Validation of the 2011 and 2016 American college of rheumatology diagnostic criteria for fibromyalgia in a Chinese population

纤维肌痛 医学 痹症科 接收机工作特性 内科学 物理疗法 结构效度 人口 切断 类风湿性关节炎 标准效度 判别效度 外部有效性 可靠性(半导体) 临床心理学 心理测量学 内部一致性 心理学 量子力学 社会心理学 物理 环境卫生 功率(物理)
作者
Juan Jiao,Zengyu Cheng,Yuya Xiao,Hui Wang,Yong-Feng Zhang,Yayun Zhao,Yuan Jia
出处
期刊:Annals of Medicine [Informa]
卷期号:55 (2)
标识
DOI:10.1080/07853890.2023.2249921
摘要

Purpose To provide a foundation for clinical diagnosis, epidemiological investigation and intervention trials, we examined the reliability and validity of the American College of Rheumatology (ACR) 2011 and 2016 survey diagnostic criteria among Chinese patients based on the fibromyalgia severity (FS) scale.Methods In this study, 200 fibromyalgia patients diagnosed according to the 1990 criteria (1990c) were matched with rheumatoid arthritis (RA) patients based on age and gender. The FS scale score and its subscales were examined to determine their correlations with the revised fibromyalgia impact questionnaire (FIQR). Receiver operator characteristic (ROC) analysis was performed, and test-retest reliability, internal consistency, and construct validity were examined.Results The area under the curve (AUC) for the ACR 2011c and 2016c was 0.870 and 0.845, respectively, and the sensitivity and specificity were 78.0% and 96.0% for the 2011c and 70.5% and 98.5% for the 2016c, respectively. The FS scale and its subscales were confirmed to exhibit good internal consistency, and they were significantly correlated with the FIQR, thereby indicating adequate construct validity. Using a lower cutoff value 11 points for the FS scale score based on the generalized pain requirement might be a more effective approach in the Chinese population; this approach yielded an AUC of 0.923 and a sensitivity of 87.0% and specificity of 97.5%.Conclusion The 2011c and 2016c are reliable instruments for diagnosing fibromyalgia patients in China. The FS scale could be a valid tool to assist in fibromyalgia diagnosis, and a cutoff value 11 points is more suitable in Chinese patients.Trial registration ClinicalTrials.gov ID: NCT03381131
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