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Collagen-related biomarkers in severe sepsis: a big stretch?

Biomedical scientists are aggressively investigating biomarkers of disease and injury. The rationale for identifying biomarkers during pathological states, such as severe sepsis, is to improve clinical prognostication and stratify therapeutic interventions for optimal recovery. An added benefit of b...

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Detalles Bibliográficos
Autores principales: Morrison, Gavin, Fraser, Douglas D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717431/
https://www.ncbi.nlm.nih.gov/pubmed/19519949
http://dx.doi.org/10.1186/cc7879
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author Morrison, Gavin
Fraser, Douglas D
author_facet Morrison, Gavin
Fraser, Douglas D
author_sort Morrison, Gavin
collection PubMed
description Biomedical scientists are aggressively investigating biomarkers of disease and injury. The rationale for identifying biomarkers during pathological states, such as severe sepsis, is to improve clinical prognostication and stratify therapeutic interventions for optimal recovery. An added benefit of biomarker studies is knowledge genesis on pathophysiological mechanisms, critical information that provides a basis for hypothesis-driven research. Unfortunately, biomarkers rarely alter our clinical approach in severe sepsis as they are often non-specific, lack adequate sensitivity and/or are difficult to measure and interpret accurately. Given the complexity and heterogeneity of severe sepsis, and the unique genetically derived susceptibilities of individuals, it is highly unlikely that one or even a handful of biomarkers will provide adequate biomedical information for clinical guidance. Thus, biomarkers will ultimately alter clinical decision making only once a panel of promising biomarkers is identified, maximizing sensitivity and specificity, and then adequately scrutinized with quantitative scoring methods over large populations of patients.
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spelling pubmed-27174312010-06-02 Collagen-related biomarkers in severe sepsis: a big stretch? Morrison, Gavin Fraser, Douglas D Crit Care Commentary Biomedical scientists are aggressively investigating biomarkers of disease and injury. The rationale for identifying biomarkers during pathological states, such as severe sepsis, is to improve clinical prognostication and stratify therapeutic interventions for optimal recovery. An added benefit of biomarker studies is knowledge genesis on pathophysiological mechanisms, critical information that provides a basis for hypothesis-driven research. Unfortunately, biomarkers rarely alter our clinical approach in severe sepsis as they are often non-specific, lack adequate sensitivity and/or are difficult to measure and interpret accurately. Given the complexity and heterogeneity of severe sepsis, and the unique genetically derived susceptibilities of individuals, it is highly unlikely that one or even a handful of biomarkers will provide adequate biomedical information for clinical guidance. Thus, biomarkers will ultimately alter clinical decision making only once a panel of promising biomarkers is identified, maximizing sensitivity and specificity, and then adequately scrutinized with quantitative scoring methods over large populations of patients. BioMed Central 2009 2009-06-02 /pmc/articles/PMC2717431/ /pubmed/19519949 http://dx.doi.org/10.1186/cc7879 Text en Copyright © 2009 BioMed Central Ltd
spellingShingle Commentary
Morrison, Gavin
Fraser, Douglas D
Collagen-related biomarkers in severe sepsis: a big stretch?
title Collagen-related biomarkers in severe sepsis: a big stretch?
title_full Collagen-related biomarkers in severe sepsis: a big stretch?
title_fullStr Collagen-related biomarkers in severe sepsis: a big stretch?
title_full_unstemmed Collagen-related biomarkers in severe sepsis: a big stretch?
title_short Collagen-related biomarkers in severe sepsis: a big stretch?
title_sort collagen-related biomarkers in severe sepsis: a big stretch?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717431/
https://www.ncbi.nlm.nih.gov/pubmed/19519949
http://dx.doi.org/10.1186/cc7879
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