Study sites
Weill Cornell Medical Center | Cleveland Clinic | Hospital of the University of Pennsylvania
Clinical evidence
Weill Cornell Medical Center | Cleveland Clinic | Hospital of the University of Pennsylvania
329 patients
Aortic aneurysm, aortic dissection, endocarditis, and valvular dysfunction
The KONECT RESILIA aortic valved conduit offers a simplified approach to root replacement, with excellent short-term outcomes reported through one year.
Yale School of Medicine, Division of Cardiac Surgery
118 patients
2021-2023
Initial findings suggest the KONECT RESILIA aortic valved conduit may offer favorable early outcomes for patients undergoing aortic root and valve replacement.
Proven performance at 7 years
*Clinical data on surgical valves with RESILIA tissue up to 7-year follow-up have been published, with additional follow-up to 10-years in progress.3




*As compared to self-assembled valved conduits
§As compard to self=assembled valved conduits with non-RESILIA valves
†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.
KONECT RESILIA Aortic Valved Conduit
Indications: For use in replacement of native or prosthetic aortic heart valves and the associated repair or replacement of a damaged or diseased ascending aorta.
Contraindications: There are no known contraindications with the use of the KONECT RESILIA aortic valved conduit.
Complications and Side Effects: Thromboembolism, valve thrombosis, hemorrhage, hemolysis, regurgitation, endocarditis, structural valve deterioration, nonstructuraldysfunction, stenosis, arrhythmia, transient ischemic attack/stroke, congestive heart failure, myocardial infarction, any of which could lead to reoperation, explantation,permanent disability, and death. Adverse events potentially associated with the use of polyester vascular grafts 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, any of which could lead to re-operation, explantation, permanent disability, and death.
CAUTION: US law restricts this device to sale by or on the order of a physician. See instructions for use for full prescribing information.
PP-US--4852