Evidence map›Paper›PMID 42853851›Full record

ArticlePLOS global public health2026

Outdoor attractive targeted sugar bait Phase III trials for malaria control in Kenya, Mali, and Zambia: An individual participant data meta-analysis.

Ruth A Ashton, Daniel P McDermott, Fousseyni Kane, Sophie Sarrassat, Angela Harris, Christen Fornadel, Joseph Wagman, Javan Chanda, Megan Littrell, Feiko O Ter Kuile and 9 more

Abstract read
In one paragraph

Article in PLOS global public 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

19 authors.

Ruth A AshtonCentre for Applied Malaria Research and Evaluation, Celia Scott Weatherhead School of Public Health & Tropical Medicine at Tulane University, New Orleans, Louisiana, United States of America.ORCID https://orcid.org/0000-0002-7248-7730
Daniel P McDermottDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Fousseyni KaneUniversity Clinical Research Centre, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.ORCID https://orcid.org/0000-0002-9967-7956
Sophie SarrassatInternational Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology and International Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID https://orcid.org/0000-0001-6872-6455
Angela HarrisInnovative Vector Control Consortium, Liverpool, United Kingdom.
Christen FornadelInnovative Vector Control Consortium, Liverpool, United Kingdom.
Joseph WagmanIndependent Consultant, Washington, District of Columbia, United States of America.
Javan ChandaIndependent Consultant, Lusaka, Zambia.
Megan LittrellPATH, Washington, District of Columbia, United States of America.ORCID https://orcid.org/0009-0004-3663-132X
Feiko O Ter KuileKenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
Aaron M SamuelsMalaria Branch, Division of Parasitic Diseases and Malaria, National Center for Emerging and Zoonotic Infectious Diseases, U.S. Centers for Disease Control and Prevention, Kisumu, Kenya.ORCID https://orcid.org/0000-0002-8355-8186
Eric OchomoDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Thomas S ChurcherSchool of Public Health, Imperial College, London, United Kingdom.
Joseph BiggsInternational Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology and International Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Sarah G StaedkeDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Seydou DoumbiaUniversity Clinical Research Centre, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Immo KleinschmidtInternational Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology and International Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID https://orcid.org/0000-0002-2422-9008
Joshua YukichCentre for Applied Malaria Research and Evaluation, Celia Scott Weatherhead School of Public Health & Tropical Medicine at Tulane University, New Orleans, Louisiana, United States of America.ORCID https://orcid.org/0000-0002-6160-5295
Thomas P EiseleCentre for Applied Malaria Research and Evaluation, Celia Scott Weatherhead School of Public Health & Tropical Medicine at Tulane University, New Orleans, Louisiana, United States of America.ORCID https://orcid.org/0000-0002-2205-622X

Funding

Bill & Melinda Gates Foundation INV-007509
6 · The paper itself

Abstract

Attractive targeted sugar baits (ATSB) are a potential new class of vector control tool that act through an "attract and kill" mechanism on mosquitoes. We conducted a meta-analysis using data from three large-scale Phase III trials of the Westham Sarabi v1.2 ATSB (0.11% dinotefuran) conducted in Kenya, Mali, and Zambia, to determine the effect of the intervention on clinical malaria incidence in children, Plasmodium falciparum infection prevalence, and dominant vector species parity, abundance, landing rate, and sporozoite positivity. The Sarabi ATSB was deployed on exterior walls at the rate of two per residential structure. Aggregated and individual-level meta-analyses were completed for each of the six trial outcomes, comprising 6981 person-years of follow-up for clinical malaria incidence (primary epidemiological outcome) and 19443 Anopheles for parity assessment (primary entomological outcome). Post-hoc analyses included assessment of dose-response relationships between coverage-adjusted intervention density and clinical malaria incidence. There were no statistically significant differences between arms in any of the epidemiological or entomological outcomes. There was statistically significant evidence of a 19% reduction in clinical malaria incidence for every 10 bait stations per hectare increase observed in spatial density (IRR 0.81, 95% CI 0.74-0.89, p < 0.001), provided that the ATSB were in good condition. This finding suggests that there may be deployment approaches or dosing strategies under which ATSB tools could be efficacious, although threshold spatial densities could not be determined from available data. This meta-analysis furthermore highlights important recommendations for future cluster-randomized trials of vector control interventions, including conducting comprehensive baseline data collection to identify cluster outliers or sites with differences in vector bionomics, and collecting a limited set of entomological outcomes in all trial clusters to ensure an adequately powered and balanced analysis of entomological effects.

Identifiers

PMID42853851
PMCPMC13652216

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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.