Symptomatic and asymptomatic episodes of transient
myocardial ischemia are well-known risk factors in patients with
coronary artery disease. In a single-blind, randomized, and placebo-controlled study, the efficacy and safety of
gallopamil was studied during a 1-week treatment period in 25 patients with high-grade
coronary artery stenosis and frequent, exercise-induced episodes of
myocardial ischemia. Eighteen patients were men, and seven patients were women; the mean age +/- SD was 59 +/- 7 years. After a 1-week run-in period (days 1-7), all patients were treated with
gallopamil 50 mg t.i.d. (days 8-14) and placebo t.i.d. (days 15-21) or vice versa. Twenty-four-hour Holter monitoring, exercise testing, and adverse effects were controlled at days 7, 14, and 21. During the run-in period, all patients suffered a mean of 5.9 +/- 2.9 episodes of transient
myocardial ischemia, mean ischemic duration was 38 +/- 29 min/day.
Gallopamil increased exercise tolerance from 7.9 to 9.8 min (+24%, p < 0.05) and resulted in reduction of the weekly usage of short-acting
nitrates by 45% compared to placebo. During 24-h Holter monitoring, mean heart rate at the onset of ST-segment depression increased from 106 to 118 beats/min (p < 0.05). The frequency of daily ischemic episodes was reduced after
gallopamil administration from 6.1 to 3.9 episodes/day (-37%, p < 0.05), the total ischemic burden decreased for symptomatic episodes by -54% (p < 0.05) and for asymptomatic episodes by 29% (p < 0.05).
Gallopamil modified the circadian distribution of ischemic episodes by modifying the morning peak of transient
myocardial ischemia.(ABSTRACT TRUNCATED AT 250 WORDS)