Why the study?
Does abciximab reduce the composite of death, myocardial infarction, and urgent target-vessel revascularization in patients with coronary artery disease undergoing elective percutaneous coronary intervention after pretreatment with clopidogrel?
Does abciximab reduce the composite of death, myocardial infarction, and urgent target-vessel revascularization in patients with coronary artery disease undergoing elective percutaneous coronary intervention after pretreatment with clopidogrel?
In low-to-intermediate risk patients undergoing elective PCI who are pretreated with a high loading dose of clopidogrel, the addition of abciximab provides no clinical benefit at 30 days and increases the risk of profound thrombocytopenia.
No benefit from adding abciximab after clopidogrel in elective PCI; challenges routine glycoprotein IIb/IIIa inhibitor use in low-to-intermediate risk patients.
BACKGROUND: Whether the glycoprotein IIb/IIIa inhibitor abciximab is beneficial in patients undergoing elective percutaneous coronary intervention after pretreatment with clopidogrel is unknown. METHODS: We enrolled 2159 patients with coronary artery disease who underwent a percutaneous coronary intervention: 1079 patients were randomly assigned in a double-blind manner to receive abciximab and 1080 patients to receive placebo. All patients were pretreated with a 600-mg dose of clopidogrel at least two hours before the procedure. The primary end point of the trial was the composite of death, myocardial infarction, and urgent target-vessel revascularization within 30 days after randomization. RESULTS: The incidence of the primary end point was 4 percent (45 patients) in the abciximab group, as compared with 4 percent (43 patients) in the placebo group (relative risk, 1.05; 95 percent confidence interval, 0.69 to 1.59; P=0.82). Most adverse events were myocardial infarctions: the incidence was 4 percent (40 patients) in the abciximab group and 4 percent (41 patients) in the placebo group (P=0.91). Twelve patients (1 percent) in the abciximab group and eight patients (1 percent) in the placebo group had major bleeding complications (P=0.37). Profound thrombocytopenia occurred in 10 patients (1 percent) in the abciximab group but in none in the placebo group (P=0.002). CONCLUSIONS: Our data suggest that in patients at low-to-intermediate risk who undergo elective percutaneous coronary intervention after pretreatment with a high loading dose of clopidogrel, abciximab is associated with no clinically measurable benefit within the first 30 days.
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Kastrati et al. (2004) studied this question.
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