Failure to follow ordered care for skin, falls, medication parameters, ear care, and weights
Summary
The facility failed to timely address a resident’s skin condition for a resident with quadriplegia who was frequently incontinent of urine and dependent for toilet hygiene. A skin sweep and risk assessment identified an open area on the left gluteal area that was moisture associated skin damage, but the record did not show physician notification or a new treatment order on that date. The wound was later documented as a new in-house acquired incontinence-associated dermatitis wound with measurements of 2.35 cm by 5.9 cm by 0.1 cm. The resident stated he had an open area on his buttocks, staff were caring for the wound, and he did not feel he was getting changes as often as he needed. The facility also failed to ensure fall interventions were implemented for a resident at risk for falls related to a history of falls, ataxia, and orthostatic hypotension. The care plan included interventions such as removing pedals from the wheelchair and using a soft touch call light. However, the resident was observed multiple times with his feet on the wheelchair pedals, and a push-button call light was present on the bed instead of the soft touch call light. The DON stated the resident had been moved closer to the nurses’ station and the soft touch call light had not been moved with him, and that he had started using foot pedals after a fractured ankle in late January 2026. The facility failed to obtain a resident’s heart rate and follow medication hold parameters for Metoprolol. The resident’s care plan and physician’s order required holding the medication for SBP below 110, DBP below 60, or HR below 60. The MAR documented blood pressures but did not document heart rates for several medication administrations, and the resident received Metoprolol on multiple dates when the DBP was below 60. The DON stated the order had been entered into the electronic health record with blood pressure parameters but not the resident’s heart rates. Additional failures included not addressing a resident’s ear wax buildup and not ensuring weights were obtained and provider notification occurred for a resident receiving furosemide for weight gain and edema. One resident was observed with a large amount of wax in both ears, including thick darker wax at the start of the ear canal and a ball of dry wax hanging in the left ear. Another resident had documented weight gains over the ordered notification thresholds, but the record did not show the physician was notified or that PRN furosemide was administered as ordered. The DON also stated weights for several dates could not be provided and there was no documentation that the provider had been notified when weights were within the ordered parameters.
Penalty
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