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Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis

Presepsin has been proposed as an early indicator for diagnosis and prognosis in sepsis. We aimed to evaluate the prognostic accuracy of presepsin levels and additional value for identifying high-risk patients when taken together with the current sepsis criteria. This was a single-center, prospectiv...

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Autores principales: Park, Jong Eun, Lee, Beomki, Yoon, Sun Joo, Park, Chi-Min, Jung, Chul Won, Ahn, Myung-Ju, Park, Hyung-Doo, Hwang, Sung Yeon, Shin, Tae Gun, Kang, Eun-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469631/
https://www.ncbi.nlm.nih.gov/pubmed/34572261
http://dx.doi.org/10.3390/biomedicines9091076
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author Park, Jong Eun
Lee, Beomki
Yoon, Sun Joo
Park, Chi-Min
Jung, Chul Won
Ahn, Myung-Ju
Park, Hyung-Doo
Hwang, Sung Yeon
Shin, Tae Gun
Kang, Eun-Suk
author_facet Park, Jong Eun
Lee, Beomki
Yoon, Sun Joo
Park, Chi-Min
Jung, Chul Won
Ahn, Myung-Ju
Park, Hyung-Doo
Hwang, Sung Yeon
Shin, Tae Gun
Kang, Eun-Suk
author_sort Park, Jong Eun
collection PubMed
description Presepsin has been proposed as an early indicator for diagnosis and prognosis in sepsis. We aimed to evaluate the prognostic accuracy of presepsin levels and additional value for identifying high-risk patients when taken together with the current sepsis criteria. This was a single-center, prospective, observational study of patients with suspected sepsis. The primary outcome was 28-day mortality. The prognostic performance of presepsin was evaluated by the area under the receiver operating characteristic curve (AUC), according to the sepsis definition using the Sequential Organ Failure Assessment (SOFA) score change (delta SOFA ≥ 2) and lactate level ≥ 2 mmol/L. A total of 755 patients were included. The AUC of presepsin for predicting 28-day mortality was 0.747. Presepsin showed adequate prognostic accuracy regardless of the delta SOFA score or lactate level. High presepsin levels (>755 pg/mL) showed an independent association with 28-day mortality (adjusted odds ratio: 5.17), and significant differences in mortality were observed, even in patients with non-sepsis low lactate level. Compared with a single criterion of the delta SOFA score or lactate, the addition of the high presepsin criterion significantly increased discrimination. Presepsin showed fair prognostic performance regardless of the clinical sepsis criteria. Complementary use of presepsin with the Sepsis-3 criteria may identify more high-risk septic patients and provide useful prognostic information.
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spelling pubmed-84696312021-09-27 Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis Park, Jong Eun Lee, Beomki Yoon, Sun Joo Park, Chi-Min Jung, Chul Won Ahn, Myung-Ju Park, Hyung-Doo Hwang, Sung Yeon Shin, Tae Gun Kang, Eun-Suk Biomedicines Article Presepsin has been proposed as an early indicator for diagnosis and prognosis in sepsis. We aimed to evaluate the prognostic accuracy of presepsin levels and additional value for identifying high-risk patients when taken together with the current sepsis criteria. This was a single-center, prospective, observational study of patients with suspected sepsis. The primary outcome was 28-day mortality. The prognostic performance of presepsin was evaluated by the area under the receiver operating characteristic curve (AUC), according to the sepsis definition using the Sequential Organ Failure Assessment (SOFA) score change (delta SOFA ≥ 2) and lactate level ≥ 2 mmol/L. A total of 755 patients were included. The AUC of presepsin for predicting 28-day mortality was 0.747. Presepsin showed adequate prognostic accuracy regardless of the delta SOFA score or lactate level. High presepsin levels (>755 pg/mL) showed an independent association with 28-day mortality (adjusted odds ratio: 5.17), and significant differences in mortality were observed, even in patients with non-sepsis low lactate level. Compared with a single criterion of the delta SOFA score or lactate, the addition of the high presepsin criterion significantly increased discrimination. Presepsin showed fair prognostic performance regardless of the clinical sepsis criteria. Complementary use of presepsin with the Sepsis-3 criteria may identify more high-risk septic patients and provide useful prognostic information. MDPI 2021-08-24 /pmc/articles/PMC8469631/ /pubmed/34572261 http://dx.doi.org/10.3390/biomedicines9091076 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Park, Jong Eun
Lee, Beomki
Yoon, Sun Joo
Park, Chi-Min
Jung, Chul Won
Ahn, Myung-Ju
Park, Hyung-Doo
Hwang, Sung Yeon
Shin, Tae Gun
Kang, Eun-Suk
Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis
title Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis
title_full Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis
title_fullStr Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis
title_full_unstemmed Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis
title_short Complementary Use of Presepsin with the Sepsis-3 Criteria Improved Identification of High-Risk Patients with Suspected Sepsis
title_sort complementary use of presepsin with the sepsis-3 criteria improved identification of high-risk patients with suspected sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469631/
https://www.ncbi.nlm.nih.gov/pubmed/34572261
http://dx.doi.org/10.3390/biomedicines9091076
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