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935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata

BACKGROUND: Saprochaete clavata, an ascomycetous yeast intrinsically resistant to echinocandins, is a rare yet emerging pathogen associated with invasive infections in immunosuppressed patients, particularly those with haematological malignancies. It is commonly misidentified as the closely-related...

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Autores principales: Chan, Xin Hui S, Cubillo-Garcia, Cristina, Ali, Shanom, Gorton, Rebecca, Rhodes, Johanna, Choy, Bennett, Fisher, Matthew, Thomson, Kirsty, Gant, Vanya, Stone, Neil, Satta, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8644122/
http://dx.doi.org/10.1093/ofid/ofab466.1130
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author Chan, Xin Hui S
Cubillo-Garcia, Cristina
Ali, Shanom
Gorton, Rebecca
Rhodes, Johanna
Choy, Bennett
Fisher, Matthew
Thomson, Kirsty
Gant, Vanya
Stone, Neil
Satta, Giovanni
author_facet Chan, Xin Hui S
Cubillo-Garcia, Cristina
Ali, Shanom
Gorton, Rebecca
Rhodes, Johanna
Choy, Bennett
Fisher, Matthew
Thomson, Kirsty
Gant, Vanya
Stone, Neil
Satta, Giovanni
author_sort Chan, Xin Hui S
collection PubMed
description BACKGROUND: Saprochaete clavata, an ascomycetous yeast intrinsically resistant to echinocandins, is a rare yet emerging pathogen associated with invasive infections in immunosuppressed patients, particularly those with haematological malignancies. It is commonly misidentified as the closely-related S. capitata. Outbreaks have been associated with a high mortality rate of >50%, due in part to delayed diagnosis and resistance to commonly-used antifungals. Environmental source identification is challenging, although dishwashers and milk flasks have been implicated in previous hospital clusters. METHODS: We describe a cluster of five haematology-oncology patients with disseminated S. clavata infections between April 2020 and April 2021 following current or recent admissions to the same ward. RESULTS: All had prolonged (median=24 days, range=9-210) and profound immunosuppression from chemotherapy and/or stem cell transplantation for acute myeloid leukaemia (n=3) or lymphoma (n=2) at the time of culture positivity. Four were severely neutropaenic (median=0.08/mm(3), range=0.01-0.26). Median patient age was 62 years (range=58-73). S. clavata was isolated from blood (n=3), urine (n=2), and liver tissue (n=1) samples. Whole genome sequencing of these isolates was performed to confirm the presence of an outbreak. All patients received empirical treatment with intravenous caspofungin before culture-guided therapy with intravenous liposomal amphotericin B +/- oral flucytosine. Two of the five patients died although both had advanced refractory malignancy. Detailed environmental sampling of fridges/freezers, drains, and vents in patient rooms and clean areas for handling or storage of food and medication failed to identify a clear point source despite isolation of multiple environmental organisms. No further cases have emerged after intensification of the cleaning regimen in these areas. CONCLUSION: Our experience highlights the emerging threat of drug-resistant yeasts particularly in the immunocompromised. Management of such outbreaks requires a multidisciplinary approach incorporating antifungal stewardship, infection control, and environmental microbiology, alongside close clinical liaison between haemato-oncologists and infection specialists. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-86441222021-12-06 935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata Chan, Xin Hui S Cubillo-Garcia, Cristina Ali, Shanom Gorton, Rebecca Rhodes, Johanna Choy, Bennett Fisher, Matthew Thomson, Kirsty Gant, Vanya Stone, Neil Satta, Giovanni Open Forum Infect Dis Poster Abstracts BACKGROUND: Saprochaete clavata, an ascomycetous yeast intrinsically resistant to echinocandins, is a rare yet emerging pathogen associated with invasive infections in immunosuppressed patients, particularly those with haematological malignancies. It is commonly misidentified as the closely-related S. capitata. Outbreaks have been associated with a high mortality rate of >50%, due in part to delayed diagnosis and resistance to commonly-used antifungals. Environmental source identification is challenging, although dishwashers and milk flasks have been implicated in previous hospital clusters. METHODS: We describe a cluster of five haematology-oncology patients with disseminated S. clavata infections between April 2020 and April 2021 following current or recent admissions to the same ward. RESULTS: All had prolonged (median=24 days, range=9-210) and profound immunosuppression from chemotherapy and/or stem cell transplantation for acute myeloid leukaemia (n=3) or lymphoma (n=2) at the time of culture positivity. Four were severely neutropaenic (median=0.08/mm(3), range=0.01-0.26). Median patient age was 62 years (range=58-73). S. clavata was isolated from blood (n=3), urine (n=2), and liver tissue (n=1) samples. Whole genome sequencing of these isolates was performed to confirm the presence of an outbreak. All patients received empirical treatment with intravenous caspofungin before culture-guided therapy with intravenous liposomal amphotericin B +/- oral flucytosine. Two of the five patients died although both had advanced refractory malignancy. Detailed environmental sampling of fridges/freezers, drains, and vents in patient rooms and clean areas for handling or storage of food and medication failed to identify a clear point source despite isolation of multiple environmental organisms. No further cases have emerged after intensification of the cleaning regimen in these areas. CONCLUSION: Our experience highlights the emerging threat of drug-resistant yeasts particularly in the immunocompromised. Management of such outbreaks requires a multidisciplinary approach incorporating antifungal stewardship, infection control, and environmental microbiology, alongside close clinical liaison between haemato-oncologists and infection specialists. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2021-12-04 /pmc/articles/PMC8644122/ http://dx.doi.org/10.1093/ofid/ofab466.1130 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Abstracts
Chan, Xin Hui S
Cubillo-Garcia, Cristina
Ali, Shanom
Gorton, Rebecca
Rhodes, Johanna
Choy, Bennett
Fisher, Matthew
Thomson, Kirsty
Gant, Vanya
Stone, Neil
Satta, Giovanni
935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata
title 935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata
title_full 935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata
title_fullStr 935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata
title_full_unstemmed 935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata
title_short 935. A Hospital Cluster of the Emerging Drug-resistant Yeast Saprochaete clavata
title_sort 935. a hospital cluster of the emerging drug-resistant yeast saprochaete clavata
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8644122/
http://dx.doi.org/10.1093/ofid/ofab466.1130
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