Cargando…

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...

Descripción completa

Detalles Bibliográficos
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
Descripción
Sumario: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.