Mitral Regurgitation in Low-Flow, Low-Gradient Aortic Stenosis Patients Undergoing TAVR: Insights From the TOPAS-TAVI 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:
09 03 2020
Historique:
received: 12 08 2019
revised: 11 10 2019
accepted: 15 11 2019
pubmed: 18 2 2020
medline: 21 10 2020
entrez: 17 2 2020
Statut: ppublish

Résumé

This study sought to determine the incidence, clinical impact, and changes over time of mitral regurgitation (MR) in patients with low-flow, low-gradient aortic stenosis (LFLG-AS) undergoing transcatheter aortic valve replacement (TAVR). Few data exist on the clinical impact and changes in severity over time of MR in patients with LFLG-AS undergoing TAVR. A total of 308 TAVR candidates with LFLG-AS were included. Patients were categorized according to MR severity at baseline, and presence of MR improvement at 12-month follow-up. Clinical outcomes were assessed at 1 and 12 months (+ echocardiography), and yearly thereafter. Baseline mild and moderate-to-severe MR were present in 118 (38.3%) and 115 (37.3%) patients, respectively. MR was of functional and mixed etiology in 77.2% and 22.7% of patients, respectively. A total of 131 patients (42.5%) died after a median follow-up of 2 (1 to 3) years. Baseline moderate-or-greater MR had no impact on mortality (hazard ratio [HR]: 1.34; 95% confidence interval [CI]: 0.72 to 2.48) or heart failure hospitalization (HR: 1.02; 95% CI: 0.49 to 2.10). At 1-year follow-up, MR improved in 44.3% of patients and remained unchanged/worsened in 55.7%. The lack of MR improvement was associated with a higher risk of all-cause and cardiac mortality (HR: 2.02; 95% CI: 1.29 to 3.17; HR: 3.03; 95% CI: 1.27 to 7.23, respectively), rehospitalization for cardiac causes (HR: 1.50; 95% CI: 1.04 to 2.15), and an increased overall-mortality/heart failure rehospitalization (HR: 1.94; 95% CI: 1.25 to 3.02). A higher baseline left ventricular end-diastolic diameter and a higher increase in left ventricular ejection fraction were found to be independent predictors of MR improvement at 1-year follow-up (odds ratio: 0.69; 95% CI: 0.51 to 0.94; and odds ratio: 0.81; 95% CI: 0.67 to 0.96, respectively). Most TAVR candidates with LFLG-AS had some degree of MR, of functional origin in most cases. MR improved in about one-half of patients, with larger left ventricular size and a higher increase in left ventricular ejection fraction post-TAVR determining MR improvement over time. The lack of MR improvement at 1 year was associated with poorer outcomes.

Sections du résumé

OBJECTIVES
This study sought to determine the incidence, clinical impact, and changes over time of mitral regurgitation (MR) in patients with low-flow, low-gradient aortic stenosis (LFLG-AS) undergoing transcatheter aortic valve replacement (TAVR).
BACKGROUND
Few data exist on the clinical impact and changes in severity over time of MR in patients with LFLG-AS undergoing TAVR.
METHODS
A total of 308 TAVR candidates with LFLG-AS were included. Patients were categorized according to MR severity at baseline, and presence of MR improvement at 12-month follow-up. Clinical outcomes were assessed at 1 and 12 months (+ echocardiography), and yearly thereafter.
RESULTS
Baseline mild and moderate-to-severe MR were present in 118 (38.3%) and 115 (37.3%) patients, respectively. MR was of functional and mixed etiology in 77.2% and 22.7% of patients, respectively. A total of 131 patients (42.5%) died after a median follow-up of 2 (1 to 3) years. Baseline moderate-or-greater MR had no impact on mortality (hazard ratio [HR]: 1.34; 95% confidence interval [CI]: 0.72 to 2.48) or heart failure hospitalization (HR: 1.02; 95% CI: 0.49 to 2.10). At 1-year follow-up, MR improved in 44.3% of patients and remained unchanged/worsened in 55.7%. The lack of MR improvement was associated with a higher risk of all-cause and cardiac mortality (HR: 2.02; 95% CI: 1.29 to 3.17; HR: 3.03; 95% CI: 1.27 to 7.23, respectively), rehospitalization for cardiac causes (HR: 1.50; 95% CI: 1.04 to 2.15), and an increased overall-mortality/heart failure rehospitalization (HR: 1.94; 95% CI: 1.25 to 3.02). A higher baseline left ventricular end-diastolic diameter and a higher increase in left ventricular ejection fraction were found to be independent predictors of MR improvement at 1-year follow-up (odds ratio: 0.69; 95% CI: 0.51 to 0.94; and odds ratio: 0.81; 95% CI: 0.67 to 0.96, respectively).
CONCLUSIONS
Most TAVR candidates with LFLG-AS had some degree of MR, of functional origin in most cases. MR improved in about one-half of patients, with larger left ventricular size and a higher increase in left ventricular ejection fraction post-TAVR determining MR improvement over time. The lack of MR improvement at 1 year was associated with poorer outcomes.

Identifiants

pubmed: 32061600
pii: S1936-8798(19)32582-8
doi: 10.1016/j.jcin.2019.11.042
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

567-579

Subventions

Organisme : CIHR
ID : FDN-143225
Pays : Canada

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Afonso B Freitas-Ferraz (AB)

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

Stamatios Lerakis (S)

Emory University Hospital, Atlanta, Georgia.

Henrique Barbosa Ribeiro (H)

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

Martine Gilard (M)

CHU Brest, Brest, France.

João L Cavalcante (JL)

University of Pittsburgh/UPMC, Pittsburgh, Pennsylvania.

Raj Makkar (R)

Cedars Sinai Hospital, Los Angeles, California.

Howard C Herrmann (HC)

University of Pennsylvania Medical Center, Philadelphia, Pennsylvania.

Stephan Windecker (S)

Bern University Hospital, Bern, Switzerland.

Maurice Enriquez-Sarano (M)

Mayo Clinic, Rochester, Minnesota.

Asim N Cheema (AN)

St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.

Luis Nombela-Franco (L)

Hospital Clínico San Carlos - Madrid, Madrid, Spain.

Ignacio Amat-Santos (I)

Hospital Clinico Universitario de Valladolid, Valladolid, Spain.

Antonio J Muñoz-García (AJ)

Hospital Virgen de la Victoria, Malaga, Spain.

Bruno Garcia Del Blanco (B)

Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Alan Zajarias (A)

Washington University School of Medicine, St. Louis, Missouri.

John C Lisko (JC)

Emory University Hospital, Atlanta, Georgia.

Salim Hayek (S)

Emory University Hospital, Atlanta, Georgia.

Vasilis Babaliaros (V)

Emory University Hospital, Atlanta, Georgia.

Florent Le Ven (F)

CHU Brest, Brest, France.

Thomas G Gleason (TG)

University of Pittsburgh/UPMC, Pittsburgh, Pennsylvania.

Tarun Chakravarty (T)

Cedars Sinai Hospital, Los Angeles, California.

Wilson Y Szeto (WY)

University of Pennsylvania Medical Center, Philadelphia, Pennsylvania.

Marie-Annick Clavel (MA)

Quebec Heart & Lung Institute, Laval University, Quebec City, Quebec, Canada; Mayo Clinic, Rochester, Minnesota.

Alberto de Agustin (A)

Hospital Clínico San Carlos - Madrid, Madrid, Spain.

Vicenç Serra (V)

Hospital Universitari Vall d'Hebron, Barcelona, Spain.

John T Schindler (JT)

University of Pittsburgh/UPMC, Pittsburgh, Pennsylvania.

Abdellaziz Dahou (A)

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

Mohamed-Salah Annabi (MS)

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

Emilie Pelletier-Beaumont (E)

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

Philippe Pibarot (P)

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

Josep Rodés-Cabau (J)

Quebec Heart & Lung Institute, Laval University, Quebec City, Quebec, Canada. Electronic address: josep.rodes@criucpq.ulaval.ca.

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