Effect of Empagliflozin on Heart Failure Outcomes After Acute Myocardial Infarction: Insights from the EMPACT-MI Trial.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
06 Apr 2024
Historique:
medline: 6 4 2024
pubmed: 6 4 2024
entrez: 6 4 2024
Statut: aheadofprint

Résumé

Empagliflozin reduces the risk of heart failure events in patients with type 2 diabetes at high cardiovascular risk, chronic kidney disease, and in those with prevalent heart failure irrespective of ejection fraction. While EMPACT-MI showed empagliflozin does not reduce the risk of the composite of hospitalization of heart failure and all-cause mortality, the impact of empagliflozin on first and recurrent heart failure events in patients after myocardial infarction is unknown. EMPACT-MI was a double-blind, randomized, placebo-controlled, event-driven trial that randomized 6522 patients hospitalized for acute myocardial infarction at risk for heart failure based on newly developed left ventricular ejection fraction of <45% and/or signs or symptoms of congestion to receive empagliflozin 10 mg daily or placebo within 14 days of admission. In prespecified secondary analyses, treatment groups were analyzed for heart failure outcomes. Over a median of follow-up of 17.9 months, the risk for first heart failure hospitalization and total heart failure hospitalizations was significantly lower in the empagliflozin compared with the placebo group (118 (3.6%) vs. 153 (4.7%) patients with events, HR 0.77 [95% CI 0.60, 0.98], P=0.031 for first heart failure hospitalization and 148 vs. 207 events, RR 0.67 [95% CI 0.51, 0.89], P=0.006 for total heart failure hospitalizations). Subgroup analysis showed consistency of empagliflozin benefit across clinically relevant patient subgroups for first and total heart failure hospitalizations. Post-discharge need for new use of diuretics, renin-angiotensin modulators, and mineralocorticoid receptor antagonists were less in patients randomized to empagliflozin than placebo (all p<0.05). In patients after acute myocardial infarction with left ventricular dysfunction or congestion, empagliflozin reduced the risk of heart failure.

Sections du résumé

BACKGROUND BACKGROUND
Empagliflozin reduces the risk of heart failure events in patients with type 2 diabetes at high cardiovascular risk, chronic kidney disease, and in those with prevalent heart failure irrespective of ejection fraction. While EMPACT-MI showed empagliflozin does not reduce the risk of the composite of hospitalization of heart failure and all-cause mortality, the impact of empagliflozin on first and recurrent heart failure events in patients after myocardial infarction is unknown.
METHODS METHODS
EMPACT-MI was a double-blind, randomized, placebo-controlled, event-driven trial that randomized 6522 patients hospitalized for acute myocardial infarction at risk for heart failure based on newly developed left ventricular ejection fraction of <45% and/or signs or symptoms of congestion to receive empagliflozin 10 mg daily or placebo within 14 days of admission. In prespecified secondary analyses, treatment groups were analyzed for heart failure outcomes.
RESULTS RESULTS
Over a median of follow-up of 17.9 months, the risk for first heart failure hospitalization and total heart failure hospitalizations was significantly lower in the empagliflozin compared with the placebo group (118 (3.6%) vs. 153 (4.7%) patients with events, HR 0.77 [95% CI 0.60, 0.98], P=0.031 for first heart failure hospitalization and 148 vs. 207 events, RR 0.67 [95% CI 0.51, 0.89], P=0.006 for total heart failure hospitalizations). Subgroup analysis showed consistency of empagliflozin benefit across clinically relevant patient subgroups for first and total heart failure hospitalizations. Post-discharge need for new use of diuretics, renin-angiotensin modulators, and mineralocorticoid receptor antagonists were less in patients randomized to empagliflozin than placebo (all p<0.05).
CONCLUSIONS CONCLUSIONS
In patients after acute myocardial infarction with left ventricular dysfunction or congestion, empagliflozin reduced the risk of heart failure.

Identifiants

pubmed: 38581389
doi: 10.1161/CIRCULATIONAHA.124.069217
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Adrian F Hernandez (AF)

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

Jacob A Udell (JA)

Women's College Hospital and Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, ON, Canada.

W Schuyler Jones (WS)

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

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.

Mark C Petrie (MC)

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

Josephine Harrington (J)

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

Michaela Mattheus (M)

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

Svenja Seide (S)

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

Isabella Zwiener (I)

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 Goodman (S)

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; 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.

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)

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

Béla Merkely (B)

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

Puja B Parikh (PB)

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

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 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; 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.

Javed Butler (J)

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

Classifications MeSH