Pressure ulcer care, risk scoring, and wound treatment failures
Summary
The facility failed to provide pressure ulcer care according to practitioner orders and failed to accurately assess and monitor residents at risk for skin breakdown. The report states that the facility did not perform treatment for pressure ulcers according to the practitioner’s orders for one resident, did not accurately complete and score the Braden Scale for two residents, and did not evaluate, implement, and monitor interventions to prevent pressure ulcer development and promote wound healing for four residents. The cited policy required admission and weekly skin risk assessments, comprehensive skin checks, and individualized repositioning and support surfaces based on risk factors. One resident had dementia, adult failure to thrive, frequent bladder incontinence, weight loss, and moisture-associated skin damage. The care plan identified risk for pressure ulcer development and later documented an unstageable deep tissue injury to the buttocks. Weekly skin/wound observations repeatedly noted a current skin issue but did not identify the type, size, or characteristics of the wound. The resident’s Calmoseptine treatment was discontinued, and the record showed the resident did not receive the treatment after that point until a new deep tissue injury to the right gluteal fold was identified. The resident then developed worsening buttock wounds, was sent to the hospital with purulent drainage and septic shock, and underwent incision, drainage, and debridement of a stage 4 sacral pressure ulcer with bone at the base of the wound. Another resident had PVD, ESRD, diabetes, and MASD. After returning from the hospital, the resident’s Braden Scale was incorrectly scored as not requiring skin integrity interventions, even though the score should have been 12. The record showed no skin evaluations for 12 days between weekly checks, and a right heel deep tissue injury was later identified. The ordered Prevalon boots were not in the room on one occasion, and observations showed the resident’s heel protector was not consistently on the foot while the resident was in bed. The wound was still present and covered with black eschar during later observation. A third resident had PVD and diabetes and was readmitted with a left foot wound. The resident’s Braden Scale showed moderate risk, and the care plan included a Prevalon boot while in bed. The TAR showed the ordered treatment for the left foot pressure ulcer was not started until two days after the wound was identified and three days after readmission. The TAR also showed the Prevalon boot order was not administered during the month. Observations showed the resident in bed without the boot, with the heel resting on the mattress, and the wound remained present. A fourth resident had quadriplegia, a history of pressure ulcers, and bilateral plantar foot pressure ulcers. The resident’s Braden Scale later showed mild risk, but staff confirmed the score was incorrect because the resident had sensory impairment and existing pressure ulcers. The ordered wound care was not followed because staff used Opticell AG dressing instead of the ordered Aquacel dressing. Staff also observed the resident in bed without pressure-relieving boots, with both plantar surfaces touching the mattress, and the ADON confirmed uncertainty about what interventions had been implemented to prevent the second foot ulcer from developing.
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