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Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia

Background: Tuberculosis (TB) and HIV are epidemiologically associated, and their co-dynamics suggest that the two diseases are directly related at the population level and within the host. However, there is no or little information on the joint spatial patterns of the two diseases in Ethiopia. The...

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Autores principales: Gemechu, Leta Lencha, Debusho, Legesse Kassa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680430/
https://www.ncbi.nlm.nih.gov/pubmed/36412600
http://dx.doi.org/10.3390/diseases10040106
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author Gemechu, Leta Lencha
Debusho, Legesse Kassa
author_facet Gemechu, Leta Lencha
Debusho, Legesse Kassa
author_sort Gemechu, Leta Lencha
collection PubMed
description Background: Tuberculosis (TB) and HIV are epidemiologically associated, and their co-dynamics suggest that the two diseases are directly related at the population level and within the host. However, there is no or little information on the joint spatial patterns of the two diseases in Ethiopia. The main objective of the current study was to assess the spatial co-clustering of TB and HIV cases simultaneously in Ethiopia at the district level. Methods: District-level aggregated data collected from the national Health Management Information System (HMIS) for the years 2015 to 2018 on the number of TB cases enrolled in directly observed therapy, short course (DOTS) who were tested for HIV and the number of HIV patients enrolled in HIV care who were screened for TB during their last visit to health care facilities were used in this study. The univariate and bivariate global and local Moran’s I indices were applied to assess the spatial clustering of TB and HIV separately and jointly. Results: The results of this study show that the two diseases were significantly (p-value [Formula: see text]) spatially autocorrelated at the district level with minimum and maximum global Moran’s I values of 0.407 and 0.432 for TB, 0.102 and 0.247 for HIV, and 0.152 and 0.251 for joint TB/HIV. The district-level TB/HIV spatial co-clustering patterns in Ethiopia in most cases overlapped with the hot spots of TB and HIV. The TB/HIV hot-spot clusters may appear due to the observed high TB and HIV prevalence rates in the hot-spot districts. Our results also show that there were low-low TB/HIV co-clusters or cold spots in most of the Afar and Somali regions, which consistently appeared for the period 2015–2018. This may be due to very low notifications of both diseases in the regions. Conclusions: This study expanded knowledge about TB and HIV co-clustering in Ethiopia at the district level. The findings provide information to health policymakers in the country to plan geographically targeted and integrated interventions to jointly control TB and HIV.
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spelling pubmed-96804302022-11-23 Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia Gemechu, Leta Lencha Debusho, Legesse Kassa Diseases Article Background: Tuberculosis (TB) and HIV are epidemiologically associated, and their co-dynamics suggest that the two diseases are directly related at the population level and within the host. However, there is no or little information on the joint spatial patterns of the two diseases in Ethiopia. The main objective of the current study was to assess the spatial co-clustering of TB and HIV cases simultaneously in Ethiopia at the district level. Methods: District-level aggregated data collected from the national Health Management Information System (HMIS) for the years 2015 to 2018 on the number of TB cases enrolled in directly observed therapy, short course (DOTS) who were tested for HIV and the number of HIV patients enrolled in HIV care who were screened for TB during their last visit to health care facilities were used in this study. The univariate and bivariate global and local Moran’s I indices were applied to assess the spatial clustering of TB and HIV separately and jointly. Results: The results of this study show that the two diseases were significantly (p-value [Formula: see text]) spatially autocorrelated at the district level with minimum and maximum global Moran’s I values of 0.407 and 0.432 for TB, 0.102 and 0.247 for HIV, and 0.152 and 0.251 for joint TB/HIV. The district-level TB/HIV spatial co-clustering patterns in Ethiopia in most cases overlapped with the hot spots of TB and HIV. The TB/HIV hot-spot clusters may appear due to the observed high TB and HIV prevalence rates in the hot-spot districts. Our results also show that there were low-low TB/HIV co-clusters or cold spots in most of the Afar and Somali regions, which consistently appeared for the period 2015–2018. This may be due to very low notifications of both diseases in the regions. Conclusions: This study expanded knowledge about TB and HIV co-clustering in Ethiopia at the district level. The findings provide information to health policymakers in the country to plan geographically targeted and integrated interventions to jointly control TB and HIV. MDPI 2022-11-17 /pmc/articles/PMC9680430/ /pubmed/36412600 http://dx.doi.org/10.3390/diseases10040106 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gemechu, Leta Lencha
Debusho, Legesse Kassa
Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia
title Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia
title_full Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia
title_fullStr Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia
title_full_unstemmed Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia
title_short Spatial Co-Clustering of Tuberculosis and HIV in Ethiopia
title_sort spatial co-clustering of tuberculosis and hiv in ethiopia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680430/
https://www.ncbi.nlm.nih.gov/pubmed/36412600
http://dx.doi.org/10.3390/diseases10040106
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