Failure to Provide Contracture Management Devices
Summary
The facility failed to ensure residents with limited range of motion received appropriate treatment and services to increase range of motion and/or prevent further decrease in range of motion for three residents with contractures or limited ROM. The deficiency involved Resident #53, Resident #64, and Resident #103, each of whom had documented contractures or ROM limitations and were observed without the ordered or expected contracture-management devices in place. Resident #53 had diagnoses including cerebral infarction, contractures of both hands, aphasia, and anxiety disorder. Her OT discharge summary stated a long-term goal for her to safely wear a hand roll on the right hand and a palm guard splint on the left hand for up to 8 hours to manage contracture and prevent skin breakdown. However, progress notes did not show refusals of the hand roll or splint, and multiple observations showed both contracted hands without the palm guard splint or hand roll in place while she was in bed or in a broda chair. Staff interviews indicated she was often combative and that staff sometimes could not apply the devices, but the nursing staff were responsible for applying them and documenting refusals. The DON and Administrator stated staff were expected to apply the hand roll and palm guard splint to residents with contractures. Resident #64 had diagnoses including right-hand contracture, muscle wasting and atrophy, and atrial fibrillation. Her MDS indicated a contracture, but her care plan lacked information regarding contracture management. OT records showed she had previously received treatment for her contracture and had progressed to using a hand splint for 4 hours, yet observations on 3/16/26 and 3/17/26 showed her right hand contracted without a hand splint in place. During interview, the resident stated she had previously used a hand roll daily and that it had been about 6 months since she last had one in her hand. The Director of Rehab and facility leadership stated nursing staff were responsible for ensuring residents on the contracture list received appropriate care and that the resident had a splint she was supposed to be wearing daily. Resident #103 had a diagnosis of left-hand contracture. His MDS reflected functional limitation in ROM, and his OT discharge summary showed a goal for him to tolerate wearing a resting hand splint to the left hand for 8 hours. The care plan and order summary did not address contracture management, and there were no ADL tasks for application of a contracture device. Observations on 3/16/26 and 3/17/26 showed his left hand curled into a fist with no splint or device on the hand or arm, and he stated he did not wear a splint even at night. Staff interviews indicated therapy had previously communicated that the splint should be worn when sitting up and removed in bed, but nursing staff were responsible for applying and maintaining the device after therapy discharge. The DON and Administrator stated nursing staff were responsible for ensuring contracture management devices were used as directed.
Penalty
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