Lancet. 2012 Jun 23;379(9834):2352-63. doi: 10.1016/S0140-6736(12)60768-5. Epub 2012 May 23.
Thrombolysis is of net benefit in patients with acute ischaemic stroke, who are younger than 80 years of age and are treated within 4·5 h of onset. The third International Stroke Trial (IST-3) sought to determine whether a wider range of patients might benefit up to 6 h from stroke onset.
In this international, multicentre, randomised, open-treatment trial, patients were allocated to 0·9 mg/kg intravenous recombinant tissue plasminogen activator (rt-PA) or to control. The primary analysis was of the proportion of patients alive and independent, as defined by an Oxford Handicap Score (OHS) of 0-2 at 6 months. The study is registered, ISRCTN25765518.
3035 patients were enrolled by 156 hospitals in 12 countries. All of these patients were included in the analyses (1515 in the rt-PA group vs 1520 in the control group), of whom 1617 (53%) were older than 80 years of age. At 6 months, 554 (37%) patients in the rt-PA group versus 534 (35%) in the control group were alive and independent (OHS 0-2; adjusted odds ratio [OR] 1·13, 95% CI 0·95-1·35, p=0·181; a non-significant absolute increase of 14/1000, 95% CI -20 to 48). An ordinal analysis showed a significant shift in OHS scores; common OR 1·27 (95% CI 1·10-1·47, p=0·001). Fatal or non-fatal symptomatic intracranial haemorrhage within 7 days occurred in 104 (7%) patients in the rt-PA group versus 16 (1%) in the control group (adjusted OR 6·94, 95% CI 4·07-11·8; absolute excess 58/1000, 95% CI 44-72). More deaths occurred within 7 days in the rt-PA group (163 [11%]) than in the control group (107 [7%], adjusted OR 1·60, 95% CI 1·22-2·08, p=0·001; absolute increase 37/1000, 95% CI 17-57), but between 7 days and 6 months there were fewer deaths in the rt-PA group than in the control group, so that by 6 months, similar numbers, in total, had died (408 [27%] in the rt-PA group vs 407 [27%] in the control group).
For the types of patient recruited in IST-3, despite the early hazards, thrombolysis within 6 h improved functional outcome. Benefit did not seem to be diminished in elderly patients.
UK Medical Research Council, Health Foundation UK, Stroke Association UK, Research Council of Norway, Arbetsmarknadens Partners Forsakringsbolag (AFA) Insurances Sweden, Swedish Heart Lung Fund, The Foundation of Marianne and Marcus Wallenberg, Polish Ministry of Science and Education, the Australian Heart Foundation, Australian National Health and Medical Research Council (NHMRC), Swiss National Research Foundation, Swiss Heart Foundation, Assessorato alla Sanita, Regione dell'Umbria, Italy, and Danube University.
在年龄小于 80 岁且发病后 4.5 小时内接受治疗的急性缺血性脑卒中患者中,溶栓治疗具有净获益。第三次国际脑卒中试验(IST-3)旨在确定更广泛的患者是否可能在发病后 6 小时内受益。
在这项国际性、多中心、随机、开放性治疗试验中,患者被分配接受 0.9mg/kg 静脉注射重组组织型纤溶酶原激活剂(rt-PA)或安慰剂。主要分析是发病 6 个月时采用牛津残疾评分(OHS)为 0-2 的存活且独立的患者比例。该研究已在 ISRCTN 注册,编号为 ISRCTN25765518。
在 12 个国家的 156 家医院共纳入 3035 名患者。所有这些患者都纳入了分析(rt-PA 组 1515 例,对照组 1520 例),其中 1617 例(53%)年龄大于 80 岁。发病 6 个月时,rt-PA 组 554 例(37%)患者存活且独立(OHS 0-2;调整后的优势比[OR]为 1.13,95%CI 0.95-1.35,p=0.181;绝对差异增加 14/1000,95%CI -20 至 48)。有序分析显示 OHS 评分有显著变化;常见 OR 为 1.27(95%CI 1.10-1.47,p=0.001)。发病后 7 天内发生致命或非致命性症状性颅内出血的患者在 rt-PA 组为 104 例(7%),对照组为 16 例(1%)(调整后的 OR 为 6.94,95%CI 4.07-11.8;绝对增加 58/1000,95%CI 44-72)。rt-PA 组发病后 7 天内死亡的患者多于对照组(163 例[11%]),rt-PA 组调整后的 OR 为 1.60,95%CI 1.22-2.08,p=0.001;绝对增加 37/1000,95%CI 17-57),但在发病后 7 天至 6 个月期间,rt-PA 组的死亡人数少于对照组,因此到 6 个月时,总死亡人数相似(rt-PA 组 408 例[27%],对照组 407 例[27%])。
对于 IST-3 招募的患者类型,尽管存在早期风险,但发病后 6 小时内溶栓治疗可改善功能结局。在老年患者中,溶栓治疗的获益似乎没有减少。
英国医学研究理事会、英国健康基金会、英国中风协会、挪威研究理事会、瑞典 AFA 保险公司、瑞典心脏肺基金会、Marianne 和 Marcus Wallenberg 基金会、波兰科学和教育部、澳大利亚心脏基金会、澳大利亚国家健康与医学研究理事会(NHMRC)、瑞士国家研究基金会、瑞士心脏基金会、乌姆布里亚地区评估署、意大利和多瑙河大学。