Procedural, 30-day and one year outcome following CoreValve or Edwards transcatheter aortic valve implantation: results of the Belgian national registry

Jan Bosmans(Antwerp University Hospital), J. Kefer(UCLouvain), Bernard De Bruyne(Onze Lieve Vrouwziekenhuis Hospital), Paul Herijgers(KU Leuven), Charlotte Dubois(KU Leuven), V. Legrand(University of Liège), Stephan Verheye(ZNA Middelheim Hospital), Inez Rodrigus(Antwerp University Hospital), for the Belgian TAVI Registry Participants
Interactive Cardiovascular and Thoracic Surgery
February 24, 2011
Cited by 221Open Access
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Abstract

We report clinical outcomes following transcatheter aortic valve implantation (TAVI), using the CoreValve revalving system (18 Fr transfemoral or subclavian) or the Edwards Sapien valve (22 Fr transfemoral or 24 Fr transapical) as part of a Belgian prospective nonrandomized multicentre registry. All 15 Belgian centres performing TAVI participated to this registry (seven exclusively Edwards Sapien, eight exclusively CoreValve). All consecutive high-risk symptomatic patients with severe aortic stenosis were evaluated by a heart team and screened for eligibility for TAVI. Three hundred and twenty-eight patients underwent TAVI with CoreValve (ns141; eight subclavian and 133 transfemoral) or Edwards Sapien (ns187; 99 transfemoral and 88 transapical) up to April 2010. Procedural success was 97%. Onemonth survival was 88% for the Edwards and 89% for the CoreValve treated patients. One-month mortality was both related to cardiac and non-cardiac reasons. Overall one-year survival was 78% in the CoreValve transfemoral treated patients, 100% in the CoreValve subclavian treated patients, 82% in the Edwards transfemoral treated patients and 63% in the Edwards transapical treated patients. This mid-term mortality was mainly related to age-related, non-cardiac complications.


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