Your browser doesn't support javascript.
loading
The Effects of Angiotensin Receptor-Neprilysin Inhibition on Major Coronary Events in Patients With Acute Myocardial Infarction: Insights From the PARADISE-MI Trial.
Mehran, Roxana; Steg, Philippe Gabriel; Pfeffer, Marc A; Jering, Karola; Claggett, Brian; Lewis, Eldrin F; Granger, Christopher; Køber, Lars; Maggioni, Aldo; Mann, Douglas L; McMurray, John J V; Rouleau, Jean-Lucien; Solomon, Scott D; Ducrocq, Gregory; Berwanger, Otavio; De Pasquale, Carmine G; Landmesser, Ulf; Petrie, Mark; Leng, David Sim Kheng; van der Meer, Peter; Lefkowitz, Martin; Zhou, Yinong; Braunwald, Eugene.
Afiliação
  • Mehran R; The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York (R.M.).
  • Steg PG; Université Paris-Cité, AP-HP (Assistance Publique-Hôpitaux de Paris), FACT (French Alliance for Cardiovascular Trials) and INSERM U-1148, France (P.G.S.).
  • Pfeffer MA; Cardiovascular Division, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (M.A.P., K.J., B.C., S.D.S., E.B.).
  • Jering K; Cardiovascular Division, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (M.A.P., K.J., B.C., S.D.S., E.B.).
  • Claggett B; Cardiovascular Division, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (M.A.P., K.J., B.C., S.D.S., E.B.).
  • Lewis EF; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford University, Palo Alto, CA (E.F.L.).
  • Granger C; Duke University Medical Center, Durham, NC (C.G.).
  • Køber L; Professor of Cardiology, Department of Clinical Medicine, University of Copenhagen, Denmark (L.K.).
  • Maggioni A; ANMCO Research Center, Heart Care Foundation, Florence, Italy (A.M.).
  • Mann DL; Washington University Medical Center, St Louis, MO (D.L.M.).
  • McMurray JJV; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Scotland (J.J.V.M., M.P.).
  • Rouleau JL; Montréal Heart Institute, University of Montréal, Quebec, Canada (J.-L.R.).
  • Solomon SD; Cardiovascular Division, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (M.A.P., K.J., B.C., S.D.S., E.B.).
  • Ducrocq G; Département de Cardiologie, Hôpital Bichat Assistance Publique Hôpitaux de Paris. France (G.D.).
  • Berwanger O; Academic Research Organization (ARO), Hospital Israelita Albert Einstein, São Paulo-SP, Brazil (O.B.).
  • De Pasquale CG; Department of Cardiovascular Medicine, Flinders Medical Centre, Adelaide, South Australia (C.G.D.P.).
  • Landmesser U; Department of Cardiology, Charité-Universitätsmedizin Berlin, Germany (U.L.).
  • Petrie M; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Scotland (J.J.V.M., M.P.).
  • Leng DSK; National Heart Centre Singapore, (D.S.K.L.).
  • van der Meer P; Department of Cardiology, University Medical Center Groningen, University of Groningen, The Netherlands (P.v.d.M.).
  • Lefkowitz M; Novartis Pharmaceutical Corporation, East Hanover, NJ (M.L., Y.Z.).
  • Zhou Y; Novartis Pharmaceutical Corporation, East Hanover, NJ (M.L., Y.Z.).
  • Braunwald E; Cardiovascular Division, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (M.A.P., K.J., B.C., S.D.S., E.B.).
Circulation ; 146(23): 1749-1757, 2022 12 06.
Article em En | MEDLINE | ID: mdl-36321459
ABSTRACT

BACKGROUND:

In patients who survive an acute myocardial infarction (AMI), angiotensin-converting enzyme inhibitors decrease the risk of subsequent major cardiovascular events. Whether angiotensin-receptor blockade and neprilysin inhibition with sacubitril/valsartan reduce major coronary events more effectively than angiotensin-converting enzyme inhibitors in high-risk patients with recent AMI remains unknown. We aimed to compare the effects of sacubitril/valsartan on coronary outcomes in patients with AMI.

METHODS:

We conducted a prespecified analysis of the PARADISE-MI trial (Prospective ARNI vs ACE Inhibitors Trial to Determine Superiority in Reducing Heart Failure Events After MI), which compared sacubitril/valsartan (97/103 mg twice daily) with ramipril (5 mg twice daily) for reducing heart failure events after myocardial infarction in 5661 patients with AMI complicated by left ventricular systolic dysfunction, pulmonary congestion, or both. In the present analysis, the prespecified composite coronary outcome was the first occurrence of death from coronary heart disease, nonfatal myocardial infarction, hospitalization for angina, or postrandomization coronary revascularization.

RESULTS:

Patients were randomly assigned at a median of 4.4 [3.0-5.8] days after index AMI (ST-segment-elevation myocardial infarction 76%, non-ST-segment-elevation myocardial infarction 24%), by which time 89% of patients had undergone coronary reperfusion. Compared with ramipril, sacubitril/valsartan decreased the risk of coronary outcomes (hazard ratio, 0.86 [95% CI, 0.74-0.99], P=0.04) over a median follow-up of 22 months. Rates of the components of the composite outcomes were lower in patients on sacubitril/valsartan but were not individually significantly different.

CONCLUSIONS:

In survivors of an AMI with left ventricular systolic dysfunction and pulmonary congestion, sacubitril/valsartan-compared with ramipril-reduced the risk of a prespecified major coronary composite outcome. Dedicated studies are necessary to confirm this finding and elucidate its mechanism. REGISTRATION URL https//www. CLINICALTRIALS gov; Unique identifier NCT02924727.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2022 Tipo de documento: Article