Incomplete Care Planning and Failure to Implement Ordered Monitoring and Treatments
Summary
The facility failed to develop and implement comprehensive care plans for three residents. For one resident with diagnoses including bipolar disorder, depression, generalized anxiety disorder, post-traumatic disorder, vascular dementia with anxiety, and major depressive disorder, the care plan included interventions to monitor and document adverse reactions to antidepressant therapy and to monitor and record mood changes, depression, anxiety, sadness, and related symptoms. However, the medical record contained no documentation that these monitoring interventions were completed, and the DON confirmed that no such documentation could be found in the EMR. For another resident with apraxia following cerebral infarction, dysarthria, and right-sided weakness/paralysis after a stroke, the resident was observed in bed wearing only an adult brief, lying flat on his back with heels not elevated, in a very warm room, with an unpleasant body odor, unkempt appearance, dry and chapped lips, and overgrown toenails. A Styrofoam cup on the bedside table contained only a small amount of water. The resident was unable to verbally respond but could answer simple questions by nodding or shaking his head, indicated that he was thirsty, stated he had not been receiving showers, and said he needed assistance with eating and drinking. He also indicated that he did not have a communication board and could not hold a cup to drink independently. For a third resident with recent admissions related to acute on chronic respiratory failure with hypoxia and hypercapnia, CO2 narcosis, sleep apnea, morbid obesity, COPD, respiratory failure with hypoxia dependent on oxygen, anxiety, and depression, the resident reported that staff had not assisted with use of the ordered BIPAP machine since returning from the hospital. The machine was found in the closet. The care plan identified a potential for difficulty breathing related to CHF, COPD, chronic respiratory failure, and OSA and included BIPAP per MD order, but the ADON verified that after the hospital readmissions the BIPAP was not re-ordered even though the resident remained on the care plan and staff were expected to follow it.
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