Failure to Document Required Medication Monitoring and Other Ordered Care
Summary
The facility failed to ensure services met professional standards of quality for multiple residents by not documenting required non-pharmacological interventions and by not documenting required side effect monitoring for psychotropic and antianxiety medications. Resident 15, Resident 58, and Resident 8 were all documented as severely cognitively impaired on MDS assessments, and each had physician orders for PRN opioid pain medication along with orders for staff to provide and document non-pharmacological interventions to reduce pain. Review of the TARs for these residents showed no documentation that staff attempted any non-pharmacological interventions, even though PRN oxycodone or morphine was administered multiple times during the reviewed periods. The facility also failed to document required side effect monitoring for psychotropic and antianxiety medications. Resident 17 was prescribed olanzapine and sertraline, Resident 6 was prescribed buspirone, Resident 58 was prescribed venlafaxine, Seroquel, and lorazepam, and Resident 8 was prescribed Risperdal and lorazepam. Physician orders directed staff to monitor for medication side effects every shift and document whether symptoms were observed or not observed. Review of the residents’ TARs showed no documentation that staff recorded whether side effects had or had not been observed for any of the ordered medications. The RCM confirmed that staff had not documented the required observations and stated the order did not provide space for staff to enter + or -. The facility also had expired lab specimen test tubes in both the North Hall and South Hall medication rooms. During observations, expired green top and blue top test tubes were found in the medication rooms, and staff confirmed that licensed nurses used those test tubes for drawing labs before they were picked up by the lab courier. In addition, Resident 5 had an incomplete wound healing supplement order that did not identify the supplement or dose, yet nurses signed the MAR as if the unidentified supplement had been administered daily. Resident 5 also had an order for an alternating low air loss mattress to be checked every shift, but observations showed the mattress display was set to 340 pounds with a flashing low-pressure alert while nurses had signed that the settings were verified as ordered.
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