Evidence map›Paper›PMID 25575618›Full record

ArticleThe Lancet. Infectious diseases2015

Spatiotemporal spread of the 2014 outbreak of Ebola virus disease in Liberia and the effectiveness of non-pharmaceutical interventions: a computational modelling analysis.

Stefano Merler, Marco Ajelli, Laura Fumanelli, Marcelo F C Gomes, Ana Pastore Y Piontti, Luca Rossi, Dennis L Chao, Ira M Longini, M Elizabeth Halloran, Alessandro Vespignani

Abstract read
In one paragraph

Article in The Lancet. Infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 4 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

118 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  19. Ecohydrology 2.0.Rendiconti Lincei. Scienze fisiche e naturali · 2022
    Review
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58 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Stefano MerlerBruno Kessler Foundation, Trento, Italy.
Marco AjelliBruno Kessler Foundation, Trento, Italy.
Laura FumanelliBruno Kessler Foundation, Trento, Italy.
Marcelo F C GomesLaboratory for the Modeling of Biological and Socio-Technical Systems, Northeastern University, Boston, MA, USA.
Ana Pastore Y PionttiLaboratory for the Modeling of Biological and Socio-Technical Systems, Northeastern University, Boston, MA, USA.
Luca RossiInstitute for Scientific Interchange, Torino, Italy.
Dennis L ChaoVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Ira M LonginiDepartment of Biostatistics, College of Public Health, Health Professions, and Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA.
M Elizabeth HalloranVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Biostatistics, University of Washington, Seattle, WA, USA.
Alessandro VespignaniLaboratory for the Modeling of Biological and Socio-Technical Systems, Northeastern University, Boston, MA, USA; Institute for Quantitative Social Sciences at Harvard University, Cambridge, MA, USA. Electronic address: a.vespignani@neu.edu.

Funding

Understanding Transmission with Integrated Genetic and Epidemiologic InferenceU54GM111274 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI VESPIGNANI, ALESSANDRO · 2014 to 2018
$12.5M
NIGMS NIH HHS U54 GM111274NIGMS NIH HHS U54-GM111274
6 · The paper itself

Abstract

backgroundThe 2014 epidemic of Ebola virus disease in parts of west Africa defines an unprecedented health threat. We developed a model of Ebola virus transmission that integrates detailed geographical and demographic data from Liberia to overcome the limitations of non-spatial approaches in projecting the disease dynamics and assessing non-pharmaceutical control interventions.

methodsWe modelled the movements of individuals, including patients not infected with Ebola virus, seeking assistance in health-care facilities, the movements of individuals taking care of patients infected with Ebola virus not admitted to hospital, and the attendance of funerals. Individuals were grouped into randomly assigned households (size based on Demographic Health Survey data) that were geographically placed to match population density estimates on a grid of 3157 cells covering the country. The spatial agent-based model was calibrated with a Markov chain Monte Carlo approach. The model was used to estimate Ebola virus transmission parameters and investigate the effectiveness of interventions such as availability of Ebola treatment units, safe burials procedures, and household protection kits.

findingsUp to Aug 16, 2014, we estimated that 38·3% of infections (95% CI 17·4-76·4) were acquired in hospitals, 30·7% (14·1-46·4) in households, and 8·6% (3·2-11·8) while participating in funerals. We noted that the movement and mixing, in hospitals at the early stage of the epidemic, of patients infected with Ebola virus and those not infected was a sufficient driver of the reported pattern of spatial spread. The subsequent decrease of incidence at country and county level is attributable to the increasing availability of Ebola treatment units (which in turn contributed to drastically decreased hospital transmission), safe burials, and distribution of household protection kits.

interpretationThe model allows assessment of intervention options and the understanding of their role in the decrease in incidence reported since Sept 7, 2014. High-quality data (eg, to estimate household secondary attack rate, contact patterns within hospitals, and effects of ongoing interventions) are needed to reduce uncertainty in model estimates.

fundingUS Defense Threat Reduction Agency, US National Institutes of Health.

Indexed as

Disease OutbreaksCommunicable Disease ControlDisease Transmission, InfectiousHemorrhagic Fever, EbolaHumansLiberiaModels, StatisticalSpatio-Temporal Analysis

Identifiers

PMID25575618
PMCPMC4409131

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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.