Department of Radiology and Nuclear Medicine, Leiden University Medical Center, the Netherlands (A.C.G.M.v.E.).
Department of Neurology, Haaglanden Medical Center (HMC), The Hague, the Netherlands (I.v.d.W.).
Stroke. 2021 Mar;52(3):781-788. doi: 10.1161/STROKEAHA.120.030210. Epub 2021 Feb 22.
Multiple trials have shown the efficacy and safety of endovascular therapy (EVT) of acute ischemic stroke in adults. Trials in children are lacking and only case reports and case series exist. However, the long-term outcome of children with acute ischemic stroke can be devastating with significant mortality and morbidity. In this study, we describe the safety and efficacy of EVT in children with anterior circulation acute ischemic stroke who were included in the MR CLEAN Registry (Multicenter Randomized Clinical Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands).
Patients under the age of 18 years who were treated with EVT for acute ischemic stroke between March 2014 and July 2017 were retrospectively reviewed up to 6 months after EVT. Nine children, aged 13 months to 16 years (median 14 years, interquartile range, 3-15 years), underwent EVT. Stroke cause was thromboembolism in children with end-stage heart failure on left ventricular assist device (4 of these 9 cases). Median time from onset to imaging was 133 minutes. Four children received intravenous alteplase before EVT, with median onset to needle time of 165 minutes. In all but one patient, EVT was technically successful. No major periprocedural complications occurred.
At 24 hours after EVT, 3 children completely recovered and 4 children showed partial recovery (median National Institutes of Health Stroke Scale, 3.5), whereas 2 patients on left ventricular assist device died within the first week due to the occurrence of multiple strokes. One patient on left ventricular assist device developed a fatal massive intracranial hemorrhage and another child died due to left ventricular assist device-related complications. Among the 5 stroke survivors, all had a favorable outcome (modified Rankin Scale score, 0-2) at 6 months follow-up.
EVT of children with acute ischemic stroke seems safe and feasible. However, these findings should be interpreted with caution as more and larger studies are needed to clarify the trade-off between risks and benefits of this treatment.
多项试验已经证明了血管内治疗(EVT)对成人急性缺血性脑卒中的疗效和安全性。但儿童的相关试验较少,仅有病例报告和病例系列研究。然而,儿童急性缺血性脑卒中的长期预后可能是灾难性的,死亡率和发病率都很高。在本研究中,我们描述了荷兰 MR CLEAN 登记处(多中心急性缺血性脑卒中血管内治疗随机临床试验)中纳入的急性前循环缺血性脑卒中儿童接受 EVT 治疗的安全性和疗效。
回顾性分析了 2014 年 3 月至 2017 年 7 月期间因急性缺血性脑卒中接受 EVT 治疗的年龄小于 18 岁的患者,随访时间最长为 EVT 后 6 个月。9 名年龄在 13 个月至 16 岁(中位数 14 岁,四分位距 3-15 岁)的儿童接受了 EVT 治疗。9 例患儿中,4 例因左心室辅助装置(LVAD)终末期心力衰竭导致血栓栓塞性脑卒中(其中 4 例)。发病至影像学检查的中位数时间为 133 分钟。4 例患儿在 EVT 前接受了静脉注射阿替普酶,中位发病至针时间为 165 分钟。除 1 例患者外,其余患者 EVT 均达到技术成功。没有发生重大围手术期并发症。
EVT 后 24 小时,3 名患儿完全恢复,4 名患儿部分恢复(中位数国立卫生研究院卒中量表评分 3.5),而 2 名 LVAD 患儿在第一周内因发生多次脑卒中死亡。1 名 LVAD 患儿发生致命性大量颅内出血,另 1 名患儿因 LVAD 相关并发症死亡。在 5 名存活的脑卒中患儿中,所有患儿在 6 个月随访时的结局良好(改良 Rankin 量表评分 0-2)。
EVT 治疗儿童急性缺血性脑卒中似乎是安全可行的。然而,由于需要更多和更大的研究来阐明这种治疗方法的风险与获益之间的权衡,因此这些发现应谨慎解释。