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

被引:0
|
作者
Boiago, Mauro [1 ,2 ]
Bellamoli, Michele [1 ]
De Biase, Chiara [1 ]
Beneduce, Alessandro [1 ]
Alonso, Lola Gutierrez [1 ]
Laforgia, Pietro [1 ]
Feliachi, Souehib [1 ]
Oliva, Omar Alessandro [1 ]
Dumonteil, Nicolas [1 ]
Tchetche, Didier [1 ]
机构
[1] Clin Pasteur, Grp Cardiovasc Intervent, Toulouse, France
[2] Clin Pasteur, Grp Cardiovasc Intervent, 45 Ave Lombez, F-31076 Toulouse 03, France
关键词
balloon-expandable valve; bicuspid aortic valve; self-expanding valve; transcatheter aortic valve implantation; END-POINT DEFINITIONS; REPLACEMENT; ASSOCIATION; MORTALITY; STENOSIS;
D O I
10.1002/ccd.31041
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionBicuspid 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.
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收藏
页码:1004 / 1014
页数:11
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