Section of Interventional Cardiology, MedStar Washington Hospital Center, Washington, DC.
Section of Interventional Cardiology, MedStar Washington Hospital Center, Washington, DC.
Am J Cardiol. 2021 Aug 15;153:129-134. doi: 10.1016/j.amjcard.2021.05.028. Epub 2021 Jul 2.
The efficacy of early administration of dual antiplatelet therapy (DAPT) for secondary prevention after acute ischemic stroke or transient ischemic attack (TIA) is uncertain. This systematic review and meta-analysis compares the safety and efficacy of early administration (<24 hours) of DAPT (using either clopidogrel or ticagrelor with aspirin) versus single antiplatelet therapy (SAPT; aspirin alone) in acute non-cardioembolic ischemic stroke or TIA, incorporating data from large randomized controlled trials. Published trials fulfilling our criteria were identified from an electronic search of MEDLINE, with key words including: "clopidogrel or ticagrelor", "aspirin", "ischemic stroke", "transient ischemic attack", and "randomized controlled trial". Included were 3 randomized controlled trials of 21,067 patients assessing early administration (<24 hours from symptom onset) of DAPT versus SAPT in non-cardioembolic acute ischemic stroke or TIA. Our efficacy outcomes were ischemic stroke and all-cause mortality. Our safety outcome was severe bleeding. We performed a meta-analysis to pool results with a hierarchical Bayesian random-effects model. Dual antiplatelet therapy significantly reduced the risk of ischemic stroke (hazard ratio [HR], 0.73; 95% credible interval [CrI]: 0.54, 0.97), while increasing the risk of severe bleeding (HR, 2.48; 95% CrI: 1.07, 5.26). There was a non-significant numerical trend toward increased mortality with DAPT (HR, 1.29; 95% CrI: 0.73, 2.23). These observations were robust under the sensitivity analysis. In the present systematic review and meta-analysis of randomized controlled trials, DAPT reduced the risk of ischemic stroke at the cost of an increase in severe bleeding. Additional trials examining the ideal timing of DAPT administration are needed to thoroughly investigate the role, if any, of routine DAPT in patients with non-cardioembolic ischemic stroke or high-risk TIA.
早期应用双联抗血小板治疗(DAPT)对急性缺血性卒中和短暂性脑缺血发作(TIA)后的二级预防的疗效尚不确定。本系统评价和荟萃分析比较了早期(发病后<24 小时)应用 DAPT(氯吡格雷或替格瑞洛联合阿司匹林)与单一抗血小板治疗(SAPT;单独使用阿司匹林)治疗急性非心源性缺血性卒中和 TIA 的安全性和疗效,纳入了来自大型随机对照试验的数据。使用 MEDLINE 电子搜索,以“氯吡格雷或替格瑞洛”、“阿司匹林”、“缺血性卒中”、“短暂性脑缺血发作”和“随机对照试验”等关键词,确定符合我们标准的已发表试验。纳入了 3 项评估急性非心源性缺血性卒中和 TIA 中早期(发病后<24 小时)应用 DAPT 与 SAPT 的 21067 例患者的随机对照试验。我们的疗效结局是缺血性卒中和全因死亡率。我们的安全性结局是严重出血。我们采用分层贝叶斯随机效应模型进行荟萃分析以汇总结果。双联抗血小板治疗显著降低了缺血性卒中的风险(风险比[HR],0.73;95%可信区间[CrI]:0.54,0.97),同时增加了严重出血的风险(HR,2.48;95% CrI:1.07,5.26)。DAPT 治疗的死亡率呈增加的非显著数值趋势(HR,1.29;95% CrI:0.73,2.23)。在敏感性分析中,这些观察结果仍然稳健。在本系统评价和荟萃分析中,DAPT 降低了缺血性卒中的风险,但增加了严重出血的风险。需要进一步的临床试验来检查 DAPT 应用的理想时机,以彻底研究常规 DAPT 在非心源性缺血性卒中和高危 TIA 患者中的作用。