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Updated: May 25, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Pharmacodynamic effects of clopidogrel in pediatric cardiac patients: a comparative study of platelet aggregation
Lisa K Jennings1, Alan D Michelson, Mary V Jacoski
1Vascular Biology Center of Excellence, University of Tennessee Health Science Center , Memphis, TN 38163, USA. ljennings@uthsc.edu
Insights
Pediatric cardiac patients show lower platelet aggregation (PA) than adults, with high variability. This explains why lower clopidogrel doses are effective in children, achieving similar platelet inhibition.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Hematology
Background:
- Limited data exist on pediatric platelet aggregation (%PA), especially in cardiac patients and response to clopidogrel.
- Understanding %PA is crucial for optimizing antiplatelet therapy in children.
Purpose of the Study:
- To estimate the normal range of %PA in pediatric patients.
- To measure the effect of clopidogrel on %PA in the PICOLO trial.
Main Methods:
- Assessed %PA induced by adenosine diphosphate (ADP) and thrombin receptor-activating peptide (TRAP) using light transmission aggregometry.
- Measured percent inhibition of platelet aggregation (%IPA) after clopidogrel administration in pediatric cardiac patients.
Main Results:
- ADP-induced %PA was lower in neonates and infants/toddlers compared to adults.
- TRAP-induced platelet aggregation was also lower in pediatric groups than adults.
- High variability in %PA and %IPA was observed, with some children showing minimal response to clopidogrel.
Conclusions:
- Pediatric cardiac patients exhibit lower baseline %PA than adults.
- The high variability in %PA and %IPA in children necessitates careful dosing of clopidogrel.
- Lower baseline %PA in children supports the lower effective clopidogrel dose (0.20 mg/kg/day) compared to adults.
Abstract:
Little data on pediatric percent platelet aggregation (%PA) exist in the literature, particularly in cardiac patients and in response to clopidogrel. The objectives were to estimate the %PA range expected in pediatric patients and to measure the clopidogrel effect on %PA in the PICOLO (Platelet Inhibition in Children on Clopidogrel) trial. To estimate a neonatal/infant %PA response range, %PA induced by 5 µM adenosine diphosphate (ADP) was assessed using light transmission aggregometry in 16 cord and 11 normal adult blood samples and prior to clopidogrel therapy in 49 neonatal and 49 infant/toddler cardiac patients enrolled in PICOLO. The %PA induced by 5 µM thrombin receptor-activating peptide (TRAP) was also assessed for 10 neonates and 21 infants/toddlers enrolled in PICOLO and compared with 11 adult samples. Percent inhibition of platelet aggregation (%IPA) induced by 5 µM ADP at steady-state clopidogrel levels was assessed in 33 neonates and 39 infants/toddlers. ADP-induced %PA was lowest in cord blood samples, intermediate in study neonates and infants/toddlers, and highest in adults. Similarly, TRAP-induced platelet aggregation was lower in neonates and infants/toddlers than adults. For all groups, %PA and %IPA were highly variable, with 11% of neonates and 13% of infants/toddlers showing <10% IPA. In conclusion, ADP- and TRAP-induced %PA is lower in pediatric cardiac patients than normal adults, but highly variable in both. The lower baseline %PA may explain why the pediatric clopidogrel dose providing 30-50% IPA (0.20 mg/kg/day) is lower than a simple weight-based extrapolation of the adult dose (75 mg/day) providing similar inhibition.
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