Outcomes in acute carotid-related stroke eligible for mechanical reperfusion: SAFEGUARD-STROKE Registry.

Lukasz Tekieli, Karolina Dzierwa, Iris Q Grunwald, Adam Mazurek, Malgorzata Urbanczyk-Zawadzka, Lukasz Wiewiorka, R Pawel Banys, Wladyslaw Dabrowski, Anna Podlasek, Ewa Weglarz, Justyna Stefaniak, Rafal T Nizankowski, Piotr Musialek
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引用次数: 0

Abstract

Background: Carotid-related strokes (CRS) are largely unresponsive to intravenous thrombolysis and are often large and disabling. Little is known about contemporary CRS referral pathways and proportion of eligible patients who receive emergency mechanical reperfusion (EMR).

Methods: Referral pathways, serial imaging, treatment data, and neurologic outcomes were evaluated in consecutive CRS patients presenting over 18 months in catchment area of a major carotid disease referral center with proximal-protected CAS expertise, on-site neurology, and stroke thrombectomy capability (Acute Stroke of CArotid Artery Bifurcation Origin Treated With Use oF the MicronEt-covered CGUARD Stent - SAFEGUARD-STROKE Registry; companion to SAFEGUARD-STROKE Study NCT05195658).

Results: Of 101 EMR-eligible patients (31% i.v.-thrombolyzed, 39.5% women, age 39-89 years, 94.1% ASPECTS 9-10, 90.1% pre-stroke mRS 0-1), 57 (56.4%) were EMR-referred. Referrals were either endovascular (Comprehensive Stroke Centre, CSC, 21.0%; Stroke Thrombectomy-Capable CAS Centre, STCC, 70.2%) or to vascular surgery (VS, 1.8%), with >1 referral attempt in 7.0% patients (CSC/VS or VS/CSC or CSC/VS/STCC). Baseline clinical and imaging characteristics were not different between EMR-treated and EMR-untreated patients. EMR was delivered to 42.6% eligible patients (emergency carotid surgery 0%; STCC rejections 0%). On multivariable analysis, non-tandem CRS was a predictor of not getting referred for EMR (OR 0.36; 95%CI 0.14-0.93, P=0.03). Ninety-day neurologic status was profoundly better in EMR-treated patients; mRS 0-2 (83.7% vs. 34.5%); mRS 3-5 (11.6% vs. 53.4%), mRS 6 (4.6% vs. 12.1%); P<0.001 for all.

Conclusions: EMR-treatment substantially improves CRS neurologic outcomes but only a minority of EMR-eligible patients receive EMR. To increase the likelihood of brain-saving treatment, EMR-eligible stroke referral and management pathways, including those for CSC/VS-rejected patients, should involve stroke thrombectomy-capable centres with endovascular carotid treatment expertise.

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符合机械再灌注条件的急性颈动脉相关中风患者的预后:SAFEGUARD-STROKE 登记。
背景:颈动脉相关性脑卒中(CRS)对静脉溶栓大多无反应,而且往往是大面积的致残性脑卒中。目前,人们对 CRS 的转诊途径以及符合条件的患者接受急诊机械再灌注(EMR)的比例知之甚少:方法:在一个拥有近端保护 CAS 专业技术、现场神经内科和卒中血栓切除术能力的主要颈动脉疾病转诊中心的覆盖区内,对 18 个月内连续出现的 CRS 患者的转诊途径、连续影像学检查、治疗数据和神经系统结果进行了评估(使用微粒覆盖的 CGUARD 支架治疗的急性颈动脉分叉源性卒中 - SAFEGUARD-STROKE 登记;SAFEGUARD-STROKE 研究 NCT05195658 的配套研究)。结果:101例符合EMR条件的患者(31%静脉溶栓,39.5%女性,年龄39-89岁,94.1% ASPECTS 9-10,90.1%卒中前mRS 0-1)中,57例(56.4%)为EMR转诊患者。转诊为血管内治疗(综合卒中中心,CSC,21.0%;卒中血栓切除CAS中心,STCC,70.2%)或血管外科治疗(VS,1.8%),其中7.0%的患者转诊次数超过1次(CSC/VS或VS/CSC或CSC/VS/STCC)。接受EMR治疗和未接受EMR治疗的患者的基线临床和成像特征没有差异。42.6%的合格患者接受了EMR治疗(颈动脉急诊手术为0%;STCC拒绝率为0%)。在多变量分析中,非串联 CRS 是未转诊 EMR 的预测因素(OR 0.36;95%CI 0.14-0.93,P=0.03)。接受过EMR治疗的患者90天后的神经系统状况明显好转:mRS 0-2 (83.7% vs. 34.5%);mRS 3-5 (11.6% vs. 53.4%);mRS 6 (4.6% vs. 12.1%);PC结论:EMR治疗可显著改善CRS的神经功能预后,但只有少数符合EMR条件的患者接受了EMR治疗。为提高救脑治疗的可能性,符合 EMR 条件的卒中转诊和管理路径(包括 CSC/VS 被拒患者的转诊和管理路径)应包括具备卒中血栓切除术能力、拥有颈动脉血管内治疗专业技术的中心。
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