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The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study

Hematosepsis is a systemic inflammatory response syndrome (SIRS) with suspected or confirmed infection, which is the most common infectious disease in clinical neonatal intensive care unit. As the rapid development of neonatal hematosepsis caused by various basic diseases, the mortality rate is high...

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Autores principales: Xiao, Ting, Chen, Li-Ping, Zhang, Li-hua, Lai, Fu-Huang, Zhang, Li, Qiu, Qun-feng, Que, Rong-Liang, Xie, SiSi, Wu, Ding-Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419931/
https://www.ncbi.nlm.nih.gov/pubmed/28471985
http://dx.doi.org/10.1097/MD.0000000000006823
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author Xiao, Ting
Chen, Li-Ping
Zhang, Li-hua
Lai, Fu-Huang
Zhang, Li
Qiu, Qun-feng
Que, Rong-Liang
Xie, SiSi
Wu, Ding-Chang
author_facet Xiao, Ting
Chen, Li-Ping
Zhang, Li-hua
Lai, Fu-Huang
Zhang, Li
Qiu, Qun-feng
Que, Rong-Liang
Xie, SiSi
Wu, Ding-Chang
author_sort Xiao, Ting
collection PubMed
description Hematosepsis is a systemic inflammatory response syndrome (SIRS) with suspected or confirmed infection, which is the most common infectious disease in clinical neonatal intensive care unit. As the rapid development of neonatal hematosepsis caused by various basic diseases, the mortality rate is high, and there are some sequelae. We report the lasted study to date with 96 cases from Fujian Longyan First Hospital between 2013 and 2015. The aim of our study is to explore the value of soluble cluster of differentiation 14 subtype (sCD14-ST) in whole blood for differential diagnosis of neonatal hematosepsis at an early stage, and used in evaluation of the severity about sepsis combined with acute physiology and chronic health evaluation II (APACHE-II) score, procalcitonin (PCT), C reactive protein (CRP), and leukocyte (WBC). In our cohort, all cases met the diagnostic criteria for hematosepsis specific for newborns. We selected 42 neonates with hematosepsis, 54 neonates with nonhematosepsis, 44 noninfectious SIRS neonates, and 53 healthy neonatal controls. Which were determined the sCD14-ST, PCT, CRP, and WBC of all samples before treatment. Then assign the APACHE-II score for the all samples before and after treatment. The study shows, sCD14-ST levels were significantly higher in hematosepsis than nonhematosepsis group (t = −2.112, P = .041). Meanwhile, sCD14-ST levels were significantly higher in neonatal hematosepsis than in noninfectious SIRS group and controls (χ(2) = 57.812, 68.944, P < .01). However, sCD14-ST in hematosepsis group was positively correlated with APACHE-II score (R-value = 0.415, P < .01). During treatment, the sCD14-ST level was decreased obviously along with APACHE-II score, PCT, CRP, and WBC (χ(2) = 35.019, 78.399, 52.363, 25.912, 7.252, all P values <.01). The area under the curve (AUC) of sCD14-ST was 0.942. The differences in ROC(AUC) of sCD14-ST compared with PCT, CRP, and WBC were statistically significant (Z = −6.034, −4.474, −5.722, all P values <.01). The sensitivity and specificity of sCD14-ST were 95.2% and 84.9%, respectively. sCD14-ST could be a blood biomarker for early identification and disease valuation in newborns hematosepsis infection; and its diagnostic value is superior to other laboratory indexes.
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spelling pubmed-54199312017-05-11 The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study Xiao, Ting Chen, Li-Ping Zhang, Li-hua Lai, Fu-Huang Zhang, Li Qiu, Qun-feng Que, Rong-Liang Xie, SiSi Wu, Ding-Chang Medicine (Baltimore) 4100 Hematosepsis is a systemic inflammatory response syndrome (SIRS) with suspected or confirmed infection, which is the most common infectious disease in clinical neonatal intensive care unit. As the rapid development of neonatal hematosepsis caused by various basic diseases, the mortality rate is high, and there are some sequelae. We report the lasted study to date with 96 cases from Fujian Longyan First Hospital between 2013 and 2015. The aim of our study is to explore the value of soluble cluster of differentiation 14 subtype (sCD14-ST) in whole blood for differential diagnosis of neonatal hematosepsis at an early stage, and used in evaluation of the severity about sepsis combined with acute physiology and chronic health evaluation II (APACHE-II) score, procalcitonin (PCT), C reactive protein (CRP), and leukocyte (WBC). In our cohort, all cases met the diagnostic criteria for hematosepsis specific for newborns. We selected 42 neonates with hematosepsis, 54 neonates with nonhematosepsis, 44 noninfectious SIRS neonates, and 53 healthy neonatal controls. Which were determined the sCD14-ST, PCT, CRP, and WBC of all samples before treatment. Then assign the APACHE-II score for the all samples before and after treatment. The study shows, sCD14-ST levels were significantly higher in hematosepsis than nonhematosepsis group (t = −2.112, P = .041). Meanwhile, sCD14-ST levels were significantly higher in neonatal hematosepsis than in noninfectious SIRS group and controls (χ(2) = 57.812, 68.944, P < .01). However, sCD14-ST in hematosepsis group was positively correlated with APACHE-II score (R-value = 0.415, P < .01). During treatment, the sCD14-ST level was decreased obviously along with APACHE-II score, PCT, CRP, and WBC (χ(2) = 35.019, 78.399, 52.363, 25.912, 7.252, all P values <.01). The area under the curve (AUC) of sCD14-ST was 0.942. The differences in ROC(AUC) of sCD14-ST compared with PCT, CRP, and WBC were statistically significant (Z = −6.034, −4.474, −5.722, all P values <.01). The sensitivity and specificity of sCD14-ST were 95.2% and 84.9%, respectively. sCD14-ST could be a blood biomarker for early identification and disease valuation in newborns hematosepsis infection; and its diagnostic value is superior to other laboratory indexes. Wolters Kluwer Health 2017-05-05 /pmc/articles/PMC5419931/ /pubmed/28471985 http://dx.doi.org/10.1097/MD.0000000000006823 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 4100
Xiao, Ting
Chen, Li-Ping
Zhang, Li-hua
Lai, Fu-Huang
Zhang, Li
Qiu, Qun-feng
Que, Rong-Liang
Xie, SiSi
Wu, Ding-Chang
The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study
title The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study
title_full The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study
title_fullStr The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study
title_full_unstemmed The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study
title_short The clinical significance of sCD14-ST for blood biomarker in neonatal hematosepsis: A diagnostic accuracy study
title_sort clinical significance of scd14-st for blood biomarker in neonatal hematosepsis: a diagnostic accuracy study
topic 4100
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419931/
https://www.ncbi.nlm.nih.gov/pubmed/28471985
http://dx.doi.org/10.1097/MD.0000000000006823
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