Department of Medicine, St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Stroke. 2012 May;43(5):1315-22. doi: 10.1161/STROKEAHA.111.646265. Epub 2012 Feb 3.
Tools to predict the clinical response after intravenous thrombolytic therapy (tPA) are scarce. The iScore is an existing validated tool to estimate outcomes after an acute ischemic stroke. The purpose of this study was to determine the ability of the iScore to predict clinical response and risk of hemorrhagic transformation after tPA.
We applied the iScore (www.sorcan.ca/iscore) to patients presenting with an acute ischemic stroke at 11 stroke centers in Ontario, Canada, between 2003 and 2009 identified from the Registry of the Canadian Stroke Network. A cohort of patients with stroke treated at 154 centers in Ontario was used for external validation. We compared outcomes between patients receiving and not receiving tPA after adjusting for differences in baseline characteristics using propensity-score matching. Patients were stratified into 3 a priori defined groups according to stroke severity using the iScore.
Among 12 686 patients with an acute ischemic stroke, 1696 (13.4%) received intravenous thrombolysis. Higher iScores were associated with poor outcomes in both the tPA and non-tPA groups (P<0.001). Among those at low and medium risk based on their iScores, tPA use was associated with a benefit in the primary outcome (relative risk, 0.74 for those with low-risk iScores; 95% CI, 0.67-0.84; relative risk, 0.88 for those with medium risk iScores; 95% CI, 0.84-0.93). There was no difference in clinical outcomes between matched patients receiving and not receiving tPA in the highest iScore group (relative risk, 0.97; 95% CI, 0.94-1.01). Similar results were observed for disability at discharge and length of stay. The incident risk of neurological deterioration and hemorrhagic transformation (any or symptomatic) with tPA increased with the iScore risk. Results were similar in the validation cohort for risk of poor outcome with tPA by iScore level.
The iScore may be used to predict clinical response and risk of hemorrhagic complications after tPA for an acute ischemic stroke. Patients with high iScores may not have a clinically meaningful benefit from intravenous tPA at the time of carrying a higher risk of hemorrhagic complications.
目前缺乏用于预测静脉溶栓治疗(tPA)后临床反应的工具。iScore 是一种现有的用于评估急性缺血性脑卒中后结局的验证工具。本研究旨在确定 iScore 预测 tPA 后临床反应和出血性转化风险的能力。
我们在加拿大安大略省的 11 个卒中中心应用 iScore(www.sorcan.ca/iscore),从加拿大卒中网络的注册系统中确定了 2003 年至 2009 年间就诊的急性缺血性卒中患者。使用安大略省 154 个中心治疗的卒中患者队列进行外部验证。我们通过倾向评分匹配,调整基线特征差异后,比较接受和未接受 tPA 的患者的结局。根据 iScore 确定的卒中严重程度,患者分为 3 个预先定义的组。
在 12686 例急性缺血性卒中患者中,1696 例(13.4%)接受了静脉溶栓治疗。iScore 较高的患者在接受 tPA 和未接受 tPA 的患者中结局均较差(均 P<0.001)。在基于 iScore 低危和中危的患者中,tPA 使用与主要结局的获益相关(低危 iScore 的相对风险为 0.74,95%CI,0.67-0.84;中危 iScore 的相对风险为 0.88,95%CI,0.84-0.93)。在 iScore 最高的组中,接受和未接受 tPA 的匹配患者的临床结局无差异(相对风险为 0.97,95%CI,0.94-1.01)。在出院时残疾和住院时间方面也观察到类似的结果。随着 iScore 风险的增加,tPA 后神经功能恶化和出血性转化(任何部位或症状性)的风险也增加。在验证队列中,根据 iScore 水平,tPA 治疗的不良结局风险也有类似的结果。
iScore 可用于预测急性缺血性卒中 tPA 后临床反应和出血性并发症的风险。iScore 较高的患者接受静脉 tPA 治疗可能不会带来有临床意义的获益,同时出血性并发症的风险更高。