Smith B J
Department of Emergency Medicine, Sutherland Hospital, Taren Point NSW, Australia.
J Accid Emerg Med. 1999 Nov;16(6):407-11. doi: 10.1136/emj.16.6.407.
To compare outcomes from accelerated alteplase (recombinant tissue plasminogen activator, t-PA) and streptokinase use in acute myocardial infarction.
Review of available studies identified by Medline and other literature searches that met the criteria of being a prospective, randomised clinical trial enrolling over 1000 patients with acute myocardial infarction. The studies had to contain an intervention arm comprising accelerated infusion t-PA, or an intervention arm comprising streptokinase provided accelerated t-PA that was compared in the same trial. Interventions compared were streptokinase 1.5 million units given over one hour compared with accelerated t-PA infusion, with concomitant use of aspirin and heparin, and main outcome measure of 30 day mortality.
Four studies met prespecified criteria, these being the GUSTO I, GUSTO IIb Angioplasty Substudy, GUSTO III, and COBALT trials. There was a total study population of 64,387 patients of whom 20,251 received streptokinase, 19,474 received t-PA, with others receiving different treatment. Pooled data show that accelerated t-PA produces a marginal 30 day mortality advantage compared with streptokinase (6.6% v 7.3%, p = 0.02, Bonferroni adjusted p = 0.12, that is borderline significance, relative risk 0.918, 95% confidence interval 0.854 to 0.986). Any benefit is attributable entirely to patients recruited in the United States in the GUSTO I study. There is an increased incidence of stroke with t-PA.
The data do not consistently show a 30 day mortality benefit from using t-PA compared with streptokinase in acute myocardial infarction, but do show increased risk of stroke. Streptokinase can be considered the thrombolytic agent of choice.
比较加速使用阿替普酶(重组组织型纤溶酶原激活剂,t-PA)和链激酶治疗急性心肌梗死的疗效。
通过检索Medline及其他文献,回顾符合纳入1000例以上急性心肌梗死患者的前瞻性随机临床试验标准的现有研究。这些研究必须包含一个使用加速静脉输注t-PA的干预组,或一个使用链激酶的干预组,且加速t-PA在同一试验中进行比较。比较的干预措施为1小时内静脉输注150万单位链激酶与加速t-PA静脉输注,并同时使用阿司匹林和肝素,主要结局指标为30天死亡率。
四项研究符合预定标准,即GUSTO I、GUSTO IIb血管成形术亚组研究、GUSTO III和COBALT试验。总研究人群为64387例患者,其中20251例接受链激酶治疗,19474例接受t-PA治疗,其他患者接受不同治疗。汇总数据显示,与链激酶相比,加速t-PA在30天死亡率方面有微弱优势(6.6%对7.3%,p = 0.02,经Bonferroni校正p = 0.12,即临界显著性,相对风险0.918,95%置信区间0.854至0.986)。任何益处完全归因于GUSTO I研究中在美国招募的患者。使用t-PA后中风发生率增加。
数据并未一致显示在急性心肌梗死中使用t-PA与链激酶相比有30天死亡率获益,但确实显示中风风险增加。链激酶可被视为首选溶栓药物。