Angiotensin-converting enzyme inhibitors in heart failure: blood pressure changes after the first dose.

Am Heart J

Department of Medicine and Therapeutics, Gardiner Institute, University of Glasgow, Scotland.

Published: September 1993

AI Article Synopsis

  • ACE inhibitors block the formation of angiotensin II, helping to lower blood pressure and improve heart failure symptoms, ultimately enhancing patient survival.
  • Despite being generally well-tolerated, there is a risk of hypotension following the first dose, which can lead to complications, though most reports are anecdotal.
  • A double-blind study with 72 heart failure patients found varying blood pressure responses to different ACE inhibitors, with captopril causing a quick drop and enalapril leading to a longer-lasting effect, while further research is ongoing to better understand these differences.

Article Abstract

Angiotensin-converting enzyme (ACE) inhibitors prevent the formation of angiotensin II in the circulation and a range of tissues. ACE inhibitors not only are effective, well-tolerated antihypertensive drugs but also improve symptoms and signs in patients with congestive cardiac failure. In addition, they improve long-term survival in these latter patients. Although ACE inhibitors are relatively free of side effects in patients with heart failure, hypotension after the first dose has been reported that may lead to symptomatic renal, cardiac, or cerebral hypoperfusion. Most reports have been uncontrolled and anecdotal. We report a double-blind placebo-controlled study in a parallel group of patients with cardiac failure (New York Heart Association classes II through IV). In total, 72 patients (6 groups of 12) were studied after either placebo, captopril, 6.25 mg, enalapril, 2.5, or perindopril, 2 mg orally, enalaprilat 1.5 mg, or perindoprilat, 1.0 mg intravenously. The blood pressure responses differed between the groups, with a short-lived early fall after captopril and a long-lasting fall after enalapril, whereas perindopril was no different from placebo. There was no significant difference between the two active intravenous regimens. Plasma ACE measurements suggested that the relative doses used were at least comparable. Further studies are in progress to investigate the mechanisms underlying the differential hemodynamic responses and also to explore the clinical relevance to safety and efficacy in the management of heart failure.

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http://dx.doi.org/10.1016/0002-8703(93)90932-yDOI Listing

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