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Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms

BACKGROUND: Infections caused by multiply drug resistant organisms such as extended spectrum beta-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae are increasing. Carbapenems (imipenem and meropenem) are the antibiotics commonly used to treat these agents. There is limited clini...

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Autores principales: Mody, Rupal M, Erwin, Daniel P, Summers, Amy M, Carrero, Hector A, Selby, Edward B, Ewell, Allesa J, Moran, Kimberly A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894638/
https://www.ncbi.nlm.nih.gov/pubmed/17553151
http://dx.doi.org/10.1186/1476-0711-6-6
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author Mody, Rupal M
Erwin, Daniel P
Summers, Amy M
Carrero, Hector A
Selby, Edward B
Ewell, Allesa J
Moran, Kimberly A
author_facet Mody, Rupal M
Erwin, Daniel P
Summers, Amy M
Carrero, Hector A
Selby, Edward B
Ewell, Allesa J
Moran, Kimberly A
author_sort Mody, Rupal M
collection PubMed
description BACKGROUND: Infections caused by multiply drug resistant organisms such as extended spectrum beta-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae are increasing. Carbapenems (imipenem and meropenem) are the antibiotics commonly used to treat these agents. There is limited clinical data regarding the efficacy of the newest carbapenem, ertapenem, against these organisms. Ertapenem susceptibility of ESBL-producing E. coli and K. pneumoniae clinical isolates were evaluated and compared to imipenem to determine if imipenem susceptibility could be used as a surrogate for ertapenem susceptibility. METHODS: 100 ESBL isolates (n = 34 E. coli and n = 66 K. pneumoniae) collected from 2005–2006 clinical specimens at WRAMC were identified and tested for susceptibility by Vitek Legacy [bioMerieux, Durham, NC]. Ertapenem susceptibility was performed via epsilometer test (E-test) [AB Biodisk, Solna, Sweden]. RESULTS: 100% of ESBL isolates tested were susceptible to ertapenem. 100% of the same isolates were also susceptible to imipenem. CONCLUSION: These results, based on 100% susceptibility, suggest that ertapenem may be an alternative to other carbapenems for the treatment of infections caused by ESBL-producing E. coli and K. pneumoniae. Clinical outcomes studies are needed to determine if ertapenem is effective for the treatment of infection caused by these organisms. However, due to lack of resistant isolates, we are unable to conclude whether imipenem susceptibility accurately predicts ertapenem susceptibility.
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spelling pubmed-18946382007-06-19 Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms Mody, Rupal M Erwin, Daniel P Summers, Amy M Carrero, Hector A Selby, Edward B Ewell, Allesa J Moran, Kimberly A Ann Clin Microbiol Antimicrob Research BACKGROUND: Infections caused by multiply drug resistant organisms such as extended spectrum beta-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae are increasing. Carbapenems (imipenem and meropenem) are the antibiotics commonly used to treat these agents. There is limited clinical data regarding the efficacy of the newest carbapenem, ertapenem, against these organisms. Ertapenem susceptibility of ESBL-producing E. coli and K. pneumoniae clinical isolates were evaluated and compared to imipenem to determine if imipenem susceptibility could be used as a surrogate for ertapenem susceptibility. METHODS: 100 ESBL isolates (n = 34 E. coli and n = 66 K. pneumoniae) collected from 2005–2006 clinical specimens at WRAMC were identified and tested for susceptibility by Vitek Legacy [bioMerieux, Durham, NC]. Ertapenem susceptibility was performed via epsilometer test (E-test) [AB Biodisk, Solna, Sweden]. RESULTS: 100% of ESBL isolates tested were susceptible to ertapenem. 100% of the same isolates were also susceptible to imipenem. CONCLUSION: These results, based on 100% susceptibility, suggest that ertapenem may be an alternative to other carbapenems for the treatment of infections caused by ESBL-producing E. coli and K. pneumoniae. Clinical outcomes studies are needed to determine if ertapenem is effective for the treatment of infection caused by these organisms. However, due to lack of resistant isolates, we are unable to conclude whether imipenem susceptibility accurately predicts ertapenem susceptibility. BioMed Central 2007-06-06 /pmc/articles/PMC1894638/ /pubmed/17553151 http://dx.doi.org/10.1186/1476-0711-6-6 Text en Copyright © 2007 Mody et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mody, Rupal M
Erwin, Daniel P
Summers, Amy M
Carrero, Hector A
Selby, Edward B
Ewell, Allesa J
Moran, Kimberly A
Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
title Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
title_full Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
title_fullStr Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
title_full_unstemmed Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
title_short Ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
title_sort ertapenem susceptibility of extended spectrum beta-lactamase-producing organisms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894638/
https://www.ncbi.nlm.nih.gov/pubmed/17553151
http://dx.doi.org/10.1186/1476-0711-6-6
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