Int J Angiol 2017; 26(03): 186-190
DOI: 10.1055/s-0037-1601872
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Aneurysmal Degeneration of the Brachial Artery after Vascular Access Creation: Surgical Treatment Results

Sérgio Teixeira
1   Department of Angiology and Vascular Surgery, Centro Hospitalar do Porto – Hospital de Santo António, Porto, Portugal
,
Pedro Sá Pinto
1   Department of Angiology and Vascular Surgery, Centro Hospitalar do Porto – Hospital de Santo António, Porto, Portugal
,
Carlos Veiga
1   Department of Angiology and Vascular Surgery, Centro Hospitalar do Porto – Hospital de Santo António, Porto, Portugal
,
Ivone Silva
1   Department of Angiology and Vascular Surgery, Centro Hospitalar do Porto – Hospital de Santo António, Porto, Portugal
,
Rui Almeida
1   Department of Angiology and Vascular Surgery, Centro Hospitalar do Porto – Hospital de Santo António, Porto, Portugal
› Author Affiliations
Further Information

Publication History

Publication Date:
11 April 2017 (online)

Abstract

True peripheral artery aneurysms proximal to a longstanding arteriovenous fistula is a well-recognized complication. Late aneurysmal degeneration is rare. This study analyzed the characteristics, therapeutic options, and outcomes of true donor brachial artery aneurysms (DBAA) after arteriovenous fistula (AVF) for hemodialysis. We retrospectively collected the data of patients with DBAA after AVF creation, surgically repaired between January 2001 and September 2015. We excluded patients with pseudoaneurysms, anastomotic aneurysms, and infected aneurysms. We recorded patient's demographics, type of access, aneurysm characteristics, symptoms, treatment, and follow-up. Ten patients were treated for aneurysmal degeneration of the brachial artery. Average aneurysm diameter was 37.5 mm. All cases had, at least, one previous distal AVF, ligated or thrombosed, at the time of diagnosis. The first access was created in mean 137 months before the diagnosis of DBAA. Nine patients had previous medical history of renal transplant and were under immunosuppressive therapy. All patients were symptomatic at the time of diagnosis. In all cases, the treatment was aneurysmectomy followed by interposition bypass. One patient developed a postoperative hematoma with the need of surgical drainage. At 50 months of follow-up, one patient was submitted to percutaneous angioplasty due to an anastomotic stenosis. No other complications occurred during the entire follow-up period (mean: 69 months). The pathogenesis underlying DBAA remains unclear. Increased blood flow after AVF creation, immunosuppressive therapy, and ligation/thrombosis of the AVF may contribute to aneurysm formation. Surgical treatment by aneurysmectomy and bypass, with autogenous conducts, is a safe and effective option.

 
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