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306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood
BACKGROUND: Diagnosis of bloodstream infections (BSI) and treatment with appropriate antimicrobials is dependent upon fast and accurate information about the microorganism(s). The long time taken for a blood culture result, microbial identification and antimicrobial susceptibility testing (AST), can...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777626/ http://dx.doi.org/10.1093/ofid/ofaa439.349 |
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author | Kadoom, Aram Lockhart, Daniel Kadoom, Yassar Fauci, Sonia La Rodgers, Andrew Turner, James Bennett, Helen Jay, Paul Thaker, Sumi Mullen, William |
author_facet | Kadoom, Aram Lockhart, Daniel Kadoom, Yassar Fauci, Sonia La Rodgers, Andrew Turner, James Bennett, Helen Jay, Paul Thaker, Sumi Mullen, William |
author_sort | Kadoom, Aram |
collection | PubMed |
description | BACKGROUND: Diagnosis of bloodstream infections (BSI) and treatment with appropriate antimicrobials is dependent upon fast and accurate information about the microorganism(s). The long time taken for a blood culture result, microbial identification and antimicrobial susceptibility testing (AST), can lead to poor antimicrobial stewardship. Many antimicrobial change decisions are based on the results of a Gram stain, with this being the first result available. Having results from a rapid test, direct from blood, which can confirm BSI and characterize the causative pathogen(s) would provide an improvement in antimicrobial stewardship and patient care. METHODS: SepsiSTAT(®) is a rapid molecular test, developed by Momentum Bioscience Ltd, for the detection of BSI, with a time-to-result of < 4 hours. It uses whole blood to detect viable microorganisms whilst also providing molecular characterization. Microorganisms are extracted from the sample using a proprietary process involving capture on magnetic microbeads. This is followed by Enzymatic Template Generation and Amplification (ETGA(®)) for ultra-sensitive, universal detection of viable bacterial and fungal species, based on detecting microbial DNA polymerase activity. Simultaneously, molecular characterization also provides genus/species identification. The detection limits of SepsiSTAT(®) were evaluated for a broad panel of microorganisms, representing 80% of BSI reported to Public Health England (2018 report). RESULTS: These results show a median detection limit (n=5) of < 10 cfu/mL in blood for microorganisms representing 77.4% of reported BSI, including key organisms such as E. coli, S. epidermidis and C. albicans. Notably, S. aureus, P. aeruginosa, E. faecalis, P. mirabilis and S. marcescens were all detected at < 1 cfu/mL. CONCLUSION: SepsiSTAT(®) can detect microbes in low numbers, with a turnaround time substantially faster than traditional blood culture. Future development will aim to shorten time-to-results to < 3 hours, further benefiting patient outcomes and antimicrobial stewardship. Future studies in a clinical setting will seek to further demonstrate the efficacy and rapid turnaround time of the SepsiSTAT(®) test. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-7777626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77776262021-01-07 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood Kadoom, Aram Lockhart, Daniel Kadoom, Yassar Fauci, Sonia La Rodgers, Andrew Turner, James Bennett, Helen Jay, Paul Thaker, Sumi Mullen, William Open Forum Infect Dis Poster Abstracts BACKGROUND: Diagnosis of bloodstream infections (BSI) and treatment with appropriate antimicrobials is dependent upon fast and accurate information about the microorganism(s). The long time taken for a blood culture result, microbial identification and antimicrobial susceptibility testing (AST), can lead to poor antimicrobial stewardship. Many antimicrobial change decisions are based on the results of a Gram stain, with this being the first result available. Having results from a rapid test, direct from blood, which can confirm BSI and characterize the causative pathogen(s) would provide an improvement in antimicrobial stewardship and patient care. METHODS: SepsiSTAT(®) is a rapid molecular test, developed by Momentum Bioscience Ltd, for the detection of BSI, with a time-to-result of < 4 hours. It uses whole blood to detect viable microorganisms whilst also providing molecular characterization. Microorganisms are extracted from the sample using a proprietary process involving capture on magnetic microbeads. This is followed by Enzymatic Template Generation and Amplification (ETGA(®)) for ultra-sensitive, universal detection of viable bacterial and fungal species, based on detecting microbial DNA polymerase activity. Simultaneously, molecular characterization also provides genus/species identification. The detection limits of SepsiSTAT(®) were evaluated for a broad panel of microorganisms, representing 80% of BSI reported to Public Health England (2018 report). RESULTS: These results show a median detection limit (n=5) of < 10 cfu/mL in blood for microorganisms representing 77.4% of reported BSI, including key organisms such as E. coli, S. epidermidis and C. albicans. Notably, S. aureus, P. aeruginosa, E. faecalis, P. mirabilis and S. marcescens were all detected at < 1 cfu/mL. CONCLUSION: SepsiSTAT(®) can detect microbes in low numbers, with a turnaround time substantially faster than traditional blood culture. Future development will aim to shorten time-to-results to < 3 hours, further benefiting patient outcomes and antimicrobial stewardship. Future studies in a clinical setting will seek to further demonstrate the efficacy and rapid turnaround time of the SepsiSTAT(®) test. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7777626/ http://dx.doi.org/10.1093/ofid/ofaa439.349 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 Kadoom, Aram Lockhart, Daniel Kadoom, Yassar Fauci, Sonia La Rodgers, Andrew Turner, James Bennett, Helen Jay, Paul Thaker, Sumi Mullen, William 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood |
title | 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood |
title_full | 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood |
title_fullStr | 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood |
title_full_unstemmed | 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood |
title_short | 306. Rapid Detection Of Bloodstream Infections, Including Molecular Characterization, From Whole Blood |
title_sort | 306. rapid detection of bloodstream infections, including molecular characterization, from whole blood |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777626/ http://dx.doi.org/10.1093/ofid/ofaa439.349 |
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