Spatiotemporal variability in case fatality ratios for 2013–2016 Ebola epidemic in West Africa
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Published version
Author(s)
Forna, Alpha
Dorigatti, Ilaria
Nouvellet, Pierre
Donnelly, Christl
Type
Journal Article
Abstract
Background: For the 2013–2016 Ebola epidemic in West Africa, the largest Ebola virus disease (EVD)
epidemic to date, we aim to analyse the patient mix in detail to characterise key sources of
spatiotemporal heterogeneity in the case fatality ratios (CFR).
Methods: We applied a non-parametric Boosted Regression Trees (BRT) imputation approach for patients
with missing survival outcomes and adjusted for model imperfection. Semivariogram analysis and
kriging were used to investigate spatiotemporal heterogeneities.
Results: CFR estimates varied significantly between districts and over time over the course of the
epidemic. BRT modelling accounted for most of the spatiotemporal variation and interactions in CFR, but
moderate spatial autocorrelation remained for distances up to approximately 90 km. Combining districtlevel CFR estimates and kriged district-level residuals provided the best linear unbiased predicted map of
CFR accounting for the both explained and unexplained spatial variation. Temporal autocorrelation was
not observed in the district-level residuals from the BRT estimates.
Conclusions: This study provides new insight into the epidemiology of the 2013–2016 West African Ebola
epidemic with a view of informing future public health contingency planning, resource allocation and
impact assessment. The analytical framework developed in this analysis, coupled with key domain
knowledge, could be deployed in real time to support the response to ongoing and future outbreaks.
epidemic to date, we aim to analyse the patient mix in detail to characterise key sources of
spatiotemporal heterogeneity in the case fatality ratios (CFR).
Methods: We applied a non-parametric Boosted Regression Trees (BRT) imputation approach for patients
with missing survival outcomes and adjusted for model imperfection. Semivariogram analysis and
kriging were used to investigate spatiotemporal heterogeneities.
Results: CFR estimates varied significantly between districts and over time over the course of the
epidemic. BRT modelling accounted for most of the spatiotemporal variation and interactions in CFR, but
moderate spatial autocorrelation remained for distances up to approximately 90 km. Combining districtlevel CFR estimates and kriged district-level residuals provided the best linear unbiased predicted map of
CFR accounting for the both explained and unexplained spatial variation. Temporal autocorrelation was
not observed in the district-level residuals from the BRT estimates.
Conclusions: This study provides new insight into the epidemiology of the 2013–2016 West African Ebola
epidemic with a view of informing future public health contingency planning, resource allocation and
impact assessment. The analytical framework developed in this analysis, coupled with key domain
knowledge, could be deployed in real time to support the response to ongoing and future outbreaks.
Date Issued
2020-04-01
Date Acceptance
2020-01-22
Citation
International Journal of Infectious Diseases, 2020, 93, pp.48-55
ISSN
1201-9712
Publisher
Elsevier
Start Page
48
End Page
55
Journal / Book Title
International Journal of Infectious Diseases
Volume
93
Copyright Statement
© 2020 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Sponsor
Medical Research Council (MRC)
Wellcome Trust
Grant Number
MR/R015600/1
213494/Z/18/Z
Subjects
Case fatality ratio
Ebola
Spatiotemporal analysis
Variogram
West Africa
0605 Microbiology
1108 Medical Microbiology
1117 Public Health and Health Services
Microbiology
Publication Status
Published
Date Publish Online
2020-01-28