Evidence map›Paper›PMID 37774732›Full record

ReviewThe Lancet. Child & adolescent health2023

Paediatric acute hepatitis of unknown aetiology: a national surveillance investigation in the USA during 2021 and 2022.

Jordan Cates, Julia M Baker, Olivia Almendares, Neha Balachandran, Erin R McKeever, Anita K Kambhampati, Caelin Cubenas, Jan Vinjé, Jennifer L Cannon, Preeti Chhabra and 9 more

Open access · greenAbstract readReview
In one paragraph

Review in The Lancet. Child & adolescent health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Jordan CatesDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA. Electronic address: ncirddvdgast@cdc.gov.
Julia M BakerDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA; Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Olivia AlmendaresDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Neha BalachandranDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA; Cherokee Nation Assurance, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Erin R McKeeverDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Anita K KambhampatiDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Caelin CubenasDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jan VinjéDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jennifer L CannonDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA; CDC Foundation, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Preeti ChhabraDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Brandi FreemanDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Sarah Reagan-SteinerNational Center for Immunization and Respiratory Diseases; Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Julu BhatnagarNational Center for Immunization and Respiratory Diseases; Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Paul A GastañaduyDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Hannah L KirkingDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
David SugermanDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Umesh D ParasharDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jacqueline E TateDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Hepatitis of Unknown Etiology Group
Centers for Disease Control and Prevention · USFoundation Center · USEpidemic Intelligence Service · USNational Center for Immunization and Respiratory Diseases · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

backgroundAdenovirus is a known cause of hepatitis in immunocompromised children, but not in immunocompetent children. In April, 2022, following multiple reports of hepatitis of unknown aetiology and adenovirus viraemia in immunocompetent children in the USA and UK, the US Centers for Disease Control and Prevention (CDC) and jurisdictional health departments initiated national surveillance of paediatric acute hepatitis of unknown aetiology. We aimed to describe the clinical and epidemiological characteristics of children identified with hepatitis of unknown aetiology between Oct 1, 2021, and Sept 30, 2022, in the USA and to compare characteristics of those who tested positive for adenovirus with those who tested negative.

methodsIn this national surveillance investigation in the USA, children were identified for investigation if they were younger than 10 years with elevated liver transaminases (>500 U/L) who had an unknown cause for their hepatitis and onset on or after Oct 1, 2021. We reviewed medical chart abstractions, which included data on demographics, underlying health conditions, signs and symptoms of illness, laboratory results, vaccination history, radiological and liver pathology findings, diagnoses and treatment received, and outcomes. Caregiver interviews were done to obtain information on symptoms and health-care utilisation for the hepatitis illness, medical history, illness in close contacts or at school or daycare, diet, travel, and other potential exposures. Blood, stool, respiratory, and tissue specimens were evaluated according to clinician discretion and available specimens were submitted to CDC for additional laboratory testing or pathology evaluation.

findingsSurveillance identified 377 patients from 45 US jurisdictions with hepatitis of unknown aetiology with onset from Oct 1, 2021, to Sept 30, 2022. The median age of patients was 2·8 years (IQR 1·2-5·0) and 192 (51%) were male, 184 (49%) were female, and one patient had sex unknown. Only 22 (6%) patients had a notable predisposing underlying condition. 347 patients (92%) were admitted to hospital, 21 (6%) subsequently received a liver transplant, and nine (2%) died. Among the 318 patients without notable underlying conditions, 275 were tested for adenovirus. Of these 116 (42%) had at least one positive specimen, and species F type 41 was the most frequent type identified (19 [73%] of 26 typed specimens were HAdV-41). Proportions of patients who had acute liver failure, received a liver transplant, and died were similar between those who tested positive for adenovirus compared with those who tested negative. Adenovirus species F was detected by polymerase chain reaction in nine pathology liver evaluations, but not by immunohistochemistry in seven of the nine with adequate liver tissue available. Interviews with caregivers yielded no common exposures.

interpretationAdenovirus, alone or in combination with other factors, might play a potential role in acute hepatitis among immunocompetent children identified in this investigation, but the pathophysiologic mechanism of liver injury is unclear. To inform both prevention and intervention measures, more research is warranted to determine if and how adenovirus might contribute to hepatitis risk and the potential roles of other pathogens and host factors.

fundingNone.

Indexed as

HepatitisMalariaChildChild Day Care CentersChild, PreschoolFemaleHospitalizationHumansInfantMaleTravelUnited States

Identifiers

PMID37774732
PMCPMC11088931
OpenAlexW4387037209

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.