Improper Reuse of Single-Use Decloggers and Incorrect Tube Feeding Formula Administration
Summary
Surveyors identified that single-use enteral feeding tube declogging devices were being retained and apparently reused for a resident with a gastrostomy tube, contrary to manufacturer instructions. One resident with severe cognitive impairment and a history of gastrostomy tube use was observed lying in bed with tube feeding infusing, and a soiled clear plastic bag hanging on the wall behind the head of the bed contained two long, thin plastic declogging stylets with dried tan feeding residue. The manufacturer's package in the bag clearly stated the declogger was intended for single use only. A nurse present at the time reported that night-shift staff were responsible for maintaining the decloggers and that they were used for one week, and she did not remove the soiled decloggers during that observation. On a subsequent observation, the previously seen soiled decloggers were no longer present, and the nurse reported she had removed and discarded them and hung new supplies. Multiple staff interviews revealed inconsistent understanding of the decloggers' proper use: some nurses stated they always used a new declogger and discarded it immediately after use, while another nurse who worked nights stated she believed the devices were reusable and would need to ask how many times they could be reused. The Central Supply Manager confirmed that only single-use decloggers were stocked and pointed out the manufacturer’s warning label that they should be discarded after a single use. The Unit Manager, Nurse Practitioner, and Interim DON each stated they were unaware that staff had been retaining or reusing single-use decloggers and affirmed that staff were expected to follow manufacturer instructions. Surveyors also found that another resident with a gastrostomy tube, who was cognitively intact and received all nutrition and hydration via the tube, was not administered the tube feeding formula specified in the physician’s order. The resident’s order required Diabetasource 1.2 at 80 ml/hr over 20 hours daily, with documentation on the MAR. The MAR showed that the ordered Diabetasource 1.2 feeding was signed out as started, but observation revealed the resident was actually receiving IsoSource 1.5 at 80 ml/hr, as labeled on the feeding container. The nurse who hung the feeding stated she believed IsoSource and Diabetasource were equivalent because they were from the same manufacturer and, based on that assumption, hung IsoSource 1.5 instead of the ordered Diabetasource 1.2. The Registered Dietitian and Medical Director later confirmed there are differences between the two formulas and that Diabetasource 1.2 was the appropriate formula for the resident’s diabetes diagnosis.
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