Refined staging classification of cardiac damage associated with aortic stenosis and outcomes after transcatheter aortic valve implantation.


Journal

European heart journal. Quality of care & clinical outcomes
ISSN: 2058-1742
Titre abrégé: Eur Heart J Qual Care Clin Outcomes
Pays: England
ID NLM: 101677796

Informations de publication

Date de publication:
28 Oct 2021
Historique:
received: 11 03 2021
revised: 04 05 2021
accepted: 03 06 2021
pubmed: 5 6 2021
medline: 30 3 2022
entrez: 4 6 2021
Statut: ppublish

Résumé

A new staging classification of aortic stenosis (AS) characterizing the extent of cardiac damage was established and validated in patients undergoing transcatheter aortic valve implantation (TAVI). We aimed to validate an updated classification system in patients undergoing TAVI. In a prospective TAVI registry, AS patients were categorized into the following stages: no cardiac damage (Stage 0), left ventricular damage (Stage 1), left atrial or mitral valve damage (Stage 2), pulmonary vasculature or tricuspid valve damage (Stage 3), or right ventricular (RV) damage or low-flow state (Stage 4). Stage 3 was sub-divided into Stage 3a (≤moderate pulmonary hypertension) and Stage 3b (severe pulmonary hypertension). Stage 4 was sub-divided into Stage 4a (low-flow without RV dysfunction), Stage 4b (RV dysfunction without low-flow), and Stage 4c (RV dysfunction with low-flow). The primary endpoint was all-cause death at 1 year. Among 1156 eligible patients, 14 were classified as Stage 0, 38 as Stage 1, 105 as Stage 2278 as Stage 3, and 721 as Stage 4. There was a stepwise increase in mortality according to advancing stages of cardiac damage: 3.9% (Stage 0-1), 9.6% (Stage 2), 14.1% (Stage 3), and 17.4% (Stage 4) (P = 0.002). After multivariable adjustment, only Stage 3b, Stage 4b, and Stage 4c conferred a significantly increased risk of mortality compared to Stage 0-1. More than one-third of patients had advanced cardiac damage (severe pulmonary hypertension or RV dysfunction) before TAVI, associating with a five- to seven-fold increased risk of mortality at 1 year. https://www.clinicaltrials.gov. NCT01368250.

Identifiants

pubmed: 34086888
pii: 6292114
doi: 10.1093/ehjqcco/qcab041
doi:

Banques de données

ClinicalTrials.gov
['NCT01368250']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

532-541

Commentaires et corrections

Type : CommentIn

Informations de copyright

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2021. For permissions, please email: journals.permissions@oup.com.

Auteurs

Taishi Okuno (T)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Dik Heg (D)

CTU, University of Bern, Bern, Switzerland.

Jonas Lanz (J)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Fabien Praz (F)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Nicolas Brugger (N)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Stefan Stortecky (S)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Stephan Windecker (S)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Thomas Pilgrim (T)

Department of Cardiology, Inselspital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

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