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Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study

BACKGROUND: The early recognition and management of sepsis improves outcomes. Biomarkers may help in identifying earlier sub-clinical signs of sepsis. We explored the potential of serial measurements of C-reactive protein (CRP), procalcitonin (PCT) and pancreatic stone protein (PSP) for the early re...

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Autores principales: Pugin, Jérôme, Daix, Thomas, Pagani, Jean-Luc, Morri, Davide, Giacomucci, Angelo, Dequin, Pierre-François, Guitton, Christophe, Que, Yok-Ai, Zani, Gianluca, Brealey, David, Lepape, Alain, Creagh-Brown, Ben, Wyncoll, Duncan, Silengo, Daniela, Irincheeva, Irina, Girard, Laurie, Rebeaud, Fabien, Maerki, Iwan, Eggimann, Philippe, François, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056692/
https://www.ncbi.nlm.nih.gov/pubmed/33879189
http://dx.doi.org/10.1186/s13054-021-03576-8
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author Pugin, Jérôme
Daix, Thomas
Pagani, Jean-Luc
Morri, Davide
Giacomucci, Angelo
Dequin, Pierre-François
Guitton, Christophe
Que, Yok-Ai
Zani, Gianluca
Brealey, David
Lepape, Alain
Creagh-Brown, Ben
Wyncoll, Duncan
Silengo, Daniela
Irincheeva, Irina
Girard, Laurie
Rebeaud, Fabien
Maerki, Iwan
Eggimann, Philippe
François, Bruno
author_facet Pugin, Jérôme
Daix, Thomas
Pagani, Jean-Luc
Morri, Davide
Giacomucci, Angelo
Dequin, Pierre-François
Guitton, Christophe
Que, Yok-Ai
Zani, Gianluca
Brealey, David
Lepape, Alain
Creagh-Brown, Ben
Wyncoll, Duncan
Silengo, Daniela
Irincheeva, Irina
Girard, Laurie
Rebeaud, Fabien
Maerki, Iwan
Eggimann, Philippe
François, Bruno
author_sort Pugin, Jérôme
collection PubMed
description BACKGROUND: The early recognition and management of sepsis improves outcomes. Biomarkers may help in identifying earlier sub-clinical signs of sepsis. We explored the potential of serial measurements of C-reactive protein (CRP), procalcitonin (PCT) and pancreatic stone protein (PSP) for the early recognition of sepsis in patients hospitalized in the intensive care unit (ICU). METHODS: This was a multicentric international prospective observational clinical study conducted in 14 ICUs in France, Switzerland, Italy, and the United Kingdom. Adult ICU patients at risk of nosocomial sepsis were included. A biomarker-blinded adjudication committee identified sepsis events and the days on which they began. The association of clinical sepsis diagnoses with the trajectories of PSP, CRP, and PCT in the 3 days preceding these diagnoses of sepsis were tested for markers of early sepsis detection. The performance of the biomarkers in sepsis diagnosis was assessed by receiver operating characteristic (ROC) analysis. RESULTS: Of the 243 patients included, 53 developed nosocomial sepsis after a median of 6 days (interquartile range, 3–8 days). Clinical sepsis diagnosis was associated with an increase in biomarkers value over the 3 days preceding this diagnosis [PSP (p = 0.003), PCT (p = 0.025) and CRP (p = 0.009)]. PSP started to increase 5 days before the clinical diagnosis of sepsis, PCT 3 and CRP 2 days, respectively. The area under the ROC curve at the time of clinical sepsis was similar for all markers (PSP, 0.75; CRP, 0.77; PCT, 0.75). CONCLUSIONS: While the diagnostic accuracy of PSP, CRP and PCT for sepsis were similar in this cohort, serial PSP measurement demonstrated an increase of this marker the days preceding the onset of signs necessary to clinical diagnose sepsis. This observation justifies further evaluation of the potential clinical benefit of serial PSP measurement in the management of critically ill patients developing nosocomial sepsis. Trial registration The study has been registered at ClinicalTrials.gov (no. NCT03474809), on March 16, 2018. https://www.clinicaltrials.gov/ct2/show/NCT03474809?term=NCT03474809&draw=2&rank=1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03576-8.
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spelling pubmed-80566922021-04-21 Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study Pugin, Jérôme Daix, Thomas Pagani, Jean-Luc Morri, Davide Giacomucci, Angelo Dequin, Pierre-François Guitton, Christophe Que, Yok-Ai Zani, Gianluca Brealey, David Lepape, Alain Creagh-Brown, Ben Wyncoll, Duncan Silengo, Daniela Irincheeva, Irina Girard, Laurie Rebeaud, Fabien Maerki, Iwan Eggimann, Philippe François, Bruno Crit Care Research BACKGROUND: The early recognition and management of sepsis improves outcomes. Biomarkers may help in identifying earlier sub-clinical signs of sepsis. We explored the potential of serial measurements of C-reactive protein (CRP), procalcitonin (PCT) and pancreatic stone protein (PSP) for the early recognition of sepsis in patients hospitalized in the intensive care unit (ICU). METHODS: This was a multicentric international prospective observational clinical study conducted in 14 ICUs in France, Switzerland, Italy, and the United Kingdom. Adult ICU patients at risk of nosocomial sepsis were included. A biomarker-blinded adjudication committee identified sepsis events and the days on which they began. The association of clinical sepsis diagnoses with the trajectories of PSP, CRP, and PCT in the 3 days preceding these diagnoses of sepsis were tested for markers of early sepsis detection. The performance of the biomarkers in sepsis diagnosis was assessed by receiver operating characteristic (ROC) analysis. RESULTS: Of the 243 patients included, 53 developed nosocomial sepsis after a median of 6 days (interquartile range, 3–8 days). Clinical sepsis diagnosis was associated with an increase in biomarkers value over the 3 days preceding this diagnosis [PSP (p = 0.003), PCT (p = 0.025) and CRP (p = 0.009)]. PSP started to increase 5 days before the clinical diagnosis of sepsis, PCT 3 and CRP 2 days, respectively. The area under the ROC curve at the time of clinical sepsis was similar for all markers (PSP, 0.75; CRP, 0.77; PCT, 0.75). CONCLUSIONS: While the diagnostic accuracy of PSP, CRP and PCT for sepsis were similar in this cohort, serial PSP measurement demonstrated an increase of this marker the days preceding the onset of signs necessary to clinical diagnose sepsis. This observation justifies further evaluation of the potential clinical benefit of serial PSP measurement in the management of critically ill patients developing nosocomial sepsis. Trial registration The study has been registered at ClinicalTrials.gov (no. NCT03474809), on March 16, 2018. https://www.clinicaltrials.gov/ct2/show/NCT03474809?term=NCT03474809&draw=2&rank=1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03576-8. BioMed Central 2021-04-20 /pmc/articles/PMC8056692/ /pubmed/33879189 http://dx.doi.org/10.1186/s13054-021-03576-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Pugin, Jérôme
Daix, Thomas
Pagani, Jean-Luc
Morri, Davide
Giacomucci, Angelo
Dequin, Pierre-François
Guitton, Christophe
Que, Yok-Ai
Zani, Gianluca
Brealey, David
Lepape, Alain
Creagh-Brown, Ben
Wyncoll, Duncan
Silengo, Daniela
Irincheeva, Irina
Girard, Laurie
Rebeaud, Fabien
Maerki, Iwan
Eggimann, Philippe
François, Bruno
Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
title Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
title_full Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
title_fullStr Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
title_full_unstemmed Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
title_short Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
title_sort serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056692/
https://www.ncbi.nlm.nih.gov/pubmed/33879189
http://dx.doi.org/10.1186/s13054-021-03576-8
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