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Assessment of Platelet Function on Whole Blood by Multiple Electrode Aggregometry in High-Risk Patients With Coronary Artery Disease Receiving Antiplatelet Therapy
125
Citations
34
References
2009
Year
Heart FailureResidual Platelet ReactivityPlatelet FunctionWhole BloodPharmacotherapyMultiple Electrode AggregometryCoronary Artery DiseaseAcute Myocardial InfarctionThrombosisHematologyClinical ChemistryMultiplate IpaPlatelet AntagonistAtherosclerosisCardiologyVascular BiologyPharmacologyLight Transmission AggregometryThrombopoiesisCardiovascular DiseaseBlood PlateletMedicineAnticoagulantEmergency MedicineAnesthesiology
This study sought to compare Multiplate impedance platelet aggregometry (IPA) with light transmission aggregometry (LTA) and the PFA-100 for determining the prevalence of residual platelet reactivity (RPR) by the Multiplate IPA in 297 patients with acute coronary syndrome receiving dual antiplatelet therapy. Aggregations were induced by adenosine-5 diphosphate (ADP), arachidonic acid, and collagen. PFA-100 closure times were measured by collagen and ADP and epinephrine (CEPI) cartridges. Significant correlations were observed between Multiplate IPA and LTA after all stimulations (P < .0001) and between Multiplate IPA (arachidonate and collagen) and PFA-100 CEPI closure time (P < .0001 for both). Cutoff values of Multiplate IPA (for all stimulations) were calculated for the identification of RPR. Between the Multiplate IPA and LTA good agreement was found with all 3 agonists (P < .0001 for all). Multiplate IPA might represent a reliable, handy, rapid tool to monitor antiplatelet therapy in clinical practice and for clinical investigations.
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