Left Ventricular Function, Congestion, and Effect of Empagliflozin on Heart Failure Risk After Myocardial Infarction.

acute myocardial infarction congestion empagliflozin heart failure left ventricular dysfunction

Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
01 Apr 2024
Historique:
received: 22 02 2024
revised: 25 03 2024
accepted: 26 03 2024
medline: 9 4 2024
pubmed: 9 4 2024
entrez: 8 4 2024
Statut: aheadofprint

Résumé

Empagliflozin reduces the risk of heart failure (HF) hospitalizations but not all-cause mortality when started within 14 days of acute myocardial infarction (AMI). To evaluate the association between left ventricular ejection fraction (LVEF), congestion, or both on outcomes and the impact of empagliflozin in reducing HF risk post-MI. In the EMPACT-MI trial, patients were randomized within 14 days of an AMI complicated by either newly reduced LVEF<45%, congestion, or both to empagliflozin 10 mg daily or placebo and followed for a median of 17.9 months. Among 6522 patients, the mean baseline LVEF was 41%+9%; 2648 patients (40.6%) presented with LVEF<45% alone, 1483 (22.7%) presented with congestion alone, and 2181 (33.4%) presented with both. Among patients in the placebo arm, multivariable adjusted risk for each 10-point reduction in LVEF included all-cause death or HF hospitalization (hazard ratio [HR] 1.49; 95%CI, 1.31-1.69; P<0.0001), first HF hospitalization (HR, 1.64; 95%CI, 1.37-1.96; P<0.0001), and total HF hospitalizations (rate ratio [RR], 1.89; 95%CI, 1.51-2.36; P<0.0001). Presence of congestion was also associated with a significantly higher risk for each of these outcomes (HR 1.52, 1.94, and RR 2.03, respectively). Empagliflozin reduced the risk for first (HR 0.77, 95%CI 0.60-0.98) and total (RR 0.67, 95%CI 0.50-0.89) HF hospitalization, irrespective of LVEF or congestion or both. The safety profile of empagliflozin was consistent across baseline LVEF and irrespective of congestion status. In patients with AMI, severity of LV dysfunction and the presence of congestion was associated with worse outcomes. Empagliflozin reduced first and total HF hospitalizations across the range of LVEF with and without congestion.

Sections du résumé

BACKGROUND BACKGROUND
Empagliflozin reduces the risk of heart failure (HF) hospitalizations but not all-cause mortality when started within 14 days of acute myocardial infarction (AMI).
OBJECTIVE OBJECTIVE
To evaluate the association between left ventricular ejection fraction (LVEF), congestion, or both on outcomes and the impact of empagliflozin in reducing HF risk post-MI.
METHODS METHODS
In the EMPACT-MI trial, patients were randomized within 14 days of an AMI complicated by either newly reduced LVEF<45%, congestion, or both to empagliflozin 10 mg daily or placebo and followed for a median of 17.9 months.
RESULTS RESULTS
Among 6522 patients, the mean baseline LVEF was 41%+9%; 2648 patients (40.6%) presented with LVEF<45% alone, 1483 (22.7%) presented with congestion alone, and 2181 (33.4%) presented with both. Among patients in the placebo arm, multivariable adjusted risk for each 10-point reduction in LVEF included all-cause death or HF hospitalization (hazard ratio [HR] 1.49; 95%CI, 1.31-1.69; P<0.0001), first HF hospitalization (HR, 1.64; 95%CI, 1.37-1.96; P<0.0001), and total HF hospitalizations (rate ratio [RR], 1.89; 95%CI, 1.51-2.36; P<0.0001). Presence of congestion was also associated with a significantly higher risk for each of these outcomes (HR 1.52, 1.94, and RR 2.03, respectively). Empagliflozin reduced the risk for first (HR 0.77, 95%CI 0.60-0.98) and total (RR 0.67, 95%CI 0.50-0.89) HF hospitalization, irrespective of LVEF or congestion or both. The safety profile of empagliflozin was consistent across baseline LVEF and irrespective of congestion status.
CONCLUSIONS CONCLUSIONS
In patients with AMI, severity of LV dysfunction and the presence of congestion was associated with worse outcomes. Empagliflozin reduced first and total HF hospitalizations across the range of LVEF with and without congestion.

Identifiants

pubmed: 38588929
pii: S0735-1097(24)06757-3
doi: 10.1016/j.jacc.2024.03.405
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Jacob A Udell (JA)

Women's College Hospital and Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, ON, Canada;. Electronic address: jay.udell@utoronto.ca.

Mark C Petrie (MC)

School of Cardiovascular and Medical Sciences, British Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

W Schuyler Jones (WS)

Division of Cardiology, Duke University Department of Medicine, Durham, NC, USA, and Duke University Medical Center, Duke Clinical Research Institute, Durham, NC, USA.

Stefan D Anker (SD)

Department of Cardiology (CVK) of German Heart Center Charité; Berlin Institute of Health Center for Regenerative Therapies (BCRT), German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin, Berlin, Germany.

Josephine Harrington (J)

Division of Cardiology, Duke University Department of Medicine, Durham, NC, USA, and Duke University Medical Center, Duke Clinical Research Institute, Durham, NC, USA.

Michaela Mattheus (M)

Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany.

Svenja Seide (S)

Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany.

Offer Amir (O)

Heart Institute, Hadassah Medical Center, The Hebrew University of Jerusalem, Jerusalem, Israel.

M Cecilia Bahit (MC)

INECO Neurociencias Oroño, Fundación INECO, Rosario, Santa Fe, Argentina.

Johann Bauersachs (J)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Antoni Bayes-Genis (A)

Heart Institute, Hospital Universitari Germans Trias i Pujol, Barcelona, Spain, and Department of Medicine, Universitat Autònomoa de Barcelona, Barcelona, Spain.

Yundai Chen (Y)

Department of Cardiology, the First Medical Center of Chinese PLA General Hospital, Beijing, China.

Vijay K Chopra (VK)

Max Super Speciality Hospital, Saket, New Delhi, India.

Gemma Figtree (G)

Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.

Junbo Ge (J)

Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, National Clinical Research Center for Interventional Medicine, Shanghai, China.

Shaun G Goodman (SG)

Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta; Division of Cardiology, Department of Medicine, St Michael's Hospital, Unity Health Toronto and Peter Munk Cardiac Centre, University Health Network, University of Toronto, Toronto, ON, Canada.

Nina Gotcheva (N)

Department of Cardiology, MHAT "National Cardiology Hospital" EAD, Sofia, Bulgaria.

Shinya Goto (S)

Department of Medicine (Cardiology), Tokai University School of Medicine, Isehara, Japan.

Tomasz Gasior (T)

Boehringer Ingelheim International GmbH, Ingelheim, Germany, and Collegium Medicum - Faculty of Medicine, WSB University, Dabrowa Gornicza, Poland.

Waheed Jamal (W)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.

James L Januzzi (JL)

Division of Cardiology, Harvard Medical School and Massachusetts General Hospital, Boston, MA, USA.

Myung Ho Jeong (MH)

Chonnam National University Hospital and Medical School, Gwangju, Republic of Korea.

Yuri Lopatin (Y)

Volgograd State Medical University, Volgograd, Russia.

Renato D Lopes (RD)

Division of Cardiology, Duke University Department of Medicine, Durham, NC, USA, and Duke University Medical Center, Duke Clinical Research Institute, Durham, NC, USA.

Béla Merkely (B)

Heart and Vascular Center, Semmelweis University, Budapest, Hungary.

Monica Martinez-Traba (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.

Puja B Parikh (PB)

Division of Cardiovascular Medicine, Department of Medicine, State University of New York at Stony Brook, Stony Brook, NY, USA.

Alexander Parkhomenko (A)

The Ukrainian Institute of Cardiology n. a. M.D. Strazhesko, AMS Ukraine, Kyiv, Ukraine.

Piotr Ponikowski (P)

Institute of Heart Diseases, Wroclaw Medical University, Wroclaw, Poland.

Xavier Rossello (X)

Hospital Universitari Son Espases, Health Research Institute of the Balearic Islands, University of the Balearic Islands, Palma de Mallorca, Spain.

Morten Schou (M)

Department of Cardiology, Herlev and Gentofte University Hospital, Copenhagen, Denmark.

Dragan Simic (D)

Department of Cardiovascular Diseases, University Clinical Center Belgrade, Serbia.

Philippe Gabriel Steg (PG)

Université Paris-Cité, FACT (French Alliance for Cardiovascular Trials), INSERM U-1148, AP-HP, Hôpital Bichat, Paris, France.

Joanna Szachniewicz (J)

Jan Mikulicz-Radecki University Clinical Hospital, Wroclaw, Poland.

Peter van der Meer (P)

Department of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.

Dragos Vinereanu (D)

University of Medicine and Pharmacy Carol Davila, University and Emergency Hospital of Bucharest, Bucharest, Romania.

Shelley Zieroth (S)

Section of Cardiology, Max Rady College of Medicine, University of Manitoba, Winnipeg, MB, Canada.

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany, and First Department of Medicine, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.

Mikhail Sumin (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.

Deepak L Bhatt (DL)

Mount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Adrian F Hernandez (AF)

Division of Cardiology, Duke University Department of Medicine, Durham, NC, USA, and Duke University Medical Center, Duke Clinical Research Institute, Durham, NC, USA.

Javed Butler (J)

Baylor Scott and White Research Institute, Dallas, TX, USA, and Department of Medicine, University of Mississippi, Jackson, MS, USA.

Classifications MeSH