Abstract

ObjectivesTo describe the ophthalmological characteristics in a Juvenile idiopathic arthritis (JIA) cohort and to evaluate how therapeutic advances have changed the course of the uveitis.MethodsAnalysis of a retrospective cohort study of consecutive JIA pediatric patients including JIA-associated uveitis (JIA-U) and comparison with a previous study in the same uveitis center assessed before the wide-spread of biological therapy.ResultsThe total of 49 JIA patients were analyzed, of whom 18 JIA-U, compared with a JIA-U past cohort of 66 patients. Systemic corticosteroids were used significantly less in the current JIA-U group (p = 0.008) than in the past one. JIA-U present cohort was on therapy more frequently with conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) than the past group (p = 0.039), mostly treated with methotrexate (93.3%). Furthermore, a larger use of biologic disease-modifying anti-rheumatic drugs (bDMARDs) was described in the current JIA-U group (p = 0.005) also associated with csDMARDs (p = 0.003). Adalimumab was used more (72.7%) in the present JIA-U cohort compared to a larger treatment with infliximab (61.5%) in the past (p = 0.005). Higher number of uveitis recurrences was observed in the previous cohort compared to the current one (p = 0.005). Fewer complications were described in this study than in the previous: posterior synechiae (p = 0.007), cataract (p < 0.001), band keratopathy (p < 0.001), and elevated intraocular pressure (IOP) (p = 0.047).ConclusionCurrent therapies reduced the uveitis recurrences and ocular complications including cataract due also to the lower use of corticosteroids. The new close collaboration with the pediatric rheumatologic center in the same University has contributed to the care improvement and decrease of uveitis complications.

Highlights

  • Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease in children with an incidence of 8.2 (7.5–9.0)/100000 cases under 16 years of age, and an annual prevalence of approximately 70.2 (16–140)/100000 [1]

  • The present cohort included 49 children with a diagnosis of JIA according to the International League of Associations for Rheumatology criteria [12]

  • Patients affected from JIA associated with uveitis were 18/49 (36.7%) (On a total of 31 eyes) while 31/49 (63.3%) children had only a diagnosis of JIA

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Summary

Introduction

JIA is the most common chronic rheumatic disease in children with an incidence of 8.2 (7.5–9.0)/100000 cases under 16 years of age, and an annual prevalence of approximately 70.2 (16–140)/100000 [1]. Sometimes systemic corticosteroids are used for a short time in severe disease, but the step is usually the immunosuppressive therapy, as disease-modifying anti-rheumatic drugs (DMARDs), mainly using methotrexate (MTX), or other immunosuppressive drugs in MTX-resistant cases [6]. This therapy is usually able to solve the recalcitrant cases achieving a good control of the uveitis in approximately 70–80% of patients within 3–4 months [7, 8]. TNF-a blocking agents are the main biologics used as treatment of chronic childhood uveitis in unresponsive JIA uveitis cases other biological drugs options are available [9,10,11,12]

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