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Left Ventricular Function, Congestion, and Effect of Empagliflozin on Heart Failure Risk After Myocardial Infarction.
Udell, Jacob A; Petrie, Mark C; Jones, W Schuyler; Anker, Stefan D; Harrington, Josephine; Mattheus, Michaela; Seide, Svenja; Amir, Offer; Bahit, M Cecilia; Bauersachs, Johann; Bayes-Genis, Antoni; Chen, Yundai; Chopra, Vijay K; Figtree, Gemma; Ge, Junbo; Goodman, Shaun G; Gotcheva, Nina; Goto, Shinya; Gasior, Tomasz; Jamal, Waheed; Januzzi, James L; Jeong, Myung Ho; Lopatin, Yuri; Lopes, Renato D; Merkely, Béla; Martinez-Traba, Monica; Parikh, Puja B; Parkhomenko, Alexander; Ponikowski, Piotr; Rossello, Xavier; Schou, Morten; Simic, Dragan; Steg, Philippe Gabriel; Szachniewicz, Joanna; van der Meer, Peter; Vinereanu, Dragos; Zieroth, Shelley; Brueckmann, Martina; Sumin, Mikhail; Bhatt, Deepak L; Hernandez, Adrian F; Butler, Javed.
Afiliação
  • Udell JA; Women's College Hospital, University of Toronto, Toronto, Ontario, Canada; Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, Ontario, Canada. Electronic address: jay.udell@utoronto.ca.
  • Petrie MC; School of Cardiovascular and Medical Sciences, British Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
  • Jones WS; Division of Cardiology, Duke University Department of Medicine, Durham, North Carolina, USA; Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina, USA.
  • Anker SD; Department of Cardiology, German Heart Center Charité, Charité Universitätsmedizin, Berlin, Germany; Berlin Institute of Health Center for Regenerative Therapies, German Centre for Cardiovascular Research partner site Berlin, Charité Universitätsmedizin, Berlin, Germany.
  • Harrington J; Division of Cardiology, Duke University Department of Medicine, Durham, North Carolina, USA; Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina, USA.
  • Mattheus M; Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany.
  • Seide S; Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany.
  • Amir O; Heart Institute, Hadassah Medical Center, The Hebrew University of Jerusalem, Jerusalem, Israel.
  • Bahit MC; INECO Neurociencias Oroño, Fundación INECO, Rosario, Santa Fe, Argentina.
  • Bauersachs J; Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
  • Bayes-Genis A; Heart Institute, Hospital Universitari Germans Trias i Pujol, Barcelona, Spain; Department of Medicine, Universitat Autònomoa de Barcelona, Barcelona, Spain.
  • Chen Y; Department of Cardiology, the First Medical Center of Chinese PLA General Hospital, Beijing, China.
  • Chopra VK; Max Super Speciality Hospital, Saket, New Delhi, India.
  • Figtree G; Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
  • Ge J; Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, National Clinical Research Center for Interventional Medicine, Shanghai, China.
  • Goodman SG; Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, Ontario, Canada; Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada; Division of Cardiology, Department of Medicine, St Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
  • Gotcheva N; Department of Cardiology, MHAT National Cardiology Hospital EAD, Sofia, Bulgaria.
  • Goto S; Department of Medicine (Cardiology), Tokai University School of Medicine, Isehara, Japan.
  • Gasior T; Collegium Medicum - Faculty of Medicine, WSB University, Dabrowa Gornicza, Poland; Boehringer Ingelheim International GmbH, Ingelheim, Germany.
  • Jamal W; Boehringer Ingelheim International GmbH, Ingelheim, Germany.
  • Januzzi JL; Division of Cardiology, Harvard Medical School and Massachusetts General Hospital, Boston, Massachusetts, USA; Heart Failure and Biomarker Trials, Baim Institute for Clinical Research, Boston, Massachusetts, USA.
  • Jeong MH; Chonnam National University Hospital and Medical School, Gwangju, Republic of Korea.
  • Lopatin Y; Volgograd State Medical University, Volgograd, Russia.
  • Lopes RD; Division of Cardiology, Duke University Department of Medicine, Durham, North Carolina, USA; Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina, USA.
  • Merkely B; Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
  • Martinez-Traba M; Boehringer Ingelheim International GmbH, Ingelheim, Germany.
  • Parikh PB; Division of Cardiovascular Medicine, Department of Medicine, State University of New York at Stony Brook, Stony Brook, New York, USA.
  • Parkhomenko A; M.D. Strazhesko Ukrainian Institute of Cardiology, AMS Ukraine, Kyiv, Ukraine.
  • Ponikowski P; Institute of Heart Diseases, Wroclaw Medical University, Wroclaw, Poland.
  • Rossello X; Hospital Universitari Son Espases, Health Research Institute of the Balearic Islands, University of the Balearic Islands, Palma de Mallorca, Spain.
  • Schou M; Department of Cardiology, Herlev and Gentofte University Hospital, Copenhagen, Denmark.
  • Simic D; Department of Cardiovascular Diseases, University Clinical Center, Belgrade, Serbia.
  • Steg PG; Université Paris-Cité, FACT (French Alliance for Cardiovascular Trials), INSERM U-1148, AP-HP, Hôpital Bichat, Paris, France.
  • Szachniewicz J; Jan Mikulicz-Radecki University Clinical Hospital, Wroclaw, Poland.
  • van der Meer P; Department of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
  • Vinereanu D; University of Medicine and Pharmacy Carol Davila, University and Emergency Hospital of Bucharest, Bucharest, Romania.
  • Zieroth S; Section of Cardiology, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Brueckmann M; Boehringer Ingelheim International GmbH, Ingelheim, Germany; First Department of Medicine, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.
  • Sumin M; Boehringer Ingelheim International GmbH, Ingelheim, Germany.
  • Bhatt DL; Mount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Hernandez AF; Division of Cardiology, Duke University Department of Medicine, Durham, North Carolina, USA; Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina, USA.
  • Butler J; Baylor Scott and White Research Institute, Dallas, Texas, USA; Department of Medicine, University of Mississippi, Jackson, Mississippi, USA.
J Am Coll Cardiol ; 83(23): 2233-2246, 2024 Jun 11.
Article em En | MEDLINE | ID: mdl-38588929
ABSTRACT

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).

OBJECTIVES:

This study sought to evaluate the association of left ventricular ejection fraction (LVEF), congestion, or both, with outcomes and the impact of empagliflozin in reducing HF risk post-AMI.

METHODS:

In the EMPACT-MI (Trial to Evaluate the Effect of Empagliflozin on Hospitalization for Heart Failure and Mortality in Patients with Acute Myocardial Infarction) 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 were followed up for a median of 17.9 months.

RESULTS:

Among 6,522 patients, the mean baseline LVEF was 41 ± 9%; 2,648 patients (40.6%) presented with LVEF <45% alone, 1,483 (22.7%) presented with congestion alone, and 2,181 (33.4%) presented with both. Among patients in the placebo arm of the trial, multivariable adjusted risk for each 10-point reduction in LVEF included all-cause death or HF hospitalization (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). The 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 hospitalizations, irrespective of LVEF or congestion, or both. The safety profile of empagliflozin was consistent across baseline LVEF and irrespective of congestion status.

CONCLUSIONS:

In patients with AMI, the severity of left ventricular 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. (Trial to Evaluate the Effect of Empagliflozin on Hospitalization for Heart Failure and Mortality in Patients with Acute Myocardial Infarction [EMPACT-MI]; NCT04509674).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos Benzidrílicos / Função Ventricular Esquerda / Inibidores do Transportador 2 de Sódio-Glicose / Glucosídeos / Insuficiência Cardíaca / Infarto do Miocárdio Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos Benzidrílicos / Função Ventricular Esquerda / Inibidores do Transportador 2 de Sódio-Glicose / Glucosídeos / Insuficiência Cardíaca / Infarto do Miocárdio Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Coll Cardiol Ano de publicação: 2024 Tipo de documento: Article