Uyttenboogaart Maarten, Koch Marcus W, Koopman Karen, Vroomen Patrick C A J, De Keyser Jacques, Luijckx Gert-Jan
Department of Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Arch Neurol. 2008 May;65(5):607-11. doi: 10.1001/archneur.65.5.noc70077. Epub 2008 Mar 10.
There is some uncertainty whether prior use of antiplatelet (AP) drugs increases the risk of symptomatic intracerebral hemorrhage (SICH) and influences functional outcome in patients with ischemic stroke treated with intravenous thrombolysis.
To assess whether prior use of AP drugs is related to outcome following intravenous tissue plasminogen activator therapy in patients with ischemic stroke.
DESIGN, SETTING, AND PATIENTS: A single-center prospective observational cohort study of the relation between prior AP therapy, occurrence of SICH, and functional outcome of consecutive patients with ischemic stroke undergoing intravenous thrombolysis with tissue plasminogen activator in a university hospital between April 1, 2002, and November 30, 2006.
The occurrence of SICH and favorable outcome reflecting independence defined as a modified Rankin Scale score of 2 or lower at 3 months.
Of the 301 patients who received intravenous tissue plasminogen activator, 89 used AP drugs prior to thrombolysis. Symptomatic intracerebral hemorrhage occurred in 12 patients (13.5%; 95% confidence interval, 7.8%-22.3%) who had received AP drugs and in 6 patients (2.8%; 95% confidence interval, 1.2%-6.2%) without prior AP therapy (P = .001). Multivariate analysis revealed that prior AP therapy was an independent predictor of SICH (odds ratio, 6.0; 95% confidence interval, 2.0-17.1). Nonetheless, prior AP therapy was independently associated with a favorable outcome (odds ratio, 2.0; 95% confidence interval, 1.0-4.3).
Despite a higher incidence of SICH, the net benefit of intravenous tissue plasminogen activator therapy for acute ischemic stroke was greater in patients using AP drugs.
对于抗血小板(AP)药物的既往使用是否会增加症状性脑出血(SICH)的风险以及影响接受静脉溶栓治疗的缺血性脑卒中患者的功能结局,目前存在一些不确定性。
评估缺血性脑卒中患者在静脉注射组织纤溶酶原激活剂治疗后,既往使用AP药物是否与结局相关。
设计、地点和患者:一项单中心前瞻性观察性队列研究,研究对象为2002年4月1日至2006年11月30日期间在一所大学医院接受组织纤溶酶原激活剂静脉溶栓的连续性缺血性脑卒中患者,探讨既往AP治疗、SICH的发生与功能结局之间的关系。
SICH的发生情况以及反映独立性的良好结局,定义为3个月时改良Rankin量表评分为2分或更低。
在接受静脉注射组织纤溶酶原激活剂的301例患者中,89例在溶栓前使用了AP药物。接受过AP药物治疗的患者中有12例(13.5%;95%置信区间,7.8%-22.3%)发生了症状性脑出血,而未接受过AP药物治疗的患者中有6例(2.8%;95%置信区间,1.2%-6.2%)发生了症状性脑出血(P = 0.001)。多因素分析显示,既往AP治疗是SICH的独立预测因素(比值比,6.0;95%置信区间,2.