Evidence map›Paper›PMID 42380856›Full record

ArticleMalaria journal2026

Clinical malaria recurrence and associated factors in infancy following IPTp-DP versus IPTp-SP in Busia, Uganda; a secondary analysis using the Conditional Frailty model.

Edward Ikoona, Adoke Yeka, Charles Natuhamya, Samuel Munyole, Fiona Agweng, Paul Mubiri, Josephine Tumuhamye, John Ssenkusu

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Article in Malaria journal, 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Edward IkoonaMakerere University School of Public Health, Kampala, Uganda. ed.ikoona@gmail.com.
Adoke YekaMakerere University School of Public Health, Kampala, Uganda.
Charles NatuhamyaUganda Youth Development Link, P.O. Box 12659, Kampala, Uganda.ORCID http://orcid.org/0000-0001-7415-094X
Samuel MunyoleMakerere University School of Public Health, Kampala, Uganda.
Fiona AgwengMakerere University School of Public Health, Kampala, Uganda.
Paul MubiriInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Josephine TumuhamyeMakerere University School of Public Health, Kampala, Uganda.
John SsenkusuMakerere University School of Public Health, Kampala, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn sub-Saharan Africa, malaria remains a leading cause of morbidity and mortality in children under five. Recurrent malaria not only increases the risk of severe anaemia and developmental delays in infants, but also presents unique challenges for statistical modelling, as episodes are often correlated. Studies have explored malaria dynamics in infants but gaps remain in contextualizing specific risk factors and how they influence malaria recurrence using appropriate modelling techniques that account for correlation. This study compared malaria recurrence among study infants and explored associated risk factors.

methodsThis was a secondary analysis of data from the PROMOTE trial conducted in Busia district, Uganda. A total of 640 infants born to women who received IPTp-DP or IPTp-SP were followed-up for 12 months. These infants experienced a total of 997 malaria episodes. To also assess dependence in malaria episodes and between-infant heterogeneity, the conditional frailty model was used. The PWP-gap time and Frailty only models were used to confirm the true underlying type of event dependence.

resultsIPTp-DP was associated with a modest but non-statistically significant reduction in recurrent malaria hazard compared with IPTp-SP (HR = 0.94, 95% CI 0.82-1.07). Compared with infants whose mothers had no education, infants born to mothers with primary, secondary and higher education had 21%, 42%, and 48% lower hazards of malaria recurrence. Infants whose mothers were 30-45 years had a 28% lower hazard of malaria recurrence compared to those of mothers 16-19 years (HR = 0.72, 95% CI 0.53-0.97). Multigravida mothers had 36% increased hazard of malaria recurrence in their infants compared with primi-gravida mothers (HR = 1.36, 95% CI 1.02-1.80). Infants living 3-5 km from a health facility had 40% greater hazard of malaria recurrence compared with infants in less than 1km (HR = 1.40, 95% CI 1.11-1.77). Malaria episodes were correlated but there was weak non-statistically significant evidence of residual between-infant heterogeneity.

conclusionsCompared with IPTp-SP, IPTp-DP did not significantly reduce malaria recurrence in infants. Maternal education, maternal age, and distance to health center were associated with the hazard of malaria recurrence in infants. Recurrent malaria episodes were correlated, with evidence of event dependence across successive episodes.

Indexed as

AntimalarialsMalariaAdultDrug CombinationsFemaleHumansInfantMalePyrimethamineRecurrenceRisk FactorsSecondary Data AnalysisSulfadoxineUgandaYoung AdultAntimalarialsDrug Combinationsfanasil, pyrimethamine drug combinationPyrimethamineSulfadoxineA new malaria episodeBetween-infant heterogeneityHazardInfantMalaria recurrence

Identifiers

PMID42380856
PMCPMC13584279

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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.