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Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures

BACKGROUND: Sepsis represents a time-sensitive disease requiring early therapeutical intervention to avoid adverse patient outcomes. Rapid microbiological diagnosis is essential to investigate sepsis aetiological agents. The FAST™ system (Qvella, ON, Canada) provides a concentrated microbial suspens...

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Autores principales: Maddalena, Calvo, Giuseppe, Migliorisi, Perez, Marianna, Guido, Scalia, Stefania, Stefani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422792/
https://www.ncbi.nlm.nih.gov/pubmed/37568240
http://dx.doi.org/10.1186/s12941-023-00617-8
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author Maddalena, Calvo
Giuseppe, Migliorisi
Perez, Marianna
Guido, Scalia
Stefania, Stefani
author_facet Maddalena, Calvo
Giuseppe, Migliorisi
Perez, Marianna
Guido, Scalia
Stefania, Stefani
author_sort Maddalena, Calvo
collection PubMed
description BACKGROUND: Sepsis represents a time-sensitive disease requiring early therapeutical intervention to avoid adverse patient outcomes. Rapid microbiological diagnosis is essential to investigate sepsis aetiological agents. The FAST™ system (Qvella, ON, Canada) provides a concentrated microbial suspension, known as a Liquid Colony™ (LC), directly from positive blood samples (PBCs) in 30–40 min to perform rapid identification (ID) and antimicrobial susceptibility testing (AST). METHODS: Qvella’s FAST™ System and FAST PBC Prep cartridges were tested on PBCs from the Policlinico Hospital of Catania during a six-month study. Two millilitres of PBC were converted into an LC for rapid ID and AST using Bruker Biotyper Sirius MALDI and BD Phoenix systems. Standard of care (SOC) methods were used as a reference, requiring 48–72 h. Agreement between the innovative technology and the standard method was calculated. RESULTS: FAST System processing was performed on 100 monomicrobial PBCs. Median turnaround times from blood cultures flagging positive to ID and AST completion were 2 and 26 h respectively. Therefore, the LC procedure was 24 h faster than the median turnaround times for SOC methods. 100% ID identification concordance was observed across 48 Gram-negative bacteria, 42 Gram-positive bacteria and 11 yeast for the genus level. 78% of Gram-negative and 95% of Gram-positive bacteria were resistant to ≥ 2 antimicrobial agents, including 45% (15/33) carbapenem-resistant enteric Gram-negative bacteria and 90% (28/31) oxacillin-resistant staphylococci. An AST essential agreement of 100% was observed due to the absence of MIC discrepancies > 1-fold dilution. Categorical errors were not observed due to the absence of MIC categorization discordances. Yeast AST was not performed. CONCLUSIONS: The Qvella FAST System produces an LC that reliably reflects the MALDI spectra and phenotypic antimicrobial susceptibility profile of microbial cells growing in the blood culture. Timely processing of PBCs with the Qvella FAST System enables sepsis diagnostic confirmation 1 day sooner than the standard methods. In line with these results, it is vital now to focus attention on establishing best practices for incorporating this strategic tool into the clinical microbiology laboratory workflow.
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spelling pubmed-104227922023-08-13 Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures Maddalena, Calvo Giuseppe, Migliorisi Perez, Marianna Guido, Scalia Stefania, Stefani Ann Clin Microbiol Antimicrob Research BACKGROUND: Sepsis represents a time-sensitive disease requiring early therapeutical intervention to avoid adverse patient outcomes. Rapid microbiological diagnosis is essential to investigate sepsis aetiological agents. The FAST™ system (Qvella, ON, Canada) provides a concentrated microbial suspension, known as a Liquid Colony™ (LC), directly from positive blood samples (PBCs) in 30–40 min to perform rapid identification (ID) and antimicrobial susceptibility testing (AST). METHODS: Qvella’s FAST™ System and FAST PBC Prep cartridges were tested on PBCs from the Policlinico Hospital of Catania during a six-month study. Two millilitres of PBC were converted into an LC for rapid ID and AST using Bruker Biotyper Sirius MALDI and BD Phoenix systems. Standard of care (SOC) methods were used as a reference, requiring 48–72 h. Agreement between the innovative technology and the standard method was calculated. RESULTS: FAST System processing was performed on 100 monomicrobial PBCs. Median turnaround times from blood cultures flagging positive to ID and AST completion were 2 and 26 h respectively. Therefore, the LC procedure was 24 h faster than the median turnaround times for SOC methods. 100% ID identification concordance was observed across 48 Gram-negative bacteria, 42 Gram-positive bacteria and 11 yeast for the genus level. 78% of Gram-negative and 95% of Gram-positive bacteria were resistant to ≥ 2 antimicrobial agents, including 45% (15/33) carbapenem-resistant enteric Gram-negative bacteria and 90% (28/31) oxacillin-resistant staphylococci. An AST essential agreement of 100% was observed due to the absence of MIC discrepancies > 1-fold dilution. Categorical errors were not observed due to the absence of MIC categorization discordances. Yeast AST was not performed. CONCLUSIONS: The Qvella FAST System produces an LC that reliably reflects the MALDI spectra and phenotypic antimicrobial susceptibility profile of microbial cells growing in the blood culture. Timely processing of PBCs with the Qvella FAST System enables sepsis diagnostic confirmation 1 day sooner than the standard methods. In line with these results, it is vital now to focus attention on establishing best practices for incorporating this strategic tool into the clinical microbiology laboratory workflow. BioMed Central 2023-08-11 /pmc/articles/PMC10422792/ /pubmed/37568240 http://dx.doi.org/10.1186/s12941-023-00617-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Maddalena, Calvo
Giuseppe, Migliorisi
Perez, Marianna
Guido, Scalia
Stefania, Stefani
Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
title Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
title_full Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
title_fullStr Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
title_full_unstemmed Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
title_short Evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
title_sort evaluation of the liquid colony for identification and antimicrobial susceptibility testing directly from positive blood cultures
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422792/
https://www.ncbi.nlm.nih.gov/pubmed/37568240
http://dx.doi.org/10.1186/s12941-023-00617-8
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