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.

ASAIO Journal (American Society for Artificial Internal Organs : 1992)
|March 1, 2018
PubMed

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.

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