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Comparative activity of carbapenem testing (the COMPACT study) in Turkey
BACKGROUND: Recent evidence indicates that Gram-negative bacterial pathogens, the most common of which are Pseudomonas spp., Enterobacteriaceae, and Acinetobacter baumannii, are frequent causes of hospital-acquired infections. This study aims to evaluate the in vitro activity of doripenem and compar...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298475/ https://www.ncbi.nlm.nih.gov/pubmed/22340940 http://dx.doi.org/10.1186/1471-2334-12-42 |
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author | Leblebicioglu, Hakan Cakir, Nedim Celen, Mustafa Kurt, Halil Baris, Hakan Laeuffer, Joerg |
author_facet | Leblebicioglu, Hakan Cakir, Nedim Celen, Mustafa Kurt, Halil Baris, Hakan Laeuffer, Joerg |
author_sort | Leblebicioglu, Hakan |
collection | PubMed |
description | BACKGROUND: Recent evidence indicates that Gram-negative bacterial pathogens, the most common of which are Pseudomonas spp., Enterobacteriaceae, and Acinetobacter baumannii, are frequent causes of hospital-acquired infections. This study aims to evaluate the in vitro activity of doripenem and comparator carbapenem antibiotics against Gram-negative clinical isolates collected from COMParative Activity of Carbapenem Testing (COMPACT) study centres in Turkey. METHODS: Ten centres in Turkey were invited to submit Pseudomonas aeruginosa, Enterobacteriaceae, and other Gram-negative isolates from intensive care unit (ICU)/non-ICU patients with complicated intra-abdominal infections, bloodstream infections, or nosocomial pneumonia, including ventilator-associated pneumonia, between May and October 2008. Susceptibility was determined by each centre using E-test. A central laboratory performed species confirmation as well as limited susceptibility and quality-control testing. RESULTS: Five hundred and ninety six isolates were collected. MIC(90 )values for doripenem, meropenem, and imipenem, respectively, were 32, ≥ 64, and ≥ 64 mg/L against Pseudomonas spp.; 0.12, 0.12, and 0.5 mg/L against Enterobacteriaceae; and ≥ 64 mg/L for each against other Gram-negative isolates. In determining the susceptibility of hospital isolates of selected Gram-negative pathogens to doripenem, imipenem, and meropenem, we found that against all pathogens combined, the MIC(90 )for ICU compared with non-ICU isolates was higher. CONCLUSIONS: Doripenem showed similar or slightly better activity than meropenem and better activity than imipenem against the Gram-negative pathogens collected in Turkey. |
format | Online Article Text |
id | pubmed-3298475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32984752012-03-10 Comparative activity of carbapenem testing (the COMPACT study) in Turkey Leblebicioglu, Hakan Cakir, Nedim Celen, Mustafa Kurt, Halil Baris, Hakan Laeuffer, Joerg BMC Infect Dis Research Article BACKGROUND: Recent evidence indicates that Gram-negative bacterial pathogens, the most common of which are Pseudomonas spp., Enterobacteriaceae, and Acinetobacter baumannii, are frequent causes of hospital-acquired infections. This study aims to evaluate the in vitro activity of doripenem and comparator carbapenem antibiotics against Gram-negative clinical isolates collected from COMParative Activity of Carbapenem Testing (COMPACT) study centres in Turkey. METHODS: Ten centres in Turkey were invited to submit Pseudomonas aeruginosa, Enterobacteriaceae, and other Gram-negative isolates from intensive care unit (ICU)/non-ICU patients with complicated intra-abdominal infections, bloodstream infections, or nosocomial pneumonia, including ventilator-associated pneumonia, between May and October 2008. Susceptibility was determined by each centre using E-test. A central laboratory performed species confirmation as well as limited susceptibility and quality-control testing. RESULTS: Five hundred and ninety six isolates were collected. MIC(90 )values for doripenem, meropenem, and imipenem, respectively, were 32, ≥ 64, and ≥ 64 mg/L against Pseudomonas spp.; 0.12, 0.12, and 0.5 mg/L against Enterobacteriaceae; and ≥ 64 mg/L for each against other Gram-negative isolates. In determining the susceptibility of hospital isolates of selected Gram-negative pathogens to doripenem, imipenem, and meropenem, we found that against all pathogens combined, the MIC(90 )for ICU compared with non-ICU isolates was higher. CONCLUSIONS: Doripenem showed similar or slightly better activity than meropenem and better activity than imipenem against the Gram-negative pathogens collected in Turkey. BioMed Central 2012-02-16 /pmc/articles/PMC3298475/ /pubmed/22340940 http://dx.doi.org/10.1186/1471-2334-12-42 Text en Copyright ©2012 Leblebicioglu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Leblebicioglu, Hakan Cakir, Nedim Celen, Mustafa Kurt, Halil Baris, Hakan Laeuffer, Joerg Comparative activity of carbapenem testing (the COMPACT study) in Turkey |
title | Comparative activity of carbapenem testing (the COMPACT study) in Turkey |
title_full | Comparative activity of carbapenem testing (the COMPACT study) in Turkey |
title_fullStr | Comparative activity of carbapenem testing (the COMPACT study) in Turkey |
title_full_unstemmed | Comparative activity of carbapenem testing (the COMPACT study) in Turkey |
title_short | Comparative activity of carbapenem testing (the COMPACT study) in Turkey |
title_sort | comparative activity of carbapenem testing (the compact study) in turkey |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298475/ https://www.ncbi.nlm.nih.gov/pubmed/22340940 http://dx.doi.org/10.1186/1471-2334-12-42 |
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