Use of FibroScan in Liver Disease
FibroScan (transient elastography) should be used as a second-line test after initial risk stratification with FIB-4 in patients with NAFLD, metabolic syndrome, diabetes, or obesity, and as a first-line assessment in patients with chronic hepatitis B or C, or those with harmful alcohol use. 1
Algorithmic Approach to FibroScan Use
Step 1: Initial Risk Stratification
Calculate FIB-4 first in all patients with suspected liver disease using routine labs (AST, ALT, platelet count, age). 1, 2 This inexpensive point-of-care test should precede FibroScan in most cases to avoid unnecessary testing and costs.
- For NAFLD patients without diabetes or metabolic syndrome: If FIB-4 <1.3, repeat in 2-3 years without FibroScan 1
- For NAFLD patients with diabetes or ≥2 metabolic risk factors: If FIB-4 ≥1.3, proceed to FibroScan 1
- For patients ≥65 years old: Use FIB-4 cutoff of 2.0 instead of 1.3 to exclude advanced fibrosis 1
- For FIB-4 >2.67: Consider direct hepatology referral regardless of FibroScan results 1
Step 2: When to Order FibroScan
Proceed directly to FibroScan without FIB-4 in these populations:
- Chronic hepatitis B or C: All patients require FibroScan to guide antiviral therapy decisions 1, 2
- Harmful alcohol use: Patients drinking ≥35 units/week (women) or ≥50 units/week (men) 1, 2
- "Gray zone" hepatitis B patients: Those with ALT 1-2 times upper limit of normal to determine if antiviral therapy should be initiated 1
Use FibroScan after FIB-4 in these populations:
- NAFLD with indeterminate FIB-4 (1.3-2.67): Proceed to FibroScan for further risk stratification 1
- Type 2 diabetes with suspected NAFLD: Even with borderline FIB-4, as 69.2% have NASH and 41.0% have advanced fibrosis 2
- Metabolic syndrome (≥2 risk factors): Obesity, hypertension, dyslipidemia, prediabetes 1
Step 3: Patient Preparation
Patients must fast for at least 3-4 hours before FibroScan to avoid falsely elevated liver stiffness measurements. 2, 3 Food intake increases hepatic blood flow and can overestimate fibrosis stage, particularly problematic when measurements fall near clinical decision thresholds.
For alcohol-related liver disease, ideally perform FibroScan after 2 weeks of abstinence as recent alcohol consumption falsely elevates liver stiffness. 2
Step 4: Interpretation of Results
Technical validity requirements must be met:
- ≥10 successful measurements obtained 1, 2, 3
- Success rate ≥60% 1, 2
- Interquartile range (IQR) <30% of median value 1, 2
If these criteria are not met, the result is unreliable and should not guide clinical decisions. 2, 4
For NAFLD/Metabolic Syndrome:
- <8.0 kPa: Rules out advanced fibrosis with 93% sensitivity; repeat in 2-3 years if metabolic risk factors persist 1, 2, 3
- 8.0-12.0 kPa: Indeterminate risk; refer to hepatologist for monitoring and re-evaluation in 2-3 years 1
- >12.0 kPa: High risk for advanced fibrosis/cirrhosis; refer to hepatologist for consideration of liver biopsy or MR elastography 1
- ≥15 kPa: Highly suggestive of compensated advanced chronic liver disease (cACLD), especially if platelet count <150,000 1
For Chronic Hepatitis B or C:
- >7.0 kPa: Indicates significant fibrosis (≥F2) 2, 3
- >12.5 kPa: Indicates cirrhosis; initiate HCC surveillance and variceal screening 2, 3, 4
For Cirrhosis Surveillance:
- >20-25 kPa: Diagnoses clinically significant portal hypertension; requires endoscopic variceal screening per Baveno criteria 1, 2
Step 5: Follow-Up Intervals
Low-risk patients (FibroScan <8.0 kPa):
- Repeat FIB-4 and/or FibroScan in 2-3 years if metabolic risk factors persist 1
- Repeat in 3-5 years if risk factors are well-controlled 1, 2
Patients with NASH and/or fibrosis: Monitor annually 1
Patients with NASH cirrhosis: Monitor at 6-month intervals 1
Patients with previous advanced fibrosis/cirrhosis: Continue hepatological follow-up despite successful antiviral therapy or decrease in noninvasive test results 1
Critical Confounding Factors and Pitfalls
FibroScan results can be falsely elevated by:
- Active hepatic inflammation or acute hepatitis: Can produce falsely cirrhotic-range values 2, 3, 4
- Extrahepatic cholestasis or biliary obstruction: Falsely elevates stiffness 2, 3, 4
- Right heart failure or passive congestion: Increases liver stiffness independent of fibrosis 2, 4
- Recent food intake: Mandatory 3-4 hour fast 2, 3
- Recent alcohol use: Ideally test after 2 weeks abstinence 2
Technical limitations:
- Obesity (BMI >28 kg/m²): May require XL probe; failure rates 4.3-10.5% in Western populations 2, 4, 5
- Ascites: Cannot perform FibroScan reliably 2, 4
- Narrow intercostal spaces: May cause failed acquisition 2, 4
The most common error is performing FibroScan without adequate fasting, which leads to overestimation of fibrosis stage and inappropriate escalation of care. 2
When FibroScan Results Trigger Specialist Referral
Immediate hepatology referral indicated for:
- FibroScan >12.0-12.5 kPa suggesting advanced fibrosis/cirrhosis 1, 3
- FibroScan ≥15 kPa with platelet count <150,000 (highly suggestive of cACLD) 1
- FibroScan >20-25 kPa indicating clinically significant portal hypertension 1, 2
- Discordant results between FIB-4 and FibroScan requiring liver biopsy 1
Hepatology referral for monitoring:
- FibroScan 8.0-12.0 kPa (indeterminate risk) 1
- Chronic hepatitis B "gray zone" patients with FibroScan showing significant fibrosis 1
Special Populations
Type 2 diabetes patients warrant particular attention as they have high rates of NASH (69.2%) and advanced fibrosis (41.0%) even with borderline FIB-4 scores. 1, 2 Screening for diabetes is mandatory in all NAFLD patients using fasting glucose, HbA1c, or 75g OGTT in high-risk groups. 1
Patients with congenital bleeding disorders previously exposed to HBV/HCV should be screened for additional chronic liver damage risk factors and evaluated with FibroScan even if asymptomatic with normal liver tests. 1
Type 1 diabetes patients should only be screened for fibrosis if additional risk factors present (obesity, incidental steatosis, elevated aminotransferases), as NAFLD prevalence is much lower than in type 2 diabetes. 1