Guidelines for the diagnosis and treatment of acute encephalopathy in childhood.
Brain edema
Coma
Cytokine storm
Excitotoxicity
Intensive care
Metabolic disorder
Neuroimaging
Status epilepticus
Targeted temperature management
Journal
Brain & development
ISSN: 1872-7131
Titre abrégé: Brain Dev
Pays: Netherlands
ID NLM: 7909235
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
18
06
2020
revised:
04
08
2020
accepted:
04
08
2020
pubmed:
25
8
2020
medline:
1
9
2021
entrez:
25
8
2020
Statut:
ppublish
Résumé
The cardinal symptom of acute encephalopathy is impairment of consciousness of acute onset during the course of an infectious disease, with duration and severity meeting defined criteria. Acute encephalopathy consists of multiple syndromes such as acute necrotizing encephalopathy, acute encephalopathy with biphasic seizures and late reduced diffusion and clinically mild encephalitis/encephalopathy with reversible splenial lesion. Among these syndromes, there are both similarities and differences. In 2016, the Japanese Society of Child Neurology published 'Guidelines for the Diagnosis and Treatment of Acute Encephalopathy in Childhood', which made recommendations and comments on the general aspects of acute encephalopathy in the first half, and on individual syndromes in the latter half. Since the guidelines were written in Japanese, this review article describes extracts from the recommendations and comments in English, in order to introduce the essence of the guidelines to international clinicians and researchers.
Identifiants
pubmed: 32829972
pii: S0387-7604(20)30215-1
doi: 10.1016/j.braindev.2020.08.001
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
2-31Informations de copyright
Copyright © 2020 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.