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欧洲急性卒中协作研究（ＥＣＡＳＳ）和（美国）国立神经病与卒中研究院（ＮＩＮＤＳＳ）两项研究由于原始资料设计存在差异未能进行直接比较，主要是由于治疗时间窗不同（ＥＣＡＳＳ：＜６ｈ；ＮＩＮＤＳＳ：≤９０ｍｉｎ／≤３ｈ）和ｒｔＰＡ剂量的不同（ＥＣＡＳＳ：...
Two studies from the European Cooperative Acute Stroke Study (ECASS) and the National Institute of Neurological and Stroke Studies (NINDSS) failed to make direct comparisons due to differences in original data design, mainly due to different treatment time windows (ECASS: <6 h; NINDSS : ≤ 90min / ≤ 3h) and rt-PA dose difference (ECASS: ...