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Stroke thrombolysis in the Philippines

机译:菲律宾中风溶栓

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Background & Objective: Currentlythere is limitedintervention for acute ischemic stroke. Recombinant tissue plasminogen activator (rTPA) has been approved for immediate recanalization after a steno-occlusive lesion of cerebral vessels. rTPA has shown its efficacy and safety from several clinical trials. The present study reports our experience with intravenous rTPA from several centers in the Philippines.Method:This is a retrospective cohort study consisting of 157 patients who qualified to receive rTPA following the NINDS trial inclusion and exclusion criteria. The primary outcome is in-hospital and 3-months mortality. Other outcome measures were determined: intracranial hemorrhage secondary to hemorrhagic conversion and functional outcome as measured by modified Rankin Scale. Additionally, standard dose (0.9mg/kg) was compared to low dose (0.6mg/kg) of rTPA in terms of mortality, intracranial bleeding and functional outcome.Results:The in-hospital mortality was seen in 23 (14.6%) and total death within 3 months was 18.3%. Independent patient (mRS 0-2) was seen in 69 (51.1%) at discharge and 95 (73.1%) at 3 months. Intracranial bleeding due to asymptomatic hemorrhagic transformation occurred in 39 (24.8%) and symptomatic hemorrhagic transformation was seen in 19 (12.1%). Conclusion: Comparing our results with SITS-MOST and Cochrane collaborations, our data showed that we have more independent patients however death and intracranial bleeding was noted to be high in our cohort of patients. Additionally, the study showed more independent patients in the low dose group.
机译:背景与目的:目前对急性缺血性中风的干预措施有限。重组组织纤溶酶原激活剂(rTPA)已被批准用于脑血管狭窄闭塞性病变后的立即再通。 rTPA已通过多项临床试验证明了其功效和安全性。本研究报告了我们在菲律宾多个中心进行静脉rTPA治疗的经验。方法:这是一项回顾性队列研究,由157名符合NINDS试验纳入和排除标准的患者接受rTPA治疗。主要结果是住院和3个月的死亡率。确定了其他结局指标:通过改良的Rankin量表对继发于出血性转化的颅内出血和功能结局进行了评估。此外,在死亡率,颅内出血和功能预后方面,将标准剂量(0.9mg / kg)与低剂量(0.6mg / kg)的rTPA进行了比较。结果:23例(14.6%)的住院死亡率被发现3个月内死亡总数为18.3%。出院时发现独立患者(mRS 0-2)的比例为69(51.1%),3个月时为95(73.1%)。无症状出血性转化引起的颅内出血发生率为39(24.8%),有症状出血性转化发生为19(12.1%)。结论:将我们的结果与SITS-MOST和Cochrane合作进行比较,我们的数据显示我们有更多的独立患者,但是死亡和颅内出血在我们的患者队列中很高。此外,研究显示低剂量组中有更多独立患者。

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