Healthcare Industry News: nitinol stent
News Release - February 20, 2014
Gore REVISE Clinical Study Demonstrates Superiority of GORE VIABAHN EndoprosthesisGORE Device Outperforms Standard Treatment Option for Stenoses or Thrombotic Occlusions
FLAGSTAFF, Ariz. & PHOENIX--(Healthcare Sales & Marketing Network)--W. L. Gore & Associates (Gore) today announced that it will present the results of the Gore REVISE Clinical Study, the only randomized, controlled study of stent-grafts to investigate both stenotic and thrombotic occlusive arteriovenous (AV) access patients. The results showed that the GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface is superior to percutaneous transluminal angioplasty (PTA) – the current standard of care for treating stenoses or thrombotic occlusions. The results of the Gore REVISE Clinical study will be presented at the 10th Annual Scientific Meeting of the American Society of Diagnostic and Interventional Nephrology (ASDIN) in Phoenix.
Key Points from the Gore REVISE Clinical Study:
- Statistical superiority over the PTA group in target lesion primary patency over a 24 month follow-up period (p = 0.008)
- Non-inferiority in terms of freedom from major device, treatment, or procedure related adverse events as compared to the PTA group (p
- Greater primary patency for both thrombotic and non-thrombotic patients as compared to PTA
- A reduction in the number of repeat interventions per patient as compared to the PTA group necessary to maintain access secondary patency
- No reported fractures crossing the elbow
The GORE VIABAHN Endoprosthesis is the lowest profile, most flexible, self-expanding, small-diameter, endoprosthesis available and the only stent or stent-graft to receive approval for the superficial femoral artery (SFA), iliac artery, and AV Access. It is constructed with a durable, reinforced, biocompatible, expanded polytetrafluoroethylene (ePTFE) liner and attached to an external nitinol stent structure. The ePTFE luminal surface of the GORE VIABAHN Endoprosthesis features the CARMEDA® BioActive Surface (CBAS® Heparin Surface) for sustained anti-thrombotic bioactivity.
“With the Gore REVISE Clinical Study, we wanted to set out and prove not only that the GORE VIABAHN Endoprosthesis can successfully treat stenoses or thrombotic occlusions, but that the device is superior to the current standard of care,” said Ray Swinney, Business Unit Leader for the Gore Peripheral Interventional Business Unit. “Investing in clinical studies such as REVISE allows Gore to provide physicians with superior technology that is supported by trusted clinical data. In doing so, we can help physicians better serve the needs of their patients, particularly those with challenging anatomies that may not have been eligible for stent-graft procedures until now.”
About W. L. Gore & Associates
The Gore Medical Products Division has provided creative therapeutic solutions to complex medical problems for more than 35 years. During that time, more than 35 million innovative Gore Medical Devices have been implanted, saving and improving the quality of lives worldwide. The extensive Gore Medical family of products includes vascular grafts, endovascular and interventional devices, surgical meshes for hernia repair, soft tissue reconstruction, staple line reinforcement and sutures for use in vascular, cardiac, and general surgery. Gore is one of a select few companies to appear on all of the U.S. “100 Best Companies to Work For” lists since the rankings debuted in 1984. For more information, visit www.goremedical.com.
GORE®, VIABAHN®, and designs are trademarks of W. L. Gore & Associates, Inc. Carmeda® and CBAS ® are trademarks Carmeda AB, a wholly owned subsidiary of W. L. Gore & Associates, Inc.
Source: W. L. Gore
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