Baird Institute for Applied Heart and Lung Surgical Research, Newtown, Australia.
J Thorac Cardiovasc Surg. 2011 May;141(5):1134-44. doi: 10.1016/j.jtcvs.2010.07.001. Epub 2010 Dec 17.
We performed the present systematic review and meta-analysis of randomized and nonrandomized comparative studies in an attempt to compare the safety and efficacy of drug-eluting stents with coronary artery bypass grafting for patients with coronary artery disease.
Twenty-five eligible comparative studies (1 randomized and 24 nonrandomized) were assessed. Two reviewers independently appraised each study. Meta-analysis was performed by combining the results of reported incidence of morbidity, mortality, and repeat revascularization. The relative risk was used as a summary statistic.
In these 25 studies 34,278 patients were compared, of whom 18,538 received drug-eluting stents and 15,740 underwent coronary artery bypass grafting. It must be acknowledged that this comparison represented a selected group of patients who received drug-eluting stents or underwent coronary artery bypass grafting. The accumulative incidences of all-cause mortality at 12 months (4.5% vs 4.0%, P = .92) and 24 months (6.2% vs 8.4%, P = .27) and 30-day myocardial infarction (1.4% vs 2.0%, P = .60) were similar, respectively, between the drug-eluting stent and coronary artery bypass grafting groups. Drug-eluting stents were associated with lower rates of all-cause mortality at 30 days (0.9% vs 2.3%, P < .001), stroke (0.4% vs 1.7%, P < .001), and 30-day major adverse cardiac and cerebrovascular events (3.6% vs 5.5%, P < .04). However, the coronary artery bypass grafting group had a lower incidence of postprocedural myocardial infarction (5.5% vs 4.7%, P = .03), repeat revascularization (22.2% vs 4.1%, P < .001), and 12-month major adverse cardiac and cerebrovascular events (16.7% vs 10.5%, P < .001). Subgroup analysis of patients with multivessel coronary artery disease showed similar results.
Drug-eluting stents are associated with less periprocedural risks but a higher incidence of postprocedural myocardial infarction, repeat revascularization, and 12-month major adverse cardiac and cerebrovascular events compared with coronary artery bypass grafting.
我们进行了这项系统评价和荟萃分析,纳入了随机和非随机对照研究,旨在比较药物洗脱支架与冠状动脉旁路移植术治疗冠心病患者的安全性和疗效。
评估了 25 项符合条件的对照研究(1 项随机对照研究和 24 项非随机对照研究)。两位评审员独立评估了每一项研究。通过合并报告发病率、死亡率和再次血运重建的结果进行荟萃分析。使用相对风险作为汇总统计量。
在这 25 项研究中,比较了 34278 例患者,其中 18538 例接受药物洗脱支架治疗,15740 例接受冠状动脉旁路移植术。必须承认,这种比较代表了一组接受药物洗脱支架或冠状动脉旁路移植术的选择性患者。12 个月(4.5%比 4.0%,P=.92)和 24 个月(6.2%比 8.4%,P=.27)全因死亡率以及 30 天心肌梗死(1.4%比 2.0%,P=.60)的累积发生率在药物洗脱支架组和冠状动脉旁路移植术组之间相似。药物洗脱支架与 30 天全因死亡率(0.9%比 2.3%,P<.001)、卒中和 30 天主要心脏和脑血管不良事件(3.6%比 5.5%,P<.04)发生率较低相关。然而,冠状动脉旁路移植术组术后心肌梗死(5.5%比 4.7%,P=.03)、再次血运重建(22.2%比 4.1%,P<.001)和 12 个月主要心脏和脑血管不良事件(16.7%比 10.5%,P<.001)发生率较低。多支血管病变患者的亚组分析显示了类似的结果。
与冠状动脉旁路移植术相比,药物洗脱支架与围手术期风险较低相关,但与术后心肌梗死、再次血运重建和 12 个月主要心脏和脑血管不良事件发生率较高相关。