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Dapagliflozin in patients with heart failure and previous myocardial infarction: A participant-level pooled analysis of DAPA-HF and DELIVER.
Peikert, Alexander; Vaduganathan, Muthiah; Claggett, Brian L; Kulac, Ian J; Foà, Alberto; Desai, Akshay S; Jhund, Pardeep S; Carberry, Jaclyn; Lam, Carolyn S P; Kosiborod, Mikhail N; Inzucchi, Silvio E; Martinez, Felipe A; de Boer, Rudolf A; Hernandez, Adrian F; Shah, Sanjiv J; Køber, Lars; Ponikowski, Piotr; Sabatine, Marc S; Petersson, Magnus; Langkilde, Anna Maria; McMurray, John J V; Solomon, Scott D.
Afiliación
  • Peikert A; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Vaduganathan M; University Heart Center Graz, Department of Cardiology, Medical University of Graz, Graz, Austria.
  • Claggett BL; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Kulac IJ; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Foà A; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Desai AS; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Jhund PS; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Carberry J; BHF Glasgow Cardiovascular Research Center, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
  • Lam CSP; BHF Glasgow Cardiovascular Research Center, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
  • Kosiborod MN; National Heart Centre Singapore & Duke-National University of Singapore, Singapore, Singapore.
  • Inzucchi SE; University of Groningen, University Medical Center Groningen, Department of Cardiology, Groningen, The Netherlands.
  • Martinez FA; Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO, USA.
  • de Boer RA; Yale School of Medicine, New Haven, CT, USA.
  • Hernandez AF; Universidad Nacional de Córdoba, Córdoba, Argentina.
  • Shah SJ; Department of Cardiology, Thoraxcenter, Erasmus MC, Rotterdam, The Netherlands.
  • Køber L; Duke University Medical Center, Durham, NC, USA.
  • Ponikowski P; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Sabatine MS; Department of Cardiology, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
  • Petersson M; Department of Heart Disease, Wroclaw Medical University, Wroclaw, Poland.
  • Langkilde AM; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • McMurray JJV; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Solomon SD; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Eur J Heart Fail ; 26(4): 912-924, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38487939
ABSTRACT

AIMS:

Patients with heart failure (HF) and history of myocardial infarction (MI) face a higher risk of disease progression and clinical events. Whether sodium-glucose cotransporter 2 inhibitors may modify clinical trajectory in such individuals remains incompletely understood. METHODS AND

RESULTS:

The DAPA-HF and DELIVER trials compared dapagliflozin with placebo in patients with symptomatic HF with left ventricular ejection fraction (LVEF) ≤40% and > 40%, respectively. In this pooled participant-level analysis, we assessed efficacy and safety outcomes by history of MI. The primary outcome in both trials was the composite of cardiovascular death or worsening HF. Of the total of 11 007 patients, 3731 (34%) had a previous MI and were at higher risk of the primary outcome across the spectrum of LVEF in covariate-adjusted models (hazard ratio [HR] 1.12, 95% confidence interval [CI] 1.02-1.24). Dapagliflozin reduced the risk of the primary outcome to a similar extent in patients with (HR 0.83, 95% CI 0.72-0.96) and without previous MI (HR 0.76, 95% CI 0.68-0.85; pinteraction = 0.36), with consistent benefits on key secondary outcomes as well. Serious adverse events did not occur more frequently with dapagliflozin, irrespective of previous MI.

CONCLUSION:

History of MI confers increased risks of adverse cardiovascular outcomes in patients with HF across the LVEF spectrum, even among those with preserved ejection fraction. Dapagliflozin consistently and safely reduces the risk of cardiovascular death or worsening HF, regardless of previous MI.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases / 6_other_circulatory_diseases Asunto principal: Volumen Sistólico / Compuestos de Bencidrilo / Inhibidores del Cotransportador de Sodio-Glucosa 2 / Glucósidos / Insuficiencia Cardíaca / Infarto del Miocardio Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Heart Fail Asunto de la revista: CARDIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases / 6_other_circulatory_diseases Asunto principal: Volumen Sistólico / Compuestos de Bencidrilo / Inhibidores del Cotransportador de Sodio-Glucosa 2 / Glucósidos / Insuficiencia Cardíaca / Infarto del Miocardio Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Heart Fail Asunto de la revista: CARDIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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