PT - JOURNAL ARTICLE AU - Craig Haifer AU - Colleen R Kelly AU - Sudarshan Paramsothy AU - David Andresen AU - Lito E Papanicolas AU - Genevieve L McKew AU - Thomas J Borody AU - Michael Kamm AU - Samuel P Costello AU - Jane M Andrews AU - Jakob Begun AU - Hiu Tat Chan AU - Susan Connor AU - Simon Ghaly AU - Paul DR Johnson AU - Daniel A Lemberg AU - Ramesh Paramsothy AU - Andrew Redmond AU - Harsha Sheorey AU - David van der Poorten AU - Rupert W Leong TI - Australian consensus statements for the regulation, production and use of faecal microbiota transplantation in clinical practice AID - 10.1136/gutjnl-2019-320260 DP - 2020 May 01 TA - Gut PG - 801--810 VI - 69 IP - 5 4099 - http://gut.bmj.com/content/69/5/801.short 4100 - http://gut.bmj.com/content/69/5/801.full SO - Gut2020 May 01; 69 AB - Objective Faecal microbiota transplantation (FMT) has proved to be an extremely effective treatment for recurrent Clostridioides difficile infection, and there is interest in its potential application in other gastrointestinal and systemic diseases. However, the recent death and episode of septicaemia following FMT highlights the need for further appraisal and guidelines on donor evaluation, production standards, treatment facilities and acceptable clinical indications.Design For these consensus statements, a 24-member multidisciplinary working group voted online and then convened in-person, using a modified Delphi approach to formulate and refine a series of recommendations based on best evidence and expert opinion. Invitations to participate were directed to Australian experts, with an international delegate assisting the development. The following issues regarding the use of FMT in clinical practice were addressed: donor selection and screening, clinical indications, requirements of FMT centres and future directions. Evidence was rated using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) system.Results Consensus was reached on 27 statements to provide guidance on best practice in FMT. These include: (1) minimum standards for donor screening with recommended clinical selection criteria, blood and stool testing; (2) accepted routes of administration; (3) clinical indications; (4) minimum standards for FMT production and requirements for treatment facilities acknowledging distinction between single-site centres (eg, hospital-based) and stool banks; and (5) recommendations on future research and product development.Conclusions These FMT consensus statements provide comprehensive recommendations around the production and use of FMT in clinical practice with relevance to clinicians, researchers and policy makers.