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Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles

Determination of the susceptibility profile of isolates of Candida from blood culture bottles is extremely important for correctly guiding patient pharmacotherapy. The aim of this study was to compare the results of analysis of Candida isolated directly from blood culture bottles by the VITEK MS MAL...

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Autores principales: Celestino de Souza, Ândrea, Goldani, Luciano Z., Roesch, Eliane Würdig, Lutz, Larissa, Barth, Patricia Orlandi, André de Souza Sampaio, Paulo, Aquino, Valério Rodrigues, Pereira, Dariane Castro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610690/
https://www.ncbi.nlm.nih.gov/pubmed/34824584
http://dx.doi.org/10.1155/2021/9364231
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author Celestino de Souza, Ândrea
Goldani, Luciano Z.
Roesch, Eliane Würdig
Lutz, Larissa
Barth, Patricia Orlandi
André de Souza Sampaio, Paulo
Aquino, Valério Rodrigues
Pereira, Dariane Castro
author_facet Celestino de Souza, Ândrea
Goldani, Luciano Z.
Roesch, Eliane Würdig
Lutz, Larissa
Barth, Patricia Orlandi
André de Souza Sampaio, Paulo
Aquino, Valério Rodrigues
Pereira, Dariane Castro
author_sort Celestino de Souza, Ândrea
collection PubMed
description Determination of the susceptibility profile of isolates of Candida from blood culture bottles is extremely important for correctly guiding patient pharmacotherapy. The aim of this study was to compare the results of analysis of Candida isolated directly from blood culture bottles by the VITEK MS MALDI-TOF identification system and the fluconazole disk diffusion assay with those of standard identification methods. Testing directly from the bottle allowed results 24 to 48 hours quicker than the standard method. There was a categorical agreement of 51.64% (47 of 91 samples) between the results of analysis directly from the bottle and analysis by the standard method. Regarding species identification, there was 96.15% agreement for Candida parapsilosis (25 of 26 samples). Categorical agreement between the rapid and standard disk diffusion methods was 95%, and the agreement between the rapid disk diffusion method and the broth microdilution method was 97%. Only minor errors in the rapid method were observed: 3 (5%) in the standard disk diffusion method and 2 (3%) in the broth microdilution method. Our study concluded that the rapid disk diffusion method for fluconazole is a fast, easy, reproducible, and consistent method. Its timely implementation for testing antifungal agents in the clinical microbiology laboratory can help reduce profile release times, thus helping to determine the most appropriate antifungal treatment.
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spelling pubmed-86106902021-11-24 Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles Celestino de Souza, Ândrea Goldani, Luciano Z. Roesch, Eliane Würdig Lutz, Larissa Barth, Patricia Orlandi André de Souza Sampaio, Paulo Aquino, Valério Rodrigues Pereira, Dariane Castro Int J Microbiol Research Article Determination of the susceptibility profile of isolates of Candida from blood culture bottles is extremely important for correctly guiding patient pharmacotherapy. The aim of this study was to compare the results of analysis of Candida isolated directly from blood culture bottles by the VITEK MS MALDI-TOF identification system and the fluconazole disk diffusion assay with those of standard identification methods. Testing directly from the bottle allowed results 24 to 48 hours quicker than the standard method. There was a categorical agreement of 51.64% (47 of 91 samples) between the results of analysis directly from the bottle and analysis by the standard method. Regarding species identification, there was 96.15% agreement for Candida parapsilosis (25 of 26 samples). Categorical agreement between the rapid and standard disk diffusion methods was 95%, and the agreement between the rapid disk diffusion method and the broth microdilution method was 97%. Only minor errors in the rapid method were observed: 3 (5%) in the standard disk diffusion method and 2 (3%) in the broth microdilution method. Our study concluded that the rapid disk diffusion method for fluconazole is a fast, easy, reproducible, and consistent method. Its timely implementation for testing antifungal agents in the clinical microbiology laboratory can help reduce profile release times, thus helping to determine the most appropriate antifungal treatment. Hindawi 2021-11-16 /pmc/articles/PMC8610690/ /pubmed/34824584 http://dx.doi.org/10.1155/2021/9364231 Text en Copyright © 2021 Ândrea Celestino de Souza et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Celestino de Souza, Ândrea
Goldani, Luciano Z.
Roesch, Eliane Würdig
Lutz, Larissa
Barth, Patricia Orlandi
André de Souza Sampaio, Paulo
Aquino, Valério Rodrigues
Pereira, Dariane Castro
Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles
title Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles
title_full Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles
title_fullStr Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles
title_full_unstemmed Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles
title_short Evaluation of Identification and Susceptibility for Candida Spp. Isolated Directly from Positive Blood Culture Bottles
title_sort evaluation of identification and susceptibility for candida spp. isolated directly from positive blood culture bottles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610690/
https://www.ncbi.nlm.nih.gov/pubmed/34824584
http://dx.doi.org/10.1155/2021/9364231
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