Alfred Hospital, Melbourne, Australia; Monash University, Melbourne, Australia.
Monash University, Melbourne, Australia; Monash Medical Centre, Clayton, Australia.
J Thorac Cardiovasc Surg. 2019 Feb;157(2):633-640. doi: 10.1016/j.jtcvs.2018.08.114. Epub 2018 Sep 28.
Aspirin may reduce the risk of vascular graft thrombosis after cardiovascular surgery. We previously reported the 30-day results of a trial evaluating aspirin use before coronary artery surgery. Here we report the 1-year outcomes evaluating late thrombotic events and disability-free survival.
Using a factorial design, we randomly assigned patients undergoing coronary artery surgery to receive aspirin or placebo and tranexamic acid or placebo. The results of the aspirin comparison are reported here. The primary 1-year outcome was death or severe disability, the latter defined as living with a modified Katz activities of daily living score < 8. Secondary outcomes included a composite of myocardial infarction, stroke and death from any cause through to 1 year after surgery.
Patients were randomly assigned to aspirin (1059 patients) or placebo (1068 patients). The rate of death or severe disability was 4.1% in the aspirin group and 3.5% in the placebo group (relative risk, 1.17; 95% confidence interval, 0.76-1.81; P = .48). There was no significant difference in the rates of myocardial infarction (P = .11), stroke (P = .086), or death (P = .24), or a composite of these cardiovascular end points (P = .68). With the exception of those with a low European System for Cardiac Operative Risk Evaluation score (P = .03), there were no interaction effects on these outcomes with tranexamic acid (all tests of interaction P > .10).
In patients undergoing coronary artery surgery, preoperative aspirin did not reduce death or severe disability, or thrombotic events through to 1 year after surgery.
阿司匹林可能会降低心血管手术后血管移植物血栓形成的风险。我们之前报告了评估冠状动脉手术前使用阿司匹林的试验的 30 天结果。在这里,我们报告了评估晚期血栓事件和无残疾生存的 1 年结果。
我们采用析因设计,随机分配接受冠状动脉手术的患者接受阿司匹林或安慰剂和氨甲环酸或安慰剂。这里报告阿司匹林比较的结果。主要 1 年结局是死亡或严重残疾,后者定义为日常生活活动改良 Katz 评分<8。次要结局包括手术后 1 年内心肌梗死、中风和任何原因导致的死亡的复合结局。
患者被随机分配至阿司匹林组(1059 例)或安慰剂组(1068 例)。阿司匹林组的死亡或严重残疾发生率为 4.1%,安慰剂组为 3.5%(相对风险,1.17;95%置信区间,0.76-1.81;P=0.48)。心肌梗死发生率(P=0.11)、中风发生率(P=0.086)或死亡率(P=0.24)或这些心血管终点的复合结局发生率(P=0.68)无显著差异。除欧洲心脏手术风险评估系统评分低的患者(P=0.03)外,氨甲环酸对这些结局无交互作用(所有交互作用检验 P>0.10)。
在接受冠状动脉手术的患者中,术前阿司匹林并未降低手术后 1 年内的死亡或严重残疾或血栓事件发生率。