F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
K

Failure in Medication Monitoring and Lab Management

Highland Pines Rehabilitation CenterClearwater, Florida Survey Completed on 04-17-2025

Summary

The facility failed to effectively monitor adverse events, specifically in the management of medication levels for multiple residents. This deficiency was highlighted by the case of a resident whose medication levels were not adequately monitored, leading to a significant medical event. The resident was admitted with various medical diagnoses and had specific medication orders that were not consistently followed. Laboratory results indicating low medication levels were not communicated to the physician, and necessary consultations were not obtained, resulting in the resident experiencing a severe medical episode that required transfer to a higher level of care. The report details multiple instances where the facility did not maintain effective systems for monitoring and reporting adverse events. Several residents had medication levels that were either not checked or not reported to the appropriate medical personnel, leading to suboptimal management of their conditions. The facility's process for handling lab orders and results was inadequate, with orders not being entered into the lab portal, results not being communicated to providers, and critical lab values not being addressed in a timely manner. Interviews with facility staff, including the Director of Nursing and other medical personnel, revealed systemic failures in the lab process and medication management. There was a lack of accountability and oversight in ensuring that lab results were reviewed and acted upon. The facility's Quality Assurance and Performance Improvement (QAPI) plan did not adequately address these issues, leading to a breakdown in the monitoring and management of residents' health care needs.

Plan Of Correction

QAPI/N 901 QA Program 1. What corrective action(s) will be accomplished for those residents found to have been affected by the deficient practices? Residents #5 and #10 no longer reside in the facility. Laboratory orders for medication management were received for residents #1, #2, #3, #4, #6, #7, #8, #9, and #11. Results of labs were reported to resident physicians, documented in the clinical record, and new orders were transcribed as indicated. Consult was for resident #1 as requested by physician. 2. How will you identify other residents having potential to be affected by the same practice and what corrective actions will be taken? A facility-wide audit of current residents on medications was conducted by the Director of Nursing/designee to ensure that residents on medications had appropriate lab monitoring orders in place and that any consults that were previously ordered were scheduled. Any residents identified without lab monitoring orders or fully executed consults were reported to physician and new orders transcribed as indicated. 3. What measures will be put into place or what systematic changes will you make to ensure that the practice does not recur? The Regional Nurse Consultant educated the Nursing Home Administrator and Director of Nursing on ensuring that an effective Quality Assurance program is in place as it pertains to the care of residents with a diagnosis, ensuring that lab orders are in place to monitor medication levels, physicians are notified of abnormal lab values or refused labs, documentation of physician notification of lab levels and new orders is recorded in the resident clinical record, and that consultation orders for or other outside providers are executed appropriately. 4. How the corrective action(s) will monitor to ensure the practice will not recur, i.e., what quality assurance program will be put in place(s); will be accomplished for those residents: Director of Nursing/Designee will randomly audit residents on medications to ensure that appropriate lab orders for monitoring medication levels are in place and consultation orders for outside providers are completed weekly for four weeks and then monthly for two months. Results of the audits will be submitted by the Director of Nursing/designee to the Quality Assessment, Assurance, and Compliance Committee monthly for three months for further recommendations and guidance.

Removal Plan

  • Regional Nurse Consultant educated the Administrator and Director of Nursing on ensuring that an effective Quality Assurance and Performance Improvement Plan is in place to ensure the safety of all residents.
  • Administrator educated 100% of the members of the Quality Assurance and Assessment Committee on ensuring that an effective Quality Assurance and Performance Improvement Plan is in place to ensure the safety of all residents.
  • Adhoc meeting held with interdisciplinary team and Medical director related to lab process monitoring and MD notification. Another Adhoc meeting was held on lab process/lab monitoring, following physician orders, clinical morning meeting process with review of lab binder, lab access availability audit.
  • Daily audits were conducted on lab process with no new findings.
  • Process Change: Administrator is responsible for ensuring that an effective Quality Assurance and Performance Improvement Plan is in place to ensure the safety of all residents.
  • All education and in-service sign in sheets were reviewed and validated for 13 out of 13 members of the Quality Assurance and Assessment Committee on ensuring that an effective Quality Assurance and Performance Improvement Plan is in place to ensure the safety of all residents.
  • Interviews were conducted with the Nursing Home Administrator, members of the interdisciplinary team, the Assistant Director of Nursing, and the DON. The staff members were able to verbalize they had been trained and were knowledgeable about the new policies.

Penalty

Inspection fine: $182,782
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The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.

Resources

Below are regulatory guidelines relevant to this citation:

See other F0867 citations
QAPI Monitoring Deficiencies for Skin Assessments and Food Sanitation
F
F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
Short Summary

QAPI monitoring was deficient when the facility failed to ensure performance improvement activities were properly implemented and tracked for incomplete skin assessments and food labeling issues in the snack room. The CEO stated there were three PIPs, but benchmark measurements were not consistently documented, one PIP remained active after completion because the facility did not want to fall off track, and the current measurement method did not adequately track whether improvement had occurred since implementation.

No penalty information released
tooltip icon
The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.
Failure to Develop a Staffing PIP
F
F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
Short Summary

The facility failed to develop and implement a PIP for staffing concerns after those issues were identified in QAPI. The DON stated staffing had been discussed, but no current staffing PIP existed, and later said a PIP was not started because the owner said there was no staffing issue. The Administrator reported short staffing for about a month, with call outs and no shows worsening after delayed paychecks, and staff said staffing concerns were discussed in QAPI along with efforts to find solutions and hire CNAs and nurses.

No penalty information released
tooltip icon
The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.
QAPI Committee Failed to Address Long Call Light Wait Times
E
F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
Short Summary

QAPI failed to address resident concerns about long call light wait times, which were linked to cares not being performed and toileting tasks not being completed in a timely manner. QAPI notes showed repeated discussion of call light delays over several months, including a 9-minute response goal, follow-up by nurse managers, daily report review, and adding management staff around mealtimes, but there was no discussion about increasing facility staffing related to the concern.

No penalty information released
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The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.
Failure to Maintain Clean and Homelike Environment
D
F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
Short Summary

Failure to Maintain Clean and Homelike Environment: Surveyors found that resident rooms, shower rooms, and common areas were not kept clean and homelike, with black buildup in grout, damaged grout, chipped floor tiles, and dusty ceiling vents. On revisit, the same environmental deficiency recurred, showing the facility did not sustain compliance with the cleanliness requirement.

No penalty information released
tooltip icon
The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.
QAPI Program Failed to Analyze Repeated Incontinence Care Neglect
F
F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
Short Summary

QAPI Program Failed to Analyze Repeated Incontinence Care Neglect: Multiple FRIs substantiated repeated failures to provide incontinence care, including not honoring a resident’s bedpan preference and instructing the resident to urinate in an incontinence brief. Although the facility used audits, staff education, and disciplinary action, the audit tool lacked meaningful documentation, and QAPI minutes did not include data analysis, RCA, or a PIP/action plan for the recurring incontinence care issues.

No penalty information released
tooltip icon
The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.
Ineffective QAPI Oversight and Tracking of Performance Improvement Plans
F
F0867 F867: Set up an ongoing quality assessment and assurance group to review quality deficiencies and develop corrective plans of action.
Short Summary

Ineffective QAPI oversight and tracking of PIPs: The facility’s QAPI minutes showed multiple ongoing PIPs for concerns such as staffing, hand hygiene, incontinence care, care conferences, tray accuracy, narcotic counts, HR, and showers, but many lacked measurable goals, dates, or a designated point person. Prior action items were not shown to be revisited or followed through in later meetings, and the Administrator, DON, and Corporate RN acknowledged that not all concerns were turned into PIPs. Several of the same issues later appeared as survey deficiencies.

No penalty information released
tooltip icon
The penalty, as released by CMS, applies to the entire inspection this citation is part of, covering all citations and f-tags issued, not just this specific f-tag. For the complete original report, please refer to the 'Details' section.
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