Evidence map›Paper›PMID 30157921›Full record

ArticleBMC medicine2018

Local and regional dynamics of chikungunya virus transmission in Colombia: the role of mismatched spatial heterogeneity.

Sean M Moore, Quirine A Ten Bosch, Amir S Siraj, K James Soda, Guido España, Alfonso Campo, Sara Gómez, Daniela Salas, Benoit Raybaud, Edward Wenger and 2 more

Abstract read
In one paragraph

Article in BMC medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
–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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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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.

Sean M MooreDepartment of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA. smoore15@nd.edu.
Quirine A Ten BoschDepartment of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA.
Amir S SirajDepartment of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA.
K James SodaDepartment of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA.
Guido EspañaDepartment of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA.
Alfonso CampoSubdirección de Análisis de Riesgo y Respuesta Inmediata en Salud Pública, Instituto Nacional de Salud de Colombia, Bogotá, Colombia.
Sara GómezGrupo de Enfermedades Transmisibles, Instituto Nacional de Salud de Colombia, Bogotá, Colombia.
Daniela SalasGrupo de Enfermedades Transmisibles, Instituto Nacional de Salud de Colombia, Bogotá, Colombia.
Benoit RaybaudInstitute for Disease Modeling, Bellevue, WA, USA.
Edward WengerInstitute for Disease Modeling, Bellevue, WA, USA.
Philip WelkhoffInstitute for Disease Modeling, Bellevue, WA, USA.
T Alex PerkinsDepartment of Biological Sciences and Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA. taperkins@nd.edu.ORCID http://orcid.org/0000-0002-7518-4014

Funding

Defense Advanced Research Projects Agency D16AP00114
6 · The paper itself

Abstract

backgroundMathematical models of transmission dynamics are routinely fitted to epidemiological time series, which must inevitably be aggregated at some spatial scale. Weekly case reports of chikungunya have been made available nationally for numerous countries in the Western Hemisphere since late 2013, and numerous models have made use of this data set for forecasting and inferential purposes. Motivated by an abundance of literature suggesting that the transmission of this mosquito-borne pathogen is localized at scales much finer than nationally, we fitted models at three different spatial scales to weekly case reports from Colombia to explore limitations of analyses of nationally aggregated time series data.

methodsWe adapted the recently developed Disease Transmission Kernel (DTK)-Dengue model for modeling chikungunya virus (CHIKV) transmission, given the numerous similarities of these viruses vectored by a common mosquito vector. We fitted versions of this model specified at different spatial scales to weekly case reports aggregated at different spatial scales: (1) single-patch national model fitted to national data; (2) single-patch departmental models fitted to departmental data; and (3) multi-patch departmental models fitted to departmental data, where the multiple patches refer to municipalities within a department. We compared the consistency of simulations from fitted models with empirical data.

resultsWe found that model consistency with epidemic dynamics improved with increasing spatial granularity of the model. Specifically, the sum of single-patch departmental model fits better captured national-level temporal patterns than did a single-patch national model. Likewise, multi-patch departmental model fits better captured department-level temporal patterns than did single-patch departmental model fits. Furthermore, inferences about municipal-level incidence based on multi-patch departmental models fitted to department-level data were positively correlated with municipal-level data that were withheld from model fitting.

conclusionsOur model performed better when posed at finer spatial scales, due to better matching between human populations with locally relevant risk. Confronting spatially aggregated models with spatially aggregated data imposes a serious structural constraint on model behavior by averaging over epidemiologically meaningful spatial variation in drivers of transmission, impairing the ability of models to reproduce empirical patterns.

Indexed as

AnimalsChikungunya FeverChikungunya virusColombiaHumansMosquito VectorsSpatial AnalysisAedes aegyptiAggregation biasArbovirusChikungunyaColombiaEpidemicMathematical modelSpatial scaleTransmission dynamics

Identifiers

PMID30157921
PMCPMC6116375

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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.