Transcatheter Versus Surgical Aortic Valve Replacement in Patients With Complex Coronary Artery Disease.


Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
22 11 2021
Historique:
received: 25 08 2021
accepted: 31 08 2021
entrez: 19 11 2021
pubmed: 20 11 2021
medline: 1 4 2022
Statut: ppublish

Résumé

The aim of this study was to compare, in a cohort of patients with complex coronary artery disease (CAD) and severe aortic stenosis (AS), the clinical outcomes associated with transfemoral transcatheter aortic valve replacement (TAVR) (plus percutaneous coronary intervention [PCI]) versus surgical aortic valve replacement (SAVR) (plus coronary artery bypass grafting [CABG]). Patients with complex CAD were excluded from the main randomized trials comparing TAVR with SAVR, and no data exist comparing TAVR + PCI vs SAVR + CABG in such patients. A multicenter study was conducted including consecutive patients with severe AS and complex CAD (SYNTAX [Synergy Between PCI with Taxus and Cardiac Surgery] score >22 or unprotected left main disease). A 1:1 propensity-matched analysis was performed to account for unbalanced covariates. The rates of major adverse cardiac and cerebrovascular events (MACCE), including all-cause mortality, nonprocedural myocardial infarction, need for new coronary revascularization, and stroke, were evaluated. A total of 800 patients (598 undergoing SAVR + CABG and 202 undergoing transfemoral TAVR + PCI) were included, and after propensity matching, a total of 156 pairs of patients were generated. After a median follow-up period of 3 years (interquartile range: 1-6 years), there were no significant differences between groups for MACCE (HR for transfemoral TAVR vs SAVR: 1.33; 95% CI: 0.89-1.98), all-cause mortality (HR: 1.25; 95% CI: 0.81-1.94), myocardial infarction (HR: 1.16; 95% CI: 0.41-3.27), and stroke (HR: 0.42; 95% CI: 0.13-1.32), but there was a higher rate of new coronary revascularization in the TAVR + PCI group (HR: 5.38; 95% CI: 1.73-16.7). In patients with severe AS and complex CAD, TAVR + PCI and SAVR + CABG were associated with similar rates of MACCE after a median follow-up period of 3 years, but TAVR + PCI recipients exhibited a higher risk for repeat coronary revascularization. Future trials are warranted.

Sections du résumé

OBJECTIVES
The aim of this study was to compare, in a cohort of patients with complex coronary artery disease (CAD) and severe aortic stenosis (AS), the clinical outcomes associated with transfemoral transcatheter aortic valve replacement (TAVR) (plus percutaneous coronary intervention [PCI]) versus surgical aortic valve replacement (SAVR) (plus coronary artery bypass grafting [CABG]).
BACKGROUND
Patients with complex CAD were excluded from the main randomized trials comparing TAVR with SAVR, and no data exist comparing TAVR + PCI vs SAVR + CABG in such patients.
METHODS
A multicenter study was conducted including consecutive patients with severe AS and complex CAD (SYNTAX [Synergy Between PCI with Taxus and Cardiac Surgery] score >22 or unprotected left main disease). A 1:1 propensity-matched analysis was performed to account for unbalanced covariates. The rates of major adverse cardiac and cerebrovascular events (MACCE), including all-cause mortality, nonprocedural myocardial infarction, need for new coronary revascularization, and stroke, were evaluated.
RESULTS
A total of 800 patients (598 undergoing SAVR + CABG and 202 undergoing transfemoral TAVR + PCI) were included, and after propensity matching, a total of 156 pairs of patients were generated. After a median follow-up period of 3 years (interquartile range: 1-6 years), there were no significant differences between groups for MACCE (HR for transfemoral TAVR vs SAVR: 1.33; 95% CI: 0.89-1.98), all-cause mortality (HR: 1.25; 95% CI: 0.81-1.94), myocardial infarction (HR: 1.16; 95% CI: 0.41-3.27), and stroke (HR: 0.42; 95% CI: 0.13-1.32), but there was a higher rate of new coronary revascularization in the TAVR + PCI group (HR: 5.38; 95% CI: 1.73-16.7).
CONCLUSIONS
In patients with severe AS and complex CAD, TAVR + PCI and SAVR + CABG were associated with similar rates of MACCE after a median follow-up period of 3 years, but TAVR + PCI recipients exhibited a higher risk for repeat coronary revascularization. Future trials are warranted.

Identifiants

pubmed: 34794656
pii: S1936-8798(21)01682-4
doi: 10.1016/j.jcin.2021.08.073
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2490-2499

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Alperi was supported by a research grant from the Martín Escudero Foundation. Dr Rodés-Cabau holds the Research Chair “Fondation Famille Jacques Larivière” for the Development of Structural Heart Disease Interventions; and has received institutional research grants from Edwards Lifesciences and Medtronic. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Alberto Alperi (A)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Siamak Mohammadi (S)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Francisco Campelo-Parada (F)

Rangueil University Hospital, Toulouse, France.

Erika Munoz-Garcia (E)

Hospital Universitario Virgen de la Victoria, Malaga, Spain.

Luis Nombela-Franco (L)

Cardiovascular Institute, Hospital Clinico San Carlos, IdISSC, Madrid, Spain.

Laurent Faroux (L)

Reims University Hospital, Reims, France.

Gabriela Veiga (G)

Hospital Marques de Valdecilla, Santander, Spain.

Vicenç Serra (V)

Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Quentin Fischer (Q)

Assistance Publique-Hôpitaux de Paris, Bichat Hospital, Paris, France.

Isaac Pascual (I)

Hospital Universitario Central de Asturias, Oviedo, Spain.

Luis Asmarats (L)

Hospital Santa Creu i Sant Pau, Barcelona, Spain.

Enrique Gutiérrez (E)

Hospital Gregorio Maranon, Madrid, Spain.

Ander Regueiro (A)

Hospital Clinic de Barcelona, Barcelona, Spain.

Victoria Vilalta (V)

Hospital Germans Trias i Pujol, Badalona, Spain.

Henrique B Ribeiro (HB)

Instituto do Coração (InCor), Heart Institute, University of Sao Paulo, Sao Paulo, Brazil.

Anthony Matta (A)

Rangueil University Hospital, Toulouse, France.

Antonio Munoz-Garcia (A)

Hospital Universitario Virgen de la Victoria, Malaga, Spain.

German Armijo (G)

Cardiovascular Institute, Hospital Clinico San Carlos, IdISSC, Madrid, Spain.

Damien Metz (D)

Reims University Hospital, Reims, France.

Jose M De la Torre Hernandez (JM)

Hospital Marques de Valdecilla, Santander, Spain.

Eduard Rodenas-Alesina (E)

Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Marina Urena (M)

Assistance Publique-Hôpitaux de Paris, Bichat Hospital, Paris, France.

Cesar Moris (C)

Hospital Universitario Central de Asturias, Oviedo, Spain.

Dabit Arzamendi (D)

Hospital Santa Creu i Sant Pau, Barcelona, Spain.

Pedro Perez-Fuentes (P)

Hospital Clinic de Barcelona, Barcelona, Spain.

Eduard Fernandez-Nofrerias (E)

Hospital Germans Trias i Pujol, Badalona, Spain.

Diego Carter Campanha-Borges (DC)

Instituto do Coração (InCor), Heart Institute, University of Sao Paulo, Sao Paulo, Brazil.

Jules Mesnier (J)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Pierre Voisine (P)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Eric Dumont (E)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Dimitri Kalavrouziotis (D)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Josep Rodés-Cabau (J)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada; Hospital Clinic de Barcelona, Barcelona, Spain. Electronic address: josep.rodes@criucpq.ulaval.ca.

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Classifications MeSH