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Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease
BACKGROUND: Fecal microbiota transplantation (FMT) is a well-established therapeutic option for patients with antibiotic resistant Clostridioides difficile infection (CDI). However, the efficacy of FMT in patients with chronic liver disease remains elusive. AIMS: We studied the effect of FMT on chro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007953/ https://www.ncbi.nlm.nih.gov/pubmed/32047670 http://dx.doi.org/10.1155/2020/1874570 |
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author | Meighani, Alireza Alimirah, Maryam Ramesh, Mayur Salgia, Reena |
author_facet | Meighani, Alireza Alimirah, Maryam Ramesh, Mayur Salgia, Reena |
author_sort | Meighani, Alireza |
collection | PubMed |
description | BACKGROUND: Fecal microbiota transplantation (FMT) is a well-established therapeutic option for patients with antibiotic resistant Clostridioides difficile infection (CDI). However, the efficacy of FMT in patients with chronic liver disease remains elusive. AIMS: We studied the effect of FMT on chronic liver disease (CLD) patients with CDI at our tertiary medical center. METHODS: A cohort of all patients who received FMT from December 2012 to May 2014 for refractory or recurrent CDI was identified. Patients were monitored for a year after FMT. Descriptive analysis was conducted to compare the effect of FMT in patients with and without CLD. RESULTS: A total of 201 patients with CDI received FMT, 14 of which had a history of CLD. Nine of these patients exhibited cirrhosis of the liver with a mean Child-Turcotte-Pugh score of 8. CDI development in these patients was associated with recent exposure to antibiotics and was observed to be significantly different between both groups (17% of CLD patients vs. 58% in the general cohort, p = 0.01). Four patients with CLD received >1 FMT, of which 2 did not respond to treatment. There was no significant difference between patients with liver disease and the rest of the cohort with regard to FMT response (12/14 (87%) vs. 164/187 (88%), p = 0.01). Four patients with CLD received >1 FMT, of which 2 did not respond to treatment. There was no significant difference between patients with liver disease and the rest of the cohort with regard to FMT response (12/14 (87%) vs. 164/187 (88%), CONCLUSION: FMT is a safe and effective therapy against CDI for patients with CLD and cirrhosis. |
format | Online Article Text |
id | pubmed-7007953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-70079532020-02-11 Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease Meighani, Alireza Alimirah, Maryam Ramesh, Mayur Salgia, Reena Int J Hepatol Research Article BACKGROUND: Fecal microbiota transplantation (FMT) is a well-established therapeutic option for patients with antibiotic resistant Clostridioides difficile infection (CDI). However, the efficacy of FMT in patients with chronic liver disease remains elusive. AIMS: We studied the effect of FMT on chronic liver disease (CLD) patients with CDI at our tertiary medical center. METHODS: A cohort of all patients who received FMT from December 2012 to May 2014 for refractory or recurrent CDI was identified. Patients were monitored for a year after FMT. Descriptive analysis was conducted to compare the effect of FMT in patients with and without CLD. RESULTS: A total of 201 patients with CDI received FMT, 14 of which had a history of CLD. Nine of these patients exhibited cirrhosis of the liver with a mean Child-Turcotte-Pugh score of 8. CDI development in these patients was associated with recent exposure to antibiotics and was observed to be significantly different between both groups (17% of CLD patients vs. 58% in the general cohort, p = 0.01). Four patients with CLD received >1 FMT, of which 2 did not respond to treatment. There was no significant difference between patients with liver disease and the rest of the cohort with regard to FMT response (12/14 (87%) vs. 164/187 (88%), p = 0.01). Four patients with CLD received >1 FMT, of which 2 did not respond to treatment. There was no significant difference between patients with liver disease and the rest of the cohort with regard to FMT response (12/14 (87%) vs. 164/187 (88%), CONCLUSION: FMT is a safe and effective therapy against CDI for patients with CLD and cirrhosis. Hindawi 2020-01-27 /pmc/articles/PMC7007953/ /pubmed/32047670 http://dx.doi.org/10.1155/2020/1874570 Text en Copyright © 2020 Alireza Meighani et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Meighani, Alireza Alimirah, Maryam Ramesh, Mayur Salgia, Reena Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease |
title | Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease |
title_full | Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease |
title_fullStr | Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease |
title_full_unstemmed | Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease |
title_short | Fecal Microbiota Transplantation for Clostridioides Difficile Infection in Patients with Chronic Liver Disease |
title_sort | fecal microbiota transplantation for clostridioides difficile infection in patients with chronic liver disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007953/ https://www.ncbi.nlm.nih.gov/pubmed/32047670 http://dx.doi.org/10.1155/2020/1874570 |
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