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Efficacy and Safety of Sacubitril/Valsartan in Japanese Patients With Chronic Heart Failure and Reduced Ejection Fraction - Results From the PARALLEL-HF Study.
Tsutsui, Hiroyuki; Momomura, Shin-Ichi; Saito, Yoshihiko; Ito, Hiroshi; Yamamoto, Kazuhiro; Sakata, Yasushi; Desai, Akshay Suvas; Ohishi, Tomomi; Iimori, Takayuki; Kitamura, Toshihito; Guo, Weinong.
Afiliação
  • Tsutsui H; Department of Cardiovascular Medicine, Faculty of Medical Sciences, Kyushu University.
  • Momomura SI; Saitama Citizens Medical Center.
  • Saito Y; Department of Cardiovascular Medicine, Nara Medical University.
  • Ito H; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Yamamoto K; Department of Cardiovascular Medicine and Endocrinology and Metabolism, Tottori University.
  • Sakata Y; Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
  • Desai AS; Cardiovascular Division, Brigham and Women's Hospital.
  • Ohishi T; Novartis Pharma K.K.
  • Iimori T; Novartis Pharma K.K.
  • Kitamura T; Novartis Pharma K.K.
  • Guo W; Novartis Pharmaceutical Corporation.
Circ J ; 85(5): 584-594, 2021 04 23.
Article em En | MEDLINE | ID: mdl-33731544
ABSTRACT

BACKGROUND:

In the Prospective Comparison of angiotensin receptor neprilysin inhibitor (ARNI) With ACEi to Determine Impact on Global Mortality and Morbidity in Heart Failure (PARADIGM-HF) study, treatment with sacubitril/valsartan reduced the primary outcome of cardiovascular (CV) death and heart failure (HF) hospitalization compared with enalapril in patients with chronic HF and reduced ejection fraction (HFrEF). A prospective randomized trial was conducted to assess the efficacy and safety of sacubitril/valsartan in Japanese HFrEF patients.Methods and 

Results:

In the Prospective comparison of ARNI with ACEi to determine the noveL beneficiaL trEatment vaLue in Japanese Heart Failure patients (PARALLEL-HF) study, 225 Japanese HFrEF patients (New York Heart Association [NYHA] class II-IV, left ventricular ejection fraction [LVEF] ≤35%) were randomized (1 1) to receive sacubitril/valsartan 200 mg bid or enalapril 10 mg bid. Over a median follow up of 33.9 months, no significant between-group difference was observed for the primary composite outcome of CV death and HF hospitalization (HR 1.09; 95% CI 0.65-1.82; P=0.6260). Early and sustained reductions in N-terminal pro-brain natriuretic peptide (NT-proBNP) from baseline were observed with sacubitril/valsartan compared with enalapril (between-group difference Week 2 25.7%, P<0.01; Month 6 18.9%, P=0.01, favoring sacubitril/valsartan). There was no significant difference in the changes in NYHA class and Kansas City Cardiomyopathy Questionnaire (KCCQ) clinical summary score at Week 8 and Month 6. Sacubitril/valsartan was well tolerated with fewer study drug discontinuations due to adverse events, although the sacubitril/valsartan group had a higher proportion of patients with hypotension.

CONCLUSIONS:

In Japanese patients with HFrEF, there was no difference in reduction in the risk of CV death or HF hospitalization between sacubitril/valsartan and enalapril, and sacubitril/valsartan was safe and well tolerated.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Circ J Assunto da revista: ANGIOLOGIA / CARDIOLOGIA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Circ J Assunto da revista: ANGIOLOGIA / CARDIOLOGIA Ano de publicação: 2021 Tipo de documento: Article