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

Platelets
|February 8, 2012
PubMed

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.

Related Concept Videos

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight, compared...
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses a challenge in...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
Pharmacodynamics in Geriatric Patients: Effects of Age01:27

Pharmacodynamics in Geriatric Patients: Effects of Age

Age-related pharmacokinetic changes are extensively documented, but understanding age-related pharmacodynamic alterations is relatively limited. This knowledge gap can be partly attributed to the complexity of developing appropriate measures of drug responses compared to bioanalytical methods for determining drug concentrations.Most information regarding age-related differences in human pharmacodynamics originates from cross-sectional studies. However, these studies assume that observed mean...