Incomplete dialysis communication and missing bedside emergency kits
Summary
The facility failed to provide safe, appropriate hemodialysis care and services for multiple residents receiving dialysis. The report states that the facility did not ensure a hemodialysis emergency kit was available at the bedside for Residents 14, 26, 39, and 97. Resident 39 had a right upper chest perma-catheter and Resident 97 had an AV shunt in the left arm; both stated they went to hemodialysis on Tuesdays, Thursdays, and Saturdays. Resident 14 had a right thigh perma-catheter and Resident 26 had a right upper chest perma-catheter. Staff confirmed that the emergency kit should have been available at the bedside for use if bleeding occurred at the dialysis access site. For Resident 41, the dialysis communication record was incomplete and the hemodialysis center’s recommendation to hold metoprolol on dialysis days was not followed as documented. The record showed missing post-dialysis assessments, missing access-site documentation, and missing post-dialysis weights on multiple dialysis communication forms. The hemodialysis center documented that blood pressure medications should not be given on dialysis days to prevent hypotension, and later documented to hold metoprolol, iron, and ESA on a dialysis day; however, the MAR showed metoprolol was administered that morning. The medical record did not show that the center’s recommendations were communicated to the physician on those days. The record also failed to show nursing documentation of monitoring the dialysis access site, even though the care plan addressed access-site monitoring. For Resident 49, the dialysis communication forms were incomplete and inaccurate, with multiple missing post-dialysis assessments, missing vital signs, missing access-site documentation, and missing nurse signatures. The resident had ESRD and received hemodialysis three times weekly. The resident was also on a 1500 mL/day fluid restriction with orders to record intake and output. During observation, a water pitcher was present at the bedside without graduated measurement, and staff stated the resident was on fluid restriction and should not have a water pitcher at bedside. The record also showed intake and output was not recorded on several dates, and staff stated the resident drank from the pitcher and from meal trays. For Resident 72, the dialysis communication record was also incomplete and inaccurate, with missing dialysis end times and missing or inconsistent documentation of catheter location/status and post-dialysis assessments on several forms.
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