Evidence map›Paper›PMID 25149479›Full record

ArticleMalaria journal2014

Development and validation of climate and ecosystem-based early malaria epidemic prediction models in East Africa.

Andrew K Githeko, Laban Ogallo, Martha Lemnge, Michael Okia, Ednah N Ototo

Abstract readValidation Study
In one paragraph

Article in Malaria journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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  3. Predicting Infectious Diseases: A Bibliometric Review on Africa.International journal of environmental research and public health · 2022
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Andrew K GithekoKenya Medical Research Institute, Centre for Global Health Research, (KEMRI) Climate and Human Health Research Unit, PO Box 1578, Kisumu, Kenya. githeko@yahoo.com.
Laban Ogallo
Martha Lemnge
Michael Okia
Ednah N Ototo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria epidemics remain a serious threat to human populations living in the highlands of East Africa where transmission is unstable and climate sensitive. An existing early malaria epidemic prediction model required further development, validations and automation before its wide use and application in the region. The model has a lead-time of two to four months between the detection of the epidemic signal and the evolution of the epidemic. The validated models would be of great use in the early detection and prevention of malaria epidemics.

methodsConfirmed inpatient malaria data were collected from eight sites in Kenya, Tanzania and Uganda for the period 1995-2009. Temperature and rainfall data for the period 1960-2009 were collected from meteorological stations closest to the source of the malaria data. Process-based models were constructed for computing the risk of an epidemic in two general highland ecosystems using temperature and rainfall data. The sensitivity, specificity and positive predictive power were used to validate the models.

resultsDepending on the availability and quality of the malaria and meteorological data, the models indicated good functionality at all sites. Only two sites in Kenya had data that met the criteria for the full validation of the models. The additive model was found most suited for the poorly drained U-shaped valley ecosystems while the multiplicative model was most suited for the well-drained V-shaped valley ecosystem. The +18°C model was adaptable to any of the ecosystems and was designed for conditions where climatology data were not available. The additive model scored 100% for sensitivity, specificity and positive predictive power. The multiplicative model had a sensitivity of 75% specificity of 99% and a positive predictive power of 86%.

conclusionsThe additive and multiplicative models were validated and were shown to be robust and with high climate-based, early epidemic predictive power. They are designed for use in the common, well- and poorly drained valley ecosystems in the highlands of East Africa.

Indexed as

EpidemicsEpidemiologic MethodsClimateEcosystemForecastingHumansKenyaMalariaModels, StatisticalPredictive Value of TestsSensitivity and SpecificityTanzaniaTemperatureUganda

Identifiers

PMID25149479
PMCPMC4158077

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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.