Wander Guards Not Properly Positioned or Monitored for Residents at Risk for Elopement
Summary
The facility failed to ensure adequate supervision and proper use of wander guards for residents at risk for elopement. The report states that 3 of 3 residents at risk for wandering or elopement did not have their assistance devices positioned or monitored as ordered, and that staff did not follow the manufacturer’s instructions for the wander guard system. Facility policy required wander guards to be applied per care plan, tested at door areas, and maintained through regular inspection and testing, while the manufacturer’s guide stated the facility was responsible for regular inspection, testing, and cleaning of the system and that transmitters should alarm when a resident wearing one is within 4 feet of a monitored door. One resident with unspecified dementia and severely impaired cognition had physician orders and care plan directions for a wander guard to be checked every shift, yet the surveyor could not find the device on the resident during observation. A CNA later confirmed the resident was not wearing a wander guard and checked the resident’s wheelchair and walker without finding one. An ADON also could not locate the device and suggested it may have been moved when the wheelchair changed, while the software system still showed the wander guard as being in the resident’s room. Staff reported that nurses were to check the software weekly, but the Maintenance Director stated the software was only checked with updates and that nurses only looked at it if an alarm activated. Another resident with diagnoses including unspecified dementia, heart failure, and atrial fibrillation had orders for a wander guard to be placed on the outside aspect of the walker for best alarm activation and to be checked every shift. The surveyor observed the wander guard attached to the walker’s metal bar rather than on the resident, and staff stated the resident did not have one on the body. When the ADON and Maintenance Director tested the walker at the exit door, the alarm did not sound until the walker or the staff member was already at or beyond the doorway. The surveyor also observed a resident with diabetes, anemia, and atrial fibrillation whose wander guard was attached to the wheelchair metal frame and not on the resident, and the tester used to check the device had a 9V battery that expired in 12/2023. Staff gave inconsistent responses about who maintained the tester, and the Maintenance Director stated he did not know the battery was expired.
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