Evidence map›Paper›PMID 34315475›Full record

Trial reportMalaria journal2021

Effect of seasonal malaria chemoprevention plus azithromycin on Plasmodium falciparum transmission: gametocyte infectivity and mosquito fitness.

Koudraogo Bienvenue Yaméogo, Rakiswendé Serge Yerbanga, Seydou Bienvenu Ouattara, Franck A Yao, Thierry Lefèvre, Issaka Zongo, Frederic Nikièma, Yves Daniel Compaoré, Halidou Tinto, Daniel Chandramohan and 4 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

14 authors.

Koudraogo Bienvenue YaméogoInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso. yamkbienvenue@yahoo.fr.
Rakiswendé Serge YerbangaInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Seydou Bienvenu OuattaraInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Franck A YaoInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Thierry LefèvreInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Issaka ZongoInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Frederic NikièmaInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Yves Daniel CompaoréInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.
Halidou TintoInstitut de Recherche en Sciences de la Santé, Nanoro, Burkina Faso.
Daniel ChandramohanLondon School of Hygiene and Tropical Medicine, London, UK.
Brian GreenwoodLondon School of Hygiene and Tropical Medicine, London, UK.
Adrien M G BelemUniversité Nazi Boni, Bobo-Dioulasso, Burkina Faso.
Anna CohuetMIVEGEC, University of Montpellier, IRD, CNRS, Montpellier, France.
Jean Bosco OuédraogoInstitut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso.

Funding

Institut de Recherche pour le Developpement JEAI grant
6 · The paper itself

Abstract

backgroundSeasonal malaria chemoprevention (SMC) consists of administration of sulfadoxine-pyrimethamine (SP) + amodiaquine (AQ) at monthly intervals to children during the malaria transmission period. Whether the addition of azithromycin (AZ) to SMC could potentiate the benefit of the intervention was tested through a double-blind, randomized, placebo-controlled trial. The effect of SMC and the addition of AZ, on malaria transmission and on the life history traits of Anopheles gambiae mosquitoes have been investigated.

methodsThe study included 438 children randomly selected from among participants in the SMC + AZ trial and 198 children from the same area who did not receive chemoprevention. For each participant in the SMC + AZ trial, blood was collected 14 to 21 days post treatment, examined for the presence of malaria sexual and asexual stages and provided as a blood meal to An. gambiae females using a direct membrane-feeding assay.

resultsThe SMC treatment, with or without AZ, significantly reduced the prevalence of asexual Plasmodium falciparum (LRT X

conclusionThis study demonstrates that SMC may contribute to a reduction in human to mosquito transmission of P. falciparum, and the reduced mosquito longevity observed for females fed on treated blood may increase the benefit of this intervention in control of malaria. The addition of AZ to SPAQ in SMC appeared to enhance the infectivity of gametocytes providing further evidence that this combination is not an appropriate intervention.

Indexed as

Genetic FitnessMalaria, FalciparumAmodiaquineAnimalsAntimalarialsAzithromycinChemopreventionChild, PreschoolCulicidaeDrug CombinationsHumansPlasmodium falciparumPyrimethamineSeasonsSulfadoxineAmodiaquineAntimalarialsAzithromycinDrug Combinationsfanasil, pyrimethamine drug combinationPyrimethamineSulfadoxineAzithromycinGametocytesSeasonal malaria chemopreventionTransmission

Identifiers

PMID34315475
PMCPMC8314489

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.