J Am Coll Cardiol. 1988 Dec;12(6 Suppl A):3A-13A. doi: 10.1016/0735-1097(88)92635-6.
17,187 patients entering 417 hospitals up to 24 h (median 5 h) after the onset of suspected acute myocardial infarction were randomized, with placebo control, between i) a 1 h intravenous infusion of 1.5 million units of streptokinase; ii) 1 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%) vascular deaths among patients allocated streptokinase infusion versus 1029/8595 (12.0%) among those allocated placebo infusion (odds reduction: 25% +/- 4; 2p less than 0.00001); 804/8587 (9.4%) vascular deaths among patients allocated aspirin tablets versus 1016/8600 (11.8%) among those allocated placebo tablets (odds reduction: 23% +/- 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 death appeared to be additive: 343/4292 (8.0%) among patients allocated both active agents versus 568/4300 (13.2%) among those allocated neither (odds reduction: 42% +/- 5; 95% confidence limits 34% to 50%). There was evidence of benefit rom each agent even for patients treated late after pain onset (odds reduction at 0-4, 5-12, and 13-24 h: 35% +/- 6, 16% +/- 7 and 21% +/- 12 for streptokinase alone; 25% +/- 7,21% +/- 7 and 21% +/- 12 for aspirin alone; and 53% +/- 8,32% +/- 9 and 38% +/- 15 for the combination of streptokinase and aspirin). Streptokinase was associated with an excess of bleeds requiring transfusion (0.5% versus 0.2%) and of confirmed cerebral hemorrhage (0.1% versus 0.0%), but with fewer other strokes (0.6% versus 0.8%). These "other" strokes may have included a few undiagnosed cerebral hemorrhages, but still there was no increase in total strokes (0.7% streptokinase versus 0.8% placebo infusion). Aspirin significantly reduced nonfatal reinfarction (1.0% versus 2.0%) and nonfatal stroke (0.3% versus 0.6%), and was not associated with any significant increase in cerebral hemorrhage or in bleeds requiring transfusion. An excess of nonfatal 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% versus 2.9%), strokes (0.6% versus 1.1%), and deaths (8.0% versus 13.2%) than those allocated neither.(ABSTRACT TRUNCATED AT 250 WORDS)
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)入院的患者,进行随机分组并设置安慰剂对照,分组情况如下:i)静脉输注150万单位链激酶1小时;ii)服用160毫克/天的肠溶阿司匹林1个月;iii)同时接受两种活性治疗;或iv)两种治疗均不接受。单独使用链激酶和单独使用阿司匹林均使5周血管死亡率显著降低:接受链激酶输注的患者中有791/8592(9.2%)发生血管死亡,而接受安慰剂输注的患者中有1029/8595(12.0%)发生血管死亡(比值降低:25%±4;P<0.00001);接受阿司匹林片治疗的患者中有804/8587(9.4%)发生血管死亡,而接受安慰剂片治疗的患者中有1016/8600(11.8%)发生血管死亡(比值降低:23%±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有343/4292(8.0%)发生血管死亡,而未接受任何治疗的患者中有568/4300(13.2%)发生血管死亡(比值降低:42%±5;95%置信区间为34%至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有益效果(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%±6、16%±7和21%±12;阿司匹林单独使用时分别为:25%±7、21%±7和21%±12;链激酶和阿司匹林联合使用时分别为:53%±8、32%±9和38%±15)。链激酶与需要输血的出血事件(0.5%对0.2%)及确诊的脑出血()0.1%对0.0%)增多相关,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被诊断出的脑出血,但总体中风发生率并未增加(链激酶组为0.7%,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多的情况,但添加阿司匹林后似乎完全避免了这种情况。接受链激酶和阿司匹林联合治疗的患者发生再梗死(1.8%对2.9%)、中风(0.6%对1.1%)和死亡()8.0%对13.2%)的情况显著少于未接受任何治疗的患者。(摘要截选至250字)