Eggers Jürgen, König Inke R, Koch Björn, Händler Götz, Seidel Günter
Department of Neurology, Asklepios Hospital Hamburg North, Tangstedter Landstrasse 400, D-22417 Hamburg, Germany.
Stroke. 2008 May;39(5):1470-5. doi: 10.1161/STROKEAHA.107.503870. Epub 2008 Mar 13.
Sonothrombolysis is a new treatment approach in acute ischemic stroke. The results of a monocenter, randomized clinical study are presented.
Subjects with acute middle cerebral artery main stem occlusion were randomized into a target group receiving 1-hour transcranial continuous insonation using a 1.8-MHz Doppler ultrasound (US) probe or a control group. All underwent standard thrombolysis with intravenous recombinant tissue-type plasminogen activator.
Thirty-seven subjects were included; 19 subjects were treated in the target (US) group and 18 in the control (no-US) group, all with no residual flow in the middle cerebral artery main stem occlusion (Thrombolysis in Brain Ischemia recanalization grade 0). Compared with the no-US group, the US group showed greater improvement in National Institutes of Health Stroke Scale values at days 1 and 4 and a higher median Thrombolysis in Brain Ischemia grade 1 hour after recombinant tissue-type plasminogen activator initiation. Recanalization (complete or partial) after 1 hour occurred in 57.9% of the US group and 22.2% of the no-US group (P=0.045). After 90 days, 4 subjects from the US group had a modified Rankin Score <or=1 (none from the no-US group) and 8 had a Barthel Index >or=95 (none from the no US group; P=0.106 and P=0.003, respectively). Three subjects from the US group (15.8%) developed a symptomatic intracranial hemorrhage as did one (5.6%) in the no-US group (P=0.60).
This small randomized study indicates a beneficial impact of transcranial ultrasound on recanalization and short-term outcome in subjects with middle cerebral artery main stem occlusion and recombinant tissue-type plasminogen activator treatment.
超声溶栓是急性缺血性卒中的一种新治疗方法。本文展示了一项单中心随机临床研究的结果。
将急性大脑中动脉主干闭塞的受试者随机分为目标组和对照组,目标组使用1.8兆赫兹多普勒超声探头进行1小时经颅连续超声照射,对照组则不进行该操作。所有受试者均接受静脉注射重组组织型纤溶酶原激活剂的标准溶栓治疗。
共纳入37名受试者;目标(超声)组治疗19名受试者,对照组(无超声)治疗18名受试者,所有受试者大脑中动脉主干闭塞处均无残余血流(脑缺血溶栓再通分级为0级)。与无超声组相比,超声组在第1天和第4天的美国国立卫生研究院卒中量表评分改善更大,且在重组组织型纤溶酶原激活剂开始使用1小时后的脑缺血溶栓分级中位数更高。超声组1小时后再通(完全或部分)发生率为57.9%,无超声组为22.2%(P = 0.045)。90天后,超声组有4名受试者改良Rankin量表评分≤1(无超声组无此情况),8名受试者巴氏指数≥95(无超声组无此情况;P分别为0.106和0.003)。超声组有3名受试者(15.8%)发生有症状性颅内出血,无超声组有1名受试者(5.6%)发生(P = 0.60)。
这项小型随机研究表明,经颅超声对大脑中动脉主干闭塞且接受重组组织型纤溶酶原激活剂治疗的受试者的再通及短期预后有有益影响。