Five-Year Outcomes and Prognostic Value of Feature-Tracking Cardiovascular Magnetic Resonance in Patients Receiving Early Prereperfusion Metoprolol in Acute Myocardial Infarction.


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 10 2020
Historique:
received: 04 05 2020
revised: 20 07 2020
accepted: 20 07 2020
pubmed: 21 8 2020
medline: 13 11 2020
entrez: 22 8 2020
Statut: ppublish

Résumé

The aim of the present study was to investigate the long-term impact of early intravenous metoprolol in ST-segment elevation myocardial infarction (STEMI) patients in terms of left ventricular (LV) strain with feature-tracking cardiovascular magnetic resonance (CMR) and its association with prognosis. A total of 270 patients with first anterior STEMI enrolled in the randomized METOCARD-CNIC clinical trial, assigned to receive up to 15 mg intravenous metoprolol before primary percutaneous coronary intervention versus conventional STEMI therapy, were included. LV global circumferential (GCS) and longitudinal (GLS) strain were assessed with feature-tracking CMR at 1 week after STEMI in 215 patients. The occurrence of major adverse cardiac events (MACE) at 5-year follow-up was the primary end point. Among 270 patients enrolled, 17 of 139 patients assigned to metoprolol arm and 31 of 131 patients assigned to control arm experienced MACE (hazard ratio [HR] 0.500, 95% confidence interval [CI] 0.277 to 0.903; p = 0.022). Impaired LV GCS and GLS strain were significantly associated with increased occurrence of MACE (GCS: HR 1.208, 95% CI 1.076 to 1.356, p =0.001; GLS: HR 1.362, 95% CI 1.180 to 1.573, p < 0.001). On multivariable analysis, LV GLS provided incremental prognostic value over late gadolinium enhancement (LGE) and LV ejection fraction (LVEF) (LGE + LVEF chi-square = 12.865, LGE + LVEF + GLS chi-square = 18.459; p =0.012). Patients with GLS ≥-11.5% (above median value) who received early intravenous metoprolol were 64% less likely to experience MACE than their counterparts with same degree of GLS impairment (HR 0.356, 95% CI 0.129 to 0.979; p = 0.045). In conclusion, early intravenous metoprolol has a long-term beneficial prognostic effect, particularly in patients with severely impaired LV systolic function. LV GLS with feature-tracking CMR early after percutaneous coronary intervention offers incremental prognostic value over conventional CMR parameters in risk stratification of STEMI patients.

Identifiants

pubmed: 32819681
pii: S0002-9149(20)30771-2
doi: 10.1016/j.amjcard.2020.07.037
pii:
doi:

Substances chimiques

Antihypertensive Agents 0
Metoprolol GEB06NHM23

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-47

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Tomaž Podlesnikar (T)

Department of Cardiology, Heart Lung Center, Leiden University Medical Center, Leiden, The Netherlands; University Medical Centre Maribor, Maribor, Slovenia; Internal Medicine Clinic, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Gonzalo Pizarro (G)

CentroNacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain; CIBER de enfermedades CardioVasculares (CIBERCV), Madrid, Spain; Ruber Juan Bravo Hospital Universidad Europea, Madrid, Spain.

Rodrigo Fernández-Jiménez (R)

CentroNacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain; CIBER de enfermedades CardioVasculares (CIBERCV), Madrid, Spain; Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.

Jose M Montero-Cabezas (JM)

Department of Cardiology, Heart Lung Center, Leiden University Medical Center, Leiden, The Netherlands.

Javier Sánchez-González (J)

Philips Healthcare, Madrid, Spain.

Chiara Bucciarelli-Ducci (C)

Bristol Heart Institute, Bristol NIHR Cardiovascular Research Centre, University of Bristol and University Hospitals Bristol NHS Trust, Bristol, United Kingdom.

Nina Ajmone Marsan (N)

Department of Cardiology, Heart Lung Center, Leiden University Medical Center, Leiden, The Netherlands.

Zlatko Fras (Z)

Internal Medicine Clinic, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Jeroen J Bax (JJ)

Department of Cardiology, Heart Lung Center, Leiden University Medical Center, Leiden, The Netherlands.

Valentin Fuster (V)

CentroNacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain; Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.

Borja Ibáñez (B)

CentroNacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain; CIBER de enfermedades CardioVasculares (CIBERCV), Madrid, Spain; IIS-Fundación Jiménez Díaz University Hospital, Madrid, Spain.

Victoria Delgado (V)

Department of Cardiology, Heart Lung Center, Leiden University Medical Center, Leiden, The Netherlands. Electronic address: v.delgado@lumc.nl.

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