Prognostic Usefulness of Myocardial Work in Patients With Heart Failure and Reduced Ejection Fraction Treated by Sacubitril/Valsartan.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
15 06 2020
Historique:
received: 23 01 2020
revised: 19 03 2020
accepted: 20 03 2020
pubmed: 20 4 2020
medline: 1 9 2020
entrez: 20 4 2020
Statut: ppublish

Résumé

The noninvasive assessment of myocardial work (MW) by pressure-strain loops analysis (PSL) is a relative new tool for the evaluation of myocardial performance. Sacubitril/Valsartan is a treatment for heart failure with reduced ejection fraction (HFrEF) which has a spectacular effect on the reduction of cardiovascular events (major adverse cardiovascular events [MACEs]). This study aimed to evaluate the short- and medium-term effect of Sacubitril/Valsartan treatment on MW parameters and the prognostic value of MW in this specific group of patients. Seventy-nine patients with HFrEF (mean age: 66 ± 12 years; LV ejection fraction: 28% ± 9%) were prospectively included in the study and treated with Sacubitril/Valsartan. Echocardiographic examination was performed at baseline, and after 6- and 12-month of therapy with Sacubitril/Valsartan. Sacubitril/Valsartan significantly increased myocardial constructive work (CW) (1023 ± 449 vs 1424 ± 484 mm Hg%, p <0.0001) and myocardial work efficiency (WE) [87 (78to 90) vs 90 (86 to 95), p <0.0001]. During FU (2.6 ± 0.9 years), MACEs occurred in 13 (16%) patients. After correction for LV size, LV ejection fraction and WE, global myocardial constructive work (CW) was the only predictor of MACEs [hazard ratio [HR] 0.99 (0.99 to 1.00), p = 0.04]. A CW <910 mm Hg identified patients at particularly increase risk of MACEs [HR 11.09 (1.45 to 98.94), p = 0.002, log-rank test p <0.0001]. In conclusion, in patients with HFrEF who receive a comprehensive background beta-blocker and mineral-corticoid receptor antagonist therapy, Sacubitril/Valsartan induces a significant improvement of myocardial CW and WE. In this population, the estimation of CW before the initiation of Sacubitril/Valsartan allows the prediction of MACEs.

Identifiants

pubmed: 32305222
pii: S0002-9149(20)30281-2
doi: 10.1016/j.amjcard.2020.03.031
pii:
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Tetrazoles 0
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1856-1862

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Yanis Bouali (Y)

University of Rennes, CHU Rennes, Rennes, France.

Erwan Donal (E)

University of Rennes, CHU Rennes, Rennes, France.

Alban Gallard (A)

University of Rennes, CHU Rennes, Rennes, France.

Clément Laurin (C)

University of Rennes, CHU Rennes, Rennes, France.

Arnaud Hubert (A)

University of Rennes, CHU Rennes, Rennes, France.

Auriane Bidaut (A)

University of Rennes, CHU Rennes, Rennes, France.

Christophe Leclercq (C)

University of Rennes, CHU Rennes, Rennes, France.

Elena Galli (E)

University of Rennes, CHU Rennes, Rennes, France. Electronic address: elena.galli@chu-rennes.fr.

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Classifications MeSH