Failure to Conduct Routine Inspections of Bed Rails
Summary
The facility failed to ensure routine inspections of bed/side rails were conducted as part of a regular maintenance program, leading to potential safety risks for four residents. The facility's policy on restraints and side rails did not provide guidance for routine inspections after installation, which is crucial to identify possible areas of entrapment. The FDA guidance suggests evaluating the dimensional limits of gaps in hospital beds to mitigate entrapment risks, especially for vulnerable populations such as elderly residents who are frail or have uncontrolled body movements. Resident #55, who has a history of seizures, stroke, and hemiplegia, was observed using a side rail that moved several inches when pulled, indicating a lack of secure attachment. The resident's care plan did not document the use of side rails, and there was no record of maintenance inspections for gap measurements. Similarly, Resident #32, diagnosed with Parkinson's disease and dementia, was observed with U-shaped rails raised on both sides of the bed, but there was no documentation related to the use of side rails or inspections for safety. Residents #47 and #50 also had beds with enabler rails, but their medical records lacked documentation of side rail inspections to identify entrapment areas. Interviews with facility staff, including the Maintenance Director and Administrator, revealed that there was no system in place for routine side rail inspections, and the responsibility for installation and inspection was assigned to the maintenance staff. The Administrator expected routine inspections to reduce the risk of entrapment, but this was not being implemented effectively.
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