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Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants

INTRODUCTION: The role of CD64 in late onset sepsis (LOS) in preterm infants has been described in several studies. Aim of this study was to investigate whether CD64 expression is increased in the days before clinical manifestation of LOS. METHODS: Patients with birth weight below 1,500g were eligib...

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Autores principales: Kipfmueller, Florian, Schneider, Jessica, Prusseit, Julia, Dimitriou, Ioanna, Zur, Berndt, Franz, Axel R., Bartmann, Peter, Mueller, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404048/
https://www.ncbi.nlm.nih.gov/pubmed/25894336
http://dx.doi.org/10.1371/journal.pone.0124634
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author Kipfmueller, Florian
Schneider, Jessica
Prusseit, Julia
Dimitriou, Ioanna
Zur, Berndt
Franz, Axel R.
Bartmann, Peter
Mueller, Andreas
author_facet Kipfmueller, Florian
Schneider, Jessica
Prusseit, Julia
Dimitriou, Ioanna
Zur, Berndt
Franz, Axel R.
Bartmann, Peter
Mueller, Andreas
author_sort Kipfmueller, Florian
collection PubMed
description INTRODUCTION: The role of CD64 in late onset sepsis (LOS) in preterm infants has been described in several studies. Aim of this study was to investigate whether CD64 expression is increased in the days before clinical manifestation of LOS. METHODS: Patients with birth weight below 1,500g were eligible for study participation. During routine blood sampling CD64 index was determined between day of life 4 and 28. Patients were allocated to one of four groups: (1) blood-culture positive sepsis, (2) clinical sepsis, (3) symptoms of infection without biochemical evidence of infection, or (4) patients without suspected infection. Kinetics of CD64 expression were compared during a period before and after the day of infection in the respective groups. RESULTS: 50 infants were prospectively enrolled and allocated to each group as follows: group (1) n = 7; group (2) n = 10; group (3) n = 8; and group (4) n = 25. CD64 index was elevated in 57% of patients in group (1) at least two days before infection. In contrast only 20% in the clinical sepsis group and 0% in group (3) had an elevated CD64 index in the days before infection. 10 of the 25 patients in the control group (4) presented increased CD64 index values during the study period. CONCLUSIONS: The CD64 index might be a promising marker to detect LOS before infants demonstrate signs or symptoms of infection. However, larger prospective studies are needed to define optimal cut-off values and to investigate the role of non-infectious inflammation in this patient group.
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spelling pubmed-44040482015-05-02 Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants Kipfmueller, Florian Schneider, Jessica Prusseit, Julia Dimitriou, Ioanna Zur, Berndt Franz, Axel R. Bartmann, Peter Mueller, Andreas PLoS One Research Article INTRODUCTION: The role of CD64 in late onset sepsis (LOS) in preterm infants has been described in several studies. Aim of this study was to investigate whether CD64 expression is increased in the days before clinical manifestation of LOS. METHODS: Patients with birth weight below 1,500g were eligible for study participation. During routine blood sampling CD64 index was determined between day of life 4 and 28. Patients were allocated to one of four groups: (1) blood-culture positive sepsis, (2) clinical sepsis, (3) symptoms of infection without biochemical evidence of infection, or (4) patients without suspected infection. Kinetics of CD64 expression were compared during a period before and after the day of infection in the respective groups. RESULTS: 50 infants were prospectively enrolled and allocated to each group as follows: group (1) n = 7; group (2) n = 10; group (3) n = 8; and group (4) n = 25. CD64 index was elevated in 57% of patients in group (1) at least two days before infection. In contrast only 20% in the clinical sepsis group and 0% in group (3) had an elevated CD64 index in the days before infection. 10 of the 25 patients in the control group (4) presented increased CD64 index values during the study period. CONCLUSIONS: The CD64 index might be a promising marker to detect LOS before infants demonstrate signs or symptoms of infection. However, larger prospective studies are needed to define optimal cut-off values and to investigate the role of non-infectious inflammation in this patient group. Public Library of Science 2015-04-20 /pmc/articles/PMC4404048/ /pubmed/25894336 http://dx.doi.org/10.1371/journal.pone.0124634 Text en © 2015 Kipfmueller et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kipfmueller, Florian
Schneider, Jessica
Prusseit, Julia
Dimitriou, Ioanna
Zur, Berndt
Franz, Axel R.
Bartmann, Peter
Mueller, Andreas
Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants
title Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants
title_full Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants
title_fullStr Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants
title_full_unstemmed Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants
title_short Role of Neutrophil CD64 Index as a Screening Marker for Late-Onset Sepsis in Very Low Birth Weight Infants
title_sort role of neutrophil cd64 index as a screening marker for late-onset sepsis in very low birth weight infants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404048/
https://www.ncbi.nlm.nih.gov/pubmed/25894336
http://dx.doi.org/10.1371/journal.pone.0124634
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