Evidence map›Paper›PMID 39577971›Full record

ArticleThe Lancet. Global health2024

The epidemiological benefit of pyrethroid-pyrrole insecticide treated nets against malaria: an individual-based malaria transmission dynamics modelling study.

Thomas S Churcher, Isaac J Stopard, Arran Hamlet, Dominic P Dee, Antoine Sanou, Mark Rowland, Moussa W Guelbeogo, Basiliana Emidi, Jacklin F Mosha, Joseph D Challenger and 23 more

Abstract read
In one paragraph

Article in The Lancet. Global health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  8. Durability study of VeeralinParasites & vectors · 2025
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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

33 authors.

Thomas S ChurcherSchool of Public Health, Imperial College London, London, UK. Electronic address: thomas.churcher@imperial.ac.uk.
Isaac J StopardSchool of Public Health, Imperial College London, London, UK.
Arran HamletSchool of Public Health, Imperial College London, London, UK.
Dominic P DeeSchool of Public Health, Imperial College London, London, UK.
Antoine SanouCentre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Mark RowlandDepartment of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
Moussa W GuelbeogoCentre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Basiliana EmidiDepartment of Parasitology, National Institute for Medical Research, Mwanza Medical Research Centre, Mwanza, Tanzania.
Jacklin F MoshaDepartment of Parasitology, National Institute for Medical Research, Mwanza Medical Research Centre, Mwanza, Tanzania.
Joseph D ChallengerSchool of Public Health, Imperial College London, London, UK.
Adrian DenzSchool of Public Health, Imperial College London, London, UK.
Andrew GloverSchool of Public Health, Imperial College London, London, UK.
Giovanni D CharlesSchool of Public Health, Imperial College London, London, UK.
Emma L RussellSchool of Public Health, Imperial College London, London, UK.
Rich FitzjohnSchool of Public Health, Imperial College London, London, UK.
Pete WinskillSchool of Public Health, Imperial College London, London, UK.
Christen FornadelInnovative Vector Control Consortium, Liverpool, UK.
Tom McleanInnovative Vector Control Consortium, Liverpool, UK.
Peder DigrePATH, Washington, DC, USA.
Joseph WagmanPATH, Washington, DC, USA.
Frank MoshaDepartment of Parasitology, National Institute for Medical Research, Mwanza Medical Research Centre, Mwanza, Tanzania.
Jackie CookDepartment of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
Martin C AkogbétoCentre de Recherches Entomologiques de Cotonou, Cotonou, Benin.
Luc S DjogbenouInstitut Régional de Santé Publique, University of Abomey-Caliva, Abomey-Calavi, Benin; Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Hilary RansonVector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Philip McCallVector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Alphaxard ManjuranoDepartment of Parasitology, National Institute for Medical Research, Mwanza Medical Research Centre, Mwanza, Tanzania.
Sagnon N'FaléCentre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Natacha ProtopopoffDepartment of Disease Control, London School of Hygiene & Tropical Medicine, London, UK; Department of Parasitology, National Institute for Medical Research, Mwanza Medical Research Centre, Mwanza, Tanzania.
Manfred AccrombessiDepartment of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
Corine NguforDepartment of Disease Control, London School of Hygiene & Tropical Medicine, London, UK; Centre de Recherches Entomologiques de Cotonou, Cotonou, Benin.
Geraldine FosterVector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Ellie Sherrard-SmithSchool of Public Health, Imperial College London, London, UK.

Funding

Medical Research Council MR/T041986/1Wellcome Trust
6 · The paper itself

Abstract

backgroundInsecticide treated nets (ITNs) are the most important malaria prevention tool in Africa but the rise of pyrethroid resistance in mosquitoes is likely impeding control. WHO has recommended a novel pyrethroid-pyrrole ITN following evidence of epidemiological benefit in two cluster-randomised, controlled trials (CRTs). It remains unclear how effective more costly pyrethroid-pyrrole ITNs are compared with other tools, or whether they should be deployed when budgets are limited. We aimed to compare the epidemiological impact and cost-effectiveness of the mass distribution of pyrethroid-pyrrole ITNs relative to other ITNs over 3 years in different African settings.

methodsIn this individual-based malaria transmission dynamics modelling study we characterise the entomological impact of ITNs using data from a systematic review of experimental hut trials from across Africa. This African entomological data was used to inform an individual-based malaria transmission dynamics model, which was validated against CRT results from Benin and Tanzania. The full impact of new ITNs was quantified for trial sites and simulation was used to project impact in different settings which were included within an accessible interface (the Malaria Intervention Tool) to support National Malaria Programmes to explore how vector control tools and budgets could be allocated across regions to avert the most cases.

findingsThe model projects that distributing pyrethroid-pyrrole ITNs averted 65% (95% credible interval 48-74) of cases over 3 years in Tanzania, and 75% (28-93) in Benin. The model indicates that trials might have underestimated the benefits of switching ITNs by 12-16% over 3 years because participants stopped using trial-allocated nets. In moderate endemicity non-trial settings, pyrethroid-pyrrole ITNs are projected to reduce malaria prevalence by 25-60% and switching from pyrethroid-only ITNs is probably highly cost-effective in most locations given current prices, averting an additional 10-30% of cases.

interpretationThe benefit of pyrethroid-pyrrole ITNs varies by setting but is generally the most cost-effective indoor vector control intervention in Africa. National Malaria Programmes can strategise deployment to maximise impact. Entomological data could broadly predict epidemiological impact, although there are some inconsistencies, illustrating the challenge in capturing the dynamics across diverse settings.

fundingUnitaid, Bill & Melinda Gates Foundation, the UK Medical Research Council, Wellcome Trust, and the UK Foreign, Commonwealth & Development Office.

Indexed as

Insecticide-Treated BednetsMalariaMosquito ControlPyrethrinsAfricaAnimalsAnophelesBeninChildChild, PreschoolCost-Benefit AnalysisFemaleHumansInsecticidesMosquito VectorsTanzaniaInsecticidesPyrethrins

Identifiers

PMID39577971
PMCPMC11584316

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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.