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Nonresponders to clopidogrel therapy among Indian patients undergoing elective/adhoc angioplasty
Viji S Thomson1, Bobby John, Purendra K Pati
1Department of Cardiology, Christian Medical College and Hospital, Vellore, India. sanviji@cmcvellore.ac.in
Insights
Clopidogrel nonresponse is common in Indian patients undergoing coronary angioplasty, with significant variability in platelet inhibition. Further studies are needed to understand the clinical impact of this nonresponse.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Clopidogrel is a standard antiplatelet drug used with aspirin after coronary angioplasty.
- Limited data exists on clopidogrel nonresponse rates in Indian populations.
Purpose of the Study:
- To investigate the nonresponse rate and interpatient variability of clopidogrel therapy in Indian patients undergoing coronary angioplasty.
Main Methods:
- Platelet aggregation was measured at baseline, 2, and 24 hours after administering clopidogrel (300 mg bolus, then 75 mg daily).
- Adenosine diphosphate (ADP) at concentrations of 2.5 and 10 micromol/L was used to stimulate platelet aggregation.
- Nonresponse was defined based on observed platelet aggregation levels.
Main Results:
- Significant interpatient variability in platelet aggregation response to clopidogrel was observed.
- The nonresponse rate was 47.7% at 2 hours post-administration, decreasing to 29.2% at 24 hours.
- Platelet aggregation was maximally inhibited at 24 hours post-drug administration.
Conclusions:
- Clopidogrel nonresponse is prevalent in Indian patients undergoing coronary angioplasty.
- Wide interpatient variability in platelet inhibition exists.
- Larger studies are required to validate the clinical implications of these findings.
Background:
Clopidogrel has become the standard antiplatelet drug along with aspirin in patients undergoing coronary angioplasty; however, data regarding the nonresponse rate to clopidogrel therapy in Indian patients are limited.
Methods And Results:
Platelet aggregation was measured at baseline and 2 and 24 hours post administration of bolus dose of 300 mg clopidogrel, followed by 75 mg once daily in patients undergoing elective or adhoc coronary angioplasty. Baseline platelet aggregation with 2.5 and 10 micromol/L ADP was 27.91 +/- 20.9% and 53.45 +/- 22.44%. Platelet aggregation at 2 hours and 24 hours with 2.5 micromol/L of ADP was 19.65 +/- 16.9% and 10.44 +/- 11.9%. The corresponding values with 10 micromol of ADP were 48.81 +/- 25.3% and 27.04 +/- 22.4%. Platelet aggregation was maximally inhibited at 24 hours with both 2.5 and 10 micromol/L of ADP. Marked interpatient variability in platelet aggregation in response to clopidogrel administration was observed and varied from -43 to 65%, -32 to 85% with 2.5 micromol/L at 2 hours and 24 hours and -65 to 53%, -35 to 97% with 10 micromol/L ADP at 2 hours and 24 hours. Nonresponse rate 2 hours after clopidogrel administration was 47.7%, and decreased to 29.2% at 24 hours post drug administration.
Conclusion:
Clopidogrel nonresponse is prevalent among Indian patients, and there is wide interpatient variability in platelet inhibition among individual patients. However, the clinical implications of these findings need to be substantiated in larger studies with clinical end points.
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