Enhanced onset of platelet inhibition with a loading dose of ticlopidine in ASA-treated stable coronary patients
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Updated: Oct 28, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
1Department of Cardiology, University Hospital, Linköping, Sweden.
Insights
A loading dose of ticlopidine, combined with aspirin, significantly enhances antiplatelet effects compared to standard dosing. This approach may reduce complications associated with coronary angioplasty and stenting procedures.
Area of Science:
- Cardiology
- Pharmacology
- Thrombosis
Background:
- Antiplatelet therapy is crucial for managing complications after coronary angioplasty.
- Ticlopidine, alongside aspirin (ASA), improves outcomes post-coronary stenting, yet early complications persist.
- Standard ticlopidine administration exhibits a delayed onset of action.
Purpose of the Study:
- To evaluate the efficacy of a ticlopidine loading dose versus standard treatment in ASA-treated patients.
- To assess the impact of a loading dose on platelet inhibition before coronary procedures.
Main Methods:
- Randomized trial involving 18 stable coronary patients pre-treated with ASA.
- Comparison of standard ticlopidine (250 mg BID) versus a loading dose (1500 mg) followed by standard dosing.
- Assessment of antiplatelet effect via ADP-induced platelet fibrinogen binding after one day.
Main Results:
- Standard ticlopidine showed minimal antiplatelet effect after one day.
- The ticlopidine loading dose regimen achieved significantly greater platelet inhibition (24.9-35.3% vs. 5.6-10.6%, p<0.005).
- Loading dose resulted in superior inhibition at lower final ADP concentrations.
Conclusions:
- A loading dose of ticlopidine provides more potent and rapid platelet inhibition than standard dosing.
- Administering a ticlopidine loading dose the day before angioplasty may mitigate procedural complications.
- This strategy holds promise for improving safety in coronary interventions.
Abstract:
Antiplatelet therapy reduces the rate of complications of coronary angioplasty. Ticlopidine, in addition to acetyl salicytic acid (ASA), improves the results after coronary stenting, but early complications still occur. Ticlopidine given in the standard way has a slow onset of action. Eighteen ASA-treated stable coronary patients were randomized to standard ticlopidine treatment (250 mg twice daily) or to a loading dose of 1500 mg followed by 250 mg twice daily. After one day, standard treatment had a very modest antiplatelet effect, as assessed by ADP-induced platelet fibrinogen binding, whereas the loading dose resulted in a considerably better platelet inhibition; relative inhibition, 5.6-10.6 vs. 24.9-35.3% (p<0.005) with final ADP concentrations 3 and 0.6 microM, respectively. It is possible that a loading dose of ticlopidine, given the day before the procedure, might reduce the complications related to angioplasty and stenting.
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