Liver Function Test Flashcards

1
Q

What are the classifications of liver disease

A
  • Infection (Viral, bacterial, parasitic)
  • Toxic/drug induced
  • Autoimmune
  • Biliary tract obstruction
  • Vascular
  • Metabolic
  • Neoplastic
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2
Q

Causes of acute hepatitis

A
  • Poisoning (paracetamol)
  • Infection (Hep A-C)
  • Inadequate perfusion
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3
Q

Outcome of acute hepatitis

A
  • Resolution in majority of cases
  • Progression to acute hepatic failure
  • Progression to chronic hepatic damage
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4
Q

Common causes of chronic liver disease

A
  • Alcoholic fatty liver
  • Chronic active hepatitis
  • Primary biliary cirrhosis
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5
Q

Unusual causes of chronic liver disease

A
  • a-1 AT deficiency
  • Haemochromatosis
  • Wilson’s disease
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6
Q

Define cholestasis

A

Failure to produce/excrete bile

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7
Q

Result of cholestasis

A

Accumulation of conjugated bilirubin in the blood, leading to jaundice

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8
Q

What does liver failure result in

A
  • Inadequate synthesis of albumin, leading to oedema and ascites
  • Inadequate synthesis of clotting factors, resulting in bruising
  • Inability to eliminate bilirubin, causing jaundice
  • Inability to eliminate nitrogenous waste (e.g. ammonia) giving rise to hepatic encephalopathy
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9
Q

What do current liver function tests cover

A
  • Albumin
  • ALT (+ AST)
  • ALP (+ gamma-GT)
  • Bilirubin
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10
Q

Why measure albumin

A

Synthetic function

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11
Q

Why measure ALT

A

Aminotransferases for hepatocellular damage

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12
Q

Why measure ALP

A

For biliary epithelial damage and obstruction

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13
Q

Why measure bilirubin

A

For cholestasis

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14
Q

Advantages of current liver function tests

A
  • Cheap, widely available, interpretable

- Able to direct next subsequent investigation (e.g. imaging)

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15
Q

Disadvantages of current liver function tests

A
  • Does not assess liver function
  • Lack of complete organ specificity
  • Lack of disease specificity
  • May be over-sensitive
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16
Q

Where else is low albumin found

A
  • Post-surgical/ITU patients due to redistribution
  • Significant malnutrition
  • Nephrotic syndrome
17
Q

When is ALP raised

A
  • In liver disease due to increased synthesis

- In response to cholestasis

18
Q

When is gamma-GT raised

A
  • Cholestasis

- Affected by ingestion of alcohol/drugs such as phenytoin

19
Q

Where else is ALP present

A
  • Bone
  • Gut
  • Placenta
20
Q

Where else is gamma-GT present

A
  • Bone
  • Biliary tract
  • Pancreas
  • Kidney
21
Q

What happens to bilirubin once excreted in bile

A
  • Attacked by bacteria in colon and excreted in faeces

- Small amounts reabsorbed and excreted in urine as urobilirubin

22
Q

What can cause cholestasis

A
  • Failure by hepatocytes (intrahepatic cholestasis)

- Obstruction to bile flow (extra hepatic obstruction)

23
Q

What does an increased est ALT/ALP, normal ALT and increased ALP suggest

A

Cholestasis

24
Q

What does an increased est ALT/ALP and >10 fold increase in ALT and decrease in ALP suggest

A

Hepatocellular

25
Q

What else can cause changes in bilirubin

A
  • Haemolysis

- Gilberts syndrome

26
Q

What else can cause changes in ALP

A

Physiological e.g. pregnancy, childhood

27
Q

What else can cause changes in ALT

A

Skeletal muscle disorders e.g. MI

28
Q

What else can cause changes in gamma-GT

A
  • Alcohol

- Drugs

29
Q

When to perform caeruloplasmin/copper studies

A

Wilson’s disease

30
Q

When to perform iron studies

A

Haemochromatosis

31
Q

When to perform autoantibodies

A
  • Chronic active hepatitis

- PBC

32
Q

When to perform radiological intervention

A
  • Obstruction

- Hepatomegaly

33
Q

What is intelligent LFTs (iLFTs)

A
  • Combination of published diagnostic guidelines and expert opinion
  • Combination of biochemistry, haematology and serology in conjunction with liver ultrasound
34
Q

Who is considered for iLFTs

A

Patients with abnormal LFT’s in whom the cause in unclear (patients with frank jaundice excluded)

35
Q

First stage of iLFT

A
  • Patient specific data (age, gender, BMI, alcohol intake etc)
  • LFT and FBC performed (ALT, albumin, bilirubin, alk phos, gamma GT and platelets)
36
Q

Second stage of iLFT

A
  • If any of previous test abnormal
  • Aetiology screen (hepatitis serology, liver immunology, ferritin
  • Fibrosis staging