Lyden P, Lu M, Jackson C, Marler J, Kothari R, Brott T, Zivin J
Department of Neurology, Veterans Administration Medical Center, University of California at San Diego School of Medicine, USA.
Stroke. 1999 Nov;30(11):2347-54. doi: 10.1161/01.str.30.11.2347.
No stroke scale has been validated as an outcome measure using data from a clinical trial demonstrating a positive therapeutic effect. Therefore, we proposed to use data from the National Institute of Neurological Disorders and Stroke (NINDS) tPA Stroke Trial to determine whether the National Institutes of Health Stroke Scale (NIHSS) was valid in patients treated with tissue plasminogen activator (tPA) and to explore the underlying clinimetric structure of the NIHSS.
We performed an exploratory factor analysis of NIHSS data from Part 1 (n=291) of the NINDS tPA Stroke Trial to derive a hypothesized underlying factor structure. We then performed a confirmatory factor analysis of this structure using NIHSS data from Part 2 of the same trial (n=333). We then tested whether this final factor structure could be found in tPA- and placebo-treated patients serially over time after stroke treatment. Using 3-month outcome data, we tested for an association between the NIHSS and other measures of stroke outcome.
The exploratory analysis suggested that there were 2 factors underlying the NIHSS, representing left and right brain function, confirming the content validity of the scale. An alternative structure composed of 4 factors could be derived, with a better goodness of fit: the first 2 factors could represent left brain cortical and motor function, respectively, and the second 2 factors could represent right brain cortical and motor function, respectively. The same factor structures were then found in tPA and placebo patient groups studied serially over time, confirming the exploratory analysis. All 3-month clinical outcomes were associated with each other at subsequent time points, confirming predictive validity.
This is the first study of the validity of a stroke scale in patients treated with effective stroke therapy. The NIHSS appeared to be valid in patients with acute stroke and for finding treatment-related differences. The scale was valid when used serially over time after stroke, up to 3 months, and showed good agreement with other measures of outcome.
尚无卒中量表经临床试验数据验证可作为显示出积极治疗效果的结局指标。因此,我们提议使用美国国立神经疾病与卒中研究所(NINDS)的tPA卒中试验数据,以确定美国国立卫生研究院卒中量表(NIHSS)在接受组织纤溶酶原激活剂(tPA)治疗的患者中是否有效,并探索NIHSS潜在的计量结构。
我们对NINDS tPA卒中试验第1部分(n = 291)的NIHSS数据进行探索性因子分析,以得出一个假设的潜在因子结构。然后,我们使用同一试验第2部分(n = 333)的NIHSS数据对该结构进行验证性因子分析。然后,我们测试在卒中治疗后的一段时间内,能否在接受tPA治疗和安慰剂治疗的患者中依次发现这种最终的因子结构。利用3个月的结局数据,我们测试了NIHSS与其他卒中结局指标之间的关联。
探索性分析表明,NIHSS有两个潜在因子,分别代表左脑和右脑功能,证实了该量表的内容效度。可以得出一个由4个因子组成的替代结构,其拟合优度更好:前两个因子可分别代表左脑皮质和运动功能,后两个因子可分别代表右脑皮质和运动功能。随后在接受tPA和安慰剂治疗的患者组中依次发现了相同的因子结构,证实了探索性分析的结果。所有3个月的临床结局在后续时间点均相互关联,证实了预测效度。
这是第一项关于有效卒中治疗患者中卒中量表效度的研究。NIHSS在急性卒中患者中似乎有效,并且可用于发现治疗相关差异。该量表在卒中后长达3个月的一段时间内连续使用时有效,并且与其他结局指标显示出良好的一致性。