![]() ![]() ![]() The rate of loss and injury associated with devices attaching to beds remains relatively unchanged since 1999 when the FDA established the Hospital Bed Safety recommendations. – present risk for entrapment that can result in death or maiming. Do not allow the use of devices that slide under the mattress these devices tend to shift during use and measuring entrapment zones will not be accurate.Īny devices attaching to the bed – side rails of all sizes, halo bars, enabler bars, etc. do not use equipment intended for use at home). Only devices meeting FDA guidelines should be used and only devices intended for use in a facility (i.e. A care plan addressing use and risk reduction interventionsĪll devices attaching to the bed should be measured for entrapment zones.Documented entrapment zone measurements including measurements of the resident body parts per FDA recommendations ( ).Informed consent signed by the resident or legal representative.Risk/benefit analysis including the specific risks related to the resident’s condition.Attempts at reduction and/or rationale why reduction has not been attempted.Proof the device is the least restrictive and/or the rationale as to why it is the least restrictive if no other device was trialed.Proof of medical symptoms being treated. ![]() Surveyors are citing assist devices on beds when they do not have: Surveyors have been educated on the risks associated with these devices and instructed on how to determine if facilities are utilizing them appropriately. It is important to know that the regulations related to restraints and assist devices has not changed. These devices are being cited as restraints (F221) or potential/actual accidents (F323) due to the risk of entrapment. Providers across the country have recently experienced surveys with an emphasis on the risks of enabler bars (assistive devices). ![]()
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