Inconsistent pre-dialysis assessment and missing communication for dialysis medication
Summary
Safe, appropriate dialysis care/services were not consistently provided for a resident with end stage renal disease who received hemodialysis three times weekly and had a left upper arm AV fistula. The resident’s care plan included monitoring bruit and thrill, ensuring attendance at dialysis, and monitoring labs. However, the electronic treatment record showed multiple charting blanks for ordered checks of the AV fistula bruit and thrill, assessment of the dialysis access dressing for bleeding after return from dialysis, and removal of the dialysis access dressing four hours post-treatment. The record also showed that on multiple hemodialysis days, the resident was not assessed prior to leaving the facility for dialysis, with no documented vital signs before departure on several dates in August and September 2025. The resident had an order for Midodrine 10 mg prior to dialysis on Monday, Wednesday, and Friday, with instructions to hold the medication if systolic blood pressure was higher than 140. The eMAR reflected several instances where Midodrine was not administered and blood pressure was not documented, and one instance where it was administered with documented blood pressure readings. Dialysis progress notes did not reflect documentation of the Midodrine doses that were held or the pre-dialysis assessments conducted. During interview, the RN/UM stated that if no information was sent with the resident to the dialysis center, it meant there were no issues, and that any issue would result in a phone call. The RN/UM could not show evidence that communication with the dialysis center occurred when Midodrine was held or administered. The DON, LNHA, and regional RN were informed of the concern, and the regional RN stated the dialysis progress note was used as the communication form, but the dialysis center did not have access to the facility’s eMR where the assessment information was documented.
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