Impact of Proportionality of Secondary Mitral Regurgitation on Outcome After 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
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

715-725

Investigateurs

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.

Auteurs

Mathias Orban (M)

Medizinische Klinik und Poliklinik I, Klinikum der Universität München, Munich, Germany; Munich Heart Alliance, Partner Site German Center for Cardiovascular Disease, Munich, Germany.

Nicole Karam (N)

Department of Cardiology, European Hospital Georges Pompidou and Paris Cardiovascular Research Center, INSERM U970, Paris, France.

Edith Lubos (E)

UKE Hamburg, Klinik und Poliklinik für Allgemeine und Interventionelle Kardiologie, Hamburg, Germany.

Daniel Kalbacher (D)

UKE Hamburg, Klinik und Poliklinik für Allgemeine und Interventionelle Kardiologie, Hamburg, Germany.

Daniel Braun (D)

Medizinische Klinik und Poliklinik I, Klinikum der Universität München, Munich, Germany.

Simon Deseive (S)

Medizinische Klinik und Poliklinik I, Klinikum der Universität München, Munich, Germany.

Michael Neuss (M)

Herzzentrum Brandenburg, Medizinische Hochschule Brandenburg Theodor Fontane, Bernau, Germany.

Christian Butter (C)

Herzzentrum Brandenburg, Medizinische Hochschule Brandenburg Theodor Fontane, Bernau, Germany.

Fabien Praz (F)

Universitätsklinik für Kardiologie, Inselspital Bern, Switzerland.

Mohammad Kassar (M)

Universitätsklinik für Kardiologie, Inselspital Bern, Switzerland.

Aniela Petrescu (A)

Zentrum für Kardiologie, Johannes Gutenberg-Universität, Mainz, Germany.

Roman Pfister (R)

Department III of Internal Medicine, Heart Center, University of Cologne, Cologne, Germany.

Christos Iliadis (C)

Department III of Internal Medicine, Heart Center, University of Cologne, Cologne, Germany.

Matthias Unterhuber (M)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Philipp Lurz (P)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Holger Thiele (H)

Department of Cardiology, Heart Center Leipzig at University of Leipzig, Leipzig, Germany.

Stephan Baldus (S)

Department III of Internal Medicine, Heart Center, University of Cologne, Cologne, Germany.

Ralph Stephan von Bardeleben (R)

Zentrum für Kardiologie, Johannes Gutenberg-Universität, Mainz, Germany.

Stefan Blankenberg (S)

UKE Hamburg, Klinik und Poliklinik für Allgemeine und Interventionelle Kardiologie, Hamburg, Germany.

Steffen Massberg (S)

Medizinische Klinik und Poliklinik I, Klinikum der Universität München, Munich, Germany; Munich Heart Alliance, Partner Site German Center for Cardiovascular Disease, Munich, Germany.

Stephan Windecker (S)

Universitätsklinik für Kardiologie, Inselspital Bern, Switzerland.

Jörg Hausleiter (J)

Medizinische Klinik und Poliklinik I, Klinikum der Universität München, Munich, Germany; Munich Heart Alliance, Partner Site German Center for Cardiovascular Disease, Munich, Germany. Electronic address: joerg.hausleiter@med.lmu.de.

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