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The value of a risk model for early-onset candidemia

Bloodstream infections from Candida species are associated with an increased length of stay, increased hospital costs, and higher mortality when compared with bacterial bloodstream infections. Delayed or inappropriate therapy in candidemia leads to increased mortality, thus early recognition becomes...

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Detalles Bibliográficos
Autores principales: Sandrock, Christian, Siddiqui, Javeed
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811893/
https://www.ncbi.nlm.nih.gov/pubmed/19939291
http://dx.doi.org/10.1186/cc8127
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author Sandrock, Christian
Siddiqui, Javeed
author_facet Sandrock, Christian
Siddiqui, Javeed
author_sort Sandrock, Christian
collection PubMed
description Bloodstream infections from Candida species are associated with an increased length of stay, increased hospital costs, and higher mortality when compared with bacterial bloodstream infections. Delayed or inappropriate therapy in candidemia leads to increased mortality, thus early recognition becomes paramount. With biomarkers showing promise, blood cultures still remain the gold standard but require 24 to 72 hours for growth. The reliance on epidemiologic risk factors for the initiation of empiric antifungal therapy therefore provides the best method for early appropriate therapy. Shorr and colleagues have devised a risk score to identify patients with early-onset candidemia as defined by positive blood cultures within 2 days of admission, thus allowing for the initiation of early appropriate antifungal therapy.
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spelling pubmed-28118932010-11-16 The value of a risk model for early-onset candidemia Sandrock, Christian Siddiqui, Javeed Crit Care Commentary Bloodstream infections from Candida species are associated with an increased length of stay, increased hospital costs, and higher mortality when compared with bacterial bloodstream infections. Delayed or inappropriate therapy in candidemia leads to increased mortality, thus early recognition becomes paramount. With biomarkers showing promise, blood cultures still remain the gold standard but require 24 to 72 hours for growth. The reliance on epidemiologic risk factors for the initiation of empiric antifungal therapy therefore provides the best method for early appropriate therapy. Shorr and colleagues have devised a risk score to identify patients with early-onset candidemia as defined by positive blood cultures within 2 days of admission, thus allowing for the initiation of early appropriate antifungal therapy. BioMed Central 2009 2009-11-16 /pmc/articles/PMC2811893/ /pubmed/19939291 http://dx.doi.org/10.1186/cc8127 Text en Copyright ©2009 BioMed Central Ltd
spellingShingle Commentary
Sandrock, Christian
Siddiqui, Javeed
The value of a risk model for early-onset candidemia
title The value of a risk model for early-onset candidemia
title_full The value of a risk model for early-onset candidemia
title_fullStr The value of a risk model for early-onset candidemia
title_full_unstemmed The value of a risk model for early-onset candidemia
title_short The value of a risk model for early-onset candidemia
title_sort value of a risk model for early-onset candidemia
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811893/
https://www.ncbi.nlm.nih.gov/pubmed/19939291
http://dx.doi.org/10.1186/cc8127
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