Department of Haematology, South Eastern Area Laboratory Services (SEALS), Prince of Wales Hospital, Sydney, Australia.
N Engl J Med. 2012 Nov 22;367(21):1979-87. doi: 10.1056/NEJMoa1210384. Epub 2012 Nov 4.
Patients who have had a first episode of unprovoked venous thromboembolism have a high risk of recurrence after anticoagulants are discontinued. Aspirin may be effective in preventing a recurrence of venous thromboembolism.
We randomly assigned 822 patients who had completed initial anticoagulant therapy after a first episode of unprovoked venous thromboembolism to receive aspirin, at a dose of 100 mg daily, or placebo for up to 4 years. The primary outcome was a recurrence of venous thromboembolism.
During a median follow-up period of 37.2 months, venous thromboembolism recurred in 73 of 411 patients assigned to placebo and in 57 of 411 assigned to aspirin (a rate of 6.5% per year vs. 4.8% per year; hazard ratio with aspirin, 0.74; 95% confidence interval [CI], 0.52 to 1.05; P=0.09). Aspirin reduced the rate of the two prespecified secondary composite outcomes: the rate of venous thromboembolism, myocardial infarction, stroke, or cardiovascular death was reduced by 34% (a rate of 8.0% per year with placebo vs. 5.2% per year with aspirin; hazard ratio with aspirin, 0.66; 95% CI, 0.48 to 0.92; P=0.01), and the rate of venous thromboembolism, myocardial infarction, stroke, major bleeding, or death from any cause was reduced by 33% (hazard ratio, 0.67; 95% CI, 0.49 to 0.91; P=0.01). There was no significant between-group difference in the rates of major or clinically relevant nonmajor bleeding episodes (rate of 0.6% per year with placebo vs. 1.1% per year with aspirin, P=0.22) or serious adverse events.
In this study, aspirin, as compared with placebo, did not significantly reduce the rate of recurrence of venous thromboembolism but resulted in a significant reduction in the rate of major vascular events, with improved net clinical benefit. These results substantiate earlier evidence of a therapeutic benefit of aspirin when it is given to patients after initial anticoagulant therapy for a first episode of unprovoked venous thromboembolism. (Funded by National Health and Medical Research Council [Australia] and others; Australian New Zealand Clinical Trials Registry number, ACTRN12605000004662.).
首次发生无诱因静脉血栓栓塞的患者在停止抗凝治疗后复发的风险很高。阿司匹林可能有效预防静脉血栓栓塞的复发。
我们将 822 名完成初始抗凝治疗后首次无诱因静脉血栓栓塞的患者随机分配,接受每日 100mg 阿司匹林或安慰剂治疗,最长 4 年。主要结局是静脉血栓栓塞的复发。
在中位数为 37.2 个月的随访期间,安慰剂组 411 例患者中有 73 例(6.5%/年)和阿司匹林组 411 例患者中有 57 例(4.8%/年)发生静脉血栓栓塞复发(风险比为 0.74;95%置信区间[CI]为 0.52 至 1.05;P=0.09)。阿司匹林降低了两个预先指定的次要复合结局的发生率:静脉血栓栓塞、心肌梗死、卒中和心血管死亡的发生率降低了 34%(安慰剂组为 8.0%/年,阿司匹林组为 5.2%/年;风险比为 0.66;95%CI为 0.48 至 0.92;P=0.01),静脉血栓栓塞、心肌梗死、卒中和大出血或任何原因导致的死亡的发生率降低了 33%(风险比为 0.67;95%CI 为 0.49 至 0.91;P=0.01)。两组之间大出血或临床相关非大出血事件的发生率(安慰剂组为 0.6%/年,阿司匹林组为 1.1%/年,P=0.22)或严重不良事件发生率无显著差异。
在这项研究中,与安慰剂相比,阿司匹林并未显著降低静脉血栓栓塞复发率,但显著降低了主要血管事件的发生率,从而带来了更好的净临床获益。这些结果证实了早期关于在首次无诱因静脉血栓栓塞初始抗凝治疗后给予阿司匹林治疗可带来治疗获益的证据。(由澳大利亚国家卫生与医学研究理事会等资助;澳大利亚新西兰临床试验注册中心编号,ACTRN12605000004662。)