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Updated: May 14, 2026

Ferric Chloride-induced Murine Thrombosis Models
Published on: September 5, 2016
[Is antiplatelet therapy always effective?]
A Remková1, A Janušicová, M Remko
1HemoMedika Bratislava, Slovenska Republika. remkova@gmail.com
Monitoring individual response to antiplatelet therapy, including acetylsalicylic acid (ASA) and clopidogrel (KLP), optimizes treatment for cardiovascular patients. This approach identifies individuals who may benefit from alternative therapies like prasugrel or ticagrelor.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Antiplatelet therapy with acetylsalicylic acid (ASA) and clopidogrel (KLP) exhibits significant inter-individual response variability.
- A subset of patients demonstrates resistance to standard antiplatelet drug regimens.
- Optimizing antiplatelet therapy is crucial for high-risk cardiovascular event patients.
Purpose of the Study:
- To evaluate individual patient responses to antiplatelet therapy.
- To assess treatment efficacy in patients receiving ASA, KLP, or combination therapy.
- To identify predictors of response and resistance in cardiovascular patients.
Main Methods:
- Light transmission aggregometry was employed to measure platelet aggregation.
- VASP phosphorylation analysis was conducted in a subset of patients.
- Patient cohorts included those treated with ASA (n=131), KLP (n=51), or ASA + KLP (n=34).
Main Results:
- Good response to ASA (inhibition < 20%) was observed in 75.0% of patients; poor response (>40%) in 12.1%.
- Good response to KLP (inhibition < 60%) was achieved by 66.1%; poor response (>70%) in 20%.
- Dose adjustments (e.g., increasing KLP to 150 mg) improved response in non-responders; higher ASA doses (>100 mg) showed limited benefit.
Conclusions:
- Laboratory monitoring of individual antiplatelet response enables personalized therapy optimization.
- This monitoring can identify patients suitable for alternative antiplatelet agents like prasugrel and ticagrelor.
- Tailoring antiplatelet therapy based on individual response improves clinical outcomes in high-risk patients.
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