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Updated: May 27, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Platelet function testing in practice: a case study
Ehtisham Mahmud1, Lawrence Ang
1University of California, San Diego Medical Center, San Diego, CA, USA.
Insights
Dual antiplatelet therapy reduces ischemic events after stenting, but residual risk remains. Point-of-care testing can identify patients with high platelet reactivity, a factor in stent thrombosis.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Hematology
Background:
- Dual antiplatelet therapy (DAPT) with aspirin and a thienopyridine is standard after percutaneous coronary intervention (PCI) to reduce ischemic events.
- Despite DAPT, a residual risk of ischemic events persists, partly due to enhanced platelet reactivity.
- Variability in patient response to thienopyridines like clopidogrel is influenced by genetic, pharmacologic, and clinical factors.
Observation:
- Point-of-care platelet function testing allows for assessment of on-treatment platelet reactivity.
- These tests can identify patients who are poor responders to thienopyridine therapy.
- Two cases of stent thrombosis were investigated using the VerifyNow P2Y12 Assay®.
Findings:
- The VerifyNow P2Y12 Assay® was used to determine on-treatment platelet reactivity in patients experiencing stent thrombosis.
- This assay helped identify potential causes for the thrombotic events by assessing platelet function.
- Enhanced platelet reactivity was identified as a potential contributor to stent thrombosis in these cases.
Implications:
- Point-of-care testing can guide antiplatelet therapy adjustments in patients at high risk for thrombotic events.
- Identifying poor responders to thienopyridines may help personalize treatment strategies to mitigate residual ischemic risk.
- These findings highlight the clinical utility of rapid platelet function assays in managing patients undergoing PCI.
Abstract:
Dual antiplatelet therapy with aspirin and a thienopyridine reduces ischemic cardiovascular events following percutaneous coronary intervention. However, despite this treatment, residual risk of ischemic events persists. Among other factors, enhanced platelet reactivity after thienopyridine therapy is associated with an increased risk of ischemic cardiovascular events. A heterogeneous and variable patient response to the thienopyridine clopidogrel exists and has been attributed to a number of genetic, pharmacologic, and clinical factors. Developments in point-of-care platelet function testing allow for the assessment of on-treatment platelet reactivity after thienopyridine therapy and thus identify poor responders. We report two cases of stent thrombosis in which the bedside rapid platelet function VerifyNow P2Y12 Assay® (Accumetrics, San Diego, CA) was used to determine on-treatment platelet reactivity and identify potential etiologies of the thrombotic events.
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