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LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.

BACKGROUND: The FilmArray Pneumonia Panel (bioMérieux) is a rapid multiplex PCR aiming to increase speed and sensitivity in the microbiological diagnosis of pneumonia. This offers potential for improved antimicrobial stewardship and evidence-based antibiotic prescribing. Whether such gains can be re...

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Autores principales: Enne, Virve, Stirling, Susan, Barber, Julie, High, Juliet, Russell, Charlotte, Dresser, Kerry, Dhesi, Zaneeta, Brealey, David, Singh, Suveer, Swart, Ann Marie, Livermore, David, Gant, Vanya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753007/
http://dx.doi.org/10.1093/ofid/ofac492.1894
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author Enne, Virve
Stirling, Susan
Barber, Julie
High, Juliet
Russell, Charlotte
Dresser, Kerry
Dhesi, Zaneeta
Brealey, David
Singh, Suveer
Swart, Ann Marie
Livermore, David
Gant, Vanya
author_facet Enne, Virve
Stirling, Susan
Barber, Julie
High, Juliet
Russell, Charlotte
Dresser, Kerry
Dhesi, Zaneeta
Brealey, David
Singh, Suveer
Swart, Ann Marie
Livermore, David
Gant, Vanya
author_sort Enne, Virve
collection PubMed
description BACKGROUND: The FilmArray Pneumonia Panel (bioMérieux) is a rapid multiplex PCR aiming to increase speed and sensitivity in the microbiological diagnosis of pneumonia. This offers potential for improved antimicrobial stewardship and evidence-based antibiotic prescribing. Whether such gains can be realised in practise is uncertain, thus, we conducted a randomized controlled trial to examine this. METHODS: Adults and children in ICU with suspected hospital-acquired or ventilator-associated pneumonia were randomized to standard care or a FilmArray Pneumonia Panel PCR test at the point of care supported by an optional prescribing algorithm. Participants were followed for 28 days. FilmArray tests were run retrospectively in the control-arm but results were not provided to treating clinicians. Antimicrobial therapy was adjudged by a committee of blinded, independent microbiologists for ‘activity’ and ‘proportionality’ vs. pathogens detected in each arm regardless of the time and method by which they were found. Clinical cure was not blinded and judged by site PI according to defined clinical parameters. RESULTS: Between July 2019 and August 2021, 556 participants were randomized at 13 hospitals; 545 met eligibility criteria; 92 were children and 183 had COVID-19 at enrolment. Baseline characteristics were well balanced between study arms. In the intervention arm 76.5% of participants were judged to have received active and proportionate antibiotics at 24h vs. 55.9% in the control arm (p< 0.001); proportions at 72h were 73.4% and 58.8%, respectively p< 0.001). Site-reported clinical cure of pneumonia at 14 days was 56.7% in the intervention arm and 64.7% in the control arm (95% CI -0.15 to 0.02), with exploratory analyses suggesting site heterogeneity. 28-day mortality was 31.3% in the intervention arm and 28.2% in the control arm (p = 0.098). Median ventilator-free days by Day 21 were 2 days in both study arms. Median ICU length of stay was 14 days in both arms. CONCLUSION: Use of the FilmArray Pneumonia Panel PCR led to a significant increase in the proportion of patients receiving ‘active and proportionate’ antibiotic therapy at 24h. Reasons for lower reported clinical cure, despite better tailored antibiotic use, remain under active analysis. DISCLOSURES: Virve Enne, BSc PhD, Biomerieux: Advisor/Consultant|Biomerieux: Advisor/Consultant|Biomerieux: Grant/Research Support|Biomerieux: Grant/Research Support|Inflammatix: Grant/Research Support Juliet High, Masters in Chemistry, Biomerieux: Advisor/Consultant|Biomerieux: Grant/Research Support David Brealey, MBBSPhD, Biomerieux: Honoraria David Livermore, BSc PhD, bioMerieux: Honoraria|bioMerieux: Provision of machines/test kits for INHALE.
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spelling pubmed-97530072022-12-16 LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care. Enne, Virve Stirling, Susan Barber, Julie High, Juliet Russell, Charlotte Dresser, Kerry Dhesi, Zaneeta Brealey, David Singh, Suveer Swart, Ann Marie Livermore, David Gant, Vanya Open Forum Infect Dis Abstracts BACKGROUND: The FilmArray Pneumonia Panel (bioMérieux) is a rapid multiplex PCR aiming to increase speed and sensitivity in the microbiological diagnosis of pneumonia. This offers potential for improved antimicrobial stewardship and evidence-based antibiotic prescribing. Whether such gains can be realised in practise is uncertain, thus, we conducted a randomized controlled trial to examine this. METHODS: Adults and children in ICU with suspected hospital-acquired or ventilator-associated pneumonia were randomized to standard care or a FilmArray Pneumonia Panel PCR test at the point of care supported by an optional prescribing algorithm. Participants were followed for 28 days. FilmArray tests were run retrospectively in the control-arm but results were not provided to treating clinicians. Antimicrobial therapy was adjudged by a committee of blinded, independent microbiologists for ‘activity’ and ‘proportionality’ vs. pathogens detected in each arm regardless of the time and method by which they were found. Clinical cure was not blinded and judged by site PI according to defined clinical parameters. RESULTS: Between July 2019 and August 2021, 556 participants were randomized at 13 hospitals; 545 met eligibility criteria; 92 were children and 183 had COVID-19 at enrolment. Baseline characteristics were well balanced between study arms. In the intervention arm 76.5% of participants were judged to have received active and proportionate antibiotics at 24h vs. 55.9% in the control arm (p< 0.001); proportions at 72h were 73.4% and 58.8%, respectively p< 0.001). Site-reported clinical cure of pneumonia at 14 days was 56.7% in the intervention arm and 64.7% in the control arm (95% CI -0.15 to 0.02), with exploratory analyses suggesting site heterogeneity. 28-day mortality was 31.3% in the intervention arm and 28.2% in the control arm (p = 0.098). Median ventilator-free days by Day 21 were 2 days in both study arms. Median ICU length of stay was 14 days in both arms. CONCLUSION: Use of the FilmArray Pneumonia Panel PCR led to a significant increase in the proportion of patients receiving ‘active and proportionate’ antibiotic therapy at 24h. Reasons for lower reported clinical cure, despite better tailored antibiotic use, remain under active analysis. DISCLOSURES: Virve Enne, BSc PhD, Biomerieux: Advisor/Consultant|Biomerieux: Advisor/Consultant|Biomerieux: Grant/Research Support|Biomerieux: Grant/Research Support|Inflammatix: Grant/Research Support Juliet High, Masters in Chemistry, Biomerieux: Advisor/Consultant|Biomerieux: Grant/Research Support David Brealey, MBBSPhD, Biomerieux: Honoraria David Livermore, BSc PhD, bioMerieux: Honoraria|bioMerieux: Provision of machines/test kits for INHALE. Oxford University Press 2022-12-15 /pmc/articles/PMC9753007/ http://dx.doi.org/10.1093/ofid/ofac492.1894 Text en © The Author(s) 2022. 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 Abstracts
Enne, Virve
Stirling, Susan
Barber, Julie
High, Juliet
Russell, Charlotte
Dresser, Kerry
Dhesi, Zaneeta
Brealey, David
Singh, Suveer
Swart, Ann Marie
Livermore, David
Gant, Vanya
LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
title LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
title_full LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
title_fullStr LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
title_full_unstemmed LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
title_short LB2304. INHALE WP3: Results of a multi-centre randomised controlled trial (INHALE) testing the utility of rapid multiplex PCR at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
title_sort lb2304. inhale wp3: results of a multi-centre randomised controlled trial (inhale) testing the utility of rapid multiplex pcr at point-of-care for the antibiotic management of hospital-acquired and ventilator-associated pneumonia in critical care.
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753007/
http://dx.doi.org/10.1093/ofid/ofac492.1894
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