Laboratory Tests for Biliary Hepatitis
For patients with suspected biliary hepatitis, a comprehensive laboratory panel should include liver function tests (ALT, AST, ALP, GGT, total and direct bilirubin), complete blood count, coagulation studies, and serological markers for viral and autoimmune etiologies.
Core Laboratory Tests
Initial Assessment
Liver Function Tests:
Synthetic Function:
- Albumin
- Prothrombin time (PT)/International Normalized Ratio (INR) 1
Complete Blood Count (CBC):
- White blood cell count with differential (to assess inflammation)
- Platelet count (may be decreased in advanced liver disease) 2
Pattern Recognition
Biliary hepatitis typically presents with a cholestatic pattern:
- Elevated ALP (often >3× ULN)
- Elevated GGT (confirms hepatobiliary origin of ALP elevation)
- Variable elevation of aminotransferases (ALT/AST)
- Elevated direct bilirubin (in obstructive cases) 1
Additional Testing
Etiological Assessment
Viral Hepatitis Markers:
- Hepatitis A, B, C, E serology 1
- If HBV positive, consider HDV testing
Autoimmune Markers:
- Antimitochondrial antibody (AMA) - for primary biliary cholangitis
- Antinuclear antibody (ANA)
- Anti-smooth muscle antibody (ASMA)
- Immunoglobulin levels (IgG, IgM, IgA) 1
Other Serological Tests:
- Ceruloplasmin (Wilson's disease)
- Alpha-1 antitrypsin level
- Ferritin and iron studies 1
Pancreatic Involvement
- Amylase and lipase (to rule out pancreatitis as a cause or complication) 2
Monitoring and Follow-up Testing
- For patients with confirmed biliary hepatitis, repeat liver function tests should be performed within 1-2 weeks initially, then at intervals based on clinical response 1
- For mild elevations (Grade 1: ALT/AST > ULN – 3× ULN), repeat testing within 1-2 weeks
- For moderate elevations (Grade 2: ALT/AST > 3–5× ULN), repeat testing within 2-5 days 1
- For severe elevations (Grade 3-4: ALT/AST > 5× ULN), repeat testing within 2-3 days 1
Special Considerations
Drug-Induced Biliary Hepatitis
If drug-induced biliary injury is suspected:
- Document all medications, including over-the-counter drugs and supplements
- Consider drug-specific monitoring protocols (e.g., immune checkpoint inhibitors have specific monitoring requirements) 1
Pre-existing Liver Disease
For patients with pre-existing liver disease:
- Establish baseline values from multiple measurements (at least 2 weeks apart)
- Use relative changes rather than absolute values (e.g., ALT >3× baseline or >300 U/L) 1
- Consider ALP isoenzyme fractionation to confirm hepatobiliary origin 1
Clinical Pearls
- A combination of ALT ≥3× ULN plus total bilirubin ≥2× ULN (Hy's Law criteria) indicates severe liver injury with poor prognosis and requires immediate action 1
- Serial measurements are more informative than single readings 2
- GGT should be measured alongside ALP to confirm hepatobiliary origin of ALP elevation 1
- Direct bilirubin helps differentiate between hepatic and post-hepatic causes of jaundice 2
- In patients with Gilbert's syndrome, direct bilirubin should be used for decision-making rather than total bilirubin 1
By systematically applying these laboratory tests, clinicians can effectively diagnose biliary hepatitis, determine its etiology, assess its severity, and monitor treatment response.