Care Plan Not Revised for Abdominal Binder and G-Tube Monitoring
Summary
The facility did not ensure that 1 of 18 residents reviewed had a care plan revised after assessment or as determined by the resident’s needs. The resident had diagnoses including hemiplegia/hemiparesis following cerebral infarction with right-sided paralysis, dysphagia, aphasia, type 2 diabetes mellitus, protein-calorie malnutrition, Alzheimer’s disease, and dementia. The resident’s admission MDS indicated severely impaired cognition with a BIMS score of 0 and total assistance needed for all ADLs. The resident was admitted with a G-tube for continuous feedings, a foley catheter, and an activated POA. The resident’s care plan included a need for a feeding tube/potential for complications of feeding tube use related to swallowing impairment and documented that the resident pulled at the G-tube at times, with an intervention for an abdominal binder to keep the G-tube from being pulled out. A physical restraint assessment documented that the abdominal binder was to be worn at all times to prevent dislodgement of the G-tube, with monitoring and opening of the binder every 2 hours. A physician order also directed that the abdominal binder be released for 15 minutes every 2 hours, with skin and circulation checks and notification of the MD/NP if changes were noted. During survey interviews and observations, multiple staff stated the resident was not wearing an abdominal binder and that they had not seen one in the resident’s room. One LPN stated the resident did not wear an abdominal binder and had never pulled at the tubing, while another LPN stated the resident had worn one in the beginning but no longer did because the resident never pulled or tried to remove the tubing. The DON and LPN unit manager stated the resident never came to the facility with an order to wear an abdominal binder and that the order had been obtained to address the POA’s concern. Survey review of the MAR/TAR showed staff initialing the binder being taken off every 2 hours per order, even though staff could not confirm the resident was actually wearing it, and the care plan was not revised to clearly reflect the resident’s current need or lack of need for the abdominal binder.
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