MINI-CASSIA CARE CENTER

1729 MILLER STREET EAST, BURLEY, ID 83318 (208) 678-9474
For profit - Corporation 68 Beds CASCADES HEALTHCARE Data: November 2025
Trust Grade
20/100
#73 of 79 in ID
Last Inspection: May 2025

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

Overview

Mini-Cassia Care Center in Burley, Idaho, has a Trust Grade of F, indicating poor performance with significant concerns about care quality. Ranked #73 out of 79 facilities in Idaho and #2 out of 2 in Cassia County, this facility is in the bottom half of options available. The trend is worsening, with issues increasing from 1 in 2023 to 9 in 2025, highlighting growing problems. While staffing is rated 3 out of 5 stars, the high turnover rate of 65% is concerning, as it exceeds the state average of 47%. Notably, the facility has no fines on record, which is a positive aspect, but there are serious concerns such as residents suffering falls without proper assessment and inadequate care leading to pressure ulcers.

Trust Score
F
20/100
In Idaho
#73/79
Bottom 8%
Safety Record
High Risk
Review needed
Inspections
Getting Worse
1 → 9 violations
Staff Stability
⚠ Watch
65% turnover. Above average. Higher turnover means staff may not know residents' routines.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Idaho facilities.
Skilled Nurses
✓ Good
Each resident gets 44 minutes of Registered Nurse (RN) attention daily — more than average for Idaho. RNs are trained to catch health problems early.
Violations
⚠ Watch
31 deficiencies on record. Higher than average. Multiple issues found across inspections.
★☆☆☆☆
1.0
Overall Rating
★★★☆☆
3.0
Staff Levels
★★★★☆
4.0
Care Quality
★☆☆☆☆
1.0
Inspection Score
Stable
2023: 1 issues
2025: 9 issues

The Good

  • 4-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record

Facility shows strength in quality measures, fire safety.

The Bad

1-Star Overall Rating

Below Idaho average (3.2)

Significant quality concerns identified by CMS

Staff Turnover: 65%

19pts above Idaho avg (46%)

Frequent staff changes - ask about care continuity

Chain: CASCADES HEALTHCARE

Part of a multi-facility chain

Ask about local staffing decisions and management

Staff turnover is elevated (65%)

17 points above Idaho average of 48%

The Ugly 31 deficiencies on record

3 actual harm
May 2025 9 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

Safe Environment (Tag F0584)

Could have caused harm · This affected 1 resident

Based on observation, review of the Centers for Medicare and Medicaid Services (CMS) State Operations Manual (SOM), Appendix PP, and resident and staff interviews, it was determined the facility faile...

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Based on observation, review of the Centers for Medicare and Medicaid Services (CMS) State Operations Manual (SOM), Appendix PP, and resident and staff interviews, it was determined the facility failed to ensure the residents had an environment where housekeeping and maintenance services provided a sanitary shower room in good repair. This was true for 1 of 4 showers used in the facility. This deficient practice created the potential for psychosocial harm if residents felt they were not provided the same homelike environment as other residents. Findings include: On 5/27/25 at 5:10 PM, it was observed the main shower in the south wing had brown and black spots resembling mold on the floor of the shower and near the drain. The shower chairs had a ring of red built up residue on the underside portion of the seat. The edge of the shower wall bar did not have an end cap cover, and a sharp metal ridge was observed. On 5/30/25 at 10:33 AM, the CRN and DON stated the shower was in disrepair and should have been closed. The DON stated there would not be a build-up of mold/dirt if the showers were cleaned between uses and deep cleaned every day. On 5/30/25 at 11:15 AM, the Administrator confirmed the main shower room on the south wing was not clean or in good repair.
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

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #20 was admitted to the facility on [DATE], with multiple diagnoses including bipolar disorder. An Annual MDS Assess...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #20 was admitted to the facility on [DATE], with multiple diagnoses including bipolar disorder. An Annual MDS Assessment, dated 3/23/25, documented no at A1500, a PASRR level II was not completed. Resident #20's medical record included documentation of a PASRR level I screening, dated 8/20/21, which identified she had a serious mental illness diagnosis of bipolar disorder. Resident #20's medical record included documentation of an abbreviated PASRR level II screening, dated 8/23/21, which identified she had a diagnosis of serious mental illness per PASRR criteria. On 5/29/25 at 3:28 PM the Regional MDS Nurse stated in 2021, Resident #20's MDS documented yes at A1500, a PASRR level II had been completed, but beginning in 2022, it was marked no in error and it should have been corrected. Based on review of the Resident Assessment Instrument (RAI) Manual, record review, and staff interview, it was determined the facility failed to ensure residents' Minimum Data Set (MDS) assessment included correct information. This was true for 2 of 14 residents (#2 and #20) whose records were reviewed for accuracy. This deficient practice had the potential for negative outcomes if residents were not monitored due to inaccurate assessments. Findings include: The RAI Manual, revised 10/1/24, documented section A1500, PASRR (Preadmission Screening and Resident Review), was to be coded yes when a PASRR level II screening determined a resident had a serious mental illness and/or intellectual disability, or related condition. 1. Resident #2 was admitted to the facility on [DATE], for care following a fracture and had multiple diagnoses including bipolar disorder (a mental health condition characterized by extreme mood swings including emotional highs or lows) and generalized anxiety disorder. Resident #2's medical record included documentation of a PASRR level I screening, dated 8/6/24, which identified she had serious mental illness diagnoses of bipolar disorder and anxiety. Resident #2's medical record included documentation of an abbreviated PASRR level II screening, dated 8/6/24, which identified she had diagnoses of serious mental illness per PASRR criteria. Resident #2's admission MDS Assessment, dated 8/7/24, documented section A1500, PASRR Is the resident currently considered by the state level II PASRR process to have a serious mental illness and/or intellectual disability, or a related condition? The answer for this question was documented as no. On 5/29/25 at 3:17 PM, the Regional MDS Nurse stated, Resident #2 has a PASRR level II, so the MDS at A1500 should be answered yes to reflect her serious mental illness diagnoses.
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

PASARR Coordination (Tag F0644)

Could have caused harm · This affected 1 resident

Based on review of the CMS SOM, Appendix PP, record review, and staff interview, it was determined the facility failed to ensure 1 of 14 residents (Resident #21), mental health needs were evaluated th...

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Based on review of the CMS SOM, Appendix PP, record review, and staff interview, it was determined the facility failed to ensure 1 of 14 residents (Resident #21), mental health needs were evaluated through the State's level II PASRR process. This deficient practice had the potential to cause harm if the resident's mental health needs were not adequately met. Findings include: Resident #21 was admitted to the facility 8/16/23, with multiple diagnoses including major depressive disorder and post-traumatic stress disorder (PTSD). A PASRR level II, dated 8/16/23, documented, A 30-day exemption rehabilitation - if [Resident #21] stays (30 days) past admission, please submit most current MDS, physician's order, social notes and psych[iatric] information to [agency name]. If discharged , please notify [agency name] per information below. A PASRR level II, dated 5/13/25, documented Resident #21 had serious mental health diagnoses including depression, anxiety, PTSD, and the PASRR level II was forwarded to [agency name] for further review. On 5/29/25 at 10:42 AM the Administrator stated Resident #21 had received a 30-day PASRR level II exemption due to medical issues. An updated PASRR level II was completed on 5/13/25. On 5/29/25 at 1:44 PM, the Resident Services Director (RSD) stated Resident #21 was given a 30-day exemption on admission for a PASRR level II, and the PASRR level II should have been submitted when Resident #21 stayed past 30-days in September 2023.
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0645 (Tag F0645)

Could have caused harm · This affected 1 resident

Based on staff interview and record review, it was determined the facility failed to ensure PASRR's were completed for 1 of 14 residents (Resident #40) reviewed for PASRR's. This deficient practice ha...

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Based on staff interview and record review, it was determined the facility failed to ensure PASRR's were completed for 1 of 14 residents (Resident #40) reviewed for PASRR's. This deficient practice had the potential for more than minimal harm when if residents required, but did not receive, specialized services for mental health while residing in the facility. Findings include: Resident #40 was admitted to the facility 5/6/22, with multiple diagnoses including Alzheimer's disease, depression, and anxiety. A Psychiatric Progress Note, dated 6/24/22, documented Resident #40 had mental health diagnoses of anxiety, insomnia, and dementia with behavioral disturbances and was taking Trazodone (antidepressant medication) 25 mg at bedtime and Seroquel (antipsychotic medication) 50 mg at bedtime. Resident #40's PASRR level I from Nevada documented No MI [mental illnesses], MR [intellectual disability], RC [related conditions] or Dementia, and was not referred for further evaluation. Resident #40's care plan, initiated on 5/19/22, documented she had Alzheimer's and dementia with behavior disturbances, anxiety, restlessness, and agitation. Interventions included administer antidepressant and antipsychotic medications. Resident #40's admission MDS Assessment, dated 5/13/22, documented the following: -She was not cognitively intact. -She had hallucinations and delusions with behavioral symptoms directed at others (threatening, screaming, cursing at others), and her behavioral symptoms significantly interfered with her participation in activities or social interactions. -She received antipsychotic medication on 7 out of the 7 previous days. On 5/29/25 at 3:15 PM, the Regional MDS Nurse stated, the Nevada PASRR level I for Resident #40 was wrong. She added, this resident should have had a PASRR Level I and II for Idaho when she was admitted to the facility, and the facility did not complete them.
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0655 (Tag F0655)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #27 was admitted to the facility on [DATE], with multiple diagnoses including low back pain, fracture of the right l...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #27 was admitted to the facility on [DATE], with multiple diagnoses including low back pain, fracture of the right leg, altered mental status, diabetes, and opioid dependence. Resident #27's medical record did not document a baseline care plan was completed. On 5/29/25 at 1:28 PM, the DON stated a baseline care plan was not completed for Resident #27. Based on record review, policy review, and staff interview, it was determined the facility failed to ensure a baseline care plan was developed within 48 hours of residents' admission. This was true for 2 of 14 residents (#1 and #27) reviewed for baseline care plans. This failure created the potential for harm if the care plan failed to provide direction for care. Findings include: The facility's Baseline Care Plans policy (undated) documented a baseline plan of care to meet the resident's immediate health and safety needs is developed for each resident within 48 hours of admission. 1. Resident #1 was admitted to the facility on [DATE], with multiple diagnoses including schizophrenia, anxiety disorder, and neuroleptic induced parkinsonism (a condition where individuals develop parkinsonian symptoms as a side effect of taking certain medications). Resident #1's medical record did not document a baseline care plan was completed. On 5/29/25 at 1:26 PM, the DON stated a baseline care plan was not completed for Resident #1.
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

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, the CMS SOM review, and staff interview, it was determined the facility failed to ensure re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, the CMS SOM review, and staff interview, it was determined the facility failed to ensure resident centered care plans were comprehensively written. This was true for 1 of 14 residents(Resident #34) whose care plans were reviewed. This deficient practice placed the resident at risk for harm when their care plan did not reflect the care necessary. Findings include: Resident #34 was admitted to the facility on [DATE], for care following a stroke affecting her right side, with multiple diagnoses including diabetes, high blood pressure, and chronic obstructive pulmonary disease (COPD, a chronic lung disease causing irreversible lung and airway damage making it hard to breathe). On 5/28/25 at 8:34 AM, Resident #34 stated the swelling in her right leg had increased over the past few weeks, and elevating her legs in bed helped a little bit, but not enough. Physician's orders, dated 8/27/22, documented give Lasix 40 mg (a diuretic) by mouth in the morning for edema. Physician's orders, dated 4/17/24, documented the following: - Aldactone 25 mg (a diuretic): Give 1 tablet by mouth in the morning for edema. - Lasix 40 mg: Give 40 mg by mouth one time a day for edema. - Lasix 20 mg: Give 20 mg by mouth one time a day for edema. Resident #34's care plan did not document any interventions or treatment planning related to edema. On 5/30/25 at 10:15 AM, the DON stated Resident #34's edema treatment and interventions were not care planned, and they should have been.
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, it was determined the facility failed to ensure services provided met professional s...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, it was determined the facility failed to ensure services provided met professional standards. This was true for 1 of 14 residents (Resident #43) whose physician orders were reviewed. This failure placed Resident #43 at risk for harm from overmedication when his seizure medication orders were not clarified. Findings include: Resident #43 was admitted to the facility on [DATE], with multiple diagnoses including a seizure disorder, dementia with agitation, and right sided hemiplegia (a form of paralysis to one side of the body). Resident #43's record documented the following physicians' orders for controlled substance emergency seizure medications, dated 11/22/24: - lorazepam oral concentrate 2 mg/ml, give 1 ml by mouth as needed for seizures, may repeat 1 time in 15 minutes if seizure activity continues, - midazolam nasal solution 5 mg/0.1 ml, give 1 spray in 1 nostril every 10 minutes as needed for non-intractable epilepsy (seizures that can be managed medically, either through medication, surgery, or other treatments). On 5/30/25 at 11:30 AM, the DON stated Resident #43's emergency seizure medication orders should have included directions for which medication to administer first, were not specific enough, and needed to be clarified.
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, medication error reports, and staff interview, it was determined the facility failed to ensure residents...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, medication error reports, and staff interview, it was determined the facility failed to ensure residents were protected from significant medication errors. This was true for 5 of 5 residents (#10, #23, #31, #34, and #44) reviewed for medication errors. This deficient practice created the potential for harm if residents received medications not as prescribed. Findings include: 1. Resident #10 was admitted to the facility on [DATE] with multiple diagnoses including, Alzheimer's disease, schizophrenia, and muscle spasms. Resident #10's record documented a physician's order for lorazepam 2 mg/ml, give 0.5 ml twice a day for anxiety. A Medication Error and Analysis report, dated 12/23/24, documented Resident #10 received 1 ml of lorazepam in error on the following dates and times: -On 12/21/24 at 5:00 AM -On 12/21/24 at 12:00 PM -On 12/21/24 at 7:00 PM -On 12/22/24 at 12:00 PM On 5/30/25 at 9:30 AM, the DON confirmed Resident #10 was administered the wrong dose of lorazepam on 12/21/24 and 12/22/24. 2. Resident #23 was admitted to the facility on [DATE], with multiple diagnoses including, seizures, alcohol abuse, and nicotine dependence. Resident #23's record documented a physician's order for Norco (a narcotic pain medication) 10-325 mg, one tablet twice per day for pain. A Medication Error and Analysis report, dated 3/4/25, documented a medication error occurred on 3/4/25. Resident #23 was administered another resident's Norco 5-325 mg in error. On 5/30/25 at 9:33 AM, the DON confirmed Resident #23 was administered the wrong dose of Norco on 3/4/25. 3. Resident #31 was admitted to the facility on [DATE], with multiple diagnoses including arthritis of left shoulder, anxiety, and schizophrenia. Resident #31's record documented a physician's order for Norco 5-325 mg, one tablet four times a day for pain. A Medication Error and Analysis report, dated 1/6/25, documented a medication error occurred on 1/6/25. Resident #31 was administered another resident's Norco 10-325 mg. On 5/30/25 at 9:36 AM, the DON confirmed Resident #31 was administered the wrong dose of Norco on 1/6/25. 4. Resident #34 was admitted to the facility on [DATE], with multiple diagnoses including stroke, diabetes, and arthritis of the left shoulder. Resident #34's record documented a physician's order for Norco 5-325 mg, one every 6 hours as needed for pain. A Medication Error and Analysis report dated 1/21/25, documented a medication error occurred on 1/21/25 when Resident #34 was administered another resident's Norco 10-325 mg. On 5/30/25 at 9:39 AM, the DON confirmed Resident #34 was administered the wrong dose of Norco on 1/21/25. 5. Resident #44 was admitted to the facility on [DATE], with multiple diagnoses including schizophrenia, diabetes, and opioid dependence. Resident #44's record documented a physician's order for lorazepam 1 mg, one time a day for anxiety. A Medication Error and Analysis report dated 4/9/25, documented a medication error occurred on 4/9/25. Resident #44 was administered oxycodone 10 mg and did not receive their lorazepam as prescribed. On 5/30/25 at 9:42 AM, the DON confirmed Resident #44 was administered the wrong medication on 4/9/25.
CONCERN (F) 📢 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 most or all residents

Based on observation, FDA Food Code, and staff interview, it was determined the facility failed to ensure kitchen equipment was cleaned. These deficiencies had the potential to affect the 56 residents...

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Based on observation, FDA Food Code, and staff interview, it was determined the facility failed to ensure kitchen equipment was cleaned. These deficiencies had the potential to affect the 56 residents who consumed food prepared by the facility. This placed residents at risk for potential foodborne illnesses and adverse health outcomes. Findings include: The FDA Food Code Section 4-602.12 Cooking and Baking Equipment documented food-contact surfaces of cooking equipment must be cleaned to prevent encrustation's that may impede heat transfer necessary to adequately cook food. Encrusted equipment may also serve as an insect attractant when not in use. On 5/30/25 at 10:40 AM, it was observed the baking sheet used to make honey buns had a black residue along the edge of the pan, which flaked off with minimal abrasion. Two skillets had a ring of dark, encrusted residue around the majority of the pan's interior and exterior surfaces. The dark, encrusted residue did not scrape off. On 5/30/25 at 10:55 AM, the Food Services Manager stated the pans should not have the black, encrusted coating, and they should be replaced.
Feb 2023 1 deficiency
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0940 (Tag F0940)

Could have caused harm · This affected 1 resident

Based on observation, record review, personnel record review, and staff interview, it was determined the facility failed to ensure staff were trained to provide assistance with feeding for 1 of 2 staf...

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Based on observation, record review, personnel record review, and staff interview, it was determined the facility failed to ensure staff were trained to provide assistance with feeding for 1 of 2 staff (Staff A) who were observed during meals. The lack of training had the potential for poor clinical outcomes to residents including choking and aspiration. Findings include: On 2/15/23 at approximately 12:30 PM, Staff A was observed sitting at a table in the middle of the common area seated next to Resident #8 in the behavioral unit. Staff A was assisting with feeding Resident #8. Later the same day at 5:45 PM, Staff A was again observed sitting at the same table in the common area assisting with feeding Resident #8. On 2/16/23 at 9:15 AM, Staff A was observed sitting at a table in the middle of the common area seated next to Resident #8 in the behavioral unit. Staff A was assisting with feeding Resident #8. During an interview on 2/16/23 at 11:35 AM, Staff A stated he was a Visual Aide. He stated he was assigned to 4 residents. Staff A stated he pays attention to those 4 residents to ensure they are dressed and out of bed, prevent potential falls, assisting with feeding, and intervening from potential negative interactions between residents if necessary. A request was made for the job description of Visual Aides and Staff A's training and education. On 2/17/23 at 10:00 AM, the job description was received and stated Visual Aides were to monitor and redirect assigned residents from peers, engage them in conversation and activities, and monitor for wandering. The job description also stated if the resident required assistance with toileting or there was a potential for harm to notify co-workers. The job description did not include assistance with feeding the residents. Staff A's training and education records, received on 2/17/23 at 8:30 AM, did not include documentation of competencies and training for assistance with feeding residents. During an interview on 2/17/23 at 10:00 AM, the Administrator stated Staff A should not be assisting residents with feeding as he had not been trained. Staff A was not trained and verified as competent to assist in feeding Resident #8.
May 2022 14 deficiencies 3 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Quality of Care (Tag F0684)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, and staff interview, it was determined the facility failed to ensure professional standar...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, and staff interview, it was determined the facility failed to ensure professional standards of practice were followed for 7 of 13 residents (#6, #13, #26, #35, #44, #48, and #51) whose records were reviewed for quality of care. Specifically: - Resident #35 suffered harm when she sustained a hip fracture with pain after a fall and the fracture was not diagnosed until 10 days after the fall. - Resident #48 and #51 were at risk for undetected injury and neurological changes when fall assessments and neurological assessments were not completed after falls. - Resident #44 was at risk for undetected injury when fall assessments were not completed after falls. - Resident #13 was at risk for increased psychiatric symptoms related to missed doses of her antipsychotic medication. - Resident #51 was at risk for abnormally high or low blood sugar when his insulin was administered per physician order. - Resident #26 was at risk for abnormally low blood pressure when his blood pressure medication was not administered per physician ordered parameters. - Resident #6 was at risk for constipation or fecal impaction when physician orders for bowel care were not followed. Findings include: The facility's policy for Assessing Falls and Their Causes, revised March 2018, stated the assessment procedure after a fall included identifying the cause of a fall and fall risk within twenty-four hours and performing a post-fall evaluation. The policy further stated a Fall Risk Assessment was required when a resident fell. The facility's policy for Neurological Assessment, revised October 2010, stated a neurological assessment was completed upon physician order, following an unwitnessed fall or a fall with a suspected head injury, or when indicated by the resident's condition. The policy included a required assessment schedule as follows: - Every 15 minutes x 1 hour. - Every 30 minutes x 2 hours. - Every hour x 5 hours. - Every 8 hours x 16 hours. The facility's Fall Clinical Protocol policy, revised 3/2018, stated nursing staff monitored the neurological status of the resident if the fall was unwitnessed or if a resident hit his or her head. Staff followed up until the resident was stable and delayed complications such as late fracture, was ruled out. The policy stated delayed complications could occur within hours, days or even weeks after a fall. These policies were not followed. 1. Resident #35 was admitted to the facility on [DATE], and readmitted [DATE], with multiple diagnoses including left hip fracture, dementia, and anxiety disorder. Resident #35's quarterly MDS assessment, dated 2/9/22, documented she was severely cognitively impaired. The facility did not ensure timely treatment for Resident #35's fractured hip as follows: A progress note, dated 3/8/22 at 4:55 PM, documented Resident #35 fell as a CNA was entering her room. A nurse then entered the room and saw Resident #35 lying on the floor, crying. Resident #35 was unable to state what happened or if she was in pain. Staff used a blanket to lift Resident #35 into her Comfort Chair. Neurological checks were initiated, and the PA was notified. A progress note, dated 3/8/22 at 5:56 PM, documented the PA ordered one dose of Morphine for pain from Resident #35's fall. A progress note, dated 3/10/22 at 6:48 PM, documented Resident #35 appeared to be in pain and she was yelling and screaming. A progress note, dated 3/11/22 at 6:47 AM, documented Resident #35 had signs and symptoms of increased pain to her left hip and right upper arm. The note documented Resident #35 refused cares and screamed louder with all cares. She received two doses of Morphine Sulfate during the previous night shift. A PA note, dated 3/11/22, documented Resident #35 needed a refill of her pain medication, and ordered Morphine every two hours for pain, as needed. A progress note, dated 3/11/22 at 3:32 PM, documented Resident #35 had no latent injuries noted from her recent fall. The note documented she received Tylenol for her pain. A progress note, dated 3/12/22 at 4:30 AM, documented Resident #35 had signs and symptoms of increased pain to her left hip and right upper arm. The note documented Resident #35 refused care, turning and repositioning, and screamed louder with all cares. The note documented Resident #35 was medicated with four doses of Morphine during the previous night. A progress note, dated 3/12/22 at 5:03 PM, documented Resident #35 had no latent injuries from her fall and she received Tylenol for her pain. The note documented Resident #35 was displaying increased anxiety and was agitated throughout the shift. A progress note, dated 3/13/22 at 4:09 AM, documented Resident #35 yelled and screamed in agony with cares. The note documented Morphine was not covering her extreme pain symptoms which were documented as 8 - 10 on a 1 - 10 pain scale (a measure of pain severity, with 0 meaning no pain and 10 being the most extreme pain). The note further documented Resident #35 was screaming for an hour or two, despite being medicated, and the physician was notified. A progress note, dated 3/13/22 at 4:37 PM, documented Resident #35 had extreme pain between 8 and 10. Staff turned Resident #35 every two hours, and determined it was painful for her. A progress note, dated 3/14/22 at 1:11 PM, documented Resident #35 had been medicated with Morphine at 6:00 AM and 9:00 AM for pain and was yelling out and crying. An NP note, dated 3/14/22, documented Resident #35 had increased pain and required multiple doses of Morphine for pain control. The note documented nurses were requesting increased pain medication for Resident #35. The note documented Resident #35's left leg was shortened and externally rotated, and Resident #35 was protecting her left leg. The note further documented Resident #35 was able to point to her left hip when asked where she was hurting. The NP ordered an x-ray of Resident #35's left hip related to her fall on 3/8/22. A progress note, dated 3/15/22 at 3:44 AM, documented Resident #35 was in pain during the night shift and required several doses of morphine. The note documented the NP examined Resident #35 and determined Resident #35 needed to have an x-ray of her left hip. A progress note, dated 3/15/22 at 10:29 AM, documented Resident #35 would have an x-ray of her hip the following day. A progress note, dated 3/16/22 at 1:46 AM, documented Resident #35 tolerated an increase of Morphine, which controlled her pain for longer periods of time. A progress note, dated 3/16/22 at 3:27 PM, documented Resident #35 had her pain controlled with Tylenol and nursing staff did not need to use Morphine for her pain. The note documented an x-ray was to be taken the following day. A progress note, dated 3/18/22 at 1:52 AM, documented Resident #35 was medicated with some relief of pain in her left hip. The note documented Resident #35 screamed in agony with cares provided by staff. The note stated the x-ray report documented Resident #35 had a left hip fracture which caused her leg to turn inward. Messages were left for the facility Administrator, ADON, Resident #35's PA, and Resident #35's representative, notifying them of the fracture. A progress note, dated 3/18/22 at 2:20 AM, documented Resident #35's representative returned the facility's phone call and was informed of Resident #35's hip fracture related to the fall on 3/8/22, 10 days after the fall. A progress note, dated 3/18/22, documented the NP examined Resident #35 and her x-ray report and ordered transport for Resident #35 to the emergency room for further treatment. On 5/25/22 at 10:00 AM, the DON stated on initial examination it did not appear Resident #35 sustained injuries from her fall on 3/8/22. The DON stated Resident #35 was non-verbal and often cried out when cares were performed, making it difficult to assess the true nature of her pain. The DON stated Resident #35 was assessed every morning and it was not apparent she had a fracture. The DON stated staff were to notify her if Resident #35 had a change in condition or continued to be in severe pain. Resident #35 was harmed when she fell and sustained a hip fracture with increasing pain and did not receive treatment for the fracture until 10 days after the fall. 2. Resident #51 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including Type 2 Diabetes Mellitus with diabetic chronic kidney disease, low back pain, and hemiplegia and hemiparesis (weakness and paralysis on one side of the body) following a stroke. Resident #51's Quarterly MDS assessment, dated 5/2/22, documented he was mildly cognitively impaired. The facility did not ensure Fall Risk Assessments or Neurological Assessment were completed for Resident #51 as follows: - An I&A report, dated 10/2/21, documented Resident #51 had an unwitnessed fall at 2:00 AM. There was no Fall Risk Assessment documented in Resident #51's record after the fall. - An I&A report, dated 11/22/21, documented Resident #51 had an unwitnessed fall at 10:10 PM. There was no Fall Risk Assessment or Neurological Assessment documented in Resident #51's record after the fall. - An I&A report, dated 1/7/22, documented Resident #51 had an unwitnessed fall at 12:15 PM. There were no Neurological Assessment documented in Resident #51's record after the fall. - An I&A report, dated 1/16/22, documented Resident #51 had an unwitnessed fall at 9:54 AM. There was no Fall Risk Assessment or Neurological Assessment documented in Resident #51's record after the fall. - An I&A report, dated 1/17/22, documented Resident #51 had at 2:00 AM. There was no Neurological Assessment documented in Resident #51's record after the fall. - An I&A report, dated 5/11/22, documented Resident #51 had an unwitnessed fall at 11:50 PM. There was no Neurological Assessment documented in Resident #51's record after the fall. On 5/27/22 at 10:45 AM, the DON stated Resident #51 did not have Fall Risk Assessments or Neurological checks completed for his falls as required by their policies. 3. Resident #44 was admitted to the facility on [DATE] and readmitted on [DATE], with multiple diagnoses including right thigh muscle atrophy (a condition in which muscles shrink and cause weakness) and dementia. The facility did not ensure a Fall Risk Assessments was completed for Resident #44 as follows: - An I&A report, dated 7/11/21 at 6:05 AM, documented staff heard a loud thump and found Resident #44 sitting on the floor between the wheelchair and his bedside. Resident #44 said he slipped when coming back from the bathroom and fell. A nurse's note, dated 7/11/21 at 6:05 AM, documented that Resident #44 was observed in pain, and his left knee was swelling. Resident #44 was sent to the hospital for evaluation at 7:15 AM. A hospital Discharge summary, dated [DATE], documented Resident #44 was admitted to the hospital on [DATE] with a left femur lateral condyle (on the end of the thigh bone near the knee) fracture. He had an open reduction and internal fixation surgery for the fracture on 7/13/21 and discharged from the hospital on 7/14/21. A progress note, dated 7/15/21 at 3:53 PM, documented that Resident #44 returned from the hospital on 7/14/21. Resident #44's record did not include a Fall Risk Assessment after his fall on 7/11/21 after returning to the facility. - An I&A report, dated 9/19/21 at 7:33 AM, documented staff was alerted by Resident #44's roommate that he needed assistance. The staff found Resident #44 sitting on the floor in his room on his buttocks with his legs extended. Resident #44 said he was trying to get into his wheelchair and did not make it. There was no Fall Risk Assessment documented in Resident #44's record after his fall. On 5/26/22 at 1:05 PM, the clinical resources nurse said the Fall Risk Assessment was not completed for Resident #44's fall incidents on 7/11/21 and 9/19/21, and it should be completed within 24 hours after the fall or upon readmission. 4. Resident #48 was admitted to the facility on [DATE] and readmitted on [DATE], with multiple diagnoses including diabetes, dyskinesia (involuntary muscle movements), schizophrenia (a mental disorder characterized by continuous or relapsing episodes in which people have a disconnection from reality), and moderate intellectual disabilities. Resident #48's I&A reports, from 2/2021 to 4/2022, documented he had nine falls in approximately 14 months. There were no Fall Risk Assessments documented in Resident #48's record after the nine falls on 7/7/21, 2/18/21, 7/29/21, 10/5/21, 12/10/21, 3/20/22, and 4/15/22. Resident #48's I&A report documented he had two unwitnessed falls on 7/29/21 and 3/20/22. There was no Neurological Assessment documented in Resident #48's record after the two unwitnessed falls. On 5/25/22 at 3:15 PM, the DON said Resident #48's Fall Risk Assessments were not being completed after each of the nine falls, and they should be completed within 24 hours after the fall. On 5/25/22 at 3:15 PM, The DON said per policy, a neurological assessment should be performed after each unwitnessed fall. She said Neurological Assessments were not completed after Resident #48's unwitnessed falls on 7/29/22 and 3/20/22. 5. Resident #13 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including hemiplegia and hemiparesis (paralysis on one side of the body), schizoaffective disorder (a condition where symptoms of both psychotic and mood disorders are present together during one episode, or within a two-week period of each other), and anxiety disorder. The facility's policy for Administering Medications, revised 4/2019, stated medications were administered in accordance with prescribed orders, including any required time frame. Medication administration times were determined by resident need and benefit, not staff convenience, including enhancing optimal therapeutic effort of the medication, preventing potential medication or food preferences, or honoring resident choices and preferences. Medications were administered within one hour of their prescribed time. This policy was not followed. Resident #13's quarterly MDS assessment, dated 3/8/22, documented she was mildly cognitively impaired. A physician's order, dated 3/18/22, documented to administer Risperdal Consta suspension (medication to treat a mental disorder) intramuscularly to Resident #13 one time a day every 14 days related to schizoaffective disorder. Resident #13's MAR did not document Risperdal Consta was administered on 5/6/22 or 5/20/22. On 5/26/22 at 4:45 PM, the DON stated there was no documentation in Resident #13's MAR or in the nursing notes to determine whether or not Resident #13 received her Risperdal Consta as ordered. The facility did not administer Resident #13's Risperdal Consta as ordered by the physician. 6. Resident #51 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including Type 2 Diabetes Mellitus with diabetic chronic kidney disease, low back pain, and hemiplegia and hemiparesis (weakness and paralysis on one side of the body) following a stroke. The Mayo clinic website, accessed on 6/3/22, stated, Blood sugar that's either too high or too low for too long may cause various serious conditions, all of which can lead to a diabetic coma. The facility's policy for Administering Medications, revised 4/2019, stated medications were administered in accordance with prescribed orders, including any required time frame. Medication administration times were determined by resident need and benefit, not staff convenience, including enhancing optimal therapeutic effort of the medication, preventing potential medication or food preferences, or honoring resident choices and preferences. Medications were administered within one hour of their prescribed time. This policy was not followed. A physician's order, dated 1/18/22, documented Resident #51 was to receive Insulin Glargine (long acting insulin), 10 units subcutaneously (injection under the skin) one time a day for diabetes mellitus. The medication was ordered to be given at 7:00 AM. Resident #51's insulin glargine was not documented as given as ordered or within 1 hour per the facility policy, as follows: - Resident #51's insulin glargine was administered on 3/1/22 at 3:33 PM, greater than 8 hours from the time it was scheduled. - Resident #51's insulin glargine was administered on 3/10/22 at 3:28 PM, greater than 8 hours from the time it was scheduled. - Resident #51's insulin glargine was administered on 3/25/22 at 1:15 PM, greater than 6 hours from the time it was scheduled. - Resident #51's insulin glargine was administered on 5/15/22 at 12:11 PM, greater than 5 hours from the time it was scheduled. On 5/26/22 at 4:45 PM, the DON stated Resident #51's insulin glargine was administered late on 3/1/22, 3/10/22, 3/25/22 and 5/15/22. The facility did not administer Resident #51's insulin glargine as ordered by the physician or facility policy. 7. Resident #26 was admitted to the facility on [DATE], with multiple diagnoses including hypertension (high blood pressure). A physician's order, dated 1/19/22, documented Resident #26 was to receive metoprolol succinate (medication to lower blood pressure) ER (extended release) 25 mg, one time a day for hypertension and staff were directed to hold the medication if his pulse rate was less than 60 or if his systolic blood pressure (top number of blood pressure reading) was less than 110 mmHg (millimeters of mercury). Resident #26's May 2022 MAR, documented his systolic blood pressure was less than 110 mmHg on the following dates: -5/6/22: blood pressure was 102/60 -5/10/22: blood pressure was 101/63 -5/13/22: blood pressure was 101/59 Resident #26's May 2022 MAR, documented he received 25 mg of metoprolol, on 5/6/22, 5/10/22, and 5/13/22. On 5/25/22 at 10:32 AM, the DON stated Resident #26's metoprolol should have been withheld on the days when his systolic blood pressure was less than 110 mmHg. The facility did not follow Resident #26's physician ordered parameters when administering his blood pressure medication. 8. Resident #6 was admitted to the facility on [DATE], discharged to the hospital on 5/11/22, and readmitted on [DATE], with multiple diagnoses including schizophrenia (a mental disorder characterized by continuous or relapsing episodes in which people have a disconnection from reality), and retention of urine (difficulty urinating and completely emptying the bladder.) Resident #6's physician order included as needed bowel management orders as follows: - Day 2 no BM (bowel movement): Encourage fluids; licensed nurse to offer prunes, prune juice, or 2 tablespoons of BAP (a constipation recipe with a mix of bran, applesauce, and prune juice) by mouth from dietary. Administer Senokot (laxative and stool softener) 8.6 mg, one tablet by mouth BID (twice a day). Report any liquid stools with no formed BM to the physician as needed. Document the results of Senokot (color, odor, blood, soft, hard, large or small amounts, if gas was expelled,) as applicable, how the resident tolerates the procedure, if the Resident refuses the procedure, and why. Order start date 6/11/18. - Day 3 no BM: Encourage fluids, offer prune juice or 2 tablespoons of BAP by mouth, BID from dietary. Administer Senokot 8.6 mg one tablet by mouth BID and Glycolax (laxative) 17 gm (gram) in 8 oz (ounce) fluid by mouth BID. Report any liquid stools with no formed BM to the physician as needed for constipation. Document the results of Senokot & Glycolax (color, odor, blood, soft, hard, large, or small amounts, if gas was expelled,) as applicable, how the resident tolerates the procedure, if the resident refuses the procedure, and why. Order start date 6/11/18. - Day 4 no BM: Encourage fluids; licensed nurse to offer prunes, prune juice, or 2 tablespoons BAP by mouth BID from dietary. Administer Senokot 8.6 mg one tablet by mouth BID, Glycolax 17 gm by mouth BID, Lactulose (synthetic sugar used to treat constipation) 30 cc (cubic centimeter) by mouth BID, and Dulcolax suppository 10 mg per rectal early in the morning. If there is no BM by noon of day 4, notify the physician for further instructions. Report any liquid stools with no formed BM to the physician as needed for constipation. Document the results of Senokot, Glycolax, Lactulose & Dulcolax (stimulates bowel movement) suppository (color, odor, blood, soft, hard, large, or small amounts, if gas was expelled,) as applicable, how the resident tolerates the procedure, if the resident refuses, and why. Order start date 6/11/18. - Day 5 no BM: Continue to offer prunes, prune juice, or BAP 2 tablespoons by mouth BID, Senokot 8.6 mg by mouth BID, Glycolax 17 gm in 8 oz fluid BID, Lactulose 30 cc by mouth BID. If there is no BM, the licensed nurse will complete the assessment, listen to bowel tones and check abdominal distention, and check the rectal vault per nursing standards. If there is no BM by 2 PM on Day 5, notify the physician or further orders as needed for constipation. Document the results of Senokot, Glycolax, Lactulose, and Dulcolax suppository (color, odor, blood, soft, hard, large, or small amounts, if gas was expelled,) as applicable. How the resident tolerates the procedure, if the resident refuses, and why. Order start date 6/11/18. An ADL report for May 2022, documented Resident #6's BM as follows: - One normal medium BM on 5/3/22 and no BM for 7 days from 5/4/22 to 5/10/22. - One normal large BM on 5/17/22 and no BM for 8 days from 5/18/22 to 5/26/22. Resident #6's MAR for May 2022 did not include documentation bowel care was administered as ordered. On 5/26/22 at 5:00 PM, the DON reviewed Resident #6's MAR and record and said Resident #6's bowel management orders were not being administered and documented for May 2022. The DON said Resident #6's last BM was on 5/17/22, and she had no BM until today, 5/26/22. The DON said if Resident #6 did not have BM later today, it would be the 9th day. The DON said the nurse was to follow the bowel management order and notify the physician if the resident had no BM on the fourth day and to receive new orders.
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 record review and staff interview, it was determined the facility failed to ensure a resident received appropriate care...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, it was determined the facility failed to ensure a resident received appropriate care to prevent and treat a pressure ulcer. This was true for 1 of 2 residents (Resident #22) reviewed for wound care. This failure resulted in harm when Resident #22 developed an abrasion on his right trochanter (upper end of the thigh bone that is connected to the hip bone) which became an unstageable pressure ulcer. Findings include: The National Pressure Injury Advisory Panel website, accessed on 6/2/22, defined pressure injury as a localized damage to the skin and underlying soft tissue usually over a bony prominence or related to a medical or other device. The injury occurs as a result of intense and/or prolonged pressure or pressure in combination with shear (friction to the skin causing it to separate from the bottom layer of skin). Stages of pressure injury are as follows: Stage 1- Intact skin with localized area of non-blanchable erythema, which may appear differently in darkly pigmented skin. Presence of blanchable erythema or changes in sensation, temperature, or firmness may precede visual changes. Color changes do not include purple or maroon discoloration these may indicate deep tissue pressure injury. Stage 2- Partial thickness skin loss with exposed dermis. The wound bed is viable, pick or red, moist and may also present as an intact or ruptured serum-filled blister. Adipose (fat) is not visible and deeper tissues are not visible. Granulation tissue, slough (non-viable yellow, tan, gray, green, or brown tissue) and eschar (dead or weakened tissue that is hard or soft in texture - usually black, brown, or tan in color) are not present. These injuries commonly result from adverse microclimate and shear in the skin over the pelvis and shear in the heel. Stage 3- Full thickness loss of skin, in which adipose is visible in the ulcer and granulation tissue and epibole (rolled wound edges) are often present. Slough and/or eschar may be visible. The depth of tissue damage varies by anatomical location; areas of significant adiposity can develop deep wounds. Undermining and tunneling may occur. Fascia, muscle, tendon, ligament, cartilage and/or bone are not exposed. If slough or eschar obscures the extent of tissue loss this is an Unstageable Pressure Injury. Stage 4- Full thickness skin and tissue loss with exposed or directly palpable fascia, muscle, tendon, ligament, cartilage, or bone in the ulcer. Slough and/or eschar may be visible. Epibole (rolled edges), undermining and/or tunneling often occur. Depth varies by anatomical location. If slough or eschar obscures the extent of tissue loss this in an Unstageable Pressure Injury. Unstageable Pressure Injury: Full-thickness skin and tissue loss in which the extent of tissue damage within the ulcer cannot be confirmed because it is obscured by slough or eschar. If slough or eschar is removed, a Stage 3 or Stage 4 pressure injury will be revealed. Stable eschar (i.e. dry, adherent, intact without erythema or fluctuance) on the heel or ischemic limb should not be softened or removed. Deep Tissue Pressure Injury: Intact or non-intact skin with localized area of persistent non-blanchable deep red, maroon, purple discoloration, or epidermal separation revealing a dark wound bed or blood-filled blister. Pain and temperature change often precede skin color changes. Discoloration may appear differently in darkly pigmented skin. This injury results from intense and/or prolonged pressure and shear forces at the bone-muscle interface. Resident #22 was admitted to the facility on [DATE], with multiple diagnoses including Alzheimer's disease, high blood pressure, muscle weakness, and abnormalities of gait and mobility. An annual MDS assessment, dated 3/15/22, documented Resident #22 was severely cognitively impaired, at risk of developing pressure ulcers, and no pressure ulcers were present. Resident #22's care plan, initiated on 3/24/22, documented he was at risk for skin impairment related to his history of incontinence of bowel and bladder and due to diagnosis of Alzheimer's disease. The care plan directed staff to provide treatments as ordered, perform weekly skin assessments, check his nails to ensure they were trimmed and filed with no jagged edges, notify the provider if new areas were noted/seen, apply protective cream after each incontinent episode, and assist him with clothing changes. Weekly Skin Assessments, dated 3/7/22, 3/10/22, 3/15/22, and 3/21/22, documented Resident #22 had no alteration to skin integrity and no new skin issues were noted during a 24-hour period. A nurse practitioner's note, dated 3/21/22, documented Resident #22 had a wound to his right trochanter (bony top of the thigh bone in the hip area). The nurse practitioner directed staff to cleanse Resident #22's wound to his right hip every three days and PRN with a wound cleanser, pat dry, cover with Tegaderm (a transparent film dressing), and monitor him for signs and symptoms of infection and wound healing. A Nurse's Note, dated 3/23/22 at 1:13 PM, documented Resident #22 had a lesion (wound or injury) present to his right hip that was blanchable (the reddened area turns white when pressed on) throughout the reddened area and the top layer of the skin was missing. The note documented the reddened area matched the size and shape of the incontinence brief adhesive tab. The Nurse's Note documented when the adhesive tab was removed it took off the top layer of Resident #22's skin. The note also documented it was on the side Resident #22 preferred to lay on. The note further documented orders to clean the wound every three days with wound cleanser, pat dry with gauze, and cover the wound with Allevyn (foam dressing). Resident #22's care plan was not updated to include the lesion/wound to his right hip. A Weekly Skin Assessment, dated 3/31/22, documented Resident #22 had no alteration to skin integrity and no new skin issues were noted during a 24-hour period. A nurse practitioner's progress note, dated 4/11/22, documented Resident #22 had a 4x4 [sic] wound to his right trochanter with necrotic eschar [dead tissue] covering and surrounding erythema [redness]. The nurse practitioner documented Resident #22 would benefit from a wound specialist. The nurse practitioner directed staff to refer Resident #22 to a wound care specialist, cleanse his wound every 72 hours and PRN with wound cleanser, pat dry, apply Medi-Honey (helps create a moist wound healing environment which aids in debridement and removal of necrotic tissue), cover with Allevyn dressing, off-load Resident #22's right hip, and turn him every two hours. A physician note, dated 4/13/22 at 8:10 AM, documented an order to administer Bactrim DS (antibiotic), one tablet two times a day for 14 days to treat the wound on Resident #22's right hip. A physician assistant's note, dated 4/15/22, documented Resident #22 had severe anxiety and significant behaviors. The note stated Resident #22 would be difficult to transfer out of facility for cares, and will try to treat in house first. The physician assistant discussed Resident #22's right hip wound with the staff and documented will try to tx [treat] here first with Santyl [medicine that removes dead tissue from wounds so they can start to heal] if it does not improve will have to send out to wound care. A Nurse's Note, dated 4/22/22 at 10:32 AM, documented Resident #22's wound had changed to eschar and it was breaking-up and pink tissue was remaining, and there was no drainage. The April 2022 MAR documented Resident #22 completed his Bactrim on 4/27/22. A Nurse's Note, dated 4/30/22 at 2:23 PM, documented Resident #22's wound to his right hip was cleansed with normal saline, patted dry, Santyl was applied with a sterile cotton tipped swab, and the wound was covered with an adhesive border gauze. The note documented the wound continued to have a moderate amount of yellow/green drainage and the bandage was completely saturated. The Nurse's Note further documented Resident #22's wound had some redness to the peri-wound (tissue surrounding a wound) and he might require more frequent dressing changes due to increased drainage. A Nurse's Note, dated 5/3/22 at 4:49 PM, documented Resident #22's wound dressing was changed, and the top of the wound was black. The note documented there was redness to the outer border and no drainage was noted. Resident #22 stated the wound was tender and he appeared to feel discomfort during wound cleansing. A care plan, initiated on 5/3/22, documented Resident #22 had an unstageable area to his right hip and staff were to assess him for signs and symptoms of pain with wound care, schedule/administer analgesic (pain reliever) prior to treatment, communicate with the physician if area was not healing or worsened, perform wound care as ordered, encourage Resident #22 not to sleep on his right hip, and perform skin checks weekly. The care plan was updated five weeks after it was noted in Resident #22's record. A Weekly Wound Observation Tool, dated 5/6/22 at 12:11 PM, documented Resident #22 had an unstageable open area to his right hip that measured 5.25 cm x 1.6 cm, with black eschar that was sluffing off (shedding) and there was more pink tissue present. The wound had no drainage or odor, infection was not suspected, and it was being treated with Santyl and a hydrocolloid dressing (waterproof). A Nurse's Note, dated 5/11/22 at 4:21 PM, documented Resident #22's wound was very odorous with signs and symptoms of infection present. The note documented sluff was present to the outer bed of the wound with redness on the peri-wound. The note also documented the wound was very painful for Resident #22 and Resident #22's provider would be notified. A Weekly Wound Observation Tool, dated 5/13/22 at 10:36 AM, documented Resident #22 had an acquired unstageable open area to his right hip that measured 6.5 cm x 4.25 cm, with 70% eschar that was pulling away from the wound edges, the peri-wound was pink. Resident #22's wound had no odor or drainage, and was treated with Medi-Honey and covered with a hydrocolloid dressing. A physician assistant's note, dated 5/13/22, documented Resident #22 was seen due to staff concerns the wound looked worse, with increased drainage and smell. The note documented Resident #22 was on Bactrim prior and it seemed to help. The physician assistant assessed the wound as cellulitis and ordered Bactrim DS for 10 days and try Medi-Honey, if does not improve consider wound care next. Resident #22's wound had increased in size by 1.25 cm x 2.65 cm in 7 days. There was no documentation he was referred to a wound clinic. A nurse practitioner's note, dated 5/16/22, documented Resident #22 had increased pain to his right hip wound and was on a low dose Duragesic (skin patch containing fentanyl, an opioid/narcotic pain medication) pain patch. The note documented Resident #22 would benefit from additional pain control. Resident #22 was prescribed Tramadol (an opioid/narcotic pain medication) 50 mg, one tablet two times a day. A Weekly Wound Observation Tool, dated 5/20/22 at 10:39 AM, documented Resident #22 had an unstageable open area to his right hip that measured 6.5. cm x 4.25 cm and was treated with Santyl and a hydrocolloid dressing. The note documented the wound had no drainage or odor, and infection was not suspected. A physician's assistant order, dated 5/23/22 at 10:09 AM, documented to refer Resident #22 to the wound clinic for his right hip wound. This was ordered 22 days after it was first ordered by the nurse practitioner on 4/11/22 and nine weeks after the wound was first identified. A Nurse's Note, dated 5/23/22 at 12:01 PM, documented Resident #22 had complaints about his wound and the wound was slightly odorous, with blackened content. The note documented they would continue to monitor the wound. The May 2022 MAR, documented Resident #22 completed his second round of Bactrim on 5/26/22. On 5/26/22 at 3:25 PM, the DON stated Resident #22 went to a Wound Clinic that morning. The DON stated Resident #22's unstageable pressure ulcer to his right trochanter started as a small abrasion from the sticky part of his undergarment and he always laid on his right side. The DON stated staff encouraged Resident #22 to lay on his left side, but he always refused. When asked why Resident #22 was not referred to a wound care specialist as ordered by the nurse practitioner on 4/11/22, the DON stated Resident #22 was seeing a podiatrist for a lesion on his left big toe and also saw an eye specialist. The DON stated they wanted to avoid causing Resident #22 anxiety by leaving the facility so often. The DON stated she talked to the nurse practitioner who then ordered to clean and treat Resident #22's right hip wound with Santyl first. The DON stated Resident #22's wound started to peel from the side, then became unstable in the center. When asked about the Weekly Skin Assessment, dated 3/31/22, which documented Resident #22 had no alteration to skin integrity, and the Nurse's Note, dated 3/23/22, documented he had a lesion to his right trochanter, the DON stated she performed weekly wound assessments and documented them on paper. The DON provided Resident #22's paper wound assessment and the assessment did not include the date the abrasion was first identified. Resident #22 was harmed when the abrasion on his right hip deteriorated and became an unstageable pressure ulcer.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Accident Prevention (Tag F0689)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, review of I&A reports, and staff interview, it was determined the facility failed to ensu...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, review of I&A reports, and staff interview, it was determined the facility failed to ensure adequate supervision was provided to residents to prevent falls. This was true for 1 of 5 residents (Resident #47) reviewed for falls. This resulted in harm to Resident #47 when he sustained bruises and a fracture to his finger. Findings include: The facility's policy Fall and Fall Risk Managing, revised 3/2018, documented staff completed a fall risk assessment and enter it into the resident's medical record. Staff would identify the cause of the resident's fall and document interventions related to a resident's specific risks and causes, try to prevent the resident from falling, and try to minimize complications from falling. Staff were to implement a resident-centered fall prevention plan to reduce specific factors of falls for each resident at risk and would monitor and document each resident's response to interventions. If a resident continued to fall, staff would re-evaluate the situation and determine if interventions were appropriate or needed to be changed. This policy was not followed. Resident #47 was admitted to the facility on [DATE] and readmitted on [DATE], with multiple diagnoses including dementia with behavioral disturbance, altered mental status, bipolar disorder (a disorder associated with episodes of mood swings ranging from depressive lows to manic highs) and epilepsy (a neurological disorder that causes seizures or unusual sensations and behaviors and sometimes loss of awareness). A quarterly MDS assessment, dated 5/5/22, documented Resident #47 had severe cognitive impairment, required extensive assistance of one to two person with ADLs and set-up for eating. The MDS also documented: - He was not steady with moving from a seated to standing position but able to stabilize with human assistance. - He was not steady with walking, turning around and facing the opposite direction while walking and moving on and off the toilet but able to stabilize with human assistance. - He had two or more falls since admission. Resident #47's care plan documented he was at risk for falls related to his diagnosis of unsteady gait and epilepsy. Interventions included the following: - Encourage him to sit-up and stand slowly, initiated on 12/20/16 and revised on 7/20/18. - Fall risk assessment after any fall, quarterly and PRN, initiated on 3/9/18. - Encourage adequate hours of sleep at night and rest periods during the day, initiated on 6/5/19. - Encourage appropriate nonskid footwear when ambulating, initiated on 6/14/19. - Support bars were installed around his toilet related to his report of attempting to sit and missing the seat, initiated on 3/28/18 and revised on 12/6/19. - Continue to encourage to ask for assistance with cares to address fall risk/actual fall, initiated on 12/23/19. - Provide him a safe place to sit in his room. Physical Therapy(PT) to evaluate and treat him as needed. Remind and encourage him frequently to call for staff assistance, initiated on 5/10/19 and revised on 12/26/19. - Move nightlight from bedside to area by the sink due to bed being moved per his preference and nightlight would be near his head when he is trying to sleep, initiated on 5/20/19 and revised on 1/29/20. - Encourage him to sit all the way back on the chairs and not on the edge of the chair, initiated on 2/25/19 and revised on 4/6/20. - Assure his room is lit at night. He uses a night light in his room, initiated on 6/14/19 and revised on 4/6/20. - Remind him to slow down when changing positions, transferring and ambulating, initiated on 5/17/20. - Ensure he has a cold soda in the refrigerator at all times, initiated on 12/16/19 and revised 5/25/20. - Move him closer to the nursing station for higher observation, initiated on 8/18/21. - When he is in common area there is a Visual Aide to keep him in line of sight at all times, initiated on 11/12/21. - Bed should be in lowest position and locked when in bed, initiated on 11/12/21 - Be sure the call light is within reach and encourage him to use it for assistance as needed was initiated on 2/16/22. - Redirect/Assist him to the nearest bathroom if he is having sudden toileting needs, initiated on 2/16/22. Resident #47's record, documented he experienced a total of 7 falls in five months, as follows: A Fall Scene Investigation Report, dated 1/20/22 at 2:11 PM, documented Resident #47 had an unwitnessed fall. He was found on the floor in his room. Resident #47 stated he wanted to lay down after using the toilet. No injuries were noted. An Interdisciplinary Team (IDT) Review for the fall on 1/20/22, dated 1/27/22, documented the root cause of the fall was that Resident #47 had no safety awareness and he did not recognize his limitations. Resident #47 believed he was more independent that he really was. The IDT review documented Resident #47 was on 15 minute checks, and had a pressure sensitive alarm in his wheelchair. The IDT documented his interventions were appropriate. A Fall Scene Investigation Report, dated 4/29/22 at 1:00 AM, documented Resident #47 had a witnessed fall. Staff heard Resident #47 getting out of his bed unassisted and went to his room. Staff observed Resident #47 fall forward and hit his head on the nightstand which was next to his bed. He was assisted to a sitting position on his bed. An IDT review of the fall on 4/29/22, dated 5/6/22, documented the root cause of Resident #47's fall was he attempted to self-rise and ambulate. The IDT documented Resident #47 had 1:1 staff which would often cause him to have increased agitation at times. Resident #47 had been on 15 minutes checks in the past and no changes to him falling. Interventions were initiated to have Physical Therapy screen Resident #47. Resident #47 was evaluated on 5/2/22, 4 days prior to the IDT review. A Fall Scene Investigation Report, dated 4/29/22 at 10:03 PM, documented Resident #47 had an unwitnessed fall. Resident #47 was found on the floor next to his bathroom door. Loose watery stool was observed on the floor, on the back of his clothing, and in his wheelchair. Resident #47 stated he could no longer hold it and lost his balance. An IDT review of the fall on 4/29/22, dated 5/2/22, documented the root cause of Resident #47's fall was he had loose/watery stool and slipped in the bowel and fell. The IDT review stated it was an isolated incident. A Physical Therapy Evaluation and Plan of Treatment, dated 5/2/22, documented Resident #47 was willing to participate. However, his cognitive deficits negatively affected his overall progress. A Speech Therapy, progress note, dated 5/3/22, documented Resident #47 had severe dementia and required 24-hour care for ADLs and safety. The note stated Resident #47 and caregivers would benefit from identification of additional supports or aides to use as dementia progressed. A Fall Scene Investigation Report, dated 5/9/22 at 11:03 PM, documented Resident #47 had an unwitnessed fall. He was observed sitting on his buttocks on the floor in his room and leaning backwards in front of his endtable with socks in his hand. All three drawers of the endtable were open. Resident #47 appeared to be agitated and he was noted to have bleeding above his right eye with his right eye turning red and bruising and an abrasion was also noted above his left eye. Resident #47's right hand was noted to have some redness to his ring finger as well as to his chin, and right cheek. An IDT review for the 5/9/22 fall, dated 5/11/22, determined the root cause of Resident #47's fall was he was self-rising and attempted to ambulate and stand when he needed assistance for safety. Resident #47's physician was made aware and reviewed his medications and laboratory results. The physician gave an order for Resident #47 to see his neurologist. A Fall Scene Investigation Report, dated 5/10/22 at 6:10 PM, documented Resident #47 had a witnessed fall. He was seen leaning over to pick-up his cup off the floor and his wheelchair went out from under him and he fell on his coccyx. An IDT review of the fall on 5/10/22 at 6:10 PM, dated 5/11/22, determined the root cause of Resident #47's fall was his wheelchair rolled out from under him when he stood. A Fall Scene Investigation Report, dated 5/10/22 at 9:05 PM, documented Resident #47 had an unwitnessed fall. Resident #47 had been going to the double doors between the North and South areas of the building to wait for morning and meet with Social Services when staff heard a loud sound, went to the area and observed him on the floor. Resident #47 was mumbling and was noted to have difficulty formulating his words. An IDT review of the fall on 5/10/22 at 9:05 PM, dated 5/11/22, documented Resident #47 had been experiencing changes in his mental and physical functioning and they would continue to reach out to his neurologist for an appointment. A Fall Scene Investigation Report, dated 5/10/22 at 11:32 PM, documented Resident #47 had an unwitnessed fall. He was observed on the floor in his room between his bed and his door. Resident #47 was yelling help me over and over and it was difficult to understand what he was saying. An IDT review of the fall on 5/10/22 at 11:32 PM, dated 5/11/22, documented Resident #47 experienced an acute change of condition. Resident #47's medications were reviewed, and staff were trying to get him into his neurologist. Resident #47 experienced 3 falls on 5/10/22 between 9:05 PM and 11:32 PM. Resident #47's care plan was updated on 5/12/22, and directed staff to change his dresser to a plastic dresser to help prevent injuries. A Nurse's Note, dated 5/13/22 at 1:50 AM, stated Resident #47's physician gave an order for Resident #47 to start on Keppra (ant-epileptic) 500 mg twice a day, decrease his Dilantin (anti-convulsant) to 150 mg twice a day in two days and then check his Phenobarbital (anti-seizure) and Phenytoin (dilantin) levels in three weeks. Resident #47's care plan was updated on 5/13/22 and staff were directed to place an anti-roll back bars on his wheelchair. A physician's progress note, dated 5/13/22, documented Resident #47 injured his ring finger on his right hand during one of his falls. The physician documented Resident #47 had some swelling and bruising to the area and gave an order to x-ray Resident #47's right hand. A Physical Therapy discharge summary note, dated 5/18/22, documented Pt [patient] demonstrated progress initially with therapy with having decline and platue of progress d/t [due to] change in medical condition that nursing is currently treating. An X-ray report, dated 5/19/22, documented Resident #47 had an acute fracture right ring finger. A physician's order, dated 5/20/22, directed staff to buddy tape (act of bandaging a damaged or particularly fractured finger or toe together with a healthy one) Resident #47's fourth finger. On 5/23/22 at 12:22 PM, Resident #47 was observed in his room standing by the foot of his bed. Resident #47's bed was placed against the wall and in low position. There were two fall mats and a mattress next to his bed. On 5/26/22 at 2:57 PM, the DON stated she was informed every time Resident #47 had a fall. The DON stated Resident #47 used to have a 1:1 staff but he did not like to have a staff next to him he became more agitated, angry and combative. The DON stated a Visual Aide was provided to Resident #47 whenever he was in the common area. When asked the meaning of a Visual Aide, the DON stated it meant within the line of sight of the staff.The DON stated Resident #47 was moved to another room closer to the nurse's station, so he could be within the line of sight of the staff when they were in the nurse's station charting. When asked if there was a Visual Aide during the night, the DON stated the Visual Aide only worked until 8:00 PM. On 5/27/22 at 10:29 AM, the Administrator stated the 1:1 staff for Resident #47 was discontinued due to his behavior with the staff. The Administrator stated Resident #47 did not like to have 1:1 staff next to him, he became more agitated and angry when he had them, and he would yell and hit his 1:1 staff. The Administrator stated when they discontinued the 1:1 staff, Resident #47 started to talk and smiled at the other residents, and his wanting to leave the facility and hitting of the staff decreased. When asked the meaning of 1:1 staff supervision, the Administrator stated the staff should be within an arm's length of the resident. When asked about the Visual Aide, the Administrator stated the resident should be in the line of sight of the staff. When asked why Resident #47 was not provided with a Visual Aide while he was in his room since he had several falls in his room, the Administrator stated one of their interventions was moving Resident #47 to a room across the nurse's station, so the staff could easily see him when they were in the nurse's station. On 5/27/22 at 2:15 PM, the surveyor observed Resident #47 while he was in his room lying on his bed. Resident #47's bed was placed against the wall to the right side of his room as you enter, and he was not in direct view of the staff in the nurse's station. When the staff were in the nurse's station it was not possible for them to see Resident #47 directly, facing the nurse's station was the wall of Resident #47's room. Resident #47 experienced multiple falls which resulted in injury including a fractured finger.
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 policy review, record review, representative interview, and staff interview, it was determined the facility failed to e...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, representative interview, and staff interview, it was determined the facility failed to ensure residents' representatives were immediately notified when residents fell or had a change in condition. This was true for 2 of 2 residents (#35 and #48) whose records were reviewed for changes in condition. This deficient practice placed residents at risk of harm due to lack of advocacy and support from their representatives when they were unable to make decisions for themselves due to decreased health status and level of consciousness. Findings include: The facility's policy for Change in a Resident's Condition or Status, revised May 2017, documented the facility would notify the resident, his or her attending physician, and representative (sponsor) of changes in the resident's medical/mental condition or status. The policy stated the nurse should notify the resident's representative when the resident was involved in any accident or incident resulting in an injury, or if there was a significant change in the resident's physical, mental, or psychosocial status. The policy further stated notification should be made within 24 hours of the change in condition unless emergency notification was required. This policy was not followed. 1. Resident #35 was admitted to the facility on [DATE], and readmitted [DATE], with multiple diagnoses including left hip fracture, dementia, and anxiety disorder. Resident #35's quarterly MDS assessment, dated 2/9/22, documented she was severely cognitively impaired. A progress note, dated 3/8/22 at 4:55 PM, documented Resident #35 fell as a CNA was entering her room. A nurse entered the room and saw Resident #35 lying on the floor, crying. Resident #35 was unable to state what happened or if she was in pain. Staff used a blanket to lift Resident #35 into her chair. Neurological checks were initiated, and the PA was notified. Resident #35's record did not include documentation her representative was notified of her fall. A progress note, dated 3/8/22 at 5:56 PM, documented the PA ordered one dose of Morphine 0.25 mg for pain related to Resident #35's fall. A progress note, dated 3/10/22 at 6:48 PM, documented Resident #35 appeared to be in pain and she was yelling and screaming. Resident #35's record did not include documentation her representative was notified of her fall or her pain. A progress note, dated 3/11/22 at 6:47 AM, documented Resident #35 had signs and symptoms of increased pain to her left hip and right upper arm. The note documented Resident #35 refused cares and screamed with all cares. The note documented Resident #35 received two doses of Morphine during the previous night shift. Resident #35's record did not include documentation her representative was notified her pain or her refusals of care. A PA note, dated 3/11/22, documented Resident #35 needed a refill of her pain medication and ordered Morphine to be given every two hours for pain, as needed. Resident #35's record did not include documentation her representative was notified of her need for ongoing need for increased pain medication. A progress note, dated 3/11/22 at 3:32 PM, documented Resident #35 had no latent injuries noted from her recent fall and she received Tylenol for her pain. A progress note, dated 3/12/22 at 4:30 AM, documented Resident #35 had signs and symptoms of increased pain to her left hip and right upper arm. The note documented Resident #35 refused care, turning and repositioning, and screamed with all cares, and she was medicated with four doses of Morphine during the previous night. Resident #35's record did not include documentation her representative was notified of her increased pain or refusals of care. A progress note, dated 3/12/22 at 5:03 PM, documented Resident #35 had no latent injuries from her fall and she received Tylenol for pain. The note documented Resident #35 was displaying increased anxiety and was agitated throughout the shift. Resident #35's record did not include documentation her representative was notified of her pain or behavior. A progress note, dated 3/13/22 at 4:09 AM, documented Resident #35 yelled and screamed in agony with cares. The note documented Morphine was not covering her extreme pain symptoms which were documented as 8 - 10 on a 1 - 10 pain scale (a measure of pain severity, with 0 meaning no pain and 10 being the most extreme pain). The note further documented Resident #35 was screaming for an hour or two, despite being medicated, and the physician was notified. Resident #35's record did not include documentation her representative was notified of her pain, behavior or physician notification. A progress note, dated 3/13/22 at 4:37 PM, documented Resident #35 had extreme pain noted to be between 8 and 10. Staff turned Resident #35 every two hours, and determined it was painful for her. Resident #35's record did not include documentation her representative was notified of her pain. A progress note, dated 3/14/22 at 1:11 PM, documented Resident #35 was medicated with Morphine at 6:00 AM and 9:00 AM for pain, yelling out, and crying. Resident #35's record did not include documentation her representative was not notified of her increased pain and behavior. An NP note, dated 3/14/22, documented Resident #35 had increased pain and required multiple doses of Morphine for pain control. The note documented nurses were requesting increased pain medication for Resident #35. The NP's examination documented Resident #35's left leg was shortened and externally rotated, and Resident #35 was protecting her left leg. The examination also documented Resident #35 was able to point to her left hip when asked where she was hurting. The NP ordered an x-ray of Resident #35's left hip related to the fall on 3/8/22. Resident #35's record did not include documentation her representative was notified of her fall, her increased pain, the NP's physical findings, or the order for an x-ray. Resident #35's record did not include documentation her representative was notified of the date of the x-ray. A progress note, dated 3/15/22 at 10:29 AM, documented Resident #35 was to receive an x-ray of her hip the following day. Resident #35's record did not include documentation her representative was notified of the order for an x-ray. A progress note, dated 3/18/22 at 1:52 AM, documented Resident #35 was medicated with some relief of pain in her left hip. The note documented Resident #35 screamed in agony with cares provided by staff. The note stated the x-ray report documented Resident #35 had a left hip fracture which caused her leg to turn inward. Messages were left for the facility Administrator, ADON, Resident #35's PA, and Resident #35's representative, notifying them of the fracture. A progress note, dated 3/18/22 at 2:20 AM, documented Resident #35's representative returned the facility's phone call and was informed of Resident #35's hip fracture related to the fall on 3/8/22, 10 days after the fall. On 5/24/22 at 10:45 AM, Resident #35's representative stated she was not notified on 3/8/22 that Resident #35 had a fall. Resident #35's representative stated she did not know about Resident #35's fall, ongoing pain, or fracture until she was notified of Resident #35's x-ray results on 3/18/22. On 5/25/22 at 10:00 AM, the DON stated Resident #35's representative should have been notified of Resident #35's fall, and ongoing pain. 2. Resident #48 was admitted to the facility on [DATE], with multiple diagnoses including diabetes, dyskinesia (involuntary muscle movements), schizophrenia (a mental disorder characterized by continuous or relapsing episodes in which people have a disconnection from reality), and moderate intellectual disabilities. Quarterly MDS assessments, dated 5/4/21 and 2/22/22, documented Resident #48 was severely cognitively impaired. An I&A report, dated 7/29/21 at 4:44 PM, documented Resident #48 tripped on his own feet while using the handrail, and went down to the floor in the hallway while walking fast with shuffling feet. Resident #48's record did not include documentation his family or representative was notified of the fall. An I&A report, dated 4/15/22 at 11:00 AM, documented Resident #48 tripped over another resident's feet and fell while ambulating. He sustained a 2 cm by 1.5 cm skin tear to his left elbow. Resident #48's record did not include documentation his family or representative was notified of the fall. On 5/25/22 at 3:15 PM, the DON stated there was no documentation Resident #48's family or representative were notified of the falls on 7/29/21 and 4/15/22, and they should have been notified as soon as possible.
CONCERN (D)

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

Safe Environment (Tag F0584)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and staff interview, it was determined the facility failed to ensure residents were provide...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and staff interview, it was determined the facility failed to ensure residents were provided with a sanitary environment free of unpleasant odors. This was true for 1 of 14 residents (Resident #37) whose environment was observed. This deficient practice created the potential for diminished quality of life and psychosocial distress for Resident #37 when she was placed in a room with a strong odor of urine due to her roommate's lack of compliance with personal hygiene. Findings include: Resident #37 was admitted to the facility on [DATE], with multiple diagnoses including dementia with behavioral disturbance and catatonic (a psychomotor disorder that affects both speech and behavior functions) schizophrenia (characterized by significant impairments in the way reality is perceived and changes in behavior). A quarterly MDS assessment, dated 4/4/22, documented Resident #37 was severely cognitively impaired. Resident #37 and Resident #39 were roommates. On 5/23/22 at 12:14 PM, a strong odor of urine was noted outside of Resident #37 and #39's room. Resident #39 was in the room, sitting in her wheelchair and clutching several DVDs to her chest. Resident #37 was observed outside of the room and was walking back and forth between the dining room and her room. On 5/26/22 at 9:20 AM, Resident #39 was in the room, sitting in her wheelchair. A strong odor of urine was noted in the room. On 5/27/22 at 2:15 PM, CNA #2 stated Resident #39 would not allow help during pericare. CNA #2 stated she knew Resident #39 needed to be changed, but whenever she approached Resident #39, she would yell at her. CNA #2 stated she would ask another CNA to help her with Resident #39, but Resident #39 always refused to be changed. On 5/27/22 at 2:22 PM, CNA #9 stated it was difficult to provide pericare to Resident #39, especially when she had a bowel movement. CNA #9 stated they needed more than two CNAs to clean her up. CNA #9 stated Resident #39 would not allow them to touch her and she would say to them I can do it, I can do it. On 5/26/22 at 9:42 AM, the DON stated Resident #37 did not stay in her room much, except during the night at bedtime, and occasionally during the day when she would sleep in the afternoon. The DON stated Resident #37 and Resident #39 were roommates since she started working in the facility which was about a year ago. The DON stated Resident #37 did not express any concern regarding the smell of urine in their room. The DON stated she thought Resident #37 was desensitized to the room.
CONCERN (D)

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

Free from Abuse/Neglect (Tag F0600)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, review of the State Survey Agency's Long Term Care Reporting Portal, review of I&A report...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, record review, review of the State Survey Agency's Long Term Care Reporting Portal, review of I&A reports, and staff interview, it was determined the facility failed to ensure 3 of 14 residents (#26, #52, and #53) reviewed for abuse, neglect, and misappropriation. The facility failed to ensure residents were not abused by a staff member. This failure resulted in the potential for residents to be subjected to ongoing abuse and potential harm. Findings include: The facility's Abuse Prevention Program policy, dated 12/2016, stated, Our residents have the right to be free from abuse, neglect, misappropriation of resident property, and exploitation. The facility's policy, Recognizing Signs and Symptoms of Abuse/Neglect, dated 1/2011, stated the facility's administration protected residents from abuse by anyone, including facility staff and other residents. The policy defined abuse as willful infliction of injury, unreasonable confinement, intimidation, or punishment with resulting physical harm, pain, or mental anguish. These policies were not followed. 1. Resident #52 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including subdural hematoma (bleeding on the brain), Type 1 diabetes mellitus, and chronic obstructive pulmonary disease . Resident #52's initial MDS assessment, dated 11/22/21, documented Resident #52 was severely cognitively impaired. On 11/10/21 at 12:00 AM, the facility reported to the state survey agency's Long Term Care portal that Resident #52 struck at CNA #10. CNA #10 told Resident #52 if she kept hitting, CNA #10 would take her down. CNA #10 cursed at Resident #52 in front of other residents and faked a punch in the direction of Resident #52. It was reported that LPN #4 began yelling because he did not want to deal with Resident #52, who was a new admission. LPN #4 yelled in front of staff and other residents, stating Resident #52 needed to be kicked out. LPN #4 then wrapped his arms around Resident #52 and walked her to her room using more than necessary force. On 5/25/22 at 2:15 PM, the DON stated she received a report from staff members on 11/10/21, regarding concerns that happened the evening of 11/9/21. The DON stated she reviewed the video camera footage and began her investigation. The DON stated she immediately suspended CNA #10 and LPN #4 pending the outcome of her investigation. The DON's investigation included reviewing the video camera footage and interviewing the staff members involved in the incidents. The DON stated she interviewed CNA #10, who admitted she yelled at Resident #52 and used profanity in front of other residents. The DON stated CNA #10 was terminated from her employment. The DON stated she reviewed the camera footage and interviewed LPN #4. LPN #4 agreed he was too rough with Resident #52 when he wrapped his arms around her and walked her to her room. LPN #4 stated he was wrong for yelling in front of residents and staff, and stating Resident #52 needed to leave the facility. The DON stated LPN #4 was terminated from his employment. 2. Resident #53 was admitted to the facility on [DATE], with multiple diagnoses including dementia, anxiety disorder, and major depressive disorder. A quarterly MDS assessment, dated 2/8/22, documented Resident #53 was severely cognitively impaired. An I&A report, dated 9/7/21 at 9:00 AM, documented the DM heard a resident calling himself an A-Hole. When the DM asked the resident why he was calling himself an A-Hole, the resident said RN #3 called him an A Hole. RN #3 then left the area to assist another resident to their room. The DM sat down with Resident #53 and calmed him down. The report stated RN #3 called Resident #53 an A-Hole because he would not sit down when she asked him to sit down. The report stated Resident #53 said RN #3 did not like him and called him names. The facility's investigation report, dated 9/7/21, documented RN #3 was interviewed over the phone by the Administrator. RN #3 stated she did not call Resident #53 an A-Hole but told him to stop being an A-Hole. The Administrator explained to RN #3 that due to the occurrence of verbal abuse toward Resident #53, she would be terminated from her employment. On 5/25/22 at 9:02 AM, the DM stated she was coming back to the kitchen when she heard RN #3 call Resident #53 an Ass Hole. The DM stated she reported the incident to the Administrator during their morning meeting. The DM stated RN #3 was no longer employed in the facility. On 5/25/22 at 9:18 AM, the Administrator stated she was the Abuse Coordinator and stated all new employees were given abuse training prior to starting work in the facility. The Administrator said abuse was discussed during staff meetings on the 10th of every month and as needed. The Administrator stated the DM reported to her that RN #3 called Resident #53 an A-Hole. The Administrator stated when she called RN #3, RN #3 stated she was frustrated. The Administrator stated RN #3 was terminated from employment. 3. Resident #26 was admitted to the facility on [DATE], with multiple diagnoses including emphysema (a lung condition wherein the air sacs in the lungs are damaged causing shortness of breath), heart failure, and anxiety disorder. A significant change MDS assessment, dated 3/30/22, documented Resident #26 was cognitively intact. An I&A report, dated 1/25/22 at 8:45 PM, documented a CNA was walking down the hallway when she heard loud voices. The CNA went to the room where the voices were coming from and saw LPN #3 was face to face and yelling at Resident #26. The I&A documented [nurse name] had his hands up by the resident's face like he wanted to choke the resident. Resident #26 stated to LPN #3 to go ahead and hit him. LPN #3 then left the room. The CNA left the room and reported the incident to another licensed nurse. The other licensed nurse reported the incident to the Administrator and ADON. LPN #3 was relieved from his duty and sent home pending investigation of the incident. The facility's investigation report, dated 2/1/22, documented Resident #26 asked for his inhaler and LPN #3 did not give it to him because he had just used his inhaler. Resident #26 yelled at LPN #3 and called him names, LPN #3 yelled back at Resident #26 and had his hands close to Resident #26's face. When LPN #3 was interviewed about the incident, he stated he should not have yelled at Resident #26. The facility terminated LPN #3's employment at the facility. On 5/23/22 at 3:12 PM, Resident #26 stated he did not remember any of the staff being rude to him. On 5/25/22 at 9:26 AM, the Administrator stated LPN #3 was sent home after the incident. The Administrator stated LPN #3 had been working in the facility for about 3-4 months when the incident happened, and it was his first time working in a Skilled Nursing Facility. The Administrator stated LPN #3 was interviewed about the incident over the phone, and stated he should not have yelled at Resident #26 and understood what he did was wrong. The Administrator stated LPN #3 was terminated from his employment. The facility was cited at past non-compliance as they were found in compliance from 2/1/22. The facility implemented the following measures to ensure ongoing compliance: - The DON stated the facility conducted regular training for all staff regarding abuse and abuse prevention. The DON stated training included information on specific behaviors and dementia. The facility also provided a certified specialist to train staff about dementia. These inservices were conducted once a month and as needed. - The DON stated the staff were provided assistance with residents by the administrative staff, or if they felt stressed, the staffing coordinator worked with staff to accommodate schedule needs in order to ease burdens on staff related to potential burnout. - The DON stated the management team (Administrator, DON, ADON, Social Services Director, MDS Coordinator) worked on the floor every day and specifically worked with residents with increased behaviors in order to allow floor staff to carry on with their duties and assist other residents. - There were no I&A reports or State portal events regarding abuse, neglect, or misappropriation from 2/1/22. During survey, staff were interviewed and able to verbalize the facility's policy for identifying and reporting abuse, neglect, and misappropriation.
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, record review, review of I&A reports, and staff interview, it was determined the facility failed to ensure...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, review of I&A reports, and staff interview, it was determined the facility failed to ensure residents' care plans were revised and updated as residents' needs changed. This was true for 4 of 16 residents (#12, #20, #22, and #44) whose care plans were reviewed. This deficient practice placed residents at risk for adverse outcomes if care and services were not provided appropriately due to a lack of information in the care plan. Findings include: 2. Resident #44 was admitted to the facility on [DATE], with multiple diagnoses including right thigh muscle atrophy (a condition in which muscles shrink and cause weakness) and dementia. An MDS assessment, dated 7/21/21, documented Resident #44 was moderately cognitively impaired, he did not walk, and his ADLs had declined from his prior function of independent to extensive two-person assistance for bed mobility, transfer, toilet use, and one-person setup assistance for moving between locations in his room. Resident #44 had impaired mobility ability to his lower extremity; he was not steady moving from seat to standing position, moving on and off the toilet, and surface-to-surface transfer (transfer between bed and chair or wheelchair). An I&A report, dated 9/19/21 at 7:33 AM, documented staff was alerted by Resident #44's roommate he needed assistance. The staff found Resident #44 sitting on the floor on his buttocks with his legs extended outward upon entering the room. Resident #44 said he was trying to get into his wheelchair and did not make it. The I&A report further documented the root cause of the fall was Resident #44 was on non-weight-bearing status due to the last fall with fracture and not strong enough to transfer from his bed to the wheelchair. Resident #44's surgeon was contacted on 9/20/21 and ordered Resident #44 to be on weight-bearing as tolerated. Resident #44's care plan for the falls was updated, as follows: -Physical therapy evaluation and treatment as needed to increase strength and balance to decrease the potential for falls and to continue to promote Resident #44's independence, start date 10/28/21. -Reminded, encouraged, and assisted Resident #44 to sleep in the center of the bed, initiated 10/28/21. -Staff rearranged room for better accommodation to assess personal belongings without ambulating, initiated 10/28/21. Resident #44's care plan did not include updates on his post-fall weight-bearing status and non-weight-bearing status to alert staff to provide the level of care he needed. The care plan was not updated until 10/28/21, more than a month after he fell. On 5/27/22 at 12:50 PM, the DON reviewed Resident #44's care plan and said Resident #44's fall care plan was not revised or interventions added for his fall on 9/19/21, and when the weight-bearing status changed on 9/20/21. 3. Resident #12 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including stroke, bipolar disorder (extreme mood swings that include mania and depression), attention-deficit hyperactive disorder, anxiety disorder, and psychosis (conditions that affect the mind, or loss of contact with reality, including hallucinations or delusions). Resident #12's physician orders documented she was to receive the following medications: -Seroquel (antipsychotic), give 200 mg two times a day in the morning and before sleep for bipolar disorder, ordered on 9/25/20. -Seroquel, give 300 mg one time a day at 1:00 PM for bipolar disorder, ordered on 3/15/21. -Librium (benzodiazepine), give 10 mg three times a day for bipolar disorder, ordered on 12/2/21. -Caplyta (antipsychotic), 42 mg, give at bedtime for bipolar disorder, ordered on 12/2/21. Resident #12's psychotropic medication care plan, initiated on 8/28/18, included interventions to monitor, record occurrence of target behavior, and document per facility protocol. A PDR meeting note, dated 4/26/22, documented Resident #12 was to be monitored and her target behaviors were yelling, verbal assault, and intrusiveness. Resident #12's care plan did not include interventions to monitor her active target behavior of yelling, verbal assault, and intrusiveness, as indicated in the 4/26/22 PDR meeting note. On 5/27/22 at 12:50 PM, the DON reviewed Resident #12's care plan and said her target behavior for psychotropic medication based on the PDR meeting on 4/26/22 were yelling, verbal assault, and intrusiveness. The DON said the three target behaviors were not documented in the behavior care plan, and the care plan should be documented and updated each month after the PDR meeting. 4. Resident #22 was admitted to the facility on [DATE], with multiple diagnoses including high blood pressure, muscle weakness and abnormalities of gait and mobility. An annual MDS assessment, dated 3/15/22, documented Resident #22 was severely cognitively impaired, at risk of developing pressure ulcers and no pressure ulcers were present. A Nurse's Note, dated 3/23/22 at 1:13 PM, documented Resident #22 had a lesion (wound or injury) present to his right upper thigh bone near the hip that was blanchable throughout the reddened area and the top layer of the skin was missing. The note documented the reddened area matched the size and shape of the incontinence brief adhesive tab. The Nurse's Note documented when the adhesive tab was removed it took off the top layer of Resident #22's skin. The note also documented it was on the side Resident #22 preferred to lay on. The note further documented orders to clean the wound every three days with wound cleanser, pat dry with gauze, and cover the wound with Allevyn (foam dressing). Resident #22's care plan was not updated to include his lesion/wound to his right upper thigh and wound care. A nurse practitioner's progress note, dated 4/11/22, documented Resident #22 had a 4x4 wound to his right upper hip with necrotic eschar (blackened, dead skin tissue that is non viable due to reduced blood supply) covering and surrounding redness. The nurse practitioner documented Resident #22 would benefit from a wound specialist. The nurse practitioner directed staff to refer Resident #22 to a wound care specialist, cleanse his wound every 72 hours and PRN with wound cleanser, pat dry, apply Medi-Honey (helps create a moist wound healing environment which aids in debridement and removal of necrotic tissue) cover with Allevyn dressing, and off-load Resident #22's right hip, and turn him every two hours. A care plan, initiated on 5/3/22, documented Resident #22 had an unstageable area to his right hip and staff were directed to assess him for signs and symptoms of pain with wound care, schedule/administer analgesic (pain reliever) prior to treatment, communicate with the physician if area was not healing or became worse, perform wound care as ordered, encourage him to not sleep on his right hip and perform skin checks weekly. Resident #22's care plan was updated on 5/3/22, to include his lesion/wound to his right trochanter which was five weeks after it was noted in the 3/23/22 nursing notes. On 5/26/22 at 3:25 PM, the DON stated Resident #22's unstageable pressure ulcer (an ulcer that has full thickness tissue loss but is ether covered by extensive necrotic tissue or eschar) to his right hip started as a small abrasion from the sticky part of his undergarment. The DON stated residents' care plans were updated quarterly and PRN. When asked about Resident #22's abrasion to his right trochanter not being included in his care plan which later progressed to an unstageable pressure ulcer, the DON stated Resident #22's care plan was updated on 5/3/22 to include his unstageable wound on his right hip. When asked why Resident #22's care plan was not updated when they first identified his wound, the DON did not provide an answer. 1. Resident #20 was admitted to the facility on [DATE], with multiple diagnoses including unspecified dementia with behavior disturbance, Type 2 diabetes mellitus, major depression, and morbid obesity. Resident #20's MDS admission assessment, dated 3/18/22, documented she was able to eat independently with set up assistance. Resident #20's weight record at admission documented her weight was 137 lbs., which was within her Ideal Body Weight (IBW) range of 127 lbs. to 153 lbs. Resident #20's care plan for nutrition, initiated 3/23/22, stated she had unplanned and unexpected weight gain related to severe obesity due to excess calories, and her goal was not to develop complications from weight gain. Resident #20's nutritional interventions, initiated 3/23/22, included the following: - Monitor and record food intake at each meal. - Monitor/record Resident #20's eating habits and patterns to assist in determining the cause of overeating. - Monitor/record/report to MD as needed situations leading to increased food consumption, reasons for weight gain, and significant weight changes. - Serve diet as ordered: controlled carbohydrate, regular texture and thin liquids. On 5/14/22, Resident #20's weight was documented at 123 lbs. Resident #20 had a weight loss of 10.22% between 3/11/22 and 5/14/22. A dietitian's progress note, dated 5/25/22, documented a conversation with Resident #20 and her daughter regarding her weight loss. Resident #20 spoke Spanish, so translation was conducted by her daughter. Food preferences were discussed with Resident #20 and her daughter, and Resident #20's daughter stated Resident #20 might eat softer, smaller, portions of food. She stated Resident #20 had no problem with the food, she just wanted to go home. The note documented the family brought food in over the weekend and Resident #20 did not eat the food. On 5/25/22, Resident #20's physician ordered a Fortified Controlled Carbohydrate Diet (CCHO), mechanical soft (minced and moist texture), regular consistency, and snack between meals for 72 hours as a trial, to see if her intake would increase. On 5/26/22 at 9:00 AM, CNA #10 stated Resident #20 did not usually eat much at breakfast and she did not touch the food the family brought in over the weekend. On 5/26/22 at 12:00 PM, Resident #20 was observed eating her lunch in her room. Resident #20 received ground barbequed pork, barbequed beans, and broccoli. She used her fork to eat two bites of her meal and then stopped eating. On 5/26/22 at 4:00 PM, the DON reviewed Resident #20's nutrition care plan. The DON stated she would expect Resident #20 to have a care plan for weight loss, and not weight gain.
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 in policy review, observation, record review, and staff interview, it was determined the facility failed to ensure residen...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based in policy review, observation, record review, and staff interview, it was determined the facility failed to ensure residents received respiratory care for a resident receiving oxygen by nasal cannula. This was true for 1 of 2 residents (Resident #26) reviewed for respiratory care. This deficient practice had the potential for harm if the residents experienced discomfort from non-humidified oxygen. Findings include: The Infection Prevention and Control Regarding Oxygen Use policy and procedure, revised October 2010, directed staff to check and make sure the water level in the humidifying jar was high enough that the water bubbles as oxygen flows through, and to periodically re-check the water level in the humidifying jar. This policy was not followed. Resident #26 was admitted to the facility on [DATE], with multiple diagnoses including emphysema (a lung condition wherein the air sacs in the lungs are damaged causing shortness of breath), heart failure, and anxiety disorder. A significant change MDS assessment, dated 3/30/22, documented Resident #26 was cognitively intact and received oxygen. A physician order, dated 3/8/22, documented he was to receive oxygen 5 liters/minute continuously via nasal cannula and to change his oxygen tubing, humidifier, and clean the filter on the first and 15th of the month and as needed. On 5/23/22 at 11:30 AM, Resident #26 was in bed sleeping and receiving oxygen via nasal cannula. The humidifier (container of water attached to the oxygen concentrator) was empty. On 5/24/22 at 10:34 AM, the DON was in Resident #26's room and was checking his oxygen saturation. The DON stated the humidifier should not be left empty and should be changed on the first and 15th of each month and when needed.
CONCERN (D)

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

Medication Errors (Tag F0758)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, it was determined the facility failed to ensure a resident receiving PRN lorazepam (...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, it was determined the facility failed to ensure a resident receiving PRN lorazepam (anti-anxiety) had clinical rationale supporting the continued use of the medication beyond 14 days. This was true for 1 of 9 residents (Resident #39) reviewed for unnecessary medications. This deficient practice had the potential for Resident #39 to experience adverse effects from unnecessary psychotropic medications. Findings include: Resident #39 was admitted to the facility on [DATE], with multiple diagnoses including anxiety disorder. An annual MDS assessment, dated 4/14/22, documented Resident #39 had severe cognitive impairment and received anti-anxiety medication on 7 of the previous 7 days. A physician order dated 5/3/22, documented Resident #39 was to receive lorazepam 1 mg, one tablet orally every 12 hours as needed for agitation and psychosis. There was no documentation in Resident #39's record to support the continuation of lorazepam beyond 14 days. On 5/27/22 at 11:46 AM, the DON reviewed Resident #39's record and stated she did not find the documentation supporting the need for the use of lorazepam beyond 14 days. The DON stated Resident #39's order should include a stop date for the use of lorazepam.
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, policy review, and staff interview, it was determined the facility failed to ensure infection control measures were consistently implemented and maintained to provide a safe and ...

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Based on observation, policy review, and staff interview, it was determined the facility failed to ensure infection control measures were consistently implemented and maintained to provide a safe and sanitary environment during perineal care. This was true for 1 of 1 resident (Resident #55) whose perineal care was observed. This failure created the potential for negative outcomes by exposing a resident to the risk of infection and cross-contamination. Findings include: The facility's Handwashing/Hand Hygiene policy, revised August 2019, stated the use of gloves did not replace hand washing/hand hygiene and directed staff to perform hand hygiene before moving from a contaminated body site to a clean body site during resident care. This policy was not followed. Infection control measures were not consistently implemented and maintained to provide a safe and sanitary environment during perineal care, as follows: On 8/23/22 at 2:15 PM, Resident #55 was observed during perineal care. CNA #1 had gloves on and unfastened Resident #55's brief which was soiled with feces. CNA #1 wiped her perineal area and then NA #1 wiped Resident #55's buttock area with a cleansing wipe five times and then removed the soiled incontinence brief. CNA #1 then asked NA #1 to get the barrier cream. NA #1 retrieved the barrier cream and squeezed the cream on CNA #1 gloved right hand. CNA #1 applied the barrier cream to Resident #55's gluteal fold area and thighs. Then NA #1 placed a clean incontinence brief next to Resident #55 and tucked it in under Resident #55 and then flattened the incontinence brief by running both her gloved hands over the brief. CNA #1 and NA #1 then assisted Resident #55 to turn to her back and fastened her incontinence brief. During the perineal care observation, CNA #1 did not change her gloves or perform hand hygiene before applying the barrier cream to Resident #55 and NA #1 did not change her gloves or perform hand hygiene before handling the clean incontinence brief. On 8/23/22 at 3:35 PM, NA #1 and CNA #1 were asked about hand hygiene while performing perineal care. NA #1 stated she did not perform hand hygiene or change her gloves during Resident #55's perineal care. NA #1 stated she performed hand hygiene whenever she felt her hands were dirty. CNA #1 stated hand hygiene should be performed before and after having resident contact. CNA #1 stated she did not change her gloves or perform hand hygiene before applying the barrier cream to Resident #55's gluteal area and thighs, CNA #1 stated she should have removed her gloves, performed hand hygiene and donned new gloves before applying the cream. The facility failed to ensure infection control measures were consistently implemented and maintained to provide a safe and sanitary environment during Resident #55's perineal care.
CONCERN (E)

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

Deficiency F0552 (Tag F0552)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, policy review, and staff interview, it was determined the facility failed to ensure informed consent was...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, policy review, and staff interview, it was determined the facility failed to ensure informed consent was obtained prior to initiation of medications for 5 of 15 residents (#6, #12, #17, #37, and #47) reviewed for unnecessary medications. This deficient practice placed residents at risk for receiving medications without knowledge of why the medication was prescribed, the expected benefits, and the risks associated with the medications. Findings include: The facility's policy Psychotropic Medication Informed Consent, Dose Reduction and Behavior Monitoring, undated, documented the following: - An informed consent was obtained for all facility residents using psychotropic medication for each medication class, including antipsychotic, anxiolytic, mood stabilizer, sedative/hypnotic, and antidepressant, used for the treatment of residents. - The facility informed the resident and/or responsible party of the psychotropic medication ordered by the physician and explained the rationale for its use. The resident and/or the responsible party, along with the physician, would establish and agree upon appropriate treatment goals associated with the psychotropic medication. - The resident or responsible party was informed of potential adverse side effects associated with the psychotropic medication. - Psychotropic medication use, treatment goals, efficacy in addressing target symptoms or distressed behaviors and continued need, was reviewed with the resident or responsible party quarterly and as needed to ensure ongoing understanding and consent. This policy was not followed. 1. Resident #17 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including hemiplegia and hemiparesis (paralysis and weakness on one side of the body) following a stroke, psychosis, and Type 2 diabetes. A physician's order, dated 5/29/18, documented to administer Fluoxetine (an antidepressant) 20 mg, 1.5 tablet by mouth one time a day for bipolar symptoms. A physician's order, dated 10/29/19, documented to administer a Depakote Tablet (an anticonvulsant) 1000 mg orally two times a day to Resident #17 related to intermittent explosive disorder (IED - a mental health condition marked by frequent impulsive anger outbursts or aggression). A physician's order, dated 10/27/20, documented to administer Chlorpromazine (an antipsychotic) 300 mg by mouth at bedtime and 50 mg and one tablet two times a day by mouth to Resident #17 for IED. Resident #17's record did not include an authorization or consent for the use of psychoactive medications for behavior. On 5/26/22 at 4:00 PM, the Administrator confirmed there was no authorization for the use of the psychoactive medications for Resident #17. 2. The facility used a consent form for all medications, entitled Psychoactive Medication Authorization. The consent read: I (resident name), or (name), a legal representative for the above resident, have been informed of the potential negative outcome with the use of psychoactive medication(s). These may include, but are not limited to: Incontinence, decreased mobility, symptoms of depression and withdrawal, reduced social contact, sedation, injury or death. Please refer to back of this page for further risks and benefits. I, and/or my legal representative, understand the facility will utilized [sic] the lowest possible therapeutic dosage and understand my right to participate in this decision. The consent contained blank lines for medications to be added, titled Psychoactive medications in use: Medication, Classification. Diagnosis. The consent form included the potential risks and benefits on the back of the form, as follows: - Potential Risks included: increased confusion, agitation, combativeness, weakness, incontinence, constipation, loss of ability to walk and independence, risk of skin problems, depression, sedation/drowsiness, dry mouth, blurred vision, nausea, vomiting, dizziness, and postural hypertension. - Potential Benefits included: decreased weeping, crying, yelling, nervousness, sleeplessness, hallucinations, paranoia, confusion, feeling of hopelessness, refusal of care, combativeness, verbal/physical abuse to staff and residents, increased feelings of well-being, decreased delusions, isolation, suicidal ideations, increased muscular control. The consent forms did not include an area or section to document the specific risks and benefits for individual medications. Examples include: a. Resident #12 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including stroke, bipolar disorder (extreme mood swings that include mania and depression), attention-deficit hyperactive disorder, anxiety disorder, and psychosis (conditions that affect the mind, or loss of contact with reality, including hallucinations or delusions). Resident #12's physician orders documented she was to receive the following medications: - Seroquel (an antipsychotic), give 200 mg, 1 tablet by mouth in the morning and before sleep for bipolar disorder, ordered on 9/25/20. - Seroquel give 300 mg, 1 tablet by mouth at 1:00 PM for bipolar disorder, ordered on 3/15/21. - Librium (benzodiazepines), give 10 mg, 1 capsule by mouth three times a day for bipolar disorder, ordered on 12/2/21. - Caplyta (antipsychotic) give 42 mg by mouth at bedtime for bipolar disorder, ordered on 12/2/21. Resident #12's Psychoactive Medication Authorization form, dated 9/4/20, included one consent for two medications (Seroquel and Librium) and included instructions to refer to the back of the consent for further information about risks. Resident #12's Psychoactive Medication Authorization form, dated 2/24/21, included consent for Rexulti (antipsychotic), and a hand-written note dated 3/30/21, documenting Resident #12's family was verbally notified Rexulti was discontinued and Caplyta was started. The consent included instructions to refer to the back of the consent for further information about risks. The Drugs.com website, accessed 6/6/22, stated the common side effects were different for the three medications, as follows: - Seroquel: uncontrolled muscle movements in the face, mask-like appearance of the face, trouble swallowing, problems with speech, a light-headed feeling, blurred vision, tunnel vision, eye pain, seeing halos around lights, severe nervous system reaction (very stiff muscles, high fever, sweating, confusion, fast or uneven heartbeats, tremors, fainting,) high blood sugar (increased thirst, increased urination, hunger, dry mouth, fruity breath odor, drowsiness, dry skin, blurred vision, weight loss,) low blood cell counts (sudden weakness or ill feeling, fever, chills, cold or flu symptoms, cough, sore throat, red or swollen gums, painful mouth sores, skin sores, trouble breathing,) speech problems, dizziness, drowsiness, tiredness, lack of energy, stuffy nose, increased appetite, weight gain, upset stomach, vomiting, constipation, dry mouth, and problems moving. - Librium: severe drowsiness, slurred speech, slow heart rate, slow breathing (breathing may stop), problems with memory or concentration, unusual changes in mood or behavior, thoughts of suicide or hurting yourself, problems with balance or muscle movement, confusion, excitement, paranoia, anger, aggression, stomach pain, loss of appetite, drowsiness or dizziness, and confusion. - Caplyta: feeling unsteady, feeling like fainting, uncontrolled muscle movements in the face (chewing, lip-smacking, frowning, tongue movement, blinking, eye movement,) tightness in your neck or throat, trouble swallowing, trouble breathing or speaking, seizure, high blood sugar (increased thirst, increased urination, dry mouth, fruity breath odor,) low white blood cell counts - fever, chills, mouth sores, skin sores, sore throat, cough, trouble breathing,) severe nervous system reaction (stiff muscles, high fever, sweating, confusion, fast or uneven heartbeats, tremors, feeling like fainting,) weight gain, and drowsiness. The consent form did not document specific risks or potential side effects for each of the medications prescribed for Resident #12. b. Resident #6 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including schizophrenia (a mental disorder characterized by continuous or relapsing episodes of psychosis) and retention of urine (difficulty urinating and completely emptying the bladder.) Resident #6's physician orders documented she was to receive the following medications: - Clonazepam (a benzodiazepine) 1 mg, give 1 tablet by mouth two times a day for agitation, ordered on 5/19/22. - Invega (an antipsychotic), give 9 mg by mouth at bedtime for schizophrenia, ordered on 5/19/22. Resident #6's Psychoactive Medication Authorization form, dated 5/18/22, included one consent for both medications and included instructions to refer to the back of the consent for further information about risks. The Drugs.com website, accessed 6/6/22, stated the common side effects were different for these two classes of medications, as follows: - Clonazepam: new or worsening seizures, severe drowsiness, weak or shallow breathing, unusual changes in mood or behavior, confusion, paranoia, nightmares, hallucinations, thoughts of suicide or self-injury, unusual or involuntary eye movements, drowsiness or dizziness, feeling tired or depressed, memory problems, problems with walking or coordination. - Invega: difficulty with speaking, drooling, fast pounding, irregular heartbeat, increased body movements, loss of balance control, muscle trembling, jerking, stiffness, shuffling walk, stiffness of the limbs, twisting movements of the body, uncontrolled movements. The consent form did not document specific risks or potential side effects for each of the medications prescribed for Resident #6. c. Resident #37 was admitted to the facility on [DATE], with multiple diagnoses including dementia with behavioral disturbance, catatonic schizophrenia (characterized by significant impairments in the way reality is perceived and changes in behavior, combined with a psychomotor disorder that affects both speech and behavior functions), and insomnia. A quarterly MDS assessment, dated 4/5/22, documented Resident #37 had severe cognitive impairment and received anti-anxiety, anti-depression and antipsychotic medications on 7 of the previous 7 days. A physician order documented Resident #37 was to receive the following medications: - Invega 12 mg, one time a day for catatonic schizophrenia, ordered 12/28/21. - Ativan (anti-anxiety) 1 mg two times a day for anxiety, ordered 1/24/22. - Trazodone (antidepressant) 50 mg at bedtime for insomnia, ordered on 4/20/22. A Psychoactive Medication Authorization form, dated 2/24/21, signed by Resident #37, included one consent for three medications (Invega, Ativan, and Trazodone) and included instructions to refer to the back of the consent for further information about risks. The Drugs.com website, accessed on 6/6/22, stated the common side effects were different for these three classes of medications, as follows: - Invega: difficulty with speaking, drooling, fast pounding, irregular heartbeat, increased body movements, loss of balance control, muscle trembling, jerking, stiffness, shuffling walk, stiffness of the limbs, twisting movements of the body, uncontrolled movements. - Ativan: severe drowsiness, unusual changes in mood or behavior, being agitated or talkative; sudden restless feeling or excitement; thoughts of suicide or hurting one's self; confusion, aggression, hallucinations; sleep problems; vision changes; or dark urine or jaundice (yellowing of the skin or eyes). - Trazodone: blurred vision, dizziness, drowsiness, headache, nausea, vomiting, dry mouth, fainting, edema, confusion, diarrhea, low blood pressure, insomnia, sedated state, and rapid heartbeat. The consent form did not document specific risks or potential side effects for each of the medications prescribed for Resident #37. d. Resident #47 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including dementia, and bipolar disorder (a disorder associated with episodes of mood swings ranging from depressive lows to manic highs). A quarterly MDS assessment, dated 5/5/22, documented Resident #47 had severe cognitive impairment and received antipsychotic and anti-anxiety medications on 7 of the previous 7 days. Resident #47's physician's orders documented Resident #47 was to receive the following medications: - Invega (antipsychotic) 3 mg, one tablet by mouth once a day for schizophrenia, ordered 2/19/21. - Invega Suspension (antipsychotic) 234 mg/1.5 ml Prefilled Syringe, inject intramuscularly one time a day starting on the 14th and ending on the 14th of every month related to bipolar disorder, ordered 5/21/21. - Ativan (anti-anxiety) 0.25 mg tablet give 0.5 mg by mouth two times a day for anxiety, ordered 10/13/21. A Psychoactive Medication Authorization form, dated 2/25/22, signed by Resident #47's representative, documented Resident #47 used Ativan and Invega medications. The consent included instructions to refer to the back of the consent for further information about risks. The Drugs.com website, accessed on 6/6/22, stated the common side effects were different for the two classes of medications, as follows: - Invega: difficulty with speaking, drooling, fast pounding, irregular heartbeat, increased body movements, loss of balance control, muscle trembling, jerking, stiffness, shuffling walk, stiffness of the limbs, twisting movements of the body, uncontrolled movements. - Ativan: severe drowsiness, unusual changes in mood or behavior, being agitated or talkative; sudden restless feeling or excitement; thoughts of suicide or hurting one's self; confusion, aggression, hallucinations; sleep problems; vision changes; or dark urine or jaundice (yellowing of the skin or eyes). On 5/26/22 at 4:50 PM, the DON stated the facility's informed consent form combined the benefits and potential negative outcomes of the medications and it was generic. The DON stated the informed consent should have the black box warnings and the benefits specific for each type of medication and should not be combined in one form.
CONCERN (E)

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

ADL Care (Tag F0677)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, policy review, record review, and staff interview, it was determined the facility failed to ensure residen...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, policy review, record review, and staff interview, it was determined the facility failed to ensure residents were provided with baths/showers and personal hygiene consistent with their needs. This was true for 9 of 13 residents (#4, #6, #13, #16, #26, #35, #44, #48 and #51) reviewed for ADLs. This failure created the potential for residents to experience embarrassment, isolation, decreased sense of self-worth, and/or skin impairment due to lack of personal hygiene. Findings include: The facility's policy, Activities of Daily Living, revised 3/2018, stated residents would be provided with care, treatment and services as appropriate to maintain or improve their ability to carry out activities of daily living. Residents who were unable to carry out activities of daily living independently received the services necessary to maintain good nutrition, grooming, and personal and oral hygiene. Hygiene was defined as including bathing, dressing, grooming, and oral care. This policy was not followed. 1. Residents were not bathed regularly according to their preferences and care plans. Examples include: a. Resident #4 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including hemiplegia and hemiparesis (weakness and paralysis on one side of the body) following a stroke, chronic obstructive pulmonary disease (COPD - a chronic inflammatory lung disease that causes obstructed airflow from the lungs), and dementia, Resident #4's annual MDS assessment, dated 11/16/21, documented she was severely cognitively impaired. Resident #4's quarterly MDS assessment, dated 2/16/22, did not document her cognition, and stated she needed extensive assistance for her ADL needs. Resident #4's care plan for ADLs, dated 3/2/22, stated she required the assistance of one staff member for bathing. Staff should provide a sponge bath for Resident #4 if bathing could not be tolerated. Resident #4's ADL flow sheet documented she was to be bathed twice a week and as needed. The following documentation was included for the months of 2/2022, 3/2022, and 4/2022: - Resident #4 received a bath on 2/1/22. Her next bath was on 2/9/22, eight days later. Resident #4's bathing was listed as NA on 2/5/22, 2/6/22, and 2/7/22. - Resident #4 received a bath on 2/18/22. Her next bath was on 2/25/22, seven days later. Resident #4's bathing was listed as NA on 2/19/22, 2/23/22, and 2/24/22. - Resident #4 received a bath on 3/5/22. Her next bath was on 3/10/22, five days later. Resident #4's bathing was listed as NA on 3/6/22, 3/7/22, and 3/9/22. - Resident #4 received a bath on 3/24/22. Her next bath was on 4/9/22, 16 days later. Resident #4's bathing was listed as NA on 3/25/22, 3/26/22, 3/27/22, 3/28/22, 3/29/22, 3/30/22, 3/31/22, 4/1/22, 4/2/22, 4/3/22, 4/4/22, 4/5/22, 4/6/22, 4/7/22, and 4/8/22. b. Resident #13 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including hemiplegia and hemiparesis (weakness and paralysis on one side of the body), schizoaffective disorder (a condition where symptoms of both psychotic and mood disorders are present together during one episode, or within a two-week period of each other), anxiety disorder, and unspecified injury of head. Resident #13's quarterly MDS assessment, dated 3/8/22, documented she needed extensive assistance for her ADL needs. Resident #13's care plan for ADLs, dated 10/14/15 and revised 12/14/21, stated she required limited to extensive assistance of one staff member for bathing three times per week. Resident #13's ADL flow sheet documented she was to be bathed three times a week and as needed. The following documentation was included for the months of 2/2022, 3/2022, 4/2022, and 5/2022: - Resident #13 received a bath on 2/4/22. Her next bath was on 2/9/22, five days later. Resident #13's bathing was marked NA on 2/1/22, 2/2/22, 2/3/22, 2/5/22, 2/6/22, and 2/8/22. - Resident #13 received a bath on 2/18/22. Her next bath was on 2/24/22, six days later. Resident #13's bathing was marked NA on 2/19/22, 2/20/22, 2/21/22, 2/22/22, and 2/23/22. - Resident #13 received a bath on 4/2/22. Her next bath was on 4/11/22, nine days later. Resident #13's bathing was marked NA on 4/3/22, 4/4/22, 4/5/22, 4/6/22, 4/7/22, 4/8/22, 4/9/22, and 4/10/22. - Resident #13 received a bath on 5/6/22. Her next bath was on 5/17/22, 11 days later. Resident #13's bathing was marked NA on 5/7/22, 5/8/22, 5/9/22, 5/10/22, 5/11/22, 5/12/22, 5/13/22, 5/14/22, 5/15/22, and 5/16/22. c. Resident #16 was admitted to the facility on [DATE], with multiple diagnoses including spinal muscle atrophy (a genetic [inherited] neuromuscular disease that causes muscles to become weak and waste away) and schizophrenia (a mental disorder in which people interpret reality abnormally and may result in hallucinations, delusions, and extremely disordered thinking and behavior that impairs daily functioning). Resident #16's quarterly MDS assessment, dated 3/8/22, documented she needed set-up and supervision assistance for her ADL needs. Resident #16's ADL care plan stated she required limited assistance of one staff with showers/bathing twice a week and as necessary. Staff were to provide a sponge bath when a full bath or shower could not be tolerated. Resident #16's ADL flow sheet for the months of 2/2022, 3/2022, and 4/2022 documented the following: - Resident #16 received a bath on 2/1/22. Her next bath was on 2/13/22, 12 days later. Resident #16's ADL flow sheet was marked NA on 2/4/22, 2/5/22, 2/7/22, 2/10/22, and 2/11/22. - Resident #16 received a bath on 2/18/22. Her next bath was on 3/10/22, 19 days later. Resident #16's ADL flow sheet was marked NA on 2/19/22, 2/22/22, 2/23/22, 2/24/22, and 3/2/22. Resident #16 refused a bath on 3/3/22. Resident #16's ADL flow sheet was marked NA on 3/4/22, 3/5/22, 3/6/22, 3/7/22, and 3/9/22. - Resident #16 received a bath on 3/14/22. Her next bath was on 3/19/22, five days later. Resident #16's ADL flow sheet was marked NA on 3/15/22, 3/16/22, 3/17/22, and 3/18/22. - Resident #16 received a bath on 3/23/22. Her next bath was on 3/31/22, seven days later. Resident #16's ADL flow sheet was marked NA on 3/24/22, 3/25/22, 3/26/22, 3/27/22, 3/28/22, 3/29/22, and 3/30/22. - Resident #16's received a bath on 3/31/22. Her next bath was on 4/11/22, ten days later. Resident #16's ADL flow sheet was marked NA on 4/1/22, 4/2/22, 4/3/22, and 4/4/22. Resident #16 refused a bath on 4/5/22. Resident #16's ADL flow sheet was marked NA on 4/6/22, 4/7/22, 4/8/22, 4/9/22, and 4/10/22. d. Resident #35 was admitted to the facility on [DATE] and readmitted on [DATE], with multiple diagnoses including left hip fracture, dementia, and anxiety disorder. Resident #35's quarterly MDS assessment, dated 2/9/22, documented she needed extensive assistance for her ADL needs. Resident #35's care plan for ADLs, dated 11/17/21, documented she needed extensive assistance of one staff member with personal hygiene. Resident #35's care plan for ADLs did not document how often she should be bathed. Resident #35's ADL flow sheet for bathing for the months of 2/2022, 3/2022, 4/2022, and 5/2022, did not document how often she should be bathed, and documented the following: - Resident #35 received a bath on 2/5/22. Her next bath was on 2/13/22, eight days later. Resident #35's ADL flow sheet for bathing was marked NA on 2/6/22, 2/7/22, 2/8/22, 2/9/22, 2/10/22, 2/11/22, and 2/12/22. - Resident #35 received a bath on 2/18/22. Her next bath was on 2/25/22, seven days later. Resident #35's ADL flow sheet for bathing was marked NA on 2/19/22, 2/20/22, 2/21/22, 2/22/22, 2/23/22, and 2/24/22. - Resident #35's received a bath on 3/15/22. Her next bath was on 3/28/22, 13 days later. Resident #35's ADL flow sheet for bathing documented NA on 3/16/22, 3/17/22, 3/18/22. Resident #35 was out of the facility from 3/18/22 to 3/23/22. Resident #35's ADL flow sheet for bathing was marked NA on 3/23/22, 3/24/22, 3/25/22, 3/26/22 and 3/27/22. - Resident #35 received a bath on 3/28/22. Her next bath was on 4/16/22, 18 days later. Resident #35's ADL flow sheet for bathing was marked NA on 3/29/22, 3/30/22, 3/31/22, 4/1/22, 4/2/22, 4/3/22, 4/4/22, 4/5/22, 4/6/22, 4/7/22, 4/8/22, 4/9/22, 4/10/22, 4/11/22, 4/12/22, 4/13/22, and 4/15/22. - Resident #35 received a bath on 5/6/22. Her next bath was on 5/17/22, 11 days later. Resident #35's ADL flow sheet for bathing was marked NA for 5/7/22, 5/8/22, 5/9/22, 5/10/22, 5/11/22, 5/12/22, 5/13/22, 5/14/22, 5/15/22, and 5/16/22. e. Resident #51 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including Type 2 diabetes, chronic kidney disease, low back pain, and hemiplegia and hemiparesis (weakness and paralysis on one side of the body) following a stroke. Resident #51's quarterly MDS assessment, dated 5/2/22, documented he needed set-up and supervision assistance for his ADL needs. Resident #51's care plan for ADLs documented he required extensive assistance with bathing. Resident #51's care plan for behavior documented if he resisted ADLs, reassure him, leave him and return 5-10 minutes later and try again. Resident #51's ADL flow sheet for bathing did not document how often he was to be bathed. Resident #51's flow sheet for 2/2022, 3/2022, and 4/2022, documented the following: - Resident #51 received a bath on 2/1/22. His next bath was on 2/13/22, 12 days later. Resident #51's ADL flow sheet for bathing was marked NA on 2/1/22, and 2/2/22. Resident #51 refused a bath 2/3/22 and 2/4/22. Resident #51's ADL flow sheet for bathing was marked NA on 2/5/22, 2/6/22, 2/7/22, 2/8/22, 2/9/22, 2/10/22, 2/11/22, and 2/12/22. - Resident #51 received a bath on 2/15/22. His next bath was on 2/25/22, ten days later. Resident #51's ADL flow sheet for bathing documented NA on 2/16/22, 2/17/22, 2/18/22, 2/19/22, 2/20/22, 2/21/22, 2/23/22, and 2/24/22. - Resident #51 received a bath on 2/25/22. His next bath was on 3/3/22, six days later. Resident #51's ADL flow sheet for bathing documented NA on 2/26/22, 2/27/22, 2/28/22, and 3/1/22. Resident #51 refused to bathe 3/2/22. - Resident #51 received a bath on 3/3/22. His next bath was on 3/10/22, seven days later. Resident #51's ADL flow sheet for bathing documented NA on 3/4/22, 3/5/22, 3/6/22, 3/7/22, and 3/9/22. - Resident #51 received a bath on 3/23/22. His next bath was on 3/31/22, eight days later. Resident #51's ADL flow sheet for bathing documented NA on 3/24/22, 3/25/22, 3/26/22, 3/27/22, 3/29/22 and 3/30/22. - Resident #51 received a bath on 3/31/22. His next bath was on 4/14/22, 14 days later. Resident #51's ADL flow sheet for bathing documented NA on 4/1/22, 4/2/22, 4/3/22, 4/4/22, 4/5/22, 4/6/22, 4/7/22, 4/8/22, 4/9/22, 4/10/22, 4/11/22, 4/12/22, and 4/13/22. - Resident #51 received a bath on 4/14/22. His next bath was on 4/24/22, ten days later. Resident #51's ADL flow sheet for bathing documented NA on 4/15/22, 4/16/22, 4/17/22, 4/19/22, and 4/20/22. Resident #51 refused a bath on 4/21/22. Resident #51's ADL flow sheet for bathing documented NA on 4/23/22. - Resident #51 received a bath on 5/11/22. His next bath was on 5/17/22, six days later. Resident #51's ADL flow sheet for bathing documented NA on 5/12/22, 5/13/22, 5/14/22, 5/15/22, and 5/16/22. f. Resident #6 was admitted to the facility on [DATE], and readmitted on [DATE], with multiple diagnoses including schizophrenia (a mental disorder characterized by continuous or relapsing episodes in which people have a disconnection from reality) and retention of urine (difficulty urinating and completely emptying the bladder). A quarterly MDS assessment, dated 2/10/22, documented Resident #6 was moderately cognitively impaired. She required setup assistance for bed mobility, toileting, dressing, eating, personal hygiene, and bathing. A care plan, dated 5/17/22, documented Resident #6 did not walk. She required two-person assistance for bed mobility and transfer and one-person physical assistance for hygiene and bathing. Resident #6's ADL flow sheet for bathing for 3/2022, 4/2022, and 5/2022, documented the following: - Resident #6 received a bath on 3/3/22. Her next bath was on 3/10/22, 7 days later. - Resident #6 received a bath on 3/28/22, and refused a bath on 4/5/22. Her next bath was on 4/24/22, 34 days later. - Resident #6 received a bath on 4/29/22. Her next bath was on 5/4/22, 5 days later. - Resident #6 received a bath on 5/19/22. Her next bath was on 5/26/22, 7 days later. On 5/27/22 at 12:39 PM, the DON said Resident #6's bathing days were every Monday and Thursday. The DON reviewed Resident #6's record and confirmed the days that baths were not given. g. Resident #48 was admitted to the facility on [DATE], with multiple diagnoses including diabetes, dyskinesia (involuntary muscle movements), schizophrenia (a mental disorder characterized by continuous or relapsing episodes in which people have a disconnection from reality), and moderate intellectual disabilities. Resident #48's quarterly MDS assessment, dated 2/2/22 and 5/5/22, documented he was severely cognitively impaired and required one-person physical assistance for bathing. An ADL care plan, initiated on 2/16/22, stated Resident #48 required limited assistance from two caregivers to bathe two times a week and as needed depending on his behaviors. Resident #48's ADL flow sheet for bathing for 3/2022 and 4/2022 documented the following: - Resident #48 refused a bath on 3/2/22 and 3/7/22. His next bath was on 3/10/22, 10 days later. - Resident #48 received a bath on 3/20/22. He refused a shower on 3/25/22 and 3/26/22. His next bath was on 3/31/22, 11 days later. Resident #48 received his next bath on 4/13/22, 13 days later. - Resident #48 received a bath on 4/16/22 and refused a bath on 4/21/22. His next bath was on 4/24/22, 8 days later. On 5/27/22 at 12:39 PM, the DON said Resident #48's bathing days were every Wednesday and Saturday. The DON reviewed Resident #48's record and confirmed the baths were not given. h. Resident #44 was admitted to the facility on [DATE], with multiple diagnoses including right thigh muscle atrophy (a condition in which muscles shrink and cause weakness) and dementia. A quarterly MDS assessment, dated 4/23/22, documented Resident #44 was moderately cognitively impaired and he required one-person physical assistance for bathing. An ADL care plan, initiated 1/27/22, stated Resident #44 required one staff member to assist with dressing, washing, and helping him in and out of the shower. Resident #44's ADL Flow sheet fort bathing for 4/2022 and 5/2022 documented the following: - Resident #44 received a bath on 4/1/22. His next bath was on 4/8/22, 7 days later. Resident #44's next bath was on 4/19/22, 11 days later. - Resident #44 received a shower on 4/26/22. His next bath was on 5/2/22, 6 days later. Resident #44's next bath was on 5/8/22, 5 days later. - Resident #44 received a bath on 5/20/22. His next bath was on 5/25/22, 5 days later. On 5/27/22 at 12:39 PM, the DON said Resident #44's shower schedule was every Tuesday and Friday. The DON reviewed Resident #44's record and confirmed the showers were not given. On 5/27/22 at 2:00 PM, the DON stated residents should be bathed consistently at least twice a week. The DON stated if a resident refused to be bathed, staff should offer a bath to residents at a different time, re-approach the resident again, offer a different type of bathing (e.g., shower or bed bath), and refusals should be documented in the ADL flow sheet. The DON stated documentation of NA was not appropriate. Residents did not receive their bath or shower as stated in their care plan or per facility policy. 2. Resident #26 was admitted to the facility on [DATE], with multiple diagnoses including emphysema (a lung condition wherein the air sacs [alveoli] in the lungs are damage causing shortness of breath), heart failure and anxiety disorder. A quarterly MDS assessment, dated 1/12/22, documented Resident #26 was cognitively intact and required one-person assistance with personal hygiene and bathing. On 5/23/22 at 8:35 AM, Resident #26 was observed in his room sitting by the edge of his bed. Resident #26's beard was thick, and part of his mustache covered his upper lip. Resident #26 stated he wanted his beard to be shaved but not his mustache. Resident #26 stated he asked the CNA to shave him many times in the past and was told by the CNA they would shave him. Resident #26 stated the CNA did not come back. On 5/25/22 at 9:53 AM, LPN #1 asked Resident #26 why he was not shaved. Resident #26 stated he had been asking the staff to shave him, but nobody would give him a shave. LPN #1 stated she was not aware Resident #26 wanted to be shaved. LPN #1 stated she would inform the CNAs that Resident #26 needed to be shaved. On 5/25/22 at 9:59 AM, CNA #8 and CNA #2 stated Resident #26 refused to be shaved a lot of times. On 5/26/22 at 8:28 AM, Resident #26 was in his room eating breakfast. Resident #26's chin had been shaved and his mustache trimmed. When asked if he was glad he had been shaved, Resident #26 touched his chin and stated, Oh yeah.
CONCERN (E)

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

Food Safety (Tag F0812)

Could have caused harm · This affected multiple residents

Based on observation, policy review, and staff interview, it was determined the facility failed to ensure measures were in place to prevent possible cross-contamination from dirty to clean areas in th...

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Based on observation, policy review, and staff interview, it was determined the facility failed to ensure measures were in place to prevent possible cross-contamination from dirty to clean areas in the kitchen. This had the potential to affect 51 residents residing in the facility who consumed food prepared by the facility. This placed residents at risk for potential contamination of food and adverse health outcomes, including food-borne illnesses. Findings include: The facility's Infection Prevention and Control policy on personal hygiene, adopted 10/2017, documented all staff were to practice frequent and appropriate handwashing and hand hygiene, and should be aware of contact with contaminated articles and equipment. The policy was not followed. On 5/26/22 at 12:00 PM, [NAME] #1 was observed washing pots and pans in the 3-compartment sink. [NAME] #1 rinsed food off the dishes and carried them to the dish machine. [NAME] #1 placed the dishes in the dish machine, then returned to the sink and continued to rinse dirty dishes. When the dish machine had finished, [NAME] #1 removed the clean dishes and set them on a rack to dry. [NAME] #1 did not perform hand hygiene after washing and rinsing dirty dishes and before removing clean dishes from the dish machine. [NAME] #1 continued to rinse dirty dishes, place them in the dish machine, and remove clean dishes from the dish machine for 15 minutes, until 12:15 PM. [NAME] #1 did not perform hand hygiene between handling dirty dishes and removing the clean dishes from the dish machine. On 5/26/22 at 12:15 PM, [NAME] #1 stated he did not wash or sanitize his hands between handling dirty dishes and clean dishes. [NAME] #1 stated he did not do the dish position often. [NAME] #1 stated he probably had been told at some time to wash or sanitize hands between handling dirty dishes and clean dishes. On 5/26/22 at 12:18 PM, the DM stated hand hygiene should be performed between the handling of dirty and clean dishes. The DM stated hands should be washed before clean dishes were removed from the dish machine and set out to dry or put away.
CONCERN (E)

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

Deficiency F0883 (Tag F0883)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, record review, and policy review, it was determined the facility failed to develop and implement proce...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, record review, and policy review, it was determined the facility failed to develop and implement processes to minimize the risk of residents acquiring, transmitting or experiencing complications from Pneumococcal pneumonia. The facility failed to implement an immunization program that tracked residents' Pneumococcal vaccine status, so immunization could be offered or provided as indicated. This was true for 1of 7 residents (Resident #26) reviewed for Pneumococcal vaccination and had the potential to affect all residents residing in the facility. Findings include: The Centers for Disease Control and Prevention (CDC) website, last reviewed 1/24/22, and accessed on 6/8/22, documented two types of pneumococcal vaccines available as follows: - Pneumococcal conjugate vaccines (PCV13, PCV15, and PCV20) - Pneumococcal polysaccharide vaccine (PPSV23) The CDC recommended the Pneumococcal vaccination for all adults [AGE] years old or older as follows: - For adults 65 years or older who have not previously received any pneumococcal vaccine, give one dose of PCV 15 or PCV 20. If PCV13 is used, this should be followed by a dose of PPSV23 at least one year later. If PCV20 is used, a dose of PPSV23 is not indicated. - For adults 65 years or older who have only received PPSV23, may receive one dose of PCV15 or PCV20 at least one year after the most recent PPSV23 vaccination. Regardless of if PCV15 or PCV20 is given, an additional dose of PPSV23 is not recommended since they already received it. - For adults [AGE] years old or older who have only received PCV13, one dose of PCV20 may be used if PPSV23 is not available. If PCV20 is used, their pneumococcal vaccinations are complete. The facility's Infection Prevention and Control policy and procedure regarding Pneumococcal Immunizations, adopted 10/2017, documented the residents shall be offered Pneumococcal Polysaccharide Vaccine (PPSV 23) and/or Pneumococcal Conjugate Vaccine (PCV 13) per CDC guidelines unless it was contraindicated, This guidance and policy were not followed: Resident #26 (over [AGE] years old) was admitted to the facility on [DATE], with multiple diagnoses emphysema (a lung condition wherein the air sacs in the lungs are damage causing shortness of breath), heart failure, and anxiety disorder. A quarterly MDS assessment, dated 1/22/22, documented Resident #26 was not offered the Pneumococcal immunization. Resident #26's record did not include documentation he received a pneumococcal immunization. On 5/27/22 at 1:00 PM, the IP stated she did not know Resident #26 was not offered the pneumococcal immunization. When asked if she was tracking the residents' immunizations, the IP stated resident records had all the vaccines the residents received. The IP was unable to provide a tracking system that showed who received the vaccines, which vaccine was received, when the next vaccination was due, and who refused and the reason for the refusal. The facility failed to have a system which identified and tracked pneumococcal immunizations for residents.
Apr 2019 7 deficiencies
CONCERN (D)

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

Transfer Requirements (Tag F0622)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, policy review, and record review, it was determined the facility failed to ensure information was prov...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, policy review, and record review, it was determined the facility failed to ensure information was provided to the receiving hospital for emergent situations of 1 of 1 resident (#4) reviewed for transfers. This deficient practice had the potential to cause harm if the resident was not treated in a timely manner due to lack of information. Findings include: The facility's Transfer and Discharge policy, revised 9/1/14, documented when it was necessary to transfer or discharge a resident to a hospital, staff were to: *notify the resident's attending physician *notify the receiving facility that the transfer was being made *prepare a transfer form to send with the resident Resident #4 was readmitted to the facility on [DATE], with multiple diagnoses including urinary tract infection and stroke with hemiplegia (paralysis) on the left side. A Nursing Progress Note, dated 4/7/19 at 3:00 AM, documented Resident #4 had an elevated temperature, complained of abdominal pain, and not feeling well. The physician assistant was notified and ordered Resident #4's transfer to the hospital. Resident #4 was transported to the hospital via emergency transport. The progress note also documented a report was called to the emergency room nurse. Resident #4's medical record did not document information was provided to the hospital to ensure a safe and effective transition of care. On 4/11/19 at 9:49 AM, the DON said the facility sent the face sheet, physician's orders, Physician's Order Scope of Treatment (POST), History and Physical, and the most recent progress note, with Resident #4 to the hospital. On 4/11/19 at 10:37 AM, the Regional Nurse said the facility did not retain a copy of the medical records sent and did not document what was sent.
CONCERN (D)

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

Deficiency F0625 (Tag F0625)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, policy review, and record review, it was determined the facility failed to ensure a bed-hold policy wa...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, policy review, and record review, it was determined the facility failed to ensure a bed-hold policy was provided to a resident or their representative upon transfer to the hospital. This was true for 1 of 1 resident (#4) reviewed for transfers. This deficient practice created the potential for harm if residents were not informed of their right to return to their former bed/room at the facility within a specified time and may cause psychosocial distress if not informed they may be charged to reserve their bed/room. Findings include: The facility's Bed-Hold readmission policy, revised on 12/19/16, documented the facility will reserve the bed of a resident who has been transferred to a hospital or left the facility with expectation of returning in the near future, as long as payment was made in advance to reserve the bed. Resident #4 was readmitted to the facility on [DATE], with multiple diagnoses including urinary tract infection and stroke with hemiplegia (paralysis) on the left side. A Nursing Progress Note, dated 4/7/19 at 3:00 AM, documented Resident #4 was transferred to the hospital. Resident #4's medical record did not include documentation she or her representative received a bed-hold notification when she was transferred to the hospital. On 4/11/19 at 9:56 AM, RN #1 said she was not aware of the facility's bed-hold policy. On 4/11/19 at 10:13 AM, the Regional Nurse said the facility could not locate a copy of a bed-hold policy provided to Resident #4 when she was transferred to the hospital on 4/7/19.
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 staff interview and record review, it was determined the facility failed to ensure residents' care plans were updated t...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview and record review, it was determined the facility failed to ensure residents' care plans were updated to include resident-specific behaviors and interventions related to the use of antipsychotic medication. This was true for 1 of 12 residents (Resident #13) whose care plans were reviewed. This failure created the potential for residents to receive unnecessary antipsychotic medication. Findings include: Resident #13 was admitted to the facility on [DATE], with multiple diagnosis including dementia with behavioral disturbances, and weakness. Resident #13's Quarterly MDS assessment, dated 1/15/19, documented Resident #13 experienced severe cognitive impairment with depressed mood. A physician's order, dated 10/30/18, documented Resident #13 was to receive Seroquel 100 mg every morning, and Seroquel XR (extended release), 50 mg every night for treatment of depression. Resident #13's care plan, revised on 1/24/19, did not include resident-specific depressive mood/behavior symptoms staff were to monitor her for or interventions staff were to implement to prevent and respond to them. On 4/10/19 at 2:49 PM, LPN #1 stated Resident #13's depression symptoms were exhibited by tearful and angry outbursts. LPN #1 said Resident #13's care plan did not include interventions related to her depression. On 4/10/19 at 3:02 PM , the DON stated Resident #13's care plan did not include interventions related to her depression.
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, staff interview, record review, and policy review, it was determined the facility failed to ensure infection control measures were consistently implemented for hand hygiene durin...

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Based on observation, staff interview, record review, and policy review, it was determined the facility failed to ensure infection control measures were consistently implemented for hand hygiene during perineal care (peri-care), and care of urinary tubing and the urine collection bag. This was true for 1 of 12 residents (Resident #9) reviewed for infection control. These deficient practices created the potential for harm by exposing residents to the risk of infection and cross contamination. Findings include: 1. The facility's Infection Control Hand Hygiene policy, dated 6/2015, documented all staff members were to follow handwashing and/or hand hygiene procedures to prevent the spread of infection. Hand hygiene or hand washing were to be completed after contact of body fluids or secretions, and the removal of gloves. On 4/9/19 at 10:55 AM, CNA #1 and CNA #2 were observed performing peri-care for Resident #9. After completing the peri-care, CNA #1 placed a new brief on Resident #9. CNA #1 did not remove her gloves or perform hand hygiene after completing the peri-care and before she applied the new brief. CNA #1 then was observed to perform hand hygiene, don new gloves and place soiled linen into a laundry bag. CNA #1 then placed a clean shirt on Resident #9. CNA #1 did not remove her gloves and perform hand hygiene after handling the soiled linen and placing a clean shirt on Resident #9. On 4/9/19 at 11:14 AM, CNA #1 stated she missed opportunities for hand hygiene and glove changes after Resident #9's peri-care, and handling dirty linen. 2. The facility's Infection Prevention and Control policy, dated 10/2017, documented to keep urinary collection bags and the tubing off the floor as part of ensuring appropriate techniques in the care and maintenance of foley (urinary) catheters. On 4/8/19 at 1:54 PM, Resident #9's urine collection bag and tubing were observed dragging on the floor. On 4/9/19 at 10:52 AM, Resident #9's urine collection bag and tubing were observed lying on the floor next to his bed. On 4/9/19 at 10:52 AM, CNA #1 stated Resident #9's urine collection bag and tubing were lying on floor next to Resident #9's bed, and they should not have touched the floor.
CONCERN (E)

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

Menu Adequacy (Tag F0803)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, review of recipes, and staff interviews, the facility failed to ensure menus were updated to reflect the r...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, review of recipes, and staff interviews, the facility failed to ensure menus were updated to reflect the residents' dietary needs. This affected 7 of 7 (#7, #13, #16, #32, #34, #42, and #50) residents who required fortified foods. This failed practice had the potential for harm if residents were dissatisfied with their meals or experienced weight loss. Findings include: a. Resident #7 was admitted to the facility on [DATE], with diagnoses that included nausea, heart failure, and chronic obstructive pulmonary disease. A physician's order, dated 1/4/19, documented Resident #7 required fortified foods with her meals for a consistent carbohydrate diet. b. Resident #13 was admitted to the facility on [DATE], with diagnoses that included heart disease and dementia. A physician's order, dated 12/28/18, documented Resident #13 required fortified foods with her meals with a regular mechanical soft meats diet, due to her teeth. c. Resident #16 was admitted to the facility on [DATE], with diagnoses that included pain and dementia. A physician's order, dated 1/25/19, documented Resident #16 required fortified foods with his meals for a regular diet. d. Resident #32 was admitted to the facility on [DATE], with diagnoses that included dysphagia (loss of or deficiency in the power to use or understand language as a result of injury to or disease of the brain), heartburn, nutritional anemia, and dementia. A physician's order, dated 1/4/19, documented Resident #32 required fortified foods with her meals for a regular finger food diet to promote intake. e. Resident #34 was admitted to the facility on [DATE], with diagnoses that included nutritional and metabolic disease, heartburn, and dementia. A physician's order, dated 2/22/19, documented Resident #34 required fortified foods with her meals for a regular pureed diet to promote weight maintenance. f. Resident #42 was admitted to the facility on [DATE], with diagnoses that included epilepsy. A physician's order, dated 3/11/19, documented Resident #42 required fortified foods with her meals for a regular diet. g. Resident #50 was admitted to the facility on [DATE], with diagnoses that included brain and skin cancer and seizures. A physician's order, dated 4/8/19, documented Resident #50 required fortified foods with her meals for a regular diet to discourage weight loss. The facility's Fortified Recipes included milkshakes, pudding parfaits, mashed potatoes, hot cereal, creamed soup, streusel topping, and milk. On 4/10/19 at 10:58 AM, [NAME] #2 was observed placing the lunch meal items into the steam table compartments. The meal consisted of pork loin, roasted potatoes, sautéed zucchini, scalloped apples, dinner roll, Swedish meat balls, parsley herbed noodles, and broccoli florets. The steam table included mechanical soft options and pureed options. The steam table did not include fortified food items. On 4/10/19 at 1:55 PM, [NAME] #2 stated she did not know how to prepare fortified food. She said the kitchen was not currently providing fortified foods to residents. [NAME] #2 stated the previous CDM never provided the education on preparing fortified foods. [NAME] #2 stated there were a few residents who required fortified foods and none of them were receiving them. On 4/10/19 at 3:50 PM, the Interim CDM stated she became aware this week that the kitchen staff was not providing fortified foods to residents and she was currently in the process of teaching kitchen staff how to prepare fortified food items. On 4/11/19 at 9:04 AM, the RD stated the facility had recipes for fortified mashed potatoes, eggs, cereals, and pudding. The RD stated she implemented the fortified foods program in November of 2018 and she discussed with the previous CDM about implementing the program. The RD stated she was unaware the program was not implemented.
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, temperature log review, resident interview, Resident Group interview, and staff interview, it was determined the facility failed to ensure palatable food was served. This directl...

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Based on observation, temperature log review, resident interview, Resident Group interview, and staff interview, it was determined the facility failed to ensure palatable food was served. This directly impacted 3 of 3 (#40, #41, and #44) residents in Resident Group interview and had the potential to affect the other 45 residents who dined in the facility. This failed practice had the potential to negatively affect residents' nutritional status and psychosocial well-being. Findings include: a. Review of the Resident Council Meeting Minutes documented the following concerns with the food. - 11/5/18: Six residents were in attendance and concerns with the food included a lack of flavor and appearance, not happy with the temperatures, and the meat tough. - 12/3/18: Six residents were in attendance and concerns with the food included sandwiches with dry and hard bread, grilled cheese sandwiches offered without cheese, meet is too tough, and meals were unappealing, and the residents would not feed the food to their dogs. The meeting minutes documented the concerns from last month still were not dealt with and there were issues with the food. - 1/7/19: Five residents were in attendance and concerns with the food included the vegetables were too mushy and residents wanted baked potatoes, spaghetti, potato salad, BBQ, chef salads, other vegetable options, and meat with breakfast. - 2/4/19: Nine residents were in attendance and concerns with the food included the food temperatures were not good, the food was cold, and the food was horrible. The meeting minutes documented the food temperature concerns from last month were still not dealt with and there continued to be an issue with the temperatures of the food. - 3/4/19: Nine residents were in attendance and the meeting minutes documented the food temperature concerns from last month were still not dealt with and there continued to be an issue with the temperatures of the food. - 4/1/19: Eight residents were in attendance and concerns with the food included the food was terrible. The meeting minutes documented the food temperature concerns from last month were still not dealt with and there continued to be an issue with the temperatures of the food. b. On 4/9/19 at 10:54 AM, during the Resident Group interview, Residents #40, #41, and #44 said the food was an issue and had been an ongoing issue for months. The residents stated the food was not good and they had spoken to the Dietitian about their concerns and nothing had changed. The residents stated the hot food was served cold and the warm food was served cold. The residents stated the food that was supposed to be cold warmed up before they received it, such as the ice cream. c. On 4/10/19 at 10:58 AM, [NAME] #2 was observed placing the lunch meal items into the steam table compartments. Steam could be seen on the left side of the steam table and the right side was observed without steam drifting up. There was a cold breeze coming from above and blowing directly onto the right side of the steam table. On 4/10/19 at 11:13 AM, [NAME] #2 was observed uncovering the food items on the steam table and started preparing pureed breads to add to the steam table. On 4/10/19 at 11:18 AM, [NAME] #2 began assessing the temperatures of the foods most of the food items where within appropriate temperatures. The ground pork was assessed at 143 degrees F, a potato dish was assessed at 156 degrees F, and the baked fruit was assessed at 103 degrees F. On 4/10/19 at 11:30 AM, the food remained uncovered and the cool breeze continued to blow onto the left side of the steam table. On 4/10/19 at 11:39 AM, the Interim CDM stated she did notice the cool breeze blowing onto the food on the left side of the steam table and she stated the food was uncoverd which could allow heat to escape. The Interim CDM assessed the temperature of the steam table water and it was 178 degrees F. The Interim CDM stated the water temperature should be 190 degrees F minimally. d. On 4/10/19 at 12:04 PM, the Interim CDM stated the facility was missing multiple days of temperature logs. She provided copies of the last four months' worth of temperature logs that she could locate. The Interim CDM stated the previous CDM was on maternity leave and according to the staff, the previous CDM had not provided adequate training to new staff on how to and when to assess temperatures of the food items before service. The facility's Meal Temperature logs were not completed at each meal as follows: - Lunch and dinner not assessed: 1/13/19 and 1/15/19 - Dinner not assessed: 1/1/19, 1/4/19, 1/5/19, 1/6/19, 1/7/19, 1/8/19, 1/10/19, 1/11/19, 1/12/19, 1/14/19, 1/16/19, 1/17/19, 1/18/19, 1/21/19, 1/22/19, 1/23/19, 1/24/19, 2/9/19, 3/31/19, 4/2/19, 4/3/19, and 4/10/19 - Breakfast not assessed: 4/9/19 - Temperatures were not assessed for all three meals: 1/19/19, 1/20/19, 1/25/19 through 2/8/19, 2/10/19 through 3/30/19, 4/1/19, and 4/4/19 through 4/8/19 - The temperature of the milk was not assessed on 1/19/19, 1/20/19, and 1/25/19 through 4/10/19. - The cold food items temperature was higher than 41 degrees on 1/24/19 when the milk was 46 degrees F. - The facility assessed the meal temperatures 57 out of 300 opportunities or 19%. On 4/10/19 at 3:50 PM, the Interim CDM stated the exhaust fan was blowing cold air onto the food and the steam table. The Interim CDM stated when the exhaust fan was turned off and the food was covered the food items retained their heat. The Interim CDM stated she educated the staff on the appropriate way to maintain temperatures of the food items on the steam table.
CONCERN (F)

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

Food Safety (Tag F0812)

Could have caused harm · This affected most or all residents

Based on observation, review of facility policy, [NAME] Cleaning list, temperature logs, sanitation logs, and the 2017 FDA Food Code, and staff interview, it was determined the facility failed to ensu...

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Based on observation, review of facility policy, [NAME] Cleaning list, temperature logs, sanitation logs, and the 2017 FDA Food Code, and staff interview, it was determined the facility failed to ensure food was handled properly and maintained according to safe practices. This was true when Potentially Hazardous Food (PHF) cold food temperatures were not maintained at safe temperatures. In addition, the facility failed to ensure measures were in place to prevent possible cross-contamination of dirty to clean areas in the kitchen and the kitchen was routinely cleaned. These failed practices placed 11 of 11 sample residents (#16, #18, #27, #28, #29, #32, #36, #37, #40, #41, and #47) who dined in the facility and the other 36 residents who dined in the facility, at risk of adverse health outcomes. Findings include: 1. The facility's Environment and Equipment policies, both dated May 2014, documented the equipment and the physical kitchen were cleaned after each use. The policies documented the kitchen staff were responsible for notifying maintenance when repairs were needed. Kitchen cleanliness Inspection: On 4/8/19 at 2:46 PM, the kitchen was observed with multiple unclean surfaces, unsafe thawing practices, and food and grease debris on and in equipment and on the floor as follows: * The wood cabinets which contained spices were observed with a greasy substance covering the doors and the cupboard surfaces. The wood was exposed; which created a porous surface for bacteria to reside. The grease could be felt when their surfaces were touched. The oven was observed with a greasy substance covering the front door handles and surface. The microwave had a yellow butter like substance on the inside top of the unit and the toaster oven had blackish brown food debris inside the unit. * Food debris and a layer of dirt were observed under the three-compartment sink, behind the ice machine, under the refrigerators, in the dishroom, in the pantry, under the stove, and under the steam table. Food debris particles were observed as small dark pellets, dust, grease, patches of sticky orange substances, multiple patches of black spills of fluids, onion skin, bread crumbs, and more. * There were three large packages of meat observed sitting in two separate sinks. One sink had two packages of frozen meat thawing without being immersed in water. The other sink had one package of frozen meat thawing with a thin stream of cold water running onto the meat and the drain was not plugged. * Two refrigerators were observed with sticky food spills and food debris throughout the units. * The recessed holding compartments of the steam table, for the metal food trays, was observed filled with water and had a slimy brown substance covering the entire bottom and approximately 1 1/2 inches to the water line. When the steam table was in use, trays containing food items were placed over the recessed areas and kept warm by the steam generated by the table. The observations above presented potential areas for bacterial growth, unsafe thawing practices, and subsequent spread of food-borne illnesses. On 4/8/19 at 2:46 PM, the facility's April 2019 Cook's Cleaning List documented the following cleaning tasks. * Daily cleaning tasks included cleaning the sinks, grill, stove, can opener, and ensuring the doors were shut. * AM [NAME] cleaning tasks included cleaning the microwave, fridges, toasters, produce fridge, and knife rack. * PM cook cleaning tasks included cleaning the steam table, dry bins, garbage cans, walls, shelves above the grill, and floors. * Friday tasks included cleaning the doors, windows, pan shelves, cupboards, can shelves, and the ice machine. * Sunday and Wednesday tasks included cleaning the freezer and pantry area. The April 2019 Cook's Cleaning List documented the Daily and AM [NAME] cleaning tasks were completed the 1st through the 3rd and the 4th through the 8th were blank. The PM [NAME] tasks were completed the 1st, and 4th through the 8th, the 2nd and 3rd were blank. The Friday and Sundays and Wednesdays tasks were blank. The Facility's Sanitizing Bucket Log documented the amount of sanitizer in Parts per Million (PPM) for the sanitizer buckets. The log was completed the 1st through the 3rd for the breakfast and lunch shifts and the 4th through the 8th were blank. The log was completed the 1st through the 7th for the dinner shift and the 8th was blank. The Facility's Dish Machine Log documented the staff assessed the PPM sanitizer level used for the dishwashing wares, and the water temperatures of the wash and rinse cycles. The log was completed for breakfast, lunch, and dinner on the 1st, 2nd, 7th and 8th. The log was incomplete on the 3rd and 4th for lunch and the 5th and 6th were incomplete for breakfast and lunch. On 4/8/19 at 2:53 PM, [NAME] #2 was observed writing in the missing holes on the Sanitizer Bucket Log. She stated she forgot to complete the documentation when she worked on the 6th through the 8th. She stated someone else worked on the 4th and the 5th and that individual never completed the logs, so she filled in those days too. [NAME] #2 stated she should not have completed the missing information for the 4th through the 8th. On 4/8/19 at 2:55 PM, [NAME] #2 observed the Cleaning Log with the surveyor and stated she forgot to complete the Cook's Cleaning Log for the 6th through the 8th. [NAME] #2 was asked to provide a copy of the Cleaning Log, however, when she provided a copy of the Cook's Cleaning Log it now contained her initials on the 6th through the 8th. [NAME] #2 stated she filled in the missing information on 4/8/19 prior to making the copy. On 4/8/19 at 2:55 PM, [NAME] #1 was asked to provide a copy of the Dish Machine Log and she stated there was missing information on multiple days. On 4/8/19 at 3:16 PM, the Administrator stated [NAME] #2 should not have filled in the missing information and he would address the issue with the kitchen. The Administrator stated the current food service company was being replaced with a new company due to concerns. 2. The 2017 FDA Food Code, Chapter 3, Part 3-5, Limitation of Growth of Organisms of Public Health Concern, subpart 3-501.12 Time/Temperature Control for Safety Food, documents refrigerated foods are to be maintained at 5 C (41 F [Fahrenheit]) or less. The facility's Cold Food Storage policy, dated May 2014, documented the food service department was responsible for maintaining all perishable foods at 41 F or less. The policy documented the food service department would ensure the thermometers were accurate and temperatures of the refrigerator and freezers were assessed daily and recorded. The facility's Food brought by Family/Visitors policy, revised February 2014, documented perishable foods would be used by the use by date and thrown out if the items exceeded the use by date. The policy documented potentially hazardous foods that were left out longer than 2 hours without appropriate refrigeration would be discarded. Multiple Kitchen Inspections documented multiple refrigerator units' temperatures were greater than 41 degrees F and contained PHF food items as follows: * On 4/8/19 at 2:49 PM, the kitchen refrigerator unit on the right was observed at 50 degrees F and refrigerator unit on the left was observed at 45 degrees F. Food items in the units consisted of milk (PHF), pudding (PHF), salads (PHF), juices, meats (PHF), cottage cheese (PHF), and more. * On 4/8/19 at 2:55 PM, a copy of the Refrigerator Temperature Logs for the two units were requested and they documented the following temperatures out of range. The unit on the right: - 4/1/19: the AM shift was not assessed, and the PM documented 42 degrees F - 4/2/19: 42 degrees F, AM shift and the PM documented 45 degrees F - 4/3/19: the PM documented 42 degrees F - 4/4/19: the AM shift was not assessed, and the PM documented 45 degrees F - 4/5/19: the AM shift was not assessed, and the PM documented 48 degrees F - 4/6/19: the AM and PM shifts documented 42 degrees F - 4/7/19: the AM shift documented 43 degrees F and the PM documented 45 degrees F - 4/8/19: the AM shift was not assessed * On 4/9/19 at 11:29 AM, the kitchen refrigerator unit on the left was observed within appropriate temperature range and the unit on the right was observed at 45 degrees F. Two containers of milk (PHF), one from the front and the back were assessed by the Interim CDM. The milk from the front of the unit was assessed at 44 degrees F and the milk from the back of the unit was assessed at 45.2 degrees F. The CDM stated she would move the food items to ensure they were within temperature range and notified the Maintenance Director to correct the issue. * On 4/9/19 at 12:47 PM, the small countertop, two-foot-high refrigerators on the halls were observed to be unclean, with outdated foods, the temperature logs lacked documentation, and temperatures out or range, as follows: South Hall refrigerator: - The fridge was observed with a 1-2-inch-thick buildup of ice in the freezer section. Food items could not fit well into the opening. - There were spills of brown sticky liquids and food debris in the unit. - There were three outdated milks with a use by dated of 4/2/19 and 11 outdated Strawberry Ensures with a use by date of 9/1/18. - The Temperature log was incomplete on the AM shifts of the 1st, 4th, and 5th, the PM shifts of the 2nd, 3rd, and 8th. - The temperature was greater than 41 degrees F on 4/4/19: 42 degrees F and 4/7/19 at 48 degrees F. - The fridge contained food items of milk (PHF), sodas, and nutritional supplements. North Hall refrigerator: - The fridge was observed with a 1-2-inch-thick buildup of ice in the freezer section. Food items could not fit well into the opening. - There were spills of sticky liquids and food debris in the unit. - There was a case of outdated chocolate Glucerna dated 12/1/18. - The Temperature log for April 2019 lacked documentation on the AM shift on the 1st, 4th, and 5th and on the PM shift on the 2nd and the 3rd. - The temperature was greater than 41 degrees F on 4/1/19 at 45 degrees F, 4/2/19 at 42 degrees F, 4/3/19 at 43 degrees F, 4/4/19 at 48 degrees F, 4/5/19 at 45 degrees F, and 4/6/19 at 42 degrees F AM shift, and 43 degrees F on the PM shift. The fridge contained food items of milk (PHF), sodas, and nutritional supplements. On 4/9/19 at 1:22 PM, [NAME] #1 stated the temperatures of the refrigerators were inappropriate and the kitchen staff were to assess the temperatures of the units. [NAME] #1 stated if concerns were identified they should report issues to maintenance. [NAME] #1 stated all facility staff should ensure food items were not retained beyond their expiration dates. On 4/10/19 at 3:38 PM, the Maintenance Director stated he monitored the kitchen refrigerators on a monthly basis. The Maintenance Director stated he did not monitor the hall refrigerators as part of his monthly checklist. He stated the staff were to let him know when the refrigerator units were not working, and he had not received any notices of the units not working until during the survey. He stated he had a refrigerator repair man in to fix the kitchen unit on 4/9/19 and 4/10/19. The Maintenance Rounds documented the kitchen refrigerators were assessed on 3/4/19. The log did not document what the units were running at or the appropriate temperatures for the units. 3. The facility's Infection Control: Hand Hygiene policy, revised September 2014, documented staff needed to perform hand hygiene after handling soiled equipment or utensil. On 4/10/19 at 8:31 AM, [NAME] #2 was observed on the dirty side of the dish room scrubbing dishes and rinsing off dishes before running them through the dish machine. [NAME] #2 was not wearing gloves or an apron to protect her clothes. [NAME] #2 left the dirty dish area and pushed a cart of clean dishes into the kitchen and began putting pots, pans, a knife, and other dishes into their spots. [NAME] #2 did not perform hand hygiene when she moved from the dirty to clean areas. At the time of the observation, [NAME] #2 stated she should have cleaned her hands. On 4/10/19 at 8:37 AM, the Interim CDM stated [NAME] #2 should have cleaned her hands and she would have [NAME] #2 rewash the dishes. 4. The facility had people enter the kitchen without wearing hair or bread restraints. On 4/10/19 at 8:51 AM, the Coffee Delivery person walked into the kitchen with a full beard and mustache, and a full head of hair not restrained in a hair net or beard or mustache restraints. On 4/10/19 at 8:55 AM, the Interim CDM stated anyone entering the kitchen should be wearing hair restraints and beard restraints if applicable.
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

  • "Why is there high staff turnover? How do you retain staff?"
  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • No fines on record. Clean compliance history, better than most Idaho facilities.
Concerns
  • • Multiple safety concerns identified: 3 harm violation(s). Review inspection reports carefully.
  • • 31 deficiencies on record, including 3 serious (caused harm) violations. Ask about corrective actions taken.
  • • Grade F (20/100). Below average facility with significant concerns.
  • • 65% turnover. Above average. Higher turnover means staff may not know residents' routines.
Bottom line: Trust Score of 20/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Mini-Cassia's CMS Rating?

CMS assigns MINI-CASSIA CARE CENTER an overall rating of 1 out of 5 stars, which is considered much below average nationally. Within Idaho, 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 Mini-Cassia Staffed?

CMS rates MINI-CASSIA CARE CENTER's staffing level at 3 out of 5 stars, which is average compared to other nursing homes. Staff turnover is 65%, which is 19 percentage points above the Idaho average of 46%. High turnover can affect care consistency as new staff learn residents' individual needs.

What Have Inspectors Found at Mini-Cassia?

State health inspectors documented 31 deficiencies at MINI-CASSIA CARE CENTER during 2019 to 2025. These included: 3 that caused actual resident harm and 28 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Mini-Cassia?

MINI-CASSIA CARE 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 CASCADES HEALTHCARE, a chain that manages multiple nursing homes. With 68 certified beds and approximately 56 residents (about 82% occupancy), it is a smaller facility located in BURLEY, Idaho.

How Does Mini-Cassia Compare to Other Idaho Nursing Homes?

Compared to the 100 nursing homes in Idaho, MINI-CASSIA CARE CENTER's overall rating (1 stars) is below the state average of 3.2, staff turnover (65%) is significantly higher than the state average of 46%, and health inspection rating (1 stars) is much below the national benchmark.

What Should Families Ask When Visiting Mini-Cassia?

Based on this facility's data, families visiting should ask: "How do you ensure continuity of care given staff turnover, and what is your staff retention strategy?" "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 facility's high staff turnover rate.

Is Mini-Cassia Safe?

Based on CMS inspection data, MINI-CASSIA CARE 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 Idaho. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Mini-Cassia Stick Around?

Staff turnover at MINI-CASSIA CARE CENTER is high. At 65%, the facility is 19 percentage points above the Idaho average of 46%. High turnover means new staff may not know residents' individual needs, medications, or preferences. It can also be disorienting for residents, especially those with dementia who rely on familiar faces. Families should ask: What is causing the turnover? What retention programs are in place? How do you ensure care continuity during staff transitions?

Was Mini-Cassia Ever Fined?

MINI-CASSIA CARE CENTER has no federal fines on record. CMS issues fines when nursing homes fail to meet care standards or don't correct problems found during inspections. The absence of fines suggests the facility has either maintained compliance or corrected any issues before penalties were assessed. This is a positive indicator, though families should still review recent inspection reports for the full picture.

Is Mini-Cassia on Any Federal Watch List?

MINI-CASSIA CARE 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.