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Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome
Sepsis-related acute respiratory distress syndrome (ARDS) has worse clinical outcomes than non-sepsis-related ARDS. Presepsin is known to be elevated in sepsis, but little is known about its discriminatory ability and prognostic evaluation in patients with sepsis-related ARDS. This study was a multi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272415/ https://www.ncbi.nlm.nih.gov/pubmed/32499573 http://dx.doi.org/10.1038/s41598-020-66121-7 |
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author | Zhao, Jiangnan Tan, Yan Wang, Li Shi, Yi |
author_facet | Zhao, Jiangnan Tan, Yan Wang, Li Shi, Yi |
author_sort | Zhao, Jiangnan |
collection | PubMed |
description | Sepsis-related acute respiratory distress syndrome (ARDS) has worse clinical outcomes than non-sepsis-related ARDS. Presepsin is known to be elevated in sepsis, but little is known about its discriminatory ability and prognostic evaluation in patients with sepsis-related ARDS. This study was a multicenter prospective cohort study of 225 consecutive ARDS patients. Patients with sepsis-related ARDS had higher presepsin levels than patients with non-sepsis-related ARDS (P < 0.001). The area under the receiver operating characteristic (ROC) curve of presepsin (0.81) was significantly greater than that of PCT (0.62) in diagnosing sepsis-related ARDS (P = 0.001). Among patients with sepsis-related ARDS, presepsin levels were significantly higher in non-survivors than in survivors (P < 0.001). Presepsin was found to be an independent predictor of in-hospital mortality in sepsis-related ARDS. Based on ROC analysis, the addition of presepsin improved discrimination based on SOFA or APACHE II scores from 0.77 to 0.87 or 0.73 to 0.85 (all P < 0.05), respectively. The levels of plasma presepsin were positively correlated with disease severity, as determined by the SOFA score in the sepsis-related ARDS group (P < 0.001). Presepsin is a valuable biomarker for early stratification of sepsis-related ARDS. Higher plasma presepsin levels are associated with increased mortality in sepsis-related ARDS. |
format | Online Article Text |
id | pubmed-7272415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72724152020-06-05 Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome Zhao, Jiangnan Tan, Yan Wang, Li Shi, Yi Sci Rep Article Sepsis-related acute respiratory distress syndrome (ARDS) has worse clinical outcomes than non-sepsis-related ARDS. Presepsin is known to be elevated in sepsis, but little is known about its discriminatory ability and prognostic evaluation in patients with sepsis-related ARDS. This study was a multicenter prospective cohort study of 225 consecutive ARDS patients. Patients with sepsis-related ARDS had higher presepsin levels than patients with non-sepsis-related ARDS (P < 0.001). The area under the receiver operating characteristic (ROC) curve of presepsin (0.81) was significantly greater than that of PCT (0.62) in diagnosing sepsis-related ARDS (P = 0.001). Among patients with sepsis-related ARDS, presepsin levels were significantly higher in non-survivors than in survivors (P < 0.001). Presepsin was found to be an independent predictor of in-hospital mortality in sepsis-related ARDS. Based on ROC analysis, the addition of presepsin improved discrimination based on SOFA or APACHE II scores from 0.77 to 0.87 or 0.73 to 0.85 (all P < 0.05), respectively. The levels of plasma presepsin were positively correlated with disease severity, as determined by the SOFA score in the sepsis-related ARDS group (P < 0.001). Presepsin is a valuable biomarker for early stratification of sepsis-related ARDS. Higher plasma presepsin levels are associated with increased mortality in sepsis-related ARDS. Nature Publishing Group UK 2020-06-04 /pmc/articles/PMC7272415/ /pubmed/32499573 http://dx.doi.org/10.1038/s41598-020-66121-7 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhao, Jiangnan Tan, Yan Wang, Li Shi, Yi Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
title | Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
title_full | Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
title_fullStr | Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
title_full_unstemmed | Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
title_short | Discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
title_sort | discriminatory ability and prognostic evaluation of presepsin for sepsis-related acute respiratory distress syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272415/ https://www.ncbi.nlm.nih.gov/pubmed/32499573 http://dx.doi.org/10.1038/s41598-020-66121-7 |
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