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Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections

BACKGROUND: Candida bloodstream infections (CBSI) continue to be associated with high mortality, despite changes in antifungal treatment and diagnostics. METHODS: All patients age 18 or greater with a first episode of CBSI by blood culture from 1/2002 to 1/2015, admitted to Barnes-Jewish Hospital, a...

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Autores principales: Lin, Charlotte, Kronen, Alyssa, Hsueh, Kevin, Powderly, William, Spec, Andrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632270/
http://dx.doi.org/10.1093/ofid/ofx163.005
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author Lin, Charlotte
Kronen, Alyssa
Hsueh, Kevin
Powderly, William
Spec, Andrej
author_facet Lin, Charlotte
Kronen, Alyssa
Hsueh, Kevin
Powderly, William
Spec, Andrej
author_sort Lin, Charlotte
collection PubMed
description BACKGROUND: Candida bloodstream infections (CBSI) continue to be associated with high mortality, despite changes in antifungal treatment and diagnostics. METHODS: All patients age 18 or greater with a first episode of CBSI by blood culture from 1/2002 to 1/2015, admitted to Barnes-Jewish Hospital, a tertiary referral hospital in St. Louis, MO, were included. We collected data on demographics, comorbidities, laboratory values, vital signs, indwelling devices, and medical treatments of interest from the electronic medical record. We analyzed the potential predictor variables using univariate logistic regression. Variables associated with mortality were considered for model inclusion. The final model was built using multivariable binary logistic regression. A predictive equation was created, and a receiver–operator curve (ROC) was calculated to determine the appropriate cut-off points and c-statistic. RESULTS: Of the 1873 episodes of CBSI identified, 789 (42%) resulted in death in 90 days. The variables included in this model were age (40–49: OR 0.463, 95% CI 0.291–0.736; 50–69: 0.542, 0.342–0.860; ≥70: 0.560, 0.400–0.785); history of CAD (1.616, 1.171–2.230), chronic liver disease (2.247, 1.327–3.806); maximum heart rate (1.496, 1.126–1.989) and temperature (0.537, 0.408–0.708); AST (1.817, 1.343–2.459) and platelet count (1.563, 1.178–2.073); the presence of ventilator (1.847, 1.321–2.582), urinary catheter (1.365, 1.008–1.847), two or more central lines (1.658, 1.020–2.694); removal of lines after positive culture (0.259, 0.181–0.370); ophthalmology consult during admission (0.441, 0.329–0.592); thoracentesis/chest tube (3.827, 1.550–9.448); diagnosis of secondary malignancy (2.131, 1.488–3.053); whether antimetabolites (2.119, 1.353–3.318), dapsone (4.507, 1.450–14.012), linezolid (1.605, 1.059–2.435), quinolones (1.384, 0.998–1.920) were ordered 90 days before positive culture. An ROC curve was calculated with an internal c-statistic of 0.806. CONCLUSION: We created a risk predictive model for 90-day mortality in patients with CBSI, with 81% probability of predicting mortality. This model can lead to development of point-of-care applications to aid decision-making regarding escalation/de-escalation of care. DISCLOSURES: W. Powderly, Merck: Grant Investigator and Scientific Advisor, Consulting fee and Research grant Gilead: Scientific Advisor, Consulting fee Astellas: Grant Investigator, Research grant A. Spec, Astellas: Grant Investigator, Grant recipient
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spelling pubmed-56322702017-10-12 Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections Lin, Charlotte Kronen, Alyssa Hsueh, Kevin Powderly, William Spec, Andrej Open Forum Infect Dis Abstracts BACKGROUND: Candida bloodstream infections (CBSI) continue to be associated with high mortality, despite changes in antifungal treatment and diagnostics. METHODS: All patients age 18 or greater with a first episode of CBSI by blood culture from 1/2002 to 1/2015, admitted to Barnes-Jewish Hospital, a tertiary referral hospital in St. Louis, MO, were included. We collected data on demographics, comorbidities, laboratory values, vital signs, indwelling devices, and medical treatments of interest from the electronic medical record. We analyzed the potential predictor variables using univariate logistic regression. Variables associated with mortality were considered for model inclusion. The final model was built using multivariable binary logistic regression. A predictive equation was created, and a receiver–operator curve (ROC) was calculated to determine the appropriate cut-off points and c-statistic. RESULTS: Of the 1873 episodes of CBSI identified, 789 (42%) resulted in death in 90 days. The variables included in this model were age (40–49: OR 0.463, 95% CI 0.291–0.736; 50–69: 0.542, 0.342–0.860; ≥70: 0.560, 0.400–0.785); history of CAD (1.616, 1.171–2.230), chronic liver disease (2.247, 1.327–3.806); maximum heart rate (1.496, 1.126–1.989) and temperature (0.537, 0.408–0.708); AST (1.817, 1.343–2.459) and platelet count (1.563, 1.178–2.073); the presence of ventilator (1.847, 1.321–2.582), urinary catheter (1.365, 1.008–1.847), two or more central lines (1.658, 1.020–2.694); removal of lines after positive culture (0.259, 0.181–0.370); ophthalmology consult during admission (0.441, 0.329–0.592); thoracentesis/chest tube (3.827, 1.550–9.448); diagnosis of secondary malignancy (2.131, 1.488–3.053); whether antimetabolites (2.119, 1.353–3.318), dapsone (4.507, 1.450–14.012), linezolid (1.605, 1.059–2.435), quinolones (1.384, 0.998–1.920) were ordered 90 days before positive culture. An ROC curve was calculated with an internal c-statistic of 0.806. CONCLUSION: We created a risk predictive model for 90-day mortality in patients with CBSI, with 81% probability of predicting mortality. This model can lead to development of point-of-care applications to aid decision-making regarding escalation/de-escalation of care. DISCLOSURES: W. Powderly, Merck: Grant Investigator and Scientific Advisor, Consulting fee and Research grant Gilead: Scientific Advisor, Consulting fee Astellas: Grant Investigator, Research grant A. Spec, Astellas: Grant Investigator, Grant recipient Oxford University Press 2017-10-04 /pmc/articles/PMC5632270/ http://dx.doi.org/10.1093/ofid/ofx163.005 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Lin, Charlotte
Kronen, Alyssa
Hsueh, Kevin
Powderly, William
Spec, Andrej
Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections
title Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections
title_full Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections
title_fullStr Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections
title_full_unstemmed Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections
title_short Risk Predictive Model for 90-Day Mortality in Candida Bloodstream Infections
title_sort risk predictive model for 90-day mortality in candida bloodstream infections
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632270/
http://dx.doi.org/10.1093/ofid/ofx163.005
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