Failure to Update and Implement Comprehensive Pain Management for a Resident with Worsening Chronic Pain
Summary
The deficiency involves the facility’s failure to provide safe, appropriate, and person‑centered pain management for a resident with chronic pain conditions, in accordance with the resident’s goals, preferences, and comprehensive care plan. The resident was admitted with fibromyalgia, anxiety disorder, major depressive disorder, and rheumatoid arthritis affecting multiple sites, and was receiving PT/OT. The care plan identified actual pain related to RA and fibromyalgia and included interventions such as administering analgesia per orders, evaluating effectiveness of pain interventions, and observing and reporting changes in function and behavior. An initial pain evaluation dated 4/7/25 showed a mild pain risk score, and the EMR flagged that an additional pain evaluation due 7/7/25 was more than 260 days overdue, indicating that updated pain assessments were not completed as scheduled. Over time, the resident’s pain increased, particularly after a RA medication that had been effective was discontinued because insurance would no longer pay for it. Nursing notes documented ongoing complaints of left hip pain, back pain with crying when sitting up, and episodes of knee and leg pain where the resident reported that pills were not helping. The resident was frequently using scheduled and PRN pain medications, including acetaminophen, gabapentin, and hydromorphone, with documented pain scores ranging from 3 to 10. The quarterly MDS dated 11/20/25 documented no pain in the last 5 days and no interference with sleep or therapy, but a subsequent quarterly pain interview on 11/26/25 documented frequent pain, difficulty sleeping due to pain, and a pain intensity of 7 (severe), with daily vocal complaints of pain. Despite this, there were no updates to the care plan to reflect severe daily pain or to add new interventions, and the pain interview lacked documentation of interventions or their effectiveness. By the time of the annual MDS on 2/28/26, the resident was documented as frequently having severe pain that interfered with sleep, therapy, and day‑to‑day activities, and the pain CAA directed staff to proceed to care plan with an objective of improvement and symptom relief. However, surveyor review showed the care plan had not been updated to address the change from no pain on the earlier MDS to severe, function‑impacting pain, and there were no new interventions or assessment of what pain level was tolerable or acceptable to the resident until a late nursing order on 3/19/26 set an acceptable pain level at 4/10. From 3/1/26 to 3/25/26, the resident received frequent PRN hydromorphone (43 doses) and PRN acetaminophen in addition to scheduled medications, with multiple instances where the pain goal was not met, yet there was no documentation that non‑pharmacological interventions were implemented despite an active order listing repositioning, distraction, warm blankets, back rubs, ice, and other measures. The resident reported that pain had worsened, that she sometimes used a cream and lying down for relief, and that she attended fewer activities because of pain. At exit, the facility had not provided information explaining why the resident’s increased pain and frequency were not comprehensively assessed, why the care plan was not updated with additional interventions beyond oral medications, or why alternatives to the discontinued RA medication with previously good effect were not pursued.
Penalty
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