About reye's syndrome
What is reye's syndrome?
Reye's syndrome is a rare and severe illness affecting children.
- Reye's syndrome is associated with viral infection and aspirin use.
- Patients with Reye's syndrome present with vomiting and mental-status changes.
- Diagnosing Reye's syndrome primarily depends on the clinical history of symptoms.
- The most common abnormal laboratory tests with Reye's syndrome include elevated liver enzymes, elevated ammonia levels, and low serum glucose levels.
- Treatment is supportive, and even with treatment severe cases result in permanent brain damage and death.
- Since educating parents about the dangers of aspirin use, the incidence of Reye's syndrome has decreased markedly.
What is Reye's syndrome?
Reye's syndrome is a rare but often severe and even fatal illness that primarily occurs in children and adolescents. Children diagnosed with Reye's syndrome generally present with vomiting and mental-status changes. The illness can resolve spontaneously or progress to coma and death. Although the cause is still unclear, studies have identified that there is a relationship between some viral infections and the use of aspirin medications. The CDC recommended educating parents about the dangers of treating children with aspirin in the 1980s, and now the disease occurs very rarely. The syndrome was initially described in 1963 by Dr. Ralph Douglas Reye.
What are the symptoms for reye's syndrome?
Rapid breathing symptom was found in the reye's syndrome condition
In Reye's syndrome, a child's blood sugar level typically drops while the levels of ammonia and acidity in his or her blood rise. At the same time, the liver may swell and develop fatty deposits. Swelling may also occur in the brain, which can cause seizures, convulsions or loss of consciousness.
The signs and symptoms of Reye's syndrome typically appear about three to five days after the onset of a viral infection, such as the flu (influenza) or chickenpox, or an upper respiratory infection, such as a cold.
Initial signs and symptoms
For children younger than age 2, the first signs of Reye's syndrome may include:
- Diarrhea
- Rapid breathing
For older children and teenagers, early signs and symptoms may include:
- Persistent or continuous vomiting
- Unusual sleepiness or lethargy
Additional signs and symptoms
As the condition progresses, signs and symptoms may become more serious, including:
- Irritable, aggressive or irrational behavior
- Confusion, disorientation or hallucinations
- Weakness or Paralysis in the arms and legs
- Seizures
- Excessive lethargy
- Decreased level of consciousness
These signs and symptoms require emergency treatment.
When to see a doctor
Early diagnosis and treatment of Reye's syndrome can save a child's life. If you suspect that your child has Reye's syndrome, it's important to act quickly.
Seek emergency medical help if your child:
- Has Seizures or convulsions
- Loses consciousness
Contact your child's doctor if your child experiences the following after a bout with the flu or chickenpox:
- Vomits repeatedly
- Becomes unusually sleepy or lethargic
- Has sudden behavior changes
What are the causes for reye's syndrome?
The exact cause of Reye's syndrome is unknown, although several factors may play a role in its development. Reye's syndrome seems to be triggered by using aspirin to treat a viral illness or infection — particularly flu (influenza) and chickenpox — in children and teenagers who have an underlying fatty acid oxidation disorder.
Fatty acid oxidation disorders are a group of inherited metabolic disorders in which the body is unable to break down fatty acids because an enzyme is missing or not working properly. A screening test is needed to determine if your child has a fatty acid oxidation disorder.
In some cases, Reye's syndrome may be an underlying metabolic condition that's unmasked by a viral illness. Exposure to certain toxins — such as insecticides, herbicides and paint thinner — also may contribute to Reye's syndrome.
What are the treatments for reye's syndrome?
Although there has been extensive research into the cause of Reye's syndrome, it is still not completely understood. As mentioned above, the use of aspirin or aspirin-containing medications to treat children with some viral infections including chickenpox, influenza, and gastroenteritis has been shown to be associated with the development of the disease. Ultimately, the causes of symptoms associated with Reye's syndrome relate to dysfunction of the liver and a resultant increase in serum ammonia levels and other toxins. These toxins cause increased pressure in the brain and swelling, leading to brain dysfunction and can progress to death.
What are the risk factors for reye's syndrome?
The following factors — usually when they occur together — may increase your child's risk of developing Reye's syndrome:
- Using aspirin to treat a viral infection, such as flu, chickenpox or an upper respiratory infection
- Having an underlying fatty acid oxidation disorder
Is there a cure/medications for reye's syndrome?
Reye’s syndrome has become less common. This is because doctors and parents no longer routinely give aspirin to children.
If your child has a headache, it’s usually best to stick to acetaminophen (Tylenol) for treatment. However, make certain to use only the recommended amount. Too much Tylenol can damage the liver.
If a child’s pain or fever is not diminished by Tylenol, see a doctor.
Reye’s syndrome is rarely fatal. However, it can cause varying degrees of permanent brain damage. Take your child to the emergency room immediately if you see signs of:
- confusion
- lethargy
- other mental symptoms