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  3. Transcatheter aortic valve implantation vs. surgical aortic valve replacement for treatment of severe aortic stenosis: a meta-analysis of randomized trials.
 

Transcatheter aortic valve implantation vs. surgical aortic valve replacement for treatment of severe aortic stenosis: a meta-analysis of randomized trials.

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BORIS DOI
10.7892/boris.86095
Date of Publication
December 14, 2016
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Departement Klinische...

Contributor
Siontis, Georgios
Universitätsklinik für Kardiologie
Praz, Fabien Daniel
Universitätsklinik für Kardiologie
Pilgrim, Thomas
Universitätsklinik für Kardiologie
Mavridis, Dimitris
Verma, Subodh
Salanti, Georgiaorcid-logo
Departement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
Institut für Sozial- und Präventivmedizin (ISPM)
Berner Institut für Hausarztmedizin (BIHAM)
Søndergaard, Lars
Jüni, Peter
Windecker, Stephan
Universitätsklinik für Kardiologie
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
European Heart Journal
ISSN or ISBN (if monograph)
0195-668X
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/eurheartj/ehw225
PubMed ID
27389906
Uncontrolled Keywords

Aortic stenosis

Meta-analysis

Randomized controlled...

Surgical aortic valve...

Transcatheter aortic ...

Transcatheter aortic ...

Description
AIMS

In view of the currently available evidence from randomized trials, we aimed to compare the collective safety and efficacy of transcatheter aortic valve implantation (TAVI) vs. surgical aortic valve replacement (SAVR) across the spectrum of risk and in important subgroups.

METHODS AND RESULTS

Trials comparing TAVI vs. SAVR were identified through Medline, Embase, and Cochrane databases. The primary outcome was death from any cause at 2 years. We performed random-effects meta-analyses to combine the available evidence and to evaluate the effect in different subgroups. This systematic review and meta-analysis is registered with PROSPERO (CRD42016037273). We identified four eligible trials including 3806 participants, who were randomly assigned to undergo TAVI (n = 1898) or SAVR (n = 1908). For the primary outcome of death from any cause, TAVI when compared with SAVR was associated with a significant 13% relative risk reduction [hazard ratio (95% CI): 0.87 (0.76-0.99); P = 0.038] with homogeneity across all trials irrespective of TAVI device (Pinteraction = 0.306) and baseline risk (Pinteraction = 0.610). In subgroup analyses, TAVI showed a robust survival benefit over SAVR for patients undergoing transfemoral access [0.80 (0.69-0.93); P = 0.004], but not transthoracic access [1.17 (0.88-1.56); P = 0.293] (Pinteraction = 0.024) and in female [0.68 (0.50-0.91); P = 0.010], but not male patients [0.99 (0.77-1.28); P = 0.952] (Pinteraction = 0.050). Secondary outcomes of kidney injury, new-onset atrial fibrillation, and major bleeding favoured TAVI, while major vascular complications, incidence of permanent pacemaker implantation, and paravalvular regurgitation favoured SAVR.

CONCLUSION

Compared with SAVR, TAVI is associated with a significant survival benefit throughout 2 years of follow-up. Importantly, this superiority is observed irrespective of the TAVI device across the spectrum of intermediate and high-risk patients, and is particularly pronounced among patients undergoing transfemoral TAVI and in females.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/143864
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
Siontis EurHeartJ 2016.pdftextAdobe PDF701.35 KBpublishedOpen
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