Oral, frozen fecal microbiota transplant (FMT) capsules for recurrent Clostridium difficile infection
Autor: | Jess L. Kaplan, Jasmin Mahabamunuge, Joanne Levin, Ilan Youngster, Hannah Systrom, Hamed Khalili, Elizabeth L. Hohmann, Jenny Sauk |
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Jazyk: | angličtina |
Předmět: |
Male
Antibiotics Administration Oral Pilot Projects Fecal microbiota transplant Feces 0302 clinical medicine Oral administration Recurrence Freezing Clinical endpoint 030212 general & internal medicine Child Aged 80 and over Medicine(all) Microbiota General Medicine Clostridium difficile Fecal Microbiota Transplantation Middle Aged 3. Good health Anti-Bacterial Agents Treatment Outcome Cohort 030211 gastroenterology & hepatology Female Research Article Adult medicine.medical_specialty Adolescent medicine.drug_class Capsules 03 medical and health sciences Young Adult Refractory Internal medicine Drug Resistance Bacterial medicine Humans Adverse effect Aged Retrospective Studies business.industry Clostridioides difficile Immunology Clostridium Infections Feasibility Studies Microbiome business |
Zdroj: | BMC Medicine |
ISSN: | 1741-7015 |
DOI: | 10.1186/s12916-016-0680-9 |
Popis: | Background Fecal microbiota transplantation (FMT) has been shown to be safe and effective in treating refractory or relapsing C. difficile infection (CDI), but its use has been limited by practical barriers. We recently reported a small preliminary feasibility study using orally administered frozen fecal capsules. Following these early results, we now report our clinical experience in a large cohort with structured follow-up. Methods We prospectively followed a cohort of patients with recurrent or refractory CDI who were treated with frozen, encapsulated FMT at our institution. The primary endpoint was defined as clinical resolution whilst off antibiotics for CDI at 8 weeks after last capsule ingestion. Safety was defined as any FMT-related adverse event grade 2 or above. Results Overall, 180 patients aged 7–95 years with a minimal follow-up of 8 weeks were included in the analysis. CDI resolved in 82 % of patients after a single treatment, rising to a 91 % cure rate with two treatments. Three adverse events Grade 2 or above, deemed related or possibly related to FMT, were observed. Conclusions We confirm the effectiveness and safety of oral administration of frozen encapsulated fecal material, prepared from unrelated donors, in treating recurrent CDI. Randomized studies and FMT registries are still needed to ascertain long-term safety. |
Databáze: | OpenAIRE |
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