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Risk factors for microbiologic failure in children with Enterobacter species bacteremia
BACKGROUND: Enterobacter species are an important cause of healthcare-associated bloodstream infections (BSI) in children. Up to 19% of adult patients with Enterobacter BSI have recurrence of infection resistant to third-generation cephalosporins (3GCs) while on therapy with a 3GC. Data are lacking...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496803/ https://www.ncbi.nlm.nih.gov/pubmed/34618858 http://dx.doi.org/10.1371/journal.pone.0258114 |
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author | Boguniewicz, Juri Revell, Paula A. Scheurer, Michael E. Hulten, Kristina G. Palazzi, Debra L. |
author_facet | Boguniewicz, Juri Revell, Paula A. Scheurer, Michael E. Hulten, Kristina G. Palazzi, Debra L. |
author_sort | Boguniewicz, Juri |
collection | PubMed |
description | BACKGROUND: Enterobacter species are an important cause of healthcare-associated bloodstream infections (BSI) in children. Up to 19% of adult patients with Enterobacter BSI have recurrence of infection resistant to third-generation cephalosporins (3GCs) while on therapy with a 3GC. Data are lacking regarding the incidence of and risk factors for recurrence of infection in children with Enterobacter BSI. METHODS: We conducted a retrospective case-control study of patients aged ≤21 years old admitted to Texas Children’s Hospital from January 2012 through December 2018 with Enterobacter BSI. The primary outcome was microbiologic failure from 72 hours to 30 days after the initial BSI (cases). The secondary outcome was isolation of a 3GC non-susceptible Enterobacter sp. from a patient with an initial 3GC-susceptible isolate. RESULTS: Twelve patients (6.7%) had microbiologic failure compared to 167 controls without microbiologic failure. Of the 138 patients (77.1%) with an Enterobacter sp. isolate that was initially susceptible to 3GCs, 3 (2.2%) developed a subsequent infection with a non-susceptible isolate. Predictors of microbiologic failure were having an alternative primary site of infection besides bacteremia without a focus or an urinary tract infection (OR, 9.64; 95% CI, 1.77–52.31; P < 0.01) and inadequate source control (OR, 22.16; 95% CI, 5.26–93.36; P < 0.001). CONCLUSIONS: Source of infection and adequacy of source control are important considerations in preventing microbiologic failure. In-vitro susceptibilities can be used to select an antibiotic regimen for the treatment of Enterobacter BSI in children. |
format | Online Article Text |
id | pubmed-8496803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84968032021-10-08 Risk factors for microbiologic failure in children with Enterobacter species bacteremia Boguniewicz, Juri Revell, Paula A. Scheurer, Michael E. Hulten, Kristina G. Palazzi, Debra L. PLoS One Research Article BACKGROUND: Enterobacter species are an important cause of healthcare-associated bloodstream infections (BSI) in children. Up to 19% of adult patients with Enterobacter BSI have recurrence of infection resistant to third-generation cephalosporins (3GCs) while on therapy with a 3GC. Data are lacking regarding the incidence of and risk factors for recurrence of infection in children with Enterobacter BSI. METHODS: We conducted a retrospective case-control study of patients aged ≤21 years old admitted to Texas Children’s Hospital from January 2012 through December 2018 with Enterobacter BSI. The primary outcome was microbiologic failure from 72 hours to 30 days after the initial BSI (cases). The secondary outcome was isolation of a 3GC non-susceptible Enterobacter sp. from a patient with an initial 3GC-susceptible isolate. RESULTS: Twelve patients (6.7%) had microbiologic failure compared to 167 controls without microbiologic failure. Of the 138 patients (77.1%) with an Enterobacter sp. isolate that was initially susceptible to 3GCs, 3 (2.2%) developed a subsequent infection with a non-susceptible isolate. Predictors of microbiologic failure were having an alternative primary site of infection besides bacteremia without a focus or an urinary tract infection (OR, 9.64; 95% CI, 1.77–52.31; P < 0.01) and inadequate source control (OR, 22.16; 95% CI, 5.26–93.36; P < 0.001). CONCLUSIONS: Source of infection and adequacy of source control are important considerations in preventing microbiologic failure. In-vitro susceptibilities can be used to select an antibiotic regimen for the treatment of Enterobacter BSI in children. Public Library of Science 2021-10-07 /pmc/articles/PMC8496803/ /pubmed/34618858 http://dx.doi.org/10.1371/journal.pone.0258114 Text en © 2021 Boguniewicz et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Boguniewicz, Juri Revell, Paula A. Scheurer, Michael E. Hulten, Kristina G. Palazzi, Debra L. Risk factors for microbiologic failure in children with Enterobacter species bacteremia |
title | Risk factors for microbiologic failure in children with Enterobacter species bacteremia |
title_full | Risk factors for microbiologic failure in children with Enterobacter species bacteremia |
title_fullStr | Risk factors for microbiologic failure in children with Enterobacter species bacteremia |
title_full_unstemmed | Risk factors for microbiologic failure in children with Enterobacter species bacteremia |
title_short | Risk factors for microbiologic failure in children with Enterobacter species bacteremia |
title_sort | risk factors for microbiologic failure in children with enterobacter species bacteremia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496803/ https://www.ncbi.nlm.nih.gov/pubmed/34618858 http://dx.doi.org/10.1371/journal.pone.0258114 |
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