Evidence map›Paper›PMID 41199390›Full record

ArticleJournal of medical case reports2025

The first Mpox case in Zambia: a case report.

Musole Chipoya, Cephas Sialubanje, Daliso Ngulube, Muzala Kapin'a, Joseph Chikuluma, Chipo Mambo, Kelvin Mwangilwa, Davie Simwaba, Dabwitso Banda, Nyambe Sinyange and 1 more

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Musole ChipoyaZambia National Public Health Institute, Lusaka, Zambia. musolechipoya@gmail.com.ORCID http://orcid.org/0000-0001-5103-9042
Cephas SialubanjeZambia National Public Health Institute, Lusaka, Zambia.
Daliso NgulubeMinistry of Health, Lusaka, Zambia.
Muzala Kapin'aZambia National Public Health Institute, Lusaka, Zambia.
Joseph ChikulumaUniversity of Zambia, Lusaka, Zambia.
Chipo MamboZambia National Public Health Institute, Lusaka, Zambia.
Kelvin MwangilwaZambia National Public Health Institute, Lusaka, Zambia.
Davie SimwabaZambia National Public Health Institute, Lusaka, Zambia.
Dabwitso BandaZambia National Public Health Institute, Lusaka, Zambia.
Nyambe SinyangeZambia National Public Health Institute, Lusaka, Zambia.
Roma ChilengiZambia National Public Health Institute, Lusaka, Zambia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMpox, a viral infection caused by an Orthopoxvirus, has reemerged outside its historically endemic regions in Central and West Africa. This geographical expansion introduces a potential risk of transmission in Zambia, where geographic proximity and active trade routes increase vulnerability. We report the first confirmed case of Mpox in Zambia, involving a 32-year-old Tanzanian cross-border truck driver who presented to Mukando Health Post in Central Province, on 4 October 2024. CASE PRESENTATION: We present a 32-year-old male patient of African descent whose symptoms included a history of 3-day fever, itchy rash, joint pains, fatigue, and sore throat. Physical examination revealed a papular rash over the face, trunk, and extremities with extension to the palms but spared the soles of the feet. No lesions were noted in either the mucosal or genital areas. However, enlarged lymph nodes were palpable in the cervical region. Biological specimens were collected and submitted to Zambia National Public Health Reference Laboratory. Samples collected, including oral swabs in transport media, whole blood, skin scrapping from lesions, swabs from lesions, and urine samples. Analytics conducted on the samples included testing for polymerase chain reaction for Mpox, human immunodeficiency virus, rapid plasma reagin for syphilis, and hepatitis B and C. Contact tracing identified both primary and secondary contacts. Polymerase chain reaction confirmed Mpox DNA in initial whole blood, with persistent detection in skin lesions and throat swabs. The patient was commenced on symptomatic treatment with benzyl benzoate, paracetamol, ibuprofen, chlorpheniramine, and phenoxymethylpenicillin and continued the same treatment after the confirmation of Mpox diagnosis. He was advised to continue good hygiene practice and remain in isolation to prevent transmission to others. None of the 22 traced contacts reported any symptoms nor tested positive.

conclusionOur report emphasizes the transmission risk for Mpox in traditionally nonendemic areas resulting from cross-border movement. This highlights the need for countries to strengthen surveillance systems resulting in increased sensitivity, specificity, and timeliness required for early detection and response to Mpox. A multifaceted collaborative approach is required between countries to ensure formalized cross-border collaboration, strengthening health-seeking behavior through deployment of mobile clinics, and utilization of digital platforms risk communication and community engagement. Improved supply chain management for laboratory reagents, sample collection, and personal protective equipment coupled with training of health workers is crucial for adequate preparedness and successful containment of outbreaks. These initiatives, collectively undertaken, will result in a robust response system safeguarding public health and preventing emerging threats such as Mpox from becoming endemic.

Indexed as

Mpox, MonkeypoxAdultHumansMaleZambiaCross-border transmissionInternational health regulations (IHR)MpoxOrthopoxvirusSurveillanceTruck driver

Identifiers

PMID41199390
PMCPMC12590703

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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.