Aortic valve replacement was performed by the use of the Medtronic self-expanding CoreValve and Evolut devices (Medtronic Inc., Minneapolis, MN, United States, n = 341, 97.1%), the Edwards Sapien S3 (Edwards Lifesciences SA, CA, United-States, n = 28, 7.9%) or the Boston neo Accurate (Boston Scientific AG, MA, United States, n = 5, 1.5%). Device implantation success was systematically evaluated for all interventions according to the Valve Academic Research Consortium-2 consensus Document criteria (19 (link)).
Evolut
Manufactured by Medtronic
Sourced in United States
The Evolut is a lab equipment product designed and manufactured by Medtronic. It is a compact and versatile device that serves as a platform for various laboratory applications. The core function of the Evolut is to provide a reliable and precise solution for sample processing and analysis in research and clinical settings.
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2 protocols using evolut
1
Transcatheter Aortic Valve Replacement Devices
2
Transcatheter Aortic Valve Implantation
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Balloon predilatation of the AoV was performed in 72% of patients. Medtronic CoreValve, Medtronic Engager, and Medtronic Evolut valves were implanted in 61, 6, and 5 patients, respectively. Edwards SAPIEN, SAPIEN 3, and SAPIEN XT valves were implanted in 87, 8, and 1 patients, respectively. Femoral, apical, axillar, and transaortic accesses were used in 107, 48, 11, and 2 patients, respectively. Valve sizes of 23, 26, 29, and 31 were used and were based on the CT-measured perimeter of the aortic annulus, per vendor recommendations. Balloon postdilatation was performed in 21% of patients, with significant aortic paravalvular leak as the leading indication.
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