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Antiplatelet therapy in the prevention of stroke
1Department of Neurology, Rhode Island Hospital-Brown University, Providence.
Insights
Aspirin effectively reduces vascular events in atherosclerosis patients. Ticlopidine offers superior stroke prevention compared to aspirin, with manageable side effects.
Area of Science:
- Cardiovascular Medicine
- Neurology
- Pharmacology
Background:
- Atherosclerosis poses significant risks for vascular events like stroke and mortality.
- Aspirin (acetylsalicylic acid) is a widely used antiplatelet agent for secondary prevention.
- The efficacy of other agents like sulfinpyrazone, dipyridamole, and ticlopidine requires comparison with aspirin.
Purpose of the Study:
- To evaluate the effectiveness of aspirin in preventing vascular outcomes in patients with atherosclerosis.
- To compare the efficacy of ticlopidine, sulfinpyrazone, and dipyridamole against aspirin and placebo in stroke prevention.
- To assess the benefit-risk ratio of ticlopidine in patients with a history of thromboembolic stroke.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials comparing antiplatelet agents.
- Analysis of data from trials such as the Ticlopidine Aspirin Stroke Study (TASS) and the Canadian-American Ticlopidine Study (CATS).
- Evaluation of cerebrovascular events, stroke, myocardial infarction, and vascular mortality as primary outcomes.
Main Results:
- Aspirin reduces vascular events by approximately 25%, with specific risk reductions for stroke (30%) and vascular mortality (15%).
- Ticlopidine demonstrated superior efficacy over aspirin in preventing stroke, showing a risk reduction of 42-47% in the TASS study.
- Sulfinpyrazone and dipyridamole did not show significant additional benefits when compared to aspirin alone.
Conclusions:
- Aspirin is a cornerstone therapy for preventing atherothrombotic events.
- Ticlopidine is a more effective alternative to aspirin for stroke prevention, despite a low risk of reversible neutropenia.
- Further research, like the European Stroke Prevention Study II, is ongoing to clarify the roles of combination therapies.
Abstract:
Aspirin (acetylsalicylic acid) is effective in reducing vascular outcome events in patients with atherosclerosis: a relative risk reduction of about 30% for stroke, 22% for stroke and death, and 15% for vascular mortality. It is probable that low and high dose aspirin are similar in efficacy. Complications are more frequent with high dose aspirin than with low doses. Four randomised trials evaluating sulfinpyrazone vs placebo, and 3 trials evaluating sulfinpyrazone vs aspirin, showed more cerebrovascular events in the sulfinpyrazone group than in the aspirin and placebo groups. One small trial comparing dipyridamole with placebo in patients with cerebrovascular disease found no difference between the 2 groups in outcome. No other studies have compared dipyridamole alone with placebo or aspirin. The European Stroke Prevention Study II is currently in progress and is comparing dipyridamole + aspirin, dipyridamole, aspirin, and placebo. In the first year, the Ticlopidine Aspirin Stroke Study (TASS) showed a 42% risk reduction for stroke and death using the efficacy analysis and a 47% risk reduction for stroke and stroke death. Ticlopidine was more effective than aspirin in reducing stroke in both males and females. Apart from a reversible severe neutropenia in 0.86% of patients, ticlopidine-related adverse effects were relatively benign and reversible. The Canadian-American Ticlopidine Study (CATS) compared ticlopidine with placebo in patients with completed major strokes. The cumulative event rates for the primary outcome events of stroke, myocardial infarction and vascular death, using the efficacy approach, show clear evidence of separation almost immediately after randomisation, consistent with a constant risk reduction of about 30% in the ticlopidine group. These data provide strong evidence that ticlopidine conveys a clinically important reduction in the risk of thromboembolic events in patients with a history of completed thromboembolic stroke. In conclusion, aspirin is effective in preventing atherothrombotic morbidity and mortality. It reduces the overall vascular event rate by about 25%. Sulfinpyrazone and dipyridamole appear to add nothing important over aspirin alone. Ticlopidine is more effective than aspirin in preventing stroke. The modest, reversible risk of neutropenia, affecting less than 1% of patients, makes the benefit: risk ratio a reasonable one.
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