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Alteplase and ischaemic stroke: have new reviews of old data helped?

机译:阿替普酶和缺血性中风:对旧数据的新评论有帮助吗?

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Background Thrombolysis for stroke is still not widely used as current recommendations restrict treatment to selected patients. In general, these are patients who can be assessed quickly by specialised stroke teams, have intracranial haemorrhage excluded by appropriate brain imaging, and are treated with alteplase (recombinant tissue plasminogen activator; rt-PA) within 3 h of symptom onset. There is, however, still much debate regarding the scope of treatment and the reorganisation of services required to support an effective service.Recent developments Two recent publications have helped clarify some issues. The first was an individual-patient data meta-analysis of the alteplase trials. These analyses suggest treatment effects beyond the usual 3 h time window, but other than time to treatment no other factors influenced the effects of treatment. The second publication was a reanalysis of the original National Institute of Neurological Disorders and Stroke (NINDS) alteplase trial, done after criticism of the original study. The reanalysis confirmed that there was significant baseline imbalance of stroke severity between treatment and control groups in the NINDS trial, but established that this did not materially affect the positive results of the trial. However, the recording of blood pressure in the study was found to be inconsistent and therefore unsuitable for reanalysis. The previously published data on recommendations for blood-pressure control, arising from the NINDS trial, needs to be reconsidered in this light. Both studies included too few patients to provide reliable data on which clinical and radiological features influence the response to alteplase.
机译:背景技术中风的溶栓治疗仍未得到广泛应用,因为当前的建议将治疗限于特定患者。通常,这些患者可以通过专门的中风团队快速评估,通过适当的脑成像排除颅内出血,并在症状发作后3小时内用阿替普酶(重组组织纤溶酶原激活物; rt-PA)治疗。但是,关于有效范围所需要的治疗范围和服务重组,仍然存在很多争论。最近的发展最近有两本出版物帮助阐明了一些问题。首先是阿替普酶试验的个体患者数据荟萃分析。这些分析表明治疗效果超出了通常的3小时时间范围,但是除了治疗时间以外,没有其他因素影响治疗效果。第二份出版物是对原始的美国国家神经疾病和中风研究所(NINDS)阿替普酶试验的重新分析,该试验是在对原始研究提出批评之后进行的。重新分析证实,在NINDS试验中,治疗组和对照组之间存在严重的基线卒中严重性失衡,但确定这不会对试验的阳性结果产生实质性影响。但是,研究中发现的血压记录不一致,因此不适合进行重新分析。有鉴于此,需要重新考虑之前发表的有关NINDS试验的血压控制建议数据。两项研究都包括很少的患者,无法提供有关临床和放射学特征影响对阿替普酶反应的可靠数据。

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