PT - JOURNAL ARTICLE AU - Ajay Tambralli AU - Timothy Beukelman AU - Peter Weiser AU - Thomas Prescott Atkinson AU - Randy Quentin Cron AU - Matthew Laurence Stoll TI - High Doses of Infliximab in the Management of Juvenile Idiopathic Arthritis AID - 10.3899/jrheum.130133 DP - 2013 Aug 15 TA - The Journal of Rheumatology PG - jrheum.130133 4099 - http://www.jrheum.org/content/early/2013/08/10/jrheum.130133.short 4100 - http://www.jrheum.org/content/early/2013/08/10/jrheum.130133.full AB - Objective To review our experiences with high-dose infliximab (IFX) to treat juvenile idiopathic arthritis (JIA). We routinely use high doses of IFX (10–20 mg/kg) in children with recalcitrant or highly active JIA. Although biologics have revolutionized treatment of JIA, many patients have active disease despite therapy. Studies have shown benefits of high-dose IFX in several conditions, including inflammatory bowel disease, psoriasis, and idiopathic uveitis. The safety and effectiveness of high-dose IFX have not been evaluated in JIA. Methods We performed a retrospective review of children with JIA who received IFX ≥ 10 mg/kg. We recorded all serious adverse events (SAE), medically important infections, and infusion reactions. We also recorded the physician global assessment of disease activity (MD global) and active joint count (AJC) at initiation of high-dose IFX and 3, 6, and 12 months thereafter. Results Fifty-eight subjects received a total of 1064 infusions over 95 person-years. There were a total of 9 SAE (9.5/100 person-yrs), 7 of which were potentially related to therapy, and 6 infusion reactions (0.5%), none constituting anaphylaxis. Statistically significant improvements were observed in the AJC (median 0, range 0–31, vs 2, 0–39) and MD global (12, 2–31, vs 22, 5–80) over the first year. Conclusion High-dose IFX appears safe in the management of JIA. Future prospective controlled studies are necessary to evaluate its safety and efficacy.