Department of Geriatrics, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230022 China.
Chin Med J (Engl). 2013;126(9):1750-4.
The combination of cilostazol, aspirin and clopidogrel (triple antiplatelet therapy, TAT) after a percutaneous coronary intervention has been used as an alternative therapy. We performed a meta-analysis to evaluate the efficacy and safety of TAT for patients after percutaneous coronary intervention (PCI).
We systematically searched Pubmed, Embase and Web of Science databases to identify all randomized controlled trials (RCTs) that compared dual antiplatelet therapy (DAT) with and without cilostazol after PCI. All analyses were conducted using Review Manager 5.0.
The final analysis consisted of 4474 patients from ten studies. The combined results suggested that there was a lower risk of cardiac death (relative risk (RR) = 0.55, 95% confidence interval (CI): 0.31 - 0.98, P < 0.05) and major adverse cardiac events (MACEs) (RR = 0.63, 95% CI: 0.54 - 0.74, P < 0.05) in patients treated with TAT as compared to those with DAT follow-ups after six months to one year; no significant difference was observed in bleeding and non-fatal myocardial infarction (MI) (RR = 1.14, 95% CI: 0.80 - 1.64, P > 0.05; RR = 0.87, 95% CI: 0.42 - 1.83, P > 0.05). However, the rate of adverse drug reaction was higher in patients receiving TAT than in patients receiving DAT (RR = 2.21, 95% CI: 1.84 - 2.66, P < 0.05). Moreover, there was a lower risk of stent thrombosis in patients treated with TAT as compared to those treated with DAT (RR = 0.44, 95% CI: 0.21 - 0.94, P < 0.05). The TAT group had a reduced risk of target lesion revascularization (TLR) (RR = 0.60, 95% CI: 0.43 - 0.82, P = 0.001) and target vessel revascularization (TVR) than the DAT group (RR = 0.56, 95% CI: 0.45 - 0.71, P < 0.05). The number of MACEs was lower for patients in the TAT group than in the DAT group with diabetes mellitus sub-analysis (RR = 0.41, 95% CI: 0.28 - 0.61, P < 0.05). But no significant difference was observed between the two groups regarding MACEs in patients with drug-eluting stent implantations (RR = 0.82, 95% CI: 0.65 - 1.03, P > 0.05).
TAT could significantly reduce the rates of MACEs and cardiac death in comparison to DAT, but more attention should be paid to adverse side effects of the drugs.
在经皮冠状动脉介入治疗(PCI)后,联合使用西洛他唑、阿司匹林和氯吡格雷(三联抗血小板治疗,TAT)已被用作替代疗法。我们进行了一项荟萃分析,以评估 TAT 对 PCI 后患者的疗效和安全性。
我们系统地检索了 Pubmed、Embase 和 Web of Science 数据库,以确定所有比较 PCI 后双联抗血小板治疗(DAT)与不联合西洛他唑的随机对照试验(RCT)。所有分析均使用 Review Manager 5.0 进行。
最终分析纳入了来自 10 项研究的 4474 名患者。综合结果表明,TAT 组患者在 6 个月至 1 年随访期间心脏死亡(相对风险(RR)=0.55,95%置信区间(CI):0.31 - 0.98,P < 0.05)和主要不良心脏事件(MACEs)(RR = 0.63,95%CI:0.54 - 0.74,P < 0.05)的风险较低;但在出血和非致死性心肌梗死(MI)方面,TAT 组与 DAT 组无显著差异(RR = 1.14,95%CI:0.80 - 1.64,P > 0.05;RR = 0.87,95%CI:0.42 - 1.83,P > 0.05)。然而,TAT 组患者的药物不良反应发生率高于 DAT 组(RR = 2.21,95%CI:1.84 - 2.66,P < 0.05)。此外,TAT 组患者的支架血栓形成风险低于 DAT 组(RR = 0.44,95%CI:0.21 - 0.94,P < 0.05)。TAT 组患者的靶病变血运重建(TLR)(RR = 0.60,95%CI:0.43 - 0.82,P = 0.001)和靶血管血运重建(TVR)(RR = 0.56,95%CI:0.45 - 0.71,P < 0.05)风险低于 DAT 组。糖尿病亚组分析显示,TAT 组患者的 MACE 发生率低于 DAT 组(RR = 0.41,95%CI:0.28 - 0.61,P < 0.05)。但在药物洗脱支架植入患者中,两组间 MACE 发生率无显著差异(RR = 0.82,95%CI:0.65 - 1.03,P > 0.05)。
与 DAT 相比,TAT 可显著降低 MACE 和心脏死亡的发生率,但应更加关注药物的不良反应。