Abstract

Visceral Leishmaniasis is a very dangerous form of leishmaniasis and, shorn of appropriate diagnosis and handling, it leads to death and physical disability. Depicting the spatiotemporal pattern of disease is important for disease regulator and deterrence strategies. Spatiotemporal modeling has distended broad veneration in recent years. Spatial and spatiotemporal disease modeling is extensively used for the analysis of registry data and usually articulated in a hierarchical Bayesian framework. In this study, we have developed the hierarchical spatiotemporal Bayesian modeling of the infected rate of Visceral leishmaniasis in Human (VLH). We applied the Stochastics Partial Differential Equation (SPDE) approach for a spatiotemporal hierarchical model for Visceral leishmaniasis in human (VLH) that involves a GF and a state process is associated with an autoregressive order one temporal dynamics and the spatially correlated error term, along with the effect of land shield, metrological, demographic, socio-demographic and geographical covariates in an endemic area of Amhara regional state, Ethiopia. The model encompasses a Gaussian Field (GF), affected by an error term, and a state process described by a first-order autoregressive dynamic model and spatially correlated innovations. A hierarchical model including spatially and temporally correlated errors was fit to the infected rate of Visceral leishmaniasis in human (VLH) weekly data from January 2015 to December 2017 using the R package R-INLA, which allows for Bayesian modeling using the stochastic partial differential equation (SPDE) approach. We found that the mean weekly temperature had a significant positive association with infected rate of VLH. Moreover, net migration rate, clean water coverage, average number of households, population density per square kilometer, average number of persons per household unit, education coverage, health facility coverage, mortality rate, and sex ratio had a significant association with the infected rate of visceral leishmaniasis (VLH) in the region. In this study, we investigated the dynamic spatiotemporal modeling of Visceral leishmaniasis in Human (VLH) through a stochastic partial differential equation approach (SPDE) using integrated nested Laplace approximation (INLA). Our study had confirmed both metrological, demographic, sociodemographic and geographic covariates had a significant association with the infected rate of visceral leishmaniasis (VLH) in the region.

Highlights

  • Visceral leishmaniasis is the second most parasitic killer in the globe next to malaria, responsible for an estimated 200,000 to 400,000 infections each year globally [1, 2]

  • We considered the average weekly infected rate of Visceral Leishmaniasis (VLH) from the first week of January 2015 to last week of December 2017 with T = 156 weeks, at every m = 10 locations and 5 validation sites in Amhara Regional State, Ethiopia, including geographical, socioeconomic, metrological covariates, spatial coordinates and temporal dynamics

  • The data for this study is provided by the University of Gondar Leishmaniasis research center, Ethiopian Central Statistical Agency (CSA) and Amhara Regional Health Bureau

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Summary

Introduction

Visceral leishmaniasis is the second most parasitic killer in the globe next to malaria, responsible for an estimated 200,000 to 400,000 infections each year globally [1, 2]. About 9095% of visceral leishmaniasis infections is contributed by most Sub-saharan countries, Asian and Latin American, According to the study by [3, 4]. Based on the species of Leishmania parasites and other immunological and epidemiological aspects, Leishmania infection can lead to cutaneous (CL), mucocutaneous (MCL) or visceral leishmaniasis (VL) [5]. Leishmaniasis is a group of diseases caused by protozoan parasites of the genus Leishmania that are transmitted between humans and other mammalian hosts by phlebotomine sand flies [5], this human infection caused by over 20 species [5, 6]. Depicting the spatiotemporal pattern of disease is important for disease regulator

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