Stay Ahead of Compliance with Monthly Citation Updates


In your State Survey window and need a snapshot of your risks?

Survey Preparedness Report

One Time Fee
$79
  • Last 12 months of citation data in one tailored report
  • Pinpoint the tags driving penalties in facilities like yours
  • Jump to regulations and pathways used by surveyors
  • Access to your report within 2 hours of purchase
  • Easily share it with your team - no registration needed
Get Your Report Now →

Monthly citation updates straight to your inbox for ongoing preparation?

Monthly Citation Reports

$18.90 per month
  • Latest citation updates delivered monthly to your email
  • Citations organized by compliance areas
  • Shared automatically with your team, by area
  • Customizable for your state(s) of interest
  • Direct links to CMS documentation relevant parts
Learn more →

Save Hours of Work with AI-Powered Plan of Correction Writer


One-Time Fee

$49 per Plan of Correction
Volume discounts available – save up to 20%
  • Quickly search for approved POC from other facilities
  • Instant access
  • Intuitive interface
  • No recurring fees
  • Save hours of work
F0605
D

Failure to Document Rationale and Gradual Dose Reduction for Psychotropic Medications

Franklin, Minnesota Survey Completed on 05-28-2025

Penalty

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.

Summary

The facility failed to ensure that as-needed (PRN) antipsychotic medications were limited to a 14-day period and that clinical rationale was documented for continuation beyond this timeframe. For two residents, there was no evidence in the medical records to support the ongoing use of PRN psychotropic medications past 14 days, nor was there documentation of a gradual dose reduction (GDR) or appropriate indication for use. Pharmacy reconciliation reports repeatedly requested clinical rationale and GDRs, but the facility did not respond or provide the required documentation. One resident, who was moderately cognitively impaired and had multiple diagnoses including anemia, heart failure, renal insufficiency, diabetes, hyperlipidemia, and anxiety, was prescribed alprazolam PRN with no documented rationale for use beyond 14 days. Another resident, who was severely cognitively impaired with diagnoses including peripheral vascular disease, arthritis, Alzheimer's, and anxiety, was prescribed multiple psychotropic medications, including haloperidol and olanzapine, with no clinical rationale for their continued use past 14 days. Additionally, there was no evidence of a GDR for the resident's antidepressant, and morphine was prescribed with an inappropriate indication of dementia. The consulting pharmacist confirmed that the required clinical rationales and GDRs were missing from the medical records and that multiple requests for this information had gone unanswered. The DON also confirmed the lack of documentation and was unsure who was responsible for completing pharmacy reviews, as the previous DON had left unexpectedly. Facility policy required documentation of rationale for extended psychotropic use and GDRs, but these requirements were not met for the residents reviewed.

An unhandled error has occurred. Reload 🗙