Evidence map›Paper›PMID 42660167›Full record

ArticleThe Lancet. Global health2026

Prevalence, characteristics, and clinical course of mpox-related ophthalmic disease (MBOTE-EYE): a prospective cohort study in South Kivu, Democratic Republic of the Congo.

Theophile Kabesha, Christophe Van Dijck, Samuel Mudwanga, Sarah Houben, Yves Mujula, Papy Munganga, Jean-Claude Tshomba, Guy Mukari, Tony Wawina-Bokalanga, Eddy Kinganda-Lusamaki and 21 more

Abstract read
In one paragraph

Article in The Lancet. Global health, 2026. 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

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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

31 authors.

Theophile KabeshaFaculty of Medicine, Université Officielle de Bukavu, Bukavu, Democratic Republic of the Congo.
Christophe Van DijckDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Data Science Institute, I-BioStat, Hasselt University, Hasselt, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Samuel MudwangaFaculty of Medicine, Université Officielle de Bukavu, Bukavu, Democratic Republic of the Congo.
Sarah HoubenDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Yves MujulaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Papy MungangaNational Police Hospital, Goma, Democratic Republic of the Congo.
Jean-Claude TshombaRodolphe Mérieux Institute, Institut National de Recherche Biomédicale, Goma Laboratory, Goma, Democratic Republic of the Congo.
Guy MukariNational Program for HIV/AIDS, Ministry of Public Health, Kinshasa, Democratic Republic of the Congo.
Tony Wawina-BokalangaDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Eddy Kinganda-LusamakiInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo; Service de Microbiologie, Département de Biologie Médicale, Cliniques Universitaires de Kinshasa, Université de Kinshasa, Kinshasa, Democratic Republic of the Congo; TransVIHMI, Université de Montpellier, INSERM, IRD, Montpellier, France.
Bart K JacobsDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Achilleas TsoumanisDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Emmanuel Hasivirwe VakaniakiDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Anne W RimoinDepartment of Epidemiology, University of California, Los Angeles, CA, USA.
Isabel BrosiusDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Elise De VosDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Eugene BangwenDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Stefanie BrackeDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Koen VercauterenDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Jean-Claude MwanzaDepartment of Ophthalmology, University of North Carolina, Chapel Hill, NC, USA.
Deogratias B NgomaFaculty of Medicine, Catholic University of Bukavu, Bukavu, Democratic Republic of the Congo.
Patrick KatotoCenter for Tropical Diseases and Global Health, Faculty of Medicine, Catholic University of Bukavu, Bukavu, Democratic Republic of the Congo.
Steven YehTruhlsen Eye Institute, University of Nebraska Medical Center, Omaha, NE, USA.
Nelly N KabediDepartment of Ophthalmology, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Veronique NussenblattLaboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, MD, USA.
Olivier Tshiani-MbayaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo; Clinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Ian CrozierClinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Sabin Sabiti NunduDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Jason KindrachukNational Microbiology Laboratory Branch, Public Health Agency of Canada, Winnipeg, MB, Canada; Department of Medical Microbiology & Infectious Diseases, University of Manitoba, Winnipeg, MB, Canada.
Laurens LiesenborghsDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium. Electronic address: lliesenborghs@itg.be.
Placide Mbala-KingebeniInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo; University of Kinshasa Medical School, Kinshasa, Democratic Republic of the Congo; South African National Bioinformatics Institute, University of the Western Cape, Cape Town, South Africa; Department of Virology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan. Electronic address: placide.mbala@inrb.cd.

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI PENDLETON, RICHARD · 2019 to 2025
$3932.6M
NIH HHS 75N91019D00024
6 · The paper itself

Abstract

backgroundSystematic longitudinal ophthalmologist-led assessment of mpox-related ophthalmic disease (MPOXROD) is rarely reported. We aimed to characterise the prevalence and clinical course of MPOXROD under supportive management during a clade Ib outbreak.

methodsMBOTE-EYE was a substudy nested within a prospective cohort in South Kivu, Democratic Republic of the Congo. All hospitalised patients with PCR-confirmed mpox (within the last 48 h) were eligible. Participants underwent ophthalmological examination at enrolment, discharge, and days 29 and 59. Conjunctival swabs were collected for monkeypox virus PCR. Risk factors for MPOXROD were assessed using mixed-effects Poisson regression.

findingsBetween Oct 28, 2024, and June 30, 2025, 310 participants were enrolled (median age 14·0 years [IQR 2·5-25·0]; 166 [54%] female). At enrolment, conjunctival disease was present in 112 (36% [95% CI 31-42]) participants, corneal disease in 24 (8% [5-11]), and anterior uveitis in two (1% [0-2]). Overall, 134 (43% [38-49]) participants developed MPOXROD during follow-up, most often bilaterally. Blindness following ulcerative keratitis occurred in two (1% [0-3]) of 224 participants. Periorbital lesions (adjusted risk ratio [aRR] 3·65 [95% CI 2·42-5·49]) and severe acute malnutrition (aRR 3·16 [1·22-8·22]) were associated with MPOXROD. PCR was done among 89 patients and cycle threshold values below 25 occurred exclusively during active MPOXROD.

interpretationOphthalmic involvement in clade Ib mpox is common and frequently bilateral, with a substantial burden of keratitis and risk of vision loss. Systematic eye examinations should be integrated into mpox care, and targeted ophthalmic therapies should be developed.

fundingCanadian Institutes of Health Research and the International Development Research Centre, the European & Developing Countries Clinical Trials Partnership, and the Belgian Directorate-General for Development Cooperation and Humanitarian Aid.

Indexed as

Eye DiseasesMpox, MonkeypoxAdolescentAdultChildChild, PreschoolDemocratic Republic of the CongoFemaleHumansMalePrevalenceProspective StudiesRisk FactorsYoung Adult

Identifiers

PMID42660167
PMCPMC13646179

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