Failure to Monitor BP/HR for Metoprolol and to Complete GDR for Quetiapine
Summary
The facility failed to ensure a resident's drug regimen was free from unnecessary drugs when staff did not monitor blood pressure and heart rate before administering Metoprolol Succinate ER 25 mg twice daily for Resident #7, despite physician orders to hold the medication if systolic blood pressure was below 110 or heart rate was less than 60. Review of the September 2025 through December 2025 MARs showed the medication was routinely given at 9:00 AM and 5:00 PM, but there was no documentation on the MAR showing blood pressure or heart rate checks before administration. The vital sign record from September 2025 through December 2025 was inconsistent and did not show vital signs taken every day or in the evening to match the medication schedule. The pharmacist's monthly medication record reviews also reflected the concern, and the DON confirmed the finding during interview. The facility also failed to complete a gradual dose reduction for Resident #36, who was receiving quetiapine 12.5 mg nightly for vascular dementia. Resident #36 had a history of depression, falls, speech disturbance, asthma, osteoarthritis-related shoulder pain, and prior resistive behavior with care, and entered hospice care on 6/7/24, after which psychiatric services were no longer received. The record showed the resident continued on quetiapine without a gradual dose reduction, and nursing had not documented side effects or behaviors to show whether the medication was still needed. GNA staff reported the resident had been very resistive to care when first admitted but was now very cooperative, and another staff member stated the resident no longer resisted care like before.
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