Barber P Alan, Parsons Mark W, Desmond Patricia M, Bennett Donald A, Donnan Geoffrey A, Tress Brian M, Davis Stephen M
Department of Neurology, Royal Melbourne Hospital, Parkville, Vic 3050, Australia.
J Neuroimaging. 2004 Apr;14(2):123-32.
The authors used serial magnetic resonance perfusion-weighted imaging (PWI) and diffusion-weighted imaging (DWI) to determine whether major reperfusion and the attenuation of infarct expansion are associated with improved stroke outcome.
Forty-nine patients were studied with serial magnetic resonance imaging within 6 hours of stroke onset and again at 4 days (subacute studies) and 3 months (outcome studies). Two imaging parameters were examined: infarct expansion between acute and outcome studies and major reperfusion between acute and subacute studies.
Patients with major reperfusion (45% of those with acute PWI lesions) were more likely to have little or no disability at outcome (National Institutes of Health Stroke Scale [NIHSS] score < or = 4, P = .0176; Barthel Index [BI] score > or = 90, P = .0547) after adjustment for baseline differences. In contrast, patients with infarct expansion (48%) were more likely to be dead or dependent at outcome (BI < 90, P = .0414; NIHSS score P = .082; modified Rankin Scale score > 2, P < .0001). These measures were used to generate sample size calculations based on hypothetical treatment effects. Therapies postulated to double the proportion of patients with major reperfusion from one third to two thirds would require 41 patients in each group (treated and untreated) to be sufficiently powered to show a difference. Interventions postulated to halve the number of patients with infarct expansion from 50% to 25% would require 66 patients in each group to show a difference.
Infarct expansion and major reperfusion are associated with clinically meaningful changes in stroke outcome. These measures could be used as surrogate markers of outcome in late phase II proof-of-concept stroke studies designed to provide efficacy signals before embarking on large phase III studies with definitive clinical endpoints.
作者采用系列磁共振灌注加权成像(PWI)和弥散加权成像(DWI)来确定主要再灌注及梗死灶扩展的减轻是否与改善的卒中结局相关。
对49例患者在卒中发作6小时内进行系列磁共振成像检查,并在4天(亚急性期研究)和3个月(结局研究)时再次检查。检查了两个成像参数:急性研究与结局研究之间的梗死灶扩展以及急性研究与亚急性期研究之间的主要再灌注。
在对基线差异进行校正后,发生主要再灌注的患者(急性PWI病变患者中的45%)在结局时更有可能几乎没有残疾或无残疾(美国国立卫生研究院卒中量表[NIHSS]评分≤4,P = 0.0176;巴氏指数[BI]评分≥90,P = 0.0547)。相比之下,发生梗死灶扩展的患者(48%)在结局时更有可能死亡或依赖他人(BI < 90,P = 0.0414;NIHSS评分P = 0.082;改良Rankin量表评分>2,P < 0.0001)。这些测量值用于根据假设的治疗效果进行样本量计算。假设能使主要再灌注患者比例从三分之一翻倍至三分之二的治疗方法,每组(治疗组和未治疗组)需要41例患者才能有足够的检验效能显示差异。假设能使梗死灶扩展患者数量从50%减半至25%的干预措施,每组需要66例患者才能显示差异。
梗死灶扩展和主要再灌注与卒中结局的临床意义改变相关。在旨在进行具有明确临床终点的大型III期研究之前提供疗效信号的晚期II期概念验证卒中研究中,这些测量值可用作结局的替代标志物。