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Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis
The initial evaluation of a suspected sepsis in a neonate is always challenging. There are many methods to screen a neonate with suspected sepsis. One of newer method is to assess the changes in neutrophil volume conductivity and scatter. The objective of this study was to establish changes in Neutr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064568/ https://www.ncbi.nlm.nih.gov/pubmed/32157117 http://dx.doi.org/10.1038/s41598-020-61434-z |
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author | Nesargi, Prerana Niranjan, H. S. Bandiya, Prathik Benakappa, Naveen |
author_facet | Nesargi, Prerana Niranjan, H. S. Bandiya, Prathik Benakappa, Naveen |
author_sort | Nesargi, Prerana |
collection | PubMed |
description | The initial evaluation of a suspected sepsis in a neonate is always challenging. There are many methods to screen a neonate with suspected sepsis. One of newer method is to assess the changes in neutrophil volume conductivity and scatter. The objective of this study was to establish changes in Neutrophil volume conductivity scatter (VCS) in neonatal sepsis and to determine appropriate cut off levels using receiver operating characteristic (ROC) curves. Neonates with suspected sepsis were evaluated with blood counts, culture and neutrophil VCS parameters. Based on these parameters neonates were classified into sepsis group (Blood culture positive), Probable sepsis group (clinical course consistent with sepsis and positive sepsis screen and negative blood culture), No sepsis group (Clinical course not suggestive of sepsis with negative sepsis screen and blood culture). A total of 304 neonates were included in the study of which 144 were in sepsis group and 160 in no sepsis group respectively. Among the neutrophil VCS parameters there was significant difference between the groups with respect to mean neutrophil volume (MNV) and volume distribution width (VDW) (180 vs 163 vs 150) (p < 0.01). MNV and VDW had good sensitivity (95%, 82%) and specificity (86%, 74%) for diagnosis of sepsis. In conclusion, Neutrophil VCS parameters, especially MNV, can be incorporated with other sepsis screen parameters in diagnosis of neonatal sepsis. |
format | Online Article Text |
id | pubmed-7064568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70645682020-03-18 Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis Nesargi, Prerana Niranjan, H. S. Bandiya, Prathik Benakappa, Naveen Sci Rep Article The initial evaluation of a suspected sepsis in a neonate is always challenging. There are many methods to screen a neonate with suspected sepsis. One of newer method is to assess the changes in neutrophil volume conductivity and scatter. The objective of this study was to establish changes in Neutrophil volume conductivity scatter (VCS) in neonatal sepsis and to determine appropriate cut off levels using receiver operating characteristic (ROC) curves. Neonates with suspected sepsis were evaluated with blood counts, culture and neutrophil VCS parameters. Based on these parameters neonates were classified into sepsis group (Blood culture positive), Probable sepsis group (clinical course consistent with sepsis and positive sepsis screen and negative blood culture), No sepsis group (Clinical course not suggestive of sepsis with negative sepsis screen and blood culture). A total of 304 neonates were included in the study of which 144 were in sepsis group and 160 in no sepsis group respectively. Among the neutrophil VCS parameters there was significant difference between the groups with respect to mean neutrophil volume (MNV) and volume distribution width (VDW) (180 vs 163 vs 150) (p < 0.01). MNV and VDW had good sensitivity (95%, 82%) and specificity (86%, 74%) for diagnosis of sepsis. In conclusion, Neutrophil VCS parameters, especially MNV, can be incorporated with other sepsis screen parameters in diagnosis of neonatal sepsis. Nature Publishing Group UK 2020-03-10 /pmc/articles/PMC7064568/ /pubmed/32157117 http://dx.doi.org/10.1038/s41598-020-61434-z Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nesargi, Prerana Niranjan, H. S. Bandiya, Prathik Benakappa, Naveen Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis |
title | Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis |
title_full | Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis |
title_fullStr | Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis |
title_full_unstemmed | Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis |
title_short | Neutrophil Volume, conductivity and scatter (VCS) as a screening tool in neonatal sepsis |
title_sort | neutrophil volume, conductivity and scatter (vcs) as a screening tool in neonatal sepsis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064568/ https://www.ncbi.nlm.nih.gov/pubmed/32157117 http://dx.doi.org/10.1038/s41598-020-61434-z |
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