Abstract

BackgroundCarbapenem-resistant Enterobacteriaceae (CRE) have emerged as an urgent public health threat. Intestinal colonization with CRE has been identified as a risk factor for the development of systemic CRE infection, but has not been compared to colonization with third and/or fourth generation cephalosporin-resistant (Ceph-R) Enterobacteriaceae. Moreover, the risk conferred by colonization on adverse outcomes is less clear, particularly in critically ill patients admitted to the intensive care unit (ICU).MethodsWe carried out a cohort study of consecutive adult patients screened for rectal colonization with CRE or Ceph-R upon ICU entry between April and July 2013. We identified clinical variables and assessed the relationship between CRE or Ceph-R colonization and subsequent systemic CRE infection within 30 days (primary outcome) and all-cause mortality within 90 days (secondary outcome).ResultsAmong 338 ICU patients, 94 (28%) were colonized with either Ceph-R or CRE. 26 patients developed CRE infection within 30 days of swab collection; 47% (N = 17/36) of CRE-colonized and 3% (N = 2/58) of Ceph-R colonized patients. 36% (N = 13/36) of CRE-colonized patients died within 90 days compared to 31% (N = 18/58) of Ceph-R-colonized and 15% (N = 37/244) of non-colonized patients. In a multivariable analysis, CRE colonization independently predicted development of a systemic CRE infection at 30 days (aOR 10.8, 95% CI2.8–41.9, p = 0.0006); Ceph-R colonization did not (aOR 0.5, 95% CI0.1–3.3, p = 0.5). CRE colonization was associated with increased 90-day mortality in a univariable analysis (p-value 0.001), in a multivariable model, previous hospitalization and medical ICU admission were independent predictors of 90-day mortality whereas CRE colonization approached significance (aOR 2.3, 95% CI1.0–5.3, p = 0.056).ConclusionsOur study highlights the increased risk of CRE infection and mortality in patients with CRE colonization at the time of ICU admission. Future studies are needed to assess how CRE colonization can guide empiric antibiotic choices and to develop novel decolonization strategies.

Highlights

  • Carbapenem-resistant Enterobacteriaceae (CRE) have become widespread in the US, prompting the Centers for Diseases Control and Prevention (CDC) to classify them as an urgent threat to public health, its highest risk category [1]

  • The risk conferred by colonization on adverse outcomes is less clear, in critically ill patients admitted to the intensive care unit (ICU)

  • Among 338 ICU patients, 94 (28%) were colonized with either cephalosporin-resistant Enterobacteriaceae (Ceph-R) or CRE. 26 patients developed CRE infection within 30 days of swab collection; 47% (N = 17/36) of CRE-colonized and 3% (N = 2/58) of Ceph-R colonized patients. 36% (N = 13/36) of CRE-colonized patients died within 90 days compared to 31% (N = 18/58) of Ceph-R-colonized and 15% (N = 37/244) of non-colonized patients

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Summary

Introduction

Carbapenem-resistant Enterobacteriaceae (CRE) have become widespread in the US, prompting the Centers for Diseases Control and Prevention (CDC) to classify them as an urgent threat to public health, its highest risk category [1]. Patients residing in the intensive care unit (ICU) have been found to have a high burden of CRE infections as well as increased mortality [4,5,6]. In ICU patients, this risk varied widely and between 29–73% of carbapenem-resistant K. pneumoniae carriers subsequently developed infections [4, 5]. While Ceph-R colonization has similar risk factors and is associated with increased use of broad-spectrum antibiotics [21] the role of colonization with third and/or fourth generation cephalosporin-resistant Enterobacteriaceae (Ceph-R) on subsequent CRE infections is less clear. Intestinal colonization with CRE has been identified as a risk factor for the development of systemic CRE infection, but has not been compared to colonization with third and/or fourth generation cephalosporin-resistant (Ceph-R) Enterobacteriaceae. The risk conferred by colonization on adverse outcomes is less clear, in critically ill patients admitted to the intensive care unit (ICU)

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