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SSRI 暴露对缺血性脑卒中溶栓后出血并发症和结局的影响。

Effects of SSRI exposure on hemorrhagic complications and outcome following thrombolysis in ischemic stroke.

机构信息

Department of Neurology, St. John's Hospital, Medical Faculty, Sigmund Freud University Vienna, Vienna, Austria.

出版信息

Int J Stroke. 2018 Jul;13(5):511-517. doi: 10.1177/1747493017743055. Epub 2017 Nov 14.

DOI:10.1177/1747493017743055
PMID:29134925
Abstract

Background Selective serotonin reuptake inhibitors (SSRI) may interfere with platelet function, and pre-stroke SSRI treatment has been associated with increased hematoma volumes and mortality in hemorrhagic stroke patients. The effects of SSRI on the risk of hemorrhagic complications after thrombolysis in ischemic stroke patients are unclear. Aims To examine the effects of pre-stroke SSRI exposure on bleeding complications, functional outcome, and mortality following thrombolysis in ischemic stroke. Methods Data including standard demographic and clinical variables as well as baseline and follow-up stroke severity (measured by National Institutes of Health Stroke Score), functional outcome (measured by modified Rankin Scale) at 3 months, and mortality at 7 and 90 days were extracted from the Virtual International Stroke Trials Archive. Multivariable binary logistic regression was used for statistical analyses. Results Out of 1114 ischemic stroke patients treated with recombinant tissue-type plasminogen activator, 135 (12.1%) had previous SSRI exposure. Symptomatic intracranial hemorrhage occurred in 30 (2.7%) patients. Of those, 2 (1.5%, n = 135) were in the SSRI pretreatment group and 28 (2.9%, n = 979) were SSRI naive patients. Pre-stroke SSRI exposure in thrombolysed patients showed association with neither bleeding complications ( P = .58) nor functional outcome ( P = .38) nor mortality ( P = .65). Conclusions Results from this large retrospective ad hoc database cohort study indicate that pre-stroke SSRI exposure in ischemic stroke patients who receive thrombolytic treatment is not associated with bleeding complications, functional outcome, or mortality.

摘要

背景

选择性 5-羟色胺再摄取抑制剂(SSRIs)可能会干扰血小板功能,而卒中前 SSRIs 治疗与出血性卒中患者血肿体积增大和死亡率升高相关。SSRIs 对缺血性卒中溶栓后出血并发症风险的影响尚不清楚。目的:研究卒中前 SSRIs 暴露对缺血性卒中溶栓后出血并发症、功能结局和死亡率的影响。方法:从虚拟国际卒中试验档案中提取了包括标准人口统计学和临床变量以及基线和随访卒中严重程度(用国立卫生研究院卒中量表测量)、3 个月时的功能结局(用改良 Rankin 量表测量)和 7 天和 90 天的死亡率等数据。采用多变量二项逻辑回归进行统计学分析。结果:在接受重组组织型纤溶酶原激活剂治疗的 1114 例缺血性卒中患者中,有 135 例(12.1%)有卒中前 SSRIs 暴露。30 例(2.7%)患者发生症状性颅内出血。其中,2 例(1.5%,n=135)在 SSRI 预处理组,28 例(2.9%,n=979)为 SSRI 无暴露组。溶栓治疗的缺血性卒中患者的卒中前 SSRI 暴露与出血并发症(P=0.58)、功能结局(P=0.38)或死亡率(P=0.65)均无相关性。结论:这项大型回顾性特设数据库队列研究的结果表明,缺血性卒中患者在接受溶栓治疗前使用 SSRIs 与出血并发症、功能结局或死亡率无关。

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