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Updated: Jan 24, 2026

Author Spotlight: Hickman Catheter Use for Long-Term Vascular Access in a Preclinical Swine Model
Published on: March 31, 2023
A coming of age for vascular access research: the good, the bad, and the ugly!
Diego Celdran Bonafonte1, Prabir Roy-Chaudhury2
1Division of Cardiothoracic Surgery, University of Arizona College of Medicine, Tucson, Arizona, USA.
Insights
Researchers identified novel biological pathways causing arteriovenous fistula stenosis in mice. This discovery offers potential new therapeutic targets for dialysis vascular access dysfunction, a significant clinical issue.
Area of Science:
- Vascular biology and nephrology.
Background:
- Dialysis vascular access dysfunction is a major clinical challenge with high morbidity, mortality, and cost.
- Current therapies for vascular access dysfunction are limited in effectiveness.
Purpose of the Study:
- To identify novel biological pathways contributing to arteriovenous fistula stenosis in a mouse model.
- To establish a foundation for developing new therapeutic strategies for dialysis vascular access dysfunction.
Main Methods:
- High-quality scientific investigation of "mouse" arteriovenous fistula stenosis.
Main Results:
- Identification of several novel biological pathways implicated in arteriovenous fistula stenosis.
- These pathways represent potential druggable targets.
Conclusions:
- The identified pathways offer a promising substrate for innovation in treating dialysis vascular access dysfunction.
- Further research into these targets may lead to effective new therapies.
Abstract:
Dialysis vascular access dysfunction remains an important clinical problem with a very significant morbidity, mortality, and socio-economic cost. Despite the magnitude of the clinical problem, there are currently no truly effective therapies for vascular access dysfunction. Through a high-quality scientific investigation, Liang et al. have identified a number of novel biological pathways responsible for "mouse" arteriovenous fistula stenosis. We hope that the identification of these druggable pathways (targets) will allow for the development of new and effective therapies for vascular access dysfunction, through the creation of an innovation substrate for dialysis vascular access.
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