Impact of Proportionality of Secondary Mitral Regurgitation on Outcome After Transcatheter Mitral Valve Repair.
MR proportionality
echocardiography
heart failure
secondary mitral regurgitation
transcatheter mitral valve repair
Journal
JACC. Cardiovascular imaging
ISSN: 1876-7591
Titre abrégé: JACC Cardiovasc Imaging
Pays: United States
ID NLM: 101467978
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
received:
13
04
2020
revised:
07
05
2020
accepted:
19
05
2020
pubmed:
31
8
2020
medline:
28
8
2021
entrez:
31
8
2020
Statut:
ppublish
Résumé
The purpose of this paper was to evaluate the impact of proportionality of secondary mitral regurgitation (SMR) in a large real-world registry of transcatheter edge-to-edge mitral valve repair (TMVr) BACKGROUND: Differences in the outcomes of recent randomized trials of TMVr for SMR may be explained by the proportionality of SMR severity to left ventricular (LV) volume. The ratio of pre-procedural effective regurgitant orifice area (EROA) to LV end-diastolic volume (LVEDV) was retrospectively assessed in patients undergoing TMVr for severe SMR between 2008 and 2019 from the EuroSMR registry. A recently proposed SMR proportionality scheme was adapted to stratify patients according to EROA/LVEDV ratio in 3 groups: MR-dominant (MD), MR-LV-co-dominant (MLCD), and LV-dominant (LD). All-cause mortality was assessed as a primary outcome, secondary heart failure (HF) outcomes included hospitalization for HF (HHF), New York Heart Association (NYHA) functional class, N-terminal pro-B-type natriuretic peptide (NT-proBNP), 6-min-walk distance, quality of life and MR grade. A total of 1,016 patients with an EROA/LVEDV ratio were followed for 22 months after TMVr. MR was reduced to grade ≤2+ in 92%, 96%, and 94% of patients (for MD, MLCD, and LD, respectively; p = 0.18). After adjustment for covariates including age, sex, diabetes, kidney function, body surface area, LV ejection fraction, and procedural MR reduction (grade ≤2+), adjusted rates of 2-year mortality in MD patients did not differ from those for MLCD patients (17% vs. 18%, respectively), whereas it was higher in LD patients (23%; p = 0.02 for comparison vs. MD+MLCD). The adjusted first HHF rate differed between groups (44% in MD, 56% in MLCD, 29% in LD; p = 0.01) as did the adjusted time for first death or HHF rate (66% in MD, 82% in MLCD, 68% in LD; p = 0.02). Improvement of NYHA functional class was seen in all groups (p < 0.001). Values for 6-min-walk distances, quality of life and NT-proBNP improved in most patients. MD and MLCD patients had a comparable, adjusted 2-year mortality rate after TMVr which was slightly better than that of LD patients. Patients treated with TMVr had symptomatic improvement regardless of EROA/LVEDV ratio.
Identifiants
pubmed: 32861652
pii: S1936-878X(20)30620-3
doi: 10.1016/j.jcmg.2020.05.042
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
715-725Investigateurs
Mathias Orban
(M)
Lukas Stolz
(L)
Martin Orban
(M)
Daniel Braun
(D)
Michael Näbauer
(M)
Simon Deseive
(S)
Steffen Massberg
(S)
Jörg Hausleiter
(J)
Nicole Karam
(N)
Tania Puscas
(T)
Noemie Tence
(N)
Christian Latremouille
(C)
Edith Lubos
(E)
Daniel Kalbacher
(D)
Dirk Westermann
(D)
Niklas Schofer
(N)
Sebastian Ludwig
(S)
Stefan Blankenberg
(S)
Michael Neuss
(M)
Marvin Bannehr
(M)
Tanja Kücken
(T)
Christoph Edlinger
(C)
Valentin Hähnel
(V)
Christian Butter
(C)
Fabien Praz
(F)
Mohammad Kassar
(M)
Nicolas Brugger
(N)
Thomas Pilgrim
(T)
Mirjam G Winkel
(MG)
Stephan Windecker
(S)
Aniela Petrescu
(A)
Stephan von Bardeleben
(S)
Roman Pfister
(R)
Christos Iliadis
(C)
Maria Körber
(M)
Viktor Mauri
(V)
Monique Wösten
(M)
Clemens Metze Stephan Baldus
(CM)
Matthias Unterhuber
(M)
Philipp Lurz
(P)
Thilo Noack
(T)
Michael Borger
(M)
Stephan Blazek
(S)
Steffen Desch
(S)
Holger Thiele
(H)
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 This work was supported by Klinikum der Universität München. Dr. Hausleiter has received speaker honoraria from Abbott Vascular and Edwards Lifesciences. Dr. Karam has received consultant fees from Abbott Vascular. Dr. Pfister has received financial support for attending symposia by Abbot Vascular. Dr. Lurz is a consultant to Abbott Vascular, Edwards Lifesciences, and Medtronic. Dr. Windecker has received research and educational grants to his institution from Abbott, Amgen, Bayer, Bristol-Myers Squibb, Biotronik, Boston Scientific, CSL Behring, Medtronic, Edwards Lifesciences, Polares, and Sinomed. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.