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Reactive oxygen species measure for rapid detection of infection in fluids

BACKGROUND: Early detection of infection is critical to rapidly starting effective treatment. Diagnosis can be difficult, particularly in the intensive care unit (ICU) population. Because the presence of polymorphonuclear neutrophils in tissues is the hallmark of inflammatory processes, the objectiv...

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Autores principales: Bardon, Jean, Lukaszewicz, Anne-Claire, Faivre, Valérie, Huot, Benjamin, Payen, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Paris 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851674/
https://www.ncbi.nlm.nih.gov/pubmed/27130425
http://dx.doi.org/10.1186/s13613-016-0142-8
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author Bardon, Jean
Lukaszewicz, Anne-Claire
Faivre, Valérie
Huot, Benjamin
Payen, Didier
author_facet Bardon, Jean
Lukaszewicz, Anne-Claire
Faivre, Valérie
Huot, Benjamin
Payen, Didier
author_sort Bardon, Jean
collection PubMed
description BACKGROUND: Early detection of infection is critical to rapidly starting effective treatment. Diagnosis can be difficult, particularly in the intensive care unit (ICU) population. Because the presence of polymorphonuclear neutrophils in tissues is the hallmark of inflammatory processes, the objective of this proof of concept study was to determine whether the measurement of reactive oxygen species (ROS) could be an efficient diagnostic tool to rapidly diagnose infections in peritoneal, pleural and bronchoalveolar lavage (BAL) fluids in ICU patients. METHODS: We prospectively included all patients hospitalized in the 21-bed surgical ICU of a teaching hospital from June 2010 to February 2014 who presented with systemic inflammatory response syndrome with suspicion of a peritoneal or pleural fluid or pulmonary infection needing a BAL. Instantaneous basal ROS production was measured in fluids and after phorbol 12-myristate 13-acetate (PMA) stimulation. We compared patients with infected fluids to those with non-infected fluids. RESULTS: The overall ICU mortality rate was 34 %. A majority of patients were sampled following a delay of 5 days (2–12) after ICU admission, with most receiving antibiotics at the time of fluid sampling (71 %). Fluids were infected in 21/65 samples: 6/17 peritoneal fluids, 8/28 pleural fluids and 7/20 BALs. ROS production was significantly higher in the infected than in the non-infected group at baseline and after PMA stimulation in the peritoneal and pleural fluids but not in BAL. CONCLUSION: Assessing instantaneous ROS production appears as a fast and reliable diagnostic method for detecting peritoneal and pleural fluid infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-016-0142-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-48516742016-05-17 Reactive oxygen species measure for rapid detection of infection in fluids Bardon, Jean Lukaszewicz, Anne-Claire Faivre, Valérie Huot, Benjamin Payen, Didier Ann Intensive Care Research BACKGROUND: Early detection of infection is critical to rapidly starting effective treatment. Diagnosis can be difficult, particularly in the intensive care unit (ICU) population. Because the presence of polymorphonuclear neutrophils in tissues is the hallmark of inflammatory processes, the objective of this proof of concept study was to determine whether the measurement of reactive oxygen species (ROS) could be an efficient diagnostic tool to rapidly diagnose infections in peritoneal, pleural and bronchoalveolar lavage (BAL) fluids in ICU patients. METHODS: We prospectively included all patients hospitalized in the 21-bed surgical ICU of a teaching hospital from June 2010 to February 2014 who presented with systemic inflammatory response syndrome with suspicion of a peritoneal or pleural fluid or pulmonary infection needing a BAL. Instantaneous basal ROS production was measured in fluids and after phorbol 12-myristate 13-acetate (PMA) stimulation. We compared patients with infected fluids to those with non-infected fluids. RESULTS: The overall ICU mortality rate was 34 %. A majority of patients were sampled following a delay of 5 days (2–12) after ICU admission, with most receiving antibiotics at the time of fluid sampling (71 %). Fluids were infected in 21/65 samples: 6/17 peritoneal fluids, 8/28 pleural fluids and 7/20 BALs. ROS production was significantly higher in the infected than in the non-infected group at baseline and after PMA stimulation in the peritoneal and pleural fluids but not in BAL. CONCLUSION: Assessing instantaneous ROS production appears as a fast and reliable diagnostic method for detecting peritoneal and pleural fluid infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-016-0142-8) contains supplementary material, which is available to authorized users. Springer Paris 2016-04-29 /pmc/articles/PMC4851674/ /pubmed/27130425 http://dx.doi.org/10.1186/s13613-016-0142-8 Text en © Bardon et al. 2016 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.
spellingShingle Research
Bardon, Jean
Lukaszewicz, Anne-Claire
Faivre, Valérie
Huot, Benjamin
Payen, Didier
Reactive oxygen species measure for rapid detection of infection in fluids
title Reactive oxygen species measure for rapid detection of infection in fluids
title_full Reactive oxygen species measure for rapid detection of infection in fluids
title_fullStr Reactive oxygen species measure for rapid detection of infection in fluids
title_full_unstemmed Reactive oxygen species measure for rapid detection of infection in fluids
title_short Reactive oxygen species measure for rapid detection of infection in fluids
title_sort reactive oxygen species measure for rapid detection of infection in fluids
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851674/
https://www.ncbi.nlm.nih.gov/pubmed/27130425
http://dx.doi.org/10.1186/s13613-016-0142-8
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