English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Children receiving biologic DMARDs were older at enrollment (mean age 13 years versus 10 years; p <0.001) and had a longer disease duration (mean 6 years versus 4 years; p<0.001). Children with imaging evidence of joint damage (RR 1.6; 95% CI: 1.3-1.9), positive RF (RR: 1.36; 95% CI 1.1 – 1.6), or positive anti-CCP (RR: 1.35; 1.1-1.7) were more likely to have received a biologic DMARD. Children with oligoarthritis were less likely to have received a biologic DMARD than other categories. Conclusion The majority of patients with JIA enrolled into the CARRAnet registry has relatively low disease activity, minimal disability, and have received at least one DMARD. Positive anti-CCP or RF, joint damage on imaging, older age at enrollment and longer disease duration were associated with biologic DMARD use. Limitations include the underrepresentation of non-English speaking families and enrollment bias. Continued enrollment into this cohort will support future analyses with increased sample sizes and the potential for longitudinal data analysis. Disclosure

pediatric rheumatology online journal

Disease characteristics and medication use in a multicenter cohort of children with juvenile idiopathic arthritis (JIA): preliminary analyses from the CARRAnet registry