Key result
Triple antiplatelet therapy did not reduce the risk of major adverse cardiovascular events compared to dual antiplatelet therapy after PCI with a second-generation drug-eluting stent.
Why the study?
Does triple antiplatelet therapy (aspirin, clopidogrel, and cilostazol) reduce major cardiovascular events compared to dual antiplatelet therapy in patients treated with a second-generation drug-eluting stent?
Observational (n=1,248)
Yes
Does triple antiplatelet therapy (aspirin, clopidogrel, and cilostazol) reduce major cardiovascular events compared to dual antiplatelet therapy in patients treated with a second-generation drug-eluting stent?
Triple antiplatelet therapy with cilostazol does not provide additional clinical benefit over standard dual antiplatelet therapy in patients receiving second-generation drug-eluting stents.
Answers are grounded in this paper and cite their sources.
Triple therapy was not associated with lower MACE; does not support routine cilostazol addition and leaves open need for randomized confirmation.
It has been shown that triple antiplatelet therapy with cilostazol results in better clinical outcomes than dual therapy in patients treated with a first-generation drug-eluting stent (DES); however, it is unclear whether triple antiplatelet therapy has a similar efficacy after the implantation of second-generation DES.In the COACT (Cath Olic medical center percutAneous Coronary in Tervention) registry, 1248 study subjects who underwent percutaneous coronary intervention with an everolimus- or zotarolimus-eluting stent (Endeavor, Xience V, or Promus) were analyzed. The patients were divided into 2 groups after propensity score matching (n = 724; M = 422 [58.3%]; mean age = 66.1 ± 11.0 years): Group 1: patients treated with dual antiplatelet drugs (aspirin and clopidogrel; n = 362; M = 213 [58.8%]; mean age = 65.6 ± 11.7 years); Group 2: patients treated with triple antiplatelet drugs (aspirin, clopidogrel, and cilostazol; n = 362; M = 209 [57.7%]; mean age = 65.6 ± 11.7 years). The mean follow-up duration was 13 ± 10 months, and the cumulative incidence of major cardiovascular events (MACE) was 6.3% in Group 1 and 7.7% in Group 2. There were no significant differences in MACE (death, nonfatal myocardial infarction, and stroke) between the 2 groups (OR, 1.210; 95% CI: 0.772-1.898; P = 0.406). Kaplan-Meier curves for MACE did not show any survival benefit for triple antiplatelet therapy, even in patients with acute coronary syndrome.In patients treated with a second-generation DES implantation, there is no added clinical benefit to using triple rather than dual antiplatelet therapy.
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Kim et al. (2015) conducted an observational in Percutaneous coronary intervention with second-generation drug-eluting stent (n=1,248). Triple antiplatelet therapy (aspirin, clopidogrel, and cilostazol) vs. Dual antiplatelet therapy (aspirin and clopidogrel) was evaluated on Major adverse cardiovascular events (MACE), defined as death, nonfatal myocardial infarction, or stroke (OR 1.210, 95% CI 0.772-1.898, p=0.406). Triple antiplatelet therapy did not reduce the risk of major adverse cardiovascular events compared to dual antiplatelet therapy after PCI with a second-generation drug-eluting stent.
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