To prevent recurrence of
cerebral infarction (CI), the efficacy of antiplatelet
therapy, when used in combination with a
calcium antagonist, was examined. The study subjects were 57 chronic CI patients (40 men, 17 women; mean age, 68.5 years) who experienced either CI or its recurrence more than 3 months before the start of the study. They were randomly allocated into one of the following four groups for the 8-week study; group A--
ticlopidine hydrochloride 200 mg once daily and
nicardipine hydrochloride 20 mg three times daily (TID); group B--
ticlopidine hydrochloride 200 mg once daily; group C--
aspirin 81 mg once daily and
nicardipine hydrochloride 20 mg TID; or group D--
aspirin 81 mg once daily. Platelet aggregation was measured before treatment and 4 and 8 weeks after the initiation of each
therapy by using
adenosine diphosphate (
ADP) (2 microM and 0.5 microM) and
collagen (2 micrograms/mL), and evaluated in terms of percent maximum platelet aggregation. Results showed significant suppression of 2.0 microM
ADP platelet aggregation in groups A, B, and C. At 0.5-microM
ADP, only groups A and B showed significant platelet aggregation suppression. All groups showed significant suppression of
collagen platelet aggregation. In comparing single
therapy with combination
therapy, groups A and B were not significantly different from one another after 4 or 8 weeks in 2-microM
ADP or
collagen platelet aggregation suppression. In contrast, group C had significantly greater suppression of both 2-microM
ADP and
collagen aggregations compared with group D. In conclusion,
nicardipine hydrochloride administration with
aspirin may be a useful alternative
therapy for the prevention of CI recurrence.