Intravenous thrombolysis in German stroke units before and after regulatory approval of recombinant tissue plasminogen activator

被引:23
作者
Weimar, C. [1 ]
Kraywinkel, K. [1 ]
Maschke, M. [1 ]
Diener, H. -C. [1 ]
机构
[1] Univ Duisburg Gesamthsch, Dept Neurol, DE-45122 Essen, Germany
关键词
ischemic stroke; thrombolysis; door-to-needle time; outcome; cerebral hemorrhage;
D O I
10.1159/000094995
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Intravenous thrombolysis with recombinant tissue plasminogen activator (rt-PA) within 3 h after onset of focal cerebral ischemia was approved in Germany in August 2000. Methods: 11 neurology departments with acute stroke units participated in the German Stroke Study Collaboration before (n = 2,925) and after (n = 3,204) approval of rt-PA in Germany and consecutively registered all patients admitted within 24 h following acute ischemic stroke. Results: Frequency of intravenous thrombolysis in patients admitted within 24 h after symptom onset increased from 4.8% before approval to 7.9% after approval of rt-PA. Among patients treated with rtPA, age increased significantly and the delay between symptom onset and imaging was significantly shorter in the second study period. Conclusions: The observed improvement in management and quantity of intravenous thrombolysis may be explained by greater experience and greater legal security following regulatory approval of rtPA. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:429 / 431
页数:3
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