New York Methodist Hospital, Brooklyn, 11215, USA.
Am J Med. 2010 Mar;123(3):250-8. doi: 10.1016/j.amjmed.2009.08.016.
Antiplatelet therapy is the principal component of the antithrombotic regimen after acute myocardial infarction. It remains unclear whether additional chronic oral anticoagulation (OAC) improves outcomes. We set out to evaluate the risk and benefit of long-term OAC after myocardial infarction.
We pooled 10 randomized clinical trials comparing warfarin-containing regimens (OAC) with or without aspirin with non-OAC regimens with or without aspirin (No OAC) for patients with recent infarction. The primary endpoint was all-cause mortality. Other endpoints included recurrent infarction, stroke, and major bleeding. We calculated the odds ratio (OR) (fixed effect, OR <1 indicates benefit for OAC) for death and other ischemic and hemorrhagic complications at the longest interval of follow-up available.
Among 24,542 patients, 14,062 were assigned to OAC and 10,480 to no OAC. The patients were followed for 3-63 months, for 89,562 patient-years. Death occurred in 2424 patients (9.9%), 1279 OAC patients, and 1145 in the no OAC group, OR 0.97 (95% confidence interval [CI], 0.88-1.05), P=.43. Similarly, there was no effect on recurrent infarction. Stroke occurred in 578 patients (2.4%), 271 in the OAC group and 307 in the no OAC group, OR 0.75 (95% CI, 0.63-0.89), P=.001. There was substantially more major bleeding (OR 1.83 [95% CI, 1.50-2.23], P <.001) in the OAC group. Separate analyses, performed for patients (n=11,920) randomized to aspirin versus aspirin and OAC yielded very similar results.
As compared with placebo or aspirin, OAC with or without aspirin does not reduce mortality or reinfarction, reduces stroke, but is associated with significantly more major bleeding.
抗血小板治疗是急性心肌梗死后抗血栓治疗的主要组成部分。目前尚不清楚额外的慢性口服抗凝治疗(OAC)是否能改善预后。我们旨在评估心肌梗死后长期 OAC 的风险和获益。
我们汇总了 10 项比较华法林治疗方案(OAC)与 OAC 联合或不联合阿司匹林与非 OAC 治疗方案(No OAC)联合或不联合阿司匹林治疗近期心肌梗死患者的随机临床试验。主要终点是全因死亡率。其他终点包括再发梗死、卒中和大出血。我们计算了最长随访间隔可用时 OAC 死亡和其他缺血性和出血性并发症的优势比(OR)(固定效应,OR<1 表示 OAC 获益)。
在 24542 名患者中,14062 名患者被分配到 OAC 组,10480 名患者被分配到 No OAC 组。患者的随访时间为 3-63 个月,共随访 89562 患者年。2424 名患者(9.9%)发生死亡,1279 名 OAC 患者和 1145 名 No OAC 患者,OR 0.97(95%置信区间[CI],0.88-1.05),P=.43。同样,再发梗死也没有影响。578 名患者(2.4%)发生卒中,271 名 OAC 患者和 307 名 No OAC 患者,OR 0.75(95% CI,0.63-0.89),P=.001。OAC 组主要出血事件显著更多(OR 1.83 [95% CI,1.50-2.23],P<.001)。对随机接受阿司匹林与阿司匹林和 OAC 治疗的患者(n=11920)进行的单独分析得出了非常相似的结果。
与安慰剂或阿司匹林相比,OAC 联合或不联合阿司匹林并不能降低死亡率或再梗死率,降低卒中风险,但与显著更多的大出血有关。