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PMID: 16641440 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Predictors of mortality in patients with bloodstream infection due to ceftazidime-resistant Klebsiella pneumoniae.

Antimicrobial agents and chemotherapy ·Vol. 50 ·No. 5 ·2006-05-00 ·Pages 1715-20

Anderson DJ, Engemann JJ, Harrell LJ, Carmeli Y, Reller LB, Kaye KS

Abstract

Bloodstream infection (BSI) due to multidrug-resistant Klebsiella is associated with high rates of morbidity and mortality. The aim of this study was to identify predictors of in-hospital mortality among patients with BSI due to ceftazidime-resistant (CAZ-R) Klebsiella pneumoniae at a tertiary care medical center. Patients with CAZ-R K. pneumoniae BSI were identified by our microbiology laboratory between January 1995 and June 2003. Clinical data were collected retrospectively. Logistic regression was used to identify independent predictors of all causes of in-hospital mortality. Of 779 patients with K. pneumoniae BSI, 60 (7.7%) had BSI due to CAZ-R K. pneumoniae; 43 (72%) of these were nosocomial infections. Pulsed-field gel electrophoresis identified a single predominant strain in 17 (28%) patients. The in-hospital mortality rate was 43% (n = 26). Among patients with CAZ-R K. pneumoniae BSI, those who died were similar to survivors with respect to demographic, clinical, and antimicrobial susceptibility characteristics. Only 43 (72%) patients received effective therapy within 5 days of BSI. In bivariable analysis, delay in initiation of effective therapy for >72 h after diagnosis of BSI was associated with death (P = 0.03). Strain genotype was not predictive of outcome. In multivariable analysis, delay in initiation of effective therapy for >72 h after diagnosis of BSI was an independent predictor of death (odds ratio, 3.32; 95% confidence interval, 1.07 to 10.3). Thus, among patients with BSI due to CAZ-R K. pneumoniae, a delay in the initiation of effective therapy of greater than 72 h after BSI was associated with a >3-fold increase in mortality risk.

MeSH Terms
Adolescent Adult Aged Anti-Bacterial Agents/therapeutic use Bacteremia/drug therapy,epidemiology,microbiology Blood-Borne Pathogens/isolation & purification Ceftazidime/pharmacology Cohort Studies Cross Infection Drug Resistance, Bacterial Electrophoresis, Gel, Pulsed-Field Female Gram-Positive Bacterial Infections/blood,epidemiology,microbiology Hospital Mortality Humans Klebsiella Infections/blood,epidemiology,microbiology,mortality Klebsiella pneumoniae/drug effects,genetics,isolation & purification Logistic Models Male Middle Aged Mortality Retrospective Studies Risk Factors Survival Analysis United States/epidemiology
Chemicals
Anti-Bacterial Agents Ceftazidime
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Anderson Deverick J
Duke University Medical Center, Division of Infectious Disease, DUMC Box 3824, Durham, NC 27710, USA. ander077@mc.duke.edu
Engemann John J
Harrell Lizzie J
Carmeli Yehuda
Reller L Barth
Kaye Keith S
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
2006-05-00
Pages
1715-20
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC1472233
Subset
IM
Grants
NIA NIH HHS · K23 AG023621 · United States
NIA NIH HHS · K23 AG 23621-01A1 · United States
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