Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1782176805077123072 |
---|---|
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. |
format | Text |
id | pubmed-2811893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sandrockchristian thevalueofariskmodelforearlyonsetcandidemia AT siddiquijaveed thevalueofariskmodelforearlyonsetcandidemia AT sandrockchristian valueofariskmodelforearlyonsetcandidemia AT siddiquijaveed valueofariskmodelforearlyonsetcandidemia |