Key result
Triple therapy with cilostazol, aspirin, and clopidogrel reduced restenosis risk by 48% compared to dual therapy in patients post-PCI (OR: 0.52, P < 0.00001).
Why the study?
Does triple therapy (cilostazol, aspirin, and clopidogrel) improve effectiveness and safety compared to dual therapy (aspirin and clopidogrel) in patients receiving percutaneous coronary intervention?
Does triple therapy (cilostazol, aspirin, and clopidogrel) improve effectiveness and safety compared to dual therapy (aspirin and clopidogrel) in patients receiving percutaneous coronary intervention?
Adding cilostazol to aspirin and clopidogrel after PCI reduces restenosis and revascularization but increases non-bleeding adverse events like rash and gastrointestinal disorders.
Triple therapy may reduce restenosis post-PCI but increases rash and GI events; supports consensus with safety trade-offs.
The combination of cilostazol, aspirin, and clopidogrel (triple therapy) after percutaneous coronary intervention has been considered as an alternative therapy. We performed a meta‐analysis based on 8 randomized controlled trials with a total of 3332 patients to compare the effectiveness and safety of this triple therapy with traditional dual therapy (aspirin and clopidogrel). Our findings suggested that the triple therapy is more effective than dual therapy in preventing restenosis (odds ratio [OR]: 0.52, 95% confidence interval [CI]: 0.40–0.66, P < 0.00001), maintaining minimal lumen diameter (OR: 0.15, 95% CI: 0.10–0.20, P < 0.00001), and avoiding target‐vessel revascularization (OR: 0.62, 95% CI: 0.47–0.82, P = 0.001). There is also no significant difference in major adverse cardiac and cerebrovascular events between the 2 therapies, except the smaller occurrence rate of target‐lesion revascularization in the triple‐therapy group (OR: 0.42, 95% CI: 0.26–0.69, P = 0.0005). However, the triple therapy is associated with a higher level of adverse drug events, including rash (OR: 2.45, 95% CI: 1.41–4.23, P = 0.001), gastrointestinal disorders (OR: 2.59, 95% CI: 1.26–5.30, P = 0.009), and drug discontinuation (OR: 3.80, 95% CI: 1.59–9.10, P = 0.003), but it has no difference in bleeding compared with the dual therapy (OR: 1.05, 95% CI: 0.71–1.55, P = 0.80). Additional Supporting Information may be found in the online version of this article. Ping Wang, MS and Shijie Zhou, MS contributed equally to this article. The authors have no funding, financial relationships, or conflicts of interest to disclose.
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Wang et al. (2012) studied this question. Triple therapy with cilostazol, aspirin, and clopidogrel reduced restenosis risk by 48% compared to dual therapy in patients post-PCI (OR: 0.52, P < 0.00001).
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