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Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence

An increase in antibiotic usage is considered to contribute to the emergence of antimicrobial resistance. Although experts are counting on the antimicrobial stewardship programs to reduce antibiotic usage, their effect remains uncertain. In this study, we aimed to evaluate the impact of antibiotic u...

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Autores principales: Kim, Jeong Yeon, Yum, Yunjin, Joo, Hyung Joon, An, Hyonggin, Yoon, Young Kyung, Kim, Jong Hun, Sohn, Jang Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219833/
https://www.ncbi.nlm.nih.gov/pubmed/34158540
http://dx.doi.org/10.1038/s41598-021-91332-x
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author Kim, Jeong Yeon
Yum, Yunjin
Joo, Hyung Joon
An, Hyonggin
Yoon, Young Kyung
Kim, Jong Hun
Sohn, Jang Wook
author_facet Kim, Jeong Yeon
Yum, Yunjin
Joo, Hyung Joon
An, Hyonggin
Yoon, Young Kyung
Kim, Jong Hun
Sohn, Jang Wook
author_sort Kim, Jeong Yeon
collection PubMed
description An increase in antibiotic usage is considered to contribute to the emergence of antimicrobial resistance. Although experts are counting on the antimicrobial stewardship programs to reduce antibiotic usage, their effect remains uncertain. In this study, we aimed to evaluate the impact of antibiotic usage and forecast the prevalence of hospital-acquired extended spectrum β-lactamase (ESBL)—producing Escherichia coli (E. coli) using time-series analysis. Antimicrobial culture information of E. coli was obtained using a text processing technique that helped extract free-text electronic health records from standardized data. The antimicrobial use density (AUD) of antibiotics of interest was used to estimate the quarterly antibiotic usage. Transfer function model was applied to forecast relationship between antibiotic usage and ESBL-producing E. coli. Of the 1938 hospital-acquired isolates, 831 isolates (42.9%) were ESBL-producing E. coli. Both the proportion of ESBL-producing E. coli and AUD increased over time. The transfer model predicted that ciprofloxacin AUD is related to the proportion of ESBL-producing E. coli two quarters later. In conclusion, excessive use of antibiotics was shown to affect the prevalence of resistant organisms in the future. Therefore, the control of antibiotics with antimicrobial stewardship programs should be considered to restrict antimicrobial resistance.
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spelling pubmed-82198332021-06-24 Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence Kim, Jeong Yeon Yum, Yunjin Joo, Hyung Joon An, Hyonggin Yoon, Young Kyung Kim, Jong Hun Sohn, Jang Wook Sci Rep Article An increase in antibiotic usage is considered to contribute to the emergence of antimicrobial resistance. Although experts are counting on the antimicrobial stewardship programs to reduce antibiotic usage, their effect remains uncertain. In this study, we aimed to evaluate the impact of antibiotic usage and forecast the prevalence of hospital-acquired extended spectrum β-lactamase (ESBL)—producing Escherichia coli (E. coli) using time-series analysis. Antimicrobial culture information of E. coli was obtained using a text processing technique that helped extract free-text electronic health records from standardized data. The antimicrobial use density (AUD) of antibiotics of interest was used to estimate the quarterly antibiotic usage. Transfer function model was applied to forecast relationship between antibiotic usage and ESBL-producing E. coli. Of the 1938 hospital-acquired isolates, 831 isolates (42.9%) were ESBL-producing E. coli. Both the proportion of ESBL-producing E. coli and AUD increased over time. The transfer model predicted that ciprofloxacin AUD is related to the proportion of ESBL-producing E. coli two quarters later. In conclusion, excessive use of antibiotics was shown to affect the prevalence of resistant organisms in the future. Therefore, the control of antibiotics with antimicrobial stewardship programs should be considered to restrict antimicrobial resistance. Nature Publishing Group UK 2021-06-22 /pmc/articles/PMC8219833/ /pubmed/34158540 http://dx.doi.org/10.1038/s41598-021-91332-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kim, Jeong Yeon
Yum, Yunjin
Joo, Hyung Joon
An, Hyonggin
Yoon, Young Kyung
Kim, Jong Hun
Sohn, Jang Wook
Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence
title Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence
title_full Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence
title_fullStr Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence
title_full_unstemmed Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence
title_short Impact of antibiotic usage on extended-spectrum β-lactamase producing Escherichia coli prevalence
title_sort impact of antibiotic usage on extended-spectrum β-lactamase producing escherichia coli prevalence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219833/
https://www.ncbi.nlm.nih.gov/pubmed/34158540
http://dx.doi.org/10.1038/s41598-021-91332-x
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