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Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study

BACKGROUND: The BioFire® FilmArray® Blood Culture Identification Panel 1 (BF-FA-BCIP) detects microorganisms with high accuracy in positive blood cultures (BC) – a key step in the management of patients with suspected bacteraemia. We aimed to compare the time to optimal antimicrobial therapy (OAT) f...

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Autores principales: Agnetti, Jessica, Büchler, Andrea C., Osthoff, Michael, Helfenstein, Fabrice, Weisser, Maja, Siegemund, Martin, Bassetti, Stefano, Bingisser, Roland, Schaefer, Dirk J., Clauss, Martin, Hinic, Vladimira, Tschudin-Sutter, Sarah, Bättig, Veronika, Khanna, Nina, Egli, Adrian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601314/
https://www.ncbi.nlm.nih.gov/pubmed/37884860
http://dx.doi.org/10.1186/s12879-023-08732-9
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author Agnetti, Jessica
Büchler, Andrea C.
Osthoff, Michael
Helfenstein, Fabrice
Weisser, Maja
Siegemund, Martin
Bassetti, Stefano
Bingisser, Roland
Schaefer, Dirk J.
Clauss, Martin
Hinic, Vladimira
Tschudin-Sutter, Sarah
Bättig, Veronika
Khanna, Nina
Egli, Adrian
author_facet Agnetti, Jessica
Büchler, Andrea C.
Osthoff, Michael
Helfenstein, Fabrice
Weisser, Maja
Siegemund, Martin
Bassetti, Stefano
Bingisser, Roland
Schaefer, Dirk J.
Clauss, Martin
Hinic, Vladimira
Tschudin-Sutter, Sarah
Bättig, Veronika
Khanna, Nina
Egli, Adrian
author_sort Agnetti, Jessica
collection PubMed
description BACKGROUND: The BioFire® FilmArray® Blood Culture Identification Panel 1 (BF-FA-BCIP) detects microorganisms with high accuracy in positive blood cultures (BC) – a key step in the management of patients with suspected bacteraemia. We aimed to compare the time to optimal antimicrobial therapy (OAT) for the BF-FA-BCIP vs. standard culture-based identification. METHODS: In this retrospective single-centre study with a before-after design, 386 positive BC cases with identification by BF-FA-BCIP were compared to 414 controls with culture-based identification. The primary endpoint was the time from BC sampling to OAT. Secondary endpoints were time to effective therapy, length of stay, (re-)admission to ICU, in-hospital and 30-day mortality. Outcomes were assessed using Cox proportional hazard models and logistic regressions. RESULTS: Baseline characteristics of included adult inpatients were comparable. Main sources of bacteraemia were urinary tract and intra-abdominal infection (19.2% vs. 22.0% and 16.8% vs. 15.7%, for cases and controls, respectively). Median (95%CI) time to OAT was 25.5 (21.0–31.2) hours with BF-FA-BCIP compared to 45.7 (37.7–51.4) hours with culture-based identification. We observed no significant difference for secondary outcomes. CONCLUSIONS: Rapid microorganism identification by BF-FA-BCIP was associated with a median 20-h earlier initiation of OAT in patients with positive BC. No impact on length of stay and mortality was noted. TRIAL REGISTRATION: Clinicaltrials.gov, NCT04156633, registered on November 5, 2019. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08732-9.
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spelling pubmed-106013142023-10-27 Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study Agnetti, Jessica Büchler, Andrea C. Osthoff, Michael Helfenstein, Fabrice Weisser, Maja Siegemund, Martin Bassetti, Stefano Bingisser, Roland Schaefer, Dirk J. Clauss, Martin Hinic, Vladimira Tschudin-Sutter, Sarah Bättig, Veronika Khanna, Nina Egli, Adrian BMC Infect Dis Research BACKGROUND: The BioFire® FilmArray® Blood Culture Identification Panel 1 (BF-FA-BCIP) detects microorganisms with high accuracy in positive blood cultures (BC) – a key step in the management of patients with suspected bacteraemia. We aimed to compare the time to optimal antimicrobial therapy (OAT) for the BF-FA-BCIP vs. standard culture-based identification. METHODS: In this retrospective single-centre study with a before-after design, 386 positive BC cases with identification by BF-FA-BCIP were compared to 414 controls with culture-based identification. The primary endpoint was the time from BC sampling to OAT. Secondary endpoints were time to effective therapy, length of stay, (re-)admission to ICU, in-hospital and 30-day mortality. Outcomes were assessed using Cox proportional hazard models and logistic regressions. RESULTS: Baseline characteristics of included adult inpatients were comparable. Main sources of bacteraemia were urinary tract and intra-abdominal infection (19.2% vs. 22.0% and 16.8% vs. 15.7%, for cases and controls, respectively). Median (95%CI) time to OAT was 25.5 (21.0–31.2) hours with BF-FA-BCIP compared to 45.7 (37.7–51.4) hours with culture-based identification. We observed no significant difference for secondary outcomes. CONCLUSIONS: Rapid microorganism identification by BF-FA-BCIP was associated with a median 20-h earlier initiation of OAT in patients with positive BC. No impact on length of stay and mortality was noted. TRIAL REGISTRATION: Clinicaltrials.gov, NCT04156633, registered on November 5, 2019. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08732-9. BioMed Central 2023-10-26 /pmc/articles/PMC10601314/ /pubmed/37884860 http://dx.doi.org/10.1186/s12879-023-08732-9 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
Agnetti, Jessica
Büchler, Andrea C.
Osthoff, Michael
Helfenstein, Fabrice
Weisser, Maja
Siegemund, Martin
Bassetti, Stefano
Bingisser, Roland
Schaefer, Dirk J.
Clauss, Martin
Hinic, Vladimira
Tschudin-Sutter, Sarah
Bättig, Veronika
Khanna, Nina
Egli, Adrian
Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
title Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
title_full Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
title_fullStr Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
title_full_unstemmed Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
title_short Identification of microorganisms by a rapid PCR panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
title_sort identification of microorganisms by a rapid pcr panel from positive blood cultures leads to faster optimal antimicrobial therapy – a before-after study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601314/
https://www.ncbi.nlm.nih.gov/pubmed/37884860
http://dx.doi.org/10.1186/s12879-023-08732-9
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