Referral for Fatty Liver: Risk Stratification Determines Next Steps
Not all patients with fatty liver need GI referral—the decision depends entirely on fibrosis risk stratification using validated scoring systems, with high-risk patients requiring specialist evaluation while low-risk patients can be managed in primary care. 1
Initial Risk Stratification (Required for All Patients)
Calculate the FIB-4 score immediately for every patient with suspected fatty liver, even if liver enzymes are normal. 1 This score uses age, ALT, AST, and platelet count to stratify fibrosis risk. 1
Low-Risk Patients (Can Be Managed in Primary Care)
- FIB-4 <1.3 (or <2.0 if over 65 years): These patients have very low risk of advanced fibrosis (only 2.6 liver-related events per 1000 patient-years) and can be managed without specialist referral. 1
- Focus on lifestyle modifications and cardiovascular risk reduction in primary care. 1
- Repeat surveillance testing in 2-3 years to monitor for progression. 1
High-Risk Patients (Require Immediate GI/Hepatology Referral)
Refer immediately to a gastroenterologist or hepatologist if: 1
- FIB-4 score in the high-risk range 1
- Liver stiffness ≥12.0 kPa on elastography 1
- Enhanced Liver Fibrosis (ELF) score >9.5 1
- Persistently elevated liver enzymes for >6 months with no NAFLD risk factors (no diabetes, BMI <25, no dyslipidemia, no hypertension) 2
- Evidence of advanced liver disease (features of cirrhosis or portal hypertension on imaging or blood tests) 2
- Fibroscan reading >16 kPa 2
Second-Line Testing Before Referral
If initial FIB-4 is indeterminate, obtain quantitative fibrosis assessment with: 2
- Serum ELF measurements 2
- Fibroscan/ARFI elastography (use 7.1-7.9 kPa as optimal cut-off to rule out advanced fibrosis) 2
- Magnetic resonance elastography if available (most accurate imaging test, with cut-offs of 3.62-4.8 kPa for advanced fibrosis) 2
Critical Pitfalls to Avoid
Do not rely solely on liver enzymes—normal transaminases do not rule out advanced fibrosis or cirrhosis. 2 Many hepatologists over-rely on transaminases instead of metabolic risk factors when diagnosing NAFLD. 2
Do not overlook high-risk populations: 2
- Patients with type 2 diabetes have >70% prevalence of NAFLD and increased risk of advanced fibrosis 1
- Obesity (especially BMI >35) doubles the risk of liver disease at any given alcohol intake 2
Exclude significant alcohol consumption (>14 drinks/week for women, >21 drinks/week for men) before attributing fatty liver to NAFLD alone. 2, 3
Why This Matters
Advanced fibrosis dramatically increases mortality risk: 1
Early detection and specialist management can prevent progression to cirrhosis and hepatocellular carcinoma. 1 Patients with advanced fibrosis require screening for esophageal varices and hepatocellular carcinoma. 2
Special Considerations
FIB-4 and similar scores have not been validated in patients under 35 years—interpret with caution in young patients. 1
Even with negative extended liver workup and no NAFLD risk factors, adults with persistently abnormal liver tests should be referred for further evaluation, as some treatable conditions (like autoimmune liver disease) may present without typical markers. 2