Laboratory Tests for Liver Disease Follow-up
For liver disease follow-up, laboratory testing should include bilirubin, albumin, ALT, ALP, GGT, and a full blood count, along with specific tests based on the underlying liver condition. 1
Core Laboratory Panel for Liver Disease Follow-up
Standard Panel (Every 6 months)
- Liver Function Tests:
- Bilirubin (total and direct)
- Albumin
- ALT (alanine aminotransferase)
- ALP (alkaline phosphatase)
- GGT (gamma-glutamyltransferase)
- Complete Blood Count (CBC)
- Coagulation Studies:
- Prothrombin time (PT)/International Normalized Ratio (INR)
Additional Tests Based on Specific Liver Conditions
For Viral Hepatitis
- Hepatitis viral load (HBV DNA or HCV RNA)
- Alpha-fetoprotein (AFP) for hepatocellular carcinoma screening
For Autoimmune Liver Disease
- Immunoglobulin levels (IgG, IgM, IgA)
- Autoantibodies (ANA, ASMA, AMA, LKM)
For Metabolic Liver Disease
- Ferritin and transferrin saturation (hemochromatosis)
- Alpha-1-antitrypsin level
- Ceruloplasmin (Wilson's disease)
For Non-alcoholic Fatty Liver Disease (NAFLD)
- Fasting glucose
- Lipid profile
- HbA1c
Frequency of Testing
The frequency of laboratory testing should be adjusted based on:
Disease Severity:
Treatment Monitoring:
- Patients on hepatotoxic medications: Every 3 months
- Patients undergoing specific therapy (e.g., antivirals): As per treatment protocol
Disease-Specific Considerations:
Non-Laboratory Assessments to Include
- Fibrosis Assessment: Non-invasive fibrosis markers (FIB-4, NAFLD Fibrosis Score) or elastography should be performed at least annually 1
- Imaging: Liver ultrasound and/or MRI with MRCP at least annually 1
Special Considerations
For Children
- Include anti-liver kidney microsomal antibody and celiac antibodies in autoimmune panels
- Alpha-1-antitrypsin level and ceruloplasmin (for children >3 years) 1
- More frequent monitoring may be needed during growth spurts or puberty 1
For Pregnant Women with History of Liver Disease
- Follow-up clinical visit with laboratory analysis 6-8 weeks after delivery
- Second follow-up after 2-3 years due to increased risk of hepatobiliary and immune-mediated diseases 1
Common Pitfalls to Avoid
- Ignoring mild elevations: Even mild elevations can indicate significant liver disease 2
- Attributing all abnormalities to medications: Always exclude other causes 2
- Focusing only on ALT/AST: Remember that normal aminotransferases do not exclude significant fibrosis or cirrhosis 1
- Overlooking non-hepatic causes: Consider muscle or cardiac injury for AST elevations 2
- Delaying referral: Patients with signs of liver failure or persistent unexplained elevations should be promptly referred to a hepatologist 2
By following this structured approach to laboratory testing for liver disease follow-up, clinicians can effectively monitor disease progression, treatment response, and detect complications early.