Three‐year clinical outcomes after transcatheter aortic valve implantation in patients with bicuspid aortic disease: Comparison between self‐expanding and balloon‐expandable valves

Author:

Boiago Mauro1ORCID,Bellamoli Michele1,De Biase Chiara1ORCID,Beneduce Alessandro1ORCID,Alonso Lola Gutierrez1,Laforgia Pietro1,Feliachi Souehib1,Oliva Omar Alessandro1ORCID,Dumonteil Nicolas1,Tchétché Didier1

Affiliation:

1. Groupe CardioVasculaire Interventionnel Clinique Pasteur Toulouse France

Abstract

AbstractIntroductionBicuspid aortic valve (BAV) stenosis is a complex anatomical scenario for transcatheter aortic valve implantation (TAVI). Favorable short‐term clinical outcomes have been reported with TAVI in this setting, but long‐term data are scarce.MethodsWe retrospectively included, in a single‐center registry, patients with BAV stenosis who underwent TAVI before 2020. We compared patients treated with self‐expanding valves (SEV) versus balloon‐expandable valves (BEV). The primary endpoint was a composite of all‐cause mortality, stroke and need for aortic valve (AV) reintervention at 3 years. Secondary endpoints included each component of the primary endpoint, cardiovascular mortality, permanent pacemaker implantation (PPI) rate, mean gradient and ≥moderate paravalvular leak (PVL) rate.ResultsA total of 150 consecutive patients (SEV = 83, BEV = 67) were included. No significant differences were reported between SEV and BEV groups for the primary composite endpoint (SEV 35.9% vs. BEV 32%, p = 0.66), neither for clinical secondary endpoints (all‐cause mortality SEV 28.1% vs. BEV 28%, p = 0.988; cardiovascular mortality SEV 14.1% vs. BEV 20%, p = 0.399; stroke SEV 12.5% vs. BEV 6%, p = 0.342; need for AV reintervention SEV 0% vs. BEV 0%; PPI SEV 28.1% vs. BEV 24%, p = 0.620). A lower mean gradient persisted up to 3 years in the SEV group (SEV 8.8 ± 3.8 mmHg vs. BEV 10.7 ± 3.2 mmHg, p = 0.063), while no significant difference was found in the rate of ≥ moderate PVL (SEV 3/30 vs. BEV 0/25, p = 0.242).ConclusionsIn this single center registry, we observed favorable 3‐year clinical outcomes in nonselected BAV patients treated with different generation devices, without significant differences between patients receiving SEV or BEV.

Publisher

Wiley

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