Parnsiri Chairangsarit MD*, Pasiri Sithinamsuwan MD*, Suchada Niyasom MD*, Chesda Udommongkol MD*, Samart Nidhinandana MD*, Jithanorm Suwantamee MD*
Affiliation : * Division of Neurology, Department of Medicine, Phramongkutklao Hospital
Objectives : To determine efficacy and tolerability of aspirin plus dipyridamole (combination) versus aspirin
alone in acute intervention treatment after acute ischemic stoke among Thai patients.
Materials and Methods : This pilot study enrolled ischemic stroke patients within 48 hours and randomized to
aspirin 300 mg/d or combination (aspirin 300 mg/d+ standard release dipyridamole 75 mg thrice a day) and
followed up for 6 months. End points were recurrent ischemic stroke, transient ischemic attack and vascular
death. Side effects were recorded. National Institutes of Health Stroke Scale was assessed at entry and at 6
months period for determining neurological functions.
Results : Of 38 patients, mean age was 64.3 years. Male and female were 52.6% and 47.4% respectively. There
were 18 patients in the aspirin group and 20 patients in the combination group. No patient developed end
point events or no significant adverse event in both groups. The combination group showed more improve-
ment in neurological function than the aspirin group (p-value 0.009).
Conclusion : This pilot study showed equal efficacy and tolerability of the combination group and aspirin
alone in acute intervention treatment for prevention of recurrent stroke or vascular death within 6 months.
Keywords : Aspirin, Dipyridamole, Prevention, Acute intervention
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