EARLY ADMINISTRATION OF RAMIPRIL IN ACUTE MYOCARDIAL-INFARCTION - NEUROHORMONAL AND HEMODYNAMIC-EFFECTS AND TOLERABILITY

Citation
M. Vanderent et al., EARLY ADMINISTRATION OF RAMIPRIL IN ACUTE MYOCARDIAL-INFARCTION - NEUROHORMONAL AND HEMODYNAMIC-EFFECTS AND TOLERABILITY, Cardiology, 88(6), 1997, pp. 548-555
Citations number
41
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
00086312
Volume
88
Issue
6
Year of publication
1997
Pages
548 - 555
Database
ISI
SICI code
0008-6312(1997)88:6<548:EAORIA>2.0.ZU;2-U
Abstract
Although several large studies indicate a beneficial effect of angiote nsin-converting enzyme (ACE) inhibitors after myocardial infarction, t he optimal timing of therapy in terms of safety and the effects on neu rohormones during myocardial infarction are less well known. In order to investigate the effect of ramipril, administered within 24 h after myocardial infarction, on hemodynamics and neurohormones and its safet y, 20 patients with a myocardial infarction were studied. Nine patient s had an anterior, 10 an inferior, and 1 a non-Q-wave infarction. Four teen patients received thrombolytic therapy, whereas 6 did not. The in itial dose of ramipril was 1.25 mg, but was gradually increased to 5 m g during the next 4 days. Side effects did not occur. The mean arteria l pressure decreased 8 h after the first dose from 84 +/- 2 mm Hg (con trol) to 77 +/- 2 mm Hg (p < 0.05) and remained decreased thereafter. This was accompanied by a reduction in systemic resistance of 8% after 8 h and of 12% an day 2. Heart rate, cardiac and stroke indexes, and pulmonary artery and wedge pressures did not change. The ACE activity decreased within 1 h of ramipril administration with a maximum of 71% at 4 h after the second dose and remained at this level throughout the study. Angiotensin II decreased by 34% (day 2) and by 41% (day 5). Th e renin activity gradually increased from 33 +/- 7.5 to 75.4 +/- 11.5 mu M/ml on day 5, whereas epinephrine was reduced from day 2 onwards, with a maximal reduction of 71% on day 5. Arginine vasopressin was sig nificantly reduced 5 h after ramipril administration until the end of the study, with a maximum of 77% on day 3. Moreover, a late but signif icant decrease in norepinephrine occurred on day 5. Thus, oral ramipri l results in early ACE inhibition, followed by progressive attenuation of the neuroendocrine activation and a reduction in afterload during the acute phase of myocardial infarction, It is well tolerated, also i n combination with nitro-glycerin and thrombolytic therapy.