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2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates
BACKGROUND: Cefoxitin has a good in vitro activity and stability in resistance to hydrolysis by ESBLs, and is a good candidate for the treatment of urinary tract infection (UTI). However, data are scarce regarding its use in clinical practice, especially against K. pneumoniae deemed to be capable of...
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/PMC6253686/ http://dx.doi.org/10.1093/ofid/ofy210.2075 |
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author | Senard, Olivia Bouchand, Frederique Deconinck, Laurene Matt, Morgan Fellous, Lesly Rottman, Martin Perronne, Christian Dinh, Aurelien Davido, Benjamin |
author_facet | Senard, Olivia Bouchand, Frederique Deconinck, Laurene Matt, Morgan Fellous, Lesly Rottman, Martin Perronne, Christian Dinh, Aurelien Davido, Benjamin |
author_sort | Senard, Olivia |
collection | PubMed |
description | BACKGROUND: Cefoxitin has a good in vitro activity and stability in resistance to hydrolysis by ESBLs, and is a good candidate for the treatment of urinary tract infection (UTI). However, data are scarce regarding its use in clinical practice, especially against K. pneumoniae deemed to be capable of the acquirement of porin-deficient mutant. METHODS: We conducted a retrospective study from September 2014 to November 2017, in a tertiary-care hospital. We gathered all prescriptions of Cefoxitin for UTI due to ESBL isolates. We compared the clinical outcomes between E. coli and K. pneumoniae ESBL-producing isolates after a 90-day follow-up. When available, we assessed whether Cefoxitin-based regimen was associated with an emergence of resistance. To our knowledge there is no clinical data supporting a real threat of development of resistance in UTI. RESULTS: The treatment of 31 patients with a mean age of 60 ± 18 years was analyzed. We observed a clinical cure at D90 in 81.2% (n = 13/16) of cases for ESBL E. coli isolates and 85.7% (12/14) for ESBL K. pneumoniae (P = 0.72). Overall, we noted an efficacy of FOX around 83.3% (n = 25/30). [Image: see text] Median dose of Cefoxitin was 4 g (2–8). Only one patient infected by an ESBL E. coli received an oral relay with levofloxacin for 4 additional days. No adverse events were reported. One patient who relapsed, carried a K. pneumoniae isolate that became intermediate to Cefoxitin in the follow-up. CONCLUSION: In a period of major threat with a continuous increase of ESBL obliging to a policy of carbapenem-sparing regimens, it seems detrimental to deprive physicians of using Cefoxitin for ESBL Enterobacteriaceae for the treatment of UTI while our data show its efficacy. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6253686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62536862018-11-28 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates Senard, Olivia Bouchand, Frederique Deconinck, Laurene Matt, Morgan Fellous, Lesly Rottman, Martin Perronne, Christian Dinh, Aurelien Davido, Benjamin Open Forum Infect Dis Abstracts BACKGROUND: Cefoxitin has a good in vitro activity and stability in resistance to hydrolysis by ESBLs, and is a good candidate for the treatment of urinary tract infection (UTI). However, data are scarce regarding its use in clinical practice, especially against K. pneumoniae deemed to be capable of the acquirement of porin-deficient mutant. METHODS: We conducted a retrospective study from September 2014 to November 2017, in a tertiary-care hospital. We gathered all prescriptions of Cefoxitin for UTI due to ESBL isolates. We compared the clinical outcomes between E. coli and K. pneumoniae ESBL-producing isolates after a 90-day follow-up. When available, we assessed whether Cefoxitin-based regimen was associated with an emergence of resistance. To our knowledge there is no clinical data supporting a real threat of development of resistance in UTI. RESULTS: The treatment of 31 patients with a mean age of 60 ± 18 years was analyzed. We observed a clinical cure at D90 in 81.2% (n = 13/16) of cases for ESBL E. coli isolates and 85.7% (12/14) for ESBL K. pneumoniae (P = 0.72). Overall, we noted an efficacy of FOX around 83.3% (n = 25/30). [Image: see text] Median dose of Cefoxitin was 4 g (2–8). Only one patient infected by an ESBL E. coli received an oral relay with levofloxacin for 4 additional days. No adverse events were reported. One patient who relapsed, carried a K. pneumoniae isolate that became intermediate to Cefoxitin in the follow-up. CONCLUSION: In a period of major threat with a continuous increase of ESBL obliging to a policy of carbapenem-sparing regimens, it seems detrimental to deprive physicians of using Cefoxitin for ESBL Enterobacteriaceae for the treatment of UTI while our data show its efficacy. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253686/ http://dx.doi.org/10.1093/ofid/ofy210.2075 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 Senard, Olivia Bouchand, Frederique Deconinck, Laurene Matt, Morgan Fellous, Lesly Rottman, Martin Perronne, Christian Dinh, Aurelien Davido, Benjamin 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates |
title | 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates |
title_full | 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates |
title_fullStr | 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates |
title_full_unstemmed | 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates |
title_short | 2422. Efficacy of Cefoxitin for the Treatment of Urinary Tract Infection (UTI) Due to ESBL-Producing E. coli and K. pneumoniae Isolates |
title_sort | 2422. efficacy of cefoxitin for the treatment of urinary tract infection (uti) due to esbl-producing e. coli and k. pneumoniae isolates |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253686/ http://dx.doi.org/10.1093/ofid/ofy210.2075 |
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