Cardiac Death After Transcatheter Aortic Valve Replacement With Contemporary Devices.


Journal

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

Informations de publication

Date de publication:
25 09 2023
Historique:
received: 14 12 2022
revised: 14 06 2023
accepted: 09 07 2023
medline: 23 10 2023
pubmed: 28 9 2023
entrez: 27 9 2023
Statut: ppublish

Résumé

The burden of cardiac death after transcatheter aortic valve replacement (TAVR), particularly from advanced heart failure (HF) and sudden cardiac death (SCD), remains largely unknown. This study sought to evaluate the incidence and predictors of SCD and HF-related death in TAVR recipients treated with newer-generation devices. This study included a total of 5,421 consecutive patients who underwent TAVR with newer-generation devices using balloon (75.7%) or self-expandable (24.3%) valves. After a median follow-up of 2 (IQR: 1-3) years, 976 (18.0%) patients had died, 50.8% from cardiovascular causes. Advanced HF and SCD accounted for 11.6% and 7.5% of deaths, respectively. Independent predictors of HF-related death were atrial fibrillation (HR: 2.17; 95% CI: 1.47-3.22; P < 0.001), prior pacemaker (HR: 1.79; 95% CI: 1.10-2.92; P = 0.01), reduced left ventricular ejection fraction (HR: 1.08 per 5% decrease; 95% CI: 1.01-1.14; P = 0.02), transthoracic approach (HR: 2.50; 95% CI: 1.37-4.55; P = 0.003), and new-onset persistent left bundle branch block (HR: 1.85; 95% CI: 1.14-3.02; P = 0.01). Two baseline characteristics (diabetes, HR: 1.81; 95% CI: 1.13-2.89; P = 0.01; and chronic kidney disease, HR: 1.72; 95% CI: 1.02-2.90; P = 0.04) and 3 procedural findings (valve in valve, HR: 2.17; 95% CI: 1.01-4.64; P = 0.04; transarterial nontransfemoral approach, HR: 2.23; 95% CI: 1.23-4.48; P = 0.01; and periprocedural ventricular arrhythmia, HR: 7.19; 95% CI: 2.61-19.76; P < 0.001) were associated with an increased risk of SCD after TAVR. Advanced HF and SCD accounted for a fifth of deaths after TAVR in contemporary practice. Potentially treatable factors leading to increased risk of HF deaths and SCD were identified, such as arrhythmia/dyssynchrony factors for HF and valve-in-valve TAVR or periprocedural ventricular arrhythmias for SCD.

Sections du résumé

BACKGROUND
The burden of cardiac death after transcatheter aortic valve replacement (TAVR), particularly from advanced heart failure (HF) and sudden cardiac death (SCD), remains largely unknown.
OBJECTIVES
This study sought to evaluate the incidence and predictors of SCD and HF-related death in TAVR recipients treated with newer-generation devices.
METHODS
This study included a total of 5,421 consecutive patients who underwent TAVR with newer-generation devices using balloon (75.7%) or self-expandable (24.3%) valves.
RESULTS
After a median follow-up of 2 (IQR: 1-3) years, 976 (18.0%) patients had died, 50.8% from cardiovascular causes. Advanced HF and SCD accounted for 11.6% and 7.5% of deaths, respectively. Independent predictors of HF-related death were atrial fibrillation (HR: 2.17; 95% CI: 1.47-3.22; P < 0.001), prior pacemaker (HR: 1.79; 95% CI: 1.10-2.92; P = 0.01), reduced left ventricular ejection fraction (HR: 1.08 per 5% decrease; 95% CI: 1.01-1.14; P = 0.02), transthoracic approach (HR: 2.50; 95% CI: 1.37-4.55; P = 0.003), and new-onset persistent left bundle branch block (HR: 1.85; 95% CI: 1.14-3.02; P = 0.01). Two baseline characteristics (diabetes, HR: 1.81; 95% CI: 1.13-2.89; P = 0.01; and chronic kidney disease, HR: 1.72; 95% CI: 1.02-2.90; P = 0.04) and 3 procedural findings (valve in valve, HR: 2.17; 95% CI: 1.01-4.64; P = 0.04; transarterial nontransfemoral approach, HR: 2.23; 95% CI: 1.23-4.48; P = 0.01; and periprocedural ventricular arrhythmia, HR: 7.19; 95% CI: 2.61-19.76; P < 0.001) were associated with an increased risk of SCD after TAVR.
CONCLUSIONS
Advanced HF and SCD accounted for a fifth of deaths after TAVR in contemporary practice. Potentially treatable factors leading to increased risk of HF deaths and SCD were identified, such as arrhythmia/dyssynchrony factors for HF and valve-in-valve TAVR or periprocedural ventricular arrhythmias for SCD.

Identifiants

pubmed: 37758382
pii: S1936-8798(23)01056-7
doi: 10.1016/j.jcin.2023.07.015
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2277-2290

Informations de copyright

Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Mesnier was supported by a research grant from Fédération Française de Cardiologie. Dr Belahnech was supported by a research grant from Aula Vall d’Hebron. 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 and consultant/speaker fees from Edwards Lifesciences and Medtronic. Dr Ternacle has served as a consultant for Abbott. Dr Modine has served as a consultant for Abbott, Edwards Lifesciences, and Medtronic. Dr Nombela-Franco has served as a proctor for Abbott and Edwards Lifesciences. Dr Reguiero has served as a proctor for Abbott. Dr Himbert has served as a proctor for Abbott and Edwards Lifesciences. Dr Asmarats has received speaker fees from Edwards Lifesciences. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Jules Mesnier (J)

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

Julien Ternacle (J)

Hôpital Cardiologique Haut-Lévêque, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.

Asim N Cheema (AN)

Southlake Regional Health Centre, St. Michael's Hospital Toronto, Newmarket, Ontario, Canada.

Francisco Campelo-Parada (F)

Hôpital Rangueil, CHU Toulouse, Toulouse, France.

Marina Urena (M)

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

Gabriela Veiga-Fernandez (G)

Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain.

Luis Nombela-Franco (L)

Cardiovascular Institute, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria Hospital Clínico San Carlos, Madrid, Spain.

Antonio J Munoz-Garcia (AJ)

Hospital Universitario Virgen de la Victoria, Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares, Málaga, Spain.

Victoria Vilalta (V)

Department of Cardiology, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.

Ander Regueiro (A)

Cardiology Department, Instituto Clínic Cardiovascular, Hospital Clínic, Barcelona, Spain and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

David Del Val (D)

Department of Cardiology, Hospital Universitario de La Princesa, Universidad Autónoma de Madrid, Instituto de Investigación Sanitaria La Princesa, CIBER-CV, Madrid, Spain.

Lluis Asmarats (L)

Cardiology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Maria Del Trigo (M)

Servicio de Cardiología, Hospital Universitario Puerta de Hierro, Madrid, Spain.

Vicenç Serra (V)

Vall d'Hebron Research Institute, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Guillaume Bonnet (G)

Hôpital Cardiologique Haut-Lévêque, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.

Melchior Jonveaux (M)

Hôpital Cardiologique Haut-Lévêque, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.

Effat Rezaei (E)

Southlake Regional Health Centre, St. Michael's Hospital Toronto, Newmarket, Ontario, Canada.

Anthony Matta (A)

Hôpital Rangueil, CHU Toulouse, Toulouse, France.

Dominique Himbert (D)

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

Jose Maria de la Torre Hernandez (JM)

Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain.

Gabriela Tirado-Conte (G)

Cardiovascular Institute, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria Hospital Clínico San Carlos, Madrid, Spain.

Eduard Fernandez-Nofrerias (E)

Department of Cardiology, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.

Pablo Vidal (P)

Cardiology Department, Instituto Clínic Cardiovascular, Hospital Clínic, Barcelona, Spain and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Fernando Alfonso (F)

Department of Cardiology, Hospital Universitario de La Princesa, Universidad Autónoma de Madrid, Instituto de Investigación Sanitaria La Princesa, CIBER-CV, Madrid, Spain.

Lola Gutierrez-Alonso (L)

Cardiology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Juan Francisco Oteo (JF)

Servicio de Cardiología, Hospital Universitario Puerta de Hierro, Madrid, Spain.

Yassin Belahnech (Y)

Vall d'Hebron Research Institute, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Siamak Mohammadi (S)

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

François Philippon (F)

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

Thomas Modine (T)

Hôpital Cardiologique Haut-Lévêque, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.

Josep Rodés-Cabau (J)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada; Cardiology Department, Instituto Clínic Cardiovascular, Hospital Clínic, Barcelona, Spain and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. Electronic address: josep.rodes@criucpq.ulaval.ca.

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