Failure to Monitor and Document Use of a Physical Restraint
Summary
The facility failed to provide ongoing monitoring and reassessment of a physical restraint, failed to implement restraint-reduction interventions, and used a physical restraint without documentation showing it was medically necessary for one resident. The resident was admitted with multiple diagnoses including intervertebral disc degeneration of the lumbar region, hypercholesterolemia, hypertension, osteoarthritis of the left hip and knee, dementia, chronic embolism and thrombosis, Alzheimer's disease, anxiety disorders, varicose veins, and osteoporosis. The current MDS showed severe cognitive impairment, that the resident was rarely understood, and that she used a manual wheelchair operated by staff, with no physical or verbal behaviors or wandering documented. Survey observations showed the resident seated in a wheelchair with a secured lap cushion on her lap and resting against her trunk while the wheelchair was pushed up against a corner table in the dining room. On multiple observations across several days, the resident remained in the same position, including one instance where she attempted to move the secured lap cushion but was unsuccessful and another where she was sleeping in the wheelchair at the dining room table. Staff interviews indicated the device was used routinely, with one CNA stating the resident must always wear the secured lap cushion because she gets out of her wheelchair, and another CNA stating it was removed only for toileting and at bedtime. An LPN stated staff were not instructed to document the time the device was placed or removed. Record review showed a physician's order dated August 25, 2025 for a lap buddy on the wheelchair every shift, but the order did not note release of the restraint. A signed restraint evaluation dated August 19, 2025 identified the secured lap cushion as both an enabler and restraint and cited sliding out of the wheelchair as the reason for use. There was no documentation of the restraint in progress notes, no evidence of a restraint observation, no documentation of the resident's response for 72 hours after initiation, and no skin assessments related to the restraint. The care plan only stated to provide a lap buddy and did not include details about release, duration, reason, or interventions to reduce restraint use. The facility's Physical Restraint Policy required restraint observations, physician orders defining type, reason, duration, and justification, documentation of the resident's response each shift for 72 hours, temporary release at least every two hours, and care plan details reflecting restraint use and reduction efforts.
Penalty
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