Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18398
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dc.contributor.authorRoberts, Stuart K-
dc.contributor.authorLim, Ricky-
dc.contributor.authorStrasser, Simone-
dc.contributor.authorNicoll, Amanda-
dc.contributor.authorGazzola, Alessia-
dc.contributor.authorMitchell, Joanne-
dc.contributor.authorSiow, Way-
dc.contributor.authorKhoo, Tiffany-
dc.contributor.authorHamarneh, Zaki-
dc.contributor.authorWeltman, Martin-
dc.contributor.authorGow, Paul J-
dc.contributor.authorJanko, Natasha-
dc.contributor.authorTse, Edmund-
dc.contributor.authorMishra, Gauri-
dc.contributor.authorCheng, En-Hsiang-
dc.contributor.authorLevy, Miriam-
dc.contributor.authorCheng, Wendy-
dc.contributor.authorSood, Siddharth-
dc.contributor.authorSkoien, Richard-
dc.contributor.authorMitchell, Jonathan-
dc.contributor.authorZekry, Amany-
dc.contributor.authorGeorge, Jacob-
dc.contributor.authorMacQuillan, Gerry-
dc.contributor.authorWigg, Alan-
dc.contributor.authorStuart, Katherine-
dc.contributor.authorSievert, William-
dc.contributor.authorMcCaughan, Geoffrey-
dc.date2017-10-16-
dc.date.accessioned2018-08-30T05:58:46Z-
dc.date.available2018-08-30T05:58:46Z-
dc.date.issued2018-02-
dc.identifier.citationClinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association 2018; 16(2): 268-277en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18398-
dc.description.abstractLittle 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. 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. 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. 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.en_US
dc.language.isoeng-
dc.subjectImmune Suppressanten_US
dc.subjectInflammationen_US
dc.subjectPeriportal Hepatitisen_US
dc.subjectTAPESTRY Studyen_US
dc.titleEfficacy and Safety of Mycophenolate Mofetil in Patients With Autoimmune Hepatitis and Suboptimal Outcomes After Standard Therapy.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleClinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Associationen_US
dc.identifier.affiliationThe Alfred, Melbourneen_US
dc.identifier.affiliationRoyal Prince Alfred Hospital, Sydneyen_US
dc.identifier.affiliationEastern Health, Box Hill Hospital, and Monash University, Box Hillen_US
dc.identifier.affiliationStorr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Sydneyen_US
dc.identifier.affiliationFlinders Medical Centre, Adelaideen_US
dc.identifier.affiliationNepean Hospital, Sydneyen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationRoyal Adelaide Hospital, Adelaideen_US
dc.identifier.affiliationMonash Medical Centre and Monash University, Melbourneen_US
dc.identifier.affiliationPrincess Alexandra Hospital, Brisbaneen_US
dc.identifier.affiliationLiverpool Hospital, Sydneyen_US
dc.identifier.affiliationRoyal Perth Hospital, Perthen_US
dc.identifier.affiliationRoyal Melbourne Hospital, Melbourneen_US
dc.identifier.affiliationRoyal Brisbane and Women's Hospital, Brisbaneen_US
dc.identifier.affiliationNambour General Hospital, Nambouren_US
dc.identifier.affiliationSt George Hospital, Sydney, Australiaen_US
dc.identifier.affiliationSir Charles Gairdner Hospital, Perthen_US
dc.identifier.affiliationCentenary Research Institute, Sydneyen_US
dc.identifier.doi10.1016/j.cgh.2017.09.063en_US
dc.type.contentTexten_US
dc.identifier.pubmedid29050991-
dc.type.austinJournal Article-
local.name.researcherGow, Paul J
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
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