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New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma
BACKGROUND: Patients often develop infectious complications after severe trauma. No biomarkers exist that enable early identification of patients who are at risk. Neutrophils are important immune cells that combat these infections by phagocytosis and killing of pathogens. Analysis of neutrophil func...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072076/ https://www.ncbi.nlm.nih.gov/pubmed/32172430 http://dx.doi.org/10.1186/s40635-020-0299-1 |
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author | Hesselink, Lillian Spijkerman, Roy de Fraiture, Emma Bongers, Suzanne Van Wessem, Karlijn J. P. Vrisekoop, Nienke Koenderman, Leo Leenen, Luke P. H. Hietbrink, Falco |
author_facet | Hesselink, Lillian Spijkerman, Roy de Fraiture, Emma Bongers, Suzanne Van Wessem, Karlijn J. P. Vrisekoop, Nienke Koenderman, Leo Leenen, Luke P. H. Hietbrink, Falco |
author_sort | Hesselink, Lillian |
collection | PubMed |
description | BACKGROUND: Patients often develop infectious complications after severe trauma. No biomarkers exist that enable early identification of patients who are at risk. Neutrophils are important immune cells that combat these infections by phagocytosis and killing of pathogens. Analysis of neutrophil function used to be laborious and was therefore not applicable in routine diagnostics. Hence, we developed a quick and point-of-care method to assess a critical part of neutrophil function, neutrophil phagosomal acidification. The aim of this study was to investigate whether this method was able to analyze neutrophil functionality in severely injured patients and whether a relation with the development of infectious complications was present. RESULTS: Fifteen severely injured patients (median ISS of 33) were included, of whom 6 developed an infection between day 4 and day 9 after trauma. The injury severity score did not significantly differ between patients who developed an infection and patients who did not (p = 0.529). Patients who developed an infection showed increased acidification immediately after trauma (p = 0.006) and after 3 days (p = 0.026) and a decrease in the days thereafter to levels in the lower normal range. In contrast, patients who did not develop infectious complications showed high-normal acidification within the first days and increased tasset to identify patients at risk for infections after trauma and to monitor the inflammatory state of these trauma patients. CONCLUSION: Neutrophil function can be measured in the ICU setting by rapid point-of-care analysis of phagosomal acidification. This analysis differed between trauma patients who developed infectious complications and trauma patients who did not. Therefore, this assay might prove a valuable asset to identify patients at risk for infections after trauma and to monitor the inflammatory state of these trauma patients. TRIAL REGISTRATION: Central Committee on Research Involving Human Subjects, NL43279.041.13. Registered 14 February 2014. https://www.toetsingonline.nl/to/ccmo_search.nsf/Searchform?OpenForm. |
format | Online Article Text |
id | pubmed-7072076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-70720762020-03-23 New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma Hesselink, Lillian Spijkerman, Roy de Fraiture, Emma Bongers, Suzanne Van Wessem, Karlijn J. P. Vrisekoop, Nienke Koenderman, Leo Leenen, Luke P. H. Hietbrink, Falco Intensive Care Med Exp Research BACKGROUND: Patients often develop infectious complications after severe trauma. No biomarkers exist that enable early identification of patients who are at risk. Neutrophils are important immune cells that combat these infections by phagocytosis and killing of pathogens. Analysis of neutrophil function used to be laborious and was therefore not applicable in routine diagnostics. Hence, we developed a quick and point-of-care method to assess a critical part of neutrophil function, neutrophil phagosomal acidification. The aim of this study was to investigate whether this method was able to analyze neutrophil functionality in severely injured patients and whether a relation with the development of infectious complications was present. RESULTS: Fifteen severely injured patients (median ISS of 33) were included, of whom 6 developed an infection between day 4 and day 9 after trauma. The injury severity score did not significantly differ between patients who developed an infection and patients who did not (p = 0.529). Patients who developed an infection showed increased acidification immediately after trauma (p = 0.006) and after 3 days (p = 0.026) and a decrease in the days thereafter to levels in the lower normal range. In contrast, patients who did not develop infectious complications showed high-normal acidification within the first days and increased tasset to identify patients at risk for infections after trauma and to monitor the inflammatory state of these trauma patients. CONCLUSION: Neutrophil function can be measured in the ICU setting by rapid point-of-care analysis of phagosomal acidification. This analysis differed between trauma patients who developed infectious complications and trauma patients who did not. Therefore, this assay might prove a valuable asset to identify patients at risk for infections after trauma and to monitor the inflammatory state of these trauma patients. TRIAL REGISTRATION: Central Committee on Research Involving Human Subjects, NL43279.041.13. Registered 14 February 2014. https://www.toetsingonline.nl/to/ccmo_search.nsf/Searchform?OpenForm. Springer International Publishing 2020-03-14 /pmc/articles/PMC7072076/ /pubmed/32172430 http://dx.doi.org/10.1186/s40635-020-0299-1 Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Hesselink, Lillian Spijkerman, Roy de Fraiture, Emma Bongers, Suzanne Van Wessem, Karlijn J. P. Vrisekoop, Nienke Koenderman, Leo Leenen, Luke P. H. Hietbrink, Falco New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
title | New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
title_full | New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
title_fullStr | New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
title_full_unstemmed | New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
title_short | New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
title_sort | new automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072076/ https://www.ncbi.nlm.nih.gov/pubmed/32172430 http://dx.doi.org/10.1186/s40635-020-0299-1 |
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