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Review article: the modern management of autoimmune hepatitis
Author(s) -
YEOMAN A. D.,
LONGHI M. S.,
HENEGHAN M. A.
Publication year - 2010
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2010.04241.x
Subject(s) - medicine , autoimmune hepatitis , azathioprine , intensive care medicine , liver transplantation , disease , cirrhosis , tacrolimus , hepatocellular carcinoma , clinical trial , hepatitis , transplantation , immunology
Aliment Pharmacol Ther   31 , 771–787 Summary Background  The management of autoimmune hepatitis (AIH) continues to be refined. However, several issues remain unresolved, primarily as a consequence of the low incidence of the disease. This factor has contributed both to a lack of understanding of and a paucity of large scale clinical trials involving therapeutic agents. Aim  To summarize the latest evidence regarding the pathogenesis, diagnosis, therapy and long‐term management of AIH with a focus on clinical aspects of the disease. Method  We searched PUBMED for articles pertaining to AIH, its pathogenesis, treatment and clinical outcomes, combined with the authors’ own knowledge of the literature. Results  Standard therapy (corticosteroids and azathioprine) is effective in more than 80% of patients which renders study of novel agents difficult. Budesonide appears to show equivalence to prednisolone. Available, but limited, data suggest that mycophenolate mofetil, tacrolimus and ciclosporin are all variably effective second line agents. Patients with AIH and cirrhosis are at risk of hepatocellular carcinoma (HCC) and require screening. Patients with end stage liver disease represent excellent candidates for liver transplantation. Conclusions  Despite ongoing limitations in the understanding of pathogenesis and difficulties in evaluating novel therapies, the management of AIH continues to evolve slowly. Multi‐centre collaboration is necessary to obtain sufficient patient numbers to undertake good quality therapeutic studies.

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