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Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model

BACKGROUND: Prognostic biomarker research neonatal sepsis is lacking. We assessed the utility of a validated pediatric prognostic tool called PERSEVERE II that uses decision tree methodology to predict mortality at discharge in neonates who experienced sepsis. METHODS: Prospective study in a dual-ce...

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Autores principales: Al Gharaibeh, Faris N., Lahni, Patrick, Alder, Matthew N., Wong, Hector R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261505/
https://www.ncbi.nlm.nih.gov/pubmed/36513805
http://dx.doi.org/10.1038/s41390-022-02414-z
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author Al Gharaibeh, Faris N.
Lahni, Patrick
Alder, Matthew N.
Wong, Hector R.
author_facet Al Gharaibeh, Faris N.
Lahni, Patrick
Alder, Matthew N.
Wong, Hector R.
author_sort Al Gharaibeh, Faris N.
collection PubMed
description BACKGROUND: Prognostic biomarker research neonatal sepsis is lacking. We assessed the utility of a validated pediatric prognostic tool called PERSEVERE II that uses decision tree methodology to predict mortality at discharge in neonates who experienced sepsis. METHODS: Prospective study in a dual-center cohort of neonates with sepsis admitted between June 2020 and December 2021. Biomarker analysis was done on serum samples obtained at the time of evaluation for the event. RESULTS: In a cohort of 59 neonates with a mortality rate of 15.3%, PERSEVERE II was 67% sensitive and 59% specific for mortality, p 0.27. Amongst PERSEVERE II biomarkers, IL-8 showed good prognostic performance for mortality prediction with a cutoff of 300 pg/mL (sensitivity 100%, specificity 65%, negative predictive value 100%, AUC 0.87, p 0.0003). We derived a new decision tree that is neonate specific (nPERSEVERE) with improved performance compared to IL-8 (sensitivity 100%, specificity 86%, negative predictive value 100%, AUC 0.95, p <0.0001). CONCLUSIONS: IL-8 and nPERSEVERE demonstrated good prognostic performance in a small cohort of neonates with sepsis. Moving towards precision medicine in sepsis, our study proposes an important tool for clinical trial prognostic enrichment which needs to be validated in larger studies.
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spelling pubmed-102615052023-10-23 Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model Al Gharaibeh, Faris N. Lahni, Patrick Alder, Matthew N. Wong, Hector R. Pediatr Res Article BACKGROUND: Prognostic biomarker research neonatal sepsis is lacking. We assessed the utility of a validated pediatric prognostic tool called PERSEVERE II that uses decision tree methodology to predict mortality at discharge in neonates who experienced sepsis. METHODS: Prospective study in a dual-center cohort of neonates with sepsis admitted between June 2020 and December 2021. Biomarker analysis was done on serum samples obtained at the time of evaluation for the event. RESULTS: In a cohort of 59 neonates with a mortality rate of 15.3%, PERSEVERE II was 67% sensitive and 59% specific for mortality, p 0.27. Amongst PERSEVERE II biomarkers, IL-8 showed good prognostic performance for mortality prediction with a cutoff of 300 pg/mL (sensitivity 100%, specificity 65%, negative predictive value 100%, AUC 0.87, p 0.0003). We derived a new decision tree that is neonate specific (nPERSEVERE) with improved performance compared to IL-8 (sensitivity 100%, specificity 86%, negative predictive value 100%, AUC 0.95, p <0.0001). CONCLUSIONS: IL-8 and nPERSEVERE demonstrated good prognostic performance in a small cohort of neonates with sepsis. Moving towards precision medicine in sepsis, our study proposes an important tool for clinical trial prognostic enrichment which needs to be validated in larger studies. 2023-10 2022-12-13 /pmc/articles/PMC10261505/ /pubmed/36513805 http://dx.doi.org/10.1038/s41390-022-02414-z Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Al Gharaibeh, Faris N.
Lahni, Patrick
Alder, Matthew N.
Wong, Hector R.
Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model
title Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model
title_full Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model
title_fullStr Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model
title_full_unstemmed Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model
title_short Biomarkers Estimating Baseline Mortality Risk for Neonatal Sepsis: nPERSEVERE: neonate-Specific Sepsis Biomarker Risk Model
title_sort biomarkers estimating baseline mortality risk for neonatal sepsis: npersevere: neonate-specific sepsis biomarker risk model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261505/
https://www.ncbi.nlm.nih.gov/pubmed/36513805
http://dx.doi.org/10.1038/s41390-022-02414-z
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