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急性缺血性卒中的静脉注射重组组织型纤溶酶原激活剂治疗:以色列的初步经验。

Intravenous recombinant tissue plasminogen activator therapy for acute ischemic stroke: initial Israeli experience.

作者信息

Schwammenthal Yvonne, Drescher Michael J, Merzeliak Oleg, Tsabari Rakefet, Bruk Bella, Feibel Meir, Hoffman Chen, Bakon Mati, Rotstein Zeev, Chapman Joab, Tanne David

机构信息

Stroke Unit, Department of Neurology, Neurovascular Laboratory, Sheba Medical Center, Tel Hashomer, Israel.

出版信息

Isr Med Assoc J. 2004 Feb;6(2):70-4.

Abstract

BACKGROUND

Intravenous recombinant tissue plasminogen activator therapy within 3 hours of stroke onset is a proven effective treatment for acute ischemic stroke.

OBJECTIVE

To assess the feasibility and safety of rt-PA therapy for reperfusion in routine clinical practice in Israel, in the setting of a dedicated stroke unit.

METHODS

Consecutive patients presenting within less than 3 hours of stroke onset were evaluated by an emergency physician and the neurology stroke team. After brain computerized tomography, eligible patients were treated with intravenous rt-PA (0.9 mg/kg, maximum dose 90 mg) according to an in-hospital protocol corresponding to recommended criteria. Patients were admitted to the acute stroke unit. Safety and clinical outcome were routinely assessed. Recanalization was assessed by serial transcranial Doppler.

RESULTS

The study group comprised 16 patients, mean age 61 years (range 47-80 years), male to female ratio 10:6, whose median baseline National Institutes of Health stroke scale was 13 (range 6-24). They were treated within a mean door-to-CT time of 39 minutes (range 17-62 min), door-to-drug time 101 minutes (range 72-150), and stroke onset-to-drug time 151 minutes (range 90-180). There was an early improvement within 24 hours (of > or = 4 points in the NIHSS score) in 7 patients (44%) and no early deteriorations. There were no protocol deviations, no symptomatic intracranial hemorrhages, and no major systemic hemorrhage within 36 hours of rt-PA treatment. Three asymptomatic hemorrhagic transformations of the infarct were noted on routine follow-up brain CT associated with neurologic improvement. Outcome data were comparable to the National Institute of Neurological Disorders and Stroke rt-PA Stroke Study.

CONCLUSION

Intravenous rt-PA treatment within 3 hours of stroke onset in routine clinical practice in Israel is feasible and appears safe in the setting of a neurology stroke unit and team. Careful implementation of rt-PA therapy for selected patients in Israel is encouraged.

摘要

背景

在中风发作3小时内进行静脉注射重组组织型纤溶酶原激活剂治疗是急性缺血性中风的一种经证实有效的治疗方法。

目的

评估在以色列的一个专门的中风单元环境下,rt-PA治疗在常规临床实践中进行再灌注的可行性和安全性。

方法

由一名急诊医生和神经科中风团队对中风发作后不到3小时就诊的连续患者进行评估。在进行脑部计算机断层扫描后,符合条件的患者根据符合推荐标准的院内方案接受静脉注射rt-PA(0.9mg/kg,最大剂量90mg)治疗。患者被收入急性中风单元。常规评估安全性和临床结果。通过连续经颅多普勒评估再通情况。

结果

研究组包括16名患者,平均年龄61岁(范围47 - 80岁),男女比例为10:6,其基线美国国立卫生研究院中风量表中位数为13(范围6 - 24)。他们的平均门到CT时间为39分钟(范围17 - 62分钟),门到用药时间为101分钟(范围72 - 150),中风发作到用药时间为151分钟(范围90 - 180)。7名患者(44%)在24小时内有早期改善(美国国立卫生研究院中风量表评分提高≥4分),且无早期病情恶化。在rt-PA治疗36小时内无方案偏差、无症状性颅内出血和重大全身性出血。在常规随访脑部CT上发现3例梗死灶无症状性出血转化,伴有神经功能改善。结果数据与美国国立神经疾病和中风研究所rt-PA中风研究相当。

结论

在以色列的常规临床实践中,中风发作3小时内进行静脉注射rt-PA治疗是可行的,并且在神经科中风单元和团队的环境下似乎是安全的。鼓励在以色列对选定患者谨慎实施rt-PA治疗。

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