Inadequate Pain Assessment and Management
Summary
The facility did not adequately assess and provide pain management services for one resident who required such care. The resident had diagnoses including Parkinsonism, panic disorder, disorientation, generalized anxiety disorder, polyneuropathy, lumbar disc degeneration with discogenic back pain, and a brain stimulator implant. The resident’s admission MDS showed a BIMS score of 13/15, indicating cognition intact, and the resident received scheduled pain medication. The care plan identified potential pain/discomfort related to the right shoulder and directed staff to administer pain relief measures, evaluate and document effectiveness, and use appropriate pain scales and non-therapeutic interventions as needed. The resident had multiple pain-related medication orders, including PRN acetaminophen, PRN tramadol, scheduled meloxicam, topical diclofenac gel for right shoulder pain, topical muscle rub, and ice/cold compresses for the right shoulder. The PRN orders did not include clear parameters or indications for when each medication should be used. Survey review of the MAR showed repeated PRN administrations for pain, but the documentation did not include pain severity, location, or characteristics for many of the doses. Several entries documented only "pain" or a general body area, and first-time reports of pain in new locations such as the right hip, right lower rib, and right lower quadrant were not accompanied by documentation of provider notification. The resident’s follow-up PRN pain assessments also did not include intensity, severity, or characteristics of pain. The ordered non-pharmacological intervention of ice/cold compress was not administered at any time during the review period. In addition, the scheduled Voltaren gel was documented as refused on numerous occasions, but there was no documentation of provider notification, pain assessment, or alternative interventions associated with those refusals. During interview, an RN stated pain scores were not typically documented unless a MAR prompt appeared, location and characteristics were not typically assessed, and there was no known standard for choosing among multiple PRN pain medications. The RN also stated he was unaware of the ordered non-pharmacological intervention. The MD stated nursing staff were expected to use non-opioid measures first, evaluate efficacy, and then determine whether opioid medication should be used. The DON stated pain assessments should include a pain score or face scale, that PRN documentation should include location and severity if a score could not be entered, that non-pharmacological interventions should be used first, and that the provider should be notified when a resident refuses scheduled pain medication.
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