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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...

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Autores principales: Robinson, Andrew M, Medlicott, Natalie J, Ussher, James E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2016
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.
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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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