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Demystifying the global outbreak of severe acute hepatitis of unknown aetiology in children: A systematic review and meta-analysis

医学 病因学 鼻病毒 共感染 儿科 荟萃分析 肝移植 肠道病毒 免疫学 重症监护医学 移植 内科学 病毒
作者
Julie Phan,Guy D. Eslick,Elizabeth Elliott
出处
期刊:Journal of Infection [Elsevier]
卷期号:88 (1): 2-14 被引量:8
标识
DOI:10.1016/j.jinf.2023.11.011
摘要

ABSTRACT

BACKGROUND

The sudden outbreak of severe acute hepatitis of unknown aetiology (SAHUA) in the first half of 2022 affected more than 1010 children in 35 countries worldwide. Dire clinical outcomes such as acute liver failure necessitating transplantation, neurological symptoms, long-term sequelae, and death highlight the need to determine the pathogenesis of this condition. Hypotheses on the aetiology include adenovirus and SARS-CoV-2 infections and an aberrant immune response to multiple pathogen exposure following lifting of lockdown measures but further investigation is required to reach an informed consensus.

METHODS

A literature search was performed on MEDLINE and EMBASE in accordance with PRISMA guidelines for systematic reviews. Primary studies reporting data on severe acute hepatitis of unknown aetiology in children from the COVID-19 era were selected for inclusion in our review. Data on patient demographics, clinical presentation and outcomes, and diagnostic testing for coinfection were extracted. Meta-analysis used a random-effects model.

RESULTS

The 33 included studies (30 case series and 3 case-control studies) described a total of 3636 cases of SAHUA (reported 1 January 2019 to 31 December 2022), with a median age of 3.5 years. Of these, 214 children (5.9%) received a liver transplant and 66 (1.8%) died. Whilst data on diagnostic testing was incomplete, the most frequently detected coinfections were with adenovirus and/or adeno-associated virus 2 (AAV2). Other common childhood respiratory and enteric pathogens such as enterovirus, rhinovirus and herpesviruses (EBV and HHV-6) were also identified.

CONCLUSION

Coinfection with AAV2 and other common childhood pathogens may predispose children to developing this novel severe hepatitis. Altered susceptibility and response to such pathogens may be a consequence of immunological naivety following pandemic restrictions. Further investigations are needed to generate high quality evidence on aetiology for different patient demographics and geographical areas.
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