Failure to Implement Pressure Ulcer Prevention and Timely Wound Management
Summary
The deficiency involves the facility’s failure to implement appropriate pressure ulcer prevention and management for a resident who was admitted with multiple serious medical conditions and an existing pressure area. The resident was admitted from the hospital with septic shock, UTI, severe cognitive-communication deficits, diabetes, anorectal cancer with prior radiation and chemotherapy, an indwelling Foley catheter, and a gluteal cleft/coccyx pressure area being treated with Santyl. The hospital documented a Braden score of 15 (mild risk). On admission, the facility physician determined the resident could understand medical information and make decisions, and the BIMS score was 12/15, indicating moderate cognitive impairment. The facility’s pressure injury policy required a systematic approach including prompt assessment, treatment, and modification of interventions as appropriate. On admission, nursing notes documented the resident as cognitively impaired, requiring two-person assistance for transfers and toileting, and having an indwelling Foley catheter. That same night, nursing staff identified an open area on the sacral region attributed to moisture-associated skin damage (MASD), but there were no documented measurements, nor any description of odor, drainage, or wound depth. The baseline care plan intervention for this sacral MASD was to leave the area open to air, and subsequent Braden assessments on three dates in November classified the resident as low risk for pressure injury, despite the existing skin breakdown and functional limitations. The care plans and nursing interventions did not include specific preventative measures such as scheduled turning and repositioning every two hours. Later in November, weekly skin evaluations documented two new pressure wounds on the coccyx and sacrum, but again without measurements or documentation of odor, drainage, or depth, and without evidence that the physician was notified at the time of discovery. A Braden assessment on the same date showed a score of 10, indicating high risk for pressure wound development. The wound consultant’s assessment the following day identified an unstageable full-thickness sacral pressure wound measuring 6 cm by 3 cm with unknown depth and moderate serous drainage, and a Stage 3 full-thickness pressure wound on the left buttock, both described as being greater than five days in duration. Review of physician and nurse practitioner notes showed no documentation of skin changes during this period, and both the nurse practitioner and attending physician reported they had not been alerted to skin issues in November. CNA documentation showed that on multiple shifts over a 20–21 day period, staff recorded that the resident was not turned and repositioned, with numerous day, evening, and night shifts indicating “no” for turning and repositioning, demonstrating a lack of consistent implementation of pressure-relief interventions.
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