Appropriateness of Empirical Treatment and Outcome in Bacteremia Caused by Extended-Spectrum-β-Lactamase-Producing Bacteria

被引:67
作者
Frakking, Florine N. J. [1 ,3 ]
Rottier, Wouter C. [1 ,2 ]
Dorigo-Zetsma, J. Wendelien [4 ]
van Hattem, Jarne M. [5 ]
Van Hees, Babette C. [6 ]
Kluytmans, Jan A. J. W. [7 ,8 ]
Lutgens, Suzanne P. M. [7 ]
Prins, Jan M. [9 ]
Thijsen, Steven F. T. [10 ]
Verbon, Annelies [11 ]
Vlaminckx, Bart J. M. [2 ]
Stuart, James W. Cohen [1 ]
Leverstein-van Hall, Maurine A. [1 ,12 ]
Bonten, Marc J. M. [1 ,2 ]
机构
[1] Univ Med Ctr Utrecht, Dept Med Microbiol, Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] St Antonius Hosp, Dept Med Microbiol & Immunol, Nieuwegein, Netherlands
[4] Tergooi Hosp, Cent Lab Bacteriol & Serol, Hilversum, Netherlands
[5] Tergooi Hosp, Dept Internal Med, Hilversum, Netherlands
[6] Gelre Hosp, Dept Med Microbiol, Apeldoorn, Netherlands
[7] Amphia Hosp, Dept Med Microbiol & Infect Control, Breda, Netherlands
[8] Vrije Univ Amsterdam Med Ctr, Dept Med Microbiol & Infect Control, Amsterdam, Netherlands
[9] Univ Amsterdam, Acad Med Ctr, Dept Internal Med, NL-1105 AZ Amsterdam, Netherlands
[10] Diakonessen Hosp, Dept Med Microbiol & Immunol, Utrecht, Netherlands
[11] Erasmus MC, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
[12] Natl Inst Publ Hlth & Environm, NL-3720 BA Bilthoven, Netherlands
关键词
BLOOD-STREAM INFECTIONS; KLEBSIELLA-PNEUMONIAE BACTEREMIA; ESCHERICHIA-COLI; RISK-FACTORS; INHIBITOR COMBINATIONS; ANTIBIOTIC-THERAPY; ENTEROBACTERIACEAE; PREDICTORS; MORTALITY; IMPACT;
D O I
10.1128/AAC.01523-12
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
We studied clinical characteristics, appropriateness of initial antibiotic treatment, and other factors associated with day 30 mortality in patients with bacteremia caused by extended-spectrum-beta-lactamase (ESBL)-producing bacteria in eight Dutch hospitals. Retrospectively, information was collected from 232 consecutive patients with ESBL bacteremia (due to Escherichia coli, Klebsiella pneumoniae, and Enterobacter cloacae) between 2008 and 2010. In this cohort (median age of 65 years; 24 patients were <18 years of age), many had comorbidities, such as malignancy (34%) or recurrent urinary tract infection (UTI) (15%). One hundred forty episodes (60%) were nosocomial, 54 (23%) were otherwise health care associated, and 38 (16%) were community acquired. The most frequent sources of infection were UTI (42%) and intra-abdominal infection (28%). Appropriate therapy within 24 h after bacteremia onset was prescribed to 37% of all patients and to 54% of known ESBL carriers. The day 30 mortality rate was 20%. In a multivariable analysis, a Charlson comorbidity index of >= 3, an age of >= 75 years, intensive care unit (ICU) stay at bacteremia onset, a non-UTI bacteremia source, and presentation with severe sepsis, but not inappropriate therapy within <24 h (adjusted odds ratio [OR], 1.53; 95% confidence interval [CI], 0.68 to 3.45), were associated with day 30 mortality. Further assessment of confounding and a stratified analysis for patients with UTI and non-UTI origins of infection did not reveal a statistically significant effect of inappropriate therapy on day 30 mortality, and these results were insensitive to the possible misclassification of patients who had received beta-lactam-beta-lactamase inhibitor combinations or ceftazidime as initial treatment. In conclusion, ESBL bacteremia occurs mostly in patients with comorbidities requiring frequent hospitalization, and 84% of episodes were health care associated. Factors other than inappropriate therapy within <24 h determined day 30 mortality.
引用
收藏
页码:3092 / 3099
页数:8
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