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The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC
AIM: Antibiotic resistance mediated by extended-spectrum β-lactamases (ESBL) and AmpC β-lactamases is widespread and increasingly common, often rendering empiric antibiotic therapy ineffective. In septicemia, delays in initiating effective antibiotic therapy are associated with worse clinical outcom...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242201/ https://www.ncbi.nlm.nih.gov/pubmed/28116124 http://dx.doi.org/10.4155/fsoa-2016-0042 |
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author | Robinson, Andrew M Medlicott, Natalie J Ussher, James E |
author_facet | Robinson, Andrew M Medlicott, Natalie J Ussher, James E |
author_sort | Robinson, Andrew M |
collection | PubMed |
description | AIM: Antibiotic resistance mediated by extended-spectrum β-lactamases (ESBL) and AmpC β-lactamases is widespread and increasingly common, often rendering empiric antibiotic therapy ineffective. In septicemia, delays in initiating effective antibiotic therapy are associated with worse clinical outcomes. With current phenotypic antimicrobial susceptibility testing methods, there is often a delay of 18–24 h before the susceptibility of an isolate is known. RESULTS: Using an HPLC assay, breakdown of the third-generation cephalosporin cefotaxime by ESBL- and AmpC- β-lactamase-producing organisms could be detected within 90 min with 86.4% sensitivity and 100% specificity; sensitivity for ESBL detection was 100%. CONCLUSION: This assay could be readily established in any clinical laboratory with an HPLC to rapidly detect ESBL-producing Enterobacteriaceae. |
format | Online Article Text |
id | pubmed-5242201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52422012017-01-23 The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC Robinson, Andrew M Medlicott, Natalie J Ussher, James E Future Sci OA Preliminary Communication AIM: Antibiotic resistance mediated by extended-spectrum β-lactamases (ESBL) and AmpC β-lactamases is widespread and increasingly common, often rendering empiric antibiotic therapy ineffective. In septicemia, delays in initiating effective antibiotic therapy are associated with worse clinical outcomes. With current phenotypic antimicrobial susceptibility testing methods, there is often a delay of 18–24 h before the susceptibility of an isolate is known. RESULTS: Using an HPLC assay, breakdown of the third-generation cephalosporin cefotaxime by ESBL- and AmpC- β-lactamase-producing organisms could be detected within 90 min with 86.4% sensitivity and 100% specificity; sensitivity for ESBL detection was 100%. CONCLUSION: This assay could be readily established in any clinical laboratory with an HPLC to rapidly detect ESBL-producing Enterobacteriaceae. Future Science Ltd 2016-09-09 /pmc/articles/PMC5242201/ /pubmed/28116124 http://dx.doi.org/10.4155/fsoa-2016-0042 Text en © University of Otago This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Preliminary Communication Robinson, Andrew M Medlicott, Natalie J Ussher, James E The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC |
title | The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC |
title_full | The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC |
title_fullStr | The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC |
title_full_unstemmed | The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC |
title_short | The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC |
title_sort | rapid detection of cefotaxime-resistant enterobacteriaceae by hplc |
topic | Preliminary Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242201/ https://www.ncbi.nlm.nih.gov/pubmed/28116124 http://dx.doi.org/10.4155/fsoa-2016-0042 |
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