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Update on ventilator-associated pneumonia

Ventilator-associated pneumonia (VAP) is the most frequent life-threatening nosocomial infection in intensive care units. The diagnostic is difficult because radiological and clinical signs are inaccurate and could be associated with various respiratory diseases. The concept of infection-related ven...

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Autores principales: Timsit, Jean-Francois, Esaied, Wafa, Neuville, Mathilde, Bouadma, Lila, Mourvillier, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710313/
https://www.ncbi.nlm.nih.gov/pubmed/29225790
http://dx.doi.org/10.12688/f1000research.12222.1
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author Timsit, Jean-Francois
Esaied, Wafa
Neuville, Mathilde
Bouadma, Lila
Mourvillier, Bruno
author_facet Timsit, Jean-Francois
Esaied, Wafa
Neuville, Mathilde
Bouadma, Lila
Mourvillier, Bruno
author_sort Timsit, Jean-Francois
collection PubMed
description Ventilator-associated pneumonia (VAP) is the most frequent life-threatening nosocomial infection in intensive care units. The diagnostic is difficult because radiological and clinical signs are inaccurate and could be associated with various respiratory diseases. The concept of infection-related ventilator-associated complication has been proposed as a surrogate of VAP to be used as a benchmark indicator of quality of care. Indeed, bundles of prevention measures are effective in decreasing the VAP rate. In case of VAP suspicion, respiratory secretions must be collected for bacteriological secretions before any new antimicrobials. Quantitative distal bacteriological exams may be preferable for a more reliable diagnosis and therefore a more appropriate use antimicrobials. To improve the prognosis, the treatment should be adequate as soon as possible but should avoid unnecessary broad-spectrum antimicrobials to limit antibiotic selection pressure. For empiric treatments, the selection of antimicrobials should consider the local prevalence of microorganisms along with their associated susceptibility profiles. Critically ill patients require high dosages of antimicrobials and more specifically continuous or prolonged infusions for beta-lactams. After patient stabilization, antimicrobials should be maintained for 7–8 days. The evaluation of VAP treatment based on 28-day mortality is being challenged by regulatory agencies, which are working on alternative surrogate endpoints and on trial design optimization.
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spelling pubmed-57103132017-12-07 Update on ventilator-associated pneumonia Timsit, Jean-Francois Esaied, Wafa Neuville, Mathilde Bouadma, Lila Mourvillier, Bruno F1000Res Review Ventilator-associated pneumonia (VAP) is the most frequent life-threatening nosocomial infection in intensive care units. The diagnostic is difficult because radiological and clinical signs are inaccurate and could be associated with various respiratory diseases. The concept of infection-related ventilator-associated complication has been proposed as a surrogate of VAP to be used as a benchmark indicator of quality of care. Indeed, bundles of prevention measures are effective in decreasing the VAP rate. In case of VAP suspicion, respiratory secretions must be collected for bacteriological secretions before any new antimicrobials. Quantitative distal bacteriological exams may be preferable for a more reliable diagnosis and therefore a more appropriate use antimicrobials. To improve the prognosis, the treatment should be adequate as soon as possible but should avoid unnecessary broad-spectrum antimicrobials to limit antibiotic selection pressure. For empiric treatments, the selection of antimicrobials should consider the local prevalence of microorganisms along with their associated susceptibility profiles. Critically ill patients require high dosages of antimicrobials and more specifically continuous or prolonged infusions for beta-lactams. After patient stabilization, antimicrobials should be maintained for 7–8 days. The evaluation of VAP treatment based on 28-day mortality is being challenged by regulatory agencies, which are working on alternative surrogate endpoints and on trial design optimization. F1000 Research Limited 2017-11-29 /pmc/articles/PMC5710313/ /pubmed/29225790 http://dx.doi.org/10.12688/f1000research.12222.1 Text en Copyright: © 2017 Timsit JF et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Timsit, Jean-Francois
Esaied, Wafa
Neuville, Mathilde
Bouadma, Lila
Mourvillier, Bruno
Update on ventilator-associated pneumonia
title Update on ventilator-associated pneumonia
title_full Update on ventilator-associated pneumonia
title_fullStr Update on ventilator-associated pneumonia
title_full_unstemmed Update on ventilator-associated pneumonia
title_short Update on ventilator-associated pneumonia
title_sort update on ventilator-associated pneumonia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710313/
https://www.ncbi.nlm.nih.gov/pubmed/29225790
http://dx.doi.org/10.12688/f1000research.12222.1
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