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84. T2Candida Panel Use Evaluation: a Quality Improvement Project

BACKGROUND: Invasive candidiasis is a life-threatening infection with 40% mortality despite antifungal therapy[1] A retrospective chart review of results from our T2Candida Panels from March 2019 to March 2020 was conducted. We compared demographics, co-morbidities, days of antifungal use, length of...

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Autores principales: Schwarz, Erika Reategui, Rana, Meenakshi, Chasan, Rachel, Gitman, Melissa R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776192/
http://dx.doi.org/10.1093/ofid/ofaa439.129
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author Schwarz, Erika Reategui
Rana, Meenakshi
Chasan, Rachel
Gitman, Melissa R
author_facet Schwarz, Erika Reategui
Rana, Meenakshi
Chasan, Rachel
Gitman, Melissa R
author_sort Schwarz, Erika Reategui
collection PubMed
description BACKGROUND: Invasive candidiasis is a life-threatening infection with 40% mortality despite antifungal therapy[1] A retrospective chart review of results from our T2Candida Panels from March 2019 to March 2020 was conducted. We compared demographics, co-morbidities, days of antifungal use, length of stay (LOS) and mortality in patients with positive and negative assays. RESULTS: 271 assays were performed, 27 were positive and were compared to 81 negatives. Baseline demographics and co-morbidities were similar in both groups. All patients tested had >1 risk factor for candidemia. 78% were positive for C. albicans/C. tropicalis and 11% positive for C. glabrata/C. krusei and C. parapsilosis respectively. Blood cultures were positive in 8 individuals, of which 5 had a positive assay; among the other 3, one grew C. auris. All species in the T2Candida matched the blood cultures when available. β-D-glucan was positive in 82% of patients with positive T2 results vs 46% in the T2 negative group (p = 0.016). Antifungal administration within the time of assay collection was 54% in the negative group vs 74% in the positive group (p = 0.030). Mean duration of antifungal use were significantly lower in the negative group than the positive group (5.98 vs 17.55 days, p = 0.04). Demographics and Comorbidities [Image: see text] Outcomes [Image: see text] Cultures [Image: see text] CONCLUSION: T2Candida was an effective diagnostic and antimicrobial stewardship tool, leading to testing in high risk patients and reducing unnecessary antifungal use. Additional education is required for improved ordering of concurrent blood cultures. Negative results should be interpreted with caution in suspected invasive candidiasis with consideration for species not included in the panel. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-77761922021-01-07 84. T2Candida Panel Use Evaluation: a Quality Improvement Project Schwarz, Erika Reategui Rana, Meenakshi Chasan, Rachel Gitman, Melissa R Open Forum Infect Dis Poster Abstracts BACKGROUND: Invasive candidiasis is a life-threatening infection with 40% mortality despite antifungal therapy[1] A retrospective chart review of results from our T2Candida Panels from March 2019 to March 2020 was conducted. We compared demographics, co-morbidities, days of antifungal use, length of stay (LOS) and mortality in patients with positive and negative assays. RESULTS: 271 assays were performed, 27 were positive and were compared to 81 negatives. Baseline demographics and co-morbidities were similar in both groups. All patients tested had >1 risk factor for candidemia. 78% were positive for C. albicans/C. tropicalis and 11% positive for C. glabrata/C. krusei and C. parapsilosis respectively. Blood cultures were positive in 8 individuals, of which 5 had a positive assay; among the other 3, one grew C. auris. All species in the T2Candida matched the blood cultures when available. β-D-glucan was positive in 82% of patients with positive T2 results vs 46% in the T2 negative group (p = 0.016). Antifungal administration within the time of assay collection was 54% in the negative group vs 74% in the positive group (p = 0.030). Mean duration of antifungal use were significantly lower in the negative group than the positive group (5.98 vs 17.55 days, p = 0.04). Demographics and Comorbidities [Image: see text] Outcomes [Image: see text] Cultures [Image: see text] CONCLUSION: T2Candida was an effective diagnostic and antimicrobial stewardship tool, leading to testing in high risk patients and reducing unnecessary antifungal use. Additional education is required for improved ordering of concurrent blood cultures. Negative results should be interpreted with caution in suspected invasive candidiasis with consideration for species not included in the panel. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7776192/ http://dx.doi.org/10.1093/ofid/ofaa439.129 Text en © The Author 2020. 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 Poster Abstracts
Schwarz, Erika Reategui
Rana, Meenakshi
Chasan, Rachel
Gitman, Melissa R
84. T2Candida Panel Use Evaluation: a Quality Improvement Project
title 84. T2Candida Panel Use Evaluation: a Quality Improvement Project
title_full 84. T2Candida Panel Use Evaluation: a Quality Improvement Project
title_fullStr 84. T2Candida Panel Use Evaluation: a Quality Improvement Project
title_full_unstemmed 84. T2Candida Panel Use Evaluation: a Quality Improvement Project
title_short 84. T2Candida Panel Use Evaluation: a Quality Improvement Project
title_sort 84. t2candida panel use evaluation: a quality improvement project
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776192/
http://dx.doi.org/10.1093/ofid/ofaa439.129
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