Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784850869169160192 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9753007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ennevirve lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT stirlingsusan lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT barberjulie lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT highjuliet lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT russellcharlotte lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT dresserkerry lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT dhesizaneeta lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT brealeydavid lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT singhsuveer lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT swartannmarie lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT livermoredavid lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare AT gantvanya lb2304inhalewp3resultsofamulticentrerandomisedcontrolledtrialinhaletestingtheutilityofrapidmultiplexpcratpointofcarefortheantibioticmanagementofhospitalacquiredandventilatorassociatedpneumoniaincriticalcare |