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Protein C as a surrogate end-point for clinical trials of sepsis

Identification of good surrogate end-points can greatly facilitate the design of clinical trials. Using data from PROWESS and ENHANCE, Shorr and colleagues explore the potential value of several plasma biomarkers for treatment trials of activated protein C for severe sepsis. Based on the framework p...

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Detalles Bibliográficos
Autores principales: Liu, Kathleen D, Matthay, Michael A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447596/
https://www.ncbi.nlm.nih.gov/pubmed/18492215
http://dx.doi.org/10.1186/cc6859
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author Liu, Kathleen D
Matthay, Michael A
author_facet Liu, Kathleen D
Matthay, Michael A
author_sort Liu, Kathleen D
collection PubMed
description Identification of good surrogate end-points can greatly facilitate the design of clinical trials. Using data from PROWESS and ENHANCE, Shorr and colleagues explore the potential value of several plasma biomarkers for treatment trials of activated protein C for severe sepsis. Based on the framework proposed by Vasan, they tested the utility of several factors (protein C, interleukin-6, antithrombin III, prothrombin time, protein S, and d-dimers) as type 0, 1 and 2 biomarkers. Only protein C had acceptable performance characteristics as a type 2 biomarker, or surrogate end-point. The utility of protein C as a surrogate end-point for studies of severe sepsis must be validated in future prospective studies.
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spelling pubmed-24475962008-07-10 Protein C as a surrogate end-point for clinical trials of sepsis Liu, Kathleen D Matthay, Michael A Crit Care Commentary Identification of good surrogate end-points can greatly facilitate the design of clinical trials. Using data from PROWESS and ENHANCE, Shorr and colleagues explore the potential value of several plasma biomarkers for treatment trials of activated protein C for severe sepsis. Based on the framework proposed by Vasan, they tested the utility of several factors (protein C, interleukin-6, antithrombin III, prothrombin time, protein S, and d-dimers) as type 0, 1 and 2 biomarkers. Only protein C had acceptable performance characteristics as a type 2 biomarker, or surrogate end-point. The utility of protein C as a surrogate end-point for studies of severe sepsis must be validated in future prospective studies. BioMed Central 2008 2008-04-24 /pmc/articles/PMC2447596/ /pubmed/18492215 http://dx.doi.org/10.1186/cc6859 Text en Copyright © 2008 BioMed Central Ltd
spellingShingle Commentary
Liu, Kathleen D
Matthay, Michael A
Protein C as a surrogate end-point for clinical trials of sepsis
title Protein C as a surrogate end-point for clinical trials of sepsis
title_full Protein C as a surrogate end-point for clinical trials of sepsis
title_fullStr Protein C as a surrogate end-point for clinical trials of sepsis
title_full_unstemmed Protein C as a surrogate end-point for clinical trials of sepsis
title_short Protein C as a surrogate end-point for clinical trials of sepsis
title_sort protein c as a surrogate end-point for clinical trials of sepsis
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447596/
https://www.ncbi.nlm.nih.gov/pubmed/18492215
http://dx.doi.org/10.1186/cc6859
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