Published by Bupa's Health Information Team, March 2010.
This factsheet is for parents of children who have juvenile idiopathic arthritis, or who would like information about it.
Juvenile idiopathic arthritis (also known as JIA, juvenile rheumatoid arthritis and juvenile chronic arthritis) is inflammation (swelling) of the joints in children. The symptoms may last into adult life or they may disappear over time.
Arthritis is a condition that affects the joints. It means one or more of your joints are swollen, painful and stiff (inflamed). Juvenile means the arthritis affects children under 16 years. Idiopathic means the cause is unknown. JIA affects about one in 1,000 children in the UK.
JIA is a chronic condition. A chronic illness is one that lasts a long time, sometimes for the rest of the affected person's life. When describing an illness, the term chronic refers to how long a person has it, not to how serious a condition is.
There are three main types of JIA.
JIA affects all children differently. Symptoms may come and go over time with periods when they flare up and are worse. There may be times when your child has no symptoms at all - this is called remission.
The main symptoms of JIA are swollen, painful and stiff joints. The joint areas may look red and feel hot when you touch them. The exact symptoms and number of joints affected will vary depending on which type of JIA your child has.
Children with polyarticular JIA will have at least five or more joints affected including fingers and toes. Swelling and pain may also occur in hips, neck and jaw. Your child may also have other symptoms such as:
As well as joint pain, children with systemic JIA may have:
JIA may affect your child's general growth. It's possible that your child's affected limbs may develop at different rates. For example if the arthritis is particularly bad in one knee the affected leg may be slightly shorter.
Anaemia may also be a problem. Anaemia is when there are too few red blood cells or not enough haemoglobin in the blood.
There is also a risk that your child may develop inflammation of the eyes (uveitis). Make sure your child has regular eye checks with an ophthalmologist (a doctor who specialises in eye health), even if he or she doesn't have any obvious symptoms.
There is a risk that systemic JIA may affect internal organs such as the tissue that covers the heart, liver or spleen. Children with systemic JIA may need to have regular check-ups.
The cause of JIA isn't fully understood at present but it's thought to be an autoimmune disease. An autoimmune disease is a condition caused by antibodies from the immune system attacking the body. It's possible that the tendency to develop the condition is inherited. However, it's thought that other factors are likely to be involved which are responsible for setting off this reaction of your child's immune system.
Your GP will ask about your child's symptoms and examine him or her. Your GP may also ask you about your child's medical history.
There is no single test that can diagnose JIA and your GP will want to rule out other conditions that may be causing your child's symptoms. Your GP will usually refer your child to a paediatrician (a doctor who specialises in children's health).
Your child may need to have several tests, such as:
There isn't a complete cure for JIA, but there are treatments available to help control or ease the symptoms.
Your child will receive treatment from a team of health professionals. He or she will need regular check-ups to monitor his or her condition.
Regular exercise such as swimming, running or aerobics may be helpful.
Your child will be given exercises by a physiotherapist to do at home. These will aim to reduce the pain and stiffness in your child's joints. Your child will need to do these exercises every day, even though he or she may not feel like it.
Using heat treatments, such as a hot water bottle wrapped in a towel may help to ease painful and swollen joints. A cold compress, such as ice or a bag of frozen peas, wrapped in a towel may also help. Never apply ice directly to your skin as it can give you an 'ice burn' - always place a cloth between the ice and skin.
There are many different medicines available to help control symptoms, slow down or even stop the progression of JIA.
All medicines can have side-effects, some more serious than others. Always read the patient information that comes with your medicine and if you have any questions, ask your doctor or pharmacist for advice.
Most children with JIA are able to live a normal active life. For some however the symptoms may cause problems that make everyday life difficult. Your child may find it difficult to walk, bend, get dressed or even wash by themselves. There is a great deal of support available for children with JIA. As well as the team of healthcare professionals treating your child, there are support groups who can offer advice and information.
For answers to frequently asked questions on this topic, see Common questions.
For sources and links to further information, see Resources.
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This information was published by Bupa's Health Information Team and is based on reputable sources of medical evidence. It has been reviewed by appropriate medical or clinical professionals. Photos are only for illustrative purposes and do not reflect every presentation of a condition. The content is intended only for general information and does not replace the need for personal advice from a qualified health professional. For more details on how we produce our content and its sources, visit the About our Health Information page.
Publication date: March 2010
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