Predictors of Acute Neurological Worsening after Endovascular Thrombectomy.

Q1 Medicine Interventional Neurology Pub Date : 2020-01-01 Epub Date: 2019-06-18 DOI:10.1159/000499973
Jazba Soomro, Liang Zhu, Sean I Savitz, Amrou Sarraj
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引用次数: 6

Abstract

Background: Successful reperfusion after endovascular thrombectomy (EVT) correlates with good outcome. However, radiographic reperfusion does not always translate into good clinical outcomes even if the reperfusion occurs early after the stroke onset. Reasons for neurological worsening (NW) are thought to be many, such as progression of the stroke, hemorrhagic conversion post tissue plasminogen activator and/or EVT, and procedural complications such as vessel dissection or perforation, distal emboli, and re-occlusion. Data on patients worsening in the acute phase after EVT are limited.

Objective: We studied the factors associated with acute NW and also identified the predictors of NW after EVT and its association with poor outcome at discharge.

Methods: A retrospective cohort from a single comprehensive stroke center includes patients with acute ischemic stroke and large vessel occlusion in anterior and posterior circulation who presented between December 2014 and May 2017 and received EVT were reviewed. Primary outcome was defined as acute NW defined as change in NIHSS ≥4 from baseline in the first 24 h after EVT. Secondary outcome were modified Rankin scale (mRS) 0-2 at discharge and final infarct volume. Univariate and multivariate analyses were performed to evaluate clinical and radiographic variables independently correlating with NW after EVT. Receiver operating curve analysis was also performed to identify predictors.

Results: 178 patients were included in the analysis, 26 (14.7%) met the criteria for acute NW. For these 178 patients, the median age was 63 (IQR 53-74, range 26-89), baseline median NIHSS was 19 (IQR 14-24, range 5-37), ASPECTS was 8 (IQR 7-9, range 4-10), admission median systolic blood pressure (SBP) was 150 (IQR 131-170, range 94-287), and initial median blood glucose (BG) was 123 (IQR 106-157, range 69-433). The most common reasons for worsening were progression of the stroke (42.3%) and reperfusion injury PH-2 (26.9%) (p < 0.0001). Univariate logistic analysis showed that race, ASPECTS, collateral score, diabetes mellitus, admission SBP, and admission BG were associated with acute NW. In multivariate analysis, only admission BG (OR 1.00, CI 1.00-1.01, p = 0.04) was found to have a significant association with acute NW. We ran a prediction analysis for variables and found the area under the curve to be 0.75. Finally, there was strong association between NW and poor outcome at discharge (MRS 3-6, p < 0.01) by Fisher's exact test. About 46.1% in the NW group died during hospitalization compared to 10% in the non-NW group (p < 0.0001).

Conclusion: Our single-center retrospective cohort result is limited by small sample size. It showed that high admission BG is an independent predictor of NW after EVT and ultimately leads to poor outcome.

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血管内取栓后急性神经系统恶化的预测因素。
背景:血管内取栓(EVT)后再灌注成功与良好的预后相关。然而,即使再灌注发生在中风发作后的早期,影像学再灌注也不一定能转化为良好的临床结果。神经系统恶化(NW)的原因被认为有很多,如中风的进展,组织纤溶酶原激活剂和/或EVT后的出血转化,以及手术并发症,如血管剥离或穿孔,远端栓塞和再闭塞。EVT后急性期患者病情恶化的数据有限。目的:我们研究了与急性NW相关的因素,并确定了EVT后NW的预测因素及其与出院时不良预后的关系。方法:回顾性分析2014年12月至2017年5月间在某脑卒中综合中心就诊并接受EVT治疗的急性缺血性脑卒中前后循环大血管闭塞患者。主要结局定义为急性NW,定义为EVT后24小时内NIHSS较基线变化≥4。次要指标为出院时修正Rankin量表(mRS) 0-2和最终梗死体积。进行单因素和多因素分析,以评估与EVT后NW独立相关的临床和影像学变量。还进行了受试者工作曲线分析以确定预测因子。结果:178例患者纳入分析,26例(14.7%)符合急性NW标准。178例患者中位年龄为63岁(IQR 53-74,范围26-89),基线中位NIHSS为19 (IQR 14-24,范围5-37),ASPECTS为8 (IQR 7-9,范围4-10),入院中位收缩压(SBP)为150 (IQR 131-170,范围94-287),初始中位血糖(BG)为123 (IQR 106-157,范围69-433)。最常见的恶化原因是卒中进展(42.3%)和再灌注损伤PH-2 (26.9%) (p < 0.0001)。单因素logistic分析显示,种族、ASPECTS、侧支评分、糖尿病、入院收缩压和入院BG与急性NW相关。在多因素分析中,只有入院BG (OR 1.00, CI 1.00-1.01, p = 0.04)与急性NW显著相关。我们对变量进行了预测分析,发现曲线下的面积为0.75。最后,通过Fisher精确检验,NW与出院时的不良预后有很强的相关性(MRS 3-6, p < 0.01)。NW组住院期间死亡46.1%,非NW组住院期间死亡10% (p < 0.0001)。结论:我们的单中心回顾性队列结果受样本量小的限制。结果表明,高入院BG是EVT后NW的独立预测因子,并最终导致预后不良。
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Interventional Neurology
Interventional Neurology CLINICAL NEUROLOGY-
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