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High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania

Colonization of multidrug resistant (MDR) bacteria is associated with subsequent invasive infections in children with comorbidities. This study aimed to determine the resistance profile and factors associated with MDR pathogen colonization among HIV−and HIV+ children below five years of age in Mwanz...

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Autores principales: Msanga, Delfina R., Silago, Vitus, Massoza, Tulla, Kidenya, Benson R., Balandya, Emmanuel, Mirambo, Mariam M., Sunguya, Bruno, Mmbaga, Blandina Theophil, Lyamuya, Eligius, Bartlet, John, Mshana, Stephen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955874/
https://www.ncbi.nlm.nih.gov/pubmed/35335702
http://dx.doi.org/10.3390/pathogens11030379
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author Msanga, Delfina R.
Silago, Vitus
Massoza, Tulla
Kidenya, Benson R.
Balandya, Emmanuel
Mirambo, Mariam M.
Sunguya, Bruno
Mmbaga, Blandina Theophil
Lyamuya, Eligius
Bartlet, John
Mshana, Stephen E.
author_facet Msanga, Delfina R.
Silago, Vitus
Massoza, Tulla
Kidenya, Benson R.
Balandya, Emmanuel
Mirambo, Mariam M.
Sunguya, Bruno
Mmbaga, Blandina Theophil
Lyamuya, Eligius
Bartlet, John
Mshana, Stephen E.
author_sort Msanga, Delfina R.
collection PubMed
description Colonization of multidrug resistant (MDR) bacteria is associated with subsequent invasive infections in children with comorbidities. This study aimed to determine the resistance profile and factors associated with MDR pathogen colonization among HIV−and HIV+ children below five years of age in Mwanza, Tanzania. A total of 399 (HIV− 255 and HIV+ 144) children were enrolled and investigated for the presence of MDR bacteria. The median [IQR] age of children was 19 (10–36) months. Out of 27 Staphylococcus aureus colonizing the nasal cavity, 16 (59.5%) were methicillin resistant while 132/278 (47.2%) of Enterobacteriaceae from rectal swabs were resistant to third generation cephalosporins, with 69.7% (92/132) exhibiting extended spectrum beta lactamase (ESBL) phenotypes. The proportion of resistance to gentamicin, amoxicillin/clavulanic acid and meropenem were significantly higher among HIV+ than HIV− children. A history of antibiotic use in the last month OR 2.62 [1.1, 6.9] (p = 0.04) and history of a relative admitted from the same household in the past three months OR 3.73 [1.1, 13.2] (p = 0.03) independently predicted ESBL rectal colonization. HIV+ children had significantly more fecal carriage of isolates resistant to uncommonly used antibiotics. There is a need to strengthen antimicrobial stewardship and Infection Prevention and Control (IPC) programs to prevent the emergence and spread of MDR pathogens in children.
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spelling pubmed-89558742022-03-26 High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania Msanga, Delfina R. Silago, Vitus Massoza, Tulla Kidenya, Benson R. Balandya, Emmanuel Mirambo, Mariam M. Sunguya, Bruno Mmbaga, Blandina Theophil Lyamuya, Eligius Bartlet, John Mshana, Stephen E. Pathogens Article Colonization of multidrug resistant (MDR) bacteria is associated with subsequent invasive infections in children with comorbidities. This study aimed to determine the resistance profile and factors associated with MDR pathogen colonization among HIV−and HIV+ children below five years of age in Mwanza, Tanzania. A total of 399 (HIV− 255 and HIV+ 144) children were enrolled and investigated for the presence of MDR bacteria. The median [IQR] age of children was 19 (10–36) months. Out of 27 Staphylococcus aureus colonizing the nasal cavity, 16 (59.5%) were methicillin resistant while 132/278 (47.2%) of Enterobacteriaceae from rectal swabs were resistant to third generation cephalosporins, with 69.7% (92/132) exhibiting extended spectrum beta lactamase (ESBL) phenotypes. The proportion of resistance to gentamicin, amoxicillin/clavulanic acid and meropenem were significantly higher among HIV+ than HIV− children. A history of antibiotic use in the last month OR 2.62 [1.1, 6.9] (p = 0.04) and history of a relative admitted from the same household in the past three months OR 3.73 [1.1, 13.2] (p = 0.03) independently predicted ESBL rectal colonization. HIV+ children had significantly more fecal carriage of isolates resistant to uncommonly used antibiotics. There is a need to strengthen antimicrobial stewardship and Infection Prevention and Control (IPC) programs to prevent the emergence and spread of MDR pathogens in children. MDPI 2022-03-21 /pmc/articles/PMC8955874/ /pubmed/35335702 http://dx.doi.org/10.3390/pathogens11030379 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
Msanga, Delfina R.
Silago, Vitus
Massoza, Tulla
Kidenya, Benson R.
Balandya, Emmanuel
Mirambo, Mariam M.
Sunguya, Bruno
Mmbaga, Blandina Theophil
Lyamuya, Eligius
Bartlet, John
Mshana, Stephen E.
High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania
title High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania
title_full High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania
title_fullStr High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania
title_full_unstemmed High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania
title_short High Fecal Carriage of Multidrug Resistant Bacteria in the Community among Children in Northwestern Tanzania
title_sort high fecal carriage of multidrug resistant bacteria in the community among children in northwestern tanzania
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955874/
https://www.ncbi.nlm.nih.gov/pubmed/35335702
http://dx.doi.org/10.3390/pathogens11030379
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