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Effects of omecamtiv mecarbil in heart failure with reduced ejection fraction according to blood pressure: the GALACTIC-HF trial.
Metra, Marco; Pagnesi, Matteo; Claggett, Brian L; Díaz, Rafael; Felker, G Michael; McMurray, John J V; Solomon, Scott D; Bonderman, Diana; Fang, James C; Fonseca, Cândida; Goncalvesova, Eva; Howlett, Jonathan G; Li, Jing; O'Meara, Eileen; Miao, Zi Michael; Abbasi, Siddique A; Heitner, Stephen B; Kupfer, Stuart; Malik, Fady I; Teerlink, John R.
Afiliação
  • Metra M; Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
  • Pagnesi M; Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
  • Claggett BL; Division of Cardiovascular Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • Díaz R; Estudios Clinicos Latino America (ECLA), Rosario, Argentina.
  • Felker GM; Division of Cardiology, Duke University School of Medicine and Duke Clinical Research Institute, Durham, NC, USA.
  • McMurray JJV; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
  • Solomon SD; Division of Cardiovascular Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • Bonderman D; Medical University of Vienna, Vienna, Austria.
  • Fang JC; University of Utah, Salt Lake City, UT, USA.
  • Fonseca C; Hospital S. Francisco Xavier, Centro Hospitalar Lisboa Ocidental, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal.
  • Goncalvesova E; Faculty of Medicine, Comenius University, Bratislava, Slovakia.
  • Howlett JG; Division of Cardiology, Libin Cardiovascular Institute of Alberta, University of Calgary, Calgary, AB, Canada.
  • Li J; National Clinical Research Center for Cardiovascular Diseases, National Health Commission Key Laboratory of Clinical Research for Cardiovascular Medications, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • O'Meara E; Montreal Heart Institute and Université de Montréal, Montreal, QC, Canada.
  • Miao ZM; Division of Cardiovascular Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • Abbasi SA; Amgen, Inc., Thousand Oaks, CA, USA.
  • Heitner SB; Cytokinetics, Inc., South San Francisco, CA, USA.
  • Kupfer S; Cytokinetics, Inc., South San Francisco, CA, USA.
  • Malik FI; Cytokinetics, Inc., South San Francisco, CA, USA.
  • Teerlink JR; Section of Cardiology, San Francisco Veterans Affairs Medical Center and School of Medicine, University of California San Francisco, San Francisco, CA, USA.
Eur Heart J ; 43(48): 5006-5016, 2022 12 21.
Article em En | MEDLINE | ID: mdl-35675469
ABSTRACT

AIM:

Patients with heart failure with reduced ejection fraction and low systolic blood pressure (SBP) have high mortality, hospitalizations, and poorly tolerate evidence-based medical treatment. Omecamtiv mecarbil may be particularly helpful in such patients. This study examined its efficacy and tolerability in patients with SBP ≤100 mmHg enrolled in the Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure (GALACTIC-HF). METHODS AND

RESULTS:

The GALACTIC-HF enrolled patients with baseline SBP ≥85 mmHg with a primary outcome of time to cardiovascular death or first heart failure event. In this analysis, patients were divided according to their baseline SBP (≤100 vs. >100 mmHg). Among the 8232 analysed patients, 1473 (17.9%) had baseline SBP ≤100 mmHg and 6759 (82.1%) had SBP >100 mmHg. The primary outcome occurred in 715 (48.5%) and 2415 (35.7%) patients with SBP ≤100 and >100 mmHg, respectively. Patients with lower SBP were at higher risk of adverse outcomes. Omecamtiv mecarbil, compared with placebo, appeared to be more effective in reducing the primary composite endpoint in patients with SBP ≤100 mmHg [hazard ratio (HR), 0.81; 95% confidence interval (CI), 0.70-0.94] compared with those with SBP >100 mmHg (HR, 0.95; 95% CI, 0.88-1.03; P-value for interaction = 0.051). In both groups, omecamtiv mecarbil did not change SBP values over time and did not increase the risk of adverse events, when compared with placebo.

CONCLUSION:

In GALACTIC-HF, risk reduction of heart failure outcomes with omecamtiv mecarbil compared with placebo was large and significant in patients with low SBP. Omecamtiv mecarbil did not affect SBP and was well tolerated independent of SBP values.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2022 Tipo de documento: Article