How I treat juvenile idiopathic arthritis: A state of the art review
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Published on: May 16, 2025
Rolando Cimaz1, Achille Marino1, Alberto Martini2
1Azienda Oospedaliera Universitaria Anna Meyer, Florence, Italy; Università degli Studi di Firenze, Florence, Italy.
Insights
Juvenile idiopathic arthritis (JIA) is a common childhood rheumatic disease causing disability. This review offers practical treatment advice for physicians managing JIA patients to achieve remission and minimize side effects.
Area of Science:
- Pediatric Rheumatology
- Immunology
- Genetics
Background:
- Juvenile idiopathic arthritis (JIA) is the most prevalent chronic rheumatic condition in children.
- JIA presents with diverse subtypes, each having unique clinical features and underlying etiopathogenesis.
- Effective management of JIA is crucial for preventing short- and long-term disability.
Purpose of the Study:
- To offer practical, daily guidance for treating physicians managing JIA.
- To synthesize current recommendations and clinical experience for JIA management.
- To aid in achieving early and sustained remission with minimal adverse effects in pediatric patients.
Main Methods:
- Literature review of existing JIA treatment guidelines.
- Synthesis of clinical expertise from experienced rheumatologists.
- Analysis of distinct JIA disease categories and their implications.
Main Results:
- Identification of key challenges in JIA pharmacotherapy.
- Emphasis on individualized treatment strategies based on JIA subtypes.
- Highlighting the importance of timely medication adjustment.
Conclusions:
- Optimizing JIA treatment requires a nuanced approach considering disease heterogeneity.
- Physicians need practical tools to navigate medication choices for JIA.
- Early and sustained remission is achievable with informed therapeutic decisions.
Abstract:
Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease in children and an important cause of short and long-term disability. JIA encompasses several disease categories, each of which has distinct presentation, clinical manifestations, and, presumably, genetic background and etiopathogenesis. Correct choice and timely use of available medications to achieve early and sustained remission with as few side effects as possible remain challenges for the treating physician. This review aims to provide daily practical advice for the treatment of JIA patients on the basis of both our experience and existing recommendations.
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