MDS assessments failed to capture diagnoses and restraint use
Summary
The facility failed to accurately assess and code resident diagnoses related to psychotropic medication use for four residents reviewed for unnecessary medications. Resident #2’s MDS listed adjustment disorder with mixed disturbance of emotions and showed prescribed antianxiety and antidepressant medications, but the MDS did not include the diagnoses of circadian rhythm sleep disorder or major depressive disorder that were documented in the physician order report. Resident #3’s MDS listed anxiety and PTSD and showed prescribed diazepam and paroxetine for obsessive compulsive disorder, but the MDS did not include obsessive compulsive disorder. Resident #4’s MDS listed respiratory failure, tracheostomy status, ventilator dependence, and supplemental oxygen dependence, while the physician orders showed buspirone for anxiety disorder, citalopram and trazodone for depression, and diphenhydramine as needed for anxiety; the MDS did not include anxiety or depression diagnoses. Resident #7’s MDS listed acute and chronic respiratory failure, COPD, tracheostomy status, ventilator dependence, and supplemental oxygen dependence, and indicated prescribed antianxiety and antidepressant medications. The physician order report showed venlafaxine for generalized anxiety disorder and Ativan for generalized anxiety disorder, but the MDS did not include an anxiety diagnosis. During interview, the MDS Coordinator stated she coded diagnoses from the most recent physician visit progress note and verified that the diagnoses were not on Resident #2’s MDS. She also stated she coded based on prior preceptor training and had a copy of the CMS RAI Manual in her office. The DON stated the facility did not think it had an MDS RAI policy and used the CMS RAI Manual to code the MDS. The facility also failed to accurately code restraint use for two residents. Resident #51’s MDS indicated no restraints or alarms were used, but the care plan and MAR/TAR documented daily use of an abdominal binder ordered to obscure the PEG tube and prevent the resident from pulling on it. Staff interviews confirmed the binder was used throughout day and overnight shifts, and the DON stated the resident had used the abdominal binder for months, could not remove it independently, and that it was a physical restraint that should be reflected on assessments. Resident #19’s MDS also indicated no restraints or alarms were used, but the care plan and MAR/TAR documented daily use of bilateral arm immobilizers ordered to prevent the resident from pulling at tubes and injuring self. Staff interviews confirmed the immobilizers were used every day and removed every 2 hours for skin checks and ROM, and the DON stated the immobilizers were physical restraints that should be reflected on assessments.
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