Cirrhosis Flashcards

1
Q

What is cirrhosis?

A

Diffuse pathological process, characterised by fibrosis and conversion of normal liver architecture→ structurally abnormal nodules (called regenerative nodules).

Can arise from many causes and is final stage of any chronic liver disease.

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2
Q

What can cirrhosis cause?

A

PHTN, liver failure, hepatocellular carcinoma, etc.

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3
Q

Pathophysiology of cirrhosis?

A

Fibrosis occurs in most chronic liver injury→ may evolve into cirrhosis w nodule formation.

Central mechanism in hepatic fibrosis: activation of hepatic stellate cells (major source of extracellular matrix)→ accumulation of collagen in hepatic parenchyma

Overall progression→ disrupted liver blood flow→ increased portal venous pressure+ directing blood away from liver→ ascites, gastro-oesophageal varices, hepatic encephalopathy, etc

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4
Q

How can acute insults lead to acute decompensation in cirrhosis?

A

Acute insults (ie: infection)→ changes in vascular tone→ influence portal pressure→ acute decompensation

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5
Q

What is decompensated cirrhosis?

A

Acute deterioration in liver function in a patient w cirrhosis. Characterised by jaundice, ascites,hepatic encephalopathy, hepatorenal syndrome or variceal haemorrhage

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6
Q

Aetiology of cirrhosis? (lots!)

A

Any chronic liver disease
Alcoholic liver disease, non-alcoholic fatty liver disease, Hep C and B

Metabolic disorders (inclu: Wilson’s, haemochromatosis, etc)

Cholestatic and autoimmune: primary biliary cholangitis, primary sclerosing cholangitis, autoimmune hepatitis

Biliary obstruction

Hepatic venous outflow obst (R sided heart failure)

Drugs (amiodarone, methotrexate)

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7
Q

Risk factors for cirrhosis?

A

Alcohol misuse
IVDU
Unprotected intercourse
Obesity
Certain global regions where Hep B, C endemic
Blood transfusions (weak)
Tattooing (weak)

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8
Q

Abdominal/ GIT signs and symptoms of cirrhosis?

A
  • Abdominal distention (esp flanks)
  • Jaundice and pruritus
  • Haematemesis and melaena
  • Caput medusa
  • Bruising
  • Hepatomegaly and splenomegaly
  • Ascites (shifting dullness and fluid thrill) and hepatic bruit
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9
Q

Hands and nails features of cirrhosis? (3)

A

Leukonychia, palmar erythema, spider naevi

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10
Q

Facial features of cirrhosis?

A

Telangiectasia: red focal lesions resulting from irreversible dilatation of small blood vessels in skin

Bruising
Jaundiced sclera
Xanthelasma

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11
Q

Other signs and symptoms of cirrhosis? (exclu. abdominal, facial, hands and nails)

A
  • Constitutional symptoms: fatigue, weakness, weight loss
  • Peripheral oedema
  • Altered mental state (uncommon)
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12
Q

Ix: Investigations for cirrhosis?

A

Bloods
IF deranged LFTS: USS first line, CT
IF confusion with decompensated liver disease→ check blood glucose!
Endoscopy
Liver biopsy
Ascitic tap
Investigate CAUSE

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13
Q

Ix: Bloods results for cirrhosis may show?

A
  • LFTs: deranged (high AST, ALT, GGT)
  • Serum albumin and sodium: low
  • Prothrombin time: elevated
  • Platelet count: low
  • Serum AFP (alpha-fetoprotein)→ hepatocellular carcinoma; protein indicative of rapid cell division
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14
Q

Ix: USS/ CT for cirrhosis may show?

A
  • Ascites
  • Hepatomegaly
  • HCC
  • Portal HTN
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15
Q

Ix: Liver biopsy for cirrhosis may show?

A

Periportal fibrosis
Nodules

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16
Q

Ix: Investigations for potential causes of cirrhosis?

A
  • Iron studies: haemochromatosis
  • ASMA/ANA: autoimmune
  • Viral serology (Hepatitis, EBV, HIV, etc)
  • Caeruloplasmin: low levels could indicate Wilson’s disease (rare inherited disorder,copper accum in liver, brain, etc)
  • A1-antitrypsin
17
Q

First line management of cirrhosis?

A
  • Treat underlying chronic liver disease + monitor for complications + supportive care
  • Consider: sodium restriction and diuretics for ascites
18
Q

Second line management for cirrhosis?

A
  • Liver transplant (if complications/ decompensation)
  • IF not suitable for transplant: transjugular intrahepatic portosystemic shunt (TIPSS)