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静脉注射组织型纤溶酶原激活剂后疑似中风患者的安全性及预后:单中心经验

Safety and outcomes in stroke mimics after intravenous tissue plasminogen activator administration: a single-center experience.

作者信息

Lewandowski Christopher, Mays-Wilson Kathleen, Miller Joseph, Penstone Patricia, Miller Daniel J, Bakoulas Konstandinos, Mitsias Panayiotis

机构信息

Department of Emergency Medicine, Henry Ford Hospital, Detroit, Michigan.

Department of Emergency Medicine, Beaumont Hospital, Royal Oak, Michigan.

出版信息

J Stroke Cerebrovasc Dis. 2015 Jan;24(1):48-52. doi: 10.1016/j.jstrokecerebrovasdis.2014.07.048. Epub 2014 Oct 22.

Abstract

BACKGROUND

Patients with symptoms that impersonate a stroke but are later found to have an alternate diagnosis are termed stroke mimics. Stroke mimics treated with intravenous (IV) tissue plasminogen activator (t-PA) are exposed to hemorrhagic complications without benefit. The objective of this study is to describe the characteristics, safety, and outcomes of stroke mimic patients treated with t-PA within 4.5 hours.

METHODS

All patients hospitalized after IV t-PA treatment at a tertiary care hospital and primary stroke center from January 2008 through December 2011 were reviewed. Stroke mimics were determined by review of clinical and imaging findings. Stroke mimics are described and compared with acute ischemic stroke patients for demographics, clinical characteristics, and bleeding complications.

RESULTS

We identified 38 stroke mimic (12%) and 285 ischemic stroke (88%) t-PA-treated patients. Compared with ischemic stroke patients, mimic patients were younger, more often female, and reported a history of stroke more often. There were no differences in race, baseline stroke scale, or onset to treatment time. There were no intracerebral hemorrhages or deaths in the mimic patients but there were 2 systemic hemorrhages (5.2%).

CONCLUSIONS

Treatment of mimic patients with IV t-PA appears to be safe in this cohort. Concern for intracerebral hemorrhage in mimic patients need not dissuade clinicians from administering t-PA when significant concern for ischemic etiology exists.

摘要

背景

有类似中风症状但后来被确诊为其他疾病的患者被称为类中风患者。接受静脉注射(IV)组织型纤溶酶原激活剂(t-PA)治疗的类中风患者会面临出血并发症且无益处。本研究的目的是描述在4.5小时内接受t-PA治疗的类中风患者的特征、安全性和结局。

方法

回顾了2008年1月至2011年12月在一家三级医疗医院和初级卒中中心接受静脉t-PA治疗后住院的所有患者。通过回顾临床和影像学检查结果来确定类中风患者。描述类中风患者,并将其与急性缺血性中风患者在人口统计学、临床特征和出血并发症方面进行比较。

结果

我们确定了38例(12%)接受t-PA治疗的类中风患者和285例(88%)缺血性中风患者。与缺血性中风患者相比,类中风患者更年轻,女性更多,且更常报告有中风病史。在种族、基线中风量表或发病至治疗时间方面没有差异。类中风患者中没有发生脑出血或死亡,但有2例全身性出血(5.2%)。

结论

在该队列中,用静脉t-PA治疗类中风患者似乎是安全的。当对缺血性病因有重大担忧时,对类中风患者脑出血的担忧不应阻止临床医生给予t-PA治疗。

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