Reyes syndrome

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Reye's syndrome

The Columbia Encyclopedia, Sixth Edition | 2008 | The Columbia Encyclopedia, Sixth Edition. Copyright 2008 Columbia University Press. (Hide copyright information) Copyright

Reye's syndrome , rare but life-threatening disease characterized by acute encephalopathy and fatty infiltration of internal organs, especially the liver. It occurs almost entirely in children under age 15. The cause is unknown, but the disease usually follows an acute viral infection (particularly influenza or chicken pox), especially when aspirin or other salicylates have been given. The symptoms, which occur about a week after the virus infection, are vomiting and disorientation; these may be followed by seizures, coma, and respiratory arrest. Treatment is directed toward reducing brain swelling, correcting blood chemistry changes due to liver damage, and providing respiratory support if needed. Doctors recommend that children be given acetaminophen rather than aspirin for viral infections or fever .

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Reye's syndrome

A Dictionary of Nursing | 2008 | © A Dictionary of Nursing 2008, originally published by Oxford University Press 2008. (Hide copyright information) Copyright

Reye's syndrome (rayz) n. a rare disorder occurring in childhood. It is characterized by the symptoms of encephalitis combined with evidence of liver failure. Treatment is aimed at controlling cerebral oedema and correcting metabolic abnormalities, but there is a significant mortality and there may be residual brain damage. The cause is not known, but aspirin has been implicated and this drug should not be used in children below the age of 16 unless specifically indicated. [ R. D. K. Reye (1912–77), Australian histopathologist]

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