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Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections

The aim of this study was to determine the risk factors for nosocomial infections of imipenem-resistant Pseudomonas aeruginosa (IRPA). A prospective case-control study was performed at a tertiary care hospital in Ankara from January to December 2004. The patients with nosocomial P. aeruginosa infect...

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Autores principales: Onguru, Pinar, Erbay, Ayse, Bodur, Hurrem, Baran, Gulseren, Akinci, Esragul, Balaban, Neriman, Cevik, Mustafa Aydin
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610663/
https://www.ncbi.nlm.nih.gov/pubmed/19119440
http://dx.doi.org/10.3346/jkms.2008.23.6.982
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author Onguru, Pinar
Erbay, Ayse
Bodur, Hurrem
Baran, Gulseren
Akinci, Esragul
Balaban, Neriman
Cevik, Mustafa Aydin
author_facet Onguru, Pinar
Erbay, Ayse
Bodur, Hurrem
Baran, Gulseren
Akinci, Esragul
Balaban, Neriman
Cevik, Mustafa Aydin
author_sort Onguru, Pinar
collection PubMed
description The aim of this study was to determine the risk factors for nosocomial infections of imipenem-resistant Pseudomonas aeruginosa (IRPA). A prospective case-control study was performed at a tertiary care hospital in Ankara from January to December 2004. The patients with nosocomial P. aeruginosa infection were included in the study. The features of the patients with IRPA infections were compared to those with imipenem-sensitive P. aeruginosa (ISPA) infections. Only the first isolation of P. aeruginosa was considered. Nosocomial infections were defined according to Center for Disease Control (CDC) criteria. IRPA was isolated from 75 (44.1%) patients, and ISPA was isolated from 95 (55.9%) patients during the study period. IRPA were most frequently isolated from endotracheal aspirate (19%) cultures (p=0.048), whereas ISPA were most frequently isolated from urine (28%) cultures (p=0.023). In multivariate analysis, a longer duration of hospital stay until P. aeruginosa isolation (odds ratio [OR], 1.027; 95% confidence interval [CI], 1.002-1.054, p=0.034), arterial catheter administration (OR, 2.508; 95% CI, 1.062-5.920, p=0.036), vancomycin (OR, 2.882; 95% CI, 1.130-7.349, p=0.027), piperacillin-tazobactam (OR, 6.425; 95% CI, 2.187-18.875, p=0.001), and imipenem (OR, 3.580; 95% CI, 1.252-10.245, p=0.017) treatment within the 14 days before isolation of IRPA were independently associated with imipenem resistance. It was concluded that treatment with imipenem, vancomycin and piperacillin-tazobactam were major risk factors for IRPA infections in hospitalized patients. The nosocomial occurrence of IRPA was also strongly related to the duration of hospital stay, arterial catheter administration.
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spelling pubmed-26106632008-12-31 Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections Onguru, Pinar Erbay, Ayse Bodur, Hurrem Baran, Gulseren Akinci, Esragul Balaban, Neriman Cevik, Mustafa Aydin J Korean Med Sci Original Article The aim of this study was to determine the risk factors for nosocomial infections of imipenem-resistant Pseudomonas aeruginosa (IRPA). A prospective case-control study was performed at a tertiary care hospital in Ankara from January to December 2004. The patients with nosocomial P. aeruginosa infection were included in the study. The features of the patients with IRPA infections were compared to those with imipenem-sensitive P. aeruginosa (ISPA) infections. Only the first isolation of P. aeruginosa was considered. Nosocomial infections were defined according to Center for Disease Control (CDC) criteria. IRPA was isolated from 75 (44.1%) patients, and ISPA was isolated from 95 (55.9%) patients during the study period. IRPA were most frequently isolated from endotracheal aspirate (19%) cultures (p=0.048), whereas ISPA were most frequently isolated from urine (28%) cultures (p=0.023). In multivariate analysis, a longer duration of hospital stay until P. aeruginosa isolation (odds ratio [OR], 1.027; 95% confidence interval [CI], 1.002-1.054, p=0.034), arterial catheter administration (OR, 2.508; 95% CI, 1.062-5.920, p=0.036), vancomycin (OR, 2.882; 95% CI, 1.130-7.349, p=0.027), piperacillin-tazobactam (OR, 6.425; 95% CI, 2.187-18.875, p=0.001), and imipenem (OR, 3.580; 95% CI, 1.252-10.245, p=0.017) treatment within the 14 days before isolation of IRPA were independently associated with imipenem resistance. It was concluded that treatment with imipenem, vancomycin and piperacillin-tazobactam were major risk factors for IRPA infections in hospitalized patients. The nosocomial occurrence of IRPA was also strongly related to the duration of hospital stay, arterial catheter administration. The Korean Academy of Medical Sciences 2008-12 2008-12-24 /pmc/articles/PMC2610663/ /pubmed/19119440 http://dx.doi.org/10.3346/jkms.2008.23.6.982 Text en Copyright © 2008 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 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 non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Onguru, Pinar
Erbay, Ayse
Bodur, Hurrem
Baran, Gulseren
Akinci, Esragul
Balaban, Neriman
Cevik, Mustafa Aydin
Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections
title Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections
title_full Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections
title_fullStr Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections
title_full_unstemmed Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections
title_short Imipenem-Resistant Pseudomonas aeruginosa: Risk Factors for Nosocomial Infections
title_sort imipenem-resistant pseudomonas aeruginosa: risk factors for nosocomial infections
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610663/
https://www.ncbi.nlm.nih.gov/pubmed/19119440
http://dx.doi.org/10.3346/jkms.2008.23.6.982
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