Evidence map›Paper›PMID 41862968›Full record

ReviewTropical medicine and health2026

Progression from uncomplicated to severe malaria among children in settings receiving different combinations of malaria control interventions in sub-Saharan Africa: a systematic review and meta-analysis.

Erick Jacob Okek, Jeshua Jehopio, Obondo James Sande, Benson Musinguzi, Silvia Awor, Juliet Asio, Doare Kirsty Le, Julius Lutwama, Annet Kinengyere Alison, Felix Bongomin and 2 more

Abstract readReview
In one paragraph

Review in Tropical medicine and health, 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.

Erick Jacob OkekDepartment of Immunology & Molecular Biology, School of Biomedical Sciences, College of Health Sciences, Makerere University, P.O box 7072, Kampala, Uganda. okekerick@yahoo.com.
Jeshua JehopioDepartment of Immunology & Molecular Biology, School of Biomedical Sciences, College of Health Sciences, Makerere University, P.O box 7072, Kampala, Uganda.
Obondo James SandeDepartment of Immunology & Molecular Biology, School of Biomedical Sciences, College of Health Sciences, Makerere University, P.O box 7072, Kampala, Uganda.
Benson MusinguziDepartment of Immunology & Molecular Biology, School of Biomedical Sciences, College of Health Sciences, Makerere University, P.O box 7072, Kampala, Uganda.
Silvia AworFaculty of Medicine, Gulu University, P.O box 166, Laroo, Gulu City, Uganda.
Juliet AsioHIV Reference Laboratory, Department of General Virology, Uganda Virus Research Institute, P.O Box 49, Entebbe, Uganda.
Doare Kirsty LeCentre for Neonatal and Pediatric Infections, City St George's, University of London, Makerere University Johns Hopkins University, Kampala, Uganda.
Julius LutwamaDepartment of Arbovirology & Zoonotic, Uganda Virus Research Institute, P.O Box 49, Entebbe, Uganda.
Annet Kinengyere AlisonSir Albert Cook Library, College of Health Sciences, Makerere University, P.O Box 7072, Kampala, Uganda.
Felix BongominFaculty of Medicine, Gulu University, P.O box 166, Laroo, Gulu City, Uganda.
Moses OcanDepartment of Pharmacology & Therapeutics, School of Biomedical Sciences, College of Health Sciences, Makerere University, P.O box 7072, Kampala, Uganda.
Jonathan KayondoDepartment of Entomology & Parasitology, Uganda Virus Research Institute, P.O Box 49, Entebbe, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is a high variability in the pattern of deployment of combinations of malaria vectors and parasite control interventions across sub-Saharan Africa. Effects of such deployment on disease progression from uncomplicated to severe malaria (a proxy measure of naturally acquired immunity against clinical malaria) is unknown. This systematic review and meta-analysis determined the prevalence of progression from uncomplicated to severe malaria, prevalence of parasitaemia and prevalence of gametocytemia among children in settings receiving different combinations of malaria control interventions in sub-Saharan Africa.

methodsThe protocol for this review was registered by the International Prospective Register for Systematic Review (PROSPERO) with registration number CRD 42024619945. The review followed the Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) guidelines. We comprehensively searched relevant articles published in PubMed, Embase, Web of Science, Scopus and Google Scholar from 1st January 2000 to 31st December 2024. Title, abstract and full text screening were done by inserting relevant search terms and Boolean operators in the search engines of the databases. Bibliography searches of referenced literature were also done. Risk of Bias analysis was done using modified Newcastle-Ottawa tool. Random effects model, Odds ratio and pooled 95% confidence interval in STATA ver 17.0 were used to perform bivariate meta-analysis and sub-group analysis.

resultsTwelve studies involving 9,283,160 individuals were included in this review. There was no significant difference in the odds of progression from uncomplicated to severe malaria in settings receiving different combinations of malaria control interventions (OR:0.56; 95%CI 0.31 to 1.02P = 0.06). Simultaneous deployment of more combinations of malaria control interventions were associated with significantly lower odds of severe malaria(pooled OR = 0.41; 95%CI0.30,to 0.56; p < 0.00), lower odds of parasitaemia (pooled OR = 0.52; 95%CI0.38 to 0.70; p < 0.00), lower odds of uncomplicated malaria (pooled OR = 0.64; 95% CI0.43 to 0.95; p = 0.003) and a lower odds of gametocytes (pooled OR = 0.41; 95% CI 0.28 to 0.60; p < 0.00). There is no significant difference in the odds of severe malaria between settings with single versus those with no interventions (pooled OR = 0.35; 95%CI 0.11 to 1.13). Selected articles exhibited high heterogeneity.

conclusionIn comparison to single or no intervention, combination of multiple malaria control interventions significantly protects against severe malaria, parasitaemia, gametocytes and uncomplicated malaria. In comparison to single or no interventions, deployment of multiple combinations of control interventions did not offer additional protection against progression from uncomplicated to severe malaria.

Identifiers

PMID41862968
PMCPMC13003738

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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.