Why the study?
Does multiple electrode platelet aggregometry (MEA) provide more reliable monitoring of antiplatelet therapy compared to Thromboelastography Platelet Mapping (TEG/PM) in children on VAD support?
Does multiple electrode platelet aggregometry (MEA) provide more reliable monitoring of antiplatelet therapy compared to Thromboelastography Platelet Mapping (TEG/PM) in children on VAD support?
Multiple electrode platelet aggregometry appears more reliable than TEG/PM for monitoring antiplatelet therapy in pediatric patients on VAD support.
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TEG/PM and MEA comparison in small pediatric VAD cohort is hypothesis-generating; optimal monitoring strategy remains unclear.
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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Ferguson et al. (2018) studied this question.
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