Center Valve Preference and Outcomes of Transcatheter Aortic Valve Replacement: Insights From the AMTRAC Registry.


Journal

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

Informations de publication

Date de publication:
27 06 2022
Historique:
received: 18 01 2022
revised: 25 04 2022
accepted: 03 05 2022
entrez: 23 6 2022
pubmed: 24 6 2022
medline: 28 6 2022
Statut: ppublish

Résumé

Data on outcomes of transcatheter aortic valve replacement (TAVR) using balloon-expandable valves (BEVs) or self-expandable valves (SEVs) as well as the impact of center valve preference on these outcomes are limited. The aim of this study was to compare outcomes of TAVR procedures using third-generation BEVs and SEVs stratified by center valve preference. In a multicenter registry (n = 17), 13 centers exhibited valve preference (66.6%-90% of volume) and were included. Outcomes were compared between BEVs and SEVs stratified by center valve preference. In total, 7,528 TAVR procedures (3,854 with SEVs and 3,674 with BEVs) were included. The mean age was 81 years, and the mean Society of Thoracic Surgeons score was 5.2. Baseline characteristics were similar between BEVs and SEVs. Need for pacemaker implantation was higher with SEVs at BEV- and SEV-dominant centers (17.8% vs 9.3% [P < 0.001] and 12.7% vs 10.0% [P = 0.036], respectively; HR: 1.51; P for interaction = 0.021), risk for cerebrovascular accident was higher with SEVs at BEV-dominant but not SEV-dominant centers (3.6% vs 1.1% [P < 0.001] and 2.2% vs 1.4% [P = 0.162]; HR: 2.08; P for interaction < 0.01). Aortic regurgitation greater than mild was more frequent with SEVs at BEV-dominant centers and similar with BEVs regardless of center dominance (5.2% vs 2.8% [P < 0.001] and 3.4% vs 3.7% [P = 0.504], respectively). Two-year mortality was higher with SEVs at BEV-dominant centers but not at SEV-dominant centers (21.9% vs 16.9% [P = 0.021] and 16.8% vs 16.5% [P = 0.642], respectively; HR: 1.20; P for interaction = 0.032). Periprocedural outcomes, aortic regurgitation greater than mild, and 2-year mortality are worse when TAVR is performed using SEVs at BEV-dominant centers. Outcomes are similar regardless of valve type at SEV-dominant centers. The present results stress the need to account for this factor when comparing BEV and SEV outcomes. (The Aortic+Mitral Transcatheter [AMTRAC] Valve Registry; NCT04031274).

Sections du résumé

BACKGROUND
Data on outcomes of transcatheter aortic valve replacement (TAVR) using balloon-expandable valves (BEVs) or self-expandable valves (SEVs) as well as the impact of center valve preference on these outcomes are limited.
OBJECTIVES
The aim of this study was to compare outcomes of TAVR procedures using third-generation BEVs and SEVs stratified by center valve preference.
METHODS
In a multicenter registry (n = 17), 13 centers exhibited valve preference (66.6%-90% of volume) and were included. Outcomes were compared between BEVs and SEVs stratified by center valve preference.
RESULTS
In total, 7,528 TAVR procedures (3,854 with SEVs and 3,674 with BEVs) were included. The mean age was 81 years, and the mean Society of Thoracic Surgeons score was 5.2. Baseline characteristics were similar between BEVs and SEVs. Need for pacemaker implantation was higher with SEVs at BEV- and SEV-dominant centers (17.8% vs 9.3% [P < 0.001] and 12.7% vs 10.0% [P = 0.036], respectively; HR: 1.51; P for interaction = 0.021), risk for cerebrovascular accident was higher with SEVs at BEV-dominant but not SEV-dominant centers (3.6% vs 1.1% [P < 0.001] and 2.2% vs 1.4% [P = 0.162]; HR: 2.08; P for interaction < 0.01). Aortic regurgitation greater than mild was more frequent with SEVs at BEV-dominant centers and similar with BEVs regardless of center dominance (5.2% vs 2.8% [P < 0.001] and 3.4% vs 3.7% [P = 0.504], respectively). Two-year mortality was higher with SEVs at BEV-dominant centers but not at SEV-dominant centers (21.9% vs 16.9% [P = 0.021] and 16.8% vs 16.5% [P = 0.642], respectively; HR: 1.20; P for interaction = 0.032).
CONCLUSIONS
Periprocedural outcomes, aortic regurgitation greater than mild, and 2-year mortality are worse when TAVR is performed using SEVs at BEV-dominant centers. Outcomes are similar regardless of valve type at SEV-dominant centers. The present results stress the need to account for this factor when comparing BEV and SEV outcomes. (The Aortic+Mitral Transcatheter [AMTRAC] Valve Registry; NCT04031274).

Identifiants

pubmed: 35738747
pii: S1936-8798(22)00926-8
doi: 10.1016/j.jcin.2022.05.004
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04031274']

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1266-1274

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Van Miegham has received research grant support from Abbott, Boston Scientific, Edwards Lifesciences, Medtronic, PulseCath BV, and Daiichi-Sankyo; and has received advisory fees from Abbott, Boston Scientific, Ancora, Medtronic, PulseCath BV, and Daiichi-Sankyo. Dr Barbanti has received consulting fees from Edwards Lifesciences. Dr Grasso is a proctor for Abbott Vascular. Dr De Backer has received research grants and consulting fees from Abbott and Boston Scientific. Dr Andreas is a proctor for Abbott and Edwards Lifesciences; and has received advisory board fees from Medtronic. Dr Estévez-Loureiro is a consultant for Abbott Vascular and Boston Scientific. Dr Nombela-Franco has received consulting fees from Edwards Lifesciences; and is a proctor for Abbott. Dr Søndergaard has received consulting fees and/or institutional research support from Abbott, Boston Scientific, Edwards Lifesciences, Medtronic, and SMT. Dr Amat-Santos is a proctor for Boston Scientific. Dr Finkelstein is a proctor for Edwards Lifesciences and Medtronic; and has received consulting fees 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

Guy Witberg (G)

Department of Cardiology, Rabin Medical Center, Petach-Tikva, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. Electronic address: vitberguy@gmail.com.

Uri Landes (U)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Department of Cardiology, Wolfson Medical Center, Holon, Israel.

Yeela Talmor-Barkan (Y)

Department of Cardiology, Rabin Medical Center, Petach-Tikva, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Ilan Richter (I)

Department of Cardiology, Rabin Medical Center, Petach-Tikva, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Marco Barbanti (M)

Division of Cardiology, University of Catania, Catania, Italy.

Roberto Valvo (R)

Division of Cardiology, University of Catania, Catania, Italy.

Ole De Backer (O)

The Heart Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Joris F Ooms (JF)

Department of Cardiology, Thoraxcenter, Erasmus University Medical Center, Rotterdam, the Netherlands.

Fabian Islas (F)

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

Luis Marroquin (L)

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

Alexander Sedaghat (A)

Herzzentrum Bonn, Universitätsklinikum Bonn, Bonn, Germany.

Atsushi Sugiura (A)

Herzzentrum Bonn, Universitätsklinikum Bonn, Bonn, Germany.

Giulia Masiero (G)

Department of Cardiac, Thoracic and Vascular Sciences, University of Padua Medical School, Padua, Italy.

Xavier Armario (X)

Department of Cardiology, Galway University Hospital, and National University of Ireland Galway, Galway, Ireland.

Claudia Fiorina (C)

Cardiovascular Department, Spedali Civili, Brescia, Italy.

Dabit Arzamendi (D)

Hospital de Sant Creu i Sant Pau Barcelona, Barcelona, Spain.

Sandra Santos-Martinez (S)

CIBERCV, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.

Felipe Fernández-Vázquez (F)

Department of Cardiology, University Hospital of León, León, Spain.

Jose A Baz (JA)

Servicio de Cardiología, Hospital Álvaro Cunqueiro, Vigo, Pontevedra, Spain.

Klemen Steblovnik (K)

Department of Cardiology, University Medical Center, Ljubljana, Slovenia.

Victor Mauri (V)

Department of Cardiology, Heart Center, Faculty of Medicine, University of Cologne, Germany.

Matti Adam (M)

Department of Cardiology, Heart Center, Faculty of Medicine, University of Cologne, Germany.

Ilan Merdler (I)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Manuel Hein (M)

Department of Cardiology and Angiology II, University Heart Center Freiburg-Bad Krozingen, Bad Krozingen, Germany.

Philipp Ruile (P)

Department of Cardiology and Angiology II, University Heart Center Freiburg-Bad Krozingen, Bad Krozingen, Germany.

Pablo Codner (P)

Department of Cardiology, Rabin Medical Center, Petach-Tikva, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Carmelo Grasso (C)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Department of Cardiology, Wolfson Medical Center, Holon, Israel.

Luca Branca (L)

Cardiovascular Department, Spedali Civili, Brescia, Italy.

Rodrigo Estévez-Loureiro (R)

Servicio de Cardiología, Hospital Álvaro Cunqueiro, Vigo, Pontevedra, Spain.

Tomás Benito-González (T)

Department of Cardiology, University Hospital of León, León, Spain.

Ignacio J Amat-Santos (IJ)

CIBERCV, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.

Darren Mylotte (D)

Department of Cardiology, Galway University Hospital, and National University of Ireland Galway, Galway, Ireland.

Matjaz Bunc (M)

Department of Cardiology, University Medical Center, Ljubljana, Slovenia.

Giuseppe Tarantini (G)

Department of Cardiac, Thoracic and Vascular Sciences, University of Padua Medical School, Padua, Italy.

Luis Nombela-Franco (L)

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

Lars Søndergaard (L)

The Heart Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Nicolas M Van Mieghem (NM)

Department of Cardiology, Thoraxcenter, Erasmus University Medical Center, Rotterdam, the Netherlands.

Ariel Finkelstein (A)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Ran Kornowski (R)

Department of Cardiology, Rabin Medical Center, Petach-Tikva, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

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