Liver Failure Flashcards

1
Q

Definition

A

Severe liver dysfunction leading to jaundice, encephalopthy and coagulopathy

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2
Q

Classification

A

It is classified based on the time interval between the onset of jaundice and the
development of hepatic encephalopathy

o Hyperacute = < 7 days
o Acute = 1-4 weeks
o Subacute = 4-12 weeks

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3
Q

Definition (acute)

A

Acute-on-Chronic Liver Failure = acute deterioration (decompensation) in patients
with chronic liver disease

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4
Q

Aetiology (common)

A

• Viral
o Hepatitis A, B, C, D and E

• Drugs
o Paracetamol overdose
o Idiosyncratic drug reactions

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5
Q

Aetiology (less common)

A
o Autoimmune hepatitis
o Budd-Chiari syndrome
o Pregnancy-related
o Malignancy (e.g. lymphoma)
o Haemochromatosis
o Mushroom poisoning (Amanita phalloides)
o Wilson's disease
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6
Q

Pathogenesis (jaundice)

A
  • due to decreased secretion of conjugated bilirubin
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7
Q

Pathogenesis (encephalopathy)

A

• Nitrogenous products (e.g. ammonia) is absorbed in the gut and goes via
the portal circulation to the liver
• A normal liver would be able extract these harmful substances
• However, if the liver is failing, these toxic products can go through the liver
and reach the brain and exert its effects

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8
Q

Pathogenesis (coagulopathy)

A
  • Reduced synthesis of clotting factors
  • Reduced platelets
  • Platelet functional abnormalities associated with jaundice or renal failure
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9
Q

Epidemiology

A

Paracetamol overdose counts for 50% of acute liver failure in the UK

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10
Q

Presenting symptoms

A
  • May be asymptomatic
  • Fever
  • Nausea
  • Jaundice (not always)
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11
Q

Signs on physical examination

A
  • Jaundice
  • Encephalopathy
  • Asterixis
  • Fetor hepaticus
  • Ascites and splenomegaly (less common if acute or hyperacute)
  • Bruising or bleeding
  • Signs of secondary causes (e.g. bronze skin colour, Kayser-Fleisher rings)
  • Pyrexia - may indicate infection or liver necrosis
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12
Q

Investigations (to find cause)

A
o Viral serology
o Paracetamol levels 
o Autoantibodies (e.g. ASM, Anti-LKM)
o Ferritin (haemochromatosis)
o Caeruloplasmin and urinary copper (Wilson's disease)
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13
Q

Investigations (bloods)

A

o FBC
• Low Hb (if GI bleed)
• High WCC (if infection)

o U&Es
• May show renal failure (hepatorenal syndrome)

o Glucose

o LFTs
• High bilirubin
• High AST, ALT, ALP, GGT
• Low albumin

o ESR/CRP

o Coagulation screen

o ABG - to determine blood pH

o Group and save

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14
Q

Investigations (other)

A

• Liver US/CT

• Ascitic Tap
o Send for MC&S
o If neutrophils > 250/mm3 = spontaneous bacterial peritonitis

  • Doppler scan of hepatic or portal veins - check for Budd-Chiari syndrome
  • EEG - monitor encephalopathy
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15
Q

Management plan (immediate)

A

• Resuscitation - ABC
• Treat the cause if possible:
o N-acetylcysteine - treatment for paracetamol overdose

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16
Q

Management plan (treatment of complications)

A

Treatment/prevention of complications (invasive ventilation and cardiovascular
support is often required)

o Monitor - vital signs, PT, pH, creatinine, urine output, encephalopathy
o Manage encephalopathy: lactulose and phosphate enemas
o Antibiotic and antifungal prophylaxis
o Hypoglycaemia treatment
o Coagulopathy treatment - IV vitamin K, FFP, platelet infusions
o Gastric mucosa protection - PPIs or sucralfate
o AVOID sedatives or drugs metabolised by the liver
o Cerebral oedema - decrease ICP with mannitol

17
Q

Management plan (renal failure)

A

o Haemodialysis

o Nutritional support

18
Q

Management plan (surgical)

A

Liver transplant

19
Q

Possible complications

A
  • Infection
  • Coagulopathy
  • Hypoglycaemia
  • Disturbance of electrolyte balance and acid-base balance
  • Disturbance of cardiovascular system
  • Hepatorenal syndrome
  • Cerebral oedema (causing raised ICP)
  • Respiratory failure
20
Q

Prognosis

A

Depends on severity and aetiology