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Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora

BACKGROUND: The human microbiota modulates the immune system and forms the surface flora. Antibiotic administration causes dysbiosis in the intestinal flora. It is not clear if antibiotic administration in the community effects the upper airway flora in the mid-term or long-term. This study aims to...

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Autores principales: Korkmaz, Hakan, Çetinkol, Yeliz, Korkmaz, Mukadder, Çalgın, Mustafa Kerem, Arıcı, Yeliz Kaşko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750656/
https://www.ncbi.nlm.nih.gov/pubmed/34987147
http://dx.doi.org/10.12659/MSM.934931
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author Korkmaz, Hakan
Çetinkol, Yeliz
Korkmaz, Mukadder
Çalgın, Mustafa Kerem
Arıcı, Yeliz Kaşko
author_facet Korkmaz, Hakan
Çetinkol, Yeliz
Korkmaz, Mukadder
Çalgın, Mustafa Kerem
Arıcı, Yeliz Kaşko
author_sort Korkmaz, Hakan
collection PubMed
description BACKGROUND: The human microbiota modulates the immune system and forms the surface flora. Antibiotic administration causes dysbiosis in the intestinal flora. It is not clear if antibiotic administration in the community effects the upper airway flora in the mid-term or long-term. This study aims to define long-term influence of antibiotics on upper airway flora. MATERIAL/METHODS: In this prospective study, aerobic microbiological analysis of nasal and nasopharyngeal surfaces was performed. Antibiotic administration history of the last 6 months was retrieved using the social insurance database. Culture results of antibiotic-treated and antibiotic-naïve subjects were compared by Pearson’s chi-square test or Fisher’s exact test. RESULTS: A total of 210 subjects were included in the study. Normal flora were documented in 86 nasal swabs and 99 nasopharyngeal swabs. Most of the remaining cases demonstrated gram-positive bacterial overgrowth. There were 113 subjects who did not receive any antibiotic, and 93% of the remaining 97 patients received broad-spectrum antibiotics. Statistical analysis showed that nasal and nasopharyngeal flora did not change upon antibiotic administration, but antibiotic administration during the last month caused increased methicillin resistance development of coagulase-negative Staphylococcus and Staphylococcus aureus microorganisms. CONCLUSIONS: Antibiotic exposure did not lead to perturbations in general composition of upper airway flora within 6 months, although the incidence of methicillin resistance in coagulase-positive and -negative Staphylococci demonstrated significant increases when patients received antibiotic during the last month. This should be considered in case of broad-spectrum antibiotic administration, since methicillin resistance increases the morbidity and mortality of nosocomial Staphylococcus infections.
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spelling pubmed-87506562022-01-21 Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora Korkmaz, Hakan Çetinkol, Yeliz Korkmaz, Mukadder Çalgın, Mustafa Kerem Arıcı, Yeliz Kaşko Med Sci Monit Lab/In Vitro Research BACKGROUND: The human microbiota modulates the immune system and forms the surface flora. Antibiotic administration causes dysbiosis in the intestinal flora. It is not clear if antibiotic administration in the community effects the upper airway flora in the mid-term or long-term. This study aims to define long-term influence of antibiotics on upper airway flora. MATERIAL/METHODS: In this prospective study, aerobic microbiological analysis of nasal and nasopharyngeal surfaces was performed. Antibiotic administration history of the last 6 months was retrieved using the social insurance database. Culture results of antibiotic-treated and antibiotic-naïve subjects were compared by Pearson’s chi-square test or Fisher’s exact test. RESULTS: A total of 210 subjects were included in the study. Normal flora were documented in 86 nasal swabs and 99 nasopharyngeal swabs. Most of the remaining cases demonstrated gram-positive bacterial overgrowth. There were 113 subjects who did not receive any antibiotic, and 93% of the remaining 97 patients received broad-spectrum antibiotics. Statistical analysis showed that nasal and nasopharyngeal flora did not change upon antibiotic administration, but antibiotic administration during the last month caused increased methicillin resistance development of coagulase-negative Staphylococcus and Staphylococcus aureus microorganisms. CONCLUSIONS: Antibiotic exposure did not lead to perturbations in general composition of upper airway flora within 6 months, although the incidence of methicillin resistance in coagulase-positive and -negative Staphylococci demonstrated significant increases when patients received antibiotic during the last month. This should be considered in case of broad-spectrum antibiotic administration, since methicillin resistance increases the morbidity and mortality of nosocomial Staphylococcus infections. International Scientific Literature, Inc. 2022-01-06 /pmc/articles/PMC8750656/ /pubmed/34987147 http://dx.doi.org/10.12659/MSM.934931 Text en © Med Sci Monit, 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Lab/In Vitro Research
Korkmaz, Hakan
Çetinkol, Yeliz
Korkmaz, Mukadder
Çalgın, Mustafa Kerem
Arıcı, Yeliz Kaşko
Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora
title Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora
title_full Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora
title_fullStr Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora
title_full_unstemmed Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora
title_short Effect of Antibiotic Exposure on Upper Respiratory Tract Bacterial Flora
title_sort effect of antibiotic exposure on upper respiratory tract bacterial flora
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750656/
https://www.ncbi.nlm.nih.gov/pubmed/34987147
http://dx.doi.org/10.12659/MSM.934931
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