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Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii
The aim of the present study was to examine the clinical distribution and drug resistance of Acinetobacter baumannii infection, and provide evidence of clinical medication as well as the prophylaxis for the treatment of drug resistance bacteria. In total, 306 Acinetobacter baumanniis selected from r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998347/ https://www.ncbi.nlm.nih.gov/pubmed/27602085 http://dx.doi.org/10.3892/etm.2016.3513 |
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author | Ren, Guangming Zhou, Min Ding, Ning Zhou, Ning Li, Qingling |
author_facet | Ren, Guangming Zhou, Min Ding, Ning Zhou, Ning Li, Qingling |
author_sort | Ren, Guangming |
collection | PubMed |
description | The aim of the present study was to examine the clinical distribution and drug resistance of Acinetobacter baumannii infection, and provide evidence of clinical medication as well as the prophylaxis for the treatment of drug resistance bacteria. In total, 306 Acinetobacter baumanniis selected from routine culture were collected between January 2012 and December 2013, to analyze the distributions among clinical specimens and wards and their drug resistance state. Of the 306 Acinetobacter baumanniis, the main distribution of specimens was sputum, accounting for 77.78%. The distribution of administrative office was dominated by intensive care unit with a proportion of 40.0% in 2012, which rapidly increased to 60.9% in 2013, followed by neurosurgery, respiration medicine and orthopedics with proportions of 23, 12 and 9.0% in 2012 and 9.71, 8.74 and 3.88% in 2013, respectively. The Acinetobacter baumannii's drug resistance rate of Tazobactam and Piperacillin was increased from 68.0% in 2012 to 71.36% in 2013. At the same time, the drug resistance rate of imipenem was enhanced from 66.0% in 2012 to 72.81% in 2013. By 2013, the drug resistance rates of penbritin, ceftizoxime, cefotetan and macrodantin reached ≤100%. In conclusion, Acinetobacter baumannii mainly causes respiratory tract infection with severe drug resistance. The drug resistance of Acinetobacter baumannii was mainly manifested as multidrug resistance or even pan-drug resistance with an obvious increasing trend of tolerance. Thus, it is necessary to prevent and treat nosocomial infection, to minimize usage of antibiotics and to standardize medical operating, to reduce the increase in persistence. |
format | Online Article Text |
id | pubmed-4998347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-49983472016-09-06 Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii Ren, Guangming Zhou, Min Ding, Ning Zhou, Ning Li, Qingling Exp Ther Med Articles The aim of the present study was to examine the clinical distribution and drug resistance of Acinetobacter baumannii infection, and provide evidence of clinical medication as well as the prophylaxis for the treatment of drug resistance bacteria. In total, 306 Acinetobacter baumanniis selected from routine culture were collected between January 2012 and December 2013, to analyze the distributions among clinical specimens and wards and their drug resistance state. Of the 306 Acinetobacter baumanniis, the main distribution of specimens was sputum, accounting for 77.78%. The distribution of administrative office was dominated by intensive care unit with a proportion of 40.0% in 2012, which rapidly increased to 60.9% in 2013, followed by neurosurgery, respiration medicine and orthopedics with proportions of 23, 12 and 9.0% in 2012 and 9.71, 8.74 and 3.88% in 2013, respectively. The Acinetobacter baumannii's drug resistance rate of Tazobactam and Piperacillin was increased from 68.0% in 2012 to 71.36% in 2013. At the same time, the drug resistance rate of imipenem was enhanced from 66.0% in 2012 to 72.81% in 2013. By 2013, the drug resistance rates of penbritin, ceftizoxime, cefotetan and macrodantin reached ≤100%. In conclusion, Acinetobacter baumannii mainly causes respiratory tract infection with severe drug resistance. The drug resistance of Acinetobacter baumannii was mainly manifested as multidrug resistance or even pan-drug resistance with an obvious increasing trend of tolerance. Thus, it is necessary to prevent and treat nosocomial infection, to minimize usage of antibiotics and to standardize medical operating, to reduce the increase in persistence. D.A. Spandidos 2016-09 2016-07-11 /pmc/articles/PMC4998347/ /pubmed/27602085 http://dx.doi.org/10.3892/etm.2016.3513 Text en Copyright: © Ren et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Ren, Guangming Zhou, Min Ding, Ning Zhou, Ning Li, Qingling Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii |
title | Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii |
title_full | Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii |
title_fullStr | Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii |
title_full_unstemmed | Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii |
title_short | Analysis on distribution features and drug resistance of clinically isolated Acinetobacter baumannii |
title_sort | analysis on distribution features and drug resistance of clinically isolated acinetobacter baumannii |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998347/ https://www.ncbi.nlm.nih.gov/pubmed/27602085 http://dx.doi.org/10.3892/etm.2016.3513 |
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