B.1 使用 EVT 进行急性脑卒中再灌注的 CT 或 MRI 方案(COMPARE):一项国际回顾性队列研究

C Ducroux, W Boisseau, R Fahed, G Stotts, M Kyheng, J Labreuche, D. Roy, B Lapergue, A. Poppe
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引用次数: 0

摘要

背景:急性缺血性脑卒中(AIS)患者可通过计算机断层扫描(CT-CTA)或脑磁成像(MRI)选择接受再灌注治疗。本研究旨在比较 CT 和 MRI 作为接受 EVT 的 AIS 患者的主要成像方式。方法:从两个前瞻性多中心EVT队列中提取了2018年1月至2021年1月期间AIS患者的数据:法国的ETIS登记(MRI)和加拿大的OPTIMISE登记(CT)。我们收集了人口统计学、手术数据和结果。我们评估了合格成像(CT 与 MRI)与时间指标和功能结果的关联。结果:从 2018 年 1 月到 2021 年 1 月,4059 名通过 MRI 筛选的患者和 1324 名通过 CT 筛选的患者被纳入研究。两组患者的人口统计学特征相似。核磁共振成像组从成像到动脉穿刺的中位时间比CT组长37分钟。与 MRI 选择的患者相比,CT 选择的患者 90 天功能预后(mRS 0-2)更佳(48.5% vs 44.4%;调整 OR (aOR),1.54,95%CI 1.31 至 1.80,p<0.001)。结论接受EVT治疗的AIS患者如果是通过MRI而非CT选择的,那么成像到动脉穿刺的延迟时间更长,90天后的功能预后更差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
B.1 CT Or MRI protocol for acute stroke reperfusion with EVT (COMPARE): an international retrospective cohort study
Background: Patients with an acute ischemic stroke (AIS) are selected to receive reperfusion therapy using either computed tomography (CT-CTA) or magnetic brain imaging (MRI). The aim of this study was to compare CT and MRI as the primary imaging modality for AIS patients undergoing EVT. Methods: Data for AIS patients between January 2018 and January 2021 were extracted from two prospective multicenter EVT cohorts: the ETIS registry in France (MRI) and the OPTIMISE registry in Canada (CT). Demographics, procedural data and outcomes were collected. We assessed the association of qualifying imaging (CT vs. MRI) with time metrics and functional outcome. Results: From January 2018 to January 2021, 4059 patients selected by MRI and 1324 patients selected by CT were included in the study. Demographics were similar between the two groups. The median imaging-to-arterial puncture time was 37 minutes longer in the MRI group. Patients selected by CT had more favorable 90-day functional outcomes (mRS 0-2) as compared to patients selected by MRI (48.5% vs 44.4%; adjusted OR (aOR), 1.54, 95%CI 1.31 to 1.80, p<0.001). Conclusions: Patients with AIS undergoing EVT who were selected with MRI as opposed to CT had longer imaging-to-arterial-puncture delays and worse functional outcomes at 90 days.
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