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Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
A case-control study on platelet reactivity in patients with coronary stent thrombosis
H J Bouman1, J W van Werkum, N J Breet
1St Antonius Center for Platelet Function Research, St Antonius Hospital, Nieuwegein, The Netherlands.
Insights
Patients with early stent thrombosis (ST) show poor response to clopidogrel. Both early and late ST are linked to increased aspirin reactivity and higher dual antiplatelet therapy resistance.
Area of Science:
- Cardiology
- Pharmacology
- Thrombosis Research
Background:
- Stent thrombosis (ST) pathophysiology is a complex multifactorial model.
- Understanding platelet reactivity is crucial for managing ST.
- Previous research focused on single causative factors for ST.
Purpose of the Study:
- To investigate heightened platelet reactivity in patients with a history of stent thrombosis (ST).
- To assess platelet response to clopidogrel and aspirin in ST patients.
- To determine the prevalence of dual antiplatelet therapy resistance in ST survivors.
Main Methods:
- Compared platelet reactivity in 84 ST patients (41 early, 43 late) versus 103 controls.
- Assessed platelet function using optical aggregometry, VerifyNow P2Y12/aspirin, PFA-100, VASP assay, and urine 11-dehydrothromboxane B2.
- Measured reactivity before and after clopidogrel and aspirin loading doses.
Main Results:
- Early ST patients showed significantly higher on-clopidogrel platelet reactivity than controls.
- Both early and late ST patients exhibited heightened on-aspirin platelet reactivity.
- Dual antiplatelet therapy resistance was more frequent in ST patients.
Conclusions:
- Early ST is associated with a poor response to clopidogrel.
- Both early and late ST are independently linked to heightened on-aspirin platelet reactivity.
- Increased dual antiplatelet therapy resistance is a significant finding in ST patients.
Background:
The pathophysiology of stent thrombosis (ST) has evolved from the identification of single causative factors to a complex multifactorial model.
Objectives:
The aim of the present study was to investigate whether patients with a history of ST exhibit heightened platelet reactivity to clopidogrel and aspirin.
Patients/Methods:
Pretreatment and on-treatment platelet reactivity to clopidogrel and aspirin, as well as dual antiplatelet therapy resistance, was determined in 84 patients with a history of definite ST (cases: 41 early ST; 43 late ST) and in 103 control patients with a previously implanted coronary stent but no ST after the index procedure. Platelet function was evaluated with optical aggregometry, the VerifyNow P2Y12 and aspirin assays, the PFA-100 Innovance P2Y* cartridge, the flow cytometric vasodilator-stimulated phosphoprotein assay and urine 11-dehydrothromboxane B(2) measurement before and after the administration of a 600-mg loading dose of clopidogrel and 100 mg of aspirin. The study was registered at ClinicalTrials.gov, number NCT01012544.
Results:
Patients with a history of early ST clearly demonstrated higher on-clopidogrel platelet reactivity than controls. Patients with both early and late ST exhibited heightened on-aspirin platelet reactivity status, and dual antiplatelet therapy resistance was more frequent.
Conclusions:
Patients with a history of early ST exhibit a poor response to clopidogrel. Furthermore, both early and late ST are strongly and independently associated with heightened on-aspirin platelet reactivity, and dual antiplatelet therapy resistance is more frequent.
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