Majoie Charles B, Cavalcante Fabiano, Gralla Jan, Yang Pengfei, Kaesmacher Johannes, Treurniet Kilian M, Kappelhof Manon, Yan Bernard, Suzuki Kentaro, Zhang Yongwei, Li Fengli, Morimoto Masafumi, Zhang Lei, Miao Zhongrong, Rinkel Leon A, Huang Jiacheng, Otsuka Toshiaki, Wang Shouchun, Davis Stephen, Cognard Christophe, Hong Bo, Coutinho Jonathan M, Song Jiaxing, Chen Wenhuo, Emmer Bart J, Eker Omer, Zhang Liyong, Dobrocky Tomas, Nguyen Huy-Thang, Bush Steven, Peng Ya, LeCouffe Natalie E, Takeuchi Masataka, Han Hongxing, Matsumaru Yuji, Strbian Daniel, Lingsma Hester F, Nieboer Daan, Yang Qingwu, Meinel Thomas, Mitchell Peter, Kimura Kazumi, Zi Wenjie, Nogueira Raul G, Liu Jianmin, Roos Yvo B, Fischer Urs
Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, Netherlands.
Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, Netherlands.
Lancet. 2023 Sep 16;402(10406):965-974. doi: 10.1016/S0140-6736(23)01142-X. Epub 2023 Aug 25.
Intravenous thrombolysis is recommended before endovascular treatment, but its value has been questioned in patients who are admitted directly to centres capable of endovascular treatment. Existing randomised controlled trials have indicated non-inferiority of endovascular treatment alone or have been statistically inconclusive. We formed the Improving Reperfusion Strategies in Acute Ischaemic Stroke collaboration to assess non-inferiority of endovascular treatment alone versus intravenous thrombolysis plus endovascular treatment.
We conducted a systematic review and individual participant data meta-analysis to establish non-inferiority of endovascular treatment alone versus intravenous thrombolysis plus endovascular treatment. We searched PubMed and MEDLINE with the terms "stroke", "endovascular treatment", "intravenous thrombolysis", and synonyms for articles published from database inception to March 9, 2023. We included randomised controlled trials on the topic of interest, without language restrictions. Authors of the identified trials agreed to take part, and individual participant data were provided by the principal investigators of the respective trials and collated centrally by the collaborators. Our primary outcome was the 90-day modified Rankin Scale (mRS) score. Non-inferiority of endovascular treatment alone was assessed using a lower boundary of 0·82 for the 95% CI around the adjusted common odds ratio (acOR) for shift towards improved outcome (analogous to 5% absolute difference in functional independence) with ordinal regression. We used mixed-effects models for all analyses. This study is registered with PROSPERO, CRD42023411986.
We identified 1081 studies, and six studies (n=2313; 1153 participants randomly assigned to receive endovascular treatment alone and 1160 randomly assigned to receive intravenous thrombolysis and endovascular treatment) were eligible for analysis. The risk of bias of the included studies was low to moderate. Variability between studies was small, and mainly related to the choice and dose of the thrombolytic drug and country of execution. The median mRS score at 90 days was 3 (IQR 1-5) for participants who received endovascular treatment alone and 2 (1-4) for participants who received intravenous thrombolysis plus endovascular treatment (acOR 0·89, 95% CI 0·76-1·04). Any intracranial haemorrhage (0·82, 0·68-0·99) occurred less frequently with endovascular treatment alone than with intravenous thrombolysis plus endovascular treatment. Symptomatic intracranial haemorrhage and mortality rates did not differ significantly.
We did not establish non-inferiority of endovascular treatment alone compared with intravenous thrombolysis plus endovascular treatment in patients presenting directly at endovascular treatment centres. Further research could focus on cost-effectiveness analysis and on individualised decisions when patient characteristics, medication shortages, or delays are expected to offset a potential benefit of administering intravenous thrombolysis before endovascular treatment.
Stryker and Amsterdam University Medical Centers, University of Amsterdam.
血管内治疗前推荐进行静脉溶栓,但对于直接入住具备血管内治疗能力中心的患者,其价值受到质疑。现有的随机对照试验表明单纯血管内治疗并不逊色,或在统计学上尚无定论。我们组建了急性缺血性卒中改善再灌注策略协作组,以评估单纯血管内治疗与静脉溶栓联合血管内治疗相比的非劣效性。
我们进行了一项系统评价和个体参与者数据荟萃分析,以确定单纯血管内治疗与静脉溶栓联合血管内治疗相比的非劣效性。我们在PubMed和MEDLINE上检索了从数据库建立至2023年3月9日发表的文章,检索词为“卒中”“血管内治疗”“静脉溶栓”及其同义词。我们纳入了感兴趣主题的随机对照试验,无语言限制。已识别试验的作者同意参与,个体参与者数据由各试验的主要研究者提供,并由协作组集中整理。我们的主要结局是90天改良Rankin量表(mRS)评分。使用序贯回归分析,针对改善结局的调整共同优势比(acOR)的95%CI下限为0.82,评估单纯血管内治疗的非劣效性(类似于功能独立性方面5%的绝对差异)。我们对所有分析均使用混合效应模型。本研究已在国际前瞻性系统评价注册库(PROSPERO)注册,注册号为CRD42023411986。
我们识别出1081项研究,6项研究(n = 2313;1153名参与者被随机分配接受单纯血管内治疗,1160名参与者被随机分配接受静脉溶栓联合血管内治疗)符合分析条件。纳入研究的偏倚风险为低到中度。研究间的变异性较小,主要与溶栓药物的选择和剂量以及实施国家有关。接受单纯血管内治疗的参与者90天mRS评分中位数为3(IQR 1 - 5),接受静脉溶栓联合血管内治疗的参与者为2(1 - 4)(acOR 0.89,95%CI 0.76 - 1.04)。单纯血管内治疗发生任何颅内出血的频率(0.82,0.68 - 0.99)低于静脉溶栓联合血管内治疗。症状性颅内出血和死亡率无显著差异。
在直接就诊于血管内治疗中心的患者中,我们未证实单纯血管内治疗与静脉溶栓联合血管内治疗相比具有非劣效性。进一步的研究可聚焦于成本效益分析,以及在预期患者特征、药物短缺或延误将抵消血管内治疗前静脉溶栓潜在益处时的个体化决策。
史赛克公司和阿姆斯特丹大学医学中心、阿姆斯特丹大学