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
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.