首页> 外文期刊>The Lancet >The benefits and harms of intravenous thrombolysis with recombinant tissue plasminogen activator within 6 h of acute ischaemic stroke (the third international stroke trial [IST-3]): A randomised controlled trial
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The benefits and harms of intravenous thrombolysis with recombinant tissue plasminogen activator within 6 h of acute ischaemic stroke (the third international stroke trial [IST-3]): A randomised controlled trial

机译:重组组织纤溶酶原激活剂在急性缺血性中风后6小时内进行静脉溶栓治疗的利弊(第三项国际中风试验[IST-3]):一项随机对照试验

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Background Thrombolysis is of net benefi t 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 benefi t up to 6 h from stroke onset. Methods 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 defi ned by an Oxford Handicap Score (OHS) of 0-2 at 6 months. The study is registered, ISRCTN25765518. Findings 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-signifi cant absolute increase of 14/1000, 95% CI-20 to 48). An ordinal analysis showed a signifi cant 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). Interpretation For the types of patient recruited in IST-3, despite the early hazards, thrombolysis within 6 h improved functional outcome. Benefi t did not seem to be diminished in elderly patients. Funding 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.
机译:背景溶栓是急性缺血性卒中患者的净收益,这些患者年龄小于80岁,且在发病4.5小时内得到治疗。第三次国际中风试验(IST-3)试图确定在中风发作后6小时内是否会有更多患者受益。方法在这项国际性,多中心,随机,开放治疗试验中,将患者分配至0.9 mg / kg静脉内重组组织纤溶酶原激活剂(rt-PA)或进行对照。主要分析是存活和独立患者的比例,这在6个月时以牛津残障评分(OHS)为0-2进行定义。该研究已注册,ISRCTN25765518。调查结果12个国家的156家医院招募了3035名患者。所有这些患者均被纳入分析(rt-PA组为1515,对照组为1520),其中1617岁(53%)年龄在80岁以上。在6个月时,rt-PA组的554名患者(37%)与对照组的534名患者(35%)存活且独立(OHS 0-2;调整后的优势比[OR] 1.13,95%CI 0.95-1.35) ,p = 0.181;无显着绝对增加14 / 1000,95%CI-20增至48)。序数分析显示OHS分数有显着变化。普通OR 1.27(95%CI 1.10-1.47,p = 0.001)。 rt-PA组104例(7%)患者在7天内发生致命或非致命的症状性颅内出血,而对照组则为16例(1%)(校正后的OR 6.94,95%CI 4.07-11.8;绝对过量58 / 1000,95%CI 44-72)。 rt-PA组在7天内死亡的发生率(163 [11%])比对照组(107 [7%])高,校正后的OR为1.60,95%CI为1.22-2.08,p = 0.001;绝对升高37 / 1000,95%CI 17-57),但是rt-PA组的死亡人数比对照组少,因此到6个月时,死亡总数相似(408 [ rt-PA组为27%],而对照组为407 [27%]。解释对于IST-3中招募的患者类型,尽管有早期危险,但6小时内溶栓可改善功能结局。老年患者的获益似乎并未减少。资助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Arbetsmarknadens合作伙伴Forsakringsbolag(AFA)保险,瑞典心肺基金会,玛丽安和马库斯·沃伦伯格基金会,波兰科学和教育部,澳大利亚心脏基金会,澳大利亚国家卫生和医学研究委员会(NHMRC),瑞士国家研究基金会,瑞士心脏基金会,意大利安布利亚大区地区的Assessorato alla Sanita和多瑙河大学。

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