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Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates

BACKGROUND: Sepsis is a major health issue in preterm infants. Biomarkers are used to diagnose and monitor patients with sepsis, but C-reactive protein (CRP) is proven not predictive at onset of late onset neonatal sepsis (LONS) diagnosis. The aim of this study was to evaluate the association of int...

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Autores principales: Kurul, Şerife, Simons, Sinno H. P., Ramakers, Christian R. B., De Rijke, Yolanda B., Kornelisse, René F., Reiss, Irwin K. M., Taal, H. Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788923/
https://www.ncbi.nlm.nih.gov/pubmed/33407770
http://dx.doi.org/10.1186/s13054-020-03423-2
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author Kurul, Şerife
Simons, Sinno H. P.
Ramakers, Christian R. B.
De Rijke, Yolanda B.
Kornelisse, René F.
Reiss, Irwin K. M.
Taal, H. Rob
author_facet Kurul, Şerife
Simons, Sinno H. P.
Ramakers, Christian R. B.
De Rijke, Yolanda B.
Kornelisse, René F.
Reiss, Irwin K. M.
Taal, H. Rob
author_sort Kurul, Şerife
collection PubMed
description BACKGROUND: Sepsis is a major health issue in preterm infants. Biomarkers are used to diagnose and monitor patients with sepsis, but C-reactive protein (CRP) is proven not predictive at onset of late onset neonatal sepsis (LONS) diagnosis. The aim of this study was to evaluate the association of interleukin-6(IL-6), procalcitonin (PCT) and CRP with subsequent sepsis severity and mortality in preterm infants suspected of late onset neonatal sepsis. METHODS: The study was conducted at the Erasmus University Medical Center–Sophia Children’s Hospital Rotterdam. Patient data from January 2018 until October 2019 were reviewed for all preterm neonates born with a gestational age below 32 weeks with signs and symptoms suggestive of systemic infection, in whom blood was taken for blood culture and for inflammatory biomarkers determinations. Plasma IL-6 and PCT were assessed next to CRP at the moment of suspicion. We assessed the association with 7-day mortality and sepsis severity (neonatal sequential organ failure assessment (nSOFA) score, need for inotropic support, invasive ventilation and thrombocytopenia). RESULTS: A total of 480 suspected late onset neonatal sepsis episodes in 208 preterm neonates (gestational age < 32 weeks) were retrospectively analyzed, of which 143 episodes were classified as sepsis (29.8%), with 56 (11.7%) cases of culture negative, 63 (13.1%) cases of gram-positive and 24(5.0%) cases of gram-negative sepsis. A total of 24 (5.0%) sepsis episodes resulted in death within 7 days after suspicion of LONS. Both IL-6 (adjusted hazard ratio (aHR): 2.28; 95% CI 1.64–3.16; p < 0.001) and PCT (aHR: 2.91; 95% CI 1.70–5.00; p < 0.001) levels were associated with 7-day mortality; however, CRP levels were not significantly correlated with 7-day mortality (aHR: 1.16; 95% CI (0.68–2.00; p = 0.56). Log IL-6, log PCT and log CRP levels were all significantly correlated with the need for inotropic support. CONCLUSIONS: Our findings show that serum IL-6 and PCT levels at moment of suspected late onset neonatal sepsis offer valuable information about sepsis severity and mortality risk in infants born below 32 weeks of gestation. The discriminative value was superior to that of CRP. Determining these biomarkers in suspected sepsis may help identify patients with imminent severe sepsis, who may require more intensive monitoring and therapy.
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spelling pubmed-77889232021-01-07 Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates Kurul, Şerife Simons, Sinno H. P. Ramakers, Christian R. B. De Rijke, Yolanda B. Kornelisse, René F. Reiss, Irwin K. M. Taal, H. Rob Crit Care Research BACKGROUND: Sepsis is a major health issue in preterm infants. Biomarkers are used to diagnose and monitor patients with sepsis, but C-reactive protein (CRP) is proven not predictive at onset of late onset neonatal sepsis (LONS) diagnosis. The aim of this study was to evaluate the association of interleukin-6(IL-6), procalcitonin (PCT) and CRP with subsequent sepsis severity and mortality in preterm infants suspected of late onset neonatal sepsis. METHODS: The study was conducted at the Erasmus University Medical Center–Sophia Children’s Hospital Rotterdam. Patient data from January 2018 until October 2019 were reviewed for all preterm neonates born with a gestational age below 32 weeks with signs and symptoms suggestive of systemic infection, in whom blood was taken for blood culture and for inflammatory biomarkers determinations. Plasma IL-6 and PCT were assessed next to CRP at the moment of suspicion. We assessed the association with 7-day mortality and sepsis severity (neonatal sequential organ failure assessment (nSOFA) score, need for inotropic support, invasive ventilation and thrombocytopenia). RESULTS: A total of 480 suspected late onset neonatal sepsis episodes in 208 preterm neonates (gestational age < 32 weeks) were retrospectively analyzed, of which 143 episodes were classified as sepsis (29.8%), with 56 (11.7%) cases of culture negative, 63 (13.1%) cases of gram-positive and 24(5.0%) cases of gram-negative sepsis. A total of 24 (5.0%) sepsis episodes resulted in death within 7 days after suspicion of LONS. Both IL-6 (adjusted hazard ratio (aHR): 2.28; 95% CI 1.64–3.16; p < 0.001) and PCT (aHR: 2.91; 95% CI 1.70–5.00; p < 0.001) levels were associated with 7-day mortality; however, CRP levels were not significantly correlated with 7-day mortality (aHR: 1.16; 95% CI (0.68–2.00; p = 0.56). Log IL-6, log PCT and log CRP levels were all significantly correlated with the need for inotropic support. CONCLUSIONS: Our findings show that serum IL-6 and PCT levels at moment of suspected late onset neonatal sepsis offer valuable information about sepsis severity and mortality risk in infants born below 32 weeks of gestation. The discriminative value was superior to that of CRP. Determining these biomarkers in suspected sepsis may help identify patients with imminent severe sepsis, who may require more intensive monitoring and therapy. BioMed Central 2021-01-06 /pmc/articles/PMC7788923/ /pubmed/33407770 http://dx.doi.org/10.1186/s13054-020-03423-2 Text en © The Author(s) 2020 Open AccessThis 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/. 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 in a credit line to the data.
spellingShingle Research
Kurul, Şerife
Simons, Sinno H. P.
Ramakers, Christian R. B.
De Rijke, Yolanda B.
Kornelisse, René F.
Reiss, Irwin K. M.
Taal, H. Rob
Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
title Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
title_full Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
title_fullStr Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
title_full_unstemmed Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
title_short Association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
title_sort association of inflammatory biomarkers with subsequent clinical course in suspected late onset sepsis in preterm neonates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788923/
https://www.ncbi.nlm.nih.gov/pubmed/33407770
http://dx.doi.org/10.1186/s13054-020-03423-2
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