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Updated: Jul 14, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Reproducibility of platelet function testing
Megan E Hevelow1, Steven M McKenzie, Jamie E Siegel
1Cardeza Foundation for Hematologic Research, Thomas Jefferson University, Philadelphia, PA, USA. megan.hevelow@jefferson.edu
Normal variability in platelet function tests is not well-established. This study quantifies variation in platelet aggregation and release, revealing significant variability, especially with ristocetin and adenosine diphosphate, crucial for diagnosing bleeding disorders.
Area of Science:
- Hematology
- Clinical Pathology
- Diagnostic Testing
Background:
- Platelet aggregation and release studies are vital for diagnosing bleeding disorders.
- Establishing normal variability in these tests is essential for accurate interpretation.
- Previous data on intra-individual variability in platelet function assays is limited.
Purpose of the Study:
- To evaluate the intra-individual variation in platelet aggregation and release testing over a two-year period.
- To determine the intra-run variation for specific agonists and adenosine triphosphate (ATP) standards.
- To provide a basis for understanding the significance of abnormal results in patient testing.
Main Methods:
- Longitudinal study involving 5 subjects with 59 observations over 2 years.
- Platelet aggregation assays performed with various agonists.
- Platelet release studies, including adenosine triphosphate (ATP) release, were conducted.
- Intra-run variability was assessed for specific agonists and ATP standards.
Main Results:
- Average coefficients of variation (CV) for most agonist-induced platelet aggregations were below 17%.
- Significant variability was observed for ristocetin (1.0 mg/mL), with CVs ranging from 42% to 160%.
- Average CVs for platelet release tests exceeded 30%, with adenosine diphosphate (ADP) at 5 and 10 µM showing CVs of 56% and 42%, respectively.
Conclusions:
- Platelet aggregation and release tests exhibit considerable intra-individual variability.
- High variability, particularly with ristocetin and ADP, necessitates careful interpretation of results.
- Understanding this variability is critical for accurately diagnosing bleeding disorders and avoiding misinterpretation of patient data.
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