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首页> 外文期刊>American Journal of Psychiatry and Neuroscience >Efficacy and Safety of Intravenous Urokinase and Sodium Ozagrel in Acute Ischemic Stroke
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Efficacy and Safety of Intravenous Urokinase and Sodium Ozagrel in Acute Ischemic Stroke

机译:静脉尿激酶和奥扎格雷钠在急性缺血性卒中中的疗效和安全性

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摘要

Urokinase and sodium ozagrel are widely used in patients with acute ischemic stroke (AIS) in China. But the effectiveness and safety of the two combinations are not yet clear. A total of 129 AIS patients who were treated with combined intravenous (IV) urokinase and sodium ozagrel within 6 hours of onset were included in this study. All the patients were assessed with the National Institute of Health Stroke Scale (NIHSS) score at baseline, 6 hours, at hospital discharge, and 1 month after AIS. All the patients were characterized into two groups based on early response (decrease in NIHSS score ≥4 points at 6 hours) and good outcome (NIHSS score ≤ 1 at 1 month), and assessed treatment safety by evaluating intracranial hemorrhage and mortality. There were 54 patients in the good outcome group and 74 in the bad outcome group at the end. Multivariate analysis showed that shorter onset to treatment time, a lower baseline NIHSS score, and lack of large artery stenosis or occlusion werel associated with good outcome at 1 month. This study suggested that combined IV urokinase and sodium ozagrel therapy was effective and safe in treating patient with AIS within a 6-hour time window. With lower cost and a longer time window, it can be used as an alternative intravenous thrombolytic therapy in patients with AIS except rt-PA.
机译:尿激酶和奥扎格雷钠在中国广泛用于急性缺血性中风(AIS)患者。但是两种组合的有效性和安全性尚不清楚。总共129名AIS患者在发病后6小时内接受了静脉内(IV)尿激酶和奥扎格雷钠联合治疗。所有患者均在基线,出院时6小时和AIS后1个月以美国国立卫生研究院卒中量表(NIHSS)评分进行评估。根据早期反应(6小时时NIHSS评分降低≥4分)和良好的结局(1个月时NIHSS评分≤1)将所有患者分为两组,并通过评估颅内出血和死亡率评估治疗安全性。最后,良好结局组中有54例患者,不良结局组中有74例。多变量分析显示,治疗时间较短,基线NIHSS评分较低,缺乏大动脉狭窄或闭塞均与1个月的良好预后相关。这项研究表明,静脉尿激酶和奥扎格雷钠联合治疗在6小时内可有效,安全地治疗AIS患者。除rt-PA外,它还可以以较低的成本和更长的时间窗口用于AIS患者的替代静脉溶栓治疗。

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