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Evaluating of neonatal early onset sepsis through lactate and base excess monitoring

Early-onset sepsis (EOS) is one of the leading causes of neonatal death and morbidity worldwide and timely initiation of antibiotic therapy is, therefore, of paramount importance. This study aimed to evaluate the predictive effect of lactate and base excess (BE) values in the cord arterial blood gas...

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Autores principales: Yilmaz, Aslan, Kaya, Nesrin, Gonen, Ilker, Uygur, Abdulkerim, Perk, Yildiz, Vural, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491792/
https://www.ncbi.nlm.nih.gov/pubmed/37684308
http://dx.doi.org/10.1038/s41598-023-41776-0
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author Yilmaz, Aslan
Kaya, Nesrin
Gonen, Ilker
Uygur, Abdulkerim
Perk, Yildiz
Vural, Mehmet
author_facet Yilmaz, Aslan
Kaya, Nesrin
Gonen, Ilker
Uygur, Abdulkerim
Perk, Yildiz
Vural, Mehmet
author_sort Yilmaz, Aslan
collection PubMed
description Early-onset sepsis (EOS) is one of the leading causes of neonatal death and morbidity worldwide and timely initiation of antibiotic therapy is, therefore, of paramount importance. This study aimed to evaluate the predictive effect of lactate and base excess (BE) values in the cord arterial blood gas and the 6th hour of life venous blood gas analysis on clinical sepsis in newborns. This is a cohort case–control study. In this study, 104 cases were divided into clinical and suspected sepsis groups according to the evaluation at the 24th hour after delivery. Lactate and BE values were evaluated in the cord arterial blood gas analysis (ABGA) and at the postnatal 6th-hour venous blood gas. The cord ABGA and postnatal 6th-hour results were compared in the clinical and suspected sepsis groups. Clinical sepsis was found to be associated with a lactate value above 2 mMol/L at postnatal 6th-hour venous blood gas (p = 0.041). This association was the highest when the clinical sepsis group's postnatal 6th-hour lactate cut-off value was determined as 3.38 mMol/L (sensitivity 57.9% and specificity 68.5%) (p = 0.032). However, no association was found between clinical sepsis diagnosis and venous BE's value in cord ABGA at the postnatal 6th hour. We found that a venous lactate value above 3.38 mMol/L at the postnatal 6th hour was the cut-off value that could indicate early-onset clinical sepsis. However, none of the biomarkers used in diagnosing EOS can accurately show all cases.
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spelling pubmed-104917922023-09-10 Evaluating of neonatal early onset sepsis through lactate and base excess monitoring Yilmaz, Aslan Kaya, Nesrin Gonen, Ilker Uygur, Abdulkerim Perk, Yildiz Vural, Mehmet Sci Rep Article Early-onset sepsis (EOS) is one of the leading causes of neonatal death and morbidity worldwide and timely initiation of antibiotic therapy is, therefore, of paramount importance. This study aimed to evaluate the predictive effect of lactate and base excess (BE) values in the cord arterial blood gas and the 6th hour of life venous blood gas analysis on clinical sepsis in newborns. This is a cohort case–control study. In this study, 104 cases were divided into clinical and suspected sepsis groups according to the evaluation at the 24th hour after delivery. Lactate and BE values were evaluated in the cord arterial blood gas analysis (ABGA) and at the postnatal 6th-hour venous blood gas. The cord ABGA and postnatal 6th-hour results were compared in the clinical and suspected sepsis groups. Clinical sepsis was found to be associated with a lactate value above 2 mMol/L at postnatal 6th-hour venous blood gas (p = 0.041). This association was the highest when the clinical sepsis group's postnatal 6th-hour lactate cut-off value was determined as 3.38 mMol/L (sensitivity 57.9% and specificity 68.5%) (p = 0.032). However, no association was found between clinical sepsis diagnosis and venous BE's value in cord ABGA at the postnatal 6th hour. We found that a venous lactate value above 3.38 mMol/L at the postnatal 6th hour was the cut-off value that could indicate early-onset clinical sepsis. However, none of the biomarkers used in diagnosing EOS can accurately show all cases. Nature Publishing Group UK 2023-09-08 /pmc/articles/PMC10491792/ /pubmed/37684308 http://dx.doi.org/10.1038/s41598-023-41776-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yilmaz, Aslan
Kaya, Nesrin
Gonen, Ilker
Uygur, Abdulkerim
Perk, Yildiz
Vural, Mehmet
Evaluating of neonatal early onset sepsis through lactate and base excess monitoring
title Evaluating of neonatal early onset sepsis through lactate and base excess monitoring
title_full Evaluating of neonatal early onset sepsis through lactate and base excess monitoring
title_fullStr Evaluating of neonatal early onset sepsis through lactate and base excess monitoring
title_full_unstemmed Evaluating of neonatal early onset sepsis through lactate and base excess monitoring
title_short Evaluating of neonatal early onset sepsis through lactate and base excess monitoring
title_sort evaluating of neonatal early onset sepsis through lactate and base excess monitoring
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491792/
https://www.ncbi.nlm.nih.gov/pubmed/37684308
http://dx.doi.org/10.1038/s41598-023-41776-0
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