Circulation, Vol 72, 873-880, Copyright © 1985 by American Heart Association
JM Kirshenbaum, RA Kloner, EM Antman and E Braunwald
Esmolol is a new ultra short-acting (half-life [t1/2] beta 9 min) beta
1-adrenergic-receptor antagonist reported to have no intrinsic
sympathomimetic activity. The safety and efficacy of esmolol in lowering
the ventricular rate and rate-pressure product in patients with acute
myocardial infarction (n = 5), postmyocardial infarction angina (n = 10),
or acute unstable angina (n = 4), and without cardiogenic shock were
studied. After a 30 min observation period, esmolol was titrated to a
maximum dose of 300 micrograms/kg/min and infused for up to 420 min. The
ventricular rate fell from 92 +/- 11 (mean +/- SD) to 77 +/- 13 beats/min
(p less than .01) and the systolic arterial pressure decreased from 120 +/-
13 to 97 +/- 11 mm Hg (p less than .01) during the initial 30 min titration
period. There was no significant change during the maintenance phase, and
both the ventricular rate and arterial pressure returned rapidly toward
baseline values within 30 min of termination of the infusion. The cardiac
index fell from 2.8 +/- 0.6 to 2.2 +/- 0.6 liters/min/m2 (p less than .01)
during the same period, and also returned to the baseline level 30 min
after termination of the infusion. There was no significant change in the
pulmonary capillary wedge pressure, respiratory rate, or PR interval. Five
patients required termination of infusion because of hypotension and all
recovered uneventfully within 30 min of stopping the esmolol. One patient
required a brief infusion of dopamine to restore hemodynamic
stability.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Use of an ultra short-acting beta-blocker in patients with acute myocardial ischemia
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