Evidence map›Paper›PMID 40140803›Full record

ArticleMalaria journal2025

High incidence of clinical malaria among asymptomatic Plasmodium falciparum infected children receiving SMC with sulfadoxine-pyrimethamine and amodiaquine (SP + AQ) in Koulikoro, Mali.

Daouda Sanogo, Mahamoudou Toure, Moussa Keita, Fousseyni Kane, Soumba Keita, Ibrahima Sanogo, Sory Ibrahim Diawara, Cheick Oumar Tangara, Hamady Coulibaly, Bourema Cisse and 4 more

Abstract read
In one paragraph

Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Daouda SanogoWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali. sanogodd@icermali.org.
Mahamoudou ToureWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali. mah.toure@gmail.com.
Moussa KeitaWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Fousseyni KaneWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Soumba KeitaWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Ibrahima SanogoUniversity Clinical Research Center (UCRC), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Sory Ibrahim DiawaraWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Cheick Oumar TangaraWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Hamady CoulibalyWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Bourema CisseWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Sidibé M'Baye ThiamWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Mahamadou DiakiteWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Nafomon SogobaWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Seydou DoumbiaWest African International Center for Excellence in Malaria Research (WAF ICEMR), University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.

Funding

Multidisciplinary Implementation Research for malaria control and elimination in West AfricaU19AI129387 · NIAID · UNIV OF SCIENCES, TECH & TECH OF BAMAKO · PI SEYDOU DOUMBIA · 2017 to 2026
$8.2M
Training Program on Operational and Health Services Research for Malaria in MaliD43TW008652 · FIC · UNIV OF SCIENCES, TECH & TECH OF BAMAKO · PI SEYDOU DOUMBIA, Alexandre Delamou · 2010 to 2026
$3.1M
FIC NIH HHS D43 TW008652Fogarty Grant D43TW008652NIAID NIH HHS U19 AI129387NIH HHS 3U19AI129387-03S1
6 · The paper itself

Abstract

backgroundSeasonal malaria chemoprevention (SMC) with sulfadoxine-pyrimethamine and amodiaquine (SP + AQ) involves the monthly administration of therapeutic doses to children under five years of age during periods of high risk of malaria in regions where malaria transmission is highly seasonal. Current SMC guidelines recommend administering the same treatment to both non-infected and asymptomatic Plasmodium falciparum-infected children. However, a critical knowledge gap remains the impact asymptomatic infection on the efficacy of SMC in preventing clinical malaria over a four-week period. This study aimed to evaluate the risk of clinical malaria and its association with children's infection status during SMC treatment.

methodsThis study was conducted in the Koulikoro health district of Mali and focused on children under 10 years of age. A total of 726 children in 2019 and 1452 children in 2020 were randomly selected and followed throughout the SMC campaigns. The prevalence of asymptomatic P. falciparum infection was assessed in each round using microscopy prior to SMC drug administration. Children were passively monitored over a four-week period to record the incidence of clinical malaria. Data analysis was performed using R-Studio software. The risk of clinical malaria based on infection status was estimated through logistic regression analysis, and a Kaplan-Meier curve was used to compare survival times between infected and uninfected children. Proportions were compared using the Pearson Chi-square test, with statistical significance set at p < 0.05.

resultsThe average prevalence of asymptomatic P. falciparum infection was 11.0% across study years. Prevalence was notably higher among children aged 5 to 9 years old in 2019 (p < 0.001) and 2020 (p = 0.016). Asymptomatic infected children had a significantly higher risk of clinical malaria during both transmission seasons: 2019: (RR = 3.05, CI [2.04-4.72]) and 2020 (RR = 1.43, CI [1.04-1.97]). Furthermore, the time to the first malaria episode was significantly shorter among infected children in both years (p < 0.001 for 2019, p = 0.01 for 2020).

conclusionThese findings demonstrate an elevated risk of clinical malaria in asymptomatic infected children during SMC implementation. Screening and treating P. falciparum infections prior to SMC administration could substantially enhance the effectiveness of this strategy in reducing malaria morbidity in endemic areas.

Indexed as

AmodiaquineAntimalarialsAsymptomatic InfectionsChemopreventionMalaria, FalciparumPyrimethamineSulfadoxineChildChild, PreschoolDrug CombinationsFemaleHumansIncidenceInfantMaleMaliAmodiaquineAntimalarialsDrug Combinationsfanasil, pyrimethamine drug combinationPyrimethamineSulfadoxine

Identifiers

PMID40140803
PMCPMC11948680

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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.