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In Vitro Study of a Medical Device to Enhance Arteriovenous Fistula Eligibility and Maturation. | LitMetric

In Vitro Study of a Medical Device to Enhance Arteriovenous Fistula Eligibility and Maturation.

ASAIO J

From the *Flow Forward Medical, Inc. (FFM), Lowell, Massachusetts; †School of Engineering, Griffith University, Southport, Queensland, Australia; ‡Department of Internal Medicine, Roy and Lucille Carver College of Medicine, University of Iowa and Veterans Affairs Medical Center, Iowa City, Iowa; and §FFM, Olathe, Kansas.

Published: April 2016

AI Article Synopsis

Article Abstract

The arteriovenous fistula eligibility (AFE) system (Flow Forward Medical, Olathe, KS) is a small, temporary, wearable rotary blood pump system designed to rapidly dilate peripheral veins in hemodialysis patients and improve outcomes after arteriovenous fistula (AVF) creation. A benchtop pulsatile mock circulatory loop was developed to model forearm circulation and to compare the hemodynamics of the AFE system with those of a conventional radiocephalic AVF. The AFE system maintained a mean wall shear stress (mWSS) within the 2.5-7.5 Pa target range for cephalic outflow veins of 2-6 mm diameter, which when applied clinically will provide better control of mWSS during the outflow vein maturation process when compared with a conventional AVF. These results support further study to determine whether or not vein preconditioning with the AFE system under controlled levels of mWSS will promote improved AVF outcomes.

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Source
http://dx.doi.org/10.1097/MAT.0000000000000240DOI Listing

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