Improper Use and Monitoring of Mitt Restraints
Summary
The facility failed to ensure one resident was free from unnecessary restraint use and failed to follow its restraint program and policy. The resident had multiple serious diagnoses, including nontraumatic intracerebral hemorrhage, cerebral palsy, acute respiratory failure, dysphagia, dependence on ventilator status, depression, and severe cognitive impairment. The resident’s physician orders included bilateral mitts related to pulling at the trach, but the resident’s care plan did not identify restraint use, and the resident’s MDS did not code the mitt restraints. Survey observation found the resident lying in bed with bilateral mitt restraints in place, and staff were unsure why the restraints were being used. One agency RN stated she had not received restraint training from the facility and was unable to untie one mitt because it was tied so tightly that she could not fit more than two fingers under it. The surveyor observed that the mitts were not applied in a manner that allowed for easy release. It took approximately 2 to 3 minutes to untie the knots and release one restraint, and the RN retied it in a double knot. The mitts were observed to be dirty, and one mitt had dried blood on the inside where it tied around the resident’s wrist. Family members stated they had not been informed before the restraints were started, said the mitts were often left on, and reported that they had removed them in the past because they were too tight and had caused blisters. The family also stated they had been trying to get the resident transferred to another facility, but the other facility would not accept the resident while the mitts were in use. The record and interviews showed that required restraint processes were not followed. Staff and the provider were unable to identify all interventions tried before restraint use, and the restraint assessment documented that alternatives such as reorientation, toileting, pain management, diversional activity, increased supervision, non-restrictive devices, and repositioning were not attempted prior to restraint initiation. The restraint assessment, care plan, and root cause analysis were not completed until after the survey began. Survey observation also showed that the resident’s mitts were not released for more than 4 hours despite staff statements that restraints should be released every 2 hours. Multiple staff members stated they were unfamiliar with the restraint policy, unsure who was responsible for releases, and unable to produce the facility’s restraint monitoring documentation.
Penalty
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