Key result
Discontinuation of thienopyridine therapy within 6 months of drug-eluting stent implantation was the strongest predictor of stent thrombosis (HR 13.74; 95% CI 4.04-46.68; P<0.001).
Why the study?
Does discontinuation of thienopyridine therapy increase the risk of stent thrombosis in patients treated with drug-eluting stents?
Cohort (n=3,021)
Does discontinuation of thienopyridine therapy increase the risk of stent thrombosis in patients treated with drug-eluting stents?
Discontinuation of thienopyridine therapy within the first 6 months after drug-eluting stent implantation is a major risk factor for stent thrombosis, emphasizing the critical need for uninterrupted dual antiplatelet therapy during this early period.
Answers are grounded in this paper and cite their sources.
Early thienopyridine discontinuation after DES was associated with stent thrombosis; leaves open optimal DAPT duration in randomized trials.
Background— The need for prolonged aspirin and thienopyridine therapy and the risk of stent thrombosis (ST) remain as drawbacks associated with drug-eluting stents. Methods and Results— A prospective observational cohort study was conducted between June 2002 and January 2004 on 3021 patients consecutively and successfully treated in 5389 lesions with drug-eluting stents. Detailed patient information was collected on antiplatelet therapy. We analyzed the incidence of ST throughout the 18-month follow-up period and its relationship with thienopyridine therapy. ST occurred in 58 patients (1.9%) at 18 months. Forty-two patients (1.4%) experienced the event within 6 months of stent implantation. Acute myocardial infarction (fatal or nonfatal) occurred in 46 patients (79%) and death in 23 patients (39%) with ST. The median interval from discontinuation of thienopyridine therapy to ST was 13.5 days (interquartile range 5.2 to 25.7 days) for the first 6 months and 90 days (interquartile range 30 to 365 days) between 6 and 18 months. On multivariable analysis, the strongest predictor for ST within 6 months of stenting was discontinuation of thienopyridine therapy (hazard ratio, 13.74; 95% CI, 4.04 to 46.68; P <0.001). Thienopyridine discontinuation after 6 months did not predict the occurrence of ST (hazard ratio, 0.94; 95% CI, 0.30 to 2.98; P =0.92). Conclusions— Discontinuation of thienopyridine therapy was the major determinant of ST within the first 6 months, but insufficient information is available to determine whether there is benefit in continuing a thienopyridine beyond 6 months.
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Airoldi et al. (2007) conducted a cohort in Patients treated with drug-eluting stents (n=3,021). Discontinuation of thienopyridine therapy vs. Continuation of thienopyridine therapy was evaluated on Stent thrombosis within 6 months of stenting (HR 13.74, 95% CI 4.04 to 46.68, p=<0.001). Discontinuation of thienopyridine therapy within 6 months of drug-eluting stent implantation was the strongest predictor of stent thrombosis (HR 13.74; 95% CI 4.04-46.68; P<0.001).
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