Hassan Ameer E, Hassanzadeh Bahareh, Tohidi Vahid, Kirmani Jawad F
Department of Neurology and Neurosciences, University Hospital, UMDNJ, Newark, NJ, USA.
South Med J. 2010 May;103(5):398-402. doi: 10.1097/SMJ.0b013e3181d7814a.
Intravenous recombinant tissue plasminogen activator (IV rt-PA) is an effective medication currently used to treat acute ischemic stroke within three hours of symptom onset in patients with an identifiable clinical deficit measured using the National Institute of Health Stroke Scale (NIHSS).
We compared the outcomes of 27 identified patients with an NIHSS of 6 or less who received IV rt-PA for acute ischemic stroke treatment within three hours of symptom onset in our center with 24 historic controls from the nationally available National Institute of Neurological Disorders and Stroke (NINDS) study database.
The mean initial NIHSS was not significantly different in patients and control groups (mean +/- SD: 4.52 +/- 1.25 and 4.71 +/- 1.4) (P = 0.45). The mean modified Rankin score (mRS) at the time of discharge in patients and control group were 0.78 +/- 1.19 and 1.75 +/- 1.75, respectively. The mRS at discharge demonstrated a statistically significant (P < 0.03) improved clinical outcome for IV rt-PA treated group. The rate of intracranial hemorrhage (ICH) in the IV rt-PA group and control group was not significantly different (P = 1, odds ratio: 0.88, CI: 0.05-14.09).
This retrospective study demonstrates that administering intravenous rt-PA to patients with a very mild stroke (NIHSS of 6 or less) can lead to improved clinical outcome when compared to patients with similar NIHSS who have not received similar treatment.
静脉注射重组组织型纤溶酶原激活剂(IV rt-PA)是目前用于治疗急性缺血性卒中的有效药物,适用于症状发作三小时内、使用美国国立卫生研究院卒中量表(NIHSS)测得有明确临床缺损的患者。
我们将本中心27例NIHSS评分为6分及以下、在症状发作三小时内接受IV rt-PA治疗急性缺血性卒中的患者的结局,与来自全国可用的美国国立神经疾病和卒中研究所(NINDS)研究数据库的24例历史对照进行了比较。
患者组和对照组的平均初始NIHSS无显著差异(均值±标准差:4.52±1.25和4.71±1.4)(P = 0.45)。患者组和对照组出院时的平均改良Rankin量表评分(mRS)分别为0.78±1.19和1.75±1.75。出院时的mRS显示IV rt-PA治疗组的临床结局有统计学显著改善(P < 0.03)。IV rt-PA组和对照组的颅内出血(ICH)发生率无显著差异(P = 1,优势比:0.88,可信区间:0.05 - 14.09)。
这项回顾性研究表明,与未接受类似治疗、NIHSS评分相似的患者相比,对轻度卒中(NIHSS为6分及以下)患者静脉注射rt-PA可改善临床结局。