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dc.contributor.authorHussain, Nasir
dc.contributor.authorTrivedi, Palak J
dc.date.accessioned2024-02-12T12:21:43Z
dc.date.available2024-02-12T12:21:43Z
dc.date.issued2022-09-14
dc.identifier.citationHussain N, Trivedi PJ. The Inconvenient Truth of Primary Biliary Cholangitis/Autoimmune Hepatitis Overlap Syndrome. Clin Liver Dis. 2022 Nov;26(4):657-680. doi: 10.1016/j.cld.2022.06.007. Epub 2022 Sep 14en_US
dc.identifier.issn1089-3261
dc.identifier.eissn1557-8224
dc.identifier.doi10.1016/j.cld.2022.06.007
dc.identifier.pmid36270722
dc.identifier.urihttp://hdl.handle.net/20.500.14200/3643
dc.description.abstractThe term 'PBC/AIH-overlap' has been applied when features of autoimmune hepatitis (AIH), be they biochemical, serological or histological, coexist with primary biliary cholangitis (PBC), either at first presentation or sequentially during disease course. Several treatment paradigms have been proposed, extrapolated from those of the primary conditions. However, there are no randomised studies showing improved survival with combination therapy compared to bile acid monotherapy. In the absence of high-quality evidence, multidisciplinary patient-specific approaches must be used to individualise treatment pathways, with appreciation that disease phenotypes are not always static, differ in treatment responses, and have the potential to evolve over time.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.urlhttps://www.sciencedirect.com/journal/clinics-in-liver-diseaseen_US
dc.subjectMicrobiology. Immunologyen_US
dc.titleThe inconvenient truth of primary biliary cholangitis/autoimmune hepatitis overlap syndromeen_US
dc.typeArticle
dc.source.journaltitleClinics in Liver Disease
rioxxterms.versionNAen_US
dc.contributor.trustauthorHussain, Nasir
dc.contributor.trustauthorTrivedi, Palak J
dc.contributor.departmentDoctorsen_US
dc.contributor.departmentLiveren_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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