Juvenile idiopathic arthritis (JIA)
Chronic childhood arthritis (>6 weeks, onset <16y)
Overview
Arthritis persisting >6 weeks with onset before 16 years, of unknown cause, with several subtypes. Systemic JIA (Still disease) has the classic quotidian fever + salmon-pink rash; oligoarticular is the commonest and carries an uveitis risk.
Recognise
- Joint swelling/stiffness >6 weeks; morning stiffness, limp
- Oligoarticular (≤4 joints): commonest; ANTERIOR UVEITIS risk (ANA+) → needs slit-lamp screening
- Systemic (Still): daily spiking fever, salmon-pink rash, hepatosplenomegaly, serositis
- Polyarticular: ≥5 joints
Red flags
- Eye involvement (uveitis often asymptomatic → screen); macrophage activation syndrome in systemic JIA
Differentials & how to tell them apart
Investigations
Clinical (>6 weeks). Inflammatory markers, ANA (uveitis risk), rheumatoid factor (usually negative), exclude infection/malignancy; slit-lamp ophthalmology screening.
Management
NSAIDs + specialist paediatric rheumatology; uveitis screening
- 1Refer to paediatric rheumatology. NSAIDs + intra-articular steroids for symptom control.Gate: Oligoarticular / ANA-positive → regular slit-lamp screening: the uveitis is often ASYMPTOMATIC and sight-threatening
- 2Persistent/polyarticular/systemic → methotrexate then biologics; watch for macrophage activation syndrome in systemic JIA.
Key points
The uveitis of oligoarticular JIA is silent — screening prevents blindness. Systemic JIA = fever + salmon rash and can flare into macrophage activation syndrome.
Monitor & prognosis
Joint function, growth, eye screening, drug monitoring.
Many remit; uveitis and systemic disease drive morbidity.
Source: NICE; BSPAR (paediatric rheumatology)