Tekle Wondwossen G, Chaudhry Saqib A, Fatima Zara, Ahmed Maryam, Khalil Shujaat, Hassan Ameer E, Rodriguez Gustavo J, Suri Fareed K, Qureshi Adnan I
Zeenat Qureshi Stroke Research Center, University of Minnesota, Minneapolis, MN, USA.
J Vasc Interv Neurol. 2012 Jun;5(1):22-6.
A randomized double-blind trial (ECASS III) demonstrated that intravenous (IV) recombinant tissue plasminogen activator (rt-PA) administered between 3 and 4.5 hrs after the onset of symptoms significantly improved clinical outcomes in patients with acute ischemic stroke. In May 2009, the American Stroke Association guidelines recommended the use of IV rt-PA for patients presenting within 3 and 4.5 hrs after symptom onset.
To determine the rate of patients treated with IV rt-PA within the 3- and 4.5-hr time window and associated comparative outcomes in general practice.
We retrospectively reviewed all patients who were treated with IV rt-PA at two comprehensive stroke centers from September 1, 2008 to July 31, 2010 and identified a total of 98 patients. In addition, we identified patients who arrived to the ED of those centers within 2.5 to 4 hrs of symptom onset between January 1, 2007 and June 30, 2010 and received only endovascular treatment. We compared the rates of favorable outcome (determined by using modified Rankin scale 0-2 at discharge and 3-month follow-up), and National Institutes of Health Stroke Scale (NIHSS) score improvement by ≥ 4 points or 0 at discharge among patients treated with IV rt-PA within 3-4.5 hrs with those who received IV rt-PA within 0-3 hrs, and subsequently with patients presenting at similar time window treated only with endovascular treatment.
Out of the total 98 IV rt-PA treated patients, 84 of them were treated within 0-3 hrs, and 14 within the 3--4.5 hrs. Twelve patients received endovascular treatment only for the specified time window. Mean admission NIHSS score ± standard deviation (SD) was 11.90 ± 6.72, 8.57 ± 5.40, and 11.75 ± 8.06, for the 0--3, 3--4.5 hrs, and endovascular only treatment groups, respectively. Favorable clinical outcome at discharge (50% vs. 56%, p=0.77), 3 months (64% vs. 64%, p=1.0), and NIHSS score improvement (43% vs. 58%, p=0.38) were not different between those treated within 3-4.5 and 0-3 hrs time windows. There appeared to be a non-significantly higher rate of favorable outcomes at discharge (25% vs. 50%, p=0.24), and at 3 months (42% vs. 64%, p=0.43) among patients treated with IV rt-PA within 3-4.5 hrs compared with those treated with primary endovascular treatment.
An additional 14% of patients received IV rt-PA because of treatment window expansion from 3 to 4.5 hrs. Outcomes were comparable to those treated within 3 hrs of symptom onset. The shift of those patients from primary endovascular treatment does not appear to adversely affect patient outcomes.
一项随机双盲试验(ECASS III)表明,在症状发作后3至4.5小时内静脉注射重组组织型纤溶酶原激活剂(rt-PA)可显著改善急性缺血性中风患者的临床预后。2009年5月,美国中风协会指南建议对症状发作后3至4.5小时内就诊的患者使用静脉rt-PA。
确定在3至4.5小时时间窗内接受静脉rt-PA治疗的患者比例以及在一般临床实践中的相关比较结果。
我们回顾性分析了2008年9月1日至2010年7月31日期间在两个综合性中风中心接受静脉rt-PA治疗的所有患者,共识别出98例患者。此外,我们还识别出2007年1月1日至2010年6月30日期间在症状发作后2.5至4小时内到达这些中心急诊科且仅接受血管内治疗的患者。我们比较了在3至4.5小时内接受静脉rt-PA治疗的患者与在0至3小时内接受静脉rt-PA治疗的患者,以及随后在相似时间窗内仅接受血管内治疗的患者的良好预后率(出院时及3个月随访时使用改良Rankin量表0至2级确定),和出院时美国国立卫生研究院卒中量表(NIHSS)评分改善≥4分或评分为0的情况。
在总共98例接受静脉rt-PA治疗的患者中,84例在0至3小时内接受治疗,14例在3至4.5小时内接受治疗。12例患者仅在特定时间窗内接受血管内治疗。0至3小时、3至4.5小时和仅接受血管内治疗组的平均入院NIHSS评分±标准差(SD)分别为11.90±6.72、8.57±5.40和11.75±8.06。在3至4.5小时和0至3小时时间窗内接受治疗的患者之间,出院时(50%对56%,p = 0.77)、3个月时(64%对64%,p = 1.0)的良好临床预后以及NIHSS评分改善(43%对58%,p = 0.38)并无差异。与接受原发性血管内治疗的患者相比,在3至4.5小时内接受静脉rt-PA治疗的患者出院时(25%对50%,p = 0.24)和3个月时(42%对64%,p = 0.43)的良好预后率似乎略高,但差异无统计学意义。
由于治疗时间窗从3小时扩展到4.5小时,另外14%的患者接受了静脉rt-PA治疗。其预后与症状发作后3小时内接受治疗的患者相当。这些患者从原发性血管内治疗的转移似乎并未对患者预后产生不利影响。