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用于晚期窗内血栓切除术患者选择的关键随机对照试验的影像学标准。

Imaging criteria across pivotal randomized controlled trials for late window thrombectomy patient selection.

作者信息

Menon Bijoy K, Ospel Johanna Maria, McTaggart Ryan A, Nogueira Raul G, Demchuk Andrew M, Poppe Alexandre, Rempel Jeremy L, Zerna Charlotte, Joshi Manish, Almekhlafi Mohammed A, Field Thalia S, Dowlatshahi Dariush, van Adel Brian Anthony, Sauvageau Eric, Tarpley Jason, Moreira Tiago, Bang Oh Young, Heck Don, Psychogios Marios N, Tymianski Michael, Hill Michael D, Goyal Mayank

机构信息

Calgary Stroke Program, University of Calgary, Calgary, Alberta, Canada.

Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.

出版信息

J Neurointerv Surg. 2020 Nov 25. doi: 10.1136/neurintsurg-2020-016902.

Abstract

BACKGROUND

The DAWN and DEFUSE-3 trials showed the benefit of endovascular treatment (EVT) in acute ischemic stroke patients presenting beyond 6 hours from last known well (LKW) and selected by perfusion imaging criteria. The ESCAPE NA1-trial selected patients based on non-contrast CT (NCCT) Alberta Stroke Program Early CT Score (ASPECTS) and multiphase CT angiography (CTA) collateral status. This study compares baseline characteristics, workflow, and outcomes in the EVT arms of DAWN and DEFUSE-3 with late-window patients from the EVT-only arm of ESCAPE-NA1.

METHODS

Aggregate data on baseline characteristics, workflow, reperfusion quality, final infarct volume, and clinical outcomes (modified Rankin Score [mRS] at 90 days) in subjects enrolled in the DAWN and DEFUSE-3 EVT arms were compared with similar data from the ESCAPE-NA1 control arm (EVT-only arm) presenting beyond 6 hours from LKW using descriptive statistics.

RESULTS

Baseline characteristics among late-window patients in the ESCAPE NA1 trial were similar to those in the DAWN and DEFUSE-3 EVT arms. Median time from LKW-to-puncture in subjects enrolled in the ESCAPE NA1 trial was 9 hrs (IQR: 7.5-11 hours) when compared with DAWN (n=107; 12.8 hours, IQR: 10.6-16.7 hours) and DEFUSE-3 (n=92; 11.5 hours, IQR: 9.2-12.8 hours). Median post-treatment infarct-volume was largest in the ESCAPE NA1-patients (47 mL [IQR: 19-146] vs median 8 mL [IQR: 0-48] in the DAWN group and 35 mL [IQR: 18-82] in DEFUSE-3), while % mRS 0-2 at 90 days were similar across the three trials (ESCAPE NA1: 50/111 [45%], DAWN: 52/107 [49%], DEFUSE-3: 41/92 [45%]).

CONCLUSION

Patients enrolled beyond 6 hours from LKW in the ESCAPE-NA1 trial based on NCCT-ASPECTS and mCTA had similar clinical outcomes when compared with patients selected by perfusion imaging in the DAWN and DEFUSE-3 trials.

摘要

背景

DAWN和DEFUSE - 3试验显示,对于最后看起来正常(LKW)时间超过6小时且根据灌注成像标准选择的急性缺血性卒中患者,血管内治疗(EVT)有益。ESCAPE NA1试验根据非增强CT(NCCT)阿尔伯塔卒中项目早期CT评分(ASPECTS)和多期CT血管造影(CTA)侧支循环状态选择患者。本研究比较了DAWN和DEFUSE - 3试验中EVT组的基线特征、工作流程和结局与ESCAPE - NA1试验仅EVT组的晚期窗口患者。

方法

使用描述性统计方法,将DAWN和DEFUSE - 3试验EVT组患者的基线特征、工作流程、再灌注质量、最终梗死体积和临床结局(90天时改良Rankin评分[mRS])的汇总数据与ESCAPE - NA1试验对照组(仅EVT组)中LKW时间超过6小时的类似数据进行比较。

结果

ESCAPE NA1试验晚期窗口患者的基线特征与DAWN和DEFUSE - 3试验EVT组相似。ESCAPE NA1试验患者从LKW到穿刺的中位时间为9小时(IQR:7.5 - 11小时),而DAWN试验为(n = 107;12.8小时,IQR:10.6 - 16.7小时),DEFUSE - 3试验为(n = 92;11.5小时,IQR:9.2 - 12.8小时)。ESCAPE NA1试验患者治疗后的梗死体积中位数最大(47 mL [IQR:19 - 146],而DAWN组中位数为8 mL [IQR:0 - 48],DEFUSE - 3组为35 mL [IQR:18 - 82]),而90天时mRS 0 - 2的比例在三项试验中相似(ESCAPE NA1:50/111 [45%],DAWN:52/107 [49%],DEFUSE - 3:41/92 [45%])。

结论

与DAWN和DEFUSE - 3试验中通过灌注成像选择的患者相比,ESCAPE - NA1试验中基于NCCT - ASPECTS和mCTA在LKW时间超过6小时后纳入的患者具有相似的临床结局。

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