dc.contributor.author | Matthaiou, DK | en |
dc.contributor.author | Michalopoulos, A | en |
dc.contributor.author | Rafailidis, PI | en |
dc.contributor.author | Karageorgopoulos, DE | en |
dc.contributor.author | Papaioannou, V | en |
dc.contributor.author | Ntani, G | en |
dc.contributor.author | Samonis, G | en |
dc.contributor.author | Falagas, ME | en |
dc.date.accessioned | 2014-03-01T01:29:05Z | |
dc.date.available | 2014-03-01T01:29:05Z | |
dc.date.issued | 2008 | en |
dc.identifier.issn | 0090-3493 | en |
dc.identifier.uri | https://dspace.lib.ntua.gr/xmlui/handle/123456789/19128 | |
dc.subject | Acinetobacter | en |
dc.subject | Klebsiella | en |
dc.subject | Mortality | en |
dc.subject | Multiple drug resistance | en |
dc.subject | Polymyxins | en |
dc.subject | Pseudomonas | en |
dc.subject.classification | Critical Care Medicine | en |
dc.subject.other | cephalosporin derivative | en |
dc.subject.other | colistin | en |
dc.subject.other | monobactam derivative | en |
dc.subject.other | Acinetobacter baumannii | en |
dc.subject.other | adult | en |
dc.subject.other | age distribution | en |
dc.subject.other | aged | en |
dc.subject.other | antibiotic resistance | en |
dc.subject.other | antibiotic sensitivity | en |
dc.subject.other | article | en |
dc.subject.other | artificial ventilation | en |
dc.subject.other | bacterial infection | en |
dc.subject.other | bacterium isolation | en |
dc.subject.other | clinical article | en |
dc.subject.other | controlled study | en |
dc.subject.other | drug use | en |
dc.subject.other | female | en |
dc.subject.other | human | en |
dc.subject.other | intensive care unit | en |
dc.subject.other | Klebsiella pneumoniae | en |
dc.subject.other | length of stay | en |
dc.subject.other | male | en |
dc.subject.other | nonhuman | en |
dc.subject.other | priority journal | en |
dc.subject.other | Pseudomonas aeruginosa | en |
dc.subject.other | risk factor | en |
dc.subject.other | surgical technique | en |
dc.title | Risk factors associated with the isolation of colistin-resistant Gram-negative bacteria: A matched case-control study | en |
heal.type | journalArticle | en |
heal.identifier.primary | 10.1097/CCM.0B013E3181652FAE | en |
heal.identifier.secondary | http://dx.doi.org/10.1097/CCM.0B013E3181652FAE | en |
heal.language | English | en |
heal.publicationDate | 2008 | en |
heal.abstract | Objective: The emergence of multidrug-resistant Gram-negative bacteria has led to the re-use of colistin, but resistance to this agent has already been reported. We aimed to investigate the potential risk factors for the isolation of colistin-resistant Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa from hospitalized patients. Design: Matched case-control study. Setting: Tertiary care hospital in Athens, Greece. Patients: Case patients were those who had provided a clinical specimen from which a colistin-resistant K. pneumoniae, A. baumannii, or P. aeruginosa was isolated. Controls were selected from a pool of patients who had susceptible to colistin isolates and were matched (1:1) to cases for species of microorganism and site of isolation. Susceptibility to colistin was determined with the Etest. Interventions: None. Measurements and Main results: Data regarding patient demographics, comorbidities, admission to the intensive care unit, prior antibiotic use, and invasive procedures performed were analyzed as risk factors in a matched bivariable model. Variables significantly associated with colistin-resistant isolates (p < .05) were entered in a backward multivariable logistic regression model. Forty-one colistin-resistant unique patient isolates were identified from January 1, 2006, until March 31, 2007. These isolates represented infection in 35 of 41 patients. Risk factors significantly associated with the isolation of colistin-resistant isolates were age, duration of intensive care unit stay, duration of mechanical ventilation, surgical procedures, use of colistin, use of monobactams, and duration of use of third-generation cephalosporins. In the multivariable model, use of colistin was identified as the only independent risk factor (adjusted odds ratio = 7.78, p = .002). Conclusions: Colistin-resistant K. pneumoniae, A. baumannii, and P. aeruginosa pathogens may be encountered in clinical practice, in association with inappropriate colistin use. To prevent this phenomenon, colistin should be used judiciously, given that treatment options for colistin-resistant Gram-negative bacteria are limited. Copyright © 2008 by the Society of Critical Care Medicine and Lippincott Williams & Wilkins. | en |
heal.publisher | LIPPINCOTT WILLIAMS & WILKINS | en |
heal.journalName | Critical Care Medicine | en |
dc.identifier.doi | 10.1097/CCM.0B013E3181652FAE | en |
dc.identifier.isi | ISI:000253450500020 | en |
dc.identifier.volume | 36 | en |
dc.identifier.issue | 3 | en |
dc.identifier.spage | 807 | en |
dc.identifier.epage | 811 | en |
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