Juvenile idiopathic arthritis (JIA) is a heterogeneous group of diseases that affect children under 16 years of age and cause stiff or swollen joints and pain that last 6 weeks or more1,2,3.
The International League of Associations for Rheumatology (ILAR) classifies JIA into seven different types. Although chronic arthritis is mandatory for all types, they have distinct extraarticular and systemic clinical manifestations, genetic predispositions, and disease course2,3:
Arthritis usually involving the vertebral column, hips and legs.
Metacarpophalangeal
Arthritis affecting 5 joints or more during the first 6 months of disease and:
Hepatosplenomegaly
Arthritis affecting more than 1 joint with, or preceded by, fever of at least 2 weeks of duration. It is accompanied by at least one of the following: skin rash, lymph node enlargement, hepatomegaly and/or splenomegaly, or serositis.
Joint pain, stiffness and swelling1
JIA may be difficult to diagnose because some children may not complain of pain at first and joint swelling may not be obvious4.
The cause and trigger of JIA remain unclear, as it is not known what causes the immune system to malfunction in JIA2,4.
It is thought that the abnormal immune response is triggered by environmental factors in genetically susceptible individuals2.
There is strong evidence for a genetic component to the aetiology of JIA, being the strongest genetic association with genes of the major histocompatibility complex (MHC), which are central to immunity and and inflammatory processes3,5.
All types of JIA lead to a final common pathway: thickening and inflammation of the joint lining3.
Physical exam and medical history
Diagnosis of JIA based on physical exam and medical history4. The following items are essential for diagnosis and classification of JIA2:
Laboratory tests
Chlidren often test negative for blood tests that are commonly found in adults with rheumatoid arthritis such as rheumatoid factor (RF)4. Other inflammatory markers evaluated are2:
Imaging
Imaging serves to improve the certainty of a diagnosis of JIA and to evaluate joint damage2.
The best care for children with arthritis is provided by a paediatric rheumatology team that has extensive experience and can diagnose and manage the complex needs of the child and family most effectively4.
Pharmacological treatment
NSAIDs
Non-steroidal anti-inflammatory drugs are the most commonly used medicine in JIA as they have analgesic and anti-inflammatory properties5.
Corticosteroids
When only a few joints are involved, a steroid can be injected into the joint before any additional medications are given. Steroids injected into the joint do not have significant side effects4.
DMARDs
Disease-modifying anti-rheumatic drugs (DMARDs) are added as a second-line treatment when arthritis involves many joints or does not respond to steroid joint injections4. Some DMARDs are known as “biologics”, and all of them may cause side effects that need to be monitored and discussed with the paediatric rheumatologist treating your child1,4.
Physical and occupational therapies
Physical and occupational therapy can improve children’s quality of life by teaching
them ways to stay active and how to perform daily tasks with ease6
Hot and cold treatments
Heat pads or warm baths are useful for soothing stiff joints and tired muscles.
Cold is useful for acute pain6
Children with JIA should attend school, participate in extra-curricular and family activities, and live life as normally as possible4.
Exercising regularly6
Having a healthful diet6
Balancing activity with rest6
Managing stress and emotions6