Jason Leonard A, McManimen Stephanie, Sunnquist Madison, Brown Abigail, Furst Jacob, Newton Julia L, Strand Elin Bolle
Center for Community Research, DePaul University, Chicago, IL USA.
Newcastle University.
Fatigue. 2016;4(1):1-23. doi: 10.1080/21641846.2015.1124520. Epub 2016 Jan 19.
There has been considerable controversy regarding how to name and define the illnesses known as myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS). The IOM report has proposed a new clinical criteria and name for this illness, but aspects of these recommendations have been scrutinized by patients and scientists.
It is possible that both empiric and consensus approaches could be used to help settle some of these diagnostic challenges. Using patient samples collected in the United States, Great Britain, and Norway (N=556), the current study attempted to categorize patients using more general as well as more restricted case definitions.
Overall, the outcomes suggest that there might be four groupings of patients, with the broadest category involving those with chronic fatigue (N=62), defined by 6 or more months of fatigue which can be cannot be explained by medical or psychiatric conditions. A second category involves those patients that have chronic fatigue that can be explained by a medical or psychiatric condition (N=47). A third category involves more specific criteria that have been posited both by the IOM report, a Canadian Clinical Case criteria, a ME-ICC criteria and a more empiric approach. These efforts have specified domains of substantial reductions of activity, post-exertional malaise, neurocognitive impairment, and sleep dysfunction (N=346). Patients with these characteristics were more functionally impaired than those meeting just chronic fatigue criteria, < .05. Finally, those meeting even more restrictive ME criteria proposed by Ramsay, identified a smaller and even more impaired group, < .05.
The advantages of using such empirical and consensus approaches to develop reliable classification and diagnostic efforts are discussed.
关于如何命名和定义肌痛性脑脊髓炎(ME)和慢性疲劳综合征(CFS)这两种疾病一直存在很大争议。美国国家医学研究院(IOM)的报告针对这种疾病提出了新的临床标准和名称,但这些建议的某些方面受到了患者和科学家的仔细审查。
经验性方法和共识性方法都有可能用于帮助解决其中一些诊断难题。本研究使用在美国、英国和挪威收集的患者样本(N = 556),尝试采用更宽泛以及更严格的病例定义对患者进行分类。
总体而言,结果表明可能存在四类患者,最宽泛的一类包括慢性疲劳患者(N = 62),定义为疲劳持续6个月或更长时间,且无法用医学或精神疾病解释。第二类包括那些慢性疲劳可由医学或精神疾病解释的患者(N = 47)。第三类涉及美国国家医学研究院报告、加拿大临床病例标准、肌痛性脑脊髓炎国际共识标准(ME-ICC标准)以及一种更基于经验的方法所提出的更具体标准。这些标准明确了活动大幅减少、运动后不适、神经认知障碍和睡眠功能障碍等方面(N = 346)。具有这些特征的患者在功能上比仅符合慢性疲劳标准的患者受损更严重,P <.05。最后,符合拉姆齐提出的更严格的肌痛性脑脊髓炎标准的患者,构成了一个更小且受损更严重的群体,P <.05。
讨论了使用这种经验性方法和共识性方法来开展可靠的分类和诊断工作的优点。