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Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study
BACKGROUND: Candidaemia is associated with high mortality. Variables associated with mortality have been published previously, but not developed into a risk predictive model for mortality. We sought to describe the current epidemiology of candidaemia in Australia, analyse predictors of 30-day all-ca...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528341/ https://www.ncbi.nlm.nih.gov/pubmed/31113382 http://dx.doi.org/10.1186/s12879-019-4065-5 |
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author | Keighley, C. Chen, S. C-A. Marriott, D. Pope, A. Chapman, B. Kennedy, K. Bak, N. Underwood, N. Wilson, H. L. McDonald, K. Darvall, J. Halliday, C. Kidd, S. Nguyen, Q. Hajkowicz, K. Sorrell, T. C. Van Hal, S. Slavin, M. A. |
author_facet | Keighley, C. Chen, S. C-A. Marriott, D. Pope, A. Chapman, B. Kennedy, K. Bak, N. Underwood, N. Wilson, H. L. McDonald, K. Darvall, J. Halliday, C. Kidd, S. Nguyen, Q. Hajkowicz, K. Sorrell, T. C. Van Hal, S. Slavin, M. A. |
author_sort | Keighley, C. |
collection | PubMed |
description | BACKGROUND: Candidaemia is associated with high mortality. Variables associated with mortality have been published previously, but not developed into a risk predictive model for mortality. We sought to describe the current epidemiology of candidaemia in Australia, analyse predictors of 30-day all-cause mortality, and develop and validate a mortality risk predictive model. METHODS: Adults with candidaemia were studied prospectively over 12 months at eight institutions. Clinical and laboratory variables at time of blood culture-positivity were subject to multivariate analysis for association with 30-day all-cause mortality. A predictive score for mortality was examined by area under receiver operator characteristic curves and a historical data set was used for validation. RESULTS: The median age of 133 patients with candidaemia was 62 years; 76 (57%) were male and 57 (43%) were female. Co-morbidities included underlying haematologic malignancy (n = 20; 15%), and solid organ malignancy in (n = 25; 19%); 55 (41%) were in an intensive care unit (ICU). Non-albicans Candida spp. accounted for 61% of cases (81/133). All-cause 30-day mortality was 31%. A gastrointestinal or unknown source was associated with higher overall mortality than an intravascular or urologic source (p < 0.01). A risk predictive score based on age > 65 years, ICU admission, chronic organ dysfunction, preceding surgery within 30 days, haematological malignancy, source of candidaemia and antibiotic therapy for ≥10 days stratified patients into < 20% or ≥ 20% predicted mortality. The model retained accuracy when validated against a historical dataset (n = 741). CONCLUSIONS: Mortality in patients with candidaemia remains high. A simple mortality risk predictive score stratifying patients with candidaemia into < 20% and ≥ 20% 30-day mortality is presented. This model uses information available at time of candidaemia diagnosis is easy to incorporate into decision support systems. Further validation of this model is warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4065-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6528341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65283412019-05-28 Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study Keighley, C. Chen, S. C-A. Marriott, D. Pope, A. Chapman, B. Kennedy, K. Bak, N. Underwood, N. Wilson, H. L. McDonald, K. Darvall, J. Halliday, C. Kidd, S. Nguyen, Q. Hajkowicz, K. Sorrell, T. C. Van Hal, S. Slavin, M. A. BMC Infect Dis Research Article BACKGROUND: Candidaemia is associated with high mortality. Variables associated with mortality have been published previously, but not developed into a risk predictive model for mortality. We sought to describe the current epidemiology of candidaemia in Australia, analyse predictors of 30-day all-cause mortality, and develop and validate a mortality risk predictive model. METHODS: Adults with candidaemia were studied prospectively over 12 months at eight institutions. Clinical and laboratory variables at time of blood culture-positivity were subject to multivariate analysis for association with 30-day all-cause mortality. A predictive score for mortality was examined by area under receiver operator characteristic curves and a historical data set was used for validation. RESULTS: The median age of 133 patients with candidaemia was 62 years; 76 (57%) were male and 57 (43%) were female. Co-morbidities included underlying haematologic malignancy (n = 20; 15%), and solid organ malignancy in (n = 25; 19%); 55 (41%) were in an intensive care unit (ICU). Non-albicans Candida spp. accounted for 61% of cases (81/133). All-cause 30-day mortality was 31%. A gastrointestinal or unknown source was associated with higher overall mortality than an intravascular or urologic source (p < 0.01). A risk predictive score based on age > 65 years, ICU admission, chronic organ dysfunction, preceding surgery within 30 days, haematological malignancy, source of candidaemia and antibiotic therapy for ≥10 days stratified patients into < 20% or ≥ 20% predicted mortality. The model retained accuracy when validated against a historical dataset (n = 741). CONCLUSIONS: Mortality in patients with candidaemia remains high. A simple mortality risk predictive score stratifying patients with candidaemia into < 20% and ≥ 20% 30-day mortality is presented. This model uses information available at time of candidaemia diagnosis is easy to incorporate into decision support systems. Further validation of this model is warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4065-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-21 /pmc/articles/PMC6528341/ /pubmed/31113382 http://dx.doi.org/10.1186/s12879-019-4065-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Keighley, C. Chen, S. C-A. Marriott, D. Pope, A. Chapman, B. Kennedy, K. Bak, N. Underwood, N. Wilson, H. L. McDonald, K. Darvall, J. Halliday, C. Kidd, S. Nguyen, Q. Hajkowicz, K. Sorrell, T. C. Van Hal, S. Slavin, M. A. Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
title | Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
title_full | Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
title_fullStr | Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
title_full_unstemmed | Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
title_short | Candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
title_sort | candidaemia and a risk predictive model for overall mortality: a prospective multicentre study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528341/ https://www.ncbi.nlm.nih.gov/pubmed/31113382 http://dx.doi.org/10.1186/s12879-019-4065-5 |
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