Evidence map›Paper›PMID 40888503›Full record

SynthesisJournal of viral hepatitis2025

Risk Factors for Hepatitis C Virus Among the General Population in Sub-Saharan Africa-An Analysis of Systematic Review Data.

Getahun Molla Kassa, Aaron G Lim, Melaku Tileku Tamiru, Tesfa Sewunet Alamneh, Peter Vickerman, Emebet Dagne, Andargachew Mulu, Obsie Baissa, Ora Paltiel, John F Dillon and 5 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Journal of viral hepatitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Getahun Molla KassaPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-9926-7797
Aaron G LimPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Melaku Tileku TamiruDivision of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.
Tesfa Sewunet AlamnehPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-4830-931X
Peter VickermanPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-8291-5890
Emebet DagneDepartment of Internal Medicine, Institute of Health, Jimma University, Jimma, Ethiopia.
Andargachew MuluArmauer Hansen Research Institute, Addis Ababa, Ethiopia.
Obsie BaissaDepartment of Hematology and Braun School of Public Health, Faculty of Medicine, Hadassah-Hebrew University, Jerusalem, Israel.
Ora PaltielDepartment of Hematology and Braun School of Public Health, Faculty of Medicine, Hadassah-Hebrew University, Jerusalem, Israel.
John F DillonDivision of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.
Elias Ali YesufDepartment of Health Policy and Management, Institute of Health, Jimma University, Jimma, Ethiopia.
Matthew HickmanPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Josephine G WalkerPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Clare E FrenchPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
DESTINE NIHR Global Health Research Group

Funding

National Institute for Health and Care Research NIHR 133208Wellcome Trust
6 · The paper itself

Abstract

Understanding risk factors for hepatitis C virus (HCV) is critical for targeting screening and prevention. We systematically reviewed risk factors associated with HCV seroprevalence among the general population in sub-Saharan Africa (SSA). Comprehensive systematic review of HCV seroprevalence of community-based observational studies reporting HCV risk factors in SSA. Study quality was assessed using Joanna Briggs Institute tool. Random effect meta-analyses were used to estimate odds ratios (OR) with 95% confidence intervals (CI). We identified 92 studies. Higher odds of HCV seroprevalence were observed among age 21-64 (OR = 1.77, 95% CI 1.17-2.68) and 65+ groups (OR = 11.75, 95% CI 5.51-25.05) compared to those aged ≤ 20 years; not being formally educated (OR = 1.78, 95% CI 1.35-2.35) compared to secondary/above and being married (OR = 1.91, 95% CI 1.45-2.51) or divorced (OR = 3.20, 95% CI 1.91-5.36) compared to never married. Family history of HCV (OR = 1.52, 95% CI 1.17-1.96), being a person living with HIV (OR = 2.64, 95% CI 1.61-4.33) or being HBsAg positive (OR = 1.66, 95% CI 1.10-2.50) were all positively associated with increased HCV seroprevalence, as was having a history of blood transfusion (OR = 1.81, 95% CI 1.33-2.45), hospitalisation (OR = 1.55, 95% CI 1.22-1.96), medical operation (OR = 1.28, 95% CI 1.01-1.62), scarification (OR = 1.29, 95% CI 1.01-1.64) and injection drug use (OR = 7.04, 95% CI 1.16-42.68). Pilot HCV screening programmes targeting older adults and people exposed to healthcare-associated factors could potentially lead to the efficient detection of HCV cases and reduce future HCV exposures among the general population in SSA countries.

Indexed as

Hepatitis CAdultAfrica South of the SaharaFemaleHepacivirusHumansMaleMiddle AgedRisk FactorsSeroepidemiologic StudiesSystematic Reviews as TopicYoung Adultgeneral populationhepatitis Cmeta‐analysisrisk factorssub‐Saharan Africa

Identifiers

PMID40888503
PMCPMC12400790

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.