. There was a prosthetic leg on the floor next to the bedside table. During an observation on 3/7/25 at 8:40 A.M., Resident #44 was sitting in bed and said to the surveyor old leg not new one as he/she pointed to the prosthetic leg on the floor. When the surveyor asked if he/she was getting a new one, Resident #44 shook his/her head side to side and said I don't know. Review of the physician note dated 1/7/25, indicated: visit with patient today about new prosthetic. Patient stated old prosthetic is too heavy to ambulate, with increase fatigue and LE (left extremity) and low back pain. Would recommend new lighter fitting prosthetic to help increase ambulation distance and decrease pain with less caregiver asst. Review of the clinical record failed to indicate that Resident #44 had ever been evaluated for a new prosthetic leg. During an interview on 3/6/25 at 9:10 A.M., the Director of Rehab said Resident #44 may benefit from a new prosthetic leg because it is very old and he/she may have lost weight since admission and said he called the vendor last week, (approximately 2 months since the physician note recommending a newer prosthetic), but should call again to set up an evaluation. During an interview on 3/7/25 at 11:23 A.M. the Assistant Director of Nurses (ADON) said she would expect that an evaluation would be completed and said she was not aware of the recommendation. During an interview on 3/8/24 at 9:38 A.M., the Director of Nursing said that she would look into the consult for the prosthetic leg and said she would expect staff to follow up when the recommendation was made in January to start the process. During an interview on 3/10/25 at 10:28 A.M. Nurse Practitioner #1 said she would expect that recommendations would be implemented and documented in the medical chart to obtain a new prosthetic leg. c. Review of the Nurse Practitioner note dated 10/28/24, indicated, Chief complaint about shoulder pain. Assessment & Plan- bilateral shoulder pain: pt c/o (patient complained of) bilateral shoulder pain. Will order shoulder X-ray to assess for arthritis. Review of the nursing progress note dated, 11/1/24, indicated a physician order for Lidocaine patch for c/o pain to bilat (bilateral) shoulder. Review of the medical record indicated an imaging signature request form from an outside vendor dated 1/28/25, indicated, 4th request for ordering practitioner's signature. Exam date 10/29/24. Confirm this exam order by signing this document and faxing it back to imaging. The form was unsigned. During an interview on 3/7/25 11:23 A.M., the Assistant Director of Nurses (ADON) said Resident #44 should have had the X-ray completed as ordered and said she is not sure why it was not done. During an interview on 3/7/25 at 12:04 P.M., Nurse #7 said Resident #44 had an order for an X-ray but said she did not see that the X-ray was ever done. During an interview on 3/10/25 at 10:08 A.M., Nurse Practitioner #1 said Resident #44 was reporting shoulder pain and said she ordered an X-ray but was not aware that it was never done. NP #1 said the X-ray should have been obtained and followed up on and said Resident #44 has had pain in his/her shoulders and neck.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0773 (Tag F0773)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview, the facility failed to notify the Physician of critical labs for two resident...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview, the facility failed to notify the Physician of critical labs for two residents (#12, and #44) out of a total of 20 sampled residents. Specifically: 1. For Resident #12, the facility failed to alert the Physician of critically high BUN (measures how much blood urea nitrogen is in your body and can may indicated a problem with kidneys or liver) and critically low potassium (measures the electrolyte potassium in the blood that is essential for proper muscle and nerve function) results, which resulted in a delay of treatment and hospitalization for acute hypokalemia and acute kidney injury. 2. For Resident #44, the facility failed to obtain laboratory services as ordered by the Physician. Findings include: 1. Resident #12 was admitted to the facility in August 2024 with diagnoses including dementia, and chronic obstructive pulmonary disease. Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #12 is moderately cognitively impaired as evidenced by a score of 12 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam. The MDS also indicated Resident #12 requires assistance with bathing and dressing and utilizes oxygen therapy. Review of Resident #12's clinical record indicated that a blood draw was obtained on 2/26/25 at 12:20 P.M. with results reported to the facility on 2/26/25 at 4:52 P.M. that were critical: - BUN:106 (Reference range 10 - 24). Critically high. - Potassium: 2.7 (Reference range 3.3 - 5.1) Critically low. Resident #12's lab draw on 11/6/24 indicated his/her previous levels were as follows: - BUN: 19 - Potassium: 4.2 Review of the nurse progress note dated 2/26/25 at 9:09 P.M., written by Nurse #4, indicated: Resident continues on antibiotic azithromycin for PNA (pneumonia), no ill effect noted, VSS (vital signs stable). Resident compliant with meds and care, no s/sx (signs or symptoms) of hypo/hyperglycemia noted, safety maintained at all times. The nurse progress note failed to indicate Resident #12's lab results were reported to the Physician. Review of the nurse progress notes dated 2/27/25 at 10:50 A.M. written by the Director of Nursing (DON) indicated: Resident alert and able to make needs known. Continues on abx (antibiotic treatment) for pneumonia with no adverse effect. Critical lab results with BUN of 106 . Reported to provider, new order obtained from [Nurse Practitioner] to send resident to ED for evaluation. Review of the hospital paperwork dated 2/27/25 indicated the following lab results: BUN: 106 Potassium: 2.3 (a decrease from his/her potassium level on 2/26/25) Additional review of the hospital paperwork indicated Resident #12 was admitted to the hospital and diagnosed with acute hypokalemia, and acute kidney injury. During an interview on 3/6/25 at 8:14 A.M., Nurse #2 said that labs are obtained for residents on Wednesdays and Friday mornings. Nurse #2 said that labs do not usually come back until the afternoon so nurses will give report to the 3:00 P.M. - 11:00 P.M. shift to be aware of pending lab results for residents. Nurse #2 said that if labs are critical, the lab will call the facility and alert the nursing staff who will then alert the physician immediately. During an interview on 3/6/25 at 10:58 A.M., Nurse #3 said she worked the 7:00 A.M. - 3:00 P.M., shift on 2/26/25 and remembered that the lab tech arrived late that day. Nurse #3 said she told the incoming nurse (Nurse #4) that Resident #12 had pending labs. Nurse #3 said that staff would immediately call the physician if there were critical lab results for a resident. During an interview on 3/6/25 at 1:56 P.M., Nurse #4 said that he worked the 3:00 P.M. - 11:00 P.M., shift on 2/26/25. Nurse #4 said that he completely forgot to check Resident #12's labs and the DON called him on 2/27/25 and said that Resident #12's labs were critical and Resident #12 was being sent to the hospital. Nurse #4 said he did not receive a call from the lab company and he did not think that the lab faxes over results to the facility. During an interview on 3/6/25 at 11:26 A.M., the Lab Coordinator said that the lab will place three calls to the facility to alert them of any critical labs in addition to faxing over a copy of the lab results. The Lab Coordinator said that if the facility misses the call, they can still view the lab results online. The surveyor was unable to locate a physical copy of Resident #12's labs in his/her paper chart or the unit lab book. Review of the lab report indicated that calls were placed to the facility on 2/26/25 at 5:04 P.M., 5:37 P.M., and 6:29 P.M., which were unanswered. The DON was unavailable for interview. During an interview on 3/7/25 at 11:18 A.M., the Assistant Director of Nursing (ADON) said that staff should be alerting providers with critical lab results immediately. The ADON said that the DON had found that Resident #12's critical labs were not reported on 2/26/25 and she alerted Nurse Practitioner #1 on 2/27/25. During an interview on 3/10/25 at 9:36 A.M., the Nurse Practitioner said that nursing staff should immediately notify the provider with any critical lab results. The Nurse Practitioner said that she was not made aware until 2/27/25 of Resident #12's labs and she ordered the Resident be sent to the hospital. The Nurse Practitioner said that Resident #12's potassium level was too low and required hospitalization and he/she should have been sent out right away on 2/26/25. 2. Resident #44 was admitted to the facility in August 2024 with diagnoses that include, chronic kidney disease stage 4 severe, retention of urine, type 2 diabetes mellitus, and unspecified combined systolic (congestive) and diastolic (congestive) heart failure (CHF). Review of the most recent Minimum Data Set (MDS) assessment, dated 2/17/25, indicated that Resident #44 was cognitively intact as evidenced by a Brief Interview for Mental Status score of 15 out of 15. Further review of the MDS indicated Resident #44 requires substantial/maximal assistance for self-care and mobility. Review of the physician lab orders for Resident #44 indicated: Add TSH (thyroid stimulating hormone), T4 (thyroxine), D3 (vitamin D), B12, FOLATE, Fe tibc (total iron binding capacity) ferritin, HgA1c (glucose blood levels in diabetic patients) and FLP (fasting lipid profile), dated 11/8/2024. Review of the electronic medical record for Resident #44 failed to indicate the ordered labs were obtained. The surveyor was unable to locate a physical copy of Resident #44's labs in his/her paper chart or the unit lab book. During an interview on 3/6/25 at 11:34 A.M., Nurse #6 said Resident #44 was in the hospital recently and should have orders for labs because he/she had elevated levels that needed to be checked and said the Resident has kidney issues. Nurse #6 reviewed Resident #44's medical record and said she did not see any of the labs ordered on 11/8/24. Review of Resident #44's medical record indicated a physician progress note dated 10/29/24, indicated the following: Patient was transferred off hospice care. Remains the same condition but we need to regulate meds (medication) and labs. Review of the physician progress note dated 11/15/24, did not include information related to the labs that were ordered on 11/8/24. During an interview on 3/6/25 at 12:30 P.M., the Director of Nursing said Resident #44 did not have labs drawn as ordered and said she would expect the orders to be followed and monitored. During an interview on 3/7/25 at 11:00 A.M., the Assistant Director of Nurses (ADON) said Resident #44 had an order for lab draws but did not see that they were done. The ADON said staff should have notified the doctor to obtain a new order for labs. The Physician was unavailable for interview. During an interview on 3/10/25 at 10:14 A.M., Nurse Practitioner (NP) #1 said Resident #44 is very fragile and needs close monitoring due to his/her medical conditions and requires labs to be followed and monitored. NP #1 said labs should have been completed as ordered in November and said labs are checked to see if the resident needs to be transferred to the hospital for treatment. NP #1 said she was not aware that the labs in November were not completed and said Resident #44 should have had labs ordered when he/she returned from the hospital.
CONCERN (D)

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

Deficiency F0578 (Tag F0578)

Could have caused harm · This affected 1 resident

Based on record review and interview, the facility failed to accurately execute an Advanced Directive for 1 Resident (#69), out of a total sample of 20 residents. Specifically, for Resident #69 the fa...

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Based on record review and interview, the facility failed to accurately execute an Advanced Directive for 1 Resident (#69), out of a total sample of 20 residents. Specifically, for Resident #69 the facility failed to ensure the Massachusetts Medical Order for Life Sustaining Treatment (MOLST) (An Advanced Directive that is reviewed and signed as an order by a Physician/Nurse Practitioner (NP), or Physician Assistant (PA) and confirms a Resident's decisions for life sustaining treatment), was valid and signed by the Resident. Findings include: Review of the Facility's policy titled Advanced Directives, revision date September 2022, indicated the resident has the right to formulate an advanced directive, including the right to accept or refuse medical or surgical treatment. Advanced Directives are honored in accordance with state law and facility policy. Resident #69 was admitted to the facility in December 2024 and has diagnoses that include muscle wasting and atrophy, sepsis, chronic obstructive pulmonary disease, atherosclerotic heart disease and peripheral vascular disease. Review of the Minimum Data Set assessment, dated 12/25/25 indicated Resident #69 scored an 11 out of 15 on the Brief Interview for Mental Status score, indicating he/she as having moderately intact cognition. Review of Resident #69's medical record indicated the following: - A MOLST form dated 12/23/24 indicating Do Not Resuscitate, and Do Not Intubate and Ventilate, signed by a nurse practitioner and signed by a person, not the resident. - admission paperwork signed by Resident #69. Further review of the medical record failed to indicate a physician's order, or documentation to indicate Resident #69 had an invoked health care proxy agent, (an order/document that is signed by the physician, NP or PA that indicates the resident lacks the capacity to make their health care treatment decisions, allowing a designated health care agent to make informed decisions). During an interview on 3/6/25 at 12:19 P.M., the Social Worker said that Resident #69's health care proxy was not invoked, and that the person who signed the MOLST did not have the authority to make health care decisions for Resident #69, resulting in the MOLST not being valid.
CONCERN (D)

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

Notification of Changes (Tag F0580)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview, the facility failed to notify the physician of a change in condition for one ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview, the facility failed to notify the physician of a change in condition for one Resident, (#6), out of a total of 20 sampled residents. Specifically, the facility failed to notify the physician of a change in skin condition. Findings include: Review of the facility policy titled Change in a Resident's Condition or Status, dated revised December 2003 indicated that the facility shall promptly notify the resident, his or her attending physician and representative of changes in the resident's medical/mental condition and or status. Resident #6 was admitted to the facility in February 2023 with diagnoses including COPD (chronic obstructive pulmonary disease), chronic respiratory failure and schizophrenia. Review of the Minimum Data Set assessment dated [DATE], indicated that Resident #6 scored a 9 out of 15 on the Brief Interview for Mental Status exam, indicating moderately impaired cognition. During an interview on 3/4/25, at 10:47 A.M., Resident #6 said he/she has a fungal infection in his/her right groin. Resident #6 said that he/she told the nurses, but no one has obtained a nystatin powder (antifungal) for it. Resident #6 said that he/she bought Gold Bond powder, but it doesn't work. Review of the physician's orders failed to indicate an order for antifungal powder. Review of the progress notes failed to indicate that the physician was notified of Resident #6 having a reddened groin and was requesting an antifungal powder to be applied. Review of the document titled weekly Skin Review dated 2/12/25, indicated groin is pink. antifungal powder applied, no new skin issues. Review of the document titled weekly Skin Review dated 2/19/25, indicated resident groin is pink, antifungal powder applied. Review of the document titled weekly Skin Review dated 2/25/25, indicated groin is pink, antifungal powder order is in place, no new skin issues noted. During an interview on 3/06/25, at 10:11 A.M., the Regional Nurse said that the physician should have been notified of Resident #6's reddened groin.
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, record review and interview, the facility failed to ensure quality of care for two Residents (#69, and #6)...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview, the facility failed to ensure quality of care for two Residents (#69, and #6), out of a total sample of 20 residents. Specifically, 1. For Resident #69, the facility failed to ensure for Resident #69, who is treated with anticoagulant medication (a medication that hinders clotting of the blood), that areas of discoloration consistent with bruising were identified. 2. For Resident #6, the facility failed to obtain a treatment for a change in condition related to skin management. Findings include: 1. Review of the Facility's policy titled Anticoagulation - Clinical Protocol, revision date November 2018, included but was not limited to the following: Monitoring and Follow-up 5. The staff and physician will monitor for possible complications in individuals who are being anticoagulated and will manage related problems. A. If an individual on anticoagulation therapy, shows signs of excessive bruising, hematuria, hemoptysis, or other evidence of bleeding, the nurse will discuss the situation with the physician before giving the next scheduled dose of anticoagulant. Resident #69 was admitted to the facility in December 2024 and has diagnoses that include muscle wasting and atrophy, sepsis, chronic obstructive pulmonary disease, atherosclerotic heart disease and peripheral vascular disease. Review of the Minimum Data Set assessment, dated 12/25/25 indicated Resident #69 scored an 11 out of 15 on the Brief Interview for Mental Status exam, indicating he/she as having moderately intact cognition. During an observation and interview on 3/4/25 at 8:35 A.M., Resident #69 was in his/her bed. Resident #69's right arm had scattered red areas on the skin. Nurse #6 entered the room and said the Resident is on Lovanox (an anticoagulant) and administered the medication via an injection, and then she exited the room. Resident #69 said he/she transfers in out of bed with a slide board and can easily bump his/her arms. Review of Resident #69's physician's orders indicated the following: - Aspirin (a medication that can thin the blood) oral tablet delayed release 81 mg, give 1 tablet by mouth one time a day for Arterial Insufficiency, start date 12/20/2024. - Lovenox (an anticoagulation medication that hinders the clotting of blood) Injection Solution Prefilled Syringe 40 MG/0.4ML (Enoxaparin Sodium). Inject 0.4 ml subcutaneously one time a day for supplement related to ATHEROSCLEROTIC HEART DISEASE OF NATIVE CORONARY ARTERY WITHOUT ANGINA PECTORIS (I25.10) start date 12/20/24. - Clopidogrel Bisulfate Oral Tablet (an antiplatelet medication) 75 mg, give 75 mg by mouth one time a day for prophylactic use for 3 months. Start date 1/9/2025. - Monitor for Bleeding/Bruising r/t (related to) Lovenox use every shift, start 12/19/24 - Weekly skin check every shift every Thu (Thursday), start date 12/25/2024. Review of Resident #69's care plans indicated a care plan 'the Resident will not experience complications secondary to anticoagulation therapy', date initiated: 12/22/24. Goal - Resident will not develop bruising or abnormal bleeding from anticoagulant use through next review, dated initiated 12/22/24, revision date 2/28/2025. During an observation and interview on 3/6/25 at 8:48 A.M., and on 3/6/25 at 9:16 A.M., Resident #69 was in bed. His/her right arm had an increase in the number of areas of reddish discoloration on his/her right arm. Resident #69 said his/her left arm now had marks and held his/her arm up revealing red circular areas. Resident #69 said his/her arms have the areas because he/she is on a blood thinner and when he/she moves around or bangs them on the bed rail they just pop. Resident #69 said his/her right arm is worse than his/her my left arm. Resident #69's right arm had large, darker reddened discolorations, and close to his/her elbow was a small dark raised area, consistent with a scab. Resident #69 said it was a small cut. Resident #69 said the nurses knows about his/her skin. During an interview on 3/6/25 at 10:35 A.M., Certified Nursing Assistant (CNA) #1 said any changes in a resident's skin is reported to the nursing staff. CNA #1 said she is taking care of Resident #69 today and was not aware of any skin issues other than the dressings to his/her feet. The surveyor and CNA #1 went to Resident #69's room and observed both his/her arms. Resident #69 said the area on the right elbow observed with a scab has been there a few days after he/she hit it on his/her wheelchair. CNA #1 said the areas on his/her arms should be reported to nursing staff. Review of the Weekly skin review-V3, dated 3/6/25 indicated it failed to document areas of red discoloration on Resident #69's right or left arms. Review of the progress notes entered in Resident #69's medical record from 3/1/25 through 3/6/25 failed to indicate any nursing progress note related to changes in Resident #69's skin, specifically the areas of discoloration to his/her right and left arms. Nor were there any progress notes to indicate the physician was made aware of the resident's areas of discoloration on his/her right and left arms. Review of the March 2025, Medication Administration Record (MAR) indicated: Monitor for Bleeding/Bruising r/t (related to) Lovenox use every shift, start 12/19/24, and from 3/1/25 through day shift on 3/6/25, the day, evening and night shifts were checked off by nursing staff, and failed to indicate if any bleeding or bruising was noted. During an interview on 3/6/25 at 10:51 A.M., Nurse #6 said she just been informed of the bruises on Resident #69's right and left arms. Nurse #6 said the Resident is on three blood thinners and requires close monitoring to make sure he/she does not have any bruises or bleeding. Nurse #6 said the weekly skin check should include documentation of any skin changes including bruises. Nurse #6 said the MAR should include if bleeding or bruising is present due to the use of blood thinners. 2. Resident #6 was admitted to the facility in February 2023 with diagnoses including COPD (chronic obstructive pulmonary disease), chronic respiratory failure and schizophrenia. Review of the Minimum Data Set assessment dated [DATE] indicated that Resident #6 scored a 9 out of 15 on the Brief Interview for Mental Status exam, indicating moderately impaired cognition. During an interview on 3/4/25 at 10:47 A.M., Resident #6 said he/she has a fungal infection in his/her right groin. Resident #6 said that he/she told the nurses but no one has obtained a nystatin powder (an antifungal) for it. Resident #6 said that he/she bought Gold Bond powder but it doesn't work. Review of the physician's orders failed to indicate an order for antifungal powder. Review of the progress notes failed to indicate that the physician was notified of Resident #6 having a reddened groin and was requesting an anti fungal powder to be applied. Review of the document titled weekly Skin Review dated 2/12/25, indicated groin is pink. antifungal powder applied, no new skin issues. Review of the document titled weekly Skin Review dated 2/19/25, indicated resident groin is pink, antifungal powder applied. Review of the document titled weekly Skin Review dated 2/25/25, indicated groin is pink, antifungal powder order is in place, no new skin issues noted. During an interview on 3/6/25, at 9:00 A.M., Nurse #5 said that she did not know the residents very well and did not know Resident #6 had a reddened groin. Nurse #6 then said that the physician should have been notified when Resident #6's groin became reddened.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview the facility failed to ensure for one Resident (#69) that a smoking assessment...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview the facility failed to ensure for one Resident (#69) that a smoking assessment was completed and that a care plan was developed for smoking. Findings include: Review of the facility's policy titled Smoking Policy - Residents, revision date October 2023 indicted the following: The facility has established and maintains safe smoking practices. 1. Prior to and upon admission, residents are informed of the facility smoking policy, including designated smoking areas, and the extent to which the facility can accommodate their smoking or non-smoking preferences. 7. Resident smoking status is evaluated upon admission. If a smoker, the evaluation includes a. current level of tobacco consumption, b. method of tobacco consumption (traditional cigarettes electronic cigarettes, pipe, etc.) c. desire to quit smoking; and d. ability to smoke safely with or without supervision (per a completed Safe Smoking Evaluation). 9. A resident's ability to smoke safely is re-evaluated quarterly, upon significant change (physical or cognitive) and as determined by the staff. 10. Any smoking-related privileges, restrictions, and concerns (for example, need for close monitoring) are noted on the care plan, and all personnel caring for the resident shall be alerted to those issues. Resident #69 was admitted to the facility in December 2024 and has diagnoses that include muscle wasting and atrophy, sepsis, chronic obstructive pulmonary disease, atherosclerotic heart disease and peripheral vascular disease. Review of the Minimum Data Set assessment, dated 12/25/25 indicated Resident #69 scored an 11 out of 15 on the Brief Interview for Mental Status exam, indicating he/she as having moderately intact cognition. Further, the MDS indicated no tobacco use. Review of the list, not dated, provided by the facility to the surveyors on 3/4/25, indicated Resident #69 was listed as a person who smoked, requiring supervised/monitoring. Review of Resident #69's medical record indicated the following: - No person-centered care plan for smoking including individualized interventions. - No Safe Smoking Evaluation. - A smoking agreement signed by Resident #69, dated 12/23/24. -The admission Nursing assessment dated [DATE] indicated Resident #69 did not smoke. During an interview on 3/6/25 at approximately 8:37 A.M., Resident #69 said he/she smokes when his/her friend visits a few times a week, but he/she does not go out to the smoking area. During an interview on 3/6/25 at 8:19 A.M., Nurse #6 said that she was not aware that Resident #69 smoked, and that Resident #69 had told her that he/she did not smoke. During an interview on 3/6/25 at 3:02 P.M., the Social Worker said Resident #69 signed a smoking agreement upon admission. The Social Worker said at admission Resident #69 was ill and did not smoke, and when he/she began to feel better he/she resumed smoking. The Social Worker said Resident #69 may have began smoking around the end of January. The Social Worker said there was no safe smoking evaluation in Resident #69's medical record. The Social Worker said a care plan for smoking was initiated and discontinued. During an interview on 3/6/25 at 3:58 P.M., the Administrator said he added Resident #69 to the supervised smoking list because he saw him/her smoking outside with his/her friend. The Administrator said a care plan for smoking should be in place and a safe smoking evaluation should have been conducted when staff became aware that Resident #69 began to smoke.
CONCERN (D)

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

Respiratory Care (Tag F0695)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview and observation, the facility failed to provide respiratory care for three of 20 sampled resid...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview and observation, the facility failed to provide respiratory care for three of 20 sampled residents. Specifically: 1. For Resident #18, the facility failed to implement the physician's order for oxygen use. 2. For Resident #6, the facility failed to implement the physician's order for oxygen, and did not change expired oxygen tubing. 3. For Resident #12, the facility failed to obtain a physician's order for oxygen used by the Resident. Findings include: 1. Resident #18 was admitted to the facility in [DATE] and had diagnoses which included chronic obstructive pulmonary disease (COPD). Review of Resident #18's Minimum Data Set assessment dated [DATE], indicated a Brief Interview for Mental Status exam of 7, signifying severe cognitive impairment, and an active diagnosis of COPD. Review of Resident #18's respiratory care plan dated [DATE], indicated: - The Resident has oxygen therapy related to COPD. - Provide oxygen as ordered. Review of Resident #18's physician's order dated [DATE], indicated: - Oxygen via nasal cannula as needed at 2 liters per minute to maintain saturation at or above 90%. On [DATE] at 10:41 A.M., the surveyor observed Resident #18 lying awake in bed and wearing a nasal cannula. The cannula and tubing were attached to an oxygen concentrator, located on the floor by the side of the bed. The oxygen was running and set to 4 1/2 liters per minute. On [DATE] at 7:58 A.M., the surveyor observed Resident #18 asleep in bed, and wearing a nasal cannula attached to the oxygen concentrator. The concentrator was running and set to 4 1/2 liters per minute. During an interview with Nurse #2 on [DATE] at 8:05 A.M., the surveyor told her that Resident #18's oxygen was running at 4 1/2 liters per minute. Nurse #2 reviewed the Resident's physician orders and said the oxygen delivery rate should be set to 2 liters per minute. Nurse #2 accompanied the surveyor to the Resident's room and observed the oxygen concentrator was running at 4 1/2 liters per minute. During an interview with Resident #18 on [DATE] at 9:33 A.M., he/she said he/she does not adjust the oxygen level on the concentrator, and that only staff touch the concentrator. 2. Resident #6 was admitted to the facility in February 2023 with diagnoses including COPD (chronic obstructive pulmonary disease), chronic respiratory failure and schizophrenia. Review of the Minimum Data Set assessment date [DATE] indicated that Resident #6 scored a 9 out of 15 on the Brief Interview for Mental Status exam, indicating moderately impaired cognition. On [DATE], at 8:09 A.M. the surveyor observed Resident #6 in bed receiving 4.5 liters/minute of oxygen via nasal cannula. The surveyor then observed the oxygen tubing to be dated [DATE]. Review of the physician orders dated [DATE] indicated an order for O2 via nasal cannula 1 to 3 liters/minute continuous. Review of the medication administration record dated [DATE] indicated that the oxygen tubing was changed on [DATE]. Review of the care plan indicated that Resident #6 is at risk for respiratory complications r/t COPD, respiratory failure and to provide O2 therapy as ordered. During an interview on [DATE], at 9:00 A.M., Nurse #5 said that the oxygen tubing was dated [DATE] and should have been changed on [DATE]. Nurse #5 then said that the oxygen was running at 4.5 liters/minute and was ordered to be running at no higher than 3 liters/minute. Nurse #5 then said that the medical record was inaccurate because a nurse had signed off that the O2 tubing was changed on [DATE]. 3. Resident #12 was admitted to the facility in [DATE] with diagnoses including dementia, and chronic obstructive pulmonary disease. Review of the Minimum Data Set (MDS) assessment dated [DATE] indicated Resident #12 is moderately cognitively impaired as evidenced by a score of 12 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam. The MDS also indicated Resident #12 requires assistance with bathing and dressing and utilizes oxygen therapy. On [DATE], the surveyor observed Resident #12 asleep in bed wearing oxygen via nasal cannula. The surveyor was unable to observe the oxygen concentrator due to its placement under the bed. Review of Resident #12's physicians orders failed to indicate a current order for the use of oxygen. During an interview on [DATE] at 8:20 A.M., Resident #12 was observed seated in the hallway outside his/her door, not wearing 02. Resident #12 and said he/she wears oxygen at night and gave the surveyor permission to view the concentrator. The surveyor then observed the 02 concentrator running with the nasal cannula on the floor. The concentrator was set at 3 liters. Resident #12 said it should be set at 2 liters. During an interview on [DATE] at 10:16 A.M., Nurse #2 said that Resident #12 wears oxygen at night when he/she is sleeping. Nurse #2 and the surveyor reviewed the physician' orders and Nurse #2 said she could not see an order for the use of oxygen for Resident #12. Nurse #2 said residents on oxygen need a physician's order. During an interview on [DATE] at 11:25 A.M., the Assistant Director of Nursing (ADON) said that she knew Resident #12 wore oxygen at night and did not know there was no order in place.
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, record review and interview, the facility failed to ensure medications were stored as required for one Res...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interview, the facility failed to ensure medications were stored as required for one Resident (#26), out of a total sample of 20 residents. Specifically, the facility failed to ensure that medication was not left at the Resident's bedside unattended. Findings include: Review of the facility policy titled 'Medication Labeling and Storage' dated February 2023, indicated the following but was not limited to: -The facility stores all medications and biologicals in locked compartments under proper temperature, humidity and light controls. Only authorized personnel have access to keys. Resident #26 was admitted to the facility in April 2019 with diagnoses including gastro esophageal reflux disease without esophagitis. Review of Resident #26's Minimum Data Set (MDS) assessment dated [DATE] indicated the Resident scored a 15 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam indicating he/she was cognitively intact. The MDS further indicated the Resident did not reject care. On 3/4/25 at 8:09 A.M., the surveyor observed three medicine cups by the Resident's bedside table with 15 round various colored tablets, and appeared to be calcium carbonate Tums. Review of the medical record indicated the following physician order. - Calcium carbonate tablet 1250 (500 ca) mg (milligram). Give 2 tablets by mouth with meals for supplement. Review of medical record failed to indicate a resident self-medication administration assessment had been completed. During an interview on 3/6/25 at 11:04 A.M., Nurse #6 said the nurses are supposed to stay with the Resident during medication administration to ensure all medications are taken. During an interview on 3/7/25 at 11:08 A.M., the Assistant Director of Nursing (ADON) said nurses are to stay with the resident until all the medication is consumed and should not leave any medications by the bedside.
CONCERN (D)

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

Deficiency F0825 (Tag F0825)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure specialized rehab services were provided in a timely fashion...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure specialized rehab services were provided in a timely fashion for one Resident (#41) out of a total sample of 20 residents. Findings include: Resident #41 was admitted to the facility in November 2022 with diagnoses including hemiplegia and hemiparesis following cerebral infarction (stroke) affecting right dominant side. Review of Resident #41's Minimum Data Set (MDS) assessment dated [DATE] indicated the Resident had a moderate impaired cognition and scored a 10 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam. Review of Resident #41's medical record indicated the following: - Nursing note dated 2/8/25: Patient continue to c/o (complain of) pain and stiffness of left-hand joints when he/she tries to use his/her hand and bend his/her fingers. No swelling, redness or signs of trauma noted. The doctor notified new order to start patient on Biofreeze gel every 8 hours, then refer patient to OT (Occupational Therapy) [sic]. During an interview on 3/7/25 at 11:41 A.M., the Assistant Director of Nursing (ADON) said the OT evaluation was done on Tuesday 3/4/25. She further said they have not had an OT on staff and the per diem (as needed) OT staff are here at the facility only once a month. The ADON said the expectation for a therapy screen to be completed should be no more than two weeks. During an interview on 3/7/25 at 12:03 P.M., the Rehab Director said they are made aware of residents requiring therapy evaluation either by nursing staff telling them verbally, filling out a slip or during morning meeting. He further said he has not had an occupational therapist on staff, and the expectation is a resident should be evaluated as soon as possible after the initial screen request.
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** Based on record review and interview, the facility failed to ensure the accuracy of its medical records for 3 of 20 sampled resi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure the accuracy of its medical records for 3 of 20 sampled residents. Specifically: 1. For Resident #18, the facility failed to accurately document the oxygen delivery rate. 2. For Resident #6, the facility failed to accurately date oxygen tubing. 3. For Resident #1, the facility failed to accurately document wound dressing treatment. Findings include: 1. Resident #18 was admitted to the facility in April 2024 and had diagnoses which included chronic obstructive pulmonary disease (COPD). Review of Resident #18's Minimum Data Set assessment dated [DATE], indicated a Brief Interview for Mental Status exam of 7, signifying moderate cognitive impairment, and an active diagnosis of COPD. Review of Resident #18's respiratory care plan dated 10/20/24, indicated: - The Resident has oxygen therapy related to COPD. - Provide oxygen as ordered. Review of Resident #18's physician's order dated 5/14/24, indicated: - Oxygen via nasal cannula as needed at 2 liters per minute to maintain saturation at or above 90%. On 3/4/25 at 10:41 A.M., the surveyor observed Resident #18 lying awake in bed and wearing a nasal cannula. The cannula and tubing were attached to an oxygen concentrator, located on the floor by the side of the bed. The oxygen was running and set to 4 1/2 liters per minute. On 3/6/25 at 7:58 A.M., the surveyor observed Resident #18 asleep in bed, and wearing the nasal cannula, attached to the oxygen concentrator. The concentrator was running and set to 4 1/2 liters per minute. Review of Resident #18's Medication Administration Record (MAR) indicated that on 3/4/25, 3/5/25 and 3/6/25, staff documented he/she received oxygen via nasal cannula as needed at 2 liters per minute. The MAR did not indicate the Resident's oxygen was set to and running at 4 1/2 liters per minute. Review of Resident #18's nursing notes dated 3/4/25, 3/5/25 and 3/6/25, did not indicate the Resident's oxygen was set to and running at 4 1/2 liters per minute. During an interview with Nurse #2 on 3/6/25 at 8:05 A.M., the surveyor told her that Resident #18's oxygen was running at 4 1/2 liters per minute, but the MAR indicated it ran at 2 liters per minute. Nurse #2 reviewed the Resident's physician orders and said the oxygen delivery rate should be set to 2 liters per minute and that the MAR was inaccurate. Nurse #2 accompanied the surveyor to the Resident's room and observed the oxygen concentrator was running at 4 1/2 liters. During an interview with Resident #18 on 3/6/25 at 9:33 A.M., he/she said he/she does not adjust the oxygen level on the concentrator, and that only staff touch the concentrator. 2. Resident #6 was admitted to the facility in February 2023 with diagnoses including COPD (chronic obstructive pulmonary disease), chronic respiratory failure and schizophrenia. Review of the Minimum Data Set assessment date 12/25/24 indicated that Resident #6 scored a 9 out of 15 on the Brief Interview for Mental Status exam, indicating moderately impaired cognition. A. During an interview on 3/4/25, at 10:47 A.M., Resident #6 said he/she has a fungal infection in his/her right groin. Resident #6 said that he/she told the nurses but no one has obtained a nystatin powder (an anti fungal) for it. Resident #6 said that he/she bought Gold Bond powder but it doesn't work. Review of the physician's orders failed to indicate an order for fungal powder. Review of the progress notes failed to indicate that the physician was notified of Resident #6 having a reddened groin and was requesting an anti fungal powder to be applied. Review of the document titled weekly Skin Review dated 2/12/25, indicated groin is pink. antifungal powder applied, no new skin issues. Review of the document titled weekly Skin Review dated 2/19/25, indicated resident groin is pink, antifungal powder applied. Review of the document titled weekly Skin Review dated 2/25/25, indicated groin is pink, anti fungal powder order is in place, no new skin issues noted. During an interview on 3/6/25, at 10:11 A.M.,the Regional Nurse said that a doctor's order for an antifungal powder should be obtained before applying the powder. The Regional Nurse also said that the documentation should be accurate and not indicate a physician's order was in place when it was not. B. On 3/4/25 at 8:09 A.M., the surveyor observed Resident #6 in bed receiving 4.5 liters/minute of oxygen via nasal cannula. The surveyor then observed the oxygen tubing to be dated 2/24/25. Review of the physician orders dated March 2025 indicated an order for O2 via nasal cannula 1 to 3 liters/minute continuous. Review of the medication administration record dated March 2025 indicated that the oxygen tubing was changed on 3/2/25. Review of the care plan indicated that Resident #6 is at risk for respiratory complications r/t COPD, respiratory failure and to provide O2 therapy as ordered. During an interview on 3/06/25, at 9:00 A.M., Nurse #5 said that the oxygen tubing was dated 2/24/25 and should have been changed on 3/3/25. Nurse #5 then said that the oxygen was running at 4.5 liters/minute and it was ordered to be running at no higher than 3 liters/minute. Nurse #5 then said that the medical record was inaccurate because a nurse had signed off that the O2 tubing was changed on 3/3/25. 3. Resident #1 was admitted to the facility in February 2023 with diagnoses including peripheral vascular disease and lymphedema. Review of Resident #1's Minimum Data Set (MDS) assessment dated [DATE] indicated the Resident scored a 15 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam indicating he/she was cognitively intact. The MDS further indicated the Resident had wounds. On 3/4/25 at 8:13 A.M., the surveyor observed Resident #1 lying in his/her bed land the eft ankle had a border gauze dressing dated 3/2. Review of the medical record indicated the following physician order, dated 2/10/25: - Xeroform gauze, gauze island with border apply to left upper medial ankle once daily every day shift. Review of the current Treatment Administration Record (TAR) indicated the nurses had signed off that the wound dressing had been changed on 3/3/25. During an interview on 3/6/25 at 11:07 A.M., Nurse #6 said the treatment nurse does the wound treatments Monday through Friday and the floor nurses are responsible for the treatments when the wound treatment nurse is not available. She further said nurses should not document a treatment as complete if it was not completed. During an interview on 3/7/25 at 11:10 A.M., the Assistant Director of Nursing (ADON) said the floor nurses are responsible for ensuring the wound treatments are completed as ordered and document accurately.
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 record review, interview and observation, the facility failed to provide respiratory care in accordance with profession...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview and observation, the facility failed to provide respiratory care in accordance with professional standards of practice, for three of 20 sampled residents. Specifically: 1. For Resident #18, the facility failed to develop a care plan for post-traumatic stress disorder. 2. For Resident #11, the facility failed to develop a care plan for post-traumatic stress disorder. 3. For Resident #12, the facility failed to develop a care plan for suicidal ideation. 4. For Resident #44, the facility failed to develop care plans for the presence of a cardiac pacemaker. 1. Resident #18 was admitted to the facility in April 2024, with diagnoses including post-traumatic stress disorder (PTSD), anxiety and depression. Review of the Minimum Data Set assessment dated [DATE], indicated a Brief Interview for Mental Status exam of 7, signifying severe cognitive impairment, and an active diagnosis of PTSD. Review of the current care plan for PTSD/mood care dated 5/10/24, indicated: - Resident #18 was at risk for alteration in mood related to: diagnosis of Depression, PTSD. - The care plan goal: Resident will display positive affect through next review period. - Care plan intervention was limited to: Staff to report any changes in resident's mood to Social Worker, Director of Nurses and supportive services immediately for evaluation. During an interview with the Regional Nurse on 3/6/25 at 10:13 A.M., she said Resident #18's care plan for PTSD should be individualized to include specific triggers and interventions, and that the current care plan is not individualized. The Regional Nurse said the PTSD care plan should give direct care staff direction on how to manage the Resident's PTSD and associated behaviors.2. Resident #11 was admitted to the facility in July 2023 with diagnoses including post-traumatic stress disorder (PTSD), anxiety and borderline personality disorder. Review of the current care plan failed to indicate a plan of care for the diagnosis of PTSD. During an interview on 3/6/25, at 10:11 A.M., the Regional Nurse said that residents with a diagnosis of PTSD should have a care plan in place that addresses the Resident's PTSD. 3. Resident #12 was admitted to the facility in August 2024 with diagnoses including dementia, chronic obstructive pulmonary disease and suicidal ideation. Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #12 is moderately cognitively impaired as evidenced by a score of 12 out of a possible 15 on the Brief Interview for Mental Status (BIMS) exam. The MDS also indicated Resident #12 requires assistance with bathing and dressing and utilizes oxygen therapy. Review of Resident #12's discharge paperwork from the hospital indicated that he/she had a history of suicidal ideation and had been transferred to the psychiatric unit during his/her hospital stay after reporting suicidal ideation with a plan. Review of Resident #12's care plans failed to include a care plan identifying Resident #12's history of suicidal ideation or methods or means for staff to monitor for his/her mental well-being and physical safety. During an interview on 3/6/25 at 10:37 A.M., the Social Worker said residents with a history of suicidal ideation or attempt history should have care plans implemented to reflect triggers signs/symptoms and to notify the physician/administration of any changes of behaviors. The Social Worker said she was not aware Resident #12 did not have a care plan related to his/her suicidal ideation. 4. Review of the facility policy titled Pacemaker, Care of a Resident with, dated as revised December 2015, indicated the purpose of this procedure is to provide information about and guidance for the care of a resident with a pacemaker. - Pacemakers are electronic devices that artificially stimulate the heart muscle with electrical impulses when the heart rhythm is too low (bradycardia). - Pacemakers are programmed to sense the heart and respiratory rate and to administer electrical pulses when the heart rate falls below a set threshold. Complications -If the pulse generator or battery fails or if the leads become displaced the pacemaker may not work properly leading to [NAME] arrhythmias. Resident #44 was admitted to the facility in August 2024 with diagnoses that included: presence of cardiac pacemaker, unspecified combined systolic (congestive) and diastolic (congestive) heart failure, unspecified atrial fibrillation (irregular heartbeat), essential (primary) hypertension, atherosclerotic heart disease of native coronary artery (buildup of plaque restricting blood flow), and acute respiratory failure with hypoxia (lack of oxygen). Review of the most recent Minimum Data Set (MDS) assessment, dated 2/17/25, indicated that Resident #44 was cognitively intact as evidenced by a Brief Interview for Mental Status exam score of 15 out of 15. Further review of the MDS indicated the presence of a cardiac pacemaker. On 3/4/25 at 9:43 A.M., the surveyor observed Resident #44 sitting in bed. A white box was located on the nightstand next to the Resident's bed. Resident #44 said he/she has a pacemaker and but did not know who manages it. Review of Resident #44's pacemaker care plan, dated 8/27/24, indicated the Resident has a pacemaker r/t (related to) A-fib (atrial fibrillation). - Will remain free from s/sx (signs /symptoms) of pacemaker malfunction or failure through the review date. - Obtain vital signs as ordered/per facility protocol and record. Notify MD of significant nursing abnormalities. Review of Resident #44's medical record failed to indicate information on the cardiac pacemaker. During an interview on 3/6/25 at 9:48 A.M., Certified Nursing Assistant #1 said Resident #44 does not have a pacemaker. During an interview on 3/6/25 at 11:36 A.M., Nurse #6 said Resident #44 does have a pacemaker and said the care plan should be completed with information related to the pacemaker and said she did not have any additional information regarding reports in the medical record. During an interview on 3/6/25 at 12:30 P.M., the Director of Nurses said the pacemaker care plan must be updated with information on how the pacemaker is monitored and specifics of the pacemaker and monitoring orders must be in place. During an interview on 3/10/25 at 10:08 A.M., Nurse Practitioner #1 said the medical record should indicate the presence of a pacemaker, so staff are aware.
Feb 2025 3 deficiencies
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

Safe Environment (Tag F0584)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and records reviewed, for five out of thirteen resident rooms on one unit (Unit A) and for thr...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and records reviewed, for five out of thirteen resident rooms on one unit (Unit A) and for three out of three resident shower rooms, the Facility failed to ensure it provided a safe, clean, comfortable and homelike environment for its residents, when the condition of the resident shower rooms were found to be dirty and baseboard heaters in several resident rooms were in disrepair, with missing or damaged covers, both of which created potentially hazardous conditions. Findings include: Review of the Facility Policy titled Shower and Tub Room Cleaning, undated, indicated showers would be cleaned daily to remove soap scum, dirt and debris, providing a safe and sanitary place for residents to bathe. Review of a Department of Public Health (DPH) Consumer Complaint Form, dated 02/06/25, indicated the Complainant alleged that the resident showers were dirty and covered in mold and mildew. The Form further indicated the Complainant alleged that baseboard heaters in several resident rooms were broken and exposed. During an environmental tour of Unit C, on 02/20/25 at 7:54 A.M., Surveyor #2 observed the resident shower room had blackened areas in the grout between the tiles on the wall of the shower and did not appear to be cleaned on a routine basis. The shower room was poorly lit, and there were black mildew-like stains on the ceiling. During an environmental tour of Unit A, on 02/20/25 at 8:15 A.M., Surveyor #2 observed the following: - Resident shower room (near the nurses' station): The ceiling was covered with a black mildew-like substance. The air in the room was very humid, smelled musty, and the exhaust fan was not working. The base of the shower curtain was black. The air vent was caked with dust. - Resident shower room (near the Hair Salon): The shower curtain was dirty. The ceiling and the grout between the shower tiles were covered with a black mildew-like substance. - room [ROOM NUMBER]: The baseboard heater cover was hanging off. - room [ROOM NUMBER]: The baseboard heater cover was completely off, sharp edges and heating elements were exposed and accessible to residents. - room [ROOM NUMBER]: The baseboard heater cover was hanging off. - room [ROOM NUMBER]: The baseboard heater cover was hanging off. - room [ROOM NUMBER]: The baseboard heater cover was hanging off and sharp edges were exposed and accessible to residents. During an interview on 02/20/25 at 11:55 A.M., Resident #6 said the shower on Unit C was not kept clean. Resident #6 led Surveyor #3 to the shower room and showed her the black mildew-like substance that covered the grout between the shower tiles. During an interview on 02/20/25 at 9:40 A.M., the Director of Environmental Services said the expectation was for the housekeepers to clean the resident shower rooms daily. The Director of Environmental Services said that the exhaust fan in the Unit A Shower Room (near the nurses' station) was supposed to turn on automatically, but it did not operate consistently, and he had not been able to fix it. During an interview on 02/20/25 at 2:30 P.M., with the Administrator, Surveyor #2 requested copies of all Facility Policies that addressed overall general maintenance of the resident care areas and/or maintaining the baseboard heating equipment in resident rooms. The Administrator provided, and Surveyor #2 reviewed the following Facility Policies related to maintenance: - General Guidelines (Maintenance of Fire safety Equipment), October 2019 - Cleaning and Disinfection of Environmental Surfaces, August 2010 Review of Policies indicated there was no documentation to address general maintenance of the resident care areas and/or the upkeep of the baseboard heaters. The Administrator said the Facility had identified a problem with the covers on the baseboard heaters about a year ago and had planned to replace all the covers. The Administrator said that while some covers were purchased on 08/29/24, several baseboard heaters were still in need of replacement covers.
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

Deficiency F0804 (Tag F0804)

Could have caused harm · This affected multiple residents

Based on records reviewed, interviews and observations, for one of three sampled resident care units (Unit A), the Facility failed to ensure food provided to the residents was served at safe and appet...

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Based on records reviewed, interviews and observations, for one of three sampled resident care units (Unit A), the Facility failed to ensure food provided to the residents was served at safe and appetizing temperatures, when on 02/20/25, results of test tray observations indicated the food items were not served at appetizing temperatures and some of the food items were not palatable. Finding include: Review of the Facility's policy, titled Food Temperatures, undated, indicated foods will be maintained at proper temperature to ensure food safety. The point of service temperature to residents will be within the range of 120 degrees Fahrenheit (F) to 140 degrees (F) based on the resident's preference. The policy further indicated the following range of temperatures recommended for food at point of tray assembly: -Meat, portioned for service: 160 degrees (F) -Potatoes and vegetables: 160 degrees (F) Review of the Dining Committee Minutes, dated 12/16/24 and attended by 12 residents, indicated some residents stated that some meals were not up to temperature, but the residents did not specify which meal. Review of a Department of Public Health (DPH) Consumer Complaint Form, dated 02/06/25, indicated the Complainant alleged that breakfast was always cold, and dinner was inedible. During an interview on 02/20/25 at 8:08 A.M., Resident #7 (who resided on Unit A) said the food at the Facility was awful and always cold. Resident #7 said there was no variety, and the food quality was poor. During an interview on 02/20/25 at 8:15 A.M., Resident #3 (who resided on Unit A) said the quality of the food at the Facility was poor. Resident #3 showed the surveyor his/her breakfast meal which consisted of scrambled eggs and one piece of toast, which had been cut in half and toasted on only one side. On 02/20/25 at 11:31 A.M., Surveyor #1 observed the following in the facility's main kitchen: - [NAME] #1 took the temperature of the following food items in preparation to serve the lunch meal: -puree beef: 170 degrees (F) -puree carrots: 180 degrees (F) -mashed potatoes: 160 degrees (F) -hamburger: 160 degrees (F) -hot dog: 150 degrees (F) -chicken salad: 41 degrees (F) - At 11:37 A.M., the lunch line began. [NAME] #1 plated the food items and handed the plate to the Dietary Aide who put a cover over the plate and placed it in the food truck, to be delivered to the resident units. On 02/20/25 at 12:14 P.M., the second lunchtime truck for Unit A left the kitchen. At 12:14 P.M., the second lunchtime truck was observed to arrive on Unit A. Multiple staff members began passing the lunch trays out to the residents who were in their rooms. At 12:19 P.M., after the last resident meal tray was removed and served, the test tray was pulled from the truck by Nurse #1. A food test tray was then conducted on Unit A by Surveyor #1 accompanied by Nurse #1. Test Tray observations: The food temperatures were measured by Nurse #1, the food items were tasted by Surveyor #1 in the presence of Nurse #1, observations were as follows: - puree beef was 109.9 degrees (F) and tasted lukewarm - mashed potatoes were 104.4 degrees (F), were tepid, bland, and not palatable. - puree carrots were 103.6 degrees (F), were tepid and not palatable. - hot dog was 97.3 degrees (F), was cold and not palatable. - A hamburger was not provided on the test tray. - The chicken salad sandwich was dark in appearance; the portion of chicken salad in the sandwich was inadequate and did not meet the corners or edges of the bread and tasted bland. During an interview on 02/20/25 at 12:30 P.M., Resident #4 (who resided on Unit A) said the food was awful and that he/she got some kind of salad sandwich for lunch and it tasted awful. During an interview on 02/20/25 at 12:32 P.M., Resident #5 (who resided on Unit A) said the food was not good, so he/she usually requested hamburgers. During an interview on 02/20/25 at 2:38 P.M., the Food Service Director (FSD) said the hot food temperature at the time of service to residents should be 135 degrees (F). The FSD said she was not surprised that the food temperatures for the test tray were low, and she thought one of the wells in the steam table did not hold the appropriate temperature. The FSD said the food would not taste good at those temperatures (obtained during the test tray observation). During a telephone interview on 02/21/25 at 9:31 A.M., the Administrator said the facility needed a pellet system (provides an insulated base to hold the plated food ready for service). The Administrator said the plates were not kept warm because there was nothing under them.
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

Food Safety (Tag F0812)

Could have caused harm · This affected multiple residents

Based on observations, interviews and records reviewed, for the main kitchen where all food items are prepared and plated before being served to the residents, the facility failed to ensure; 1) they m...

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Based on observations, interviews and records reviewed, for the main kitchen where all food items are prepared and plated before being served to the residents, the facility failed to ensure; 1) they maintained a clean and sanitary environment in the facility's main kitchen, and 2) that kitchen (dietary) staff adhered to sanitary standards of practice during food handling when two of two cooks were observed handling food without wearing hair restraints. Findings include: Review of the Facility's policy, titled Sanitation/Infection Control, undated, indicated the following: -The Dietary Manager is responsible for supervising all sanitation and housekeeping procedures within the Dietary Department. -The Dietary Manager and consultant dietician develop a cleaning schedule. -Light daily cleaning is required for the refrigerator .outside doors on steamers and freezers are wiped off. -All work and storage areas are clean, well lit, and orderly. Review of the Facility's policy, titled Personal Hygiene, undated, indicated the key to a safe and sanitary Dietary Department is healthy employees, properly trained in safe food handling, who practice good personal hygiene. The Policy indicated if hair was long and not covered properly with a cap, a hair net must be worn. On 02/20/25 at 11:15 A.M., the surveyor observed the following in the facility's main kitchen: 1) A wall of reach-in freezers adjacent to the steam table with large areas of fingerprints and smears along five out of five doors. -Four of the five reach-in freezer doors did not have a plastic protective piece along the door handle, leaving an exposed metal edge, which created a space for debris to collect. -The reach-in refrigerator located near the exit door of the kitchen had large areas of fingerprints and smears on both doors. 2) -Dietary staff were preparing to serve the lunch meal. -Cook #1 stood behind the steam table, in front of the uncovered food items to be served for lunch, without wearing a beard net. -Cook #1 plated all the food items to be served to the residents for lunch, without wearing a beard net. -Cook #2 set up a workstation at a preparation table behind the steam table, placing several pieces of bread on the table to make sandwiches for the residents, without wearing a cap or hair net. -Cook #2 made several sandwiches to be served to the residents for lunch, without wearing a cap or hair net. During an interview on 02/20/25 at 2:38 P.M., the Food Service Director (FSD) said she had a generic cleaning schedule but needed to develop a better one. The FSD said the freezer and refrigerator doors should be cleaned every shift and that the handles on the reach-in freezer doors had been missing for a long time. The FSD said all dietary staff were supposed to wear hair and beard coverings when they were in the kitchen. The FSD said both cooks should have worn appropriate hair coverings when in the kitchen and during lunch service. During a telephone interview on 02/21/25 at 9:31 A.M., the Administrator said he expected the kitchen appliances to be clean and he did not know that the plastic coverings for the handles on the reach-in freezers were missing. The Administrator said that all dietary staff were supposed to wear appropriate hair coverings when they were in the kitchen.
Nov 2024 2 deficiencies
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

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

Based on records reviewed and interviews for two of three sampled residents (Resident #1 and Resident #2) who were assessed by nursing to be at risk for elopement, the Facility failed to ensure 1) nur...

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Based on records reviewed and interviews for two of three sampled residents (Resident #1 and Resident #2) who were assessed by nursing to be at risk for elopement, the Facility failed to ensure 1) nursing updated Resident #1's comprehensive plan of care with new interventions following an elopement on 07/07/24, and 2) nursing developed and implemented an individualized comprehensive care plan with interventions, treatment goals and outcomes that addressed Resident #2's risk for elopement. Findings include: Review of the Facility's policy titled Care Plans Comprehensive Person-Centered, dated 03/2022, included the following: -A comprehensive, person-centered care plan that includes measurable objectives and timetables to meet the resident's physical, psychosocial and functional needs is developed and implemented for each resident. -The care plan interventions are derived from a thorough analysis of the information gathered as part of the comprehensive assessment. -Assessments of residents are ongoing and care plans are revised as information about the residents and the residents' conditions change. Review of the Facility's policy titled Wandering and Elopements, dated 03/2019, indicated if a resident is identified to be at risk for wandering, elopement, or other safety issues, the resident's care plan will include strategies and interventions to maintain the resident's safety. 1) Resident #1 was admitted to the Facility in July 2023, diagnoses include hereditary ataxia (impaired balance or coordination), mild cognitive impairment, and repeated falls. Review of Resident #1's Elopement and Wander Risk Evaluation, dated 04/15/24, indicated he/she was assessed as being at high risk for elopement. Review of Resident #1's Quarterly Minimum Data Set (MDS) assessment, dated 04/17/24, indicated he/she scored a 10 out of 15 on the Brief Interview for Mental Status (BIMS) assessment (0-7 suggests severe cognitive impairment, 8-12 suggests moderate cognitive impairment, and 13-15 suggests no cognitive impairment). Review of Resident #1's Elopement Care Plan, renewed and reviewed with his/her April 2024 MDS, indicated he/she was at risk for elopement with an intervention to make the receptionist and other staff aware of his/her risk for elopement. Review of Resident #1's Nurse Progress Note, dated 07/07/24 and signed by Nurse #3, indicated Resident #1 had an argument with his/her roommate and Resident #1 attempted to leave the Facility. The Note indicated staff were able to redirect Resident #1 back into the Facility, but he/she refused to go back to his/her room and Resident #1 was moved to a different room for the night. During an interview on 11/26/24 at 3:16 P.M., Nurse #3 said she was the nurse on duty for the evening shift (3:00 P.M. through 11:00 P.M.) on 07/07/24. Nurse #3 said staff found Resident #1 outside in the parking lot adjacent to the facility, that Resident #1 was crying and said that he/she wanted to go home. Nurse #3 said staff were able to redirect Resident #1 back into the Facility. Nurse #3 said she notified the Director of Nurses (DON), Assistant Director of Nurses (ADON) and the Administrator that Resident #1 spent that night in a different room. Nurse #3 said no changes were made to Resident #1's care plan. Review of Resident #1's Elopement Care Plan, initiated 04/12/24, indicated there was no documentation to support that new interventions were implemented after his/her elopement on 07/07/24. Review of an Employee Statement, undated and signed by Certified Nurse Aide (CNA) #1, indicated CNA #1 entered Resident #1's room at 7:40 P.M. on 09/21/24, to provide him/her care, and Resident #1's roommate said Resident #1 left the building to meet his/her spouse. During a telephone interview on 11/26/24 at 4:43 P.M., Nurse #1 said he worked through a staffing agency and was on duty the evening shift of 09/21/24 and he did not know how Resident #1 was able to leave the Facility that evening, unattended by staff. Nurse #1 said it was a busy time of night when Resident #1 left the Facility. Nurse #1 said when Resident #1 returned to the Facility, he/she had bruises on his/her face and abrasions to his/her knees and palms. Nurse #1 said the abrasions were all superficial. During an interview on 11/26/24 at 3:59 P.M., the Director of Nurses (DON) said had she realized that Resident #1 was found outside of the building in the facility's parking lot on 07/07/24, she would have revised the care plan at that time to add new interventions which would have included for Resident #1 to always wear a wander guard bracelet (triggers an alarm at the exit doors) and to increase safety checks performed by staff, in an effort to prevent his/her second elopement. 2) Resident #2 was admitted to the Facility in May 2024, diagnoses include Alzheimer's Disease, repeated falls, and unsteadiness on feet. Review of Resident #2's Nursing Elopement and Wander Risk Evaluation, dated 08/26/24, indicated he/she was assessed to be at high risk for elopement. Review of Resident #2's medical record indicated there was no documentation to support that an individualized comprehensive care plan with interventions, treatment goals and outcomes that addressed his/her risk of elopement, had been developed. During an interview on 11/26/24 at 3:59 P.M., the Director of Nurses (DON) said Resident #2 should have had a care plan related to his/her risk of elopement once the risk of elopement was identified.
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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

Based on records reviewed and interviews for one of three sampled residents (Resident #1), who was assessed by nursing to be at high risk for elopement, and was moderately cognitively impaired, the Fa...

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Based on records reviewed and interviews for one of three sampled residents (Resident #1), who was assessed by nursing to be at high risk for elopement, and was moderately cognitively impaired, the Facility failed to ensure he/she was provided an adequate level of staff supervision to prevent two incidents of elopement, when on 07/07/24, Resident #1 was found out in the parking lot adjacent to the facility (unescorted by a staff member) and, on 09/21/24, Resident #1 was able to exit the facility unbeknownst to staff, was found by staff a couple of blocks away from the facility with bruises on his/her face and abrasions on his/her bilateral knees and palms. Findings include: Review of the Facility Policy titled Wandering and Elopements, dated March 2019, indicated the following: -The facility will identify residents who are at risk of unsafe wandering and strive to prevent harm while maintaining the least restrictive environment for residents. Review of the Report submitted by the facility via the Health Care Facility Reporting System (HCFRS), dated 09/21/24, indicated that at approximately 7:40 P.M., during evening rounds, the staff were unable to locate Resident #1. Further review of the Report indicated Resident #1 was found at 7:50 P.M., by a staff member, two blocks away from the facility. The Report indicated that Resident #1 said that while he/she was walking outside, he/she fell down but was able to get back up and continue walking. Resident #1 was admitted to the Facility in July 2023, diagnoses include hereditary ataxia (impaired balance or coordination), mild cognitive impairment, difficulty in walking, and repeated falls. Review of Resident #1's Nursing Elopement and Wander Risk Evaluation, dated 04/15/24, indicated he/she was assessed as being at high risk for elopement. Review of Resident #1's Quarterly Minimum Data Set (MDS) assessment, dated 04/17/24, indicated he/she scored a 10 out of 15 on the Brief Interview for Mental Status (BIMS) assessment (0-7 suggests severe cognitive impairment, 8-12 suggests moderate cognitive impairment, and 13-15 suggests no cognitive impairment). Review of Resident #1's Elopement Care Plan, reviewed and renewed with his/her April 2024 MDS, indicated he/she was at risk for elopement and included an intervention to make the receptionist (located at the building's entrance) and other staff aware of elopement risk. Review of Resident #1's Nurse Progress Note, dated 07/07/24 and signed by Nurse #3, indicated Resident #1 had an argument with his/her roommate and Resident #1 attempted to leave the facility. The Note indicated staff were able to redirect Resident #1 back into the facility, but he/she refused to go back to his/her room; Resident #1 was moved to a different room for the night. Further Review of the Note indicated the Director of Nurses (DON), Assistant Director of Nurses (ADON) and the Administrator were all notified. During an interview on 11/26/24 at 3:16 P.M., Nurse #3 said she was the nurse on duty for the evening shift (3:00 P.M. through 11:00 P.M.) on 07/07/24. Nurse #3 said staff found Resident #1 outside in the parking lot adjacent to the facility, that Resident #1 was crying and said that he/she wanted to go home. Nurse #3 said Resident #1 probably walked out of the facility's back door which was not alarmed until 8:00 P.M. Nurse #3 said staff were outside, possibly coming in at change of shift, when they saw Resident #1 in the parking lot. Nurse #3 said staff were able to redirect Resident #1 back into the facility. Nurse #3 said Resident #1 should not have been outside alone. During an interview on 11/26/24 at 3:59 P.M., the Director of Nurses (DON) said that she was notified by Nurse #3 of an incident related to Resident #1 on 07/07/24, but did not realize that Resident #1 was found in the facility's parking lot. The DON said no new interventions to prevent another elopement were added to Resident #1's care plan at that time but should have been. Review of an Employee Statement, undated and signed by Certified Nurse Aide (CNA) #1, indicated CNA #1 entered Resident #1's room at 7:40 P.M. [on 09/21/24] to assist with his/her care and Resident #1's roommate said Resident #1 left the building to meet his/her spouse. Review of an Employee Statement, dated 09/21/24 and signed by Nurse #2, indicated that around 7:40 P.M. a CNA reported to her that Resident #1 was not in his/her room and Resident #1's roommate had reported that Resident #1 left the facility to go home. The Statement indicated Nurse #2 drove down the road from the facility and found Resident #1 crossing a bridge and he/she had bruises to his/her forehead, lips, chin, and bilateral palms. During a telephone interview, which included review of his witness statement, on 11/26/24 at 4:43 P.M., Nurse #1 said he worked at the facility through a staffing agency and was on duty the evening shift of 09/21/24 and Resident #1 was on his assignment. Nurse #1 said a CNA told him that Resident #1 had left the facility alone. Nurse #1 said he began to search the inside of the building. Nurse #1 said he did not know how Resident #1 was able to leave the facility that evening, unattended by staff. Nurse #1 said it was a busy time of night when Resident #1 left. Nurse #1 said when Resident #1 returned to the facility, he/she had bruises on his/her face and abrasions to his/her knees and palms. Nurse #1 said the abrasions were all superficial. During an interview on 11/26/24 at 3:59 P.M., the Director of Nurses (DON) said if she had realized that Resident #1 was found outside of the building in the facility's parking lot on 07/07/24, she would have added new interventions which would have included for Resident #1 to always wear a wander guard bracelet (triggers alarms at the exit doors) and to increase safety checks performed by staff, in an effort to prevent future elopements.
Mar 2024 19 deficiencies 3 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Notification of Changes (Tag F0580)

A resident was harmed · This affected 1 resident

Based on interview, record and policy review, the facility failed to notify the Physician/Non-Physician Practitioner (NPP: Nurse Practitioner) of a significant change in medical condition and an elope...

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Based on interview, record and policy review, the facility failed to notify the Physician/Non-Physician Practitioner (NPP: Nurse Practitioner) of a significant change in medical condition and an elopement for two Residents (#60 and #62) out of a total sample of three closed records reviewed. Specifically, the facility staff failed to: 1. For Resident #60, identify a serious change in condition and acute decline in mental status, and notify the Physician/ NPP timely, resulting in the Resident further decompensating and being transferred to the hospital. 2. For Resident #62, notify the Physician/ NPP when the Resident with compromised medical status, and no access to prescribed medications eloped (left) the facility without a Leave of Absence (LOA) order and did not return to the facility. Findings include: 1. Review of the facility policy, Change in Resident's Condition or Status, Revised December 2023, indicated the following: The Nurse will notify the resident's attending Physician or Physician on call when there has been a (an): -Change in the resident's physical/ emotional /mental condition -Need to alter the resident's medical treatment significantly -Need to transfer the resident to a hospital/treatment center -Specific instruction to notify the physician of changes in the resident's condition Resident #60 was admitted to the facility in February 2024 with diagnoses including: Stage 4 (advanced Oxygen needs) Pulmonary Fibrosis (progressive lung disease where the lung tissue becomes damaged with fibrosis [scarring]. The thickened, stiff scar tissue makes breathing difficult for the individual, eventually resulting in shortness of breath [SOB], even at rest) and Acute on Chronic Respiratory Failure with Hypoxia (a life-threatening condition where the lungs cannot provide enough oxygen to the body or remove enough carbon dioxide from the body, that can trigger serious complications for the individual). Review of the February 2024 Physician's orders indicated the following: -Albuterol Sulfate (bronchodilator- relaxes and opens the airways) Nebulizer Solution (2.5 mg/3ml) 0.083% 1 vial inhale orally via nebulizer every 6 hours as needed (PRN) for SOB, start date 2/7/24. -O2 (Oxygen) via nasal cannula (NC) with humidification water at 3.5 liter per minute (LPM) to maintain saturation (SpO2 - measure of Oxygen in the blood as a percentage of the maximum Oxygen the blood could carry) above 90% every shift related to Acute and Chronic Respiratory Failure with Hypoxia, start date 2/14/24. Review of the Occupational Therapy Treatment Encounter dated 2/20/24, indicated: -Resident had difficulty speaking -SpO2 was 95% on 4 LPM of Oxygen (O2) and heart rate (HR) was 50 -The head of bed (HOB) was elevated approximately 45°(degree) and respiratory rate (RR) was 28 bpm (breaths per minute). -When the Resident lifted his/her right foot to don (put on) their sock, the RR increased to 40, and the HR was 49 with activity. -Lying on Left side: vitals read 85% SpO2 with 1-minute recovery to 93% SpO2 on 4 LPM O2, and HR - 64. -Lying on Right side: 79% SpO2 with 5-minute recovery to 93% SpO2 [on 4 LPM O2] and non-productive cough. -Reported to nursing. Further review of the medical record did not indicate that the Physician/NP were notified of the change in the Resident's condition reported to the nursing staff by the Occupational Therapy staff on 2/20/24. Review of the Nursing Progress Notes dated 2/21/24 at 7:37 A.M., indicated the following: -Resident is alert and oriented with baseline [sic] confusion. -Resident c/o (complaint) shortness of breath, neb (Nebulizer) treatment given at 12:00 A.M., and 6:00 A.M., with good [sic] -Very anxious, increasing of respiration [sic] noted during care Review of the Nursing Progress Notes dated 2/21/24 at 8:48 A.M., indicated the following: -Resident very SOB. -Resident experiencing very shallow breathing, appears quite anxious, respirations fluctuating mid-high 20's. -Resident unable to clearly express needs. -Resident continues with O2 at 3.5 LPM via nasal cannula, SpO2 fluctuating low-high 90's -Resident's Nurse called NP and 911 for transport (to hospital). Review of the Nursing Progress Notes indicated the following medication was administered more frequently than (every 6 hours PRN) as ordered the Physician: -Albuterol Sulfate Nebulizer Solution (2.5mg/3ml) 0.083% 1 vial inhale orally via Nebulizer every 6 hours PRN for SOB: > 2/21/24 at 00:51 A.M., > 2/21/24 at 2:27 A.M., PRN effective (Treatment repeated within 1 hour, 36 minutes) > 2/21/24 at 7:35 A.M. (Treatment repeated within 5 hours, 8 minutes) > 2/21/24 at 8:29 A.M., indicated the following: PRN was ineffective (Treatment repeated within 54 minutes) Review of the February 2024 Medication Administration Record (MAR) indicated an order for Albuterol Sulfate Nebulizer Solution (2.5mg/3ml) 0.083% 1 vial inhale orally via Nebulizer every 6 hours PRN for SOB -was given on 2/21/24 at 12:51 A.M., with diminished lung sounds before and after the Albuterol treatment -was given at 2/21/24 at 7:35 A.M., with diminished lung sounds before and after the Albuterol treatment Review of the Oxygen Care Plan, initiated 2/7/24 indicated the following: -Monitor symptoms of respiratory distress and report to MD as needed (PRN) -Oxygen via nasal cannula at 3 liters (LPM) continuously (was implemented before a Physician order for 3.5 LPM of Oxygen was obtained on 2/14/24) -Promote lung expansion and improve air exchange by positioning with proper body alignment (if tolerated, head of bed at 45°) Review of the Emergency Hospital Report, dated 2/22/24, indicated that Resident #60 was admitted with the following active diagnoses: -Sepsis (a serious condition that happens when the body's immune system has an extreme response to an infection and the body's reaction causes damage to its own tissues and organs) -Failure to Thrive (a syndrome of global decline in older adults as a worsening of physical frailty that is frequently compounded by cognitive impairment) -Weakness and increasing Shortness of Breath (abnormal respiration often characterized by the feeling of suffocation) -Influenza (flu- contagious respiratory infection caused by influenza viruses that infect the nose, throat and lungs) -Urinary Tract Infection (UTI: bacterial infection of the urinary tract) -Pneumonia (an infection of the lungs that may be caused by bacteria, viruses, fungi or aspiration [when food or liquid is accidentally inhaled into airways and lungs] and characterized by severe cough with phlegm, fever, chills and difficulty breathing). -The patient is DNR/DNI, and the prognosis is poor. During an interview on 3/21/24 at 4:11 P.M., the Assistant Director of Nurses (ADON) said that if a resident is having a change in condition, nursing staff would perform an assessment of the resident including taking vital signs to rule out any issues with the lungs. The ADON said that a resident would need a Physician's order to titrate Oxygen to maintain the SpO2 level above a certain number. If someone got a nebulizer treatment and it did not work, the facility staff should notify the Doctor of the change in respiratory status and the results after the nebulizer treatment. During a telephone interview on 3/29/24 at 12:05 P.M., Rehabilitation Service Staff (RSS) #3 said that she provided therapy treatment to Resident #60 on the morning of 2/20/24 and documented on the Occupational Therapy Treatment Encounter. RSS #3 said that the Resident was more lethargic and seemed more deconditioned (having lost physical strength through being sick, injured, or not active) than he/she had been the previous day and could not even tolerate sitting on the edge of the bed without being SOB. RSS #3 said that Resident #60's SpO2 was 79% on 4 LPM O2 and there were no orders to increase the amount of Oxygen that could be given. RSS #3 said that she was concerned enough about the Resident's change in condition that she reported her findings to the Nurse assigned to take care of the Resident that morning. During a telephone interview on 3/29/24 at 12:15 P.M., Nurse #1 said that she was assigned to the care of Resident #60 on 2/20/24 (Day shift) and that the Resident was very anxious, his/her respiratory rate had increased with any activity and the Resident had new worsening, increased confusion and SOB. When the surveyor asked Nurse #1 if she was aware of the Occupational Therapy (OT) note from 2/20/24, Nurse #1 said that OT/RSS #3 had informed her that the Resident had increased SOB with activity during the therapy session, but she did not have access to read the OT notes. Nurse #1 said that the Resident's Oxygen was set to 4 LPM, and that was outside of the 3.5 LPM that was ordered, but she was not sure how the Oxygen got set to the 4 LPM. Nurse #1 said that she did not offer the Resident an Albuterol Nebulizer at that time or notify the Physician of the change in condition, and she should have done so based on the ongoing changes with the Resident. During a telephone interview on 3/29/24 at 12:58 P.M., Nurse # 4 said that she received the Resident shift report on 2/21/24 around 7:30 A.M., and upon entering Resident #60's room sometime later, she could tell that the Resident was in distress. Nurse #4 said that she called out for help and other staff members came to assist her. Staff also placed calls to the Physician and the family. Nurse #4 said that the Resident had SOB while talking and his/her SpO2 was around 85% and RR was 28-30 bpm, rapid and shallow. Nurse #4 said that she was unable to give an Albuterol Nebulizer as one had been given already that morning. Nurse #4 said that she went back into the MAR and documented that the (last given) Nebulizer Treatment was ineffective as the prior shift Nurse had not made any post treatment notes, as required. During an interview on 3/26/24 at 10:05 A.M., Physician #2 said that if someone required a breathing [Nebulizer] treatment and it is a change [in status] for them, she would expect to be updated. During an interview on 3/26/24 at 1:15 P.M., the DON reviewed the record for Resident #60 and said that he/she had an O2 order for 3.5 LPM and that there were no titration orders to increase the O2 and if the Resident needed more O2 the Physician should have been notified. The DON further said that it appeared the Resident had a change in status and that staff should have notified the Physician sooner. 2. Review of the facility policy titled Wandering and Elopement, revised March 2019, indicated the following: -The facility will identify Residents who are at risk of unsafe wandering and strive to prevent harm while maintaining the least restrictive environment for residents. -If a resident is missing, initiate the elopement/missing resident emergency procedure: >Determine if the resident is out on an authorized leave. >If the resident was not authorized to leave, initiate a search of the building and the premises, and >If the resident is not located, notify the Administrator and the Director of Nursing Services, the resident legal representative, the attending physician, law enforcement officials and as necessary volunteer agencies. Resident #62 was admitted to the facility in December 2023, with diagnoses including Bipolar Disorder (a mental health condition that causes extreme mood swings between emotional highs and lows), Alcohol Abuse, Opioid Use, Diabetes Type 2 (a condition that happens because of a problem in the way the body regulates and uses sugar as a fuel), Osteomyelitis (Osteomyelitis is an infection in a bone.), left Diabetic foot ulcer (an open sore on the foot), Heart Failure (when the heart muscle doesn't pump blood as well as it should), muscle weakness and difficulty in walking. Review of the Absentee Register undated, indicated that Resident #62 signed out of the facility independently on 1/8/24. Review of the clinical record progress notes for Resident #62 indicated: -On 1/8/24 at 11:17 P.M., Patient left this morning to go visit family and has not return [sic]. -On 1/9/24 at 11:00 A.M., DON called Resident #62's family member and was informed that the Resident was currently with the family member and that Resident #62 would like to return to the facility. The DON informed the Resident that they would need a drug test from the Emergency Department before returning to the facility. -On 1/10/24 at 10:57 A.M., the DON informed the NP that Resident #62 had been discharged against medical advice (AMA) from the facility. During an interview on 3/26/24 at 1:15 P.M., the Director of Nurses (DON) reviewed the medical record for Resident #62 and said that Resident #62 had no Physician's order for an authorized leave as required and should have had one prior to leaving the facility. The DON further said that there was no completed assessment to indicate that Resident #62 could leave the building independently or with a responsible party. The DON reviewed his/her elopement score on admission and said that the elopement assessment was not completed on admission as required. The DON reviewed the nursing progress notes and said that the staff did not notify the Physician that Resident #62 did not return to the building as expected on 1/8/24 and should have returned. The DON further said that if a resident leaves the building without Physician orders it is considered elopement, and the staff should have followed the facility Wandering and Elopement policy, and notified the Physician, the Police and reported it to the Department of Public Health (DPH) timely but this was not done. Please Refer to F684.
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

Based on interview and record review, the facility failed to provide treatment, services and care that met professional standards of quality for one Resident (#60) out of a total sample of three disch...

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Based on interview and record review, the facility failed to provide treatment, services and care that met professional standards of quality for one Resident (#60) out of a total sample of three discharged residents, resulting in a decline in medical status and hospitalization with sepsis (a life-threatening medical emergency that occurs when an infection triggers the body's immune system to damage its own organs and tissues). Specifically, the facility staff failed to: 1. Recognize, assess, and manage pulmonary symptoms that indicated a significant change in condition for Resident #60 who had multiple pulmonary diagnoses that required immediate and appropriate interventions for symptom management. 2. Provide needed care and services for a nephrostomy tube and manage symptoms of a change in nephrostomy tube output as required. Findings include: Review of the facility policy, Change in Resident's Condition or Status, Revised December 2023, indicated the following: The Nurse will notify the Residents attending Physician or Physician on call when there has been a (an): -Change in the resident's physical/ emotional /mental condition -Need to alter the resident's medical treatment significantly Resident #60 was admitted to the facility in February 2024, with diagnoses including: Stage 4 (advanced Oxygen needs) Pulmonary Fibrosis (progressive lung disease where the lung tissue becomes damaged with fibrosis [scarring]. The thickened, stiff scar tissue makes breathing difficult for the individual, eventually resulting in shortness of breath [SOB], even at rest) and Acute on Chronic Respiratory Failure with Hypoxia (a life-threatening condition where the lungs cannot provide enough oxygen to the body or remove enough carbon dioxide from the body, that can trigger serious complications for the individual) and a Nephrostomy tube (tube used to drain urine directly from the kidneys to a collection bag outside of the body). Review of the February 2024 Physician's orders dated 2/7/24, indicated the following: -MOLST (Medical Orders for Life Sustaining Treatment - document of a patient's treatment preferences concerning life-sustaining treatment) Advanced Directive - Full Code (Resuscitate), start date 2/7/24. -Albuterol Sulfate (bronchodilator) Nebulizer Solution (2.5mg/3ml) 0.083% 1 vial inhale orally via nebulizer every 6 hours as needed for shortness of breath (SOB), start date 2/7/24 Review of the Oxygen Care Plan, initiated 2/7/24 indicated the following: -Monitor symptoms of respiratory distress and report to MD as needed (PRN) -Oxygen via nasal cannula at 3 LPM continuously (was implemented before a Physician order for 3.5 LPM of Oxygen was obtained on 2/14/24) -Promote lung expansion and improve air exchange by positioning with proper body alignment (if tolerated, head of bed at 45°) Review of the Nursing notes dated 2/7/24 indicated that Resident #60 was -Alert and oriented times (x) 3 [alert and oriented to person, place and time]. Review of Occupational Therapy Treatment Encounter dated 2/13/24 indicated a change in Resident #60's status from 2/7/24: -Patient was received in agitated mood and became increasingly agitated during encounter. -O2 set at 4 LPM Review of the February 2024 Physician's orders dated 2/13/24, indicated the following: -Oseltamivir Phosphate (antiviral medication) Oral Capsule 75 mg give one capsule by mouth one time a day once daily for 10 days prophylactic for flu (Influenza) for 10 administrations until finished, start date 2/13/24 -Glomerular Filtration Rate [(GFR) 71- is a measure of how well your kidneys are filtering.], start date 2/13/24 Review of Physical Therapy Treatment Encounter dated 2/14/24 indicated further decline in Resident #60's status from 2/13/24: -Patient presented with increased confusion, nursing notified. -Patient said they are feeling lethargic. Review of the February 2024 Physician's orders dated 2/14/24, indicated the following: -O2 (Oxygen) via nasal Cannula (NC) with humidification water at 3.5 liter per minute (LPM) to maintain saturation (SpO2 - measure of Oxygen in the blood as a percentage of the maximum Oxygen the blood could carry) above 90% every shift related to Acute and Chronic Respiratory Failure with hypoxia, start date 2/14/24. Review of the most recent Minimum Data Set (MDS) Assessment, dated 2/14/24 indicated the following: -Resident makes self-understood -Resident has clear comprehension to understand verbal content -Resident had a Brief Interview for Mental Status (BIMS) of 12 out of a total 15, indicating moderate cognitive impairment -No evidence of an acute change in mental status -Respiratory Failure (a serious condition that makes it difficult to breathe on your own. Develops when the lungs cannot provide enough oxygen to the body or remove enough carbon dioxide from the body) and a Urinary Tract Infection (UTI: bacterial infection of the urinary tract) within the last 7 days -Shortness of breath (SOB) while lying flat -Resident has an HCP- [not invoked - put into effect] Review of Physical Therapy Treatment Encounter dated 2/15/24 indicated continued decline in Resident #60's status from 2/14/24: -Multiple standing brakes [sic] due to fatigue, shortness of breath, and global weakness -Vital monitor: SP02 ranging from 80% to 97% after activity and heart rate ranging from 80 to 90 beats per minute (bpm) after all interventions. Review of the Nursing Progress Notes dated 2/17/24 indicated continued decline in Resident #60's status from 2/15/24: -Was awake at 2:30 A.M., and was confused -Pox (Pulse Oximetry/ SpO2) was 90-92% on O2 - 4 LPM via nasal cannula (higher liter flow than the 3.5 LPM ordered on 2/14/24). Review of the Nursing Progress Notes dated 2/19/24 indicated a significant change in condition for Resident #60 from 2/17/24: -Had an occasional nonproductive cough -Lung sound diminished (LSD) bilaterally -Episodes of SOB with exertion -Nephrostomy is patent 75 cubic centimeters (cc-standard unit in measuring volume), slightly dark yellow output Review of the Occupational Therapy Treatment Encounter dated 2/20/24, indicated continued decline in condition for Resident #60 from 2/19/24: -Resident had difficulty speaking -SpO2 was 95% on 4 LPM of Oxygen (O2) and heart rate (HR) was 50 -The head of bed (HOB) was elevated approximately 45°(degree) and respiratory rate (RR) was 28 bpm (breaths per minute). -When the Resident lifted his/her right foot to don (put on) their sock, the RR increased to 40, and the HR was 49 with activity. -Lying on Left side: vitals read 85% SpO2 with 1- minute recovery to 93% SpO2 on 4 LPM O2, and HR - 64. -Lying on Right side: 79% SpO2 with 5- minute recovery to 93% SpO2 [on 4 LPM O2] and non-productive cough. -Reported to nursing. Review of the Nursing Progress Notes dated 2/20/24 indicated: -The Resident was confused and wanted to get out of bed and go to his/her car. -Respirations noted to increase when getting help with morning care. Further review of the Nursing Progress Notes dated 2/20/24 indicated: -no evaluation and/or revision of interventions related to symptoms and conditions documented in the medical record from 2/13/24 - 2/20/24. -no Physician communication for alternative care options for Resident #60. Review of the Documentation of Resident Incapacitation pursuant to Massachusetts Health Care Proxy Act M.G.L.C201D, dated 2/20/24, indicated that Resident #60's HCP was invoked (allowing someone else to make healthcare decisions) due to a diagnosis of Dementia, with lifelong extent. Review of Resident #60's medical record failed to indicate any history, current or new of a diagnosis of Dementia. Review of the Nursing Progress Notes dated 2/21/24 at 7:37 A.M., indicated the following: -Resident c/o shortness of breath, neb treatment given at 12am and 6am with good [sic] -Very anxious, increasing of respiration noted during care Review of the Nursing Progress Notes dated 2/21/24 at 8:48 A.M., indicated the following: -Resident very SOB. Resident experiencing very shallow breathing, appears quite anxious, respirations fluctuating mid-high 20's. -Resident unable to clearly express needs. -Resident unable to swallow -Resident continues with continuous O2 at 3.5 liters applied via nasal cannula. -O2 sats fluctuating low to high 90's however resident still appearing very SOB, unable to get words out. -Residents' Nurse called Nurse Practitioner (NP) and 911 for transport. Review of the February 2024 Physician's orders dated 2/21/24, indicated the following: -DNR (Do Not Resuscitate)/ DNI (Do Not Intubate), may hospitalize - Health Care Proxy (HCP - an appointed individual to legally make medical decisions on a person's behalf if he/she became unable to do so) - Wife, start date 2/21/24 Review of the February 2024 Medication Administration Record (MAR) indicated the following: -Albuterol Sulfate Nebulizer Solution (2.5 mg/3 ml) 0.083% 1 vial inhale orally via nebulizer every 6 hours as needed for SOB was documented as administered on 2/21/24 at 12:51 A.M., and again at 7:35 A.M. -May send to emergency room (ER) for eval STAT (immediately) for SOB, start date of 2/21/24 at 8:17 A.M. Review of the Nursing Progress Notes dated 2/21/24 at 11:30 A.M., indicated the following: -Patient noted with increased SOB at rest and with talking, -RR 28-30 which are rapid and shallow, pox on 3.5 LPM 02 via nasal cannula (NC) - 85% -HR 102 and irregular, BP 90/58; LSD (lung sounds diminished) bilat; patient c/o SOB; -previous shift had given Albuterol nebulizer two times at 12:00 A.M., and at 6:00 A.M. -Patient having difficulty producing an effective cough Review of the Nursing Progress Notes indicated the following medication was administered more frequently than ordered: -(Albuterol Sulfate Nebulizer Solution (2.5 mg/3 ml) 0.083% 1 vial inhale orally via nebulizer every 6 hours as needed for SOB). > 2/21/24 at 00:51 A.M. > 2/21/24 at 2:27 A.M., PRN effective (given within 1 hour (hr) 36 minutes (mins) of the 00:51 A.M. treatment) > 2/21/24 at 7:35 A.M. (given within 5 hrs 9 mins of the 2:27 A.M. treatment) > 2/21/24 at 8:29 A.M., indicated the following: PRN was ineffective (given within 54 mins of the 7:35 A.M treatment). Review of the most recent Minimum Data Set (MDS) Assessment, dated 2/21/24 indicated the following: -Evidence of an acute change in mental status from the Resident's baseline -Behavior present, fluctuates (comes and goes, changes in severity) -Inattention -Disorganized thinking -Shortness of breath while lying flat, while sitting at rest, and with exertion -The Resident did not have a condition or chronic disease that may result in a life expectancy of less than six months. During an interview on 3/21/24 at 4:11 P.M., the Assistant Director of Nurses (ADON) said that if a resident is having a change in condition nursing staff would perform an assessment of the resident including taking vital signs to rule out any issues with the lungs. The ADON said that a resident would need a Physician's order to titrate Oxygen to maintain the SpO2 level above a certain number. The ADON said if a resident got a nebulizer treatment and it did not work, the facility staff should notify the Physician/Doctor of the change in respiratory status and the results after the nebulizer treatment. During an interview 3/22/24 at 9:20 A.M., Nurse #4 said that if a resident was having any changes in respiratory status, she would look for SOB, including listening to the lung sounds checking their pulse oximetry and checking the orders for O2 to see if the liter flow can be increased. Nurse #4 further said that she would call the Physician for any change in respiratory status as the resident could have over exertion, or they could have Pneumonia, which is why the assessment piece is so important. During a follow-up interview on 3/22/24 at 9:59 A.M., Nurse #4 said if a Resident had a change in mental status and was no longer alert and oriented, the nursing staff would complete a nursing assessment and would contact the Physician to inform them about the change and then the Physician may give the order to invoke the Health Care Proxy (HCP). During a telephone interview on 3/26/24 at 10:05 A.M., Physician #2 said that if someone required a breathing (Nebulizer) treatment and it is a change for them, she would expect to be updated on the Resident's condition. During a follow-up interview on 3/26/24 at 12:58 P.M., Physician #2 reviewed Resident #60's medical record and said that the facility staff did not speak to her about a change in condition and they did not ask to increase Resident #60's oxygen from 3.5 LPM to 4 LPM. Physician #2 further said that she does not recall invoking Resident #60's HCP for a change in mental status or Resident #60 having a diagnosis of Dementia. During an interview on 3/26/24 at 1:15 P.M., the Director of Nurses (DON) reviewed the record for Resident #60 and said that he/she had an O2 order for 3.5L and no titration order was noted, so if the Resident required more Oxygen the Physician should have been notified. The DON further said that staff should have notified the Physician when Resident #60 had a change in condition on 2/20/24 and they did not. During a telephone interview on 3/29/24 at 12:05 P.M., Rehabilitation Service Staff (RSS) #3 said that she provided therapy treatment to Resident #60 on the morning of 2/20/24 and documented the Resident's status on the Occupational Therapy Treatment Encounter form. RSS #3 said that the Resident was more lethargic and seemed more deconditioned (having lost physical strength through being sick, injured, or not active) than he/she had been the previous day and could not even tolerate sitting on the edge of the bed without being SOB. RSS #3 said that Resident #60's SpO2 was 79% on 4 LPM O2 and there were no orders to increase the amount of Oxygen that could be given. RSS #3 said that she was concerned enough about the Resident's change in condition that she reported her findings to the Nurse assigned to take care of the Resident that morning. During a telephone interview on 3/29/24 at 12:15 P.M., Nurse #1 said that she was assigned to the care of Resident #60 on 2/20/24 (Day shift) and that he/she was very anxious, and his/her respiratory rate had increased with any activity and the Resident had new worsening increased confusion and shortness of breath. When the surveyor asked Nurse #1 if she was aware of the Occupational Therapy (OT) note from 2/20/24, Nurse #1 said that OT had informed her that the Resident had increased SOB with activity during the therapy session, but she did not have access to read the OT notes. Nurse #1 said that the Resident's Oxygen was set to 4 LPM, and that was outside of the 3.5 LPM that was ordered, but she was not sure how the Oxygen got set to the 4 LPM. Nurse #1 said that she did not offer the Resident an Albuterol Nebulizer at that time or notify the Physician of the change in condition, and she should have done so based on the ongoing changes noted with the Resident. During a telephone interview on 3/29/24 at 12:58 P.M., Nurse #4 said that she received the Resident shift report on 2/21/24 around 7:30 A.M., and upon entering Resident #60's room sometime later, she could tell that the Resident was in distress. Nurse #4 said that she called out for help and other staff members came to assist her and placed calls to the Physician and the family. Nurse #4 said that the Resident had SOB while talking and his/her SpO2 was around 85% and RR was 28-30 bpm, rapid and shallow. Nurse #4 said that she was unable to give an Albuterol Nebulizer as one had been given already that morning. Nurse #4 said that she went back into the MAR and documented that the Albuterol Treatment given was ineffective, as the prior shift Nurse had not made any post treatment notes, as required. Review of the Emergency Hospital Report, dated 2/22/24 indicated that Resident #60 had active diagnoses of -Sepsis -Failure to Thrive (weight loss of more than 5%, decreased appetite, poor nutrition, and physical inactivity, often associated with dehydration, depression, immune dysfunction, and low cholesterol.) -Weakness and increasing Shortness of Breath (SOB: abnormal respiration often characterized by the feeling of suffocation). -Influenza (flu -contagious respiratory infection caused by influenza viruses that infect the nose, throat and lungs) -Urinary Tract Infection (UTI: bacterial infection of the urinary tract) -Pneumonia (an infection of the lungs that may be caused by bacteria, viruses, fungi or aspiration [when food or liquid is accidentally inhaled into airways and lungs] and characterized by severe cough with phlegm, fever, chills and difficulty breathing). -The patient is DNR/DNI and the prognosis is poor. 2. Review of the facility policy Nephrostomy Tube, Care of revised October 2010, indicated the following: -Check the placement of the tubing and integrity of the tape during assessments. -Drainage should be below the level of the kidneys. -There should be no kinks in the tubing. -Empty drainage bag once per shift and as needed. -Measure output every 8 hours. -Record urinary and nephrostomy output separately. -Change dressings every one to three days as ordered. -Use sterile technique during dressing changes. Review of the February 2024 Physician's orders, date 2/8/24 indicated the following: -Sodium Chloride solution 0.9% use 5 ml via irrigation in the afternoon for Nephrostomy tube -flush Nephrostomy tube with 5 ml Sodium Chloride solution 0.9% daily. Review of the Medical Record did not indicate that Physican's orders were in place for Nephrostomy site dressing changes or monitoring of the output from the Nephrostomy tube. Review of the February 2024 Medication Administration Record (MAR) indicated the following: -Sodium Chloride solution 0.9% use 5 ml via irrigation in the afternoon for Nephrostomy. -flush nephrostomy with 5 ml daily -was documented as administered from 2/9/24 through 2/20/24 Review of the Care Plan, indwelling Foley catheter and nephrostomy tube, initiated 2/7/24 indicated: -Check tubing for kinks each shift per policy -Monitor and document output as per facility policy -Nephrostomy tube dressing change as ordered. -Observe for document pain discomfort due to catheter Review of the most recent Minimum Data Set (MDS) Assessment, dated 2/14/24 indicated the following: -Urinary Tract Infection (UTI: bacterial infection of the urinary tract) within the last 7 days -Shortness of breath (SOB) while lying flat Review of the Physician Progress Note dated 2/15/24 indicated: -Nephrostomy tube draining yellow clear urine. Review of the Nursing Progress Note dated 2/17/24, indicated: -Nephrostomy tube draining yellow urine. Review of the Nursing Progress Note dated 2/19/24 indicated: -Nephrostomy is patent 75 cubic centimeters (cc-standard unit in measuring volume), slightly dark, yellow output Review of the Nursing Progress Note dated 2/21/24 indicated: -Nephrostomy tube draining 200 ml of amber urine. During an interview on 3/22/24 at 9:20 A.M., Nurse #4 said that if a resident has new or increased confusion, she would complete an assessment which would include vital signs and asking if they had burning with urination or frequency. If the resident had a Foley catheter or a Nephrostomy tube, they should be assessed for patency, drainage, sediment, cloudy urine, foul odor, and blockage by looking at their output. During a follow-up interview on 3/22/24 at 9:59 A.M., Nurse #4 said if a Resident had a change in mental status and was no longer alert and oriented, the nursing staff would complete a nursing assessment and would contact the Physician to inform them about the change and then the Physician may give the order to invoke the Health Care Proxy (HCP). During a telephone interview on 3/26/24 at 10:09 A.M., Physician #2 said that a Resident might have Dementia, or they may be sick and that could be why they were having a mental status change. When the surveyor asked about invoking the HCP for Resident #60, Physician #2 said that she would not invoke a HCP right away and that she would wait until the patient is totally incompetent, but if they are sick and are going to get better, she would not invoke the HCP as the Medical Orders for Life-Sustaining Treatment (MOLST (is one way of documenting a patient's treatment preferences concerning life-sustaining treatment) was in place already. During an interview on 3/26/24 at 1:15 P.M., the Director of Nurses (DON) reviewed the record for Resident #60 and said that Resident #60 had a nephrostomy tube in place and that she would expect to see orders for monitoring output and for administering dressing changes. She further said that she could not find evidence that there was a Physician's order for the nephrostomy tube site dressing changes or to monitor output, as expected and required. The DON further said that staff should have notified the Physician when Resident #60 had a change in condition on 2/20/24 and they did not.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Pressure Ulcer Prevention (Tag F0686)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record and policy review, the facility failed to provide necessary care and services to treat p...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record and policy review, the facility failed to provide necessary care and services to treat pressure ulcers (localized damage to the skin and/or underlying soft tissue usually over a bony prominence or related to a medical or other device) and prevent further skin and pressure injury for two Residents (#22 and #4), out of two applicable residents, out of a total sample of 17 residents. Specifically, the facility staff failed to: 1. Offload Resident #22's heels per the Physician's Order for treatment of an existing right heel ulcer, and prevent skin decline in his/her left heel. 2. Implement a turning and repositioning schedule and apply specialized boots and/or pillows to offload Resident #4's heels per the plan of care. Findings include: Review of the facility policy titled Pressure Ulcers/Skin Breakdown, revised April 2018, indicated the following: -The nursing staff and practitioner will assess and document an individual's significant risk factors for developing pressure ulcers; for example, immobility, recent weight loss, and a history of pressure ulcer(s). -The nurse shall describe and document/report the following: a. Full assessment of pressure sore including location, stage, length, width and depth, presence of exudates (any fluid that has been forced out of the tissues or blood vessels because of inflammation or injury) or necrotic (the death of most or all organs or tissue due to disease, injury or lack of blood supply) tissue; b. Pain assessment; c. Resident's mobility status; d. Current treatments, including support surfaces; and e. All active diagnoses -The Physician will identify medical interventions related to wound management. 1. Resident #22 was admitted to the facility in October 2022 with diagnoses including Diabetes (condition that results in too much sugar in the blood resulting in high blood glucose[sugar]), Cerebral Vascular Accident (CVA: stroke-interruption of the blood supply to the brain resulting in damage), Protein-calorie Malnutrition (nutritional status in which reduced availability of nutrients leads to changes in body composition and function), and need for assistance with personal care. Review of the Resident's clinical record indicated that he/she was transferred to the hospital on [DATE] and returned on 12/25/23. Further review of the clinical record indicated the Resident was identified as having a Deep Tissue Injury (DTI-purple or maroon localized area of discolored intact skin or fluid filled blister due to damage of underlying soft tissue from pressure) after the hospitalization, and was at increased risk for pressure ulcers related to his/her mobility status and medical conditions. Review of the Nursing assessment dated [DATE], indicated Resident #22 had a DTI to his/her right heel. Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated: - Resident #22 had moderate cognitive impairment as evidenced by a Brief Interview of Mental Status (BIMS) score of 11 out of a total possible 15 - had range of motion impairments affecting bilateral (both) lower extremities - required assistance from staff with upper and lower dressing, rolling side to side, lying to sitting and with transfers - was at risk for pressure ulcers - had an unstageable [full-thickness skin and tissue loss in which the extent of tissue damage within the ulcer cannot be confirmed because the wound bed is obscured by slough (yellow/white material in the wound bed) or eschar (dry/dry scab or dead skin)] pressure ulcer that was present on admission. Review of the March 2024 Physician's orders, included the following: - float heels when in bed every shift for DTI, initiated 1/4/24 - low air low mattress set at 150 every shift, initiated 3/8/24 Review of the March 2024 Treatment Administration Record (TAR) indicated the order and treatment to float Resident #22's heels while in bed every shift was administered every day, every shift from 3/1/24 through 3/21/24. Review of the current Activities of Daily Living (ADLs - tasks of everyday life including eating, bathing, dressing) Care Plan, initiated 10/5/22, indicated Resident #22 required assistance with ADLs and required the following: -Dependent on staff for grooming and hygiene -Assistance of 1-2 staff with positioning Review of the Weekly Wound assessment dated [DATE], indicated Resident #22 had the following: -Right heel DTI wound, unstageable -Preventative interventions included: > pressure distribution mattress > turning and repositioning program > elevate legs > float heels in bed and offload On 3/21/24 at 9:07 A.M., the surveyor observed Resident #22 lying in bed with the head of the bed elevated. The surveyor observed that an air mattress was in place and set to 150. During an interview at the time, Resident #22 said that he/she had an open area on the right heel which was uncomfortable when the heel was touched or moved. The Resident further said there was nothing special in place for his/her heel wound, but there was a treatment that was completed by nursing. On 3/21/24 at 9:13 A.M., Certified Nurses Aide (CNA) #6 entered Resident #22's room and showed the surveyor Resident #22's feet, which were covered with blankets. When CNA #6 lifted the bottom blankets, the surveyor observed that the Resident's heels were not offloaded, and there were no pillows or specialty devices in place to prevent the Resident's heels from laying directly on the mattress. The surveyor further observed that the Resident's feet were positioned on top of each other, that non-skid socks were in place and a gauze wrap was observed extending above the Resident's non-skid sock on the right foot. On 3/22/24 at 7:38 A.M. and 8:09 A.M., the surveyor observed Resident #22 lying in bed and the Resident's left foot was observed laying on the mattress, was not offloaded, and was further observed pressed against the foot board at the end of the bed. The surveyor observed that the Resident's right foot had a dressing wrapped around it and the right foot was laying on the mattress. On 3/22/24 at 11:38 A.M., the surveyor observed the wound dressing change of the Resident's right heel with Nurse #1 and Nurse #6. Prior to the dressing change treatment, Resident #22 was observed lying in bed on his/her right side with legs slightly bent. The Resident's left foot was bare and pressed against the foot board of the bed. Both of the Resident's feet were observed to be laying on the mattress and were not offloaded. Nurse #1 and Nurse #6 were observed to assist the Resident by shifting him/her up in bed so his/her feet were away from being positioned against the foot board of the bed, to access and complete the treatment to the right heel wound. When the surveyor asked Nurse #1 to provide an assessment of the Resident's left heel, Nurse #1 said the Resident's left heel was reddish in color compared to the bottom of his/her foot, and that the skin on the foot was dry. Nurse #6, who was still present during this time, said the Resident's heels should be offloaded and a treatment should be initiated to his/her left heel to prevent skin breakdown. Nurse #1 and Nurse #6 were observed to search the Resident's room to locate a pillow or device to offload the Resident's heels and Nurse #6 said there were no pillows present and that she would have to get one. On 3/22/24 at 12:42 P.M., the surveyor observed Resident #22 lying in bed with his/her eyes closed. The surveyor did not observe any pillows or devices offloading the Resident's heels. During an interview on 3/22/24 at 1:54 P.M., the Assistant Director of Nurses (ADON), who completed scheduled wound rounds with the Physician, said Resident #22's heels should be offloaded while in bed to prevent pressure on his/her heels. The surveyor relayed previous observations of the Resident's heels not being offloaded with the ADON who said that she would look into the matter. Review of the Weekly Wound Assessment, dated 3/22/24, indicated Resident #22 had a new suspected DTI to his/her left heel. During a follow-up interview on 3/22/24 at 3:51 P.M., the ADON said she assessed the Resident's heels, and at the time of her observation there were pillows under his/her feet to offload but that both of the Resident's feet were pressed against the foot board of the bed. The ADON said the Resident was repositioned in bed, so his/her feet were not against the foot board and a spacer was placed between the mattress and the footboard to prevent this from re-occurring. The ADON further said that the Resident's left heel was discolored and was boggy (abnormal texture of tissues characterized by sponginess), so the Physician was updated and an order was obtained for a treatment to the Resident's left heel and to implement heel protectors to both of the Resident's feet. During a follow-up interview on 3/26/24 at 1:53 P.M., the ADON said Resident #22 was unable to independently offload his/her heels when in bed and required assistance from staff to do this. 2. Resident #4 was admitted to the facility in March 2016, with diagnoses including hemiplegia (paralysis on one side of the body) affecting the left non-dominant side, CVA, abnormal posture, Adult Failure to Thrive (syndrome of weight loss, decreased appetite, poor nutrition and inactivity), pressure ulcer of the left buttock Stage 4 (full thickness tissue loss with exposed bone, tendon or muscle), and need for assistance with personal care. Review of the MDS Assessment, dated 2/28/24, indicated: -Resident #4 had significant cognitive impairment as evidenced by a BIMS score of 4 out of a possible 15 -had no rejections of care -had range of motion impairments of upper and lower extremities on one side -was dependent on staff for dressing, personal hygiene, rolling side to side -was at risk for pressure ulcers -had one unhealed Stage 4 Pressure Ulcer which was not present on admission. Review of the ADL Care Plan, initiated 3/9/16, indicated Resident #4 required assistance with ADLs related to hemiplegia and hemiparesis and included the following interventions: -Dependent on staff for transfers and positioning, initiated 12/18/23 Review of Potential for Skin Integrity Care Plan, initiated 3/9/16, included the following interventions: -Offload Resident heels using pillows/heels up on cushion ., revised 3/9/16 -Provide 2 assist with positioning and transfers .reposition at least every 2 hours while in bed ., revised 6/30/20 Review of the Actual Skin Integrity Impairment Care Plan, initiated 8/17/20, included the following interventions initiated 9/27/21: -Encourage Resident to turn and change position every 2 hours -Offload heels Review of the Wound Evaluation and Management Summary, dated 2/1/24, indicated the following: -Resident has wounds including a Stage 4 full thickness area on his/her left ischium (curved bone forming the base of each half of the pelvis) . -The plan of care included to offload the wounds, reposition per facility protocol . turn side to side and front to back in bed every 1-2 hours if able and elevate his/her legs Review of the March 2024 Physician's orders, initiated 3/17/21, included the following: -prevalon boots (type of specialized boots to offload feet) to bilateral heels -check for placement and check skin every evening and night for DTI Review of the March 2024 Medication Administration Record (MAR) and Treatment Administration Record (TAR) did not include documented evidence that the prevalon boots were ordered and applied from 3/1/24 through 3/21/24. Review of the current CNA Care Card included the following: -Encourage Resident to turn and change position 2 hours -Offload heels using pillows/heels up on cushions as Resident allows -Dependent of two staff with positioning On 3/20/24 at 4:19 P.M., the surveyor heard the Resident calling out and observed him/her lying in bed on his/her back. The surveyor observed that an air mattress was in place and set at 200. During an interview at the time, the Resident said he/she was uncomfortable and had some pain on his/her left side. The surveyor did not observe that the Resident's heels were offloaded. The surveyor exited the Resident's room and notified Nurse #1 of the Resident's concerns, and Nurse #1 responded that she would assess Resident #4. On 3/21/24 at 7:14 A.M. through 8:58 A.M., the surveyor observed the Resident lying in bed, positioned on his/her back with eyes closed. The air mattress was observed set at 200 and the head of the bed was slightly elevated. At 8:20 A.M., two CNA's entered the Resident's room and boosted him/her up in the bed prior to breakfast. The surveyor observed the Resident's feet as he/she was being boosted, and both feet were lying on the mattress, with no devices (pillows or boots) in place to offload. On 3/22/24 at 7:25 A.M. through 7:52 A.M., the surveyor observed Resident #4 lying in bed, on his/her back with eyes closed. During an interview at 7:31 A.M., the Resident said that his/her feet bothered him/her and were uncomfortable. The surveyor did not observe offloading boots in the Resident's room and when asked, the Resident said he/she was not aware of having anything for his/her feet. The surveyor requested assistance from the ADON, who was assisting with beverage pass at the time. The ADON uncovered the Resident's feet, and the surveyor observed that both of the Resident's feet were bare and lying on the mattress. The surveyor observed that a pillow was placed under the Resident's left knee. When the ADON assisted the Resident with moving his/her left foot, the Resident cried out in discomfort and said his/her left heel hurt. The ADON assessed the Resident's left heel and said there were no open areas on the Resident's left heel, and that she was going to position the pillow under the Resident's left heel so that it was offloaded and off the mattress. When the surveyor asked the ADON if the Resident was able to move the pillow which was observed previously positioned under his/her left knee, and the ADON said the Resident was unable to move his/her left side due to hemiplegia. After the Resident's left leg was repositioned with his/her left heel elevated, the Resident smiled and said that he/she felt better. The surveyor observed that the Resident's right foot remained on the mattress and was not offloaded. On 3/22/24 from 8:39 through 11:27 A.M., the surveyor observed the following: -At 8:39 A.M., the surveyor observed Resident #4 lying upright in bed, positioned on his/her back eating breakfast -At 8:52 A.M., the breakfast tray was removed, and the Resident remained in the same position -At 10:15 A.M., the Resident remained lying on his/her back in bed with eyes closed -At 11:27 A.M., two staff members entered the Resident's room, greeted the Resident and said that the wound dressings were going to be completed and then staff would get him/her out of bed. On 3/22/24 at 12:06 P.M. through 12:45 P.M., the surveyor observed Resident #4 lying in bed, and remained positioned on his/her back with eyes closed. During an interview on 3/22/24 at 12:47 P.M., CNA #2 said that she regularly worked with Resident #4 and knew him/her very well. CNA #2 said the Resident required full care, was incontinent of both urine and bowels, and was changed at 6:30 A.M.,10:30 A.M., and around 11:15/11:30 A.M., when he/she was assisted out of bed. CNA #2 said the Resident refused to get out of bed today because of complaints of pain which was reported to the Nurse. CNA #2 said the Resident was unable to move his/her left side and was unable to move about when in bed. CNA #2 further said that the Resident required the assistance of two staff for repositioning, that the staff will change his/her position when he/she calls out but staff had no schedule for repositioning. CNA #2 said if the Resident was lying in bed without yelling out or was observed to be sleeping, that indicated he/she was comfortable so staff would not move or reposition him/her. CNA #2 said that she puts a pillow under the Resident's heels when her shift was over to elevate his/her heels, but when she returns to work in the morning for her shift, she would find that the Resident's heels are not offloaded most of the time. When the surveyor asked whether the Resident had specialized boots to offload his/her feet, CNA #2 said she did not remember. On 3/26/24 at 12:10 P.M., the surveyor and Nurse #3 reviewed the Resident's clinical record and Nurse #3 said the Resident had an order for prevalon boots since 3/17/21, but the order was just added to the TAR on Friday 3/22/24. Nurse #3 said that unless the order was designated to the MAR or the TAR, it would not show up for the nursing staff to administer and sign off. When the surveyor asked about how the repositioning of residents was documented, Nurse #3 said that the CNAs document that information. Review of the CNA documentation indicated no documented evidence that repositioning had occurred every 1-2 hours per the Resident's plan of care. During an interview on 3/26/24 at 1:44 P.M., the ADON said the Resident should be repositioned every two hours or as needed and that the CNA's would document that this occurred in the medical record. The ADON said that there has been an order for the specialized boots to offload the Resident's heels for a long time, the ADON thought that she remembered seeing the boots, but would have to check. The ADON further said that the Resident was unable to reposition him/herself and was dependent on facility staff to do this for him/her. During a follow-up interview on 3/26/24 at 3:15 P.M., the ADON said she was unable to find any indication that Resident #4 was repositioned as per his/her plan of care since October 2023.
CONCERN (D)

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

Deficiency F0578 (Tag F0578)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility failed to ensure that an accurate and current copy of an Advanced...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility failed to ensure that an accurate and current copy of an Advanced Directive (legal documents that provide instructions for medical care and only go into effect if you are unable to communicate your own wishes) was maintained in the medical record for one Resident (#9), out of a total sample of 17 residents. Specifically, the facility staff failed to: -maintain accurate documentation of a Medical Orders for Life Sustaining Treatment (MOLST) form indicating the Resident's decision for Cardiopulmonary Resuscitation (CPR- an emergency lifesaving procedure performed when the heart stops beating) and Intubate (inserting a tube into the trachea to assist with breathing and ventilation) and Ventilate. -maintain accurate Physician's orders corresponding to the MOLST form relative to intubation status. The Physician's orders indicated Do Not Intubate (DNI) while the MOLST form indicated the Resident wishes to Intubate and Ventilate. Findings include: Review of the facility policy titled Advanced Directives, last revised [DATE], indicated: -If the resident or the resident's representative has executed one or more advanced directives, or executes one on admission, copies of these documents are obtained and maintained in the same section of the resident's medical record and are readily retrievable by any staff. -The Director of Nursing or designee notifies the attending Physician of advanced directives (or changes in advanced directives) so that appropriate orders can be documented in the resident's medical record and plan of care. -The resident's wishes are communicated to the resident's direct care staff and physician by placing the advance directive document in a prominent, accessible location in the medical record and discussing the resident's wishes in care plan meetings. -The plan of care for each resident is consistent with his or her documented treatment preferences and/or advanced directive. -The interdisciplinary team will review annually with the resident his or her advanced directives to ensure that such directives are still the wishes of the residents. Such reviews will be made during the annual assessment process and recorded in the medical record. -The interdisciplinary team will be informed of changes and/or revocations so that the appropriate changes can be made in the resident medical record and care plan. Resident #9 was admitted to the facility in [DATE], and had diagnoses including Dementia (a group of conditions characterized by impairment of at least two brain functions, such as memory and loss of judgment) and Adult Failure to Thrive (a syndrome of global decline in older adults as a worsening of physical frailty that is frequently compounded by cognitive impairment) Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated the Resident was severely cognitively impaired as evidenced by a Brief Interview for Mental Status (BIMS) Score of 6 out of 15 total. Review of the MOLST form dated [DATE], indicated the following: -Cardiopulmonary Resuscitation (CPR): both Do Not Resuscitate (DNR) and Attempt Resuscitation were circled, the DNR was crossed out and initialed above the crossed out item. -Intubate and Ventilate -Use Non-Invasive Ventilation -Transfer to Hospital -No dialysis -No artificial nutrition -No artificial hydration -Resident #9 had signed the MOLST -The attending physician had signed the MOLST on [DATE] at 2:00 P.M. Review of the [DATE] Physician's orders indicated: -MOLST Advanced Directives: Full Code (Attempt Resuscitation), DNI (Do Not Intubate), No Feeding Tubes, No Dialysis, initiated [DATE] and currently active. Review of Resident #9's Care Plan relative to Advanced Directives, initiated [DATE] and last revised [DATE], indicated the following: -The Resident has an Advanced Directive of Full Code (if a person's heart stopped beating and/or they stopped breathing, all resuscitation procedures will be provided to keep them alive) with DNI, no dialysis, no feeding tubes -CPR will be performed as needed -Review Advanced Directives as needed with Resident and family Further review of the medical record indicated: -Care Plan Note, dated [DATE], documented that according to the Resident's MOLST he/she remains a Full Code. -Physician's Note, dated [DATE], documented the Resident had a MOLST with request for Full Code, DNI, NTF (no tube feeding), and No Dialysis. During an interview on [DATE] at 9:24 A.M., Social Worker (SW) #1 said that if a resident was admitted to the facility and had not already completed a MOLST form, SW #1 or someone from the Nursing Department would review the MOLST with the resident, and then have the resident or their responsible party sign the MOLST as appropriate. The surveyor and SW #1 reviewed Resident #9's MOLST form dated [DATE], where DNR was indicated but crossed out and initialed above, and Full Code (Attempt Resuscitation) was also indicated. SW #1 said that when Resident #9 was admitted , he/she was self-responsible, and SW #1 assisted the Resident in completing the MOLST. SW #1 said that the initials on the form were SW #1's and when the error was made on the MOLST, a new MOLST form should have been completed but was not completed as required.
CONCERN (D)

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

Abuse Prevention Policies (Tag F0607)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility failed to provide protections for the health and welfare for resi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility failed to provide protections for the health and welfare for residents residing in the facility relative to two Residents (#32 and #48) out of a total sample of 17 sampled residents. Specifically, the facility staff failed to implement an investigation and report a resident-to-resident altercation when Residents #32 and #48 were witnessed arguing with each other and Resident #48 threatened to kill Resident #32. Findings include: Review of the facility policy titled Abuse, Neglect, Exploitation and Misappropriation Prevention Program, revised April 2021, indicated: -The purpose was to identify and investigate all possible incidents of abuse, neglect, mistreatment, or misappropriation of resident property. -Investigate and report any allegations within timeframes required by federal requirements. -Establish and implement a Quality Assurance Performance Improvement (QAPI) review and analysis of reports, allegations or findings of abuse, neglect, mistreatment, or misappropriation of property. Resident #32 was admitted to the facility in November 2023, with diagnoses including Major Depressive Disorder (a mental health disorder characterized by persistently depressed mood or loss of interest in activities, causing significant impairment in daily life), Morbid Obesity (when the weight is found to be more than 80 - 100 pounds above the individual's ideal body weight), Chronic Obstructive Pulmonary Disease (COPD - a chronic lung disease that leads to respiratory problems including obstructed airflow and difficulty breathing). Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #32 was cognitively intact as evidenced by a Brief Interview for Mental Status (BIMS) score of 13 out of a total of 15. Resident #48 was admitted to the facility in December 2023, with a diagnosis including Low Back Pain. Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #48 was cognitively intact as evidenced by a BIMS score of 15 out of a total 15. Review of the Nursing Progress Note dated 2/27/24 at 10:40 P.M., indicated Resident #48 approached Nurse #1 with a complaint that his/her roommate, Resident #32, was persistently crying and that it had been going on for two months and that Resident #48 could not take the persistent crying anymore. The Nursing Progress Note indicated that Nurse #1 and Certified Nurses Aide (CNA) #1 went to the Residents' room and observed both Residents yelling at each other with Resident #48 threatening to kill Resident #32. The Nursing Progress Note further indicated that Nurse #1 moved Resident #48 into another room and notified the Director of Nurses (DON). Review of the Social Worker (SW) Progress Note dated 2/28/24 at 7:21 A.M., indicated that Social Worker (SW) #1 met with Resident #48 to assess his/her mood since the Resident had been struggling with his/her roommate, and Resident #48 had been moved to another room the previous night. Resident #48 told SW #1 that he/she could not accommodate the roommate's behaviors anymore and preferred a room change. During a review and interview with SW #1 on 3/21/24 at 10:04 A.M., SW #1 said she should have followed-up with Resident #32, but she did not. SW #1 further said she should have referred both Resident #32 and Resident #48 for psychological evaluation, but she did not do so. During an interview on 3/21/24 at 12:47 P.M., the DON said there was no investigation completed for the resident-to-resident altercation that occurred between Resident #32 and Resident #48 on 2/27/24. The DON said the incident should have been investigated given the threat made by Resident #48, and reported to the Department of Public Health (DPH) but the investigation and reporting was not done as required. During an interview on 3/21/24 at 4:47 P.M., the facility Administrator said the altercation should have been investigated as indicated by the facility abuse policy and procedure but the facility staff did not investigate the incident. Please Refer to F609 and F610
CONCERN (D)

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

Report Alleged Abuse (Tag F0609)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility failed to identify, investigate and report an alleged violation w...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility failed to identify, investigate and report an alleged violation within the prescribed timeframe for two Residents (#32 and #48) out of a total sample of 17 residents. Specifically, the facility staff failed to identify a resident-to-resident altercation involving Resident #32 and Resident #48, as an alleged abuse violation, and investigate and report to the appropriate entities no later than 24 hours after the altercation occurred in accordance with state law. Findings include: Review of the facility's policy titled Abuse, Neglect, Exploitation and Misappropriation Prevention Program, last revised April 2021, included: -Investigate and report any allegations within timeframes required by federal requirements. Review of the facility's policy titled Abuse and Neglect - Clinical Protocol, revised September 2022, included: -The Nurse will report findings to the Physician as needed, the Physician will assess the resident/patient to verify or clarify such findings, especially if the cause or source of the problem is unclear. Review of the facility's policy titled Abuse, Neglect, Exploitation or Misappropriation - Reporting and Investigating, included: -All allegations are reported to local, state, and federal agencies (as required by current regulations) and thoroughly investigated by facility management. -All reports of resident abuse are reported within two hours. Resident #32 was admitted to the facility in November 2023, with a diagnosis including Major Depressive Disorder (a mental health disorder characterized by persistently depressed mood or loss of interest in activities, causing significant impairment in daily life). Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #32 was cognitively intact as evidenced by a Brief Interview for Mental Status (BIMS) score of 13 out of a total of 15. Resident #48 was admitted to the facility in December 2023 with a diagnosis including Low Back Pain. Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #48 was cognitively intact as evidenced by a BIMS score of 15 out of a total 15. Review of the Nursing Progress Note dated 2/27/24 at 10:40 P.M., indicated Resident #48 reported a complaint to Nurse #1 that his/her roommate, Resident #32, was persistently crying, that the crying had been going on for two months and that Resident #48 could not take Resident #32's crying anymore. The Nursing Progress Note indicated that Nurse #1 and Certified Nurses Aide (CNA) #1 went to Resident #48 and Resident #32's room and observed both Residents yelling at each other and Resident #48 threatening to kill Resident #32. The Nursing Progress Note further indicated that Nurse #1 moved Resident #48 into another room and notified the Director of Nurses (DON). During an interview on 3/21/24 at 8:55 A.M., Resident #32 said he/she remembered who his/her roommate was but did not recall why Resident #48 was moved out of the room that the two Residents shared. During an interview on 3/21/24 at 9:11 A.M., Resident #48 said he/she got tired of Resident #32 crying every day and night and could not take it anymore. During an interview on 3/21/24 at 11:38 A.M., the DON and the Regional Nurse said Nurse #1 had made them aware the night of the incident when Resident #48 was upset and had threatened Resident #32, but both Residents were calm, and the DON and the Regional Nurse did not feel the resident-to-resident altercation had risen to a level of investigation and/or reporting. During an interview on 3/21/24 at 12:09 P.M., Social Worker (SW) #1 said she was made aware of the incident (that occurred on 2/27/24) the following day on 2/28/24. SW #1 said she met with Resident #48 who confirmed that he/she was tired of Resident #32's crying and snoring. Resident #48 confirmed to SW #1 that he/she had threatened Resident #32 and would not go back to [living in] the same room with Resident #32. SW #1 further said she was unsure whether she had met with Resident #32 after the incident on 2/27/24. During a follow-up interview on 3/21/24 at 12:47 P.M., the DON said the incident should have been investigated and reported, but it was not. During an interview on 3/21/24 at 4:47 P.M., the facility Administrator said the incident should have been investigated and reported, but it was not. Please Refer to F610.
CONCERN (D)

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

Investigate Abuse (Tag F0610)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility staff failed to investigate an alleged violation of verbal abuse ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record and policy review, and interview, the facility staff failed to investigate an alleged violation of verbal abuse for two Residents (#32 and #48) out of a total sample of 17 residents. Specifically, -For Resident #32, the alleged victim, the facility staff failed to thoroughly investigate an altercation with Resident #48 that included verbal abuse and death threats, and immediately assess and evaluate Resident #32 for safety needs, increased supervision and medical treatment. -For Resident #48, the alleged perpetrator, the facility staff failed to thoroughly investigate an altercation with Resident #32 that included verbal abuse and death threats, to prevent any further potential abuse to the victim and/or other residents and implement corrective action following the investigation. Findings include: Review of the facility's policy titled Abuse, Neglect, Exploitation, and Misappropriation Prevention Program, revised April 2021, included: -Establish and maintain a culture of compassion and caring for all residents and particularly those with behavioral, cognitive, or emotional problems. -Identify and investigate all possible incidents of abuse, neglect, mistreatment, or misappropriation of resident property. -Investigate and report any allegations within timeframes required by federal requirements. Review of the facility's policy titled Abuse and Neglect - Clinical Protocol revised September 2022, included: -The Nurse will report findings to the Physician as needed, the Physician will assess the resident/patient to verify or clarify such findings, especially if the cause or source of the problem is unclear. -Along with staff and management, the Physician will help identify situations that might constitute or could be construed as neglect, for example inappropriate management of problematic behavior. -The facility management and staff will institute measures to address the needs of residents and minimize the possibility of abuse and neglect. -The staff and Physician will monitor individuals who have been abused to address any issues regarding their medical condition, mood, and function. Review of the facility's policy titled Abuse, Neglect, Exploitation or Misappropriation - Reporting and Investigating, included: -All allegations are reported to local, state, and federal agencies (as required by current regulations) and thoroughly investigated by facility management. -All reports of resident abuse are reported within two hours. Resident #32 was admitted to the facility in November 2023 with diagnoses including Major Depressive Disorder (a mental health disorder characterized by persistently depressed mood or loss of interest in activities, causing significant impairment in daily life). Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #32 was cognitively intact as evidenced by a Brief Interview for Mental Status (BIMS) score of 13 out of a total of 15. Resident #48 was admitted to the facility in December 2023 with a diagnosis including Low Back Pain. Review of the Minimum Data Set (MDS) assessment dated [DATE] indicated Resident #48 was cognitively intact as evidenced by a BIMS score of 15 out of a total of 15. Review of the Nursing Progress Note dated 2/27/24 at 10:40 P.M., indicated that Resident #48 alerted Nurse #1 that his/her roomate Resident #32, was persistently crying, the crying had been going on for two months and that Resident #48 could not take the crying anymore. The Nursing Progress Note indicated that Nurse #1 and Certified Nurses Aide (CNA) #1 went to the Residents' room and observed both Residents yelling at each other and Resident #48 threatening to kill Resident #32. The Nursing Progress Note further indicated that Nurse #1 moved Resident #48 (the alleged perpetrator) into another room and notified the Director of Nurses (DON). The Nursing Progress Note did not indicate that Nurse #1 evaluated Resident #32 to determine whether he/she felt safe, required increased supervision and/or medical treatment. During an interview on 3/21/24 at 8:55 A.M., Resident #32 said he/she remembered who his/her roommate was but did not recall why his/her roommate was moved out of the room. During an interview on 3/21/24 at 9:11 A.M., Resident #48 said he/she got tired of Resident #32's crying every day and night and could not take it anymore. Review of the Social Worker (SW) Progress Note dated 2/28/24 at 7:21 A.M., indicated that SW #1 met with Resident #48 to assess his/her mood since the Resident had been struggling with his/her roommate and had been moved to another room the previous night. Resident #48 informed SW #1 that he/she could not accommodate the roommate's behaviors anymore and preferred a room change. Further review of the Social Worker Progress Note did not indicate that SW #1 met with Resident #32 to assess his/her mood after the confrontation with Resident #48 on 2/27/24, when Resident #32 was subjected to verbal abuse and death threats from Resident #48. During an interview with SW #1 on 3/21/24 at 10:04 A.M., SW #1 said she should have followed-up with Resident #32, but she did not. SW #1 further said that she should have referred both Resident #32 and Resident #48 for psychological evaluation, but she did not. During an interview on 3/21/24 at 12:47 P.M., the DON said there was no investigation completed for the resident-to-resident altercation between Resident #32 and Resident #48 that occurred on 2/27/24. The DON said the incident should have been investigated given the death threat and reported to the Department of Public Health (DPH) but that was not done. During an interview on 3/21/24 at 4:47 P.M., the facility Administrator said the incident should have been investigated but it had not been.
CONCERN (D)

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

PASARR Coordination (Tag F0644)

Could have caused harm · This affected 1 resident

Based on interview and record review, the facility failed to coordinate an assessment with the Pre-admission Screening and Resident Review program (PASRR- is a federal requirement to help ensure that ...

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Based on interview and record review, the facility failed to coordinate an assessment with the Pre-admission Screening and Resident Review program (PASRR- is a federal requirement to help ensure that individuals who have a mental disorder or intellectual disabilities are not inappropriately placed in nursing homes for long term care. PASRR requires that: 1) all applicants to a Medicaid-certified nursing facility be evaluated for a serious mental disorder and/or intellectual disability; 2) be offered the most appropriate setting for their needs [in the community, a nursing facility, or acute care setting], and 3) receive the services they need in those settings) for one Resident (#1) out of a total sample of 17 residents. Specifically, the facility staff failed to review Resident #1 for a Level II Resident Review (person-centered assessment taking into account all relevant information) when he/she was admitted to the facility with a diagnosis of Bipolar Disorder (serious mental illness - SMI), and was being treated with an antipsychotic medication (used to treat symptoms of mental illness, including delusions [fixed, false conviction in something that is not real or and not shared by other people] and psychosis [condition of the mind resulting in difficulty determining what is real and not real]). Findings include: Resident #1 was admitted to the facility in February 2023 with diagnoses including Bipolar Disorder and Psychoactive Substance Use (a drug or other substance that affects how the brain works and causes changes in mood, awareness, thoughts, feelings, or behavior). Review of Resident #1's Level I PASRR indicated the following: -The Resident had no documented diagnosis of mental illness or mental disorder (MI/MD). -The Resident's screen for Serious Mental Illness (SMI) was negative. Review of Resident #1's Order Summary Report dated 3/21/24, indicated the Resident had a primary diagnosis of Bipolar Disorder. Review of Resident #1's March 2024 Physician orders indicated the following: -Abilify (an antipsychotic medication) Oral Tablet 30 milligrams (mg). Give one tablet by mouth once a day related to Bipolar Disorder, initiated 12/12/23. -Monitor for side effects of antipsychotic medications which may include but not limited to: dystonia, tremors, confusion, restlessness, pacing, anxiety, Tardive Dyskinesia, dry mouth. Review of Resident #1's clinical record did not provide evidence that a Level II PASRR assessment had been completed as required when the Resident had a documented SMI diagnosis. During an interview on 3/21/24 at 9:58 A.M., the Social Worker (SW) said if a resident had a negative screen for SMI and was later diagnosed with SMI, the resident would be referred to the PASRR program for review. The SW said if Resident #1 had a negative screen for SMI, then was diagnosed with Bipolar Disorder, he/she should have been referred to the PASRR program for review. The SW further said Resident #1 was admitted with the diagnosis of Bipolar Disorder from the hospital which was not indicated on the Resident's initial PASRR, and that she should have reviewed the Level I PASRR for accuracy but she did not. The SW said Resident #1 should have been referred to the PASRR program for a Level II, but as of 3/21/24, the Level II review had not been done.
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 observation, interview, record and policy review, the facility failed to ensure the plan of care was revised for one Re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record and policy review, the facility failed to ensure the plan of care was revised for one Resident (#18), out of a total sample of 17 residents. Specifically, the facility staff failed to revise Resident #18's Nutritional Care Plan to reflect current nutritional interventions of pureed diet with nectar thick liquids and nutritional supplement provided. Findings include: Review of the facility policy titled Comprehensive Person-Centered Care Plans, revised March 2022, indicated a comprehensive, person-centered care plan includes measurable objectives and timetables to meet the resident's physical, psychosocial, and functional needs is developed and implemented for each resident. The policy also included the following: -The interdisciplinary team (IDT), in conjunction with the resident and his/her family or legal representative, develops and implements a comprehensive, person-centered care plan for each resident. -The interdisciplinary team reviews and updates the care plan when there has been a significant change in the resident's condition, when the desired outcome is not met, when the resident has been readmitted to the facility from a hospital stay; and at least quarterly, in conjunction with the required quarterly Minimum Data Set (MDS) assessments. Resident #18 was admitted to the facility in September 2020, with diagnoses including Hemiplegia (paralysis on one side) after a Cerebrovascular Accident (CVA- disruption of the blood supply to the brain resulting in damage), Vascular Dementia with agitation (problems with planning or organizing, making decisions or solving problems), and need for assistance with personal care. Review of the Nutrition Care Plan, initiated 9/15/20 and last revised 12/22/23, indicated Resident #18 had poor nutritional status related to texture restrictions, poor dentition, and impaired self-feeding. The plan of care included the following interventions: -Donut to breakfast trays, ground meat sandwich to lunch and supper trays, soft foods to assist with chewing, revised 1/12/21 -Monitor for tolerance and acceptance of dysphagia (difficulty swallowing) advanced diet with ground meat, revised 9/15/20 -Provide and serve supplements as ordered: 8 ounces (oz) Ensure Plus (nutritional supplement) three times daily, revised 6/9/21 Review of the March 2024 Physician's orders included the following: -Regular pureed diet with nectar thick liquids (easily pourable and are comparable to heavy syrup found in canned fruit) consistency, initiated 1/16/24 -House supplement 4 oz (ounces) three times daily, initiated 9/26/23 Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #18: -had severe cognitive impairment as evidenced by a Brief Interview of Mental Status (BIMS) score of 4 out of a total 15 -required set up/clean up assistance with eating -was on a mechanically altered diet Review of the Nutritional Risk Evaluation dated 2/28/24, indicated the following: -Diet was pureed with nectar thick liquids . Review of the Care Plan Note, dated 3/12/24, indicated a Quarterly Care Plan Meeting was held and included the Registered Dietitian (RD). The Care Plan Note indicated that Resident #18 was on a pureed consistency diet. On 3/20/24 at 10:10 A.M., the surveyor observed the Resident lying in bed with the head of the bed elevated, and eating breakfast. The surveyor observed that the Resident's meal ticket indicated pureed consistency with nectar thick liquids. On 3/26/24 at 1:04 P.M., the surveyor and the RD reviewed Resident #18's current Nutritional Care Plan, last revised on 12/22/23, and which did not indicate regular pureed diet with nectar thick liquids and the the current nutritional supplement ordered. The RD said that the current care plan was not accurate relative to the interventions and diet consistency and needed to be revised. The RD said that care plan revisions would occur at least quarterly with the scheduled MDS Assessments or if there was a change that required the plan of care to be adjusted. Please Refer to F692
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 record review and interview, the facility failed to ensure that one Resident (#9) out of a total sample of 17 residents...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure that one Resident (#9) out of a total sample of 17 residents, with limited range of motion (ROM) received appropriate care and services to maintain and/or improve their mobility function. Specifically, the facility staff failed to have PT (Physical Therapy)/OT (Occupational Therapy) re-evaluate and implement Resident #9's therapy services following an Orthopedic Consult and recommendations, to prevent further avoidable reduction in ROM and mobility. Findings include: Resident #9 was admitted to the facility in June 2021, with diagnoses including Dementia (a decline in intellectual functioning, including problems with memory, reasoning and thinking), Adult Failure to Thrive (decreased appetite, poor nutrition, and physical inactivity, often associated with dehydration, depression, immune dysfunction, and low cholesterol), muscle wasting, muscle weakness, fracture of right femur (broken thigh bone), fracture of proximal phalanx of left index finger (broken finger), and fracture of phalanx of left ring finger (broken finger). Review of the Nursing Progress Note dated 12/13/23, indicated the Resident was observed on the floor. The Nursing Progress Note indicated further assessment was done and the Resident was experiencing pain and bruising, the Physician was notified, and the Resident was sent to the emergency room for evaluation. Review of the Physician's Note dated 12/19/23, indicated Resident #9 returned from hospitalization with a fracture of the right femur (broken thigh bone). The Resident was also required to be NWB (non-weight bearing: withholding pressure from a limb or extremity post-surgery or injury to allow healing) to their right upper extremity (arm) and needed a sling. Review of the Nursing Progress Note dated 1/8/24, indicated the Nurse responded to an alarm in Resident #9's room and found him/her on the floor and the Medical Doctor (MD) was notified. Review of the Nursing Progress Note dated 1/9/24, indicated the Resident had x-rays done of his/her hand with findings of fracture (break) of the 4th and 5th fingers with swelling. The Nursing Progress Note indicated the findings were reported to the Medical Doctor and PT (Physical Therapy)/OT (Occupational Therapy) departments. Review of the Nursing Progress Note dated 1/10/24, indicated that Resident #9 had another fall where he/she incurred fractures to two fingers and was now NWB to right upper extremity and the left upper extremity required splint/brace use. Review of the Nursing Progress Note dated 1/12/24, indicated the Nurse spoke with the Nurse Practioner (NP) and the Resident was to remain NWB to the left hand until he/she was seen by ortho (Orthopedics) for follow-up. The Nursing Progress Note further indicated that care was coordinated with PT and OT. Review of the March 2024 Physician's orders, dated 3/22/24, indicated the following: -Non-weight bearing to right upper extremity, initiated 12/19/23 and active -Left hand non-weight bearing every shift, initiated 1/9/24 and active Review of the Rehabilitation to Nursing Communication form, dated 1/17/24, indicated Resident #9: -transfers fluctuated with the assistance of 1 or 2 staff -required extensive assistance with feeding, hygiene, bathing, and dressing -was NWB to bilateral upper extremities Review of the Physical Therapy (PT) Discharge summary, dated [DATE], indicated Resident #9: -received PT services from 12/19/23 through 1/17/24 -Resident's prior level of functioning before PT service involvement was at supervision level for transfers and bed mobility. -Bilateral upper extremity NWB restrictions were impacting further progress with balance, walking, transfers, and bed mobility. -Positive gains in functional mobility with recent plateau of progress due to ongoing NWB status for right upper extremity in sling, non-weight bearing left hand due to recent 4th and 5th digit fractures, and poor out of bed tolerance with therapy participation. Review of the Nursing Progress Note dated 1/18/24, indicated the Resident had stalled therapy progress due to weight bearing status of arm/hand, was unable to return to prior level of function as expected, and that Resident #9 has had 5 falls since 12/1/23 with multiple fractures. The Nursing Progress Note further indicated a significant change MDS (Minimum Data Set) will be initiated. Review of the Occupational Therapy (OT) Discharge summary, dated [DATE], indicated Resident #9: -received OT services from 12/18/23 through 1/22/24 -prior level of functioning before OT services was toileting at a supervision level with a rolling walker -Resident has reached highest practical level with OT -Resident is NWB of bilateral upper extremities -The Resident requires maximum/total assistance for feeding/hygiene/all bilateral ADLs (activities of daily living) until weight bearing (WB) status is cleared. Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated: -the Resident had a significant change in status. -that Resident #9 was severely cognitively impaired as evidenced by a Brief Interview for Mental Status (BIMS) score of six out of a total 15. -had a fall with major injury. -was dependent on staff for eating and toileting. -required maximum assistance with bathing, dressing, and personal hygiene. -required moderate assistance from staff for bed mobility and transfers. The MDS Assessment further indicated the Resident was not walking due to safety concerns and required maximum staff assistance for wheelchair use. Review of the Orthopedic Report of Consultation, dated 1/24/24, indicated the following: -Diagnosis of healing fracture, healing right hip -Right shoulder, right elbow, left hand in good position -No pain or discomfort -Range of Motion (ROM)/Strength all areas to tolerance Review of the Nursing Progress Note dated 1/24/24 indicated: -Resident was seen by Orthopedic .findings as follows: healing right hip, right shoulder, and right elbow. -Left hand in good position. -Physician or Medical Doctor (MD) recommends ROM as tolerated. Review of the Nurse Practitioner Note dated 1/25/24, indicated: -Unsteadiness of feet, decreased mobility, deconditioning, muscle weakness: continue PT/OT evaluation and treatment as indicated. Further review of the medical record did not indicate that PT and/or OT services assessed/ re-assessed Resident #9's range of motion following the Orthopedic Consult completed on 1/24/24. During an interview on 3/26/24 at 10:09 A.M., the surveyor and the Director of Rehabilitation (DoR) reviewed the Orthopedic Consult report dated 1/24/24. The DoR said that an evaluation and assessment was not conducted by PT and OT after the Resident's Orthopedic appointment on 1/24/24 and that a PT/OT evaluation and assesment should have been completed.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, record review, and policy review, the facility failed to provide an environment that was free of potential a...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, record review, and policy review, the facility failed to provide an environment that was free of potential accidents and hazards for one Resident (#62), out of a total sample of three closed records reviewed. Specifically, for Resident #62, the facility failed to: -assess the Resident for an independent authorized leave of absence (LOA) from the facility when he/she did not have a Physician's order for LOA and a known cognitive deficit. -identify the required needs of the Resident who had multiple medical diagnoses that required ongoing monitoring, care, services and medication administration, when the Resident did not have access to prescribed medications while on LOA and required staff supervision while ambulating for partial weight bearing (PWB- when a fraction of the body's weight (e.g., 20% or 50%) can be put on the affected limb) due to a Diabetic foot ulcer (skin breakdown due to a complication from Diabetes that is associated with infection, amputation and death). -contact the Resident for 24 hours, and notify the Physician for two days, when the Resident did not return from the LOA. Findings include: Review of the facility's policy titled Wandering and Elopement, revised March 2019, indicated the following: -The facility will identify residents who are at risk of unsafe wandering and strive to prevent harm while maintaining the least restrictive environment for residents. -If a resident is missing, initiate the elopement/missing resident emergency procedure: *Determine if the resident is out on an authorized leave *If the resident was not authorized to leave, initiate a search of the building and the premises and *If the resident is not located, notify the Administrator and the Director of Nursing Services, the resident legal representative, the attending physician, law enforcement officials, and as necessary volunteer agencies. Resident #62 was admitted to the facility in December 2023 with diagnoses including bipolar disorder (a mental health condition that causes extreme mood swings between emotional highs and lows), alcohol abuse, opioid use, diabetes type 2 (DM II - condition in which the body does not produce enough insulin and has trouble controlling blood sugar levels), osteomyelitis (inflammation of bone or bone marrow due to infection), left diabetic foot ulcer, heart failure (when the heart is unable to pump blood as it should resulting in fluid buildup in the feet, arms, lungs and other organs), muscle weakness, and difficulty in walking. Review of the most recent Minimum Data Set (MDS) assessment, dated 12/21/23, indicated Resident #62 had moderate cognitive impairment as evidenced by a Brief Interview for Mental Status (BIMS) score of 10 out of a total score of 15. Further review of the MDS indicated the following: -Wandering behavior four to six days but less than daily, during the seven day look back period -Ambulated with a walker -Presence of a surgical wound -At risk for falls related to right [sic] foot wound, side effects from psychotropic medication, and wandering -At risk for injury if a fall occurs. Review of the Psychosocial Assessment, dated 12/11/23, indicated that Resident #62 was confused with short-term memory deficits. Review of the Nursing Evaluation, effective 12/11/23, indicated that the elopement/wander risk assessment was not completed on the Resident's admission to the facility. Review of the Active January 2024 Physician's orders indicated the following daily ordered medications: -PWB to left foot every shift for WB status. -Aripiprazole (anti-psychotic) 5 milligrams (mg) give one tablet once a day, related to Bipolar Disorder. -Asprin 81 mg give one tablet one time a day, related to Heart Failure. -Carevedilol (Alpha-Beta Blockers) 6.25 mg give one tablet two times a day, related to Hypertension. -Folic Acid (vitamin) 400 microgram (mcg) give one tablet, related to chronic Viral Hepatitis. -Furosemide (Diuretic [water pill]) 40 mg give one tablet two times a day, related to Heart Failure. -Neurontin (anti-convulsant) 100 mg give one capsule three times a day, related to chronic Viral Hepatitis. -Calcium Alginate with silver (a type of wound dressing that contains silver alginate [an ionic silver complex that inhibits the growth of microorganisms]) to left dorsal (top of foot) full thickness (both the epidermis and dermis layers of the skin are completely destroyed, and the damage extends down into the subcutaneous tissue, which may include fat, muscles, and even bones) foot every day shift for wound care, cleanse with normal saline, pat dry, cover with gauze. -Lantus (Insulin) 100 units (U)/Milliliter (mL) inject 30 units subcutaneously one time a day -Insulin Lispro Injection Solution 100 U/mL per sliding scale (varies the dose of Insulin base on blood glucose[sugar] levels): >70-100 blood sugar (BS): no Insulin >101-150 BS: no Insulin >151-199 BS: 1 unit >200-249 BS: 2 units >250-299 BS: 3 units >300-349 BS: 4 units >350-999 BS: 5 units and call Physician >Subcutaneously before meals 7:30 A.M., 11:30 A.M., 4:30 A.M., related to DM with foot ulcer. -Methadone (analgesic opioid agonists) 10 mg/ml give 115 mg one time a day for substance abuse Review of the January 2024 Medication Treatment Record (MAR) indicated that on 1/8/24 the Resident received the following medications: -Methadone 10 mg/ml give 115 mg -Lispro 100 Unit/mL 3 units Further review of the January 2024 MAR did not indicate that Resident #62 received his/her ordered medications for Heart Failure, Hypertension, Viral Hepatitis, Bipolar Disorder, Diabetes maintenance and foot ulcer wound care for 1/8/24 - 1/10/24 when the Resident was determined to be discharged from the facility. Review of the Physical Therapy Discharge summary, dated [DATE], indicated the following: -Patient will safely ambulate on level surfaces 250 feet using four-wheel walker (FWW) with modified independence 95% of the time while weight bearing precautions to increase independence within the facility. -Supervised assist for unlimited distances, Patient continues to require cues and reminder to maintain partial weight bearing (PWB) and use of FWW to do so. Cognitive deficits impairing follow through. -Patient requires supervision with cues to use assistive device and for PWB during ambulation outdoors/indoors and on uneven surfaces. Review of the Wound Evaluation and Management Summary, dated 1/4/24, indicated the following: -Left Distal Dorsal full thickness -Measurments of 3.5 length by (x) 0.9 width x 0.2 centimeter (cm) -Moderate serous drainage (a type of fluid that comes out of a wound with tissue damage) -Calcium Alginate with silver, apply once daily for 9 days -Elevate legs, prevent any trauma, surgery follow-up Review of the Absentee Register, undated, indicated that Resident #62 signed out of the facility independently from 12/19/23 through 1/8/24 a total of 16 times. -On 1/8/24 Resident #62 signed out at 10:30 with an approximate return of 11:00 (A.M. or P.M., was not designated) Review of the clinical record progress notes for Resident #62 indicated the following: -On 1/8/24 at 11:17 P.M., Patient left this morning to go visit family and has not return [sic] -On 1/9/24 at 11:00 A.M., Director of Nurses (DON) called Resident #62. -Resident #62 stated (to DON) they planned to come back to the facility last night, however was unable. -DON informed the Resident that he/she would require drug testing from an Emergency Room, before returning to the facility. -On 1/10/24 at 8:20 A.M., DON attempted call to Resident as he/she still has not returned to facility. -On 1/10/24 at 10:57 A.M., DON informed Nurse Practitioner (NP) that patient had been discharged against medical advice (AMA) from the facility. Review of the Current Care Plan identified that Resident #62 had a problematic manner in which the Residents' acts characterized by ineffective coping, wandering related to restlessness, initiated 1/3/24, and indicated the following: -Resident will wander only within specified boundaries thru [sic] next review date -Provide assistance in locating own room. -Provide directional cues [i.e. pictures, name on doors]. -Place familiar objects in resident surroundings. Review of the Current Care Plan further identified Resident #62 had a chronic/progressive decline in intellectual functioning characterized by: deficit in memory, judgment, decision making and thought process related to Alcoholism, initiated 12/13/23, and indicated the following: -Allow adequate time for response -Ask simple questions which require yes and no answers when possible -Break activities into manageable subtasks. Give one instruction at a time to resident. -Cue and prompt resident with simple direct verbal cues and reminders - demonstrate tasks During an interview on 3/22/24 at 1:12 P.M., the facility Administrator said when a resident has an LOA from the facility they are supposed to sign out. The Administrator said there would be a Physician's order for the resident to go LOA either with assistance or independently. The Administrator further said that if there was no Physician's order for an LOA, the facility would consider it an elopement, staff would search the grounds, perform a head count, announce over the intercom, and interview other residents. The Administrator said the facility staff would try to call the resident and then provide education about the expectations of a LOA, notify the Police, the Department of Public Health (DPH), the facility's regional management team, the Physician, and call the hospital to see if the resident was admitted there. During an interview on 3/26/24 at 10:05 A.M., Physician #2 said that residents can go out on a LOA with a Physician's order with a responsible person. Physician #2 further said that some residents go out independently but that she does not give those orders. Physician #2 said that she does not do any evaluations to determine if a resident can go out independently and that the facility determines if a resident can go on a LOA. Physician #2 said that residents should have a time frame of how long they can be out of the building on a LOA. Physician #2 said that if a resident goes out on a LOA and does not return to the facility, she would expect to be notified by staff and it would be considered an elopement. During an interview on 3/26/24 at 11:15 A.M., the DON said when a resident is admitted to the facility, the facility should perform an evalution to determine whether the Resident is independent or if they need a responsible party to have an LOA. If the resident is determined to be able to have a LOA, a Physician's order is entered into the resident's medical record. The DON further said that the Physican is the one making the final decision as to whether the resident can go on an LOA or not. When the surveyor asked the DON how it is determined which resident is independent and which resident needs a responsible party with them for a LOA, the DON said that ultimately it is the Physician's decision. The DON further said that if there was no order for a LOA, the resident would not be expected to leave the facility and if they did leave, the facility would notify the Physician and it would treated as an elopement. During a follow-up interview on 3/26/24 at 1:15 P.M., the surveyor and the DON reviewed the medical record for Resident #62 and the DON said that Resident #62 had no Physician's order for an authorized leave as required, and should have had one prior to leaving the facility. The DON further said that there was no assessment completed to indicate that Resident #62 could leave the building independently or with a responsible party. The DON reviewed Resident #62's elopement score on admission and said that the elopement assessment was not completed on admission as required. The DON reviewed the nursing progress notes and said that the staff did not notify the Physician that Resident #62 did not return to the building on 1/8/24. The DON further said that if a Resident leaves the building without authorized leave orders it is considered an elopement, and the facility staff should have notified the Physician and the Police, and reported the incident to DPH timely.
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, record and policy review, the facility failed to provide acceptable nutritional care and servic...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record and policy review, the facility failed to provide acceptable nutritional care and services for one Resident (#18), out of a total of 17 residents. Specifically, the facility staff failed to ensure that Resident #18 was provided the appropriate consistency of food and liquids as ordered by the Physician, and supervision/assistance per the plan of care, resulting in severe weight loss (greater than 7.5% in three months) for the Resident. Findings include: Review of the facility policy titled Weighing and Measuring the Resident, revised March 2011, included the following relative to reporting: -Report significant weight loss/weight gain to the nurse supervisor. -The threshold for significant unplanned and undesired weight/gain will be based on the following criteria >1 month- 5 percent (%) weight loss is significant; greater than 5% is severe >3 months- 7.5 % weight loss is significant; greater than 7.5% is severe >6 months- 10 % weight loss is significant; greater than 10% is severe -Report other information in accordance with facility policy and professional standards of care. Review of the facility policy titled Supporting Activities of Daily Living (ADL-basic and everyday skills that are essential to living including eating, dressing, toileting, personal hygiene), revised March 2018, indicated residents will be provided with care, treatment and services as appropriate to maintain or improve their ability to carry out ADLs. The policy also included the following: -Appropriate care and services will be provided for residents who are unable to carry out ADLs independently, with the consent of the resident and in accordance with the plan of care, including appropriate support and assistance with hygiene, mobility, elimination, dining, and communication . -Care and services to prevent and/or minimize functional decline . -If residents with cognitive impairment or Dementia resist care, staff will attempt to identify the underlying cause of the problem and not just assume the resident is refusing or declining care. Approaching the resident in a different way or at a different time, or having another staff member speak with the resident may be appropriate Review of the facility policy titled, Pureed Food Preparation, undated, indicated the facility will prepare foods in a manner that sustains nutritional value and taste. The food will be pureed to assure the desired consistency. Resident #18 was admitted to the facility September 2020, with diagnoses including Hemiplegia (paralysis on one side) after a Cerebrovascular Accident (CVA- disruption of the blood supply to the brain resulting in damage to specific areas of the brain), Vascular Dementia with agitation (problems with planning or organizing, making decisions or solving problems), and need for assistance with personal care. Review of the March 2024 Physician's orders included the following: -Monthly weights, initiated 4/19/18 -Regular pureed diet with nectar thick liquids (easily pourable and are comparable to heavy syrup found in canned fruit) consistency, initiated 1/16/24 Review of the current Certified Nurses Aide (CNA) Care Card (information for the staff to provide specific resident care) included the following: -Feeding/Eating: continual supervision in a small group with a 1:8 ratio at times, requires assistance of one staff to complete the meal -Document on behavior monitoring form each episode Review of the ADL Care Plan, initiated 9/15/20 and revised 2/1/23, indicated the Resident required assistance with ADLs and included the following interventions: -Re-approach if resident refuses, initiated 7/7/22 -Feeding/Eating: continual supervision in a small group with a 1:8 ratio, at times requires assistance of one staff to complete the meal, initiated 1/22/24 Review of the Nutrition Care Plan, initiated 9/15/20 and revised 12/22/23, indicated Resident #18 had poor nutritional status related to texture restrictions, poor dentition, and impaired self-feeding. The plan of care included the following interventions: -Extra pudding added to lunch and dinner meals , revised 1/12/21 -Monitor for tolerance and acceptance of [diet] , revised 9/15/20 -Provide, serve diet as ordered, monitor intake, and record every meal, revised 9/15/20 -Monitor for signs and symptoms of choking or aspiration- coughing, gagging, pocketing food. -Speech evaluation as indicated, revised 9/15/20 Review of the Minimum Data Set (MDS) assessment dated [DATE], indicated Resident #18: -had severe cognitive impairment as evidenced by a Brief Interview of Mental Status (BIMS) score of 4 out of a total 15, -had upper and lower extremity range of motion impairment on one side, -required set up/clean up assistance with eating, -was on a mechanically altered diet. Review of the Mini Nutritional Assessment, dated 2/28/24, indicated the following: -Resident had moderate decrease in food intake due to loss of appetite, digestive problems, and chewing or swallowing difficulties over the past 3 months -Weight loss greater than 3 kilograms (kg) or 6.6 pounds (lbs) -Was bed or chair bound -Had severe Dementia or depression -Score of 5 (out of 14) indicating malnourished nutritional status Review of the Nutritional Risk Evaluation, dated 2/28/24, indicated the following: -Resident's weight was 147 lbs, he/she did not have significant weight change -Diet was pureed with nectar thick liquids with variable meal intake from 25-100%, mostly greater than 50% -Extra items on lunch tray: pudding -Nutrition Plan: gradual decline in weight noted, increased risk for weight loss, choking/aspiration, decreased feeding skills, dehydration, and impaired skin. Continue with modified diet, additional nutritional interventions (house supplement and additions to meals) and encourage meals in main dining room for increased socialization. Review of the Resident weights included the following: -164.7 pounds (lbs.): 6 months ago on 9/22/23 -154.8 lbs: 3 months ago on 12/11/23 -147.3 lbs: 1 month ago on 2/1/24 -144.6 lbs: 3/18/24 (12% weight loss from 9/22/23 - 3/18/24, indicating severe weight loss) On 3/20/24 at 10:10 A.M., the surveyor observed the Resident lying in bed with the head of the bed elevated, eating breakfast. The Resident said that he/she did not like the juice because it tasted like there was rice in it. The surveyor did not observe any staff present in the room to assist the Resident. The surveyor also observed the Resident's meal ticket which indicated pureed consistency with nectar thick liquids. The pureed eggs and meat observed on the Resident's plate were not smooth and cohesive, and pieces of non-pureed food was observed throughout both the pureed eggs and meat items. The surveyor observed a partially consumed cup of thickened juice on the table. The surveyor observed Resident #18 feed his/her self in a very slow pace using the spoon provided. On 3/21/24 at 8:23 A.M. through 8:59 A.M., the surveyor observed Resident #18 lying upright in bed. The breakfast meal was placed on an overbed table in front of him/her and the surveyor observed the pureed consistency food items provided were chunky with evidence of non-puree food pieces present. During the observation, Activities Staff #1 entered the room and provided the resident with a covered glass of regular apple juice (not thickened) with a straw. During an interview at 8:55 A.M., Activities Staff #1 said that she provided the Resident with apple juice this morning at breakfast. Activities Staff #1 further said that it was a regular (not nectar thick) apple juice that was provided as she was not aware that Resident #18 needed anything different. Activities Staff #1 left the Resident's room, and the surveyor observed the Resident slowly eating and drinking and continuously chewing after taking a bite of the pureed food items on his/her plate. No staff were present to provide assistance or encouragement to Resident #18 during the observation and he/she spent most of the time not eating with hands on his/her lap. From 8:59 A.M. through 10:15 A.M., the surveyor observed the Resident closed his/her eyes and stop eating and drinking. the surveyor did not observe any staff entering the room to encourage, provide supervision or assistance to the Resident. On 3/21/24 at 12:18 P.M. through 1:02 P.M., the surveyor observed the Resident seated alone at a table in the Unit Dining Room during lunch. The lunch meal which was pureed meatloaf, mashed potatoes, pureed vegetables and a pureed fruit cup was provided to the Resident. There was no pudding provided per the nutrition plan of care. The surveyor observed that the food provided to Resident #18 had non-pureed food chunks in the fruit cup, the meatloaf, and the pureed vegetables. CNA #4 prepared the Resident's coffee and cranberry juice opening and using multiple packets of thickener. After mixing the thickener into the Resident's beverages, she left them positioned next to him/her and went to assist another resident in the dining room. At 12:32 P.M., the Resident was observed using a spoon to consume the coffee and cranberry juice which was the consistency of pudding (and not nectar consistency per the plan of care). At 12:37 P.M. the Resident picked up the glass of thickened cranberry juice and was observed to attempt to drink the thickened juice but was unable because the liquid was not moving out of the cup (due to the thickness). The surveyor observed the Resident's cheeks were sucked inward as he/she continued to attempt to drink from the cup. Staff who were present in the dining room assisting other residents did not offer assistance to Resident #18. During an interview at the time, the Resident said that the juice was hard to drink. At 12:42 P.M., the surveyor requested that the Assistant Director of Nurses (ADON) observe the Resident's liquids. During an interview and observation, the ADON said the beverages provided were pudding thick consistency and were too thick for the Resident to drink, and that the Resident was supposed to be provided with nectar thick consistency liquids. The ADON removed the pudding thick liquids from Resident #18's table and was observed to provide him/her with nectar thick apple juice and coffee. The surveyor asked the Resident if the liquids were better, and he/she nodded their head yes and was observed to pick up the nectar thick apple juice and drink without issue. The surveyor observed that after a few bites of the lunch meal, the Resident put his/her spoon down and discontinued eating. Nurse #6 approached the Resident at 1:02 P.M., and asked if he/she wanted assistance and then removed the less than half eaten plate of food. On 3/22/24 at 7:57 A.M. through 9:10 A.M., the surveyor observed Resident #18 lying upright in bed during breakfast. Nectar thick cranberry juice was provided to him/her and no staff were present in the room to assist the Resident. At 8:39 A.M., the breakfast meal was provided and contained pureed eggs, a pureed muffin, and a bowl of hot cereal. At 8:45 A.M., the Resident stopped eating and drinking and with hands on his/her lap, started to watch the television in his/her room. No staff were observed to offer assistance, provide encouragement or supervise the Resident with the breakfast meal. The surveyor observed that the Resident would occasionally take a bite of food or a drink of liquid and then pause for extended periods of time. At 9:10 A.M., CNA #5 removed Resident #18's meal tray. During an interview at the time, CNA #5 said that the Resident consumed about 50% of the breakfast meal. On 3/22/24 at 12:26 P.M. through 12:39 P.M., the surveyor observed Resident #18 eating lunch in the Unit Dining Room. A pureed meal with nectar thick liquids was provided, but no pudding was provided per the nutrition plan of care. The Resident was observed to slowly and occasionally feed self, with no assistance provided by staff. At 12:39 P.M., CNA #2 removed the Resident's meal tray. During an interview, CNA #2 said the Resident did not do very good with lunch and said he/she consumed about 25 % of the meal and drank about 1/4 cup of nectar thick liquid. During an interview on 3/22/24 at 12:58 P.M., CNA #2 said she has worked with Resident #18 for a long time and knows him/her well. CNA #2 said the Resident required assistance with ADLs, can have behaviors at times with some staff but does well with consistent staff. CNA #2 said the Resident was on a pureed with nectar thick liquid diet and would cough if the liquids were not thickened. CNA #2 further said the Resident was very slow with eating meals, and did not require assistance or supervision because he/she fed him/herself. During an interview on 3/26/24 at 12:45 P.M., the Speech Language Pathologist (SLP-specializes in communication and swallowing disorders) said that he was a Consultant with the facility two days a week and has not worked with Resident #18 for a long time. The SLP further said that pureed food consistency should be smooth, without visible lumps or pieces of food, and that the presence of skins or seeds could be problematic for potential choking or aspiration. The SLP also said the pureed consistency should not be runny, too thick, or pasty. The SLP said that he was not aware that Resident #18 was on a pureed with nectar thick liquid consistency diet, that he was a contracted employee and the facility staff would notify him with requests of which residents they wanted him to assess. The SLP said that he does not provide general education to the facility staff relative to diet and liquid consistencies but would provide specific information for a resident he had worked with relative to specific feeding/swallowing strategies. The SLP further said he thought the facility would provide general education and training for the staff about the specific diets they use as it varies from facility to facility. During an interview on 3/26/24 at 1:37 P.M., the ADON said the facility just implemented the beverage cart with meal pass, and staff from different departments assist with this process including the Administrator, Social Services, and Activities Staff. The ADON said that there was no information located on the beverage cart relative to specific resident diets (consistencies, allergies, intolerances), but that if the staff were unsure what a resident's diet was, the staff should ask the resident's Nurse for the information. The ADON further said that there was no formal training for the facility staff on modified diets, including thickened liquids, and that in the past the liquids have come pre-thickened from the kitchen, but this has not been consistent. On 3/26/24 at 1:04 P.M., the surveyor and the Registered Dietitian (RD) reviewed the Resident's clinical record. The RD said Resident #18 was hospitalized several months ago and was downgraded to a pureed diet with nectar thick liquids because of aspiration Pneumonia (when food/fluids are inhaled into the lungs causing an infection). The RD further said Resident #18 needed to be in the dining room for all meals, was able to feed him/herself but required supervision during meals and fluid intake because of his/her specialized diet. The RD said that if the Resident declined to eat in the Unit Dining Room or if community dining was suspended, then the Nurses and/or CNAs would need to ensure that supervision/assistance was provided in his/her room. The RD said that she completes weight audits monthly in the beginning of each month for the previous month and was not aware that Resident #18 had experienced severe weight loss. The surveyor relayed observations during the lunch meal and that pudding not being provided per the nutritional plan of care and the RD said that she would have to look into this concern. The RD further said she would understand why the Resident has lost weight if supervision/assistance with meals and recommended interventions were not provided, as required. Please Refer to F805
CONCERN (D)

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

Dental Services (Tag F0791)

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 dental services for two Residents (#1 and #18...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide dental services for two Residents (#1 and #18) out of a total sample of 17 residents. Specifically, the facility staff failed to: 1. Obtain consent and refer Resident #1 for dental services. 2. Implement dental recommendations for extractions as recommended by the Dentist for Resident #18. Findings include: Review of the facility policy titled Dental Services, revised December 2016, indicated: -Routine and 24-hour emergency dental services are provided to our residents through: a. A contract agreement with a licensed Dentist that comes to the facility monthly. b. Referral to the resident's personal Dentist. c. Referral to community Dentist; or d. Referral to other healthcare organizations that provide dental services. -Residents have the right to select Dentists of their choice when dental care or services are needed. -Selected Dentist must be available to provide follow-up care. -All dental services provided are recorded in the resident's medical record. A copy of the resident's dental record is provided to any facility to which the resident is transferred. 1. Resident #1 was admitted to the facility in February 2023, with diagnoses including Bipolar Disorder (mental health illness that causes dramatic shifts in a person's mood, energy and ability to think clearly), Hypertension (high blood pressure), and Metabolic Encephalopathy (a problem in the brain caused by a chemical imbalance in the blood). Review of Resident #1's Minimum Data Set (MDS) assessment dated [DATE], indicated the Resident was cognitively intact as evidenced by a Brief Interview for Mental Status (BIMS) score of 15 out of total 15. Further review of the MDS Assessment indicated that Resident #1 had natural teeth that were broken. During an interview on 3/20/24 at 4:36 P.M., Resident #1 said he/she had a broken tooth and had not seen a Dentist for a few years. Resident #1 said that he/she would like to receive dental services at the facility. During an interview on 3/21/24 at 12:30 P.M., the surveyor and Nurse #3 reviewed Resident #1's medical record. Nurse #3 said that Resident #1 did not have a signed consent to be seen by a Dentist and had not been seen by a Dentist since admission to the facility. During an interview with Medical Record Personnel #1 on 3/21/24 at 1:26 P.M., Medical Record Personnel #1 said she was responsible for obtaining consent for residents to be seen by the contracted facility Dentist but she had not obtained a consent for Resident #1. During an interview on 3/21/24 at 3:05 P.M., the Director of Nurses (DON) said the facility staff had not obtained consent for Resident #1 to be seen by the contracted facility Dentist. 2. Resident #18 was admitted to the facility in September 2020, with diagnoses including Hemiplegia (paralysis on one side) after a Cerebrovascular Accident (CVA- disruption of the blood supply to the brain resulting in damage to specific areas of the brain), Vascular Dementia with agitation (problems with planning or organizing, making decisions or solving problems), and need for assistance with personal care. Review of the Minimum Data Set (MDS) Assessment, dated 7/12/23, indicated Resident #18: -had significant cognitive impairment as evidenced by a Brief Interview of Mental Status (BIMS) score of 5 out of 15. -required substantial/maximum assistance with oral hygiene. -was on a mechanically altered diet. -had obvious or likely cavities or broken natural teeth. Review of the Oral/Dental Care Plan, initiated 7/7/23 and revised 10/19/23, indicated the Resident had oral/dental problems related to poor dentition and included the following interventions: -Coordinate arrangements for dental care, transportation as needed/as ordered, initiated 7/11/23 Review of the March 2024 Physician's orders included the following: -Dental consultation, evaluation, and treatment as needed, initiated 10/3/18 -May be seen by dental services PRN (as needed), initiated 8/3/22 Review of the current Certified Nurses Aide (CNA) Care Card (information for the staff to provide specific resident care) included the following: -Coordinate arrangements for dental care, transportation as needed/as ordered Review of the Dental Consult, dated 2/5/24, indicated Resident #18 was evaluated and the following was noted: -Condition of the Resident's teeth were poor with general breakdown -Severe inflammation of the gingiva/swollen, bleeding gums -Treatment Notes: all remaining teeth are in very poor condition. Discussed extractions with Resident to prevent further infections. Resident wishes to have all remaining teeth to be removed. -Action Required by the Nursing Home Staff: obtain signature for consent for extractions . On 3/20/24 at 10:10 A.M., the surveyor observed the Resident lying in bed with the head of the bed elevated, eating breakfast. The surveyor observed that the Resident had a few teeth which were in poor condition. During an interview on 3/26/24 at 2:50 P.M., the Director of Nurses (DON) said when dental services are in the facility, the resident recommendations are given to her or the Assistant DON (ADON), who then provide it to the Physician to approve. The DON said there have been issues with the process, it does not always work, and that recommendations have been missed. The DON said that she would check into the Resident's dental consultation recommendations from 2/5/24 and follow-up with the surveyor. During a follow-up interview on 3/26/24 at 4:00 P.M., the DON said Resident #18's dental consult dated 2/5/24 was missed and never addressed. The DON further said there was no appointment made to have the dental extractions completed, and that one was made today (3/26/24) after the surveyor inquired about the dental consultation. The DON said there were process issues when consultants come into the facility and make recommendations and how this is communicated to the facility staff.
CONCERN (D)

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

Deficiency F0805 (Tag F0805)

Could have caused harm · This affected 1 resident

Based on observation, interview, record and policy review, the facility failed to ensure that one Resident (#18) out of a total sample of 17 residents, received the appropriate consistency of mechanic...

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Based on observation, interview, record and policy review, the facility failed to ensure that one Resident (#18) out of a total sample of 17 residents, received the appropriate consistency of mechanically altered food and liquids. Specifically, the facility staff failed to ensure Resident #18 was provided the appropriate consistency of pureed food and nectar thick liquids (easily pourable and are comparable to heavy syrup found in canned fruit) when he/she had a Physician's order for the specialized diet, had poor dentition and had a history of chewing/swallowing problems putting him/her at risk for choking and aspiration (food/fluids that are inhaled into the lungs and can cause infection). Findings include: Review of the policy titled Pureed Food Preparation, undated, indicated the facility will prepare food in a manner that sustains nutritional value and taste. The food will be pureed to assure the desired consistency. Resident #18 was admitted to the September 2020, with diagnoses including Hemiplegia (paralysis on one side) after a Cerebrovascular Accident (CVA- disruption of the blood supply to the brain resulting in damage to specific areas of the brain), Vascular Dementia with agitation (problems with planning or organizing, making decisions or solving problems), and need for assistance with personal care. Review of the March 2024 Physician's orders included the following: -Regular pureed diet with nectar thick liquids consistency, initiated 1/16/24 Review of the Nutrition Care Plan, initiated 9/15/20 and revised 12/22/23, indicated Resident #18 had poor nutritional status related to texture restrictions, poor dentition and impaired self-feeding. The plan of care included the following interventions: -Monitor for tolerance and acceptance of [diet] , revised 9/15/20 -Provide, serve diet as ordered, monitor intake and record every meal, revised 9/15/20 -Monitor for signs and symptoms of choking or aspiration- coughing, gagging, pocketing food. -Speech evaluation as indicated, revised 9/15/20 Review of the Minimum Data Set (MDS) Assessment, dated 2/28/24, indicated Resident #18: -had severe cognitive impairment as evidenced by a Brief Interview of Mental Status (BIMS) score of 4 out of 15. -had upper and lower extremity range of motion impairment on one side. -required set up/clean up assistance with eating. -was on a mechanically altered diet. On 3/20/24 at 10:10 A.M., the surveyor observed the Resident reclining in bed with the head of the bed elevated, eating breakfast. The Resident said the juice he/she was drinking tasted like there was rice in it. The surveyor observed the Resident's meal ticket indicated pureed consistency with nectar thick liquids and that the pureed eggs and meat on the Resident's plate was not smooth and cohesive, with pieces of non-pureed food in both the eggs and meat. On 3/21/24 at 8:23 A.M. through 8:59 A.M., the surveyor observed Resident #18 reclining upright in bed and the breakfast meal was placed on an overbed table in front of him/her. The surveyor observed the pureed consistency food items provided for the breakfast meal were chunky with pieces of non-puree food pieces present. Activities Staff #1 entered the Resident's room and provided him/her with a covered glass of regular apple juice (not thickened) with a straw. During an interview at 8:55 A.M., Activities Staff #1 said that she provided the Resident with apple juice, that it was a regular (not nectar thick) apple juice as she was not aware that he/she needed anything different for juice. On 3/21/24 at 12:18 P.M. through 1:02 P.M., the surveyor observed the Resident seated at a table alone in the Unit Dining Room during lunch. The surveyor observed the lunch meal, which was pureed meatloaf, mashed potatoes, pureed vegetables, and pureed fruit cup, had non-pureed food chunks in the fruit cup, the meatloaf and the pureed vegetables. The surveyor observed CNA #4 preparing the Resident's coffee and cranberry juice by using multiple packets of thickener. After mixing the thickener into the Resident's beverages, CNA #4 left the beverages next to him/her and went to assist another resident in the dining room. The surveyor observed the Resident using a spoon consume the coffee and cranberry juice which both had the consistency of pudding (and not nectar per the plan of care). The Resident was further observed picking up the glass of thickened cranberry juice and attempting to drink the thickened juice without success as the liquid was not moving out of the cup (due to the thickness). During an interview at the time, the Resident said that the juice was hard to drink and the surveyor observed the Resident cheeks were sucked inward as he/she continued to try to drink from the cup, without assistance from staff who were also in the dining room assisting other residents. During an interview and observation, the ADON said the beverages provided to Resident # 18 were pudding thick consistency, were too thick as he/she should be provided nectar thick consistency liquids. The ADON provided the Resident with nectar thick apple juice and coffee which he/she was able pick up the nectar thick apple juice and drink without issue. On 3/22/24 at 12:30 P.M., the surveyor requested a pureed meal from Dietary Aide #1, who had cooked and served the meal. The surveyor observed pieces of unpureed food pieces in the green beans, pureed fish, and green particles in the mashed potatoes of the pureed meal provided. During an interview, Dietary Aide #1 said she takes the regular menu items, puts them into the food processer, adds liquids, and then uses the puree option. The surveyor and Dietary Aide #1 observed the puree fish cutlet, mashed potatoes, and pureed green beans which had been served and were still present on the serving table. Dietary Aide #1 said there were pieces of the food in the pureed fish and the pureed green beans that had not been fully pureed. Dietary Aide #1 said the pieces of green in the potatoes were cilantro, which she added for flavor. Dietary Aide #1 further said that it was difficult to fully puree the food using the equipment the facility had but thought as long as the food was mostly broken down, it was fine for the residents. When the surveyor asked what the pureed consistency should look like, Dietary Aide #1 said it should not be runny and it should be easy for the residents to swallow. On 3/26/24 at 12:21 P.M., the Food Service Director (FSD) said the pureed food consistency should not be liquidy/runny, should hold its form, like a pudding, and should not have pieces or chunks of food within it. The FSD said that the food is cooked first and then put into a food processer, which had a puree option, but it does not puree as well as it should. The FSD further said the facility used to have a commercial food processer for pureeing the food, but it broke several years ago and was replaced with the equipment the facility currently have. During an interview on 3/26/24 at 12:45 P.M., the Speech Language Pathologist (SLP-specializes in communication and swallowing disorders) said that pureed food consistency should be smooth, without visible lumps or pieces of food and that presence skins or seeds could be problematic for potential choking or aspiration. The SLP said the consistency should not be runny or too thick or pasty. The SLP said that he does not provide general education to the facility staff relative to diet and liquid consistencies but would provide specific information for a resident he had worked with relative to specific feeding/swallowing strategies for that person. During an interview on 3/26/24 at 1:37 P.M., the ADON said the facility just implemented the beverage cart with meal pass and staff from different departments assist with this process including the Administrator, Social Services, and Activities Staff. The ADON said that there is no information located on the beverage cart relative to specific resident diets (consistencies, allergies, intolerances), but that if the staff are unsure what a resident's diet is, they should ask the resident's Nurse if they are not clinical staff. The ADON said that there was no formal training for the facility staff on modified diets, including thickened liquids, and that in the past the liquids have come pre-thickened from the kitchen but this has not been consistent.
CONCERN (D)

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

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

Based on observation, interview, record and policy review, the facility failed to ensure that transmission-based precautions (TBP- implemented for patients who are known or suspected to be infected wi...

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Based on observation, interview, record and policy review, the facility failed to ensure that transmission-based precautions (TBP- implemented for patients who are known or suspected to be infected with infectious agents) were implemented in order to prevent the potential spread of infection for one Resident #22, of one applicable resident on TBP precautions, out of a total sample of 17 residents. Specifically, the facility failed to ensure that the required personal protective equipment (PPE) was worn prior to entering Resident #22's room when he/she was on Contact Precautions (prevent transmission of infectious agents which are spread by direct or indirect contact with the patient or the patient's environment) for a Clostridium difficile colitis (C-Diff: inflammation of the colon caused by bacteria causing fever, abdominal pain and diarrhea) infection. Findings include: Review of the facility policy titled Clostridium Difficile, revised October 2018, indicated: -precautions will be taken to prevent transmission to other residents. -the primary reservoirs of C-Diff are infected people and surfaces. -Spores can persist on resident-care items and surfaces for several months and are resistant to some common cleaning and disinfection methods. -Residents with diarrhea and suspected C-Diff infection are placed on Contact Precautions while awaiting laboratory results. -When caring to residents with C-Diff infection, staff is to maintain vigilant hand hygiene. -Handwashing with soap and water is superior to Alcohol Based Hand Rub (ABHR) for the mechanical removal of the C-Diff spores from the hands. Review of the facility policy titled Categories of TBP-Isolation, revised September 2022, indicated TBP are initiated: -when a resident develops signs and symptoms of a transmissible infection -arrives from admission with symptoms of infection -has a laboratory confirmed infection -and is at risk of transmitting the infection to other residents The following was referenced in the policy relative to contact precautions: >staff and visitors wear gloves when entering the room . >gloves are removed and hand hygiene is performed prior to leaving the room. >staff and visitors wear a disposable gown upon entering the room and remove prior to leaving the room. Resident #22 was admitted to the facility in October 2022, with diagnoses including Cerebrovascular Accident (CVA: interruption of the blood supply to the brain resulting in damage to specific areas of the brain), assistance with personal care, and C-Diff infection. On 3/21/24 from 7:22 A.M. through 8:57 A.M., the surveyor observed the following: -Signage posted outside of the Resident's room indicating: > Stop. Contact Precautions: Everyone must: clean hands before entering and when leaving the room; providers and staff must also: put on gloves before room entry and discard before room exit, put on a gown before entry and discard before room exit . >Wash hands with soap and water . - A bin with PPE (gown, gloves) was located outside of the Resident's room -7:44 A.M., the Administrator knocked and entered the Resident's room with only a surgical mask in place (no gown and gloves were worn) and exited a short time later, without performing hand hygiene. -7:46 A.M., Human Resources Staff knock and enter the Resident's room with only a surgical mask in place (no gloves or gown was worn). -8:50 A.M., Certified Nurses Aide (CNA) #2 knock and enter the room to collect the Resident's breakfast tray without putting on a gown and gloves as required, and exited the room shortly after, without performing hand hygiene. -8:57 A.M., Activities Staff #1 knock and enter the Resident's room to provide an activities sheet. The Activities Staff did not put on a gown or gloves prior to entering the room and exited shortly after. On 3/22/24 at 7:38 A.M., the surveyor observed Human Resource Staff knock and enter Resident #22's room without a gown or gloves worn to provide the Resident beverages for breakfast. During an interview on 3/22/24 at 7:44 A.M., Human Resource Staff said that the gown and gloves were only to be put on when entering Resident #22's room when personal care was being provided. She further said she was not sure why the Resident was on Contact Precautions but knew that it was only supposed to be worn by staff providing personal care. On 3/22/24 at 8:19 A.M., the surveyor observed CNA #5 enter the Resident's room to provide him/her with requested items for breakfast. CNA #5 did not wear a gown and gloves upon entering the room, and also did not perform hand hygiene. On 3/22/24 at 8:59 A.M., the surveyor observed the Administrator knock and enter the Resident's room. The Administrator did not put on a gown or gloves prior to entering the room. The Administrator was observed conversing while leaning over the Resident who was in bed and touching the side rail while conversing with the Resident. After a brief conversation, the Administrator exited the room without performing hand hygiene. During an interview on 3/22/24 at 1:54 P.M., the Assistant Director of Nurses (ADON) who was also the Infection Preventionist (IP) said that Resident #22 was on precautions for C-Diff infection and was actively having loose stools. During a follow-up interview on 3/26/24 at 1:53 P.M., the ADON/IP said that all staff are supposed to wear a gown and gloves prior to entering Resident #22's room because he/she was on Contact Precautions for C-Diff infection. The ADON/IP said prior to exiting the room, the gown and gloves were to be discarded and hand hygiene needed to be performed using soap and water. The ADON/IP said because of the Resident's type of infection, contact with the Resident and his/her environment can transmit the infection.
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 interview, record and document review, the facility failed to provide competent nursing staff to care for one Resident (#60), out of one applicable resident, out of a total sample of 17 resid...

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Based on interview, record and document review, the facility failed to provide competent nursing staff to care for one Resident (#60), out of one applicable resident, out of a total sample of 17 residents, who required Nephrostomy (temporary tube used to drain urine directly from the kidneys to a bag outside of the body) site care resulting in the Resident being hospitalized with multiple infections. Specifically, the facility staff failed to: -Ensure that all licensed Nursing staff caring for Resident #60 had the competency and skills required to provide care and services for a Nephrostomy tube, when nine out of 15 facility Licensed Nurses who cared for the Resident were provided with training on Nephrostomy site care. -obtain Physician orders for sterile (free from microorganisms to prevent infection) dressing changes every one to three days, and measure output from the Nephrostomy Tube every eight hours as required. Findings include: Review of the Facility Assessment, undated, indicated the following: Resident #60 was admitted to the facility February 2024, with a diagnosis of a new re-inserted Nephrostomy Tube. Review of the facility policy Nephrostomy Tube, Care of, revised October 2010, indicated the following: -Check the placement of the tubing and integrity of the tape during assessments. -Drainage should be below the level of the kidneys. -There should be no kinks in the tubing. -Empty drainage bag once per shift and as needed. -Measure output every 8 hours. -Record urinary and nephrostomy output separately. -Change dressings every one to three days as ordered. -Use sterile technique during dressing changes. Reporting pertaining to the Nephrostomy Tube: Report any of the following signs and symptoms to the Physician: >Redness, inflammation reports of pain or other signs of infection at the insertion site. >Reduced output or output below established parameters. >Inability to irrigate to signs of obstruction of the tube. >Signs of skin breakdown around the dressing site. >If the tube becomes dislodged. Review of the February 2024 Physician's orders indicated the following orders: -Sodium Chloride solution 0.9%, use 5 ml via irrigation in the afternoon for Nephrostomy [Facility policy indicated to use no more than 2-3 ml for irrigation]. -flush nephrostomy with 5 ml (Sodium Chloride solution 0.9%), daily, start date 2/8/24. Further review of the February 2024 Physician's orders failed to indicate any instructions for Nephrostomy site dressing changes or monitoring of the output from the Nephrostomy tube. Review of the February 2024 Medication Administration Record (MAR) indicated no orders for any dressing changes (including a sterile dressing) to the Nephrostomy site every one to three days as ordered per facility policy. The February 2024 MAR also did not include orders for measuring output from the Nephrostomy Tube every 8 hours per facility policy. Further review of the February 2024 MAR indicated: -Sodium Chloride solution 0.9%, use 5 ml via irrigation in the afternoon for Nephrostomy. Flush nephrostomy with 5 ml daily was documented as administered from 2/9/24 through 2/20/24. Review of the Care Plan, indwelling Foley catheter and nephrostomy tube, initiated 2/7/24 indicated: -Check tubing for kinks each shift per policy -Monitor and document output as per facility policy. -Nephrostomy tube dressing change as ordered. -Observe for/document pain discomfort due to catheter. Review of the Inservice Sign in Sheet, Nephrostomy Care- Understanding Nephrostomy Tube, How to Take Care of Percutaneous Nephrostomy Tube, when to call the Doctor for complications, dated 2/7/24, indicated that nine Licensed Nursing staff signed off as completing the training. Review of the February 2024 MAR indicated that 15 Licensed Nursing staff provided care for Resident #60. During an interview on 3/26/24 at 10:45 A.M., the Assistant Director of Nurses (ADON) said that competencies are completed when an employee is newly hired, annually, and as needed based on a Resident's new diagnosis. The ADON further said that she just completed training on Nephrostomy care with Licensed Nursing staff as the facility had a new Resident with a Nephrostomy tube. When the surveyor asked how competency of a skill is determined, the ADON said that she demonstrated the skill individually and then asked the staff to reciprocate the skill. The ADON provided the surveyor with evidence that nine out of 15 Licensed Nurses who cared for Resident #60 were provided with training on Nephrostomy site care. Review of the Emergency Hospital Report dated 2/22/24, indicated that Resident #60 had active diagnoses of -Sepsis (a life-threatening medical emergency that occurs when an infection triggers the body's immune system to damage its own organs and tissues) -Urinary Tract Infection (bacterial infection of the urinary tract) During an interview on 3/26/24 at 1:15 P.M., the Director of Nurses (DON) reviewed the clinical record for Resident #60 and said she could not find evidence of a Physician's order for providing sterile dressing changes and measuring output as expected and required for a resident with a Nephrostomy tube.
CONCERN (E)

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

Deficiency F0804 (Tag F0804)

Could have caused harm · This affected multiple residents

Based on observation, interview, record and policy review, the facility failed to provide palatable food that was within appropriate temperatures for service on one unit (A-wing) out of two units obse...

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Based on observation, interview, record and policy review, the facility failed to provide palatable food that was within appropriate temperatures for service on one unit (A-wing) out of two units observed and relative to four Resident's (#24, #27, #47, and #52) and members of a Resident Council Meeting. Specifically, the facility staff failed to: -for Resident's #47, #24, #27, and #52, provide food that was palatable and served at a safe and appetizing temperature. -for members of a Resident Council Meeting held during the recertification survey, provide food that was palatable, appetizing and served at a proper temperature. Findings include: Review of the facility policy titled Food Temperatures, undated, indicated: -foods will be maintained at proper temperature to ensure food safety. -that test trays will be made up periodically -the temperatures of the test trays, as to be served to the resident, will be recorded by the Dietary Manager. Review of the Room Test Tray Evaluation Form, undated, included the following parameters for acceptable temperatures when the food was delivered: -Entree 135 -160 degrees Fahrenheit (F) -Starch 135-160 degrees F -Hot cereal 145-160 degrees F -Beverage 40-55 degrees F (cold), 145-180 degrees F (hot) During the initial pool process on 3/20/24 from 9:06 A.M. through 10:09 A.M., the following interviews were obtained from Residents residing on the A-Wing Unit: -Resident #47 said the eggs were always cold, and the staff say they cannot reheat them. He/she also said the vegetables are always cold and mushy. -Resident #24 said the food is not hot, the A-Wing is the last unit served. -Resident #27 said the food is cold on most days, mostly at breakfast. -Resident #52 said he/she does not like the food because it is too bland and does not have enough seasoning. On 3/21/24 from 10:45 A.M. through 11:15 A.M., the survey team held a Resident Council meeting with 12 residents and the following was discussed: -The food was cold, breakfast was the coldest- particularly the eggs and the pancakes. -One resident said that there were no warmers under the plates to keep the food hot, just covers. -One resident said he/she received cold food for nine days in a row. -Several residents said there were administrative staff passing trays yesterday and today,, and that did not usually occur The surveyor requested a test tray and calibrated thermometer to be on the last meal cart delivered to the A-Wing on 3/22/24 at 7:30 A.M. The breakfast meal service on A-Wing Unit was served from 8:07 A.M. through 8:26 A.M. and the surveyor observed the following: -8:07 A.M., the first meal cart arrived on the Unit. The Director of Nurses (DON) checked the resident meal trays and tray distribution began shortly after by several staff including Social Services, Activities and Rehabilitation Staff. -8:24 A.M., the second meal cart was observed on the Unit and breakfast trays were being distributed. -8:26 A.M., all resident breakfast trays had been distributed. At 8:26 A.M., the surveyor obtained the test tray and the following temperatures were obtained with the Assistant Director of Nurses (ADON): -cream of wheat-133.2 degrees F, lukewarm, bland -pureed eggs- 122.9 degrees F, lukewarm -pureed muffin - 113.1 degrees F, lukewarm, bland -coffee- 127.2 degrees, warm During an interview on 3/22/24 at 8:31 A.M., the ADON said the plate for the test tray meal was warm but not hot. The ADON further said that she assists with passing resident meals and that the residents do complain at times that the meal is cold. The ADON said when the residents complain that the meal is cold, the staff should get another meal from the kitchen for the resident. During an interview on 3/26/24 at 12:21 P.M., the surveyor reviewed the resident concerns and the temperatures from the test tray with the Food Service Director (FSD). The FSD said she was aware of the resident's complaints of food temperatures especially in the morning. The FSD said that test trays are conducted a few times a month and they have verified issues with the temperatures concerns. The FSD said the facility does not have the metal inserts for the plates which assist in keeping the plates hot and thought that the metal inserts may be needed. The FSD further said the temperature of the hot foods when served to residents should be above 135 degrees.
CONCERN (F)

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

Deficiency F0727 (Tag F0727)

Could have caused harm · This affected most or all residents

Based on review of the facility's Licensed Nurse staff schedule, Daily Census list provided to the survey team, and interview, the facility failed to provide the services of a Registered Nurse (RN) fo...

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Based on review of the facility's Licensed Nurse staff schedule, Daily Census list provided to the survey team, and interview, the facility failed to provide the services of a Registered Nurse (RN) for at least eight consecutive hours a day, seven days a week. Specifically, the facility staff failed to: 1. Provide at least eight consecutive hours of RN services in the facility over one 24-hour period on 12/23/23, when no nurse staffing waivers were in place. 2. appropriately schedule the services of a RN when the facility scheduled the Director of Nurses (DON) as a charge nurse, providing direct resident care and the average facility resident occupancy was above 60 residents. Findings include: 1. Review of the Nursing Staff Schedule 'as worked' provided by the facility, dated 12/23/23, included no evidence that a RN worked at the facility for 8 consecutive hours on 12/23/23. During an interview on 3/26/24 at 10:53 A.M., the surveyor and the DON reviewed the schedule for 12/23/23, and the DON said there was no RN coverage scheduled until 11:00 P.M. on 12/23/23. The DON further said that she would expect to be notified by the Scheduler if there was no RN coverage in the facility so that another RN could be assigned to work and she was not aware there was no RN in the building until 11:00 P.M. on 12/23/23 until the surveyor brought it to her attention. During an interview on 3/26/24 at 11:30 A.M., Regional Nurse #1 reviewed the Nursing Staff Schedule dated 12/23/23 and said that the facility did not have a RN working for 8 consecutive hours as required on 12/23/23. 2. Review of the Nursing Administration schedule dated 2/8/24, indicated that the DON worked an assignment providing direct resident care. Review of the Daily Census dated 2/1/24 through 2/29/24 indicated that the average daily census was above 60 in February 2024. During an interview on 3/20/24 at 8:12 A.M., the Administrator said the facility had no nurse staffing waivers in place. During an interview on 3/26/24 at 10:45 A.M., the DON said that she works full-time, 40 hours a week or more as a DON. The DON further said that if the facility has staffing needs, she will have an assignment providing direct resident care. The DON said that she has taken direct resident care assignments providing medications and treatments to residents on several occasions. During an interview on 3/26/24 at 12:15 P.M., The facility Scheduler reviewed the nurse staffing schedules and said that the DON worked an assignment providing direct resident care on 2/8/24 from 3:30 P.M. until 7:30 P.M.
CONCERN (F)

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

Pharmacy Services (Tag F0755)

Could have caused harm · This affected most or all residents

Based on observation, policy review, and interview, the facility failed to accurately and safely ensure that routine and emergency medications and pharmaceutical services were provided to meet the nee...

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Based on observation, policy review, and interview, the facility failed to accurately and safely ensure that routine and emergency medications and pharmaceutical services were provided to meet the needs of each resident. Specifically, the facility staff failed to ensure that: 1. Three open medication Emergency Box Kits on one unit (A) were re-ordered as required. 2. Expired medications were removed from the medication cart on one unit (A-short) out of two units observed. Findings include: Review of the facility policy titled, Storage of Medications, dated 11/2020, indicated: -Discontinued, outdated, or deteriorated drugs or biologicals are returned to the dispensing Pharmacy or destroyed. 1. On 3/21/23 at 9:57 A.M., the surveyor and the Director of Nurses (DON) observed the Unit A medication storage room with the following: -open Emergency Box Kits with no evidence that the kits were re-ordered from the Pharmacy. >Antibiotic kit was open, dated 3/14/24. >E-Kit I2171 and E-Kit I2113 had been opened, verified by the protective seal being broken and no date indicating when it had been opened. During an interview at the time, the DON said that she was unable to determine when the E-Kit I2171 and E-Kit I2113 were opened as the reconciliation (the formal process of obtaining a complete and accurate list of each patient's current medications) from the Pharmacy was not completed to indicate what medications had been removed and for which Resident the removed medications were utilized. The DON further said that medications from E-Kits were missing and that there was no receipt indicating any of the E-kits records were faxed to the Pharmacy to request replacement medications. 2. On 3/21/24 at 10:00 A.M., the surveyor and the DON observed the medication cart on the Unit A-short. A bottle of Multivitamins with Minerals, with an expiration date of 11/13/23, was found in the top drawer of the medication cart. During an interview at the time, the DON said the Multivitamin with Minerals medication had expired and should have been removed from the medication cart.
Feb 2023 1 deficiency
CONCERN (D)

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

Deficiency F0883 (Tag F0883)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure that staff provided education and offered a Pneumococcal Vac...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure that staff provided education and offered a Pneumococcal Vaccine upon admission to the facility for one Resident (#1), out of a total sample of five residents. Findings include: Review of the facility policy titled, Pneumococcal Vaccine, revised 3/22, included, but not limited to: -Prior to or upon admission, residents are assessed for eligibility to receive the Pneumococcal vaccine series, and when indicated, are offered the vaccine series within thirty (30) days of admission to the facility unless medically contraindicated or the resident has already been vaccinated. CDC recommends Pneumococcal Conjugate Vaccines (PCV) PCV15 or PCV20 for: Adults 65 years or older Adults 19 through [AGE] years old with certain medical conditions or risk factors CDC recommends Pneumococcal Polysaccharide Vaccine (PPSV) PPSV23 for: Children 2 through [AGE] years old with certain medical conditions Adults 19 years or older who get PCV15 Resident #1 was admitted to the facility in November 2022 with a diagnosis of Hemiplegia (paralysis on one side of the body) and Hemiparesis (muscle weakness or partial paralysis on one side of the body) following a Cerebral Infarction (stroke- disrupted blood flow to the brain due to problems with the blood vessels that supply it) affecting the dominant right side. Review of the Discharge Return Anticipated Minimum Data Set (MDS) Assessment, dated 11/2022, indicated in Section O:0300 that the Resident's Pneumococcal vaccine was not up to date and the vaccine was not offered. Review of the clinical record did not contain documentation to indicate if education was provided and the Pneumococcal vaccine was offered to Resident #1 upon admission. During an interview on 2/1/23 at 1:20 P.M., the Regional Corporate Director said there was no documentation found in the clinical record to indicate the Pneumococcal vaccine was offered to Resident #1, as required.
Oct 2022 6 deficiencies
CONCERN (D)

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

Deficiency F0551 (Tag F0551)

Could have caused harm · This affected 1 resident

Based on policy review, record review and interview, the facility failed to ensure its staff obtained written consent, including education on the risks and benefits of proposed care related to the use...

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Based on policy review, record review and interview, the facility failed to ensure its staff obtained written consent, including education on the risks and benefits of proposed care related to the use of an anti-psychotic medication, from a Resident Representative, for one Resident (#20), out of a total sample to 12 Residents. Findings include: Review of the facility's policy, revised 2019, Behavioral Assessment, Intervention and Monitoring, indicated the following: -The resident and family/representatives will be informed of the resident's condition as well as the potential risks and benefits of proposed interventions. Resident # 20 was admitted to the facility in May 2022 with a diagnosis of Schizoaffective Disorder, Bipolar Type (mental health disorder that is marked by a combination of Schizophrenia symptoms, such as hallucinations or delusions, and mood disorder symptoms, such as depression or mania.) Review of an Minimum Date Set (MDS) assessment, dated 7/27/22, indicated Resident #20 had severe cognitive impairment as evidenced by a score of 3 out of 15 on the Brief Interview for Mental Status (BIMS). Review of the October 2022 Physician Orders indicated, Seroquel (an antipsychotic medication) 12.5 milligram (mg) by mouth, two times a day. Review of the October 2022 Medication Administration Record (MAR) indicated, Seroquel 12.5 mg was given twice daily, from 10/01/22 through 10/06/22. Review of the clinical record indicated that there was not a written Informed Consent for Psychotropic Administration for the use of Seroquel, signed by Resident #20's Representative. During an interview on 10/06/22 at 1:51 P.M., Nurse #1 reviewed the clinical record and said that Resident # 20 did not have a signed Informed Consent for the use of Seroquel. During an interview on 10/06/22 at 2:21 P.M., the Director of Nursing (DON) said, after reviewing the clinical record that there was not a Informed Consent, signed by the Resident's Representative, for the Seroquel that was being administered daily as ordered.
CONCERN (D)

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

Transfer Notice (Tag F0623)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure that its staff provided a written Notice of Transfer/Dischar...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure that its staff provided a written Notice of Transfer/Discharge to the Resident and/or the Resident's Representative, for one Resident (#18), out of a total sample of 12 Residents. Findings include: Resident #18 was admitted to the facility in February 2022. Review of the Minimum Data Set (MDS) assessment, dated 4/26/22, indicated an unplanned discharge to an acute hospital. Review of the April 2022 Nurses Progress Notes, indicated that Resident #18 had a change in his/her health condition, was sent to the hospital for evaluation and was subsequent admitted with Pneumonia and Anemia. The clinical record indicated the Resident had been readmitted to the facility on [DATE]. Further review of the clinical record indicated there was no Transfer/Discharge Notice for the 4/26/22 transfer. During an interview on 10/06/22 at 1:19 P.M., Social Worker (SW) #1 said that there was not a Transfer/Discharge Notice provided on 4/26/22 to the Resident or Resident's Representative, as required.
CONCERN (D)

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

Deficiency F0625 (Tag F0625)

Could have caused harm · This affected 1 resident

Based on policy review, interview and record review, the facility failed to ensure its staff provided the bed hold notice at the time of a hospital transfer, for two Residents (#41 and #18), out of 12...

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Based on policy review, interview and record review, the facility failed to ensure its staff provided the bed hold notice at the time of a hospital transfer, for two Residents (#41 and #18), out of 12 sampled residents. Findings include: Review of the facility's policy, titled Bed-Holds and Returns and dated March 2017, indicated the following: -Prior to transfers and therapeutic leaves, residents/resident representatives will be informed in writing of the bed-hold and return policy. -Prior to a transfer, written information will be given to the residents/resident representative that explain in detail: a. The rights and limitations of the resident regarding bed holds; b. The reserve bed payment policy as indicated by the state plan; c. The facility per diem rate required to hold a bed (non-Medicaid residents), or to hold a bed beyond the state bed hold period (Medicaid residents); and d. The details of the transfer (per the Notice of Transfer). 1. Resident #41 was admitted to the facility in November 2012. Review of a progress note, dated 6/16/22, indicated the Resident #41 was sent to the emergency room for an evaluation and was admitted . Review of the clinical record indicated no bed hold notice was provided to the Resident/Resident Representative, as required. During an interview on 10/06/22 at 3:50 P.M., the Director of Nurses said the bed hold notice was not issued to the Resident/Resident Representative, and should have been. 2. Resident #18 was admitted to the facility in February 2022. Review of the Minimum Data Set (MDS) assessment, dated 4/26/22, indicated an unplanned discharge to an acute hospital. Review of the clinical record indicated no evidence that a bed hold notice had been provided to the Resident/Resident Representative. During an interview on 10/06/22 at 1:19 P.M., Social Worker (SW) #1 said Resident # 18 and/or their Representative was not provided the bed hold policy at time of transfer, as required.
CONCERN (D)

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

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

Based on interview and record review the facility failed to ensure its staff accurately coded a facility acquired pressure ulcer on a Minimum Data Set (MDS) assessment for one Resident (#41) out of 12...

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Based on interview and record review the facility failed to ensure its staff accurately coded a facility acquired pressure ulcer on a Minimum Data Set (MDS) assessment for one Resident (#41) out of 12 sampled residents. Findings include: Resident #41 was re-admitted to the facility in June 2022. Review of a skin assessment, dated 7/01/22, indicated the Resident had no open areas. Review of a progress note, dated 7/08/22, indicated the Resident had a stage 2 (partial thickness loss of dermis presenting as a shallow open ulcer with a red pink wound bed, without slough/dead tissue) pressure ulcer on right buttock. Review of the wound consult, dated 8/25/22, indicated the Resident had a stage 3 (full thickness tissue loss. Subcutaneous fat may be visible but bone, tendon or muscle are not exposed. Slough may be present but does not obscure the depth of tissue loss. May include undermining and tunneling) pressure ulcer on the right buttock (same wound as the one identified on 7/08/22). Review of the MDS assessment, dated 8/31/22, indicated the Resident had a stage 3 pressure ulcer that was present on admission/readmission. During an interview on 10/06/22 at 2:58 P.M., the MDS Nurse said the MDS should have indicated the pressure ulcer was facility acquired, not present on admission or readmission.
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 observation, interview and record review, the facility failed to ensure its staff provided appropriate care and service...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure its staff provided appropriate care and services for an indwelling urinary catheter for two Residents (#16 and #18) out of four applicable sampled residents. Specifically, (1.) for Resident #16 the staff failed to (a.) ensure the catheter was changed as ordered and (b.) failed to address the Resident's non-compliance with catheter care. (2.) For Resident #18 the staff failed to obtain a Physician's order prior to changing the catheter. Findings include: 1 a. Resident #16 was admitted to the facility in May 2021 with a diagnosis including neurogenic bladder (lack of bladder control due to brain, spine or nerve damage). Review of the Minimum Data Set (MDS) assessment, dated 7/20/22, indicated the Resident was cognitively intact as evidenced by a score of 14 out of 15 on the Brief Interview for Mental Status (BIMS) assessment. Review of a progress note, dated 5/28/22, indicated the Resident was sent to the emergency room (ER) for an evaluation due to ongoing hematuria (blood in the urine). Review of the hospital Discharge summary, dated [DATE], indicated the Resident was found to have kidney stones which were blocking the suprapubic catheter (a tube that is inserted through the belly and into the bladder to drain urine) and causing decreased output and hematuria. The Resident was also found to have a Urinary Tract Infection (UTI) and was started on a seven day course of Cefpodoxime (antibiotic) 200 milligrams by mouth twice daily. Review of a urology consult, dated 6/02/22, indicated the Resident was seen for a supra pubic catheter change. It also indicated the Resident had missed his/her appointment for the catheter change on 5/05/22 and was seen in the hospital on 5/28/22 for hematuria. The plan included for the Resident to be seen by urology in one month. Review of the progress notes on 5/05/22 did not indicate that the Resident missed the urology appointment for the catheter change, why it was missed, or if the appointment was rescheduled. Review of a progress note, dated 8/11/22, indicated the Resident informed the Nurse that the catheter was leaking. The Nurse called the Urologist and their office informed the Nurse that the Resident had missed appointments on 6/30/22 and 8/04/22 for the catheter to be changed. The next available appointment was on 9/01/22. Review of the progress notes for 6/30/22 and 8/04/22 did not indicate that the Resident missed the urology appointments for the catheter changes, why they were missed, or if they were rescheduled. Review of a progress note, dated 8/16/22, indicated the Resident complained the catheter was leaking, The Director of Nurses (DON offered to change it but the Resident refused and requested numbing gel (numbing agent) that the urology office uses to be used. The Resident was assured it would be ordered and as soon as it came in, the DON would change the catheter. Review of the progress notes from 8/16/22 through 8/31/22 did not indicate an attempt to change the catheter or documentation that the Resident refused a catheter change. During an interview on 10/06/22 at 12:38 P.M., Nurse #2 said that the Resident missed two visits to Urology, 6/30/22 and 8/04/22. 1 b. Review of the facility's policy, Suprapubic Catheter Care, dated October 2010, indicated the following: -The purpose of this procedure is to prevent skin irritation around the stoma (insertion site) and to prevent infection of the resident's urinary tract. -The urinary drainage bag must be held or positioned lower than the bladder at all times to prevent the urine in the tubing and drainage bag from flowing back into the bladder. -Check the resident frequently to be sure the tubing is free from kinks. -Empty the collection bag at least every eight hours. Review of Resident #16's care plan for the Suprapubic Catheter, with goal date 11/20/22, indicated the following interventions: -catheter care as ordered -check tubing for kinks each shift/per policy -monitor and document intake and output as per facility policy -observe for and document any pain/discomfort due to catheter -observe for and report any sign and symptoms of UTI -Resident educated to not disconnect closed catheter system by him/herself (initiated 7/09/21). Further review indicated no new interventions to the care plan related to the Resident's non-compliance with catheter care. During an interview on 10/05/22 at 10:16 A.M., the Resident said he/she drains the catheter myself and said the catheter wasplugged. The Resident then lifted his/her shirt and the surveyor observed the catheter with a cap on the end (preventing the bladder to drain spontaneously into a drainage bag). The Resident said he/she would drain the urine into the toilet if he/she got the urge. During an interview on 10/06/22 at 10:49 A.M., the Resident said he/she was supposed to have the catheter changed monthly. When the surveyor asked if the catheter was plugged again, the Resident lifted up his/her shirt and the surveyor observed the catheter with a cap on the end. During an interview on 10/06/22 at 11:03 A.M., the DON said that she knew the Resident was plugging the catheter at night but had no idea he/she was doing it during the day. She said the Resident refused to have the catheter changed at the facility and she thought at one point they obtained the numbing gel but then the Resident still refused to have it changed. She said the Physician said he wasn't going to give orders for it to be changed at the facility if the Resident was going to the Urologist. The DON said there should be notes stating that the Resident went to Urology or refused etc. When the surveyor pointed out that the catheter had not been changed at either location (facility or Urology) from June 2022 to September 2022, the DON did not say anything. The DON said they have not provided any education to the Resident about emptying the catheter because they do not want him/her doing it. She said the nurses do not know if the urinary outputs the Resident tells them are accurate because he/she unplugs the catheter independently. The surveyor asked what the plan was given that the Resident was still plugging the catheter, the DON said it's behavioral. The surveyor asked if the behaviors had been care planned for non-compliance related to catheter care, or if they had involved psychiatric services to help with the non-compliance and the DON said they had not done either. She said there shouldn't be so many holes in the clinical record regarding this issue and she understood the concerns. 2. Resident #18 was admitted to the facility in February 2022 with diagnoses including Neuromuscular Dysfunction of Bladder (urinary or bladder problems due to disease or injury of the central nervous system or peripheral nerves involved in the control of urination) and Chronic Kidney Disease Stage 5 ( the kidneys have lost nearly all their ability to do their job effectively). Review of a Progress Note, dated 10/2/2022, indicated that Resident #18 had attempted to pull out his/her Foley (flexible tube that a clinician passes through the urethra into the bladder to drain urine) catheter and it was then removed by the Nurse. The note further indicated that a new Foley catheter was inserted. On 10/05/22 at 8:44 A.M., the surveyor observed Resident #18 lying down in bed in his/her room. A Foley catheter drainage bag was observed to be hooked to the side of the bed. Resident #18 said that the Foley catheter had been changed recently by a nurse in the facility. Review of the October 2022 Physician orders indicated that there was no order to insert a Foley catheter, including the catheter and balloon size. During an interview on 10/06/22 at 9:40 A.M., Nurse #1 said that the Foley catheter was recently changed and that there was no order to insert a new one. She further said that a Physician's order including the size of the catheter and the balloon, should have been obtained prior to inserting a new Foley catheter.
CONCERN (D)

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

Deficiency F0727 (Tag F0727)

Could have caused harm · This affected 1 resident

Based on interview and review of timesheets, the facility failed to ensure that the services of a Registered Nurse (RN) were used for at least eight consecutive hours a day, seven days a week from 9/4...

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Based on interview and review of timesheets, the facility failed to ensure that the services of a Registered Nurse (RN) were used for at least eight consecutive hours a day, seven days a week from 9/4/22 through 10/1/22, specifically Sunday, 9/18/22. Findings include: Review of the timesheets provided to the survey team from 9/4/22 through 10/1/22 indicated no RN was scheduled to work on Sunday, 9/18/22 on any of the three shifts indicated on the timesheet. During an interview on 10/7/22 at 10:53 A.M. the Staffing Coordinator said no RN had been scheduled for a 24 hour period on 9/18/22.
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
  • • 37% turnover. Below Massachusetts's 48% average. Good staff retention means consistent care.
Concerns
  • • Multiple safety concerns identified: 5 harm violation(s), $43,719 in fines. Review inspection reports carefully.
  • • 42 deficiencies on record, including 5 serious (caused harm) violations. Ask about corrective actions taken.
  • • $43,719 in fines. Higher than 94% of Massachusetts facilities, suggesting repeated compliance issues.
  • • Grade F (10/100). Below average facility with significant concerns.
Bottom line: Trust Score of 10/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Fitchburg Rehabilitation And Nursing Center's CMS Rating?

CMS assigns FITCHBURG REHABILITATION AND NURSING CENTER an overall rating of 1 out of 5 stars, which is considered much below average nationally. Within Massachusetts, 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 Fitchburg Rehabilitation And Nursing Center Staffed?

CMS rates FITCHBURG REHABILITATION AND NURSING CENTER's staffing level at 2 out of 5 stars, which is below average compared to other nursing homes. Staff turnover is 37%, compared to the Massachusetts average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Fitchburg Rehabilitation And Nursing Center?

State health inspectors documented 42 deficiencies at FITCHBURG REHABILITATION AND NURSING CENTER during 2022 to 2025. These included: 5 that caused actual resident harm and 37 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Fitchburg Rehabilitation And Nursing Center?

FITCHBURG REHABILITATION AND NURSING 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 EPHRAM LAHASKY, a chain that manages multiple nursing homes. With 87 certified beds and approximately 68 residents (about 78% occupancy), it is a smaller facility located in FITCHBURG, Massachusetts.

How Does Fitchburg Rehabilitation And Nursing Center Compare to Other Massachusetts Nursing Homes?

Compared to the 100 nursing homes in Massachusetts, FITCHBURG REHABILITATION AND NURSING CENTER's overall rating (1 stars) is below the state average of 2.9, staff turnover (37%) is near the state average of 46%, and health inspection rating (1 stars) is much below the national benchmark.

What Should Families Ask When Visiting Fitchburg Rehabilitation And Nursing Center?

Based on this facility's data, families visiting should ask: "Can you walk me through typical staffing levels on day, evening, and night shifts?" "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?" These questions are particularly relevant given the below-average staffing rating.

Is Fitchburg Rehabilitation And Nursing Center Safe?

Based on CMS inspection data, FITCHBURG REHABILITATION AND NURSING 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 1-star overall rating and ranks #100 of 100 nursing homes in Massachusetts. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Fitchburg Rehabilitation And Nursing Center Stick Around?

FITCHBURG REHABILITATION AND NURSING CENTER has a staff turnover rate of 37%, which is about average for Massachusetts nursing homes (state average: 46%). Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was Fitchburg Rehabilitation And Nursing Center Ever Fined?

FITCHBURG REHABILITATION AND NURSING CENTER has been fined $43,719 across 2 penalty actions. The Massachusetts average is $33,516. 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 Fitchburg Rehabilitation And Nursing Center on Any Federal Watch List?

FITCHBURG REHABILITATION AND NURSING 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.