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Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review

Antimicrobial resistance is a rising threat to global health and is associated with increased mortality. Intestinal colonisation with multidrug-resistant organisms (MDRO) can precede invasive infection and facilitates spread within communities and hospitals. Novel decolonisation strategies, such as...

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Autores principales: Bilsen, Manu P., Lambregts, Merel M.C., van Prehn, Joffrey, Kuijper, Ed J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654246/
https://www.ncbi.nlm.nih.gov/pubmed/34636363
http://dx.doi.org/10.1097/MOG.0000000000000792
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author Bilsen, Manu P.
Lambregts, Merel M.C.
van Prehn, Joffrey
Kuijper, Ed J.
author_facet Bilsen, Manu P.
Lambregts, Merel M.C.
van Prehn, Joffrey
Kuijper, Ed J.
author_sort Bilsen, Manu P.
collection PubMed
description Antimicrobial resistance is a rising threat to global health and is associated with increased mortality. Intestinal colonisation with multidrug-resistant organisms (MDRO) can precede invasive infection and facilitates spread within communities and hospitals. Novel decolonisation strategies, such as faecal microbiota transplantation (FMT), are being explored. The purpose of this review is to provide an update on how the field of FMT for MDRO decolonisation has developed during the past year and to assess the efficacy of FMT for intestinal MDRO decolonisation. RECENT FINDINGS: Since 2020, seven highly heterogenous, small, nonrandomised cohort studies and five case reports have been published. In line with previous literature, decolonisation rates ranged from 20 to 90% between studies and were slightly higher for carbapenem-resistant Enterobacteriaceae than vancomycin-resistant Enterococcus. Despite moderate decolonisation rates in two studies, a reduction in MDRO bloodstream and urinary tract infections was observed. SUMMARY AND IMPLICATIONS: Although a number of smaller cohort studies show some effect of FMT for MDRO decolonisation, questions remain regarding the true efficacy of FMT (taking spontaneous decolonisation into account), the optimal route of administration, the role of antibiotics pre and post-FMT and the efficacy in different patient populations. The observed decrease in MDRO infections post-FMT warrants further research.
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spelling pubmed-86542462021-12-15 Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review Bilsen, Manu P. Lambregts, Merel M.C. van Prehn, Joffrey Kuijper, Ed J. Curr Opin Gastroenterol GASTROINTESTINAL INFECTIONS: Edited by Mark H. Wilcox Antimicrobial resistance is a rising threat to global health and is associated with increased mortality. Intestinal colonisation with multidrug-resistant organisms (MDRO) can precede invasive infection and facilitates spread within communities and hospitals. Novel decolonisation strategies, such as faecal microbiota transplantation (FMT), are being explored. The purpose of this review is to provide an update on how the field of FMT for MDRO decolonisation has developed during the past year and to assess the efficacy of FMT for intestinal MDRO decolonisation. RECENT FINDINGS: Since 2020, seven highly heterogenous, small, nonrandomised cohort studies and five case reports have been published. In line with previous literature, decolonisation rates ranged from 20 to 90% between studies and were slightly higher for carbapenem-resistant Enterobacteriaceae than vancomycin-resistant Enterococcus. Despite moderate decolonisation rates in two studies, a reduction in MDRO bloodstream and urinary tract infections was observed. SUMMARY AND IMPLICATIONS: Although a number of smaller cohort studies show some effect of FMT for MDRO decolonisation, questions remain regarding the true efficacy of FMT (taking spontaneous decolonisation into account), the optimal route of administration, the role of antibiotics pre and post-FMT and the efficacy in different patient populations. The observed decrease in MDRO infections post-FMT warrants further research. Lippincott Williams & Wilkins 2022-01 2021-10-22 /pmc/articles/PMC8654246/ /pubmed/34636363 http://dx.doi.org/10.1097/MOG.0000000000000792 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle GASTROINTESTINAL INFECTIONS: Edited by Mark H. Wilcox
Bilsen, Manu P.
Lambregts, Merel M.C.
van Prehn, Joffrey
Kuijper, Ed J.
Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
title Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
title_full Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
title_fullStr Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
title_full_unstemmed Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
title_short Faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
title_sort faecal microbiota replacement to eradicate antimicrobial resistant bacteria in the intestinal tract – a systematic review
topic GASTROINTESTINAL INFECTIONS: Edited by Mark H. Wilcox
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654246/
https://www.ncbi.nlm.nih.gov/pubmed/34636363
http://dx.doi.org/10.1097/MOG.0000000000000792
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