Initial Medication Treatment for Autoimmune Hepatitis
Standard Induction Regimen
- The European Association for the Study of Liver Diseases (EASL) recommends starting prednisone as initial therapy followed by addition of azathioprine after two weeks, particularly when bilirubin levels are below 6 mg/dL, in patients with moderate to severe disease 1
- Combination therapy with prednisone (starting at 30 mg/day, tapering to 10 mg/day over 4 weeks) plus azathioprine (1-2 mg/kg/day) is superior to prednisone monotherapy because it produces significantly fewer corticosteroid-related side effects (10% versus 44%) while maintaining equivalent efficacy 4
Alternative Regimen for Non-Cirrhotic Patients
- Budesonide 9 mg/day plus azathioprine may be considered specifically in treatment-naive, non-cirrhotic patients with early-stage disease who are at high risk for steroid-specific side effects, such as psychosis, poorly controlled diabetes, or severe osteoporosis 1, 4
Monitoring and Response Assessment
- 80-90% of patients achieve biochemical improvement with transaminases normalizing within 6 months in most responders 1, 4
- Complete normalization of both transaminases AND IgG levels should be the goal, as persistent elevations predict relapse after treatment withdrawal, ongoing histological activity, progression to cirrhosis, and poor outcomes 1, 2
Treatment Duration
- Continue treatment for at least 2 years and for at least 12 months after normalization of liver enzymes 2, 3
Management of Non-Response
- For confirmed non-responders, increase doses of prednisolone and azathioprine (up to azathioprine 2 mg/kg/day) 1, 2, 3
Acute Severe Autoimmune Hepatitis
- Patients with acute severe AIH require immediate treatment with high-dose intravenous corticosteroids (≥1 mg/kg) as early as possible 1
Prevention of Treatment Complications
- All patients must receive calcium and vitamin D supplementation from treatment initiation, DEXA scanning for bone mineral density monitoring at 1-2 year intervals, and vaccination against hepatitis A and B early in susceptible patients 2, 3