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Updated: Feb 13, 2026

In Vitro Thrombosis Test for Ventricular Assist Devices
Published on: March 21, 2025
Monitoring of Antiplatelet Therapy in Children on Ventricular Assist Device Support: Comparison of Multiplate and
Lee P Ferguson1, Phuoc Duong2, Kim F Pearce3
1From the Department of Paediatric Intensive Care, Freeman Hospital, Newcastle upon Tyne, United Kingdom.
Insights
Multiple electrode platelet aggregometry (MEA) is more reliable than Thromboelastography Platelet Mapping (TEG/PM) for monitoring antiplatelet therapy in pediatric ventricular assist device (VAD) patients. MEA shows better dose-response and less variability than TEG/PM.
Area of Science:
- Pediatric Cardiology
- Hematology
- Biomedical Engineering
Background:
- Monitoring antiplatelet therapy is crucial for children with ventricular assist devices (VADs).
- The optimal method for assessing antiplatelet efficacy in this population remains unclear.
- Current methods may not accurately reflect platelet function in pediatric VAD patients.
Purpose of the Study:
- To compare the reliability of Thromboelastography Platelet Mapping (TEG/PM) and multiple electrode platelet aggregometry (MEA) for monitoring antiplatelet therapy in children with VADs.
- To evaluate antiplatelet dose-response relationships and intraindividual variability using both methods.
- To determine which assay is superior for guiding antiplatelet treatment in pediatric VAD support.
Main Methods:
- Retrospective analysis of 66 paired blood samples from 9 pediatric patients (<16 years) on VAD.
- Simultaneous measurement of platelet function using TEG/PM and MEA (Multiplate analyzer).
- Assessment of agreement, dose-response, and intraindividual variability for aspirin and clopidogrel.
Main Results:
- Poor agreement between TEG/PM and MEA in determining therapeutic antiplatelet response (arachidonic acid κ=0.23, ADP κ=0.13).
- Higher rates of aspirin and clopidogrel resistance detected by TEG/PM compared to MEA.
- Significant dose-response with clopidogrel and MEA (R²=0.56), but not with TEG/PM (p=0.15).
- Greater intraindividual variability in platelet reactivity measured by TEG/PM during steady-state therapy.
Conclusions:
- Multiple electrode platelet aggregometry (MEA) demonstrates greater reliability than TEG/PM for monitoring antiplatelet therapy in pediatric VAD patients.
- MEA provides more consistent and clinically relevant assessment of antiplatelet effects in this population.
- These findings suggest MEA should be preferred for optimizing antiplatelet management in children with VADs.
Abstract:
The optimal method for monitoring antiplatelet therapy in children supported with ventricular assist devices (VADs) is unknown. We conducted a retrospective study to compare Thromboelastography Platelet Mapping (TEG/PM) with multiple electrode platelet aggregometry (MEA) on a Multiplate analyzer (Roche Diagnostics, Mannheim, Germany). We analyzed data from 66 paired blood samples from 9 patients <16 years of age on VAD where platelet function was simultaneously measured with TEG/PM and MEA. Antiplatelet dose-response relationships and intraindividual variability during steady state therapy were determined. Agreement in determination of therapeutic antiplatelet therapy was poor (arachidonic acid, κ 0.23; adenosine diphosphate [ADP], κ 0.13). Rate of aspirin and clopidogrel resistance was much higher when determined using TEG/PM than MEA. In patients receiving ≥5 mg/kg/day aspirin, 72% of TEG/PM measurements showed subtherapeutic response compared with 11% of MEA measurements. There was evidence of a dose-response relationship with clopidogrel and MEA ADP-induced aggregation (R2 = 0.56; p < 0.0001); however, there was no association between dose and TEG/PM% ADP inhibition (p = 0.15). Intraindividual variability in platelet reactivity was far greater when measured by TEG/PM during steady state therapy. Multiple electrode platelet aggregometry appears to be more reliable than TEG/PM for monitoring antiplatelet therapy in children supported with VAD.
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