TY - JOUR
T1 - Bayesian epidemic models for spatially aggregated count data
AU - Malesios, Chrisovalantis
AU - Demiris, Nikolaos
AU - Kalogeropoulos, Konstantinos
AU - Ntzoufras, Ioannis
N1 - This is the peer reviewed version of the following article: Malesios, C., Demiris, N., Kalogeropoulos, K., and Ntzoufras, I. ( 2017) Bayesian epidemic models for spatially aggregated count data. Statist. Med., 36: 3216– 3230, which has been published in final form at https://doi.org/10.1002/sim.7364. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.
PY - 2017/9/10
Y1 - 2017/9/10
N2 - Epidemic data often possess certain characteristics, such as the presence of many zeros, the spatial nature of the disease spread mechanism, environmental noise, serial correlation and dependence on time‐varying factors. This paper addresses these issues via suitable Bayesian modelling. In doing so, we utilize a general class of stochastic regression models appropriate for spatio‐temporal count data with an excess number of zeros. The developed regression framework does incorporate serial correlation and time‐varying covariates through an Ornstein–Uhlenbeck process formulation. In addition, we explore the effect of different priors, including default options and variations of mixtures of g‐priors. The effect of different distance kernels for the epidemic model component is investigated. We proceed by developing branching process‐based methods for testing scenarios for disease control, thus linking traditional epidemiological models with stochastic epidemic processes, useful in policy‐focused decision making. The approach is illustrated with an application to a sheep pox dataset from the Evros region, Greece.
AB - Epidemic data often possess certain characteristics, such as the presence of many zeros, the spatial nature of the disease spread mechanism, environmental noise, serial correlation and dependence on time‐varying factors. This paper addresses these issues via suitable Bayesian modelling. In doing so, we utilize a general class of stochastic regression models appropriate for spatio‐temporal count data with an excess number of zeros. The developed regression framework does incorporate serial correlation and time‐varying covariates through an Ornstein–Uhlenbeck process formulation. In addition, we explore the effect of different priors, including default options and variations of mixtures of g‐priors. The effect of different distance kernels for the epidemic model component is investigated. We proceed by developing branching process‐based methods for testing scenarios for disease control, thus linking traditional epidemiological models with stochastic epidemic processes, useful in policy‐focused decision making. The approach is illustrated with an application to a sheep pox dataset from the Evros region, Greece.
UR - https://onlinelibrary.wiley.com/doi/full/10.1002/sim.7364
U2 - 10.1002/sim.7364
DO - 10.1002/sim.7364
M3 - Article
SN - 1097-0258
VL - 36
SP - 3216
EP - 3230
JO - Statistics in Medicine
JF - Statistics in Medicine
IS - 20
ER -