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Prevalence of multidrug‐resistant pseudomonas aeruginosa and carbapenem‐resistant enterobacteriaceae among specimens from hospitalized patients with pneumonia and bloodstream infections in the United States from 2000 to 2009
Author(s) -
Zilberberg Marya D.,
Shorr Andrew F.
Publication year - 2013
Publication title -
journal of hospital medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.128
H-Index - 65
eISSN - 1553-5606
pISSN - 1553-5592
DOI - 10.1002/jhm.2080
Subject(s) - pneumonia , medicine , pseudomonas aeruginosa , enterobacteriaceae , carbapenem resistant enterobacteriaceae , multiple drug resistance , microbiology and biotechnology , cephalosporin , antibiotics , carbapenem , antibiotic resistance , drug resistance , biology , bacteria , escherichia coli , biochemistry , genetics , gene
BACKGROUND Antimicrobial resistance complicates antibiotic selection. Pseudomonas aeruginosa (PA), common in pneumonia and blood stream infections (BSIs), is frequently resistant to multiple antimicrobial classes. Carbapenem‐resistant Enterobacteriaceae (CRE) have emerged as a pathogen of concern over the past decade. OBJECTIVE To determine the prevalence of CRE and multidrug‐resistant PA (MDR‐PA) in pneumonia and BSI hospitalizations. DESIGN Survey of data from a nationally representative sample of microbiology laboratories in 217 hospitals in the United States. METHODS/SETTING We examined Eurofins' The Surveillance Network database from 2000 to 2009 to explore the proportion of all PA in pneumonia and BSI that is MDR. We performed the same analysis for CRE as a proportion of Enterobacteriaceae . We defined MDR‐PA as any isolate resistant to ≥3 drug classes. Enterobacteriaceae were CRE if resistant to both a third generation cephalosporin and a carbapenem. RESULTS We identified 205,526 PA (187,343 pneumonia; 18,183 BSI) and 95,566 Enterobacteriaceae specimens (58,810 pneumonia; 36,756 BSI). The prevalence of MDR‐PA was ∼15‐fold higher than CRE in both infection types (pneumonia: 22.0% MDR‐PA vs 1.6% CRE; BSI: 14.7% MDR‐PA vs 1.1% CRE). There was a net rise in MDR‐PA as a proportion of all PA from 2000 to 2009 (BSI: 10.7%–13.5%; pneumonia: 19.2%–21.7%). The CRE phenotype emerged in 2002 in both infection types, peaking in 2008 at 3.6% in BSI and 5.3% in pneumonia, and stabilized thereafter. CONCLUSIONS Although CRE organisms have emerged as an important pathogen in BSI and pneumonia, MDR‐PA remains more prevalent in the United States. Journal of Hospital Medicine 2013;8:559–563. © 2013 Society of Hospital Medicine