Transcatheter Edge-to-Edge Tricuspid Repair for Severe Tricuspid Regurgitation Reduces Hospitalizations for Heart Failure.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
04 2020
Historique:
received: 10 09 2019
revised: 16 12 2019
accepted: 17 12 2019
entrez: 4 4 2020
pubmed: 4 4 2020
medline: 10 4 2021
Statut: ppublish

Résumé

The goal of this study was to evaluate the effect of transcatheter edge-to-edge tricuspid valve repair (TTVR) for severe tricuspid regurgitation (TR) on hospitalization for heart failure (HHF) and HF-related endpoints. Patients with severe TR need effective therapies beyond conservative treatment. The impact of TTVR on HHF and HF-related endpoints is unknown. Isolated TTVR was performed in 119 patients. Assessments were conducted of New York Heart Association functional class, 6-min walk distance, Minnesota Living with Heart Failure Questionnaire scores, N-terminal pro-B-type natriuretic peptide level, and medication. HHFs were analyzed in the preceding 12 months before and until the longest available follow-up after TTVR. Results were compared with those of 114 patients who underwent combined mitral and tricuspid valve repair. Procedural success with a reduction to moderate or less TR and no in-hospital death was achieved in 82% of patients. With a median follow-up of 360 days (interquartile range: 187 to 408 days), a durable TR reduction to moderate or less was achieved in 72% of patients (p < 0.001). TTVR reduced the annual rate of HHF by 22% (1.21 to 0.95 HHF/patient-year; p = 0.02), with concomitant clinical improvement in New York Heart Association functional class (patients in class II or lower: 9% to 67%; p < 0.001), 6-min walk distance (+39 m; p = 0.001), and Minnesota Living with Heart Failure Questionnaire score (-6 points; p = 0.02). N-terminal pro-B-type natriuretic peptide level decreased numerically by 783 pg/ml. Diuretic dose before TTVR was increased, but HF medication did not change after TTVR. Procedural success was associated with improved 1-year survival (79% vs. 60%; p = 0.04) and event-free-survival (death + first HHF: 67% vs. 40%; p = 0.001). Transcatheter mitral and tricuspid valve repair-treated patients had comparable outcomes. TTVR for severe TR is associated with a reduction of HHF and improved clinical outcomes.

Sections du résumé

OBJECTIVES
The goal of this study was to evaluate the effect of transcatheter edge-to-edge tricuspid valve repair (TTVR) for severe tricuspid regurgitation (TR) on hospitalization for heart failure (HHF) and HF-related endpoints.
BACKGROUND
Patients with severe TR need effective therapies beyond conservative treatment. The impact of TTVR on HHF and HF-related endpoints is unknown.
METHODS
Isolated TTVR was performed in 119 patients. Assessments were conducted of New York Heart Association functional class, 6-min walk distance, Minnesota Living with Heart Failure Questionnaire scores, N-terminal pro-B-type natriuretic peptide level, and medication. HHFs were analyzed in the preceding 12 months before and until the longest available follow-up after TTVR. Results were compared with those of 114 patients who underwent combined mitral and tricuspid valve repair.
RESULTS
Procedural success with a reduction to moderate or less TR and no in-hospital death was achieved in 82% of patients. With a median follow-up of 360 days (interquartile range: 187 to 408 days), a durable TR reduction to moderate or less was achieved in 72% of patients (p < 0.001). TTVR reduced the annual rate of HHF by 22% (1.21 to 0.95 HHF/patient-year; p = 0.02), with concomitant clinical improvement in New York Heart Association functional class (patients in class II or lower: 9% to 67%; p < 0.001), 6-min walk distance (+39 m; p = 0.001), and Minnesota Living with Heart Failure Questionnaire score (-6 points; p = 0.02). N-terminal pro-B-type natriuretic peptide level decreased numerically by 783 pg/ml. Diuretic dose before TTVR was increased, but HF medication did not change after TTVR. Procedural success was associated with improved 1-year survival (79% vs. 60%; p = 0.04) and event-free-survival (death + first HHF: 67% vs. 40%; p = 0.001). Transcatheter mitral and tricuspid valve repair-treated patients had comparable outcomes.
CONCLUSIONS
TTVR for severe TR is associated with a reduction of HHF and improved clinical outcomes.

Identifiants

pubmed: 32241534
pii: S2213-1779(20)30011-1
doi: 10.1016/j.jchf.2019.12.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-276

Commentaires et corrections

Type : CommentIn

Informations de copyright

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

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 (DZHK), Munich, Germany.

Karl-Philipp Rommel (KP)

Heart Center Leipzig at University Leipzig, Leipzig, Germany.

Edwin C Ho (EC)

Division of Cardiology, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada; Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Matthias Unterhuber (M)

Heart Center Leipzig at University Leipzig, Leipzig, Germany.

Alberto Pozzoli (A)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Kim A Connelly (KA)

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

Simon Deseive (S)

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

Christian Besler (C)

Heart Center Leipzig at University Leipzig, Leipzig, Germany.

Geraldine Ong (G)

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

Daniel Braun (D)

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

Jeremy Edwards (J)

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

Mizuki Miura (M)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Gökhan Gülmez (G)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Lukas Stolz (L)

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

Mara Gavazzoni (M)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Michel Zuber (M)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland; Division of Cardiology, University Hospital of Zurich, Zurich, Switzerland.

Martin Orban (M)

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

Michael Nabauer (M)

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

Francesco Maisano (F)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Holger Thiele (H)

Heart Center Leipzig at University Leipzig, Leipzig, 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 (DZHK), Munich, Germany.

Maurizio Taramasso (M)

Division of Cardiovascular Surgery, University Hospital of Zurich, Zurich, Switzerland.

Neil P Fam (NP)

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

Philipp Lurz (P)

Heart Center Leipzig at University Leipzig, Leipzig, Germany.

Jörg Hausleiter (J)

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

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