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
F0657
D

Failure to Notify Responsible Party and Hospice of Psychotropic Medication Discontinuation

Bakersfield, California Survey Completed on 08-19-2025

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 notify the responsible party (RP) and hospice provider when a psychotherapeutic medication, Quetiapine, was discontinued for a resident with diagnoses including senile degeneration of the brain, dementia, and major depressive disorder with severe psychotic symptoms. The resident was under hospice care and had an identified RP. The decision to discontinue the medication was made by the interdisciplinary team (IDT) following a recommendation from the physician's assistant, and the team agreed to the discontinuation. Upon review of the resident's medical record, there was no documentation that the RP or hospice provider had been informed of the medication change. The facility's policy requires the IDT, in conjunction with the resident and their family or legal representative, to develop and implement a comprehensive, person-centered care plan, including participation in care planning and notification of significant changes. The lack of documentation and notification meant that the RP and hospice provider were not included in the decision-making process regarding the resident's care.

An unhandled error has occurred. Reload 🗙