Failure to Provide Ordered Skin Assessments and Timely Pressure Injury Prevention
Summary
The deficiency involves the facility’s failure to provide ordered skin assessments, prescribed topical treatments, and timely wound identification and interventions, resulting in the development and worsening of pressure-related skin breakdown in two residents. One resident (R1) was admitted with multiple comorbidities including spinal cord disease, cervical radiculopathy, COPD, acute respiratory failure, pneumonia, morbid obesity, muscle wasting and atrophy, major depressive disorder, and diaper dermatitis. On admission, the RN documented moisture-associated skin damage (MASD) and other skin issues but did not document any pressure ulcers. Physician orders included skin assessments every shift for three days, weekly skin risk assessments for four weeks, and wound care to bilateral ischial and coccyx areas with Triad cream to open wound beds and silicone barrier cream to intact skin twice daily and as needed for incontinence. The wound nurse later documented a cluster wound on the left gluteal area but did not classify any of the resident’s wounds as pressure-related, and the resident was not listed on the facility’s pressure ulcer list for February and March. The facility’s documentation and treatment administration for R1 were incomplete or missing. The DON acknowledged missed skin assessments and missed administrations of Triad cream on the Treatment Administration Record (TAR) and stated that missing prescribed treatments could lead to worsening skin breakdown. CNA documentation for R1’s care and skin issues was not accessible in the EMR and could not be produced upon repeated surveyor requests. The Administrator could not provide a pharmacy requisition showing that Triad cream had been delivered, and there was no requisition from the pharmacy. The Administrator stated that the wound doctor had indicated Remedy Protect zinc cream was used instead of Triad cream, and acknowledged that a new order should have been obtained if a different product was being used. The nurse practitioner stated she was unaware of R1’s skin breakdown, expected staff to provide incontinence care and turning assistance, and expected the wound doctor to see R1 before the date the cluster wound was documented. Emergency room records later documented a stage 2 pressure injury of the sacral region, while the facility had not identified R1 as having a pressure ulcer. The second resident (R2) had a care plan indicating potential for pressure ulcer development related to bowel and bladder incontinence, with interventions including pressure-relieving devices to bed and chair and following facility protocols for prevention and treatment of skin breakdown. During observed incontinence care, a CNA stated R2 had intact skin and no pressure ulcers, but surveyors observed an open area on the sacral/coccyx area with beet-red peri-wound, buttocks, and perineum, and no visible protective cream or dressing in place. The RN assigned to R2 stated she did not have any residents with pressure wounds and had not been notified of any skin breakdown. Later, the wound nurse assessed R2 and identified a stage 3 pressure injury on the sacral area, with no prior documentation of a pressure wound, and stated that staff should have identified the skin breakdown before it progressed to stage 3. The nurse practitioner reported she was not made aware of R2’s stage 3 pressure wound and would have expected staff to notice the skin condition earlier. The wound nurse also stated that a low air loss mattress is a pressure-relieving device, that such mattresses are available through the facility or an outside vendor, and that she should have obtained a low air loss mattress for R2 but had not done so. Facility policies required systematic skin risk assessments, ongoing wound assessments, and implementation of prevention measures such as moisture management, friction and shear reduction, and pressure reduction, but these measures were not effectively implemented or documented for R1 and R2.
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