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Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates

BACKGROUND: Diagnosis is the most strenuous step in the evaluation of neonatal sepsis. No gold standard diagnostic method is available except for blood culture. We aimed to investigate the role of positive and negative acute phase reactants, namely presepsin and fetuin-A, in the diagnosis of culture...

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Autores principales: Değirmencioğlu, Halil, Ozer Bekmez, Buse, Derme, Turan, Öncel, Mehmet Yekta, Canpolat, Fuat Emre, Tayman, Cüneyt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683331/
https://www.ncbi.nlm.nih.gov/pubmed/31387523
http://dx.doi.org/10.1186/s12879-019-4316-5
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author Değirmencioğlu, Halil
Ozer Bekmez, Buse
Derme, Turan
Öncel, Mehmet Yekta
Canpolat, Fuat Emre
Tayman, Cüneyt
author_facet Değirmencioğlu, Halil
Ozer Bekmez, Buse
Derme, Turan
Öncel, Mehmet Yekta
Canpolat, Fuat Emre
Tayman, Cüneyt
author_sort Değirmencioğlu, Halil
collection PubMed
description BACKGROUND: Diagnosis is the most strenuous step in the evaluation of neonatal sepsis. No gold standard diagnostic method is available except for blood culture. We aimed to investigate the role of positive and negative acute phase reactants, namely presepsin and fetuin-A, in the diagnosis of culture-proven late-onset sepsis. METHODS: A prospective, case-control study with the infants ≤32 weeks of age with a diagnosis of culture-proven late-onset sepsis was designed. Twenty-nine preterm infants with similar gestational and postnatal ages without sepsis constituted the control group. Serum values of presepsin, fetuin-A, C-reactive protein and interleukin-6 were evaluated at the enrollment, third and seventh days of the diagnosis in the infants with positive blood culture results. RESULTS: First-day presepsin values were significantly higher in the culture-positive infants than the control group [1583 ng/L (1023–1731) vs. 426 ng/L (287–589), p = < 0.0001]. Presepsin was found to have an 88.9% sensitivity and 88.9% specificity with a cut-off value of 823 ng/ml for culture-proven LOS in our study, and area under the receiver-operating curve was 0.939. Fetuin-A levels were similar between the study and control groups (p > 0.05). CONCLUSION: Presepsin may be an accurate marker for both diagnosis and monitoring of treatment response for culture-proven late-onset sepsis in preterm infants. However, fetuin-A does not seem to be a useful tool for the diagnosis of sepsis.
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spelling pubmed-66833312019-08-09 Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates Değirmencioğlu, Halil Ozer Bekmez, Buse Derme, Turan Öncel, Mehmet Yekta Canpolat, Fuat Emre Tayman, Cüneyt BMC Infect Dis Research Article BACKGROUND: Diagnosis is the most strenuous step in the evaluation of neonatal sepsis. No gold standard diagnostic method is available except for blood culture. We aimed to investigate the role of positive and negative acute phase reactants, namely presepsin and fetuin-A, in the diagnosis of culture-proven late-onset sepsis. METHODS: A prospective, case-control study with the infants ≤32 weeks of age with a diagnosis of culture-proven late-onset sepsis was designed. Twenty-nine preterm infants with similar gestational and postnatal ages without sepsis constituted the control group. Serum values of presepsin, fetuin-A, C-reactive protein and interleukin-6 were evaluated at the enrollment, third and seventh days of the diagnosis in the infants with positive blood culture results. RESULTS: First-day presepsin values were significantly higher in the culture-positive infants than the control group [1583 ng/L (1023–1731) vs. 426 ng/L (287–589), p = < 0.0001]. Presepsin was found to have an 88.9% sensitivity and 88.9% specificity with a cut-off value of 823 ng/ml for culture-proven LOS in our study, and area under the receiver-operating curve was 0.939. Fetuin-A levels were similar between the study and control groups (p > 0.05). CONCLUSION: Presepsin may be an accurate marker for both diagnosis and monitoring of treatment response for culture-proven late-onset sepsis in preterm infants. However, fetuin-A does not seem to be a useful tool for the diagnosis of sepsis. BioMed Central 2019-08-06 /pmc/articles/PMC6683331/ /pubmed/31387523 http://dx.doi.org/10.1186/s12879-019-4316-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Değirmencioğlu, Halil
Ozer Bekmez, Buse
Derme, Turan
Öncel, Mehmet Yekta
Canpolat, Fuat Emre
Tayman, Cüneyt
Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates
title Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates
title_full Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates
title_fullStr Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates
title_full_unstemmed Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates
title_short Presepsin and fetuin-A dyad for the diagnosis of proven sepsis in preterm neonates
title_sort presepsin and fetuin-a dyad for the diagnosis of proven sepsis in preterm neonates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683331/
https://www.ncbi.nlm.nih.gov/pubmed/31387523
http://dx.doi.org/10.1186/s12879-019-4316-5
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