Evidence map›Paper›PMID 26248615›Full record

ArticleBMC medicine2015

Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models.

Francis Maina Ndungu, Kevin Marsh, Gregory Fegan, Juliana Wambua, George Nyangweso, Edna Ogada, Tabitha Mwangi, Chris Nyundo, Alex Macharia, Sophie Uyoga and 2 more

Abstract read
In one paragraph

Article in BMC medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Trial
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  12. Development of B Cell Memory in Malaria.Frontiers in immunology · 2019
    Review
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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.

Francis Maina NdunguKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. fndungu@kemri-wellcome.org.
Kevin MarshKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. kevin.marsh@ndm.ox.ac.uk.
Gregory FeganKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. gfegan@kemri-wellcome.org.
Juliana WambuaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. jwambua@kemri-wellcome.org.
George NyangwesoKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. gnyangweso@kemri-wellcome.org.
Edna OgadaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. eogada@gmail.com.
Tabitha MwangiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. tabsmwangi@gmail.com.
Chris NyundoKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. cnyundo@kemri-wellcome.org.
Alex MachariaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. amacharia@kemri-wellcome.org.
Sophie UyogaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. suyoga@kemri-wellcome.org.
Thomas N WilliamsKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. tom.n.williams@gmail.com.
Philip BejonKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. pbejon@kemri-wellcome.org.

Funding

Medical Research Council G1002624Medical Research Council MR/M003906/1Wellcome Trust 091758Wellcome Trust 092654Wellcome Trust B9RTIR0
6 · The paper itself

Abstract

backgroundThe distribution of Plasmodium falciparum clinical malaria episodes is over-dispersed among children in endemic areas, with more children experiencing multiple clinical episodes than would be expected based on a Poisson distribution. There is consistent evidence for micro-epidemiological variation in exposure to P. falciparum. The aim of the current study was to identify children with excess malaria episodes after controlling for malaria exposure.

methodsWe selected the model that best fit the data out of the models examined and included the following covariates: age, a weighted local prevalence of infection as an index of exposure, and calendar time to predict episodes of malaria on active surveillance malaria data from 2,463 children of under 15 years of age followed for between 5 and 15 years each. Using parameters from the zero-inflated negative binomial model which best fitted our data, we ran 100 simulations of the model based on our population to determine the variation that might be seen due to chance.

resultsWe identified 212 out of 2,463 children who had a number of clinical episodes above the 95(th) percentile of the simulations run from the model, hereafter referred to as "excess malaria (EM)". We then identified exposure-matched controls with "average numbers of malaria" episodes, and found that the EM group had higher parasite densities when asymptomatically infected or during clinical malaria, and were less likely to be of haemoglobin AS genotype.

conclusionsOf the models tested, the negative zero-inflated negative binomial distribution with exposure, calendar year, and age acting as independent predictors, fitted the distribution of clinical malaria the best. Despite accounting for these factors, a group of children suffer excess malaria episodes beyond those predicted by the model. An epidemiological framework for identifying these children will allow us to study factors that may explain excess malaria episodes.

Indexed as

Models, StatisticalAdolescentChildChild, PreschoolChild WelfareFemaleHumansInfantKenyaLongitudinal StudiesMalaria, FalciparumMalePlasmodium falciparumPoisson DistributionPrevalenceRisk Factors

Identifiers

PMID26248615
PMCPMC4527301

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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.