4.2 Article

Nationwide survey of rotavirus-associated encephalopathy and sudden unexpected death in Japan

Journal

BRAIN & DEVELOPMENT
Volume 36, Issue 7, Pages 601-607

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.braindev.2013.07.013

Keywords

Rotavirus; Encephalopathy; Sudden unexpected death; Neurological sequelae

Funding

  1. Ministry of Health, Labour and Welfare of Japan [H24-Shinko-003]

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Background: Rotavirus can cause severe complications such as encephalopathy/encephalitis and sudden unexpected death. The incidence of rotavirus-associated encephalopathy/encephalitis or sudden unexpected death remains unknown. To clarify the clinical features of rotavirus-associated encephalitis/encephalopathy and sudden unexpected death, we conducted a nationwide survey in Japan. Method: A two-part questionnaire was designed to determine the number of the cases and the clinical features of severe cases of rotavirus infection, including encephalitis/encephalopathy and sudden unexpected death, between 2009 and 2011. Result: Of the 1365 questionnaires sent to hospitals, 963 (70.5%) were returned and eligible for analysis. We determined 58 cases of rotavirus-associated encephalitis/encephalopathy and 7 cases of sudden unexpected death. These patients were diagnosed with rotavirus infection by immunochromatography. Although 36/58 (62.1%) encephalitis/encephalopathy patients had no sequelae, 15/58 (25.9%) patients had neurological sequelae, and 7/58 (12.1%) patients had fatal outcomes. Pleocytosis was observed in 9/40 (22.5%) patients and cerebrospinal fluid protein levels were elevated in only 4/40 (10%) patients. Elevated lactate dehydrogenase (LDH) (>500 IU/L) or acidemia (pH <7.15) were related to a poor prognosis. Conclusion: We estimate that annual cases of rotavirus-associated encephalitis/encephalopathy and sudden unexpected death were 44.0 and 4.9 cases in Japan, respectively. Elevated LDH (>500 IU/L) or acidemia (pH < 7.15) were related to a poor prognosis of the encephalitis/encephalopathy. (C) 2013 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

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