Endovascular therapy for acute vertebrobasilar occlusion (VERITAS): a systematic review and individual patient data meta-analysis

Raul G Nogueira, Tudor G Jovin, Xinfeng Liu, Wei Hu, Lucianne C M Langezaal, Chuanhui Li, Qiliang Dai, Chunrong Tao, Francisco J A Mont'Alverne, Xunming Ji, Rui Liu, Rui Li, Diederik W J Dippel, Chuanjie Wu, Wusheng Zhu, Pengfei Xu, Wim H van Zwam, Longfei Wu, Chao Zhang, Patrik Michel, Wouter J Schonewille
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Abstract

Background

Trials of endovascular therapy for basilar artery occlusion, including vertebral occlusion extending into the basilar artery, have shown inconsistent results. We aimed to pool data to estimate safety and efficacy and to explore the benefit across pre-specified subgroups through individual patient data meta-analysis.

Methods

VERITAS was a systematic review and meta-analysis that pooled patient-level data from trials that recruited patients with vertebrobasilar ischaemic stroke who were randomly assigned to treatment with either endovascular therapy or standard medical treatment alone. We included studies done between Jan 1, 2010, and Sept 1, 2023. The primary outcome was 90-day favourable functional status (modified Rankin Scale [mRS] score 0–3, with a score of 3 indicating moderate disability). Safety outcomes were symptomatic intracranial haemorrhage and 90-day mortality.

Findings

We screened 934 titles and abstracts. Of these, seven (<1%) full texts were screened. We included four trials (ATTENTION, BAOCHE, BASICS, and BEST). The pooled data included 988 patients (556 [56%] in the intervention groups and 432 [44%] in the control groups; median age 67 years [IQR 58–74]; 686 (69%) were male and 302 (31%) were female). 904 (91%) patients were randomly assigned within 12 h of estimated stroke onset. Three RCTs were done in a Chinese population and one included European and Brazilian patients. The proportion of patients achieving favourable functional status was higher in the endovascular therapy than control group (90-day mRS score 0–3 in 251 [45%] participants vs 128 [30%]; adjusted common odds ratio 2·41 [95% CI 1·78–3·26]; p<0·0001). Endovascular therapy led to an increase in functional independence (mRS score 0–2 in 194 [35%] participants vs 89 [21%]; 2·52 [1·82–3·48]; p<0·0001) as well as a reduction in both the degree of overall disability (2·09 [1·61–2·71]; p<0·0001) and mortality (198 [36%] of 556 patients vs 196 [45%] of 432; 0·60 [0·45–0·80]; p<0·0001) at 90 days, despite higher rates of symptomatic intracranial haemorrhage (30 [5%] of 548 vs two [<1%] of 413; 11·98 [2·82–50·81]; p<0·0001). Heterogeneity of treatment effect was noted for baseline stroke severity (uncertain effect in baseline National Institutes of Health Stroke Scale <10) and occlusion site (greater benefit with more proximal occlusions) but not across subgroups defined by age, sex, baseline posterior circulation Alberta Stroke Program Early CT Score, presence of atrial fibrillation or intracranial atherosclerotic disease, and time from onset to imaging.

Interpretation

VERITAS supports the robust benefit of endovascular therapy in patients with vertebrobasilar artery occlusion with moderate to severe symptoms, with approximately 2·5-times increased likelihood of achieving a favourable functional outcome. Despite a significant increase in symptomatic intracranial haemorrhage risk, endovascular therapy for vertebrobasilar artery occlusion was associated with a significant reduction in both overall disability and mortality. Although the benefit of endovascular therapy remains uncertain for patients vertebrobasilar artery occlusion presenting with mild stroke severity and extensive infarcts on neuroimaging, we found a significant clinical benefit across a range of patients with vertebrobasilar artery occlusion.

Funding

None.
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血管内治疗急性椎基底动脉闭塞(VERITAS):一项系统综述和个体患者数据荟萃分析
背景:血管内治疗基底动脉闭塞的试验,包括椎体闭塞延伸到基底动脉,显示出不一致的结果。我们的目的是汇集数据来评估安全性和有效性,并通过个体患者数据荟萃分析来探索预先指定的亚组的益处。方法:veritas是一项系统评价和荟萃分析,汇集了来自椎基底动脉缺血性卒中患者的试验数据,这些患者被随机分配到血管内治疗或单独标准药物治疗组。我们纳入了2010年1月1日至2023年9月1日之间完成的研究。主要终点为90天的良好功能状态(改良Rankin量表[mRS]评分0-3分,3分表示中度残疾)。安全性结果为症状性颅内出血和90天死亡率。我们筛选了934篇题目和摘要。其中,筛选了7篇(1%)全文。我们纳入了四个试验(ATTENTION、BAOCHE、BASICS和BEST)。合并数据包括988例患者,其中干预组556例(56%),对照组432例(44%);中位年龄67岁[IQR 58-74];男性686例(69%),女性302例(31%)。904例(91%)患者在估计卒中发作后12小时内被随机分配。在中国人群中进行了三项随机对照试验,其中一项包括欧洲和巴西患者。在血管内治疗中获得良好功能状态的患者比例高于对照组(251例[45%]对128例[30%]的90天mRS评分为0-3);校正常见优势比2.41 [95% CI 1.78 ~ 3.26];术;0·0001)。血管内治疗导致功能独立性增加(mRS评分0-2分194例(35%)vs 89例(21%);2·52[1·82 - 3·48];P< 0.0001)以及整体残疾程度的降低(2.09[1.61 - 2·71];P< 0.0001)和死亡率(556例患者中198例[36%]vs 432例患者中196例[45%];[0·45-0·0·80);尽管症状性颅内出血的发生率较高(548例中有30例[5%]vs 413例中有2例[<;1%];11·98 (2 * 82 - 50 * 81);术;0·0001)。基线脑卒中严重程度(基线美国国立卫生研究院卒中量表10的影响不确定)和闭塞部位(近端闭塞程度越高获益越大)均存在治疗效果的异质性,但不同亚组间的治疗效果不存在异质性,这些亚组由年龄、性别、基线后循环阿尔伯塔卒中计划早期CT评分、房颤或颅内动脉粥样硬化疾病的存在以及从发病到成像的时间定义。veritas支持血管内治疗对中度至重度椎基底动脉闭塞患者的强大益处,实现良好功能结果的可能性增加约2.5倍。尽管症状性颅内出血风险显著增加,但椎基底动脉闭塞的血管内治疗与总体残疾率和死亡率的显著降低相关。尽管血管内治疗对于表现为轻度脑卒中严重程度和神经影像学上广泛梗死的椎基底动脉闭塞患者的益处尚不确定,但我们发现椎基底动脉闭塞患者的一系列临床获益显著。
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