Jason Leonard A, Sunnquist Madison, Brown Abigail, Newton Julia L, Strand Elin Bolle, Vernon Suzanne D
DePaul University.
Newcastle University.
Fatigue. 2015 Jul;3(3):127-141. doi: 10.1080/21641846.2015.1051291.
The Institute of Medicine has recommended a change in the name and criteria for Chronic Fatigue Syndrome (CFS), renaming the illness Systemic Exertion Intolerance Disease (SEID). The new SEID case definition requires substantial reductions or impairments in the ability to engage in pre-illness activities, unrefreshing sleep, post-exertional malaise, and either cognitive impairment or orthostatic intolerance.
In the current study, samples were generated through several different methods and were used to compare this new case definition to previous case definitions for CFS, Myalgic Encephalomyelitis (ME-ICC), Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), as well as a case definition developed through empirical methods.
We used a cross-sectional design with samples from tertiary care settings, a biobank sample, and other forums. 796 patients from the US, Great Britain, and Norway completed the DePaul Symptom Questionnaire.
Findings indicated that the SEID criteria identified 88% of participants in the samples analyzed, which is comparable to the 92% that met the Fukuda criteria. The SEID case definition was compared to a four item empiric criteria, and findings indicated that the four item empiric criteria identified a smaller, more functionally limited and symptomatic group of patients.
The recently developed SEID criteria appears to identify a group comparable in size to the Fukuda et al. criteria, but a larger group of patients than the Canadian ME/CFS and ME criteria, and selects more patients who have less impairment and fewer symptoms than a four item empiric criteria.
美国医学研究所建议更改慢性疲劳综合征(CFS)的名称和标准,将该疾病重新命名为系统性劳累不耐受疾病(SEID)。新的SEID病例定义要求在从事病前活动的能力、睡眠不能解乏、劳累后不适,以及认知障碍或体位性不耐受方面有大幅降低或损害。
在本研究中,通过几种不同方法生成样本,并将这个新的病例定义与CFS、肌痛性脑脊髓炎(ME-ICC)、肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)之前的病例定义,以及通过实证方法制定的病例定义进行比较。
我们采用横断面设计,样本来自三级医疗机构、生物样本库和其他平台。来自美国、英国和挪威的796名患者完成了德保罗症状问卷。
研究结果表明,SEID标准在分析的样本中识别出88%的参与者,这与符合福田标准的92%相当。将SEID病例定义与四项实证标准进行比较,结果表明四项实证标准识别出的患者群体更小、功能受限更严重且症状更多。
最近制定的SEID标准似乎识别出了一个规模与福田等人的标准相当的群体,但比加拿大ME/CFS和ME标准识别出的患者群体更大,并且比四项实证标准选择了更多损害更小、症状更少的患者。