J Korean Neurol Assoc.  1998 Feb;16(1):21-27.

Comparative study of triflusal and ticlopidine on anti-platelet aggregatory effect and side effects

Affiliations
  • 1Department of Neurology, University of Ulsan.
  • 2Department of Neurology, Asan Medical Center.

Abstract

BACKGROUND AND PURPOSE: Platelet aggregation plays an important role in thrombogenesis. Thus antiplatelet agents, such as aspirin and ticlopidine, have been in usage to prevent for recurrent ischemic stroke. Triflusal is known to selectively inhibit cyclooxygenase in platelet rather than in vessel wall. And thus can be more beneficial in its antiplatelet aggregatory effect. There has been no comparative study between triflusal and ticlopidine on its antiplatelet aggregatory effect and side effects till now. Our comparative study between these two agents is to provide useful information on clinical utilization.
METHODS
Triflusal(900mg/day) and ticlopidine(500mg/day) were administered in 31 and 37 patients, who suffered from acute ischemic stroke. Their efficacy in platelet aggregation and the incidence of clinical and laboratory side effects were compared in one week and one month after the administration of the drugs.
RESULTS
Platelet aggregation was more effectively inhibited in triflusal group, especially induced by collagen or epinephrine(p<0.01). No significant difference was noted in the incidence of side effects in both groups. In five patients of the ticlopidine group, the drug was withdrawn due to skin rash and/or increased liver enzymes.
CONCLUSION
Triflusal had more effectively inhibited platelet aggregation in this study. Severe side effects even requiring discontinuation of the drug were noted in five patients of ticlopidine group.

Keyword

Triflusal; Ticlopidine; Platelet aggregation; Side effects

MeSH Terms

Aspirin
Blood Platelets
Collagen
Exanthema
Humans
Incidence
Liver
Platelet Aggregation
Platelet Aggregation Inhibitors
Prostaglandin-Endoperoxide Synthases
Stroke
Ticlopidine*
Aspirin
Collagen
Platelet Aggregation Inhibitors
Prostaglandin-Endoperoxide Synthases
Ticlopidine
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