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首页> 外文期刊>International journal of stroke: official journal of the International Stroke Society >Applicability of ENCHANTED trial results to current acute ischemic stroke patients eligible for intravenous thrombolysis in England and Wales: Comparison with the Sentinel Stroke National Audit Programme registry
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Applicability of ENCHANTED trial results to current acute ischemic stroke patients eligible for intravenous thrombolysis in England and Wales: Comparison with the Sentinel Stroke National Audit Programme registry

机译:魔法审判结果适用于当前急性缺血性脑卒中患者,符合英格兰和威尔士静脉溶栓的患者:与哨兵中风国家审计计划登记处比较

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Background: Randomized controlled trials provide high-level evidence, but the necessity to include selected patients may limit the generalisability of their results. Methods: Comparisons were made of baseline and outcome data between patients with acute ischemic stroke (AIS) recruited into the alteplase-dose arm of the international, multi-center, Enhanced Control of Hypertension and Thrombolysis Stroke study (ENCHANTED) in the United Kingdom (UK), and alteplase-treated AIS patients registered in the UK Sentinel Stroke National Audit Programme (SSNAP) registry, over the study period June 2012 to October 2015. Results: There were 770 AIS patients (41.2% female; mean age 72 years) included in ENCHANTED at sites in England and Wales, which was 19.5% of alteplase-treated AIS patients registered in the SSNAP registry. Trial participants were significantly older, had lower baseline neurological severity, less likely Asian, and had more premorbid symptoms, hypertension and atrial fibrillation. Although ENCHANTED participants had higher rates of symptomatic intracerebral hemorrhage than those in SSNAP, there were no differences in onset-to-treatment time, levels of disability (assessed by the modified Rankin scale) at hospital discharge, and mortality over 90 days between groups. Conclusions: Despite the high level of participation, equipoise over the dose of alteplase among UK clinician investigators favored the inclusion of older, frailer, milder AIS patients in the ENCHANTED trial.
机译:背景:随机对照试验提供高级别的证据,但包括所选患者的必要性可能会限制其结果的可恒大性。方法:对急性缺血性卒中(AIS)患者的基线和结果数据进行比较,募集到国际,多中心,增强的高血压和溶栓治疗中的高血压和溶栓卒中研究(迷惑)的患者(英国)和Alteplase治疗的AIS患者在英国Sentinel中风国家审计计划(SSNAP)注册处,2012年6月至2015年10月。结果:770名AIS患者(41.2%的女性;平均年龄72岁)包括在英格兰和威尔士的遗址迷人,这是在SSNAP登记处注册的Alteplase治疗的AIS患者的19.5%。试验参与者明显老化,基线神经系统严重程度降低,亚洲不太可能发生前膜症状,高血压和心房颤动。虽然魔法参与者的症状性脑出血率高于SSNAP中的速率较高,但在医院出院的医院出院时,疾病的疾病水平(改良Rankin规模评估)没有差异,并且在组之间的死亡率超过90天。结论:尽管参与水平高,但英国临床医生调查人员中的Alteplase剂量的等量有利于纳入迷人的试验中的较老年人,较温和的AIS患者。

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