Evidence map›Paper›PMID 41961721›Full record

ArticleMedicine2026

High risk of COVID-19 mortality in people living with advanced HIV disease in South Africa: A retrospective cohort study.

Seth Inzaule, Jassat Waasila, Ronaldo Silva, Nathan Ford, Soe Soe Thwin, Alimuddin Zumla, Meg Doherty, Janet Diaz, Silvia Bertagnolio

Abstract read
In one paragraph

Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Seth InzauleAmsterdam Institute for Global Health and Development, and Department of Global Health, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-0155-7391
Jassat WaasilaCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.ORCID 0000-0003-4279-3056
Ronaldo SilvaUNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP), Department of Sexual and Reproductive Health and Research, World Health Organization.
Nathan FordDepartment of Global HIV, STI, Hepatitis Programmes, World Health Organization, Geneva, Switzerland.
Soe Soe ThwinUNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP), Department of Sexual and Reproductive Health and Research, World Health Organization.
Alimuddin ZumlaDivision of Infection and Immunity, Center for Clinical Microbiology, University College London; and NIHR Biomedical Research Centre, UCL Hospitals NHS Foundation Trust, London, UK.ORCID 0000-0002-5111-5735
Meg DohertyDepartment of Global HIV, STI, Hepatitis Programmes, World Health Organization, Geneva, Switzerland.ORCID 0000-0003-2986-7129
Janet DiazWHO Health Emergencies Programme, World Health Organization, Geneva, Switzerland.
Silvia BertagnolioDepartment of AMR Surveillance, Prevention and Control World Health Organization, Geneva, Switzerland.ORCID 0000-0001-8416-2581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conflicting information exists in the literature regarding the relationship between HIV viral load suppression and immune suppression among people living with HIV (PLHIV) with coronavirus disease (COVID-19) comorbidity. We evaluated risk of in-hospital mortality among PLHIV with varying levels of immunosuppression and viral load in South Africa. We analyzed retrospectively collected individual-level cohort data from South Africa shared in the World Health Organization Global Clinic Platform comprising 3,10,522 hospitalized individuals, including 8191 PLHIV on antiretroviral therapy. Advanced disease was defined as CD4 counts of <200 cells/µL. The primary outcome was in-hospital mortality, defined as death within 28 days of hospital admission. Royston-Parmar survival models were used to assess the association of viral load and CD4 counts with in-hospital mortality among PLHIV on antiretroviral therapy. Models were adjusted for demographic factors, COVID-19 severity, severe acute respiratory syndrome coronavirus-2 variants, and comorbidities. Among the 8191 PLHIV with available CD4 and viral load data, 77.2% had viral suppression, and 35.9% had CD4 counts < 200 cells/μL. Compared to HIV-negative individuals, PLHIV with CD4 < 200 cells/μL and viral load ≥1000 copies/mL had a significantly higher risk of mortality (adjusted hazard ratio [aHR] 2.73, 95% CI: 2.45-3.04). Elevated mortality risk was also observed in PLHIV with CD4 < 200 cells/μL and viral load < 1000 copies/mL (aHR 2.01, 95% CI: 1.84-2.20), and those with CD4 ≥ 200 cells/μL and viral load ≥ 1000 copies/mL (aHR 1.47, 95% CI: 1.20-1.81). PLHIV with CD4 ≥ 200 cells/μL and viral suppression had the lowest, but still significant, increased in-hospital mortality risk (aHR 1.27, 95% CI: 1.18-1.36). A substantial increased risk of in-hospital mortality occurs among PLHIV with advanced HIV disease and unsuppressed viremia hospitalized with COVID-19. These findings highlight the importance of prioritizing COVID-19 vaccination and COVID-19 therapeutics for PLHIV during the post-pandemic phase. Further research is however needed to understand the high risk of mortality in virally suppressed PLHIV with CD4 ≥ 200 cells/μL.

Indexed as

COVID-19HIV InfectionsAdultCD4 Lymphocyte CountComorbidityFemaleHospital MortalityHumansMaleMiddle AgedRetrospective StudiesRisk FactorsSARS-CoV-2South AfricaViral LoadCD4COVID-19HIVPLHIVriskvaccinationviral suppression

Identifiers

PMID41961721
PMCPMC13593238

What OpenQuestion holds

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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.