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Published on: November 8, 2024
Effects of high ticlopidine doses on platelet function in acute coronary syndrome patients
Patrick Bélanger1, Donald A Palisaitis, Jean G Diodati
1Research Center, Hôpital du Sacré-Coeur de Montréal, and Faculty of Pharmacy, Université de Montréal, Montréal, Quebec, Canada.
Insights
Higher doses of ticlopidine (500 mg twice daily) combined with aspirin accelerate platelet inhibition in acute coronary syndromes. This faster platelet response is crucial for patients undergoing percutaneous coronary intervention.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Acute coronary syndromes (ACS) require rapid management to prevent adverse events.
- Platelet activation and aggregation are key contributors to ACS pathophysiology.
- Percutaneous coronary intervention (PCI) with stent placement is a common treatment for ACS.
Purpose of the Study:
- To evaluate if higher doses of ticlopidine with acetylsalicylic acid (aspirin) provide faster inhibition of platelet activation and aggregation in ACS patients.
- To compare the efficacy of ticlopidine 250 mg versus 500 mg twice daily in this patient population.
Main Methods:
- Seventeen ACS patients eligible for potential PCI were randomized.
- Patients received either ticlopidine 250 mg or 500 mg twice daily for 5 days, alongside aspirin.
- Platelet aggregation and activation were measured daily for 5 days.
Main Results:
- Ticlopidine 500 mg twice daily significantly reduced platelet activation and aggregation compared to 250 mg twice daily after 2 days.
- Mean platelet activation reduction was 17.6% (days 3-6) with the higher dose (P < 0.05).
- Mean platelet aggregation reduction was 16.9% (days 3-6) with the higher dose (P < 0.05).
Conclusions:
- Administering ticlopidine 500 mg twice daily with aspirin achieves faster and stronger platelet inhibition in ACS patients.
- This higher dosage regimen may improve outcomes for ACS patients undergoing PCI.
Background:
We investigated whether higher doses of ticlopidine combined with acetylsalicylic acid would allow a faster inhibition of platelet activation and aggregation in patients with acute coronary syndromes potentially undergoing percutaneous coronary intervention with stent placement.
Methods:
Seventeen patients presenting with acute coronary syndromes and candidates for possible percutaneous coronary intervention were randomized to ticlopidine 250 mg or 500 mg twice daily for 5 days. Platelet aggregation and activation were assessed at baseline before the first dose and daily for 5 days.
Results:
After 2 days of treatment, 500 mg twice daily of ticlopidine produced a significantly larger reduction in platelet activation and aggregation than 250 mg twice daily. Mean platelet activation was 17.6 +/- 3.3% lower with 500 mg twice daily from days 3 to 6 (P < or = 0.05). Mean platelet aggregation was 16.9 +/- 0.6% lower in patients treated with the higher dose on days 3 through 6 when compared with those on ticlopidine 250 mg twice daily (P < 0.05).
Conclusions:
A faster and stronger inhibition of platelet activation and aggregation is obtained when 500 mg twice daily of ticlopidine is administered daily in combination with acetylsalicylic acid in patients with acute coronary syndromes.
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