Key result
Adding cilostazol to dual antiplatelet therapy after PCI significantly reduced angiographic restenosis (OR 0.58; 95% CI 0.48-0.71; p<0.001) and target lesion revascularization.
Why the study?
Does adding cilostazol to dual antiplatelet therapy improve angiographic and clinical outcomes in patients undergoing PCI with stents?
Meta-Analysis (n=8,525)
Does adding cilostazol to dual antiplatelet therapy improve angiographic and clinical outcomes in patients undergoing PCI with stents?
Odds Ratio: 0.58 (95% CI 0.48–0.71)
p-value: p=< 0.001
The addition of cilostazol to dual antiplatelet therapy after PCI significantly reduces angiographic restenosis and target lesion revascularization without increasing bleeding risk.
Supports cilostazol addition to DAPT post-PCI; extends RCT evidence on angiographic outcomes.
OBJECTIVES: To evaluate the impact of cilostazol on the angiographic and clinical outcomes in patients undergoing percutaneous coronary intervention (PCI) with stents and treated with aspirin and thienopyridine. METHODS: A total of 11 randomized controlled trials including 8,525 patients comparing triple antiplatelet therapy (aspirin, thienopyridine and cilostazol) with standard dual antiplatelet therapy were included in the analysis. The primary end points were in-segment late loss and angiographic restenosis at angiographic follow-up. Secondary end points included mortality, stent thrombosis, target lesion revascularization (TLR) and major adverse cardiac events (MACE). RESULTS: Triple antiplatelet therapy was associated with a significant reduction in late loss [weighted mean difference 0.14, 95% confidence interval (CI) 0.08-0.20; p < 0.001] and angiographic restenosis [odds ratio (OR) 0.58, 95% CI 0.48-0.71; p < 0.001]. Addition of cilostazol to dual antiplatelet therapy was associated with a significant reduction in TLR (OR 0.56, 95% CI 0.41-0.77; p < 0.001) and MACE (OR 0.72, 95% CI 0.60-0.86; p < 0.001) with no differences in mortality (p = 0.29), stent thrombosis (p = 0.60) or bleeding episodes (p = 0.77). CONCLUSIONS: Cilostazol in addition to dual antiplatelet therapy appears to be effective in reducing the risk of restenosis and repeat revascularization after PCI without any significant benefits for mortality or stent thrombosis.
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Jang et al. (2012) conducted a meta-analysis in Percutaneous coronary intervention (PCI) with stents (n=8,525). Triple antiplatelet therapy (aspirin, thienopyridine and cilostazol) vs. Standard dual antiplatelet therapy was evaluated on In-segment late loss and angiographic restenosis at angiographic follow-up (OR 0.58, 95% CI 0.48-0.71, p=< 0.001). Adding cilostazol to dual antiplatelet therapy after PCI significantly reduced angiographic restenosis (OR 0.58; 95% CI 0.48-0.71; p<0.001) and target lesion revascularization.
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