The resident, identified as R390, returned from dialysis at 4:30 PM on April 1st with a pressure bandage covering his upper right arm fistula. When federal inspectors arrived the next morning at 9:00 AM, the dressing was still there.

"Staff will take it off when they have time," R390 told inspectors. He said nurses don't really check for the thrill and bruit — the palpable vibration and swooshing sound that indicate proper blood flow through the surgically created access point that keeps dialysis patients alive. "I will usually be the one that takes it off."
The charge nurse from the dialysis center was clear about the timeline when inspectors interviewed her that afternoon. Remove the pressure dressing two hours after treatment, she said. "This is to prevent clotting. If left too long, it will most likely end up clotting the access."
For dialysis patients, a clotted fistula means emergency surgery or death.
Registered Nurse 30 accompanied inspectors to R390's room that morning to confirm the dressing was still attached. When asked why, RN30 replied, "I'm not sure, I will have to check our facility's policy."
The nurse said he follows orders to observe the access site for redness, bleeding, and to check for thrill and bruit. He noted the last assessment was done at 12:10 AM — nearly nine hours earlier — and that he hadn't completed his morning assessment yet.
Treatment records showed dialysis fistula checks were supposed to happen every shift. But R390's care plan, initiated March 20th, included monitoring for infection signs like redness, swelling, and drainage. It contained no interventions for assessing thrill and bruit.
The Director of Nursing confirmed during her interview that staff should check for thrill and bruit before and after dialysis and every shift. She also acknowledged they should remove the dressing but wasn't sure how soon after dialysis.
By noon on April 2nd, inspectors observed R390's fistula without the pressure dressing.
The facility's own policy, revised in April 2018, stated that staff would "monitor and document the status of the resident's access site upon return from the dialysis treatment center to observe for bleeding or other complications." Federal inspectors determined Avalon Care Center failed to meet this standard.
The inspection also revealed staffing problems that affected rehabilitation services. The facility failed to provide sufficient nursing staff for restorative services, leaving one resident without consistent range-of-motion treatments designed to prevent physical decline.
Thirty residents in the facility's restorative nursing aide program were at risk for declining mobility due to inadequate staffing levels.
R390's case illustrated the gap between written policies and actual care. While treatment records documented regular fistula monitoring, the reality was a patient left to remove his own medical dressing because staff didn't have time.
The swooshing sound of blood flow through R390's fistula — the bruit that indicates a functioning access — went unchecked for hours past the critical window. In those extra 15 hours, the pressure dressing designed to stop bleeding after dialysis could have caused the very clotting it was meant to prevent.
For a dialysis patient, that difference between policy and practice can mean the difference between life and death.
Full Inspection Report
The details above represent a summary of key findings. View the complete inspection report for Avalon Care Center - Honolulu, LLC from 2025-04-03 including all violations, facility responses, and corrective action plans.
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