# Novel Occlusion-Reopening Technique for Perigraft Seromas in Arteriovenous Grafts: A Multicenter Case Report

**Authors:** Wenshen Pu, Yong Xu, Jiali Liu, Ling Chen, Qiquan Lai, Xuejing Gao, Bo Tu, Bo Hu, Ziming Wan

PMC · DOI: 10.1016/j.xkme.2026.101240 · 2026-01-05

## TL;DR

A new technique for treating recurring fluid collections around hemodialysis grafts shows 100% success in restoring graft function and preventing recurrence.

## Contribution

A novel occlusion-reopening technique for refractory perigraft seromas in arteriovenous grafts is introduced and validated.

## Key findings

- Technical success was achieved in all 5 patients with immediate restoration of graft function.
- No seroma recurrences occurred during follow-up, with all grafts remaining functional.
- The technique combines intentional thrombosis, surgical evacuation, and angioplasty for durable outcomes.

## Abstract

Arteriovenous grafts remain crucial for hemodialysis access despite the risk of perigraft seromas (PSs)—sterile fluid collections causing graft compression, thrombosis, and dysfunction. Current treatments (surgical drainage and compression therapy) show high recurrence rates. We describe a novel occlusion-reopening technique for refractory PSs in 5 patients receiving hemodialysis (mean age, 62.6 years) with expanded polytetrafluoroethylene AVGs. All seromas developed at arterial anastomoses (1-43 days after placement) and recurred after conventional therapies. Our protocol involved (1) intentional graft occlusion via manual compression to induce thrombosis, (2) complete surgical seroma evacuation with pseudocapsule preservation, and (3) percutaneous transluminal angioplasty using 6-mm balloons for graft reopening (see Fig 1 for details). Technical success was achieved in all cases, with immediate restoration of thrill/bruit and mean post–percutaneous transluminal angioplasty flow of 1320 mL/min. No seroma recurrences occurred during follow-up, and all AVGs remained functional. The occlusion-reopening technique addresses PS pathophysiology by eliminating fluid production through temporary thrombosis while preserving graft architecture. This approach demonstrates 100% efficacy in our series for recurrent PSs unresponsive to standard therapies, offering a reproducible solution with durable outcomes.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** polycystic kidney disease (MESH:D007690), arteriovenous fistula (MESH:D001164), chronic glomerulonephritis (MESH:D005921), AVG thrombosis (MESH:D013927), occlusion (MESH:D001157), AVG (MESH:D055589), tremor (MESH:D014202), infection (MESH:D007239), AVG occlusion (MESH:D006083), hematoma (MESH:D006406), AVG seromas (MESH:D049291), skin necrosis (MESH:D012871), diminished thrill (MESH:D015354), kidney failure (MESH:D051437), diabetes (MESH:D003920), AVG dysfunction (MESH:D055031)
- **Chemicals:** ePTFE (-), polytetrafluoroethylene (MESH:D011138)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925445/full.md

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Source: https://tomesphere.com/paper/PMC12925445