4.4 Article

Impact of hospital length of stay on the distribution of Gram negative bacteria and likelihood of isolating a resistant organism in a Canadian burn center

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BURNS
卷 42, 期 1, 页码 104-111

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ELSEVIER SCI LTD
DOI: 10.1016/j.burns.2015.07.010

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Gram negative bacteria; Length of stay; Distribution; Resistance; Prevalence; Burn

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Rationale: The impact of hospital length of stay (LOS) on the distribution and susceptibility of Gram negative bacteria (GNB) causing infection in burn patients remains unexplored. Knowledge of causative pathogens is important in guiding empiric antibiotic therapy. Objectives: To characterize the distribution of GNB causing infection and to identify changes in susceptibility with LOS in a tertiary care burn center. Methods: A retrospective review of all admissions to the Ross Tilley Burn Centre at Sunnybrook Health Sciences Centre with clinical cultures yielding GNB (duplicates excluded) between March 12, 2010 to July 17, 2013 was completed. Positive cultures were categorized into 5 clinically relevant time periods (in days) based on specimen collection date relative to the patient's date of admission: 0-7, 7-14, 14-21, 21-28, > 28. Chi-square for proportions was used to compare the time periods. Results: The proportion of patients with clinical cultures for P. aeruginosa increased with hospital LOS (0-7 days: 8% vs. > 28 days: 55%; p < 0.05). Conversely, clinical cultures for H. influenzae occurred primarily within the first 7 days of hospitalization (0-7 days: 36% vs. > 28 days: 0.7%; p < 0.05). Enterobacteriaceae isolation was highest between 7 and 14 days of hospitalization (7-14 days: 62% vs. > 28 days: 38%; p < 0.05). Antibiotic resistance was directly proportional to hospital LOS (% patients with multidrug resistant GNB increased from 6% [LOS 0-7days] to 44% [LOS > 28 days]; p < 0.05). Conclusions: This study provides objective data documenting changes in species and resistance patterns of GNB causing infection in patients admitted to a burn center as a function of hospital LOS; which may support delaying the use of broad spectrum antibiotics (e. g. carbapenems and beta-lactam/beta-lactamase inhibitors) in clinically stable patients. (C) 2015 Elsevier Ltd and ISBI. All rights reserved.

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