Literature DB >> 3883737

Long-term clinical and hemodynamic results of molsidomine treatment in patients with refractory heart failure.

J Acar, A Kulas, B Escudier.   

Abstract

In this report we describe the clinical and hemodynamic response of refractory cardiac failure to molsidomine. In the first part of the study the hemodynamic effects of a single oral dose of 2 or 4 mg of molsidomine were compared with placebo control in 23 patients. In the second phase the dose 8 to 24 mg/24 hours was used in nine patients with functional class III or IV symptoms over an average period of 28 months (range 7 to 42 months); a hemodynamic control study was performed. These data demonstrate that molsidomine has a hemodynamic effect on pulmonary artery pressure for 5 to 6 hours, that the peak effect is reached between 1 and 1 1/2 hours after oral intake, and that the clinical and hemodynamic benefits of molsidomine may be maintained in the long term in patients with particularly severe cardiac failure. The conditions of seven patients were clinically improved with treatment; significant reductions in mean right atrial, pulmonary artery, and pulmonary capillary pressures were observed.

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Year:  1985        PMID: 3883737     DOI: 10.1016/0002-8703(85)90682-9

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  3 in total

1.  Acute hemodynamic effects of molsidomine in patients with ischemic cardiomyopathy.

Authors:  D G Caralis; Z Kyriakides; C Ioakimides
Journal:  Cardiovasc Drugs Ther       Date:  1991-02       Impact factor: 3.727

2.  Haemodynamic evaluation of two regimens of molsidomine in patients with chronic congestive heart failure.

Authors:  G Lehmann; G Reiniger; A Beyerle; H Zeitler; W Rudolph
Journal:  Eur J Clin Pharmacol       Date:  1995       Impact factor: 2.953

3.  Comparison of haemodynamic effects of nifedipine and molsidomine in patients with coronary artery disease.

Authors:  M Kyriakidis; G Vyssoulis; P Sfikakis; C Kyriakidis; C Pitsavos; K Valsamis; V Nomikos; P Toutouzas
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

  3 in total

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