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Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study
C Keighley1,2,3, S C-A Chen4,5,6, D Marriott7
1Centre for Infectious Diseases and Microbiology Laboratory Services, ICPMR, New South Wales Health Pathology, Westmead Hospital, Darcy Rd, 3rd Level, ICPMR Building, Westmead, Sydney, New South Wales, 2145, Australia. Caitlin.keighley@sydney.edu.au.
Mortality in candidaemia (fungal blood infection) remains high. A new risk score helps predict 30-day mortality, aiding clinical decisions for patients with this serious infection.
Area of Science:
- Infectious Diseases
- Clinical Epidemiology
- Medical Informatics
Background:
- Candidaemia is a serious bloodstream infection with significant mortality rates.
- Previous studies identified mortality predictors but lacked a validated predictive model.
- This study aimed to update the epidemiology of candidaemia and develop a predictive tool.
Purpose of the Study:
- To describe the current epidemiology of candidaemia in Australia.
- To identify predictors of 30-day all-cause mortality.
- To develop and validate a clinical risk prediction model for candidaemia mortality.
Main Methods:
- Prospective study of adult candidaemia patients across eight Australian institutions over 12 months.
- Multivariate analysis of clinical and laboratory variables at diagnosis to identify mortality predictors.
- Development and validation of a risk score using receiver operating characteristic curves and a historical dataset.
Main Results:
- A total of 133 patients were included; 31% experienced 30-day all-cause mortality.
- Factors associated with increased mortality included older age, ICU admission, and specific comorbidities.
- A validated risk score was developed, stratifying patients into low (<20%) and high (≥20%) predicted 30-day mortality risk.
Conclusions:
- Candidaemia continues to be associated with high mortality.
- A simple, validated risk score is presented to aid in stratifying patient mortality risk at diagnosis.
- The model's ease of integration into decision support systems warrants further validation.
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