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alcohol-associated hepatitis

in review 4 min read Updated 2026-08-18
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alcohol-associated hepatitis

Acute jaundice in the setting of heavy alcohol use with a characteristic AST:ALT ratio ≥1.5–2:1 and both values <400 U/L. Severity determines management: MDF ≥32 or MELD >20 defines severe disease warranting prednisolone ± IV NAC. Reassess at day 4–7 with the Lille score — stop steroids if ≥0.45 (non-responder). Nutrition is as important as pharmacotherapy. Always rule out spontaneous bacterial peritonitis before starting steroids.


diagnosis

Clinical diagnosis — biopsy rarely needed unless presentation is atypical.

criterionthreshold
onset of jaundicewithin 60 days of heavy alcohol use
alcohol intake>40 g/day (women), >60 g/day (men) for ≥6 months
AST>50 U/L
AST:ALT ratio≥1.5–2:1
both AST and ALT<400 U/L
total bilirubin>51 µmol/L
the AST:ALT ratio

Alcohol depletes hepatic pyridoxal-5’-phosphate (vitamin B6 cofactor for ALT) and causes mitochondrial injury preferentially releasing AST. If ALT exceeds AST, reconsider the diagnosis — think viral hepatitis, DILI, or MASLD with a superimposed insult.

what to rule out first

  • Infection: diagnostic paracentesis if ascites present — steroids are contraindicated with active SBP
  • Other liver injury: hepatitis B/C serologies, acetaminophen level, lipase, RUQ ultrasound (biliary obstruction, hepatic vein thrombosis)
  • Sepsis workup: blood cultures, urine cultures, CXR

severity scoring

scoresevere thresholduse
Maddrey discriminant function (MDF)≥32traditional; identifies candidates for steroids
MELD>20better validated for mortality prediction

MDF=4.6×(PTpatientPTcontrol)+total bilirubin (mg/dL)\text{MDF} = 4.6 \times (\text{PT}_{\text{patient}} - \text{PT}_{\text{control}}) + \text{total bilirubin (mg/dL)}

The original formula uses mg/dL — divide SI bilirubin (µmol/L) by 17.1 before plugging in.

Non-severe AH (MDF <32, MELD ≤20): supportive care, nutrition, alcohol cessation. No steroids.


management of severe AH

nutrition

Aggressive enteral nutrition is non-negotiable — malnutrition is universal and independently predicts mortality.

  • 35 kcal/kg/day, 1.2–1.5 g/kg/day protein
  • NG feeding if oral intake inadequate
  • Do not restrict protein (encephalopathy in AH is driven by liver failure, not protein load)

pharmacotherapy

Prednisolone 40 mg PO daily × 28 days (or IV methylprednisolone 32 mg if unable to take PO)

  • Use prednisolone (not prednisone) — does not require hepatic conversion
  • ± IV N-acetylcysteine (NAC) for the first 5 days improves 1-month survival when combined with steroids (Nguyen-Khac, NEJM 2011)
contraindications to steroids
  • Active uncontrolled infection, sepsis, or SBP
  • Active GI bleeding
  • Severe AKI (creatinine >221 µmol/L in some protocols)
  • HBV reactivation risk

Always tap the ascites before starting steroids. Treating SBP with steroids on board is a setup for septic death.

lille score — day 4–7 reassessment

Reassess steroid response using the Lille score (incorporates change in bilirubin from baseline):

Lille scoreinterpretationaction
<0.16complete respondercontinue prednisolone for full 28 days
0.16–0.44partial respondercontinue; benefit still likely
≥0.45non-responderstop steroids — continued exposure adds infection risk without survival benefit

Non-responders with MELD ≥26 should be evaluated for early liver transplantation at centres with established protocols for selected patients.

what does not work

  • Pentoxifylline — no mortality benefit (STOPAH, NEJM 2015)
  • G-CSF — insufficient evidence; not recommended
  • Prophylactic antibiotics — no proven role in the absence of documented infection

early liver transplantation

Historically, a 6-month abstinence rule excluded most severe AH patients from transplant. Multiple centres now offer early transplantation for steroid non-responders with:

  • first liver-related decompensation
  • supportive social environment
  • no other severe psychiatric or substance use disorder
  • formal psychosocial and addiction assessment

This remains centre-specific and not universally available in Canada.


common traps

  • Starting steroids before ruling out infection — paracentesis and cultures first, always
  • Using prednisone instead of prednisolone — in a failing liver, conversion is impaired
  • Continuing steroids past day 7 in a non-responder — Lille ≥0.45 means stop; harm exceeds benefit
  • Confusing AH with decompensated alcohol-related cirrhosis — AH is an acute inflammatory syndrome superimposed on (or triggering) liver failure; management differs from chronic decompensation
  • Restricting protein for encephalopathy — worsens malnutrition and outcomes

related: approach to elevated liver enzymes · cirrhosis · decompensated cirrhosis · spontaneous bacterial peritonitis · hepatorenal syndrome

Key references

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