Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/36973
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dc.contributor.authorSiow W.en
dc.contributor.authorSkoien R.en
dc.contributor.authorMitchell J.en
dc.contributor.authorZekry A.en
dc.contributor.authorGeorge J.en
dc.contributor.authorMacQuillan G.en
dc.contributor.authorWigg A.en
dc.contributor.authorStuart K.en
dc.contributor.authorMcCaughan G.en
dc.contributor.authorSievert W.en
dc.contributor.authorLim R.en
dc.contributor.authorStrasser S.en
dc.contributor.authorNicoll A.en
dc.contributor.authorGazzola A.en
dc.contributor.authorRoberts S.K.en
dc.contributor.authorKhoo T.en
dc.contributor.authorHamarneh Z.en
dc.contributor.authorWeltman M.en
dc.contributor.authorGow P.en
dc.contributor.authorJanko N.en
dc.contributor.authorTse E.en
dc.contributor.authorMishra G.en
dc.contributor.authorCheng E.-H.en
dc.contributor.authorLevy M.en
dc.contributor.authorCheng W.en
dc.contributor.authorSood S.en
dc.date.accessioned2021-05-14T12:33:35Zen
dc.date.available2021-05-14T12:33:35Zen
dc.date.copyright2018en
dc.date.created20180423en
dc.date.issued2018-04-23en
dc.identifier.citationClinical Gastroenterology and Hepatology. 16 (2) (pp 268-277), 2018. Date of Publication: February 2018.en
dc.identifier.issn1542-3565en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36973en
dc.description.abstractBackground & Aims: Little is known about outcomes of patients with autoimmune hepatitis (AIH) who have a suboptimal outcome to standard therapy and are then given mycophenolate mofetil as rescue therapy. We evaluated the efficacy and safety of mycophenolate mofetil in patients failed by or intolerant to corticosteroids, with or without azathioprine. Method(s): We performed a retrospective study of 105 patients with AIH who received mycophenolate mofetil therapy after an inadequate response or intolerance to standard therapy (98% received combination therapy with corticosteroids plus thiopurines). Patients were recruited from 17 liver clinics via the Australian Liver Association Clinical Research Network. We reviewed records for baseline demographic features and characteristics of liver disease, initial therapy, mycophenolate mofetil indications, treatment outcome, and side effects. The primary outcome was biochemical remission, defined as levels of alanine and aspartate transferase and IgG level within the normal reference range, with or without normal liver histology within the first 2 years of treatment. Result(s): The indication for mycophenolate mofetil therapy was non-response to treatment for 40% of cases and intolerance to therapy for 60%. Overall, 63 patients (60%) achieved biochemical remission following a median 12 weeks treatment with mycophenolate mofetil. The proportion of patients who achieved biochemical remission was similar between patients receiving mycophenolate mofetil for non-response to standard therapy (57%) and patients with intolerance to standard therapy (62%). However, a lower proportion of patients with cirrhosis achieved biochemical remission (47%) than patients without cirrhosis (6%) (P =.07). Serious adverse events occurred in 3 patients (2.7%) including 1 death, and 10 patients (9.2%) discontinued mycophenolate mofetil because of adverse events. Conclusion(s): In this retrospective study of patients with AIH who received mycophenolate mofetil as a rescue therapy, we found the drug to be well tolerated and moderately effective, inducing biochemical remission in 60% of subjects. Rates of response are lower and rates of infection are higher in patients with AIH and cirrhosis. Prospective studies of mycophenolate mofetil are warranted for this population.Copyright © 2018 AGA Instituteen
dc.languageEnglishen
dc.languageenen
dc.publisherW.B. Saundersen
dc.relation.ispartofClinical Gastroenterology and Hepatologyen
dc.titleEfficacy and Safety of Mycophenolate Mofetil in Patients With Autoimmune Hepatitis and Suboptimal Outcomes After Standard Therapy.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.cgh.2017.09.063en
dc.publisher.placeUnited Statesen
dc.identifier.orcidStrasser, Simone; ORCID: http://orcid.org/0000-0001-6374-1525 Hamarneh, Zaki; ORCID: http://orcid.org/0000-0002-4127-8856 Stuart, Katherine; ORCID: http://orcid.org/0000-0001-8104-8919en
dc.identifier.pubmedid29050991 [http://www.ncbi.nlm.nih.gov/pubmed/?term=29050991]en
dc.identifier.source2000587702en
dc.identifier.institution(Roberts, Gazzola, Mitchell, Janko) The Alfred, Melbourne, Australia (Lim, Strasser, McCaughan) Royal Prince Alfred Hospital, Sydney, Australia (Strasser, McCaughan) Centenary Research Institute, Sydney, Australia (Nicoll, Janko) Eastern Health, Box Hill Hospital, Monash University, Box Hill, Australia (Siow, George) Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Sydney, Australia (Khoo, MacQuillan) Sir Charles Gairdner Hospital, Perth, Australia (Hamarneh, Wigg) Flinders Medical Centre, Adelaide, Australia (Weltman) Nepean Hospital, Sydney, Australia (Gow) Austin Hospital, Melbourne, Australia (Tse) Royal Adelaide Hospital, Adelaide, Australia (Mishra, Sievert) Monash Medical Centre and Monash University, Melbourne, Australia (Cheng, Stuart) Princess Alexandra Hospital, Brisbane, Australia (Levy) Liverpool Hospital, Sydney, Australia (Cheng) Royal Perth Hospital, Perth, Australia (Sood) Royal Melbourne Hospital, Melbourne, Australia (Skoien) Royal Brisbane and Women's Hospital, Brisbane, Australia (Mitchell) Nambour General Hospital, Nambour, Australia (Zekry) St George Hospital, Sydney, Australiaen
dc.description.addressS.K. Roberts, Department of Gastroenterology, The Alfred, 55 Commercial Road, Melbourne 3004, Australia. E-mail: s.roberts@alfred.org.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.subect.keywordsImmune Suppressant Inflammation Periportal Hepatitis TAPESTRY Studyen
dc.identifier.authoremailRoberts S.K.; s.roberts@alfred.org.auen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptPharmacy-
crisitem.author.deptGastroenterology and Hepatology-
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