Medications
Most children with
juvenile rheumatoid arthritis (JRA) need to take
medication to reduce inflammation and control pain and to help prevent
increasing damage to the joints. When inflammation and pain are controlled, a
child is more willing and able to do joint exercises to improve joint strength
and prevent loss of movement.
Many different medications are used to treat JRA. No single
medication works for every child. It may take some time to find the right
medication or combination of medications that best controls your child's
symptoms. Treatment is individualized for each child by his or her doctor and
parents while considering effectiveness, side effects, cost, and the type and
severity of the disease.
Medication Choices
Although treatment varies depending on the needs of the
individual child, certain medications are often tried first (first-line
medications), while others are often saved to try later if they are needed
(second-line medications).
First-line medication. Nonsteroidal
anti-inflammatory drugs (NSAIDs) are usually the first
medications tried to control JRA inflammation and symptoms. Naproxen sodium is
the most frequently used NSAID treatment for JRA. Doctors choose naproxen based
on its low incidence of side effects compared to its effectiveness.10 Ibuprofen is an effective alternative. But in general, less
than one-third of children will have significant relief from NSAIDs.5
NSAIDs and corticosteroids are most often used to control the
initial stages of
systemic JRA and may be used in children who have
pauciarticular (oligoarthritis) with shortening of the
muscles around the joints (contractures) or
polyarticular disease with joint pain and
swelling.10, 5
Second-line medication. If symptoms are
not well-controlled with NSAIDs or corticosteroids, stronger medications such
as methotrexate are often used successfully.10, 5 Methotrexate, sulfasalazine, and other second-line
medications are sometimes referred to as
disease-modifying antirheumatic drugs (DMARDs). Some
experts prefer to call them slow-acting antirheumatic drugs (SAARDs).
Some children with JRA gain significant benefit from early
methotrexate treatment. Although there is no definitive way of knowing which
children are the best candidates for early methotrexate treatment, this
practice is becoming more common in an effort to prevent joint and eye damage.
Early treatment with methotrexate is often used for polyarticular JRA.5
Biological therapy is a newer option to treat JRA, particularly
polyarticular JRA, that does not respond to other treatments. The biological
agent etanercept, which is a tumor necrosis factor (TNF) inhibitor, has had
some success in relieving symptoms and decreasing the number of flare-ups.
Other TNF inhibitors, such as infliximab, are still under study to treat
JRA.11
Medications used to treat JRA
First-line
- Nonsteroidal
anti-inflammatory drugs (NSAIDs)
- Injected
corticosteroids
Second-line
- Methotrexate
- Etanercept (Enbrel)
- Infliximab
(Remicade)
- Oral corticosteroids
Other second-line medications used less often
- Sulfasalazine
- Antimalarials (such as hydroxychloroquine sulfate
[Plaquenil]
- Adult therapies, such as cytotoxic (cell-destroying)
drugs and intravenous human immunoglobulin, that may be used for rheumatoid
arthritis in adults but are not yet proven to be safe and effective for
children with JRA
Gold salts were one of the first treatments used for joint
inflammation, and you may still hear about them. However, injected gold salts
have been replaced by methotrexate for the treatment of JRA. Gold salts taken
by mouth (oral) have not been shown to be effective for JRA.10
Medications used to treat inflammatory eye disease
- Corticosteroid
eyedrops
- Methotrexate and cyclosporine A
- Mydriatics, which are eyedrops that dilate the pupil
and keep the iris from sticking to the cornea or lens
- Tumor
necrosis factor (TNF) inhibitors. These medications are biological agents known
as anti-TNF agents because they reduce inflammation by blocking the TNF
protein.
Etanercept is an example of these medicines.
What To Think About
Annual flu shots are recommended for children who are on
long-term aspirin therapy. Children on long-term aspirin therapy who get
chickenpox or
influenza (flu) are at risk for getting Reye's
syndrome. Although there is a risk, Reye's syndrome is very rare. Very few
cases of Reye's syndrome have been reported in children with chronic arthritis
who were being treated with aspirin. If your child has been exposed to
chickenpox or flu, talk to the doctor about giving your child acetaminophen to
control pain and relieve fever until the incubation period, or the illness
itself, has passed.
Combination therapy—using methotrexate with sulfasalazine,
hydroxychloroquine, or etanercept—has been used on a limited basis to treat
JRA. Most medical experience with combination therapy is with adults; only
children with severe JRA that has not improved with methotrexate or
sulfasalazine are considered for combination treatment.
It is impossible to predict whether a child will improve with a
certain medication. Several different medications may be tried before one is
found that controls symptoms and doesn't cause side effects. It can also take
weeks to months for a medication to show effect, and symptoms may continue
during that time.