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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Internal Medicine
2016
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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. |
format | Online Article Text |
id | pubmed-4712420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
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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