Lancet. 1988 Aug 13;2(8607):349-60.
17,187 patients entering 417 hospitals up to 24 hours (median 5 hours) after the onset of suspected acute myocardial infarction were randomised, with placebo control, between: (i) a 1-hour intravenous infusion of 1.5 MU of streptokinase; (ii) one month of 160 mg/day enteric-coated aspirin; (iii) both active treatments; or (iv) neither. Streptokinase alone and aspirin alone each produced a highly significant reduction in 5-week vascular mortality: 791/8592 (9.2%) among patients allocated streptokinase infusion vs 1029/8595 (12.0%) among those allocated placebo infusion (odds reduction: 25% SD 4; 2p less than 0.00001); 804/8587 (9.4%) vascular deaths among patients allocated aspirin tablets vs 1016/8600 (11.8%) among those allocated placebo tablets (odds reduction: 23% SD 4; 2p less than 0.00001). The combination of streptokinase and aspirin was significantly (2p less than 0.0001) better than either agent alone. Their separate effects on vascular deaths appeared to be additive: 343/4292 (8.0%) among patients allocated both active agents vs 568/4300 (13.2%) among those allocated neither (odds reduction: 42% SD 5; 95% confidence limits 34-50%). There was evidence of benefit from each agent even for patients treated late after pain onset (odds reductions at 0-4, 5-12, and 13-24 hours: 35% SD 6, 16% SD 7, and 21% SD 12 for streptokinase alone; 25% SD 7, 21% SD 7, and 21% SD 12 for aspirin alone; and 53% SD 8, 32% SD 9, and 38% SD 15 for the combination of streptokinase and aspirin). Streptokinase was associated with an excess of bleeds requiring transfusion (0.5% vs 0.2%) and of confirmed cerebral haemorrhage (0.1% vs 0.0%), but with fewer other strokes (0.6% vs 0.8%). These "other" strokes may have included a few undiagnosed cerebral haemorrhages, but still there was no increase in total strokes (0.7% streptokinase vs 0.8% placebo infusion). Aspirin significantly reduced non-fatal reinfarction (1.0% vs 2.0%) and non-fatal stroke (0.3% vs 0.6%), and was not associated with any significant increase in cerebral haemorrhage or in bleeds requiring transfusion. An excess of non-fatal reinfarction was reported when streptokinase was used alone, but this appeared to be entirely avoided by the addition of aspirin. Those allocated the combination of streptokinase and aspirin had significantly fewer reinfarctions (1.8% vs 2.9%), strokes (0.6% vs 1.1%), and deaths (8.0% vs 13.2%) than those allocated neither. The differences in vascular and in all-cause mortality produced by streptokinase and by aspirin remain highly significant (2p less than 0.001 for each) after the median of 15 months of follow-up thus far available.
417家医院共纳入了17187例疑似急性心肌梗死发作后24小时内(中位数为5小时)就诊的患者,通过安慰剂对照,随机分为以下四组:(i)静脉输注1.5MU链激酶1小时;(ii)服用160mg/天的肠溶阿司匹林1个月;(iii)两种活性治疗联合使用;(iv)两种治疗均不使用。单独使用链激酶和单独使用阿司匹林均可使5周血管死亡率显著降低:接受链激酶输注的患者中,791/8592(9.2%)发生血管死亡,而接受安慰剂输注的患者中为1029/8595(12.0%)(比值降低:25%,标准差4;P<0.00001);服用阿司匹林片的患者中,804/8587(9.4%)发生血管死亡,而服用安慰剂片的患者中为1016/8600(11.8%)(比值降低:23%,标准差4;P<0.00001)。链激酶和阿司匹林联合使用的效果显著优于单独使用任何一种药物(P<0.0001)。它们对血管死亡的单独作用似乎具有相加性:接受两种活性药物治疗的患者中,343/4292(8.0%)发生血管死亡,而未接受任何治疗的患者中为568/4300(13.2%)(比值降低:42%,标准差5;95%置信区间34-50%)。即使对于疼痛发作后较晚接受治疗的患者,每种药物也都显示出了益处(链激酶单独使用时,在0-4小时、5-12小时和13-24小时的比值降低分别为:35%,标准差6;16%,标准差7;21%,标准差12;阿司匹林单独使用时分别为:25%,标准差7;21%,标准差7;21%,标准差12;链激酶和阿司匹林联合使用时分别为:53%,标准差8;32%,标准差9;38%,标准差15)。链激酶与需要输血的出血事件增加(0.5%对0.2%)和确诊脑出血增加(0.1%对0.0%)相关,但其他中风事件较少(0.6%对0.8%)。这些“其他”中风可能包括一些未确诊的脑出血,但总体中风发生率仍未增加(链激酶组为。7%,安慰剂输注组为0.8%)。阿司匹林显著降低了非致命性再梗死(1.0%对2.0%)和非致命性中风(0.3%对0.6%),且与脑出血或需要输血的出血事件显著增加无关。单独使用链激酶时报告有非致命性再梗死增加,但添加阿司匹林后似乎完全避免了这一情况。接受链激酶和阿司匹林联合治疗的患者与未接受任何治疗的患者相比,再梗死(1.8%对2.9%)、中风(0.6%对1.1%)和死亡(8.0%对13.2%)的发生率均显著降低。迄今为止,经过中位数为15个月的随访,链激酶和阿司匹林在血管死亡率和全因死亡率方面的差异仍然非常显著(每种药物的P<0.001)。