Original Article

Kidney International (2006) 70, 765–770. doi:10.1038/sj.ki.5001554; published online 28 June 2006

Minimally Invasive Limited Ligation Endoluminal-assisted Revision (MILLER) for treatment of dialysis access-associated steal syndrome

N Goel1, G A Miller1, M C Jotwani1, J Licht1, I Schur1 and W P Arnold1

1American Access Care, Brooklyn New York, USA

Correspondence: N Goel, American Access Care, 577 Prospect Ave., Brooklyn, New York 11215, USA. E-mail: drnav5487@pol.net

Received 2 January 2006; Revised 13 March 2006; Accepted 4 April 2006; Published online 28 June 2006.

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Abstract

Dialysis-associated steal syndrome (DASS) is defined as a clinical condition caused by arterial insufficiency distal to the dialysis access owing to diversion of blood into the fistula or graft. The incidence of symptomatic DASS requiring treatment is 1–8%. The etiology is iatrogenic and symptoms are quite debilitating. Banding of the access inflow has largely been abandoned because of the inherent problem with balancing fistula flow with distal flow complicated by a high incidence of subsequent access thrombosis. In this study, we are reporting a modification to the traditional banding procedure, which markedly improves banding outcomes. We are reporting 16 patients who underwent a new standardized minimally invasive banding procedure performed in an outpatient setting with minimal morbidity. This modified banding procedure requires a small (1–2 cm) skin incision for the placement of a ligature and utilizes a 4 or 5 mm diameter endoluminal balloon to achieve and standardize the desired reduction of inflow size. All 16 patients had immediate symptomatic and angiographic improvement after the procedure. Follow-up showed none of the patients had recurrence of symptoms or thrombosis of the access. In our experience, this procedure is an excellent treatment option because of its simplicity and should be considered as a first-line treatment for patients with DASS.

Keywords:

arteriovenous access, DASS, steal syndrome, DRIL, IMN

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