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A lifelong journey: Long-term perspectives on Juvenile Idiopathic Arthritis
Filipa Oliveira Ramos1, Carolina Zinterl2, João Eurico Fonseca3
1Unidade de Reumatologia Pediátrica, Hospital Universitário Santa Maria, ULS Santa Maria, Centro Académico de Medicina de Lisboa, Portugal; Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Centro Académico de Medicina de Lisboa, Portugal.
Insights
Transitioning Juvenile Idiopathic Arthritis (JIA) patients to adult care is complex. Inadequate transition leads to poor outcomes, highlighting the need for structured care and further research for better long-term management.
Area of Science:
- Rheumatology
- Pediatric Rheumatology
- Adult Rheumatology
Background:
- Juvenile Idiopathic Arthritis (JIA) is a heterogeneous group of chronic childhood inflammatory diseases with variable adult outcomes.
- Transitioning JIA patients from pediatric to adult healthcare systems presents significant challenges.
- Continuity of care is often disrupted during this transition, impacting disease management and patient health.
Purpose of the Study:
- To review the complexities and challenges associated with transitioning Juvenile Idiopathic Arthritis patients.
- To emphasize the impact of inadequate transition on disease activity, treatment adherence, and long-term outcomes.
- To highlight the need for optimized, multifaceted approaches for managing adults with JIA.
Main Methods:
- This study is a review of existing literature on Juvenile Idiopathic Arthritis transition care.
- Analysis of factors influencing disease classification, long-term outcomes, and quality of life in JIA patients.
- Synthesis of current knowledge on treatment strategies and management of comorbidities in adult JIA.
Main Results:
- Inadequate transition from pediatric to adult care results in lost follow-up, treatment cessation, and increased disease activity.
- Disease heterogeneity and evolving phenotypes complicate long-term outcome prediction in JIA.
- Despite treatment advances, many JIA patients face long-term disability and joint damage.
Conclusions:
- Optimizing long-term outcomes for adults with JIA necessitates structured transition processes, personalized treatments, and comorbidity management.
- Further research is crucial for refining predictive models and enhancing disease monitoring tools.
- A comprehensive, lifelong management strategy is essential for improving the quality of life for individuals with JIA.
Abstract:
Juvenile Idiopathic Arthritis (JIA) represents a diverse group of chronic inflammatory conditions that begin in childhood or adolescence and continue into adulthood, with varying severity and outcomes. This review discusses the complexities of transitioning JIA patients emphasizing that inadequate transition from pediatric to adult care leads to loss of follow-up, treatment discontinuation, and increased disease activity. Furthermore, challenges in disease classification hinder continuity of care across lifespan. It is also pointed out that predicting long-term outcomes in JIA remains complex due to heterogeneity and evolving phenotypes. Factors such as disease category, joint involvement, and treatment influence disease activity, functional disability, and quality of life. Despite advancements in treatment strategies, a substantial proportion of patients experience long-term disability and joint damage. Finally, it is underscored that optimising long-term outcomes in adults with JIA requires a multifaceted approach encompassing structured transition processes, personalised treatment strategies, and comprehensive management of comorbidities. Further research is needed to refine predictive models, enhance disease monitoring tools, and understand the complex interplay between disease activity, treatment response, and long-term outcomes.
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