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In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates
BACKGROUND: The purpose of this study was to define the potency of amikacin and comparator agents against a collection of blood and respiratory nosocomial isolates implicated in ICU based pulmonary infections gathered from US hospitals. METHODS: Minimum inhibitory concentrations of amikacin, aztreon...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912699/ https://www.ncbi.nlm.nih.gov/pubmed/27316973 http://dx.doi.org/10.1186/s12941-016-0155-z |
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author | Sutherland, Christina A. Verastegui, Jamie E. Nicolau, David P. |
author_facet | Sutherland, Christina A. Verastegui, Jamie E. Nicolau, David P. |
author_sort | Sutherland, Christina A. |
collection | PubMed |
description | BACKGROUND: The purpose of this study was to define the potency of amikacin and comparator agents against a collection of blood and respiratory nosocomial isolates implicated in ICU based pulmonary infections gathered from US hospitals. METHODS: Minimum inhibitory concentrations of amikacin, aztreonam, cefepime, ceftazidime, ceftolozane/tazobactam, ceftriaxone, ciprofloxacin, imipenem, meropenem, piperacillin/tazobactam and tobramycin were tested against 2460 Gram-negative isolates. Amikacin had 96 % susceptibility against the combined E. coli and K. pneumoniae isolates and 95 % susceptibility against P. aeruginosa. RESULTS: Ninety-six percent of all of isolates tested were susceptible (i.e., MICs ≤16 mg/L) to amikacin by current laboratory standards which demonstrates a high level of activity to combat infections caused by these organisms including ESBL, MDR, β-lactam and fluoroquinolone resistant strains. Moreover, 99 % of all organisms had amikacin MICs ≤64 mg/L. CONCLUSIONS: Overall, these data highlight the continued potency of amikacin and suggest that the achievable lung concentrations of approximately 5000 mg/L with the administration of the amikacin by inhalation (Amikacin Inhale, BAY41-6551) will exceed the MICs typically observed for P. aeruginosa, E. coli and K. pneumoniae in the hospital setting. |
format | Online Article Text |
id | pubmed-4912699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49126992016-06-19 In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates Sutherland, Christina A. Verastegui, Jamie E. Nicolau, David P. Ann Clin Microbiol Antimicrob Research BACKGROUND: The purpose of this study was to define the potency of amikacin and comparator agents against a collection of blood and respiratory nosocomial isolates implicated in ICU based pulmonary infections gathered from US hospitals. METHODS: Minimum inhibitory concentrations of amikacin, aztreonam, cefepime, ceftazidime, ceftolozane/tazobactam, ceftriaxone, ciprofloxacin, imipenem, meropenem, piperacillin/tazobactam and tobramycin were tested against 2460 Gram-negative isolates. Amikacin had 96 % susceptibility against the combined E. coli and K. pneumoniae isolates and 95 % susceptibility against P. aeruginosa. RESULTS: Ninety-six percent of all of isolates tested were susceptible (i.e., MICs ≤16 mg/L) to amikacin by current laboratory standards which demonstrates a high level of activity to combat infections caused by these organisms including ESBL, MDR, β-lactam and fluoroquinolone resistant strains. Moreover, 99 % of all organisms had amikacin MICs ≤64 mg/L. CONCLUSIONS: Overall, these data highlight the continued potency of amikacin and suggest that the achievable lung concentrations of approximately 5000 mg/L with the administration of the amikacin by inhalation (Amikacin Inhale, BAY41-6551) will exceed the MICs typically observed for P. aeruginosa, E. coli and K. pneumoniae in the hospital setting. BioMed Central 2016-06-17 /pmc/articles/PMC4912699/ /pubmed/27316973 http://dx.doi.org/10.1186/s12941-016-0155-z Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Sutherland, Christina A. Verastegui, Jamie E. Nicolau, David P. In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates |
title | In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates |
title_full | In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates |
title_fullStr | In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates |
title_full_unstemmed | In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates |
title_short | In vitro potency of amikacin and comparators against E. coli,K. pneumoniae and P. aeruginosa respiratory and blood isolates |
title_sort | in vitro potency of amikacin and comparators against e. coli,k. pneumoniae and p. aeruginosa respiratory and blood isolates |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912699/ https://www.ncbi.nlm.nih.gov/pubmed/27316973 http://dx.doi.org/10.1186/s12941-016-0155-z |
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