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Dynamic Multiparameter Platelet Function Assessment Using a Capacitive Biosensor
Published on: May 2, 2025
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Assessment of platelet function in patients with stroke using multiple electrode platelet aggregometry: a prospective
Ahmed Sabra1,2,3, Sophia N Stanford1,2, Sharon Storton2
1Medical School, Swansea University, Swansea, UK.
BMC Neurology
|December 13, 2016
Summary
High on-treatment platelet reactivity (HPR) is linked to adverse vascular events. Many patients on low-dose aspirin show aspirin resistance, but this decreases significantly after loading doses, suggesting potential benefits of individualized antiplatelet therapy.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- High on-treatment platelet reactivity (HPR) is associated with increased vascular events in stroke patients.
- Understanding HPR prevalence and its relation to antiplatelet (AP) drug efficacy is crucial for stroke management.
Purpose of the Study:
- To compare multiple electrode platelet aggregometry (MEA) in healthy individuals and ischemic stroke patients.
- To assess MEA differences between AP-naive patients and those on regular low-dose AP.
- To determine the prevalence of HPR at baseline and after aspirin loading doses.
Main Methods:
- Age and sex-matched study design comparing 70 ischemic stroke patients with 72 healthy controls.
- Multiple electrode platelet aggregometry (MEA) using arachidonic acid (ASPI), adenosine diphosphate (ADP), and collagen (COL) agonists.
- Blood samples collected at baseline, 24 hours, and 3-5 days post-treatment initiation.
Main Results:
- AP-naive patients exhibited significantly higher MEA results for all tested agonists compared to healthy subjects.
- A significant proportion of patients on long-term AP (33%) demonstrated aspirin resistance.
- Aspirin resistance decreased to 11.1% at 3-5 days following aspirin loading doses.
Conclusions:
- A considerable number of patients on low-dose aspirin meet criteria for aspirin resistance, though this is reduced after loading doses.
- Further research is necessary to elucidate HPR causes and the benefits of personalized AP treatment guided by platelet function testing.

