Key result
Dual nonresponsiveness to aspirin and clopidogrel is linked to ~3.2-fold higher 6-month DES thrombosis.
Why the study?
Nonresponsiveness to clopidogrel predicts DES thrombosis, but no prospective data existed regarding the incidence of dual nonresponsiveness to both aspirin and clopidogrel or its association with DES thrombosis.
Does dual nonresponsiveness to aspirin and clopidogrel increase the risk of definite/probable drug-eluting stent thrombosis in patients with successful drug-eluting stent implantation?
Cohort (n=746)
Does dual nonresponsiveness to aspirin and clopidogrel increase the risk of definite/probable drug-eluting stent thrombosis in patients with successful drug-eluting stent implantation?
Dual nonresponsiveness to aspirin and clopidogrel occurs in 6% of patients following drug-eluting stent implantation and independently identifies individuals at markedly elevated risk for stent thrombosis and cardiac mortality at 6 months.
Answers are grounded in this paper and cite their sources.
Dual nonresponsiveness may flag high-risk DES patients; leaves open whether platelet testing should guide therapy.
Objectives This study sought to determine the incidence of aspirin nonresponsiveness in addition to clopidogrel nonresponsiveness and whether this association identifies patients at an increased risk of drug-eluting stent (DES) thrombosis. Background Nonresponsiveness to clopidogrel is a predictor of DES thrombosis. No prospective data exist about the possible association of dual nonresponsiveness to clopidogrel and aspirin with DES thrombosis. Methods Platelet function was assessed after a loading dose of 600 mg clopidogrel in 746 patients who had successful DES implantation followed by 6-month dual-antiplatelet therapy. Platelet reactivity was assessed by light transmittance aggregometry using adenosine 5'-diphosphate, arachidonic acid, and collagen. The primary end point was definite/probable DES thrombosis at 6 months. The secondary end point was the composite of cardiac mortality and DES thrombosis. Results The incidence of dual nonresponsiveness to aspirin and clopidogrel was 6%. Definite/probable DES thrombosis was significantly higher in dual aspirin and clopidogrel nonresponders (11.1%) than in clopidogrel and aspirin responders (2.1%, p < 0.001), isolated clopidogrel nonresponders (2.2%, p < 0.05), or aspirin nonresponders (2.3%, p < 0.05). The incidence of the secondary end point was 4.4% in isolated clopidogrel nonresponders, 2.3% in isolated aspirin nonresponders, and 13.3% in dual aspirin and clopidogrel nonresponders. Dual clopidogrel and aspirin nonresponsiveness was an independent predictor of DES thrombosis (hazard ratio: 3.18, 95% confidence interval: 1.14 to 8.83, p = 0.027) and the composite of cardiac mortality and DES thrombosis (hazard ratio: 2.94, 95% confidence interval: 1.16 to 7.41, p = 0.022). Conclusions Dual nonresponsiveness to aspirin and clopidogrel is a relatively infrequent condition that identifies patients at a very high risk of DES thrombosis or death.
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Gori et al. (2008) conducted a cohort in Patients with successful drug-eluting stent (DES) implantation (n=746). Dual nonresponsiveness to aspirin and clopidogrel vs. Clopidogrel and aspirin responders, isolated clopidogrel nonresponders, or isolated aspirin nonresponders was evaluated on Definite/probable DES thrombosis at 6 months (HR 3.18, 95% CI 1.14-8.83, p=0.027). Dual nonresponsiveness to aspirin and clopidogrel independently predicted 6-month DES thrombosis.
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