# Severe, primary, and incidental COVID-19 in hospitalised children, South Africa: 2020–2023

**Authors:** Ameena Goga, Trisha Ramraj, Jeané Cloete, Dini Mawela, Zainab Waggie, Moherndran Archary, Kogielambal Chinniah, Prakash Jeena, Nomakhuwa E Tabane, Riana Van Zyl, Gary Reubenson, Renate Strehlau, Ute Feucht, Tarylee Reddy, Nobuhle Mchunu, Shannon Cawood, Liesl Zühlke, Kate Webb, Heather J Zar, Kirsten A Donald, Christiaan Scott, Brenda M Morrow, Thomas Aldersley, Nicolette M du Plessis, Terusha Chetty, Sithembiso Velaphi, Ziyaad Dangor, David P Moore

PMC · DOI: 10.7189/jogh.16.04009 · Journal of Global Health · 2026-01-30

## TL;DR

In South Africa, most hospitalized children with COVID-19 were severely ill, with higher severity linked to HIV status and underweight, suggesting the need for stronger child health programs.

## Contribution

The study provides insights into pediatric COVID-19 severity in a high HIV-prevalence, low-vaccination setting.

## Key findings

- Approximately 70% of SARS-CoV-2 positive children were hospitalized for primary COVID-19, with 69.3% of these cases being severe.
- Severe disease was more common in underweight children and those living with HIV, especially those not on antiretroviral therapy.
- Disease severity was highest during the ancestral SARS-CoV-2 period and decreased during the Beta, Delta, and Omicron periods.

## Abstract

Knowledge gaps persist regarding paediatric COVID-19 clinical presentation, treatment and outcomes in high HIV prevalence settings, with low COVID-19 vaccine coverage.

An ambi-directional cohort study was conducted in 13 South African public sector hospitals. Hospitalised children with SARS-CoV-2 infection or post-infection syndrome were included. Main outcomes measures included severe disease and primary COVID-19 (hospitalisation for SARS-CoV-2 infection).

There were 2363 SARS-CoV-2 positive children included (March 2020 through May 2023); median age 23.6 months (interquartile range (IQR) = 4.3–98.2 months). Excluding missing values, 1618 (68.9%) children had primary COVID-19; 1121 (69.3%) of these had severe primary COVID-19. In the primary COVID-19 group with data, 318 / 1588 (20.0%) received intensive or high care, 121/1285 (9.4%) received a blood transfusion and 48/1616 (3.0%) died. Multivariable analyses demonstrated that severe primary COVID-19 was 32% higher in children aged 29–365 days (adjusted Risk Ratio (aRR) = 1.32 (95% confidence interval (CI) = 1.13–1.55); reference: 0–28 days), 13% higher with one or more comorbidities (aRR = 1.13; CI = 1.05-1.22)), and 14–22% lower during the Beta, Delta and Omicron periods (reference: ancestral period). Amongst all hospitalised children with a positive SARS-CoV-2 test, severe disease was commoner in underweight children (aRR 1.09; CI = 1.02–1.17, P = 0.013)). Severe signs were commoner in children living with HIV (CLHIV), 88/121 (72.7%), vs. HIV uninfected 1320 / 2104 (62.7%), P = 0.026, and in antiretroviral therapy-naïve CLHIV, (37 / 41 (90.2%), vs. CLHIV on therapy 51 / 80 (63.8%), P = 0.002).

In a high HIV prevalence country, approximately 70% of children with a positive SARS-CoV-2 test were hospitalised for COVID-19 treatment; almost 70% of these children were severely ill. Controlling for other factors, disease severity was highest in the hypothesised pre-immunity Ancestral period. HIV infection and delayed ART initiation were associated with severe signs. In such settings, strengthening general child health programmes to reduce underweight and prevent or treat paediatric HIV may reduce the severity of new diseases of pandemic proportion.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** fever (MESH:D005334), bacteraemia (MESH:C531821), pain (MESH:D010146), MIS-C (MESH:C000705967), heart disease (MESH:D006331), severely ill (MESH:D045169), COVID-19 (MESH:D000086382), post-infection syndrome (MESH:D000094025), wheezing (MESH:D012135), diabetes (MESH:D003920), viral or bacterial co-infection (MESH:D014777), ill (MESH:D002908), chronic lung disease (MESH:D029424), respiratory illness (MESH:D012140), abdominal pain (MESH:D015746), death (MESH:D003643), malnutrition (MESH:D044342), ICU (MESH:C000657744), cough (MESH:D003371), joint swelling (MESH:D007592), Infectious Disease (MESH:D003141), CLHIV (MESH:D015658), neurological disease (MESH:D020271), epilepsy (MESH:D004827), hypotension (MESH:D007022), TB (MESH:D014376), asthma (MESH:D001249), infection (MESH:D007239), skin rash (MESH:D005076), Underweight (MESH:D013851), tachycardia (MESH:D013610), muscle pain (MESH:D063806)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Severe acute respiratory syndrome-related coronavirus (no rank) [taxon 694009], Human immunodeficiency virus (species) [taxon 12721], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12856961/full.md

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Source: https://tomesphere.com/paper/PMC12856961