Clinical Reference

Liver Stiffness kPa to Metavir Fibrosis Stage Conversion

Disease-specific conversion tables for MAFLD/MASLD, Hepatitis B (HBV), and Hepatitis C (HCV). Thresholds differ by aetiology — always use the correct table.

Important: kPa thresholds vary by disease aetiology, elastography system, and guideline version. These tables reflect commonly used EASL/GESA-based thresholds. Always interpret in the clinical context and refer to current guideline versions for definitive staging decisions. Thresholds for guided TE and 2D-SWE systems may differ slightly from VCTE (FibroScan) thresholds in some studies.

MAFLD / MASLD (Metabolic Fatty Liver Disease)

Based on GESA MAFLD clinical guidelines and EASL consensus. These are the most commonly encountered thresholds in Australian primary care.

LSM (kPa)Metavir StageInterpretationRecommended Action
< 8.0 kPaF0–F1No or mild fibrosisMonitor. Repeat FIB-4 in 1–2 years.
8.0–10.0 kPaF1–F2Mild to moderate fibrosisOptimise metabolic risk. Consider specialist.
10.0–12.0 kPaF2–F3Moderate to significant fibrosisSpecialist referral recommended.
12.0–15.0 kPaF3Advanced fibrosisRefer to hepatologist.
> 15.0 kPaF3–F4Advanced fibrosis / cirrhosisUrgent specialist referral.

Hepatitis B (HBV)

HBV thresholds differ from MAFLD — liver inflammation in active HBV can raise LSM independent of fibrosis. Interpret during virological suppression where possible.

LSM (kPa)Metavir StageInterpretationRecommended Action
< 6.0 kPaF0–F1No or mild fibrosisMonitor per GESA HBV guidelines.
6.0–9.0 kPaF1–F2Mild to moderate fibrosisConsider treatment initiation threshold.
9.0–12.0 kPaF2–F3Significant fibrosisTreat if not already on therapy.
> 12.0 kPaF3–F4Advanced fibrosis / cirrhosisTreat. Cirrhosis surveillance required.

Hepatitis C (HCV) — Post-Treatment Monitoring

These thresholds apply pre-DAA treatment and for post-SVR monitoring. LSM typically falls post-SVR but may remain elevated in established cirrhosis.

LSM (kPa)Metavir StageInterpretationRecommended Action
< 7.0 kPaF0–F1No or mild fibrosisTreat with DAA. Monitor post-SVR.
7.0–9.5 kPaF2Moderate fibrosisTreat. Post-SVR elastography at 6 months.
9.5–12.5 kPaF3Advanced fibrosisTreat urgently. Cirrhosis surveillance post-SVR.
> 12.5 kPaF4CirrhosisTreat. Lifelong cirrhosis surveillance required regardless of SVR.

Important Notes on kPa Interpretation

  • Inflammation elevates LSM: Active hepatitis (elevated ALT/AST) can raise liver stiffness independent of fibrosis. Interpret during periods of disease stability where possible.
  • Congestion elevates LSM: Right heart failure and hepatic venous congestion increase liver stiffness significantly — elastography in these patients may not reflect fibrosis.
  • Post-prandial state: LSM is higher within 2 hours of a large meal. Standard protocol is fasting for 2–4 hours pre-examination.
  • System-specific thresholds: Published cutoffs may differ between VCTE (FibroScan) and guided TE or 2D-SWE systems. Most published data uses VCTE. Clinically, the difference is generally not large enough to change management.
  • Baveno VII monitoring threshold: A change of ≥5 kPa between measurements is considered clinically meaningful for longitudinal monitoring (progression or regression).