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
F0552
E

Failure to Obtain Informed Consent for Psychotropic Medications

Attica, Kansas Survey Completed on 06-11-2025

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 residents and/or their representatives were fully informed and provided informed consent regarding the use of psychotropic medications, as required by facility policy. Multiple residents with diagnoses such as PTSD, anxiety, depression, panic disorder, bipolar disorder, and dementia were prescribed various psychotropic medications, including antianxiety agents, antidepressants, and antipsychotics. Despite these prescriptions, the electronic medical records (EMRs) and electronic health records (EHRs) for these residents lacked documentation that informed consent was obtained or that education was provided about the medications' benefits, risks, and alternatives. For example, one resident with PTSD, anxiety, and depression was prescribed lorazepam, mirtazapine, and sertraline, but there was no evidence in the EMR of informed consent for these medications. Another resident with panic disorder, major depressive disorder, and bipolar disorder was prescribed buspirone, desvenlafaxine, lorazepam, and olanzapine, again without documentation of informed consent. Additional residents with depression, adjustment disorder, insomnia, and dementia were also prescribed psychotropic medications such as bupropion, citalopram, and duloxetine, with no evidence that they or their representatives were informed about the medications or provided consent. Interviews with facility staff confirmed that informed consent for psychotropic medications had not been completed for these residents. The administrative nurse indicated a misunderstanding of the facility's policy, believing that consent was only necessary for new medications started at the facility, not for those continued upon admission. The facility's policy, however, clearly required informing residents, families, or representatives of the benefits, risks, and alternatives for each psychotropic medication prior to adding, discontinuing, or changing any such medication.

An unhandled error has occurred. Reload 🗙