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Macitentan in pulmonary hypertension due to left ventricular dysfunction
JL. Vachiéry, M. Delcroix, H. Al-Hiti, M. Efficace, M. Hutyra, G. Lack, K. Papadakis, LJ. Rubin,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
NLK
Free Medical Journals
od 1994 do Před 18 měsíci
Open Access Digital Library
od 1988-01-01
- MeSH
- cévní rezistence účinky léků MeSH
- dvojitá slepá metoda MeSH
- dysfunkce levé srdeční komory komplikace MeSH
- internacionalita MeSH
- krevní tlak účinky léků MeSH
- lidé MeSH
- natriuretický peptid typu B účinky léků metabolismus MeSH
- peptidové fragmenty účinky léků metabolismus MeSH
- plicní hypertenze farmakoterapie patofyziologie MeSH
- plicní tlak v zaklínění účinky léků MeSH
- pyrimidiny aplikace a dávkování MeSH
- senioři MeSH
- sulfonamidy aplikace a dávkování MeSH
- test chůzí MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
The MELODY-1 study evaluated macitentan for pulmonary hypertension because of left heart disease (PH-LHD) in patients with combined post- and pre-capillary PH.63 patients with PH-LHD and diastolic pressure gradient ≥7 mmHg and pulmonary vascular resistance (PVR) >3WU were randomised to macitentan 10 mg (n=31) or placebo (n=32) for 12 weeks. The main end-point assessed a composite of significant fluid retention (weight gain ≥5% or ≥5 kg because of fluid overload or parenteral diuretic administration) or worsening in New York Heart Association functional class from baseline to end of treatment. Exploratory end-points included changes in N-terminal pro-brain natriuretic peptide (NT-proBNP) and haemodynamics at week 12.Seven macitentan-treated and four placebo-treated patients experienced significant fluid retention/worsening functional class; treatment difference, 10.08% (95% CI -15.07-33.26; p=0.34). The difference, driven by the fluid retention component, was apparent within the first month. At week 12, versus placebo, the macitentan group showed no change in PVR, mean right atrial pressure or pulmonary arterial wedge pressure; a non-significant increase in cardiac index (treatment effect 0.4 (95% CI 0.1-0.7) L·min-1·m-2) and decrease in NT-proBNP (0.77 (0.55-1.08)) was observed. Adverse events and serious adverse events were numerically more frequent with macitentan versus placebo.Macitentan-treated patients were quantitatively more likely to experience significant fluid retention versus placebo. Macitentan resulted in no significant changes in any exploratory end-points.
Dept of Cardiology Hôpital Erasme Université Libre de Bruxelles Brussels Belgium
Dept of Cardiology Institute of Clinical and Experimental Medicine IKEM Prague Czech Republic
Dept of Clinical Development Biostatistics Actelion Pharmaceuticals Italia Imperia Italy
Dept of Clinical Research Actelion Clinical Research Inc Cherry Hill NJ USA
Dept of Global Clinical Science and Epidemiology Actelion Pharmaceuticals Ltd Allschwil Switzerland
Dept of Internal Medicine 1 Cardiology University Hospital Olomouc Olomouc Czech Republic
Dept of Respiratory Diseases KU Leuven University Hospitals of Leuven Leuven Belgium
Division of Pulmonary and Critical Care Medicine University of California San Diego La Jolla CA USA
Citace poskytuje Crossref.org
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- $a The MELODY-1 study evaluated macitentan for pulmonary hypertension because of left heart disease (PH-LHD) in patients with combined post- and pre-capillary PH.63 patients with PH-LHD and diastolic pressure gradient ≥7 mmHg and pulmonary vascular resistance (PVR) >3WU were randomised to macitentan 10 mg (n=31) or placebo (n=32) for 12 weeks. The main end-point assessed a composite of significant fluid retention (weight gain ≥5% or ≥5 kg because of fluid overload or parenteral diuretic administration) or worsening in New York Heart Association functional class from baseline to end of treatment. Exploratory end-points included changes in N-terminal pro-brain natriuretic peptide (NT-proBNP) and haemodynamics at week 12.Seven macitentan-treated and four placebo-treated patients experienced significant fluid retention/worsening functional class; treatment difference, 10.08% (95% CI -15.07-33.26; p=0.34). The difference, driven by the fluid retention component, was apparent within the first month. At week 12, versus placebo, the macitentan group showed no change in PVR, mean right atrial pressure or pulmonary arterial wedge pressure; a non-significant increase in cardiac index (treatment effect 0.4 (95% CI 0.1-0.7) L·min-1·m-2) and decrease in NT-proBNP (0.77 (0.55-1.08)) was observed. Adverse events and serious adverse events were numerically more frequent with macitentan versus placebo.Macitentan-treated patients were quantitatively more likely to experience significant fluid retention versus placebo. Macitentan resulted in no significant changes in any exploratory end-points.
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