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P696 Faecal microbiota transplantation in ultra-refractory ulcerative colitis: Retrospective analysis in a tertiary care centre

Abstract Background Colonic disbiosis is suspected to be an important factor in the physiopathology of ulcerative colitis (UC). Faecal microbiota transplantation (FMT) could play a therapeutic role because of its ability in restore a normal colonic microbiota. Some randomised trials have compared FM...

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Published in:Journal of Crohn's and colitis 2018-01, Vol.12 (supplement_1), p.S463-S463
Main Authors: Guerrero García, A, Flores de Miguel, A, Sánchez Rodríguez, E, Ríos León, R, Roy Ariño, G, Del Campo Moreno, R, Albillos Martínez, A, López-Sanromán, A
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Language:English
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Summary:Abstract Background Colonic disbiosis is suspected to be an important factor in the physiopathology of ulcerative colitis (UC). Faecal microbiota transplantation (FMT) could play a therapeutic role because of its ability in restore a normal colonic microbiota. Some randomised trials have compared FMT vs. placebo with hopeful results. Methods Observational study of patients diagnosed with ultra-refractory UC (to several lines of immunosuppressive and biological therapy) treated with FMT in a tertiary care centre. FMT was performed with stool from a single donor per procedure, according to centre protocol and exposing in vitro receptor’s mucosal lymphocytes to donor’s stool, selecting the donor with less inflammatory response (Ponce-Alonso, M. et al. ECCO 2017). Faecal filtrate was applied by colonoscopy, followed by enemas in weeks 1-2-3-4 and new colonoscopic dose in week 16. Results Four patients were included (Table 1), with a median age of 50 years. None of patients included showed an improvement in clinical activity score (Walmsley), biologic markers (C-Reactive Protein, faecal calprotectine), or colonoscopy. Conclusions In our experience, FMT was not useful in the management of ultra-refractory UC. Due to small sample size it is difficult to obtain conclusions, but maybe FMT should be employed in earlier phases of the disease.
ISSN:1873-9946
1876-4479
DOI:10.1093/ecco-jcc/jjx180.823