Chinese registry of rheumatoid arthritis (CREDIT): I. Introduction and prevalence of remission in Chinese patients with rheumatoid arthritis

To introduce the Chinese Registry of rhEumatoiD arthrITis (CREDIT), which is the first nationwide, multicentre, online rheumatoid arthritis (RA) registry in China, and to depict major cross-sectional data and treatment strategies of Chinese RA patients. RA patients who fulfilled the 2010 ACR/EULAR c...

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Veröffentlicht in:Clinical and experimental rheumatology 2018-09, Vol.36 (5), p.836-840
Hauptverfasser: Yu, Chen, Li, Mengtao, Duan, Xinwang, Fang, Yongfei, Li, Qin, Wu, Rui, Liu, Shengyun, Wang, Yongfu, Wu, Zhenbiao, Shi, Xiaofei, Jiang, Zhenyu, Wang, Yanhong, Hsieh, Evelyn D, Jin, Shangyi, Jiang, Nan, Wang, Qian, Zhao, Yan, Tian, Xinping, Zeng, Xiaofeng
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Sprache:eng
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Zusammenfassung:To introduce the Chinese Registry of rhEumatoiD arthrITis (CREDIT), which is the first nationwide, multicentre, online rheumatoid arthritis (RA) registry in China, and to depict major cross-sectional data and treatment strategies of Chinese RA patients. RA patients who fulfilled the 2010 ACR/EULAR classification criteria for rheumatoid arthritis were recruited into the registry by their rheumatologists from 144 clinical centres in China. Data, including demographics, disease characteristics, co-morbidities, treatment, and adverse reactions, were collected and documented through the predefined protocol. 8071 registered patients (F:M = 4.03:1) were registered up to May 2017. Mean age at symptom onset and at diagnosis was 46.15±14.72y and 48.68±14.54y, respectively. Point prevalence of remission (95% CIs) was 14.88% (14.10-15.66%), 4.23% (3.79-4.66%), 4.25% (3.81-4.69%), and 4.27% (3.83-4.72%) according to DAS28-CRP, CDAI, SDAI, and the 2011 ACR/EULAR remission criteria, respectively. 38.84% and 38.11% of treatment-naïve patients (n=3262) were in moderate (3.25.1) disease activity, respectively. Among treatment-naïve patients, those who were initiated on treatment with bDMARDs had higher disease activity than those who were treated with csDMARDs (p
ISSN:0392-856X