Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22605
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dc.contributor.authorHaifer, Craig-
dc.contributor.authorKelly, Colleen R-
dc.contributor.authorParamsothy, Sudarshan-
dc.contributor.authorAndresen, David-
dc.contributor.authorPapanicolas, Lito E-
dc.contributor.authorMcKew, Genevieve L-
dc.contributor.authorBorody, Thomas J-
dc.contributor.authorKamm, Michael-
dc.contributor.authorCostello, Samuel P-
dc.contributor.authorAndrews, Jane M-
dc.contributor.authorBegun, Jakob-
dc.contributor.authorChan, Hiu Tat-
dc.contributor.authorConnor, Susan-
dc.contributor.authorGhaly, Simon-
dc.contributor.authorJohnson, Paul D R-
dc.contributor.authorLemberg, Daniel A-
dc.contributor.authorParamsothy, Ramesh-
dc.contributor.authorRedmond, Andrew-
dc.contributor.authorSheorey, Harsha-
dc.contributor.authorvan der Poorten, David-
dc.contributor.authorLeong, Rupert W-
dc.date2020-02-11-
dc.date.accessioned2020-02-18T22:28:57Z-
dc.date.available2020-02-18T22:28:57Z-
dc.date.issued2020-04-03-
dc.identifier.citationGut 2020; 69(5): 801-810-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22605-
dc.description.abstractFaecal 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. 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. 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. 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.-
dc.language.isoeng-
dc.subjectClostridioides difficile-
dc.subjectFMT-
dc.subjectfaecal microbiota transplantation-
dc.subjectinflammatory bowel disease-
dc.subjectmicrobiome therapeutics-
dc.subjectstool bank-
dc.titleAustralian consensus statements for the regulation, production and use of faecal microbiota transplantation in clinical practice.-
dc.typeJournal Articleen_US
dc.identifier.journaltitleGut-
dc.identifier.affiliationWarren Alpert Medical School, Brown University, Providence, Rhode Island, USAen
dc.identifier.affiliationThe University of Adelaide, Adelaide, South Australia, Australiaen
dc.identifier.affiliationThe University of Sydney, Sydney, New South Wales, Australiaen
dc.identifier.affiliationConcord Repatriation General Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationThe University of Queensland, Brisbane, Queensland, Australiaen
dc.identifier.affiliationMater Hospital Brisbane, Brisbane, Queensland, Australiaen
dc.identifier.affiliationLiverpool Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationUniversity of New South Wales, Sydney, New South Wales, Australiaen
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSydney Children's Hospital Randwick, Randwick, New South Wales, Australiaen
dc.identifier.affiliationRoyal Brisbane and Women's Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationWestmead Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationBlacktown Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationVCS Pathology, Melbourne, Victoria, Australiaen
dc.identifier.affiliationCentre for Digestive Diseases, Sydney, New South Wales, Australiaen
dc.identifier.affiliationSt Vincent's Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationThe University of Sydney, Sydney, New South Wales, Australiaen
dc.identifier.affiliationSt Vincent's Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationConcord Repatriation General Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationSouth Australian Health and Medical Research Institute, Adelaide, South Australia, Australiaen
dc.identifier.affiliationRoyal Adelaide Hospital, Adelaide, South Australia, Australiaen
dc.identifier.affiliationThe University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationThe Queen Elizabeth Hospital, Woodville, South Australia, Australiaen
dc.identifier.affiliationBiomeBank, Adelaide, South Australia, Australiaen
dc.identifier.doi10.1136/gutjnl-2019-320260-
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-3675-6550-
dc.identifier.orcid0000-0002-9097-6028-
dc.identifier.orcid0000-0002-5838-7274-
dc.identifier.orcid0000-0002-5238-9260-
dc.identifier.orcid0000-0002-0519-4698-
dc.identifier.orcid0000-0002-2857-1812-
dc.identifier.orcid0000-0001-5256-7672-
dc.identifier.orcid0000-0001-5606-0270-
dc.identifier.orcid0000-0003-2489-6430-
dc.identifier.orcid0000-0002-1125-5362-
dc.identifier.orcid0000-0001-5944-3488-
dc.identifier.orcid0000-0001-9873-7163-
dc.identifier.pubmedid32047093-
dc.type.austinJournal Article-
local.name.researcherJohnson, Paul D R
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptInfectious Diseases-
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