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Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients

BACKGROUND: The objective of this study was to determine the main risk factors of Pseudomonas aeruginosa mutation as well as the mechanisms of acquired resistance. METHODS: We conducted a 2-year prospective study in patients who were carriers of a Pseudomonas aeruginosa strain and who had been admit...

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Autores principales: Druge, Stéphanie, Ruiz, Stéphanie, Vardon-Bounes, Fanny, Grare, Marion, Labaste, François, Seguin, Thierry, Fourcade, Olivier, Minville, Vincent, Conil, Jean-Marie, Georges, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639906/
https://www.ncbi.nlm.nih.gov/pubmed/31360523
http://dx.doi.org/10.1186/s40560-019-0390-4
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author Druge, Stéphanie
Ruiz, Stéphanie
Vardon-Bounes, Fanny
Grare, Marion
Labaste, François
Seguin, Thierry
Fourcade, Olivier
Minville, Vincent
Conil, Jean-Marie
Georges, Bernard
author_facet Druge, Stéphanie
Ruiz, Stéphanie
Vardon-Bounes, Fanny
Grare, Marion
Labaste, François
Seguin, Thierry
Fourcade, Olivier
Minville, Vincent
Conil, Jean-Marie
Georges, Bernard
author_sort Druge, Stéphanie
collection PubMed
description BACKGROUND: The objective of this study was to determine the main risk factors of Pseudomonas aeruginosa mutation as well as the mechanisms of acquired resistance. METHODS: We conducted a 2-year prospective study in patients who were carriers of a Pseudomonas aeruginosa strain and who had been admitted to a medical/surgical ICU. RESULTS: Of the 153 patients who were included, 34 had a mutation in their strain. In a multivariate analysis, a duration of ventilation > 24 days was a risk factor for mutation (risk ratio 4.29; CI 95% 1.94–9.49) while initial resistance was a protective factor (RR 0.36; CI 95% 0.18–0.71). In a univariate analysis, exposure of P. aeruginosa to ceftazidime was associated with an over-production of AmpC cephalosporinase and exposure to meropenem was associated with impermeability. A segmentation method based on the duration of ventilation (> 24 days), initial resistance, and exposure of strains to ceftazidime made it possible to predict at 83% the occurrence of mutation. CONCLUSION: The duration of ventilation and the presence of resistance as soon as P. aeruginosa is identified are predictive factors of mutation in ICU patients.
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spelling pubmed-66399062019-07-29 Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients Druge, Stéphanie Ruiz, Stéphanie Vardon-Bounes, Fanny Grare, Marion Labaste, François Seguin, Thierry Fourcade, Olivier Minville, Vincent Conil, Jean-Marie Georges, Bernard J Intensive Care Research BACKGROUND: The objective of this study was to determine the main risk factors of Pseudomonas aeruginosa mutation as well as the mechanisms of acquired resistance. METHODS: We conducted a 2-year prospective study in patients who were carriers of a Pseudomonas aeruginosa strain and who had been admitted to a medical/surgical ICU. RESULTS: Of the 153 patients who were included, 34 had a mutation in their strain. In a multivariate analysis, a duration of ventilation > 24 days was a risk factor for mutation (risk ratio 4.29; CI 95% 1.94–9.49) while initial resistance was a protective factor (RR 0.36; CI 95% 0.18–0.71). In a univariate analysis, exposure of P. aeruginosa to ceftazidime was associated with an over-production of AmpC cephalosporinase and exposure to meropenem was associated with impermeability. A segmentation method based on the duration of ventilation (> 24 days), initial resistance, and exposure of strains to ceftazidime made it possible to predict at 83% the occurrence of mutation. CONCLUSION: The duration of ventilation and the presence of resistance as soon as P. aeruginosa is identified are predictive factors of mutation in ICU patients. BioMed Central 2019-07-19 /pmc/articles/PMC6639906/ /pubmed/31360523 http://dx.doi.org/10.1186/s40560-019-0390-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Druge, Stéphanie
Ruiz, Stéphanie
Vardon-Bounes, Fanny
Grare, Marion
Labaste, François
Seguin, Thierry
Fourcade, Olivier
Minville, Vincent
Conil, Jean-Marie
Georges, Bernard
Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients
title Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients
title_full Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients
title_fullStr Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients
title_full_unstemmed Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients
title_short Risk factors and the resistance mechanisms involved in Pseudomonas aeruginosa mutation in critically ill patients
title_sort risk factors and the resistance mechanisms involved in pseudomonas aeruginosa mutation in critically ill patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639906/
https://www.ncbi.nlm.nih.gov/pubmed/31360523
http://dx.doi.org/10.1186/s40560-019-0390-4
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