Reye and Reye-like syndromes: results of a pilot study in Peninsular Malaya, 1986

Acta Paediatr Jpn. 1990 Aug;32(4):385-90. doi: 10.1111/j.1442-200x.1990.tb00850.x.

Abstract

A pilot epidemiologic study of all cases of Reye and Reye-like syndromes was undertaken at 8 representative major hospitals in Peninsular Malaya from January 1st to December 31st 1986. The cases were classified as definitive Reye's syndrome, clinical Reye's syndrome and encephalo-hepatopathies. Less than 50% of cases reviewed fulfilled the National Center for Disease Control criteria for clinical Reye's syndrome. Causes of Reye-like syndromes/encephalo-hepatopathies included fulminant hepatitis, Japanese B encephalitis, dengue, septicaemia, and complex febrile fits. It was not possible to differentiate clinical Reye's syndrome from the other encephalo-hepatopathies by either the clinical features (except for jaundice) or biochemical parameters. Liver biopsy is necessary for a definitive diagnosis of Reye's syndrome in Malaysia, because of the high prevalence of Reye-like diseases. The mortality rate in the 2 groups of patients is similar. Ingestion of salicylates was not found to be significantly associated with Reye and Reye-like syndromes in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diagnosis, Differential
  • Encephalitis / diagnosis
  • Female
  • Humans
  • Infant
  • Liver Diseases / diagnosis
  • Malaysia / epidemiology
  • Male
  • Pilot Projects
  • Prospective Studies
  • Reye Syndrome / diagnosis
  • Reye Syndrome / epidemiology*
  • Reye Syndrome / mortality