Hepatitis B virus infection in children and adolescents.
Adolescent
Alanine Transaminase
/ blood
Antiviral Agents
/ therapeutic use
Carcinoma, Hepatocellular
/ virology
Child
DNA, Viral
/ blood
Disease Progression
Female
Hepatitis B
/ diagnosis
Hepatitis B Surface Antigens
/ blood
Hepatitis B Vaccines
Humans
Infectious Disease Transmission, Professional-to-Patient
Infectious Disease Transmission, Vertical
/ prevention & control
Liver Cirrhosis
/ virology
Liver Neoplasms
/ virology
Practice Guidelines as Topic
Seroepidemiologic Studies
Journal
The lancet. Gastroenterology & hepatology
ISSN: 2468-1253
Titre abrégé: Lancet Gastroenterol Hepatol
Pays: Netherlands
ID NLM: 101690683
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
received:
25
11
2018
revised:
20
01
2019
accepted:
22
01
2019
pubmed:
16
4
2019
medline:
26
5
2020
entrez:
16
4
2019
Statut:
ppublish
Résumé
Hepatitis B virus (HBV) infection is a major cause of acute and chronic liver disease and associated morbidity and mortality worldwide. Vertical (mother-to-child) and horizontal early childhood transmission are the main routes of HBV transmission and are responsible for most chronic infections, including among adults who bear the greatest burden of morbidity and mortality. Universal hepatitis B immunisation at birth and in infancy is the key strategy for global elimination of HBV infection, and has been highly effective in reducing new vertical infections. However, global progress in scale-up of HBV testing and treatment has been slow in adults and children. In this Series paper, we summarise knowledge on the epidemiology, natural history, and treatment of chronic HBV infection in adolescents and children, and we highlight key differences from HBV infection in adults. The estimated global prevalence of HBV infection in children aged 5 years or younger is 1·3%. Most children are in the high-replication, low-inflammation phase of infection, with normal or only slightly raised aminotransferases; cirrhosis and hepatocellular carcinoma are rare. Although entecavir is approved and recommended for children aged 2-17 years, and tenofovir for those aged 12-18 years, a conservative approach to treatment initiation in children is recommended. Key actions to address current policy gaps include: validation of non-invasive tests for liver disease staging; additional immunopathogenesis studies in children with HBV infection; long-term follow-up of children on nucleoside or nucleotide analogue regimens to inform guidance on when to start treatment; evaluation of different treatment strategies for children with high rates of HBV replication; and establishment of paediatric treatment registries and international consortia to promote collaborative research.
Identifiants
pubmed: 30982722
pii: S2468-1253(19)30042-1
doi: 10.1016/S2468-1253(19)30042-1
pii:
doi:
Substances chimiques
Antiviral Agents
0
DNA, Viral
0
Hepatitis B Surface Antigens
0
Hepatitis B Vaccines
0
Alanine Transaminase
EC 2.6.1.2
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
466-476Subventions
Organisme : World Health Organization
ID : 001
Pays : International
Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2019 World Health Organization. Published by Elsevier Ltd. All rights reserved. Published by Elsevier Ltd.. All rights reserved.