Evidence map›Paper›PMID 39798583›Full record

ArticleThe Lancet. Infectious diseases2025

The effectiveness of two doses of recombinant hepatitis E vaccine in response to an outbreak in Bentiu, South Sudan: a case-control and bias indicator study.

Robin C Nesbitt, Vincent Kinya Asilaza, Catia Alvarez, Priscillah Gitahi, Patrick Nkemenang, Jetske Duncker, Melat Haile, Primitive Gakima, Joseph F Wamala, Fredrick Beden Loro and 9 more

Abstract read
In one paragraph

Article in The Lancet. Infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Robin C NesbittEpicentre, Paris, France.
Vincent Kinya AsilazaMédecins Sans Frontières, Juba, South Sudan.
Catia AlvarezGeneva Centre for Emerging Viral Diseases, Geneva University Hospitals, Geneva, Switzerland.
Priscillah GitahiMédecins Sans Frontières, Juba, South Sudan.
Patrick NkemenangMédecins Sans Frontières, Juba, South Sudan.
Jetske DunckerMédecins Sans Frontières, Juba, South Sudan.
Melat HaileMédecins Sans Frontières, Geneva, Switzerland.
Primitive GakimaMédecins Sans Frontières, Geneva, Switzerland.
Joseph F WamalaWorld Health Organization, Juba, South Sudan.
Fredrick Beden LoroWorld Health Organization, Juba, South Sudan.
Aybüke KoyuncuEpicentre, Paris, France; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Duol BiemSouth Sudan Ministry of Health, Juba, South Sudan.
Manuel AlbelaMédecins Sans Frontières, Geneva, Switzerland.
Monica RullMédecins Sans Frontières, Geneva, Switzerland.
Etienne GignouxEpicentre, Paris, France.
John RumunuSouth Sudan Ministry of Health, Juba, South Sudan.
Isabella EckerleGeneva Centre for Emerging Viral Diseases, Geneva University Hospitals, Geneva, Switzerland; Department of Medicine, University of Geneva, Geneva, Switzerland.
Iza CigleneckiMédecins Sans Frontières, Geneva, Switzerland.
Andrew S AzmanGeneva Centre for Emerging Viral Diseases, Geneva University Hospitals, Geneva, Switzerland; Médecins Sans Frontières, Geneva, Switzerland; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA; Division of Tropical and Humanitarian Medicine, Geneva University Hospitals, Geneva, Switzerland. Electronic address: azman@jhu.edu.

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundHepatitis E virus (HEV) is a leading cause of acute viral hepatitis, particularly in Asia and Africa, where HEV genotypes 1 and 2 are prevalent. Although a recombinant vaccine, Hecolin, is available, it has not been used to control outbreaks. The licensed three-dose regimen might pose challenges for it to be an impactful outbreak control tool. Our study aimed to estimate the effectiveness of two doses of Hecolin in the context of the first-ever reactive use of the vaccine.

methodsWe conducted a case-control study during an HEV outbreak in the Bentiu internally displaced persons camp, South Sudan. Patients with acute jaundice syndrome (suspected cases) seeking care at the Médecins Sans Frontières hospital were screened for study eligibility. Eligible participants were those that had been eligible for vaccination (ie, living in the camp and aged 16-40 years). Confirmed cases were defined as individuals who tested positive for hepatitis E by RT-PCR or anti-HEV IgM ELISA. Each case was matched to six controls by age, sex, pregnancy status, and residence. Self-reported vaccination status was verified through vaccination cards. The primary analysis was two-dose vaccine effectiveness, which we estimated with a matched case-control design using conditional logistic regression models. In secondary analyses we estimated vaccine effectiveness using a test-negative design and the screening method. We used test-negative cases and their matched controls as a bias indicator analysis to help quantify potential health seeking behaviour biases.

findingsBetween May 10 and Dec 30, 2022, we identified 859 patients with suspected hepatitis E. Of these, 201 met the eligibility criteria and 21 cases had laboratory confirmed hepatitis E. Among the confirmed cases, 10 (48%) were unvaccinated compared with 33 (27%) of 121 matched controls. In the primary analysis we estimated an unadjusted two-dose vaccine effectiveness of 67·8% (95% CI -28·6 to 91·9), and a two-dose vaccine effectiveness of 84·0% (-208·5 to 99·2) after adjustment for potential confounders. The bias indicator analysis suggested that test-negative cases might have been more likely to have been vaccinated than their matched community controls due to different health-care seeking behaviours, potentially meaning underestimation of effectiveness estimates. The test-negative design, which uses facility-matched controls, led to an adjusted two-dose effectiveness of 89·4% (56·4 to 98·0).

interpretationDespite the small sample size, our estimates provide evidence of effectiveness of a two-dose regimen against HEV genotype 1 during a protracted outbreak, supporting its use in similar contexts.

fundingMédecins Sans Frontières.

Indexed as

Disease OutbreaksHepatitis EVaccine EfficacyViral Hepatitis VaccinesAdolescentAdultCase-Control StudiesFemaleHepatitis E virusHumansMaleSouth SudanVaccines, SyntheticYoung AdulthecolinVaccines, SyntheticViral Hepatitis Vaccines

Identifiers

PMID39798583
PMCPMC12018298

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.