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      New automated analysis to monitor neutrophil function point-of-care in the intensive care unit after trauma

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          Abstract

          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.

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          Most cited references36

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          In vivo labeling with 2H2O reveals a human neutrophil lifespan of 5.4 days.

          Neutrophils are essential effector cells of the innate immune response and are indispensable for host defense. Apart from their antimicrobial functions, neutrophils inform and shape subsequent immunity. This immune modulatory functionality might however be considered limited because of their generally accepted short lifespan (< 1 day). In contrast to the previously reported short lifespans acquired by ex vivo labeling or manipulation, we show that in vivo labeling in humans with the use of (2)H(2)O under homeostatic conditions showed an average circulatory neutrophil lifespan of 5.4 days. This lifespan is at least 10 times longer than previously reported and might lead to reappraisal of novel neutrophil functions in health and disease.
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            Epidemiology and risk factors of sepsis after multiple trauma: an analysis of 29,829 patients from the Trauma Registry of the German Society for Trauma Surgery.

            The objectives of this study were 1) to assess potential changes in the incidence and outcome of sepsis after multiple trauma in Germany between 1993 and 2008 and 2) to evaluate independent risk factors for posttraumatic sepsis.
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              Neutrophil CD64 expression as marker of bacterial infection: a systematic review and meta-analysis.

              We performed a systematic review and meta-analysis of studies to evaluate the diagnostic accuracy of expression of CD64 on polymorphonuclear neutrophils (PMN) as a marker for bacterial infection. The analysis included studies of patients from all age groups that prospectively evaluated CD64 expression on PMNs for the diagnosis of bacterial infection. We evaluated the methodological quality of the studies according to the 25-item criteria developed by the Standards for Reporting of Diagnostic Accuracy (STARD) committee. We calculated a summary receiver operating characteristic (SROC) curve across studies included in the meta-analysis. The methodological quality score of the 13 included studies ranged from 9 to 16 points (maximum score was 25 points). The pooled sensitivity and specificity for CD64 expression on PMNs were 79% (95% CI: 70-86%) and 91% (95% CI: 85-95%), respectively. The area under curve (AUC) was 0.94. On the basis of this meta-analysis, CD64 expression on PMNs could be a useful diagnostic cell-based parameter of bacterial infections. However, published studies about this topic showed a low methodological quality. 2010 The British Infection Society. Published by Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                lilianhesselink@gmail.com
                Journal
                Intensive Care Med Exp
                Intensive Care Med Exp
                Intensive Care Medicine Experimental
                Springer International Publishing (Cham )
                2197-425X
                14 March 2020
                14 March 2020
                December 2020
                : 8
                : 12
                Affiliations
                [1 ]GRID grid.7692.a, ISNI 0000000090126352, Department of Trauma Surgery, , University Medical Center Utrecht, ; Heidelberglaan 100, 3584 CX Utrecht, the Netherlands
                [2 ]GRID grid.417100.3, ISNI 0000 0004 0620 3132, Department of Respiratory Medicine, , Wilhelmina Children’s Hospital, ; Lundlaan 6, 3584 EA Utrecht, the Netherlands
                [3 ]GRID grid.7692.a, ISNI 0000000090126352, Center for Translational Immunology, , University Medical Center Utrecht, ; Heidelberglaan 100, 3584 CX Utrecht, the Netherlands
                [4 ]GRID grid.7692.a, ISNI 0000000090126352, Department of Trauma Surgery, , University Medical Center Utrecht, ; Heidelberglaan 100, 3584 CX Utrecht, the Netherlands
                Author information
                http://orcid.org/0000-0001-8793-6650
                Article
                299
                10.1186/s40635-020-0299-1
                7072076
                32172430
                1b3c15ab-cf60-4238-be19-011b1e09b759
                © 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/.

                History
                : 29 November 2019
                : 26 February 2020
                Categories
                Research
                Custom metadata
                © The Author(s) 2020

                intensive care,trauma,infections,neutrophils,point-of-care,bedside,monitoring

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