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Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli

BACKGROUND/AIMS: The number of urinary tract infections (UTIs) caused by extended-spectrum β-lactamase-producing Escherichia coli (ESBL-EC) is increasing. In an outpatient setting, there are limited therapeutic options to treat ESBL-producing pathogens. We evaluated the outcomes of amikacin outpatie...

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Autores principales: Cho, Sung-Yeon, Choi, Su-Mi, Park, Sun Hee, Lee, Dong-Gun, Choi, Jung-Hyun, Yoo, Jin-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712420/
https://www.ncbi.nlm.nih.gov/pubmed/26767869
http://dx.doi.org/10.3904/kjim.2016.31.1.156
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author Cho, Sung-Yeon
Choi, Su-Mi
Park, Sun Hee
Lee, Dong-Gun
Choi, Jung-Hyun
Yoo, Jin-Hong
author_facet Cho, Sung-Yeon
Choi, Su-Mi
Park, Sun Hee
Lee, Dong-Gun
Choi, Jung-Hyun
Yoo, Jin-Hong
author_sort Cho, Sung-Yeon
collection PubMed
description BACKGROUND/AIMS: The number of urinary tract infections (UTIs) caused by extended-spectrum β-lactamase-producing Escherichia coli (ESBL-EC) is increasing. In an outpatient setting, there are limited therapeutic options to treat ESBL-producing pathogens. We evaluated the outcomes of amikacin outpatient parenteral antibiotic therapy (OPAT) for UTIs caused by ESBL-EC in patients not pre-treated with carbapenem. METHODS: We retrospectively evaluated the outcomes of amikacin OPAT for UTIs caused by ESBL-EC. RESULTS: From November 2011 to October 2012, eight females, who could not be hospitalized for carbapenem treatment, were treated with amikacin OPAT for nine episodes of non-bacteremic ESBL-EC UTIs. Seven of the eight patients had one or more comorbidities. Of the nine UTI cases, three had symptomatic lower UTIs and six had non-bacteremic upper UTIs. In all of the cases, symptomatic and laboratory improvements were observed following amikacin OPAT. One patient showed a delayed relapse with bilateral microabscesses 3 weeks after treatment cessation; however, a clinical and microbiological cure was eventually reached. All of the patients were able to tolerate amikacin OPAT without any significant nephrotoxicity or ototoxicity. CONCLUSIONS: Amikacin OPAT represents a feasible therapeutic option for non-bacteremic UTIs caused by ESBL-EC in settings with limited resources.
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spelling pubmed-47124202016-01-14 Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli Cho, Sung-Yeon Choi, Su-Mi Park, Sun Hee Lee, Dong-Gun Choi, Jung-Hyun Yoo, Jin-Hong Korean J Intern Med Original Article BACKGROUND/AIMS: The number of urinary tract infections (UTIs) caused by extended-spectrum β-lactamase-producing Escherichia coli (ESBL-EC) is increasing. In an outpatient setting, there are limited therapeutic options to treat ESBL-producing pathogens. We evaluated the outcomes of amikacin outpatient parenteral antibiotic therapy (OPAT) for UTIs caused by ESBL-EC in patients not pre-treated with carbapenem. METHODS: We retrospectively evaluated the outcomes of amikacin OPAT for UTIs caused by ESBL-EC. RESULTS: From November 2011 to October 2012, eight females, who could not be hospitalized for carbapenem treatment, were treated with amikacin OPAT for nine episodes of non-bacteremic ESBL-EC UTIs. Seven of the eight patients had one or more comorbidities. Of the nine UTI cases, three had symptomatic lower UTIs and six had non-bacteremic upper UTIs. In all of the cases, symptomatic and laboratory improvements were observed following amikacin OPAT. One patient showed a delayed relapse with bilateral microabscesses 3 weeks after treatment cessation; however, a clinical and microbiological cure was eventually reached. All of the patients were able to tolerate amikacin OPAT without any significant nephrotoxicity or ototoxicity. CONCLUSIONS: Amikacin OPAT represents a feasible therapeutic option for non-bacteremic UTIs caused by ESBL-EC in settings with limited resources. The Korean Association of Internal Medicine 2016-01 2015-12-28 /pmc/articles/PMC4712420/ /pubmed/26767869 http://dx.doi.org/10.3904/kjim.2016.31.1.156 Text en Copyright © 2016 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cho, Sung-Yeon
Choi, Su-Mi
Park, Sun Hee
Lee, Dong-Gun
Choi, Jung-Hyun
Yoo, Jin-Hong
Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli
title Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli
title_full Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli
title_fullStr Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli
title_full_unstemmed Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli
title_short Amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing Escherichia coli
title_sort amikacin therapy for urinary tract infections caused by extended-spectrum β-lactamase-producing escherichia coli
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712420/
https://www.ncbi.nlm.nih.gov/pubmed/26767869
http://dx.doi.org/10.3904/kjim.2016.31.1.156
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