Edwards
Lifesciences
at AATS 2022
Don't miss this year's Edwards-sponsored symposia
Visit Edwards Lifesciences at Booth #1609 at AATS 102nd Annual Meeting
Treating Mitral Regurgitation - Repair and Replace
Friday, May 13th, 2022
12:30 PM - 1:15 PM EST
Boston Sheraton Hotel Convention Center, Constitution AB
Faculty
Dr. Maurice Sarano
Dr. Kevin Accola
Dr. David Adams
Dr. Vinod Thourani
Introducing the new MITRIS RESILIA mitral valve
Saturday, May 14th, 2022
12:30 PM - 1:30 PM EST
Hynes Convention Center, Room 302
Faculty
Dr. Richard Shemin
Dr. Randolph Chitwood Jr
Dr. Gorav Ailawadi
Dr. Kevin Accola
Complex Aortic Root Care
Monday, May 16th, 2022
12:15 PM - 1:15 PM EST
Hynes Convention Center, Room 304-306
Faculty
Dr. Joseph Bavaria
Dr. Ismail El-Hamamsy
Dr. Kim de la Cruz
Dr. Eric Roselli
Visit Edwards Lifesciences at Booth #1609
Don't miss these presentations at AATS 2022 Annual Meeting:
Learn more about the HARPOON system and the RESTORE trial
CAUTION: Investigational device. Limited by Federal (United States) law to investigational use. The device is not available for marketing or commercial sale in the United States. Edwards Lifesciences is the sponsor of the RESTORE trial.
Important Safety Information: RESILIA Tissue Devices
Indications: INSPIRIS RESILIA Aortic Valve - For use in replacement of native or prosthetic aortic heart valves. KONECT RESILIA Aortic Valved Conduit - For use in replacement of native or prosthetic aortic heart valves and the associated repair or replacement of a damaged or diseased ascending aorta. MITRIS RESILIA Mitral Valve - For use in replacement of native or prosthetic mitral heart valves. Contraindications: There are no known contraindications with the use of these RESILIA tissue heart valve devices. Complications and Side Effects: INSPIRIS RESILIA Aortic Valve - Thromboembolism, valve thrombosis, hemorrhage, hemolysis, regurgitation, endocarditis, structural valve deterioration, nonstructural dysfunction, stenosis, arrhythmia, transient ischemic attack/stroke, congestive heart failure, myocardial infarction, any of which could lead to reoperation, explantation, permanent disability, and death. Additional adverse events potentially associated with the use of polyester vascular grafts in the KONECT RESILIA AVC include hemorrhage, thrombosis, graft infection, embolism, aneurysm, pseudoaneurysm, seroma, occlusion (anastomotic intimal hyperplasia), immunological reaction to collagen (shown to be a weak immunogen; infrequent, mild, localized and self-limiting), intimal peel formation, and conduit dilatation. MITRIS RESILIA Mitral Valve - Thromboembolism, valve thrombosis, hemorrhage, hemolysis, regurgitation, endocarditis, structural valve deterioration, nonstructural dysfunction, stenosis, arrhythmia, transient ischemic attack/stroke, congestive heart failure, myocardial infarction, ventricular perforation by stent posts, any of which could lead to reoperation, explantation, permanent disability, and death. Warnings: INSPIRIS RESILIA Aortic Valve - DO NOT ADJUST THE VALVE DIAMETER BY EXPANDING THE BAND PRIOR TO OR DURING IMPLANTATION OF THE SURGICAL VALVE. The expandable band is not designed to allow for compression or expansion during implantation of the surgical valve. This will cause damage to the valve and may result in aortic incompetence. DO NOT PERFORM STAND-ALONE BALLOON AORTIC VALVULOPLASTY PROCEDURES ON THIS VALVE FOR THE SIZES 19 – 25 mm as this may expand the valve causing aortic incompetence, coronary embolism or annular rupture. Valve-in-valve sizing in the INSPIRIS valve has only been tested with specific Edwards transcatheter heart valves. Use of other transcatheter valves may result in embolization of transcatheter devices anchored within or result in annular rupture.
CAUTION: Federal (USA) law restricts these devices to sale by or on the order of a physician. See Instructions for Use for full prescribing information.
Edwards, Edwards Lifesciences, the stylized E logo, HARPOON, INSPIRIS, INSPIRIS RESILIA, KONECT, KONECT RESILIA, MITRIS, MITRIS RESILIA, and RESILIA are trademarks of Edwards Lifesciences Corporation or its affiliates. All other trademarks are the property of their respective owners.
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