Published Real-World Experience Demonstrates VasQ External Support Improves Outcomes When Adopted as the Standard of Care

Published in the Journal of Vascular Access by Dr. Robert Shahverdyan, Head of Vascular Access Center at Asklepios Klinik Barmbek of Hamburg, Germany

Dr. Robert Shahverdyan, Head of Vascular Access Center at Asklepios Klinik Barmbek of Hamburg, Germany, has recently published a retrospective analysis of his first 32 consecutive radiocephalic (forearm) VasQ procedures in the Journal of Vascular Access.

The paper demonstrated that using VasQ as the standard of care for radiocephalic fistulas resulted in a significant improvement in his center’s primary fistula failure and longer-term secondary patency rates with less repeat interventions when compared to historical controls.

Radiocephalic fistulas are the preferred vascular access to facilitate dialysis treatment as compared to other modalities despite the reportedly high rates of primary failure and need for frequent interventions. Historically, the primary fistula failure rate for radiocephalic fistulas at Dr. Shahverdyan’s center before the use of VasQ was 29%, which compares well to the typically higher rates reported in the clinical literature for this type of fistula. That primary failure rate has dropped significantly to 6% since he began using VasQ as the standard of care for his radiocephalic patients.

Additionally, his rate of repeat procedures required to make the fistulas usable dropped from 0.62 per pt-yr to 0.26 per pt-yr with VasQ. For context, typically reported rates for repeat procedure are between 1 to 2 interventions per pt-yr in Europe with rates in the U.S. reported >3 per pt-yr. His data aligns well with previously reported clinical studies for VasQ for upper arm fistulas and shows that the adoption of VasQ as the standard of care improved patient outcomes of an already high-performing center.

Dr. Shahverdyan commented, “Hemodialysis patients are a particularly challenging patient population with historically poor outcomes related to vascular procedures. As surgeons, we must be skeptically optimistic about any new technology that promises better outcomes for our patients until we see it perform in a real-world setting. After a careful review of my results over the last few years, I was excited to learn of the beneficial impact VasQ has had on my hemodialysis patient outcomes and am happy that I can offer them a better option with VasQ as my new standard of care for their vascular access.”

“The results from Dr. Shahverdyan’s practice is a significant step forward for Laminate to meet our goal of providing surgeons tools to create more usable fistulas,” said Laminate CEO Tammy Gilon. “We are excited to continue to partner with physicians like Dr. Shahverdyan as they work to create functioning fistulas for each of their patients.”

Hot this week

Medtronic Expands AiBLE Spine Surgery Ecosystem with New Technologies and Siemens Healthineers Partnership

New advancements in the AiBLE Spine Surgery ecosystem build upon the company's commitment to procedural innovation and execution

Axlab, Danish Medtech Pioneer, expands to US with Advanced Robotic Tissue Sectioning for Pathology Laboratories

Kris Rokke, National Sales Director for Axlab in the US. "My team and I are extremely excited and honored about this unique opportunity to also offer this advanced technology to labs across the US and thus contribute to the pathology labs of tomorrow."

Spartan Medical Broadens Single-Use Sterile Instrument Portfolio to Improve Outcomes, Increase Efficiency, and Generate Cost Savings

Spartan Medical products portfolio of single-use, sterile med tech includes micro and minor surgical convenience kits, kerrison rongeurs, spinal and general surgical retractors, dural repair kits, synthetic biologics, and a wide range of orthopedic pre-sterilized implants and devices.

Recor Medical Supports European Society of Cardiology’s Hypertension Guidelines

Record Medical notes the new guidelines, "2024 ESC Guidelines for the management of elevated blood pressure and hypertension," have been published online and recommend the consideration of renal denervation (RDN) as a safe and effective treatment option for patients who have uncontrolled resistant hypertension or those that have uncontrolled hypertension with a higher risk of cardiovascular disease, who express a preference to undergo RDN.

ConTIPI Medical Selects EVERSANA to Support U.S. Commercialization of Non-Surgical Medical Device ProVate for Women with Pelvic Organ Prolapse

EVERSANA is a leading provider of global commercial services to the life sciences industry, to support commercialization for the ProVate device in the United States to help women experiencing pelvic organ prolapse.