Colonization with broad-spectrum cephalosporin-resistant Gram-negative bacilli in intensive care units during a nonoutbreak period: Prevalence, risk factors, and rate of infection

Citation
Emc. D'Agata et al., Colonization with broad-spectrum cephalosporin-resistant Gram-negative bacilli in intensive care units during a nonoutbreak period: Prevalence, risk factors, and rate of infection, CRIT CARE M, 27(6), 1999, pp. 1090-1095
Citations number
27
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
27
Issue
6
Year of publication
1999
Pages
1090 - 1095
Database
ISI
SICI code
0090-3493(199906)27:6<1090:CWBCGB>2.0.ZU;2-7
Abstract
Objective: To define the epidemiology of broad-spectrum cephalosporin-resis tant Gram-negative bacilli in intensive care units (ICUs) during a nonoutbr eak period, including the prevalence, the risk factors for colonization, th e frequency of acquisition, and the rate of infection. Design: Prospective cohort study, Setting: Tertiary care hospital. Patients: Consecutive patients admitted to two surgical ICUs. Main Outcome Measurements: Serial patient surveillance cultures screened fo r ceftazidime (CAZ) resistance, antibiotic and hospital exposure, and infec tions. Results: Of the 333 patients enrolled, 60 (18%) were colonized with CAZ-res istant Gram-negative bacilli (CAZ-RGN) at admission. Clinical cultures dete cted CAZ-RGN in only 5% (3/60) of these patients. By using logistic regress ion, CAZ-RGN colonization was associated with duration of exposure to cefaz olin (odds ratio, 10.3; p less than or equal to .006) and to broad-spectrum cephalosporins/penicillins (odds ratio, 2; p less than or equal to .03), A cute Physiology and Chronic Health Evaluation III(TM) score (Odds ratio, 1. 2; p less than or equal to .008), and previous hospitalization (odds ratio, 3.1; p less than or equal to .006). Of the 100 patients who remained in th e surgical ICU for greater than or equal to 3 days, 26% acquired a CAZ-RGN. Of the 14 infections caused by CAZ-RGN, 11 (79%) were attributable to the same species present in surveillance cultures at admission to the surgical ICU. Conclusions: Colonization with CAZ-RGN was common and was usually not recog nized by clinical cultures. Most patients colonized or infected with CAZ-RG N had positive surveillance cultures at the time of admission to the surgic al ICU, suggesting that acquisition frequently occurred in other wards and institutions, Patients exposed to first-generation cephalosporins, as well as broad-spectrum cephalosporins/penicillins, were at high risk of coloniza tion with CAZ-RGN. Empirical treatment of nosocomial Gram-negative infectio ns with broad-spectrum cephalosporins, especially in the critically ill pat ient, should be reconsidered.