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The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles

OBJECTIVES: With increasing antimicrobial resistance, rapid antimicrobial susceptibility testing (RAST) becomes important, especially in patients with bloodstream infections. EUCAST decided to develop a standardized rapid method, based on EUCAST disc diffusion, to offer susceptibility reports within...

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Autores principales: Jonasson, Emma, Matuschek, Erika, Kahlmeter, Gunnar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069491/
https://www.ncbi.nlm.nih.gov/pubmed/32016342
http://dx.doi.org/10.1093/jac/dkz548
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author Jonasson, Emma
Matuschek, Erika
Kahlmeter, Gunnar
author_facet Jonasson, Emma
Matuschek, Erika
Kahlmeter, Gunnar
author_sort Jonasson, Emma
collection PubMed
description OBJECTIVES: With increasing antimicrobial resistance, rapid antimicrobial susceptibility testing (RAST) becomes important, especially in patients with bloodstream infections. EUCAST decided to develop a standardized rapid method, based on EUCAST disc diffusion, to offer susceptibility reports within 4–8 h of a positive blood culture (BC). METHODS: BC bottles were spiked with clinical isolates (n = 332) of the seven most relevant sepsis pathogens with a variety of resistance mechanisms. RAST was performed directly from the bottle and zones read after 4, 6 and 8 h. Several variables were investigated, including the effect of using different BC bottles and of a 0–18 h delay between a positive signal and the performance of RAST. RESULTS: For five species, most inhibition zones could be read after 4 h. The proportion of results that could be interpreted increased from 75% at 4 h to 84% after 8 h. Categorical agreement against the reference method was good, with error rates of false susceptibility of 0.2%, 0.2% and 0.2% at 4, 6 and 8 h and false resistance of 1.2%, 0.2% and 0.1% at 4, 6 and 8 h, respectively. CONCLUSIONS: With the EUCAST RAST method, reliable AST results can be delivered within 4–8 h of positivity of BC bottles for seven important bloodstream infection pathogens. To reduce the occurrence of errors and to absorb the variability caused by using a non-standardized inoculum, material from different manufacturers and workflow-related delays, we have introduced an area in which interpretation is not permitted, the Area of Technical Uncertainty.
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spelling pubmed-70694912020-03-18 The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles Jonasson, Emma Matuschek, Erika Kahlmeter, Gunnar J Antimicrob Chemother Original Research OBJECTIVES: With increasing antimicrobial resistance, rapid antimicrobial susceptibility testing (RAST) becomes important, especially in patients with bloodstream infections. EUCAST decided to develop a standardized rapid method, based on EUCAST disc diffusion, to offer susceptibility reports within 4–8 h of a positive blood culture (BC). METHODS: BC bottles were spiked with clinical isolates (n = 332) of the seven most relevant sepsis pathogens with a variety of resistance mechanisms. RAST was performed directly from the bottle and zones read after 4, 6 and 8 h. Several variables were investigated, including the effect of using different BC bottles and of a 0–18 h delay between a positive signal and the performance of RAST. RESULTS: For five species, most inhibition zones could be read after 4 h. The proportion of results that could be interpreted increased from 75% at 4 h to 84% after 8 h. Categorical agreement against the reference method was good, with error rates of false susceptibility of 0.2%, 0.2% and 0.2% at 4, 6 and 8 h and false resistance of 1.2%, 0.2% and 0.1% at 4, 6 and 8 h, respectively. CONCLUSIONS: With the EUCAST RAST method, reliable AST results can be delivered within 4–8 h of positivity of BC bottles for seven important bloodstream infection pathogens. To reduce the occurrence of errors and to absorb the variability caused by using a non-standardized inoculum, material from different manufacturers and workflow-related delays, we have introduced an area in which interpretation is not permitted, the Area of Technical Uncertainty. Oxford University Press 2020-04 2020-02-04 /pmc/articles/PMC7069491/ /pubmed/32016342 http://dx.doi.org/10.1093/jac/dkz548 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Research
Jonasson, Emma
Matuschek, Erika
Kahlmeter, Gunnar
The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
title The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
title_full The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
title_fullStr The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
title_full_unstemmed The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
title_short The EUCAST rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
title_sort eucast rapid disc diffusion method for antimicrobial susceptibility testing directly from positive blood culture bottles
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069491/
https://www.ncbi.nlm.nih.gov/pubmed/32016342
http://dx.doi.org/10.1093/jac/dkz548
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