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Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features
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 feature...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047395/ https://www.ncbi.nlm.nih.gov/pubmed/27703997 http://dx.doi.org/10.1093/ofid/ofw136 |
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author | Paño-Pardo, José Ramón López Quintana, Beatriz Lázaro Perona, Fernando Ruiz Carrascoso, Guillermo Romero-Gómez, María Pilar Loeches Yagüe, Belén Díaz-Pollán, Beatriz Martínez-Virto, Ana Mingorance, Jesús García Rodríguez, Julio Arribas, José Ramón Gómez-Gil, Rosa |
author_facet | Paño-Pardo, José Ramón López Quintana, Beatriz Lázaro Perona, Fernando Ruiz Carrascoso, Guillermo Romero-Gómez, María Pilar Loeches Yagüe, Belén Díaz-Pollán, Beatriz Martínez-Virto, Ana Mingorance, Jesús García Rodríguez, Julio Arribas, José Ramón Gómez-Gil, Rosa |
author_sort | Paño-Pardo, José Ramón |
collection | PubMed |
description | 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 bla(OXA−48) gene was detected in 149 isolates (82.8%) followed by the bla(VIM) 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. |
format | Online Article Text |
id | pubmed-5047395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50473952016-10-04 Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features Paño-Pardo, José Ramón López Quintana, Beatriz Lázaro Perona, Fernando Ruiz Carrascoso, Guillermo Romero-Gómez, María Pilar Loeches Yagüe, Belén Díaz-Pollán, Beatriz Martínez-Virto, Ana Mingorance, Jesús García Rodríguez, Julio Arribas, José Ramón Gómez-Gil, Rosa Open Forum Infect Dis Major Articles 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 bla(OXA−48) gene was detected in 149 isolates (82.8%) followed by the bla(VIM) 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. Oxford University Press 2016-08-01 /pmc/articles/PMC5047395/ /pubmed/27703997 http://dx.doi.org/10.1093/ofid/ofw136 Text en © The Author 2016. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com. |
spellingShingle | Major Articles Paño-Pardo, José Ramón López Quintana, Beatriz Lázaro Perona, Fernando Ruiz Carrascoso, Guillermo Romero-Gómez, María Pilar Loeches Yagüe, Belén Díaz-Pollán, Beatriz Martínez-Virto, Ana Mingorance, Jesús García Rodríguez, Julio Arribas, José Ramón Gómez-Gil, Rosa Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features |
title | Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features |
title_full | Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features |
title_fullStr | Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features |
title_full_unstemmed | Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features |
title_short | Community-Onset Bloodstream and Other Infections, Caused by Carbapenemase-Producing Enterobacteriaceae: Epidemiological, Microbiological, and Clinical Features |
title_sort | community-onset bloodstream and other infections, caused by carbapenemase-producing enterobacteriaceae: epidemiological, microbiological, and clinical features |
topic | Major Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047395/ https://www.ncbi.nlm.nih.gov/pubmed/27703997 http://dx.doi.org/10.1093/ofid/ofw136 |
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