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[缺血性卒中静脉溶栓使用重组组织型纤溶酶原激活剂(rt-PA)的前提条件、适应证及禁忌证]

[Prerequisites, indications and contraindications of IV-lysis of ischemic stroke with rt-PA].

作者信息

Marx P, Hartmann A, Leistner S, Nohr R, Koennecke H C

机构信息

Neurologische Klinik und Poliklinik, Klinische Neurophysiologie, Universitätsklinikum Benjamin Franklin, Berlin.

出版信息

Fortschr Neurol Psychiatr. 2001 Aug;69(8):346-52. doi: 10.1055/s-2001-16513.

Abstract

BACKGROUND AND PURPOSE

To evaluate prerequisites, safety, and efficacy of i.v.-thrombolysis of ischemic stroke with rtPA in an academic medical center.

METHODS

Over a period of 2 years and 10 months all patients admitted with a diagnosis of stroke were recruited. Inclusion and exclusion criteria for i.v.-thrombolysis were combined from large scale randomized controlled trials, the time window, however, could be extended up to 4 hours in subjects with a negative CT-scan. Prespecified outcome parameters were the modified Rankin Scale (mRS) and the Barthel Index (BI) at 3 months, and symptomatic hemorrhagic complications. Additionally, time parameters, such as onset-admission-time, door-Ct-time, door-needle time, and onset-needle time were recorded.

RESULTS

During the reported period 103 patients underwent i.v.-thrombolysis, corresponding to 14.9% of all patients with ischemic stroke, and 47% of patients with ischemic stroke arriving in < 3 hours after symptom onset. The mean baseline NIHSS was 14, the mean mRS 13 (3-34), the mean age 70 (+/- 12) years. The following time intervals were observed: Onset-admission-time 64 min., door-CT-time 27 min., admission-needle-time 80 min., and onset-needle-time 142 min. There were 4 symptomatic intracerebral hemorrhagic transformations, including 3 parenchymal hemorrhages, 2 of them lethal, and one with almost full recovery. According to the mRS, 39% of patients had a good (mRS 0-1), 72% a good to moderate recovery (mRS 0-2). The corresponding figures for the BI were 60% BI 95-100 and 72% BI > 90. The mortality was 15%.

CONCLUSION

The i.v.-thrombolysis of ischemic stroke with rt-PA demands appropriate organisation of the pre- and in-hospital phase and can be performed safely and efficaciously in daily clinical routine if inclusion and exclusion criteria as well as all safety measures during the critical phase after therapy are strictly obeyed.

摘要

背景与目的

评估在一家学术性医疗中心使用重组组织型纤溶酶原激活剂(rtPA)对缺血性卒中进行静脉溶栓的前提条件、安全性及有效性。

方法

在2年零10个月的时间里,招募了所有诊断为卒中的住院患者。静脉溶栓的纳入和排除标准综合了大规模随机对照试验的标准,不过,对于CT扫描结果为阴性的患者,时间窗可延长至4小时。预先设定的结局参数为3个月时的改良Rankin量表(mRS)和Barthel指数(BI),以及有症状的出血性并发症。此外,还记录了一些时间参数,如发病至入院时间、入院至CT检查时间、入院至穿刺时间以及发病至穿刺时间。

结果

在报告期内,103例患者接受了静脉溶栓治疗,占所有缺血性卒中患者的14.9%,占症状发作后3小时内到达的缺血性卒中患者的47%。基线美国国立卫生研究院卒中量表(NIHSS)平均分为14分,mRS平均分为13分(3 - 34分),平均年龄为70(±12)岁。观察到以下时间间隔:发病至入院时间64分钟,入院至CT检查时间27分钟,入院至穿刺时间80分钟,发病至穿刺时间142分钟。有4例出现有症状的脑内出血转化,包括3例脑实质出血,其中2例致死,1例几乎完全康复。根据mRS,39%的患者恢复良好(mRS 0 - 1),72%的患者恢复良好至中等(mRS 0 - 2)。BI的相应数据为60%的患者BI为95 - 100,72%的患者BI > 90。死亡率为15%。

结论

使用rt - PA对缺血性卒中进行静脉溶栓需要在院前和院内阶段进行适当组织,如果严格遵守纳入和排除标准以及治疗后关键阶段的所有安全措施,在日常临床实践中可以安全有效地实施。

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