Ostomy Care Not Provided or Documented as Ordered
Summary
The facility failed to ensure ostomy care was provided as ordered and as recommended for two residents with ostomies. For one former resident with a history that included hypotension, diabetes, chronic kidney disease, cerebral infarction, sepsis with acute organ dysfunction, septic shock, endocarditis, perforated bowel, cardiac arrest, and a prolapsed ostomy, the record showed care plan interventions for emptying the ostomy bag each shift and monitoring skin around the stoma, but there was no care plan direction for changing the ostomy appliance or measuring output. The record also lacked treatment orders and documentation for the abdominal surgical incision with retention sutures that had been identified on hospital discharge instructions, and there was no order for daily stoma assessment, peristomal skin monitoring, or output monitoring as later recommended by the NP. The former resident was sent to the hospital after asking for help changing the ostomy bag multiple times during a shift, with exposed intestine noted when the bag was removed. Hospital records documented a prolapsed ostomy with approximately 7.5 to 8 inches of bowel protruding from the abdomen and a 1 cm wound dehiscence. On return to the facility, the NP documented an abdominal surgical wound and ordered ostomy care and monitoring, including daily stoma assessment, peristomal skin monitoring, and recording ostomy output every shift, but the chart contained no documentation that these orders were carried out as written. Skin checks and progress notes referenced an abdominal incision, but they did not include wound measurements, description, or details about the retention sutures. For the other resident, who had diabetes, heart failure, sepsis, hypertension, and a colostomy, the care plan included emptying the ostomy bag each shift and monitoring skin around the stoma, but there were no orders for changing the ostomy bag, monitoring the stoma site, or documenting when the appliance had last been changed. The resident stated the appliance was only changed when it ruptured or fell off and that the current bag had been worn for about a month, while the bag observed by surveyors had dark brown and black substance surrounding the appliance and on the bag. The DON confirmed there were no colostomy orders for monitoring the stoma site, emptying the bag, or changing the bag, and there was no documentation showing when the bag had last been changed.
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