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Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study

BACKGROUND AND AIMS: Intestinal parasites affect the tuberculosis disease outcome by shifting the cell‐mediated to humoral immune response and host immune system suppression. However, Mycobacterium tuberculosis (MTB) infection favors the immune escape of parasites. Hence, exploring the rate of intes...

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Autores principales: Shibabaw, Agumas, Tilahun, Mihret, Gedefie, Alemu, Sahle, Zenawork, Belete, Melaku A., Ebrahim, Hussen, Debash, Habtu, Sharew, Bekele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509650/
https://www.ncbi.nlm.nih.gov/pubmed/37736307
http://dx.doi.org/10.1002/hsr2.1569
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author Shibabaw, Agumas
Tilahun, Mihret
Gedefie, Alemu
Sahle, Zenawork
Belete, Melaku A.
Ebrahim, Hussen
Debash, Habtu
Sharew, Bekele
author_facet Shibabaw, Agumas
Tilahun, Mihret
Gedefie, Alemu
Sahle, Zenawork
Belete, Melaku A.
Ebrahim, Hussen
Debash, Habtu
Sharew, Bekele
author_sort Shibabaw, Agumas
collection PubMed
description BACKGROUND AND AIMS: Intestinal parasites affect the tuberculosis disease outcome by shifting the cell‐mediated to humoral immune response and host immune system suppression. However, Mycobacterium tuberculosis (MTB) infection favors the immune escape of parasites. Hence, exploring the rate of intestinal parasitic coinfection with pulmonary tuberculosis (PTB) and its predisposing factors to take better preventive, control, and management measures. METHODS: A facility‐based cross‐sectional study was conducted from September to December 2020 at five health institutions in Hawassa city. A total of 214 PTB patients were diagnosed using the GeneXpert assay and enrolled in this study. Demographic, clinical, and risk factors data were collected using a structured questionnaire. Stool samples were collected using a clean, labeled, and leak‐proof stool cup. Stool samples were examined using direct saline microscopy and the formal‐ether concentration technique. The data were entered and coded in SPSS software for analysis. Bivariate and multivariate logistic regression were employed to identify the associated risk factors. A p‐value less than  0.05 was considered statistically significant. RESULTS: The overall rate of intestinal parasitic‐MTB coinfection was 36.9%. The most dominant intestinal parasite was Gardia lamblia (17.8%, 38), followed by Entamoeba histolytica/dispar (9.3%, 20). Intestinal parasitosis coinfection of PTB was associated with being rural resident (adjusted odds ratio [AOR] = 2.42; 95% confidence interval [CI]: 1.23–4.8), not washing of fruits and vegetables before eating [AOR = 4.14; 95% CI: 1.92–9], being at the early stage of anti‐TB treatment [AOR = 3; 95% CI: 1.5–6.3] and presence of chronic diseases [AOR = 7; 95% CI: 3.4–14]. CONCLUSION: The burden of intestinal parasites‐MTB coinfection was high. Those who wash fruits and vegetables before eating should be encouraged, early treatment of PTB patients and avoiding the practice of open‐field defecation, especially in rural communities, is necessary. The dual effect of coinfection on disease severity and treatment success needs further cohort study.
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spelling pubmed-105096502023-09-21 Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study Shibabaw, Agumas Tilahun, Mihret Gedefie, Alemu Sahle, Zenawork Belete, Melaku A. Ebrahim, Hussen Debash, Habtu Sharew, Bekele Health Sci Rep Original Research BACKGROUND AND AIMS: Intestinal parasites affect the tuberculosis disease outcome by shifting the cell‐mediated to humoral immune response and host immune system suppression. However, Mycobacterium tuberculosis (MTB) infection favors the immune escape of parasites. Hence, exploring the rate of intestinal parasitic coinfection with pulmonary tuberculosis (PTB) and its predisposing factors to take better preventive, control, and management measures. METHODS: A facility‐based cross‐sectional study was conducted from September to December 2020 at five health institutions in Hawassa city. A total of 214 PTB patients were diagnosed using the GeneXpert assay and enrolled in this study. Demographic, clinical, and risk factors data were collected using a structured questionnaire. Stool samples were collected using a clean, labeled, and leak‐proof stool cup. Stool samples were examined using direct saline microscopy and the formal‐ether concentration technique. The data were entered and coded in SPSS software for analysis. Bivariate and multivariate logistic regression were employed to identify the associated risk factors. A p‐value less than  0.05 was considered statistically significant. RESULTS: The overall rate of intestinal parasitic‐MTB coinfection was 36.9%. The most dominant intestinal parasite was Gardia lamblia (17.8%, 38), followed by Entamoeba histolytica/dispar (9.3%, 20). Intestinal parasitosis coinfection of PTB was associated with being rural resident (adjusted odds ratio [AOR] = 2.42; 95% confidence interval [CI]: 1.23–4.8), not washing of fruits and vegetables before eating [AOR = 4.14; 95% CI: 1.92–9], being at the early stage of anti‐TB treatment [AOR = 3; 95% CI: 1.5–6.3] and presence of chronic diseases [AOR = 7; 95% CI: 3.4–14]. CONCLUSION: The burden of intestinal parasites‐MTB coinfection was high. Those who wash fruits and vegetables before eating should be encouraged, early treatment of PTB patients and avoiding the practice of open‐field defecation, especially in rural communities, is necessary. The dual effect of coinfection on disease severity and treatment success needs further cohort study. John Wiley and Sons Inc. 2023-09-20 /pmc/articles/PMC10509650/ /pubmed/37736307 http://dx.doi.org/10.1002/hsr2.1569 Text en © 2023 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Shibabaw, Agumas
Tilahun, Mihret
Gedefie, Alemu
Sahle, Zenawork
Belete, Melaku A.
Ebrahim, Hussen
Debash, Habtu
Sharew, Bekele
Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study
title Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study
title_full Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study
title_fullStr Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study
title_full_unstemmed Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study
title_short Magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in Southern Ethiopia: A cross‐sectional study
title_sort magnitude and predisposing factors of intestinal parasitosis and tuberculosis coinfection at five health institutions in southern ethiopia: a cross‐sectional study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509650/
https://www.ncbi.nlm.nih.gov/pubmed/37736307
http://dx.doi.org/10.1002/hsr2.1569
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