Assessing liver function
There is no single specific test that gives a measure of liver function, and assessment is based upon the whole clinical picture. This includes a combination of signs and symptoms, liver function tests, histopathology and imaging. Signs and symptoms include jaundice, pruritus, varices and spider naevi.Symptoms of jaundice include yellowing of skin and whites of the eyes, dark urine and pruritus |
Patients with more advanced liver impairment may have multiple symptoms and are more likely to have ascites, varices, and encephalopathy.
Liver function tests (LFTs)
Not all LFTs are specific to the liver and they should be interpreted alongside other markers of liver dysfunction and the overall clinical picture.- Bilirubin – This is a product of haemoglobin breakdown and is normally excreted in the bile. It is particularly raised in cholestasis, but can also be raised in hepatocellular disease.
- Alkaline phosphatase (ALP) – This is raised in cholestasis, since it is secreted into bile ducts, and slightly raised in hepatocellular disease. Other causes, such as bone diseases, can also increase ALP.
- Transaminases (ALT / AST) – These are markers of hepatocellular injury. Transaminases can also be raised in cardiac disease.
- Albumin – This is synthesised in the liver and has a long half-life (20 days). Although not a very specific indicator, a low albumin in association with deranged LFTs may suggest chronic liver disease/ dysfunction.
- Prothrombin time – As the liver makes clotting factors, an increased prothrombin time suggests the synthetic ability of the liver has been affected. Clotting factors have short half-lives, so changes in prothrombin time can happen quickly and can be seen in both acute and chronic liver disease.
Local LFT reference ranges may differ between hospitals and paediatric ranges may be different to those used for adults.