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Statins in Candidemia: clinical outcomes from a matched cohort study
BACKGROUND: HMG CoA reductase inhibitors (statins) in patients with bacteremic sepsis have shown significant survival benefits in several studies. There is no data on the effect of statins in candidemic patients, however in-vitro models suggest that statins interfere with ergesterol formation in the...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2894022/ https://www.ncbi.nlm.nih.gov/pubmed/20525374 http://dx.doi.org/10.1186/1471-2334-10-152 |
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author | Forrest, Graeme N Kopack, Angela M Perencevich, Eli N |
author_facet | Forrest, Graeme N Kopack, Angela M Perencevich, Eli N |
author_sort | Forrest, Graeme N |
collection | PubMed |
description | BACKGROUND: HMG CoA reductase inhibitors (statins) in patients with bacteremic sepsis have shown significant survival benefits in several studies. There is no data on the effect of statins in candidemic patients, however in-vitro models suggest that statins interfere with ergesterol formation in the wall of yeasts. METHODS: This retrospective matched- cohort study from 1/2003 to 12/2006 evaluated the effects of statins on patients with candidemia within intensive care units. Statin-users had candidemia as a cause of their systemic inflammatory response and were on statins throughout their antifungal therapy, while non-statin users were matched based on age +/- 5 years and co-morbid factors. Primary analysis was 30-day survival or discharge using bivariable comparisons. Multivariable comparisons were completed using conditional logistic regression. All variables with a p-value less than 0.10 in the bivariable comparisons were considered for inclusion in the conditional logistic model. RESULTS: There were 15 statin-users and 30 non-statin users that met inclusion criteria, all with similar demographics and co-morbid conditions except the statin group had more coronary artery disease (P < 0.01) and peripheral vascular disease (P = 0.03) and lower median APCAHE II scores (14.6 vs 17, p = 0.03). There were no differences in duration of candidemia, antifungal therapy or Candida species between the groups. Statins were associated with lower mortality on bivariable (OR 0.09, 95% CI 0.11-0.75, p = 0.03) and multivariable (OR 0.22, 95% CI 0.02-2.4, p = 0.21) analyses compared to controls; although, in the latter the protective effect lacked statistical signficance. CONCLUSION: In our small, single-center matched-cohort study, statins may provide a survival benefit in candidemia, however further studies are warranted to validate and further explore this association. |
format | Text |
id | pubmed-2894022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28940222010-06-30 Statins in Candidemia: clinical outcomes from a matched cohort study Forrest, Graeme N Kopack, Angela M Perencevich, Eli N BMC Infect Dis Research Article BACKGROUND: HMG CoA reductase inhibitors (statins) in patients with bacteremic sepsis have shown significant survival benefits in several studies. There is no data on the effect of statins in candidemic patients, however in-vitro models suggest that statins interfere with ergesterol formation in the wall of yeasts. METHODS: This retrospective matched- cohort study from 1/2003 to 12/2006 evaluated the effects of statins on patients with candidemia within intensive care units. Statin-users had candidemia as a cause of their systemic inflammatory response and were on statins throughout their antifungal therapy, while non-statin users were matched based on age +/- 5 years and co-morbid factors. Primary analysis was 30-day survival or discharge using bivariable comparisons. Multivariable comparisons were completed using conditional logistic regression. All variables with a p-value less than 0.10 in the bivariable comparisons were considered for inclusion in the conditional logistic model. RESULTS: There were 15 statin-users and 30 non-statin users that met inclusion criteria, all with similar demographics and co-morbid conditions except the statin group had more coronary artery disease (P < 0.01) and peripheral vascular disease (P = 0.03) and lower median APCAHE II scores (14.6 vs 17, p = 0.03). There were no differences in duration of candidemia, antifungal therapy or Candida species between the groups. Statins were associated with lower mortality on bivariable (OR 0.09, 95% CI 0.11-0.75, p = 0.03) and multivariable (OR 0.22, 95% CI 0.02-2.4, p = 0.21) analyses compared to controls; although, in the latter the protective effect lacked statistical signficance. CONCLUSION: In our small, single-center matched-cohort study, statins may provide a survival benefit in candidemia, however further studies are warranted to validate and further explore this association. BioMed Central 2010-06-04 /pmc/articles/PMC2894022/ /pubmed/20525374 http://dx.doi.org/10.1186/1471-2334-10-152 Text en Copyright ©2010 Forrest et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Forrest, Graeme N Kopack, Angela M Perencevich, Eli N Statins in Candidemia: clinical outcomes from a matched cohort study |
title | Statins in Candidemia: clinical outcomes from a matched cohort study |
title_full | Statins in Candidemia: clinical outcomes from a matched cohort study |
title_fullStr | Statins in Candidemia: clinical outcomes from a matched cohort study |
title_full_unstemmed | Statins in Candidemia: clinical outcomes from a matched cohort study |
title_short | Statins in Candidemia: clinical outcomes from a matched cohort study |
title_sort | statins in candidemia: clinical outcomes from a matched cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2894022/ https://www.ncbi.nlm.nih.gov/pubmed/20525374 http://dx.doi.org/10.1186/1471-2334-10-152 |
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