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2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis
BACKGROUND: Carbapenems are a class of β-lactam antibiotics which include imipenem, meropenem and ertapenem. More recently, a new oral carbapenem (faropenem) have been marketed in a limited number of countries (in particular, India and Japan). Emerging evidence demonstrates that they target the myco...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254036/ http://dx.doi.org/10.1093/ofid/ofy210.2100 |
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author | Satta, Giovanni Gonzalo, Ximena Canseco, Julio Ortiz Wey, Emmanuel Drobniewski, Francis McHugh, Timothy D |
author_facet | Satta, Giovanni Gonzalo, Ximena Canseco, Julio Ortiz Wey, Emmanuel Drobniewski, Francis McHugh, Timothy D |
author_sort | Satta, Giovanni |
collection | PubMed |
description | BACKGROUND: Carbapenems are a class of β-lactam antibiotics which include imipenem, meropenem and ertapenem. More recently, a new oral carbapenem (faropenem) have been marketed in a limited number of countries (in particular, India and Japan). Emerging evidence demonstrates that they target the mycobacterial cell wall, providing an alternative treatment for multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB), where options are limited. Compared with imipenem and meropenem (both only available as intravenous formulations), ertapenem (once daily administration) and faropenem (oral) are much more attractive alternatives for ambulatory or homecare treatment. However, there is a paucity of data on their efficacy against M. tuberculosis. The aim of this project was to test the in vitro activity of ertapenem and faropenem (with and without the addition of amoxicillin/clavulanate) against different clinical isolates of M. tuberculosis and the reference strain H37RV, to better understand their potential role as additional antibiotics in the management of drug-resistant TB. METHODS: Twenty isolates in total (19 clinical isolates, including MDR and XDR strains, plus H37Rv) were tested against different concentrations of ertapenem and faropenem (with and without the addition of amoxicillin/clavulanate). Susceptibility testing was performed using two different methods (BACTEC960 and broth microdilution). A degradation assay was also performed to evaluate the stability of ertapenem. RESULTS: Eighteen out of 20 samples were resistant to the highest concentration of ertapenem tested (including the addition of amoxicillin/clavulanate). Half of the samples tested showed some degree of susceptibility to faropenem and the addition of amoxicillin/clavulanate further reduced the MIC level in seven isolates. CONCLUSION: The results from this project have highlighted a significant level of in vitro resistance to ertapenem, whilst the clinical isolates have shown different degrees of susceptibility to faropenem. Although promising agents (in particular, faropenem), carbapenems will remain a third line choice to be used only in cases of XDR TB. There is currently no evidence to prefer the use of ertapenem despite its once daily administration. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6254036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62540362018-11-28 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis Satta, Giovanni Gonzalo, Ximena Canseco, Julio Ortiz Wey, Emmanuel Drobniewski, Francis McHugh, Timothy D Open Forum Infect Dis Abstracts BACKGROUND: Carbapenems are a class of β-lactam antibiotics which include imipenem, meropenem and ertapenem. More recently, a new oral carbapenem (faropenem) have been marketed in a limited number of countries (in particular, India and Japan). Emerging evidence demonstrates that they target the mycobacterial cell wall, providing an alternative treatment for multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB), where options are limited. Compared with imipenem and meropenem (both only available as intravenous formulations), ertapenem (once daily administration) and faropenem (oral) are much more attractive alternatives for ambulatory or homecare treatment. However, there is a paucity of data on their efficacy against M. tuberculosis. The aim of this project was to test the in vitro activity of ertapenem and faropenem (with and without the addition of amoxicillin/clavulanate) against different clinical isolates of M. tuberculosis and the reference strain H37RV, to better understand their potential role as additional antibiotics in the management of drug-resistant TB. METHODS: Twenty isolates in total (19 clinical isolates, including MDR and XDR strains, plus H37Rv) were tested against different concentrations of ertapenem and faropenem (with and without the addition of amoxicillin/clavulanate). Susceptibility testing was performed using two different methods (BACTEC960 and broth microdilution). A degradation assay was also performed to evaluate the stability of ertapenem. RESULTS: Eighteen out of 20 samples were resistant to the highest concentration of ertapenem tested (including the addition of amoxicillin/clavulanate). Half of the samples tested showed some degree of susceptibility to faropenem and the addition of amoxicillin/clavulanate further reduced the MIC level in seven isolates. CONCLUSION: The results from this project have highlighted a significant level of in vitro resistance to ertapenem, whilst the clinical isolates have shown different degrees of susceptibility to faropenem. Although promising agents (in particular, faropenem), carbapenems will remain a third line choice to be used only in cases of XDR TB. There is currently no evidence to prefer the use of ertapenem despite its once daily administration. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6254036/ http://dx.doi.org/10.1093/ofid/ofy210.2100 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Satta, Giovanni Gonzalo, Ximena Canseco, Julio Ortiz Wey, Emmanuel Drobniewski, Francis McHugh, Timothy D 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis |
title | 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis |
title_full | 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis |
title_fullStr | 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis |
title_full_unstemmed | 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis |
title_short | 2447. Ertapenem and Faropenem for the Treatment of Drug-Resistant Tuberculosis |
title_sort | 2447. ertapenem and faropenem for the treatment of drug-resistant tuberculosis |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254036/ http://dx.doi.org/10.1093/ofid/ofy210.2100 |
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