Next Generation Percutaneous AV Fistula Creation
The Velocity™ Percutaneous Arterio-Venous Fistula System
About the Velocity™ pAVF System
Despite clear benefits of initiating hemodialysis with an arteriovenous fistula (AVF) including lower mortality, less reinterventions and lower healthcare costs, few patients in the U.S. do so. The Velocity pAVF System is the next generation of vascular access systems that will address patient level and system barriers for access creation while simultaneously providing quickly functioning access with less need for reintervention.
The Velocity System is designed to provide an opportunity to streamline the process to create functional dialysis access without follow up interventions.
More than 80% of patients start dialysis with a catheter.1 Catheters are a major source of morbidity and mortality for patients on hemodialysis.2 Patients outcomes are improved when dialyzing via an AVF.3
Less than 20% of patients start dialysis with an AVF: Starting dialysis with an AVF decreases the risk of infections, hospitalizations and results in lower overall healthcare costs compared to catheters. AVF use also leads to better long-term outcomes for patients.
Late diagnosis and referral delays: Many patients with chronic kidney disease do not received kidney care soon enough, leaving not enough time to create and mature an AVF before dialysis initiation.
Maturation challenges: Traditional surgical AVFs often require 12 weeks (or longer) to mature, and during this period, patients are often dependent on catheters, exposing them to additional risks. Unfortunately, many AVFs never fully mature, rendering them unsuitable for use.
Narrowing at the artery-vein junction: The most common reason for delayed or failed AVF maturation is stenosis (narrowing) at the junction of the artery and vein. This restricts blood flow, preventing the fistula from reaching the size and flow necessary for effective dialysis access.
We need a better way: Our minimally invasive solution aims to create AVFs more efficiently by overcoming common barriers to access creation and optimizing maturation which would enable patients to start dialysis safely and effectively.
References:
- United States Renal Data System. 2024 USRDS Annual Data Report: Epidemiology of kidney disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, 2024.
- Wasse H. Catheter-related mortality among ESRD patients. Semin Dial. 2008;21(6):547-9. doi: 10.1111/j.1525-139X.2008.00500.x
- Al-Balas A, Shariff S, Lee T, Young C, Allon M. Clinical Outcomes and Economic Impact of Starting Hemodialysis with a Catheter after Predialysis Arteriovenous Fistula Creation. Am J Nephrol. 2019;50(3):221-227. doi: 10.1159/000502050.
Watch this video to learn more about the Velocity System
The VENOS-1 Clinical Study
The VENOS-1 study is a first-in-human clinical study conducted outside the U.S., with patients followed for one year (NCT05757726). The results demonstrate the potential of our minimally invasive pAVF procedure:
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100% Technical Success, highlighting the reliability of our approach.
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Rapid Maturation: Using a common definition of maturation—a blood flow of 500 mL/min and a vein diameter of 5 mm—all subjects met this endpoint by 6 weeks. The bar graph on the right compares physiologic fistula maturation with the Velocity System to surgical creation of an AVF.
% of subjects achieving unassisted physiologic maturation at 6 weeks
About Us
Our Management Team
The Venova Medical team is comprised of individuals who bring a wealth of experience that covers both medical device development and clinical expertise.
Erik van der Burg
Co-Founder, Director & CEO
Shant Vartanian, MD
Co-Founder, Director & CMO
Robert Nardelli
VP of Quality & Regulatory Affairs
Keif Fitzgerald
VP of Engineering
Board of Directors
Michael Wallace
Darshana Zaveri
Erik van der Burg
Shant Vartanian, MD
Adam Berman
Our Investors
News and Events
Venova Medical to present VENOS-1 study results during 2024 Controversies in Dialysis Access (CiDA) meeting
Venova Medical has developed the VelocityTM pAVF System, a next generation percutaneous AVF technology designed to reduce the need for reinterventions to achieve fistula maturation, maintain functionality and improve vascular access outcomes while reducing costs....
Charing Cross Symposium (CX) | April 23-25, 2024 | London, England
Venova Medical will be attending the 2024 Charing Cross Symposium (CX) being held April 23-25,2024 in London, England. The meeting will feature a presentation by Robert Shahverdyan, MD, Head of Vascular Access Center at the Asklepios Klinik Barmbek in Hamburg,...
ASDIN 20th Annual Scientific Meeting | February 23-25, 2024 | New Orleans, Louisiana
Venova Medical will be attending the 20th Annual Scientific Meeting of the American Society of Diagnostic and Interventional Nephrology (ASDIN) being held from February 23rd to 25th in New Orleans, Louisiana. Additionally, Robert Shahverdyan, MD, Head of Vascular...