急性大血管闭塞性卒中伴轻度临床症状患者血管内治疗的临床与影像学结果

Q1 Medicine
Interventional Neurology Pub Date : 2018-02-01 Epub Date: 2017-11-23 DOI:10.1159/000481205
Meredith T Bowen, Leticia C Rebello, Mehdi Bouslama, Diogo C Haussen, Jonathan A Grossberg, Nicolas A Bianchi, Samir Belagaje, Aaron Anderson, Michael R Frankel, Raul G Nogueira
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引用次数: 8

摘要

背景:最小的卒中严重程度证明血管内干预仍然是难以捉摸的。然而,相当一部分表现为大血管闭塞性卒中(LVOS)且症状轻微的患者未经治疗,面临不良预后。我们的目的是评估LVOS和低症状评分(美国国立卫生研究院卒中量表[NIHSS]评分≤8)患者接受血管内治疗(ET)的临床结果。方法:我们对2010年9月至2016年3月期间前瞻性收集的ET数据库进行回顾性分析。纳入基线NIHSS评分≤8的LVOS血管内治疗患者。收集基线患者特征、手术细节和结果参数。疗效指标为良好转归率(90天改良Rankin量表评分0-2分)和再灌注成功率(改良脑梗死治疗[mTICI]评分2b-3分)。通过实质血肿(1型实质血肿[PH-1]和2型实质血肿[PH-2])发生率和90天死亡率来评估安全性。使用逻辑回归来确定良好临床结果的预测因素。结果:共纳入935例患者;纳入72例NIHSS评分≤8分的患者。中位[IQR]年龄为61.5岁[56.2-73.0];男性39例(54%)。平均(SD)基线NIHSS评分、计算机断层扫描灌注核容积和ASPECTS分别为6.3(1.5)、7.5 mL(16.1)和8.5 mL(1.3)。28例患者(39%)静脉注射组织型纤溶酶原激活剂。闭塞部位如下:29例(40%)近端MCA-M1, 20例(28%)MCA-M2, 6例(8%)ICA末梢,9例(13%)椎基底动脉。串联闭塞7例(10%)。67例(93%)患者再灌注成功(mTICI评分2b-3);52例(72%)90天预后良好。平均最终梗死体积为32.2±59.9 mL,发生实质血肿4例(6%)。90天死亡率为10% (n = 7)。Logistic回归显示,只有再灌注成功(OR 27.7, 95% CI 1.1-655.5, p = 0.04)是预后良好的独立预测因子。结论:我们的研究结果表明,对于表现为轻度临床症状的LVOS患者,ET是安全可行的。未来的对照研究是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical and Imaging Outcomes of Endovascular Therapy in Patients with Acute Large Vessel Occlusion Stroke and Mild Clinical Symptoms.

Clinical and Imaging Outcomes of Endovascular Therapy in Patients with Acute Large Vessel Occlusion Stroke and Mild Clinical Symptoms.

Background: The minimal stroke severity justifying endovascular intervention remains elusive. However, a significant proportion of patients presenting with large vessel occlusion stroke (LVOS) and mild symptoms go untreated and face poor outcomes. We aimed to evaluate the clinical outcomes of patients presenting with LVOS and low symptom scores (National Institutes of Health Stroke Scale [NIHSS] score ≤8) undergoing endovascular therapy (ET).

Methods: We performed a retrospective analysis of a prospectively collected ET database between September 2010 and March 2016. Endovascularly treated patients with LVOS and a baseline NIHSS score ≤8 were included. Baseline patient characteristics, procedural details, and outcome parameters were collected. Efficacy outcomes were the rate of good outcome (90-day modified Rankin Scale score 0-2) and of successful reperfusion (modified Treatment in Cerebral Infarction [mTICI] score 2b-3). Safety was assessed by the rate of parenchymal hematoma (parenchymal hematoma type 1 [PH-1] and parenchymal hematoma type 2 [PH-2]) and 90-day mortality. Logistic regression was used to identify predictors of good clinical outcomes.

Results: A total of 935 patients were considered; 72 patients with an NIHSS score ≤8 were included. Median [IQR] age was 61.5 years [56.2-73.0]; 39 patients (54%) were men. Mean (SD) baseline NIHSS score, computed tomography perfusion core volume, and ASPECTS were 6.3 (1.5), 7.5 mL (16.1), and 8.5 (1.3), respectively. Twenty-eight patients (39%) received intravenous tissue plasminogen activator. Occlusions locations were as follows: 29 (40%) proximal MCA-M1, 20 (28%) MCA-M2, 6 (8%) ICA terminus, and 9 (13%) vertebrobasilar. Tandem occlusion was documented in 7 patients (10%). Sixty-seven patients (93%) achieved successful reperfusion (mTICI score 2b-3); 52 (72%) had good 90-day outcomes. Mean final infarct volume was 32.2 ± 59.9 mL. Parenchymal hematoma occurred in 4 patients (6%). Ninety-day mortality was 10% (n = 7). Logistic regression showed that only successful reperfusion (OR 27.7, 95% CI 1.1-655.5, p = 0.04) was an independent predictor of good outcomes.

Conclusion: Our findings demonstrate that ET is safe and feasible for LVOS patients presenting with mild clinical syndromes. Future controlled studies are warranted.

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Interventional Neurology
Interventional Neurology CLINICAL NEUROLOGY-
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