Evidence map›Paper›PMID 36895438›Full record

ArticleCurrent research in parasitology & vector-borne diseases2023

Assessing the variability in experimental hut trials evaluating insecticide-treated nets against malaria vectors.

Joseph D Challenger, Rebecca K Nash, Corine Ngufor, Antoine Sanou, K Hyacinthe Toé, Sarah Moore, Patrick K Tungu, Mark Rowland, Geraldine M Foster, Raphael N'Guessan and 2 more

Abstract read
In one paragraph

Article in Current research in parasitology & vector-borne diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

12 authors.

Joseph D ChallengerMedical Research Council Centre for Global Infections Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, UK.
Rebecca K NashMedical Research Council Centre for Global Infections Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, UK.
Corine NguforCentre de Recherches Entomologiques de Cotonou, Cotonou, Benin.
Antoine SanouCentre National de Recherche et de Formation sur le Paludisme, Burkina Faso.
K Hyacinthe ToéCentre National de Recherche et de Formation sur le Paludisme, Burkina Faso.
Sarah MooreVector Control Product Testing Unit (VCPTU) Ifakara Health Institute, Environmental Health, and Ecological Sciences, Bagamoyo, Tanzania.
Patrick K TunguNational Institute for Medical Research, Amani Medical Research Centre, Muheza, Tanzania.
Mark RowlandLondon School of Hygiene and Tropical Medicine, London, UK.
Geraldine M FosterVector Biology Department, Liverpool School of Tropical Medicine, Liverpool, UK.
Raphael N'GuessanLondon School of Hygiene and Tropical Medicine, London, UK.
Ellie Sherrard-SmithMedical Research Council Centre for Global Infections Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, UK.
Thomas S ChurcherMedical Research Council Centre for Global Infections Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, UK.

Funding

Medical Research Council MR/R015600/1Medical Research Council MR/T041986/1
6 · The paper itself

Abstract

Experimental hut trials (EHTs) are used to evaluate indoor vector control interventions against malaria vectors in a controlled setting. The level of variability present in the assay will influence whether a given study is well powered to answer the research question being considered. We utilised disaggregated data from 15 previous EHTs to gain insight into the behaviour typically observed. Using simulations from generalised linear mixed models to obtain power estimates for EHTs, we show how factors such as the number of mosquitoes entering the huts each night and the magnitude of included random effects can influence study power. A wide variation in behaviour is observed in both the mean number of mosquitoes collected per hut per night (ranging from 1.6 to 32.5) and overdispersion in mosquito mortality. This variability in mortality is substantially greater than would be expected by chance and should be included in all statistical analyses to prevent false precision of results. We utilise both superiority and non-inferiority trials to illustrate our methodology, using mosquito mortality as the outcome of interest. The framework allows the measurement error of the assay to be reliably assessed and enables the identification of outlier results which could warrant further investigation. EHTs are increasingly playing an important role in the evaluation and regulation of indoor vector control interventions so it is important to ensure that these studies are adequately powered.

Indexed as

AnophelesExperimental hut trialsInsecticide-treated netsLong-lasting insecticidal netsPower analysisVector control

Identifiers

PMID36895438
PMCPMC9988481

What OpenQuestion holds

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Registered trials

None linked

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.