TY - JOUR T1 - High Doses of Infliximab in the Management of Juvenile Idiopathic Arthritis JF - The Journal of Rheumatology JO - J Rheumatol SP - 1749 LP - 1755 DO - 10.3899/jrheum.130133 VL - 40 IS - 10 AU - Ajay Tambralli AU - Timothy Beukelman AU - Peter Weiser AU - Thomas Prescott Atkinson AU - Randy Quentin Cron AU - Matthew Laurence Stoll Y1 - 2013/10/01 UR - http://www.jrheum.org/content/40/10/1749.abstract N2 - 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. ER -