Khazaei Mojtaba, Davoodian Arezou, Taheri Mohammad, Ghafouri-Fard Soudeh
Neurophysiology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Neurology, Hamadan University of Medical Sciences, Hamadan, Iran.
Hum Antibodies. 2020;28(1):53-56. doi: 10.3233/HAB-190391.
One of the concerns in patients with acute ischemic stroke with former history of taking antiplatelet drugs is the risk of intracerebral hemorrhage following venous thrombolysis. The purpose of this study was to evaluate the effect of previous administration of antiplatelet drugs on adverse outcomes of recombinant tissue plasminogen activator (tPA) in patients with acute ischemic stroke.
In this study, 46 patients with the diagnosis of acute ischemic stroke were recruited. Patients were assessed in a period of three hours after stroke and received the standard dose of tPA (0.9 mg/kg). History of antiplatelet drugs, risk factors, demographic information and stroke severity were collected. The severity of the stroke was determined by the National Institutes of Health Stroke Scale (NIHSS). The outcome was assessed using the Modified Rankin Scale (MRS) and Barthel Index (BI) in the days one, 14 and 90.
Patients with history of antiplatelet drugs had an increased rate of intracranial hemorrhage [odds ratio (95% CI) = 7.3 (1.3-40.5)]. Stroke severity scores were higher in patients receiving antiplatelet drugs than the other group at discharge day and day 90. In both groups, the severity of the disease decreased with time. Mortality rate was 42.1% in patients received antiplatelet drugs and 18.5% in the other group (P> 0.05).
Based on the results of this study, patients with acute ischemic stroke and history of taking antiplatelet drugs have poor outcome following administration of standard dose of tPA.
有抗血小板药物服用史的急性缺血性脑卒中患者的一个担忧是静脉溶栓后发生脑出血的风险。本研究的目的是评估既往服用抗血小板药物对急性缺血性脑卒中患者重组组织型纤溶酶原激活剂(tPA)不良结局的影响。
本研究招募了46例诊断为急性缺血性脑卒中的患者。患者在卒中后3小时内接受评估,并接受标准剂量的tPA(0.9mg/kg)。收集抗血小板药物使用史、危险因素、人口统计学信息和卒中严重程度。卒中严重程度由美国国立卫生研究院卒中量表(NIHSS)确定。在第1天、14天和90天使用改良Rankin量表(MRS)和Barthel指数(BI)评估结局。
有抗血小板药物使用史的患者颅内出血发生率增加[比值比(95%CI)=7.3(1.3 - 40.5)]。在出院日和第90天,服用抗血小板药物的患者卒中严重程度评分高于另一组。两组患者的疾病严重程度均随时间降低。服用抗血小板药物的患者死亡率为42.1%,另一组为18.5%(P>0.05)。
基于本研究结果,有急性缺血性脑卒中和抗血小板药物服用史的患者在给予标准剂量tPA后结局较差。