What is the treatment for alcoholic hepatitis?

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Treatment of Alcoholic Hepatitis

Alcohol abstinence is the absolute cornerstone of treatment for all patients with alcoholic hepatitis, and for severe disease (mDF ≥32 or MELD >20), prednisolone 40 mg daily for 28 days should be initiated unless contraindications exist. 1, 2

Initial Assessment and Severity Stratification

Before initiating treatment, disease severity must be determined using validated scoring systems:

  • Modified Discriminant Function (mDF) ≥32 indicates severe disease requiring pharmacologic intervention 1, 2
  • MELD score >20-21 or GAHS ≥9 are alternative thresholds for defining severe disease 1, 2
  • Presence of hepatic encephalopathy alone warrants consideration of treatment regardless of other scores 1

All patients should be screened for infections at presentation with blood, urine, and ascitic fluid cultures (if ascites present), even without fever, as infection significantly worsens prognosis 2

Universal Treatment Components

Alcohol Abstinence

Complete and permanent abstinence from alcohol is mandatory - there is no safe amount of alcohol consumption after an episode of alcoholic hepatitis, as the disease can persist or redevelop with any continued drinking 1

  • Naltrexone or acamprosate may be used in combination with counseling to reduce relapse risk in patients who achieve abstinence 1
  • Baclofen has shown benefit in maintaining abstinence in patients with cirrhosis 1

Nutritional Support

Aggressive nutritional therapy is essential as most patients with severe alcoholic hepatitis are malnourished, which independently worsens outcomes 1

  • Caloric intake: 30-40 kcal/kg/day 2
  • Protein intake: 1.2-1.5 g/kg/day (up to 1.5 g/kg/day in critically ill patients) 1, 2
  • If three meals daily are insufficient, add early morning and late evening meals 1
  • Enteral nutrition improves survival regardless of steroid treatment 1

Vitamin and Mineral Supplementation

All patients require comprehensive micronutrient replacement including vitamin A, thiamine, vitamin B12, folic acid, pyridoxine, vitamin D, and zinc 1

Treatment Based on Disease Severity

Mild-Moderate Disease (mDF <32, no encephalopathy)

These patients typically improve with abstinence and nutritional support alone and do not require pharmacologic intervention 1

  • Monitor closely during hospitalization 1
  • If bilirubin decreases or mDF improves during the first week, specific medical interventions beyond nutrition are unlikely to provide benefit 1

Severe Disease (mDF ≥32 or MELD >20)

First-Line: Corticosteroids

Prednisolone 40 mg daily for 28 days (followed by discontinuation or 2-week taper) is the most extensively studied and effective treatment for severe alcoholic hepatitis 1, 2

  • Improves 28-day survival: 80-84.6% with steroids vs. 65-65.7% with placebo 1
  • Acts by reducing pro-inflammatory cytokines including TNF-α 1

Contraindications to steroids include:

  • Active gastrointestinal bleeding 1
  • Renal failure 1
  • Acute pancreatitis 1
  • Uncontrolled infection 1

Response Assessment at Day 7

Treatment response must be evaluated at day 7 using the Lille model or Early Change in Bilirubin Level (ECBL) 1, 2

  • Lille score <0.45: Good response with 85% 6-month survival - continue steroids 1, 2
  • Lille score >0.45: Poor response with only 25% 6-month survival - discontinue steroids 1, 2
  • ECBL positive (bilirubin at day 7 lower than day 1): 82% 6-month survival 1
  • ECBL negative: Only 23% 6-month survival 1

Discontinuing steroids in non-responders is critical as infection occurs more frequently in steroid non-responders, and continued steroid exposure increases risk without benefit 1

Alternative: Pentoxifylline

For patients with contraindications to steroids, pentoxifylline 400 mg orally three times daily for 4 weeks can be considered 1

  • Primarily reduces risk of hepatorenal syndrome 1
  • However, the 2014 STOPAH trial showed no mortality benefit from pentoxifylline, limiting its current role 3, 4

Critical Management Considerations

Renal Protection

Avoid nephrotoxic drugs including diuretics and iodinated contrast agents as acute kidney injury represents early multi-organ failure and dramatically worsens prognosis 2

Infection Surveillance

Monitor continuously for infections which can develop after initial diagnosis and are associated with high mortality, particularly in steroid non-responders 1, 2

Liver Transplantation

For steroid non-responders (Lille score ≥0.45), liver transplantation may offer significantly higher survival than continued medical management alone, though this requires careful patient selection and remains controversial 1, 3, 4, 5

Common Pitfalls to Avoid

  • Do not use steroids in mild disease (mDF <32 without encephalopathy) - these patients improve spontaneously and steroid risks outweigh benefits 1
  • Do not continue steroids beyond day 7 in non-responders - this only increases infection risk without improving outcomes 1
  • Do not neglect nutritional support - it is as important as pharmacologic therapy and improves outcomes independently 1
  • Do not allow partial abstinence - patients who attempt to "cut back" rather than stop completely have high recidivism rates and continued disease progression 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Initial Treatment for Alcoholic Hepatitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Alcoholic hepatitis: current challenges and future directions.

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2014

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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