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. 2016 Aug 1;3(3):ofw136.
doi: 10.1093/ofid/ofw136. eCollection 2016 Sep.

Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features

Affiliations

Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features

José Ramón Paño-Pardo et al. Open Forum Infect Dis. .

Erratum in

  • Erratum.
    [No authors listed] [No authors listed] Open Forum Infect Dis. 2017 Jun 17;4(2):ofx119. doi: 10.1093/ofid/ofx119. eCollection 2017 Spring. Open Forum Infect Dis. 2017. PMID: 28702472 Free PMC article.

Abstract

Background. Because most infections caused by carbapenemase-producing Enterobacteriaceae (CPE) begin during hospitalization, there are limited data about community-onset (CO) infections caused by CPE. Our aim is to describe the frequency of CO infections caused by CPE as well as the clinical features of CO bloodstream infections (CO-BSIs). Methods. This study includes retrospective case series of CO infections caused by CPE in a tertiary hospital from January 2010 to July 2014. Any clinical sample with a positive culture for CPE that had been ordered by primary care doctors or by doctors at the emergency room (ER) were classified as CO. Epidemiological and microbiological features of CO cases were assessed as were clinical features of CO-BSIs. Results. Of 780 clinical samples with CPE, 180 were requested at the ER or by primary care doctors (22.9%), 150 of which were produced by Klebsiella pneumoniae (83.3%). The blaOXA-48 gene was detected in 149 isolates (82.8%) followed by the blaVIM gene, 29 (16.1%). Sixty-one patients (33.9%) had a prior history of CPE infection/colonization. Thirty-four of the 119 (28.6%) patients without prior history of CPE infection/colonization did not fulfill Friedman criteria for healthcare-associated infections (HAIs). Considering previous hospitalization of up to 12 months as a criterion for defining HAI, only 16 (13.4%) cases were identified as community-acquired infections. The most frequent positive sample was urine (133 of 180; 73.9%). Twenty-one (11.7%) patients had a BSI, 9 of them secondary to urinary tract infections (42.9%). Thirty-day crude mortality among patients with BSI was 23.8% (5 of 21). Conclusions. Community-onset infections caused by CPE are an important subgroup of all CPE infections. The urinary tract is the main source. Bloodstream infections accounted for more than 10% of the cases.

Keywords: bloodstream infections; carbapenemase-producing Enterobacteriaceae; community-onset infections; epidemiology.

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Figures

Figure 1.
Figure 1.
Flow chart of patients included in the study and distribution of factors associated with healthcare among them. Abbreviations: BSI, bloodstream infection; CPE, Carbapenemase-producing Enterobacteriaceae; HCA, healthcare-associated; HULP, hospital universitario La Paz; LTCF, long-term care facility.
Figure 2.
Figure 2.
Cumulative distribution of isolates of K. pneumoniae OXA-48 belonging to ST405 (black) and ST11 (grey) sequence types in samples from ER and PCP compared with hospital isolates (inset).

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