Alcoholic Hepatitis Flashcards

1
Q

Define alcoholic hepatitis.

A

Inflammatory liver injury caused by chronic heavy intake of alcohol.

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2
Q

What are the three forms of liver disease caused by excess alcohol intake?

A

Fatty liver – occurs in women who consume >20g or men >30g of alcohol per day. Triglycerides accumulate in the liver due to defective fatty acid (+glycerol) metabolism due to mitochondrial damage(no beta oxidation due to lack of NAD+) or impairment of receptors or enzymes involved.

Alcoholic hepatitis - Lack of NAD+ causes the deranged metabolic processes to leak oxygen free radicals - which are pro-inflammatory → tissue damage Acetaldehyde is also damaging and pro-inflammatory. This is still reversible but takes some time

Liver cirrhosis - Persistent inflammation → fibroblast infiltration→ connective tissue. Irreversible

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3
Q

What is the pathophysiology of alcoholic hepatitis?

A

Defining histological features of alcoholic hepatitis are:

  1. Liver cell damage - ballooning +/- Mallory Denk bodies
  2. Inflammation
  3. Fibrosis

Fatty change may also be seen due to progression from the fatty liver stage

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4
Q

How is alcohol metabolised in the body? (2)

A

Alcohol is metabolised in the liver by 2 main pathways:

  1. Cytochrome P450 2E1 (generates free radicals through oxidation of NADPH to NADP. 2E1 is upregulated in chronic alcohol use)
  2. Alcohol dehydrogenase + Aldehyde dehydrogenase (reduce NAD —> NADH. This excess NADH:NAD ratio inhibits gluconeogenesis and promotes fatty infiltration in the liver)
  3. Hepatic macrophages only in chronic alcohol use (–> TNFalpha and reactive species production in mitochondria. Free radicals –> lipid peroxidation –> inflammation and fibrosis)
    * People with alcohol use are usually deficient in antioxidants such as glutathione and vitamin E. So oxidative stress is very damaging.*
    * Acetaldehyde can bind to cellular proteins and produce antigenic adducts –> inflammation.*
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5
Q

How common is alcoholic hepatitis?

A
  • 10-35% of heavy drinkers develop it
  • 40% of cases of alcoholic hepatitis will develop into cirrhosis
  • ALD → 3 million deaths annually worldwide.
  • Generally development of ALD is more rapid and occurs at a lower dose in women than in men.
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6
Q

What is the typical presentation of alcoholic hepatitis?

A
  • Hx of heavy alcohol intake (~15-20 years of excessive intake for development of alcoholic hepatitis)
  • May remain asymptomatic and undetected unless they present for other reasons
  • May be mild illness, nausea, malaise, epigastric pain, right hypochondriac pain and low-grade fever.
  • More severe forms: jaundice, abdominal discomfort, swelling, swollen ankles, GI bleeding.
  • There may be trigger events (e.g. aspiration pneumonia or injury)
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7
Q

What are the signs of alcoholic hepatitis on examination?

A

Signs of alcohol excess - malnourished, palmar erythema, Dupyutren’s contracture, facial talengiectasia, parotid enlargement, spider naevi, gynaecomastia, testicular atrophy, hepatomegaly, easy bruising

Signs of severe alcoholic hepatitis - febrile (50% patients), tachycardia, jaundice (>50%), bruising, encephalopathy*, ascites (30-60%), hepatomegaly (usually mild enlargement and tender on palpation), splenomegaly.

*(e.g. hepatic foetor, liver flap, drowsiness, unable to copy a 5 pointed star, disorientated)

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8
Q

What investigations would you do for alcoholic hepatitis?

A

Bloods

  • FBC - low Hb, high MCV, high WCC, low plt,
  • LFTs - AST>ALT (2:1), high Bil, low albumin, high Alk Phos, high GGT
  • U&E - urea and K+ levels tend to be low unless significant renal impairment
  • Clotting - prolonged PT is a sensitive marker of significant liver damage

Imaging

  • US - for other causes of liver damage (e.g. maligancy)
  • UGI endoscopy - for varices
  • EEG - for slow-wave activity indicative of encephalopathy

Invasive

  • Liver biopsy - percutaenous or transjugular (in presence of coagulopathy) may distinguish other causes of hepatitis
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9
Q

How do you manage alcoholic hepatitis ACUTELY?

A

Acute

  • Parenteral thiamine, Vit C and multivitamins
  • K+, Mg2+ and glucose - monitor and correct abnormalities
  • Ensure adequate urine output
  • Oral lactulose and phosphate enemas - for encephalopathy
  • Diuretics - for ascites - furosemide/spironolactone or therapeutic paracentesis
  • Glypressin and N-acetylcysteine - for hepatorenal syndrome
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10
Q

How do you manage alcoholic hepatitis (non-acutely)?

A

Treatment required:

  • Supportive
  • Stop alcohol
  • Nutrition
  • Vitamins (esp. Pabrinex containing B1 and thiamine)
  • Occasionally steroids (anti-inflammatory)

Protein restriction should be avoided unless encephalopathic

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11
Q

What are the complications of alcoholic liver disease?

A
  • Acute liver decompensation
  • Hepatorenal syndrome (renal failure secondary to advanced liver disease)
  • Cirrhosis
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12
Q

What is the prognosis with alcoholic hepatitis?

A
  • Mortality in first month is 10%, 40% in first year
  • If alcohol intake continues, most progress to cirrhosis in 1-3 years
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13
Q

What are some differentials for fatty liver disease?

A
  1. NASH
  2. Alcoholic hepatitis
  3. Kwashiorkor
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14
Q

What are the stages of alcoholic liver disease?

A
  1. Alcoholic hepatitis
  2. Chronic stable liver disease
  3. Resultant portal hypertension
  4. Liver failure (asterixis)

NB: forms are fatty liver, alcoholic hepatitis, cirrhosis.

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