In this new edition of the RESILIA Tissue Insider, we are excited to feature the recently CE‑marked KONECT RESILIA aortic valved conduit. Inside, we explore the history and development of the device, report early patient data, and share the experiences of cardiac surgeons who have implanted the device. Highlights include:
Since the first aortic aneurysm repair in 1951, aortic root replacement has evolved significantly. The latest milestone: the KONECT RESILIA aortic valved conduit – our first pre-assembled, ready-to-implant* solution with RESILIA tissue, developed to simplify bio-Bentall procedures** and support active lifestyles.
In this special edition, we hear from leading experts on the KONECT RESILIA aortic valved conduit. Professor De Paulis discusses the milestone of the first European implantation and Professor Bavaria reflects on his experience with over 400 KONECT RESILIA aortic valved conduits in the USA.
Discover more on RESILIA tissue through the current and past issues below.
*Consult instructions for use for device preparation
**As compared to self-assembled tissue valved conduits
In this issue, we report how RESILIA tissue valves are performing at 8 years in the COMMENCE trial and showcase real-world studies on these valves. We also explore the history of bioprosthetic valve innovation in the latest of our new feature articles. Other highlights include:
This healthcare professional focused booklet explores the latest clinical studies and publications involving the INSPIRIS RESILIA valve and RESILIA tissue through the review of 24 publications and abstracts.
Each reference has been summarized visually over 1 or 2 slides, for you to save time.
*Clinical data on valves with RESILIA tissue up to 7-year follow-up have been published, with additional follow-up to 10-years in progress.
Beaver T, Bavaria JE, Griffith B et al. Seven-year outcomes following aortic valve replacement with a novel tissue bioprosthesis. J Thorac Cardiovasc Surg. 2024; 168: 781–91.
†RESILIA tissue tested against tissue from commercially-available bovine pericardial valves from Edwards in a juvenile sheep model. Flameng, et al. J Thorac Cardiovasc Surg 2015;149:340–5
Refer to device instructions for use for important warnings related to VFit technology. These features have not been observed in clinical studies to establish the safety and effectiveness of the model 11500A for use in valve-in-valve procedures. VFit technology is available on sizes 19–25 mm.
Medical device for professional use. For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use (consult eifu.edwards.com where applicable).
An educational website focused on TAVI is underway
Thank you. We will keep you updated when new content is available.