Literature DB >> 2527829

Comparison of the effects of captopril and enoximone in patients with severe heart failure: a placebo controlled double-blind study.

A J Cowley1, K Stainer, R D Wynne, J M Rowley, J R Hampton.   

Abstract

The effects of enoximone, a new cyclic adenosine monophosphate phosphodiesterase inhibitor, were compared with those of captopril in a double-blind study in a group of 10 patients with severe heart failure. Four weeks treatment with enoximone improved symptom-limited exercise tolerance from a mean value of 11.33 to 13.36 minutes (P less than 0.05) and 4 weeks of captopril treatment from 11.01 to 13.92 minutes (P less than 0.05). Four of the patients had a greater exercise tolerance taking enoximone, the remaining 6 while taking captopril. Both drugs reduced perceived exertion during submaximal exercise. Minute ventilation measured at rest and during submaximal exercise was also reduced by both drugs. Resting and post exercise calf blood flow was increased to a similar extent with captopril (P less than 0.03) and enoximone (P less than 0.005). There was no difference in calf blood flow and calf vascular resistance between the drugs suggesting that the peripheral haemodynamic effects of enoximone are due to peripheral vasodilatation. Enoximone is a useful drug for the treatment of patients with severe heart failure.

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Year:  1989        PMID: 2527829     DOI: 10.1016/0167-5273(89)90010-7

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  3 in total

Review 1.  Enoximone. A review of its pharmacological properties and therapeutic potential.

Authors:  M W Vernon; R C Heel; R N Brogden
Journal:  Drugs       Date:  1991-12       Impact factor: 9.546

Review 2.  Phosphodiesterase inhibitors. Do the risks outweight the benefits?

Authors:  R Andrews; A J Cowley
Journal:  Drug Saf       Date:  1993-12       Impact factor: 5.606

3.  Circulating ACE2 activity correlates with cardiovascular disease development.

Authors:  Katalin Úri; Miklós Fagyas; Attila Kertész; Attila Borbély; Csaba Jenei; Orsolya Bene; Zoltán Csanádi; Walter J Paulus; István Édes; Zoltán Papp; Attila Tóth; Erzsébet Lizanecz
Journal:  J Renin Angiotensin Aldosterone Syst       Date:  2016-12-12       Impact factor: 1.636

  3 in total

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