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Oropharyngeal decontamination in intensive care patients: less is not more
Ventilator-associated pneumonia (VAP) is a common cause of morbidity, antibiotic use, increased length of stay and, possibly, increased mortality in ICU patients. Colonization of the oropharyngeal cavity with potentially pathogenic micro-organisms is instrumental in the pathogenesis of VAP, and sele...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784342/ https://www.ncbi.nlm.nih.gov/pubmed/19735585 http://dx.doi.org/10.1186/cc8013 |
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author | Derde, Lennie PG Bonten, Marc JM |
author_facet | Derde, Lennie PG Bonten, Marc JM |
author_sort | Derde, Lennie PG |
collection | PubMed |
description | Ventilator-associated pneumonia (VAP) is a common cause of morbidity, antibiotic use, increased length of stay and, possibly, increased mortality in ICU patients. Colonization of the oropharyngeal cavity with potentially pathogenic micro-organisms is instrumental in the pathogenesis of VAP, and selective oropharyngeal decontamination (SOD) with antibiotics (AB-SOD) or antiseptics, such as chlorhexidine gluconate (CHX-SOD), has been associated with reduced incidences of VAP. In a recent issue of Critical Care Scannapieco and colleagues investigated differences in oropharyngeal colonization between mechanically ventilated patients receiving oropharyngeal decontamination with 0.12% CHX-SOD either once or twice daily compared to placebo. CHX-SOD was associated with a reduction in Staphylococcus aureus colonization, but the study was underpowered to demonstrate a reduction in VAP incidence. We urgently need well-designed and adequately powered studies to evaluate the potential benefits of CHX-SOD on patient outcome in ICUs. |
format | Text |
id | pubmed-2784342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27843422010-09-03 Oropharyngeal decontamination in intensive care patients: less is not more Derde, Lennie PG Bonten, Marc JM Crit Care Commentary Ventilator-associated pneumonia (VAP) is a common cause of morbidity, antibiotic use, increased length of stay and, possibly, increased mortality in ICU patients. Colonization of the oropharyngeal cavity with potentially pathogenic micro-organisms is instrumental in the pathogenesis of VAP, and selective oropharyngeal decontamination (SOD) with antibiotics (AB-SOD) or antiseptics, such as chlorhexidine gluconate (CHX-SOD), has been associated with reduced incidences of VAP. In a recent issue of Critical Care Scannapieco and colleagues investigated differences in oropharyngeal colonization between mechanically ventilated patients receiving oropharyngeal decontamination with 0.12% CHX-SOD either once or twice daily compared to placebo. CHX-SOD was associated with a reduction in Staphylococcus aureus colonization, but the study was underpowered to demonstrate a reduction in VAP incidence. We urgently need well-designed and adequately powered studies to evaluate the potential benefits of CHX-SOD on patient outcome in ICUs. BioMed Central 2009 2009-09-03 /pmc/articles/PMC2784342/ /pubmed/19735585 http://dx.doi.org/10.1186/cc8013 Text en Copyright ©2009 BioMed Central Ltd |
spellingShingle | Commentary Derde, Lennie PG Bonten, Marc JM Oropharyngeal decontamination in intensive care patients: less is not more |
title | Oropharyngeal decontamination in intensive care patients: less is not more |
title_full | Oropharyngeal decontamination in intensive care patients: less is not more |
title_fullStr | Oropharyngeal decontamination in intensive care patients: less is not more |
title_full_unstemmed | Oropharyngeal decontamination in intensive care patients: less is not more |
title_short | Oropharyngeal decontamination in intensive care patients: less is not more |
title_sort | oropharyngeal decontamination in intensive care patients: less is not more |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784342/ https://www.ncbi.nlm.nih.gov/pubmed/19735585 http://dx.doi.org/10.1186/cc8013 |
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