Characterization and Clinical Impact of Bloodstream Infection Caused by Carbapenemase-Producing Enterobacteriaceae in Seven Latin American Countries

Infections caused by carbapenem-resistant Enterobacteriaceae are a public health problem associated with higher mortality rates, longer hospitalization and increased healthcare costs. We carried out a study to describe the characteristics of patients with carbapenemase-producing Enterobacteriaceae (...

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Published inPloS one Vol. 11; no. 4; p. e0154092
Main Authors Villegas, Maria Virginia, Pallares, Christian J., Escandón-Vargas, Kevin, Hernández-Gómez, Cristhian, Correa, Adriana, Álvarez, Carlos, Rosso, Fernando, Matta, Lorena, Luna, Carlos, Zurita, Jeannete, Mejía-Villatoro, Carlos, Rodríguez-Noriega, Eduardo, Seas, Carlos, Cortesía, Manuel, Guzmán-Suárez, Alfonso, Guzmán-Blanco, Manuel
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 22.04.2016
Public Library of Science (PLoS)
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Summary:Infections caused by carbapenem-resistant Enterobacteriaceae are a public health problem associated with higher mortality rates, longer hospitalization and increased healthcare costs. We carried out a study to describe the characteristics of patients with carbapenemase-producing Enterobacteriaceae (CPE) and non-CPE bloodstream infection (BSI) from Latin American hospitals and to determine the clinical impact in terms of mortality and antibiotic therapy. Between July 2013 and November 2014, we conducted a multicenter observational study in 11 hospitals from 7 Latin American countries (Argentina, Colombia, Ecuador, Guatemala, Mexico, Peru, Venezuela). Patients with BSI caused by Enterobacteriaceae were included and classified either as CPE or non-CPE based on detection of blaKPC, blaVIM, blaIMP, blaNDM and blaOXA-48 by polymerase chain reaction. Enrolled subjects were followed until discharge or death. Demographic, microbiological and clinical characteristics were collected from medical records. Both descriptive and inferential statistics were used to analyze the information. A total of 255 patients with Enterobacteriaceae BSI were included; CPE were identified in 53 of them. In vitro non-susceptibility to all screened antibiotics was higher in the patients with CPE BSI, remaining colistin, tigecycline and amikacin as the most active drugs. Combination therapy was significantly more frequent in the CPE BSI group (p < 0.001). The most common regimen was carbapenem + colistin or polymyxin B. The overall mortality was 37% (94/255). Overall and attributable mortality were significantly higher in patients with CPE BSI (p < 0.001); however, we found that patients with CPE BSI who received combination therapy and those who received monotherapy had similar mortality. After multivariate adjustment, CPE BSI (adjusted odds ratio [aOR] 4; 95% confidence interval [CI] 1.7-9.5; p = 0.002) and critical illness (aOR 6.5; 95% CI 3.1-13.7; p < 0.001) were independently associated with in-hospital mortality. This study provides valuable data on the clinical characteristics and mortality risk factors in patients with CPE BSI. We determined that CPE infection is an independent mortality predictor and thus Latin American hospitals should perform campaigns on prevention and control of CPE BSI.
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Competing Interests: MVV has received consulting honorarium and/or research grant support from Merck, Janssen-Cilag, Pfizer, MSD, AstraZeneca, Zambon and Abbott. CJP has been consultant for Merck, MSD, Pfizer, Novartis, AstraZeneca and Amarey. CHG has been consultant for MSD and Merck. CA has received consulting honorarium and/or research grant support from MSD, Pfizer, GlaxoSmithKline, AstraZeneca and Janssen-Cilag. MGB has participated in advisory boards of Pfizer, MSD and BD. All other authors reported no competing interests relevant to this article. This statement does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials.
Conceived and designed the experiments: MVV CJP KEV CHG AC. Performed the experiments: CA FR LM CL JZ CMV ERN CS MC AGS MGB. Analyzed the data: CJP KEV. Wrote the paper: CJP KEV. Discussed the results and commented on the manuscript: MVV CJP KEV CHG AC CA FR LM CL JZ CMV ERN CS MC AGS MGB.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0154092