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Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial

INTRODUCTION: Antimicrobial resistance is rising, largely due to the indiscriminate use of antimicrobials. The human gut is the largest reservoir of antibiotic resistant bacteria (ARB). Individuals colonised with ARB have the potential to spread these organisms both in the community and hospital set...

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Autores principales: Merrick, Blair, Robinson, Emily, Bunce, Catey, Allen, Liz, Bisnauthsing, Karen, Izundu, Chi Chi, Bell, Jordana, Amos, Gregory, Shankar-Hari, Manu, Goodman, Anna, Shawcross, Debbie L, Goldenberg, Simon D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7252984/
https://www.ncbi.nlm.nih.gov/pubmed/32457083
http://dx.doi.org/10.1136/bmjopen-2020-038847
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author Merrick, Blair
Robinson, Emily
Bunce, Catey
Allen, Liz
Bisnauthsing, Karen
Izundu, Chi Chi
Bell, Jordana
Amos, Gregory
Shankar-Hari, Manu
Goodman, Anna
Shawcross, Debbie L
Goldenberg, Simon D
author_facet Merrick, Blair
Robinson, Emily
Bunce, Catey
Allen, Liz
Bisnauthsing, Karen
Izundu, Chi Chi
Bell, Jordana
Amos, Gregory
Shankar-Hari, Manu
Goodman, Anna
Shawcross, Debbie L
Goldenberg, Simon D
author_sort Merrick, Blair
collection PubMed
description INTRODUCTION: Antimicrobial resistance is rising, largely due to the indiscriminate use of antimicrobials. The human gut is the largest reservoir of antibiotic resistant bacteria (ARB). Individuals colonised with ARB have the potential to spread these organisms both in the community and hospital settings. Infections with ARB such as extended spectrum beta-lactamase producing enterobacteriales (ESBL-E) and carbapenemase producing enterobacteriales (CPE) are more difficult to treat and are associated with an increased morbidity and mortality. Presently, there is no effective decolonisation strategy for these ARB. Faecal microbiota transplant (FMT) has emerged as a potential strategy for decolonisation of ARB from the human gut, however there is significant uncertainty about the feasibility, effectiveness and safety of using this approach. METHODS AND ANALYSIS: Prospective, randomised, patient-blinded, placebo-controlled feasibility trial of FMT to eradicate gastrointestinal carriage of ARB. Eighty patients with a recent history of invasive infection secondary to ESBL-E or CPE and persistent gastrointestinal carriage will be randomised 1:1 to receive encapsulated FMT or placebo. The primary outcome measure is consent rate (as a proportion of patients who fulfil inclusion/exclusion criteria); this will be used to determine if a substantive trial is feasible. Participants will be followed up at 1 week, 1 month, 3 months and 6 months and monitored for adverse events as well as gastrointestinal carriage rates of ARB after intervention. ETHICS AND DISSEMINATION: Research ethics approval was obtained by London—City and East Research Ethics Committee (ref 20/LO/0117). Trial results will be published in a peer-reviewed journal and presented at international conferences. TRIAL REGISTRATION NUMBER: ISRCTN registration number 34 467 677 and EudraCT number 2019-001618-41.
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spelling pubmed-72529842020-06-05 Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial Merrick, Blair Robinson, Emily Bunce, Catey Allen, Liz Bisnauthsing, Karen Izundu, Chi Chi Bell, Jordana Amos, Gregory Shankar-Hari, Manu Goodman, Anna Shawcross, Debbie L Goldenberg, Simon D BMJ Open Infectious Diseases INTRODUCTION: Antimicrobial resistance is rising, largely due to the indiscriminate use of antimicrobials. The human gut is the largest reservoir of antibiotic resistant bacteria (ARB). Individuals colonised with ARB have the potential to spread these organisms both in the community and hospital settings. Infections with ARB such as extended spectrum beta-lactamase producing enterobacteriales (ESBL-E) and carbapenemase producing enterobacteriales (CPE) are more difficult to treat and are associated with an increased morbidity and mortality. Presently, there is no effective decolonisation strategy for these ARB. Faecal microbiota transplant (FMT) has emerged as a potential strategy for decolonisation of ARB from the human gut, however there is significant uncertainty about the feasibility, effectiveness and safety of using this approach. METHODS AND ANALYSIS: Prospective, randomised, patient-blinded, placebo-controlled feasibility trial of FMT to eradicate gastrointestinal carriage of ARB. Eighty patients with a recent history of invasive infection secondary to ESBL-E or CPE and persistent gastrointestinal carriage will be randomised 1:1 to receive encapsulated FMT or placebo. The primary outcome measure is consent rate (as a proportion of patients who fulfil inclusion/exclusion criteria); this will be used to determine if a substantive trial is feasible. Participants will be followed up at 1 week, 1 month, 3 months and 6 months and monitored for adverse events as well as gastrointestinal carriage rates of ARB after intervention. ETHICS AND DISSEMINATION: Research ethics approval was obtained by London—City and East Research Ethics Committee (ref 20/LO/0117). Trial results will be published in a peer-reviewed journal and presented at international conferences. TRIAL REGISTRATION NUMBER: ISRCTN registration number 34 467 677 and EudraCT number 2019-001618-41. BMJ Publishing Group 2020-05-25 /pmc/articles/PMC7252984/ /pubmed/32457083 http://dx.doi.org/10.1136/bmjopen-2020-038847 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Infectious Diseases
Merrick, Blair
Robinson, Emily
Bunce, Catey
Allen, Liz
Bisnauthsing, Karen
Izundu, Chi Chi
Bell, Jordana
Amos, Gregory
Shankar-Hari, Manu
Goodman, Anna
Shawcross, Debbie L
Goldenberg, Simon D
Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial
title Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial
title_full Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial
title_fullStr Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial
title_full_unstemmed Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial
title_short Faecal microbiota transplant to ERadicate gastrointestinal carriage of Antibiotic Resistant Organisms (FERARO): a prospective, randomised placebo-controlled feasibility trial
title_sort faecal microbiota transplant to eradicate gastrointestinal carriage of antibiotic resistant organisms (feraro): a prospective, randomised placebo-controlled feasibility trial
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7252984/
https://www.ncbi.nlm.nih.gov/pubmed/32457083
http://dx.doi.org/10.1136/bmjopen-2020-038847
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