Reye's syndrome is a rare illness that can be life-threatening. The illness occurs mainly in young children and usually follows a viral infection, such as the flu, chicken pox, or upper respiratory infection. It occurs most often in children between the ages of 2 and 16 years.
The illness causes:
The exact cause of Reye's syndrome is unknown. It is believed that the use of aspirin and medicines containing aspirin may trigger its development in children. This is why children 18 years or younger should not be given aspirin in any form for any reason.
Symptoms for Reye's syndrome begin about a week after a viral infection and include:
Emergency medical care is needed when:
Children with Reye's syndrome must be hospitalized. The diagnosis is made by testing the blood and spinal fluid. A liver biopsy may also be needed. There is no cure for the illness.
Treatment consists of maintaining normal blood sugar levels and reducing pressure on the swollen brain. Most children completely recover in 2 to 3 months. Those who survive a serious attack may suffer brain damage.
The best way to reduce the risk of Reye's syndrome is never to give aspirin to any child 18 years or younger, unless otherwise specifically instructed by your healthcare provider. Reduce fever and discomfort in sick children by using acetaminophen or ibuprofen.
Medication cautions:
Disclaimer: This content is reviewed periodically and is subject to change as new health information becomes available. The information provided is intended to be informative and educational and is not a replacement for professional medical evaluation, advice, diagnosis or treatment by a healthcare professional.
HIL File CHIL3078.rf2 VRS# 7753 Data Version 7.0
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