Dialysis Care and Fluid Monitoring Deficiencies
Summary
The facility failed to provide safe, appropriate dialysis care and services for three residents receiving hemodialysis. The report states that the facility did not accurately monitor fluid intake for two residents, did not consistently monitor hemodialysis access sites for bruit, thrill, redness, swelling, bleeding, or pain, and did not document notification to the physician, dialysis facility, or nephrologist when access concerns were identified. The facility also failed to monitor one resident for extra fluids at the bedside and kept an emergency dialysis access kit in the room that did not match the resident’s access type. For one resident with a left forearm AVF and a 1200 ml fluid restriction, the record showed inconsistent fluid documentation between CNA meal documentation and the licensed nurses’ Monitor Record. The CNA documentation included multiple entries that were higher than, or not reflected in, the nursing totals, and some meal periods had no documentation. The same resident’s access monitoring was also inconsistent, with entries of N or no documentation for bruit and thrill on some shifts, and repeated documentation of pain at the access site on many shifts. The record did not show notification to the attending physician, dialysis facility, or nephrologist regarding the fluid intake concerns, absent bruit and thrill, or ongoing pain. For a second resident with a left forearm AV shunt and a 1000 ml fluid restriction, the Monitor Record showed a total fluid intake of 1040 ml on one day. The access monitoring again showed entries of N, 0, or no documentation for bruit and thrill on multiple shifts, along with repeated documentation of pain at the access site. The record did not show notification to the attending physician, dialysis facility, or nephrologist regarding the fluid intake, access findings, or pain. The DON stated she did not know why staff documented 0 or N for bruit and thrill and stated nursing interventions should have been done when the resident complained of pain. For a third resident with a left chest Permacath and a 1200 ml fluid restriction, staff observed a half-consumed bottle of soda and a cup of water at the bedside. The resident’s record did not show CNA documentation of fluid intake under Task. The resident also had a transparent bag in the room labeled as a dialysis torniquet kit, but LVN staff verified it contained supplies such as a blue torniquet and did not contain plastic clamps, and stated the torniquet would not be appropriate for a resident with a Permacath. The DON was informed and acknowledged the findings.
Penalty
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