Evidence map›Paper›PMID 42743535›Full record

ArticleJMIR research protocols2026

The Effect of Tuberculosis and HIV on the Epidemiological, Clinical, Virological, and Immunological Trajectory of COVID-19: Protocol for a Prospective Case-Ascertained and Surveillance Study.

Azaria Diergaardt, Etuhole Iipumbu, Sibongile Netha, Pieter Steenkamp, Libertina Shiweva, Balladiah Kizito, Gunar Günther, Emmanuel Nepolo, Tadesse Woldetsadik, Stefan Niemann and 2 more

Abstract read
In one paragraph

Article in JMIR research protocols, 2026. 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

12 authors.

Azaria DiergaardtSchool of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0009-0008-7495-2473
Etuhole IipumbuSchool of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0000-0002-4253-8744
Sibongile NethaSchool of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0009-0009-6401-2872
Pieter SteenkampHealth Poverty Action, Gobabis, Namibia.ORCID 0009-0001-7170-5003
Libertina ShiwevaSchool of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0009-0002-3531-8492
Balladiah KizitoVictus Global Botswana Organization, Gabarone, Botswana.ORCID 0000-0002-9905-9322
Gunar GüntherSchool of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0000-0002-2217-4322
Emmanuel NepoloSchool of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0000-0003-4302-5606
Tadesse WoldetsadikHealth Poverty Action, London, United Kingdom.ORCID 0000-0001-6357-7999
Stefan Niemann *Molecular and Experimental Mycobacteriology Group, Research Center Borstel, Borstel, Germany.ORCID 0000-0002-6604-0684
Chawangwa ModongoVictus Global Botswana Organization, Gabarone, Botswana.ORCID 0000-0002-2033-0379
Mareli Claassens *School of Medicine, University of Namibia, Bach Street, Windhoek, Namibia, +264 612063111.ORCID 0000-0002-5927-284X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The COVID-19 pandemic impacted over 620 million people, including approximately 9 million in Africa, and introduced uncertainties, especially regarding coinfection with tuberculosis (TB) or HIV. TB and HIV, both global epidemics, disproportionately affect low- and middle-income countries. Namibia and Botswana have reported high mortality rates due to TB and HIV, highlighting ongoing challenges. Objective: This paper outlines the protocol for a research study in Botswana and Namibia to address these uncertainties and enhance disease management for COVID-19, TB, and HIV, especially with coinfection. The central hypothesis is that TB or HIV coinfection increases the risk of adverse clinical, immunological, and virological COVID-19 outcomes. Methods: Core-NB is a prospective clinical cohort of patients with COVID-19 identified through facility-based surveillance. The objectives were to (1) characterize the early COVID-19 pandemic in conjunction with TB and HIV in clinical, epidemiological, virological, and immunological terms via a household transmission study; and (2) conduct targeted COVID-19 screening and testing in conjunction with TB and HIV case finding through a primary health care (PHC) facility surveillance study. For objective 1, participants were identified with reverse-transcription polymerase chain reaction (PCR) confirmation of COVID-19 at ministry of health-designated laboratories in each country. For objective 2, PHC attendees were enrolled independent of the reason for attending. Results: Index participants and consenting household contacts received home visits, including an initial enrollment visit on day 1 (the day of COVID-19 diagnosis for the index patient) and 3 follow-up visits taking place within 28 days of enrollment. Additionally, there were telephone follow-ups 3 months after enrollment. Age, sex, race, occupation, income, and educational attainment were recorded using a standardized questionnaire for all participants. Three respiratory specimens were obtained from each participant: (1) nasopharyngeal swab (SARS-CoV-2 RNA extraction and PCR); (2) sputum (GeneXpert Ultra active TB testing); and (3) extra sputum (an additional sputum sample was collected in case the GeneXpert Ultra test was positive to use for culture and drug susceptibility testing). The study was funded in October 2021, with data collection starting in June 2022 and finalized in February 2024. The household component enrolled 66 index patients with COVID-19 and 144 household contacts. In total, 1556 participants were enrolled in the PHC clinic component. The primary outcome data analyses are ongoing and expected to be published in July 2026, with secondary outcomes published in December 2026. Conclusions: This study will strengthen COVID-19, TB, and HIV diagnosis, surveillance, and control through (1) high-resolution surveillance and transmission data to establish guidelines and policies; (2) data to develop further interventions; (3) implementation of new technologies to improve care provision and boost the cooperation of stakeholders; (4) support for the development of skills and expertise in-country; and (5) contribution of evidence to build a regional network of expertise in the COVID-19, TB, and HIV coepidemics.

Indexed as

CoinfectionCOVID-19HIV InfectionsTuberculosisAdultBotswanaFemaleHumansMaleProspective StudiesSARS-CoV-2COVID-19HIV and AIDSpandemicssouthern Africatuberculosis

Identifiers

PMID42743535
PMCPMC13577614

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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.