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CPE-005 · synthetic case LIVER-FX-09

Alcohol-related liver disease predominant

About 90 g a day in a man with steatosis.

Synthetic · no real patientAuthored by Biod · reviewed by Dr. AmaralLiver engine v1.0.0

Purpose: About 90 g a day in a man with steatosis.

Inputs the engine received

Liver tests and imaging

Hepatic steatosis documented
Yes
AST
80 U/L
ALT
52 U/L
Platelets
170 ×10⁹/L

Patient

Age
49 years
Sex
Male
Alcohol intake
90 g/day

Cardiometabolic criteria

BMI
27 kg/m²

Other liver disease and context

Hepatitis B and C testing already done
Yes

What the engine reports

Priority

Advanced fibrosis likely

LV-FIB-05

A high-risk non-invasive result (or known cirrhosis) needs specialist evaluation. Confirmation of stage belongs to hepatology.

Detected clinical pattern

Alcohol-Related Liver Disease Predominant

Alcohol intake is above the MetALD range. The pattern is classified as alcohol-related liver disease.

  • Alcohol: Alcohol 90 g/day · ALD range
  • Fibrosis risk: Fibrosis risk · high

Calculations

FIB-4
3.2

Lower cutoff 1.3; high above 2.67.

Recommended next steps

For physician consideration. Urgent review always comes first.

  1. 1Consider referral to hepatology.AASLD 2023.
Evidence and rule trace · 6 rules

LV-ALC-01Alcohol intake category

Inputs: alcohol 90 g/day (male)

Alcohol-related liver disease predominant.

LV-CALC-01Derived value

Inputs: age 49 · AST 80 · ALT 52 · platelets 170

FIB-4 = 3.2

LV-FIB-01FIB-4 and its stratum

Inputs: FIB-4 3.2 · cutoff 1.3

High risk of advanced fibrosis.

LV-04ALT above the AASLD upper limit

Inputs: ALT 52 U/L (limit 33 for male)

ALT above the sex-specific upper limit.

LV-FIB-05Advanced fibrosis likely

Inputs: FIB-4 3.2

High-risk fibrosis result.

LV-REF-01Hepatology referral to consider

Inputs: advanced fibrosis likely

Referral to hepatology is reasonable to consider.

Evidence

  • EV-AASLD-2023 · Rinella ME, Neuschwander-Tetri BA, Siddiqui MS, et al. AASLD Practice Guidance on the clinical assessment and management of nonalcoholic fatty liver disease. Hepatology. 2023;77(5):1797-1835.
  • EV-DELPHI-2023 · Rinella ME, Lazarus JV, Ratziu V, et al. A multisociety Delphi consensus statement on new fatty liver disease nomenclature. Hepatology. 2023;78(6):1966-1986.
  • EV-MCPHERSON-2017 · McPherson S, Hardy T, Dufour JF, et al. Age as a confounding factor for the accurate non-invasive diagnosis of advanced NAFLD fibrosis. Am J Gastroenterol. 2017;112(5):740-751.

Physician adjudication required. Clinical decision support for physician review. This output classifies steatotic liver disease under the 2023 nomenclature and stratifies fibrosis risk. It does not stage fibrosis by itself, diagnose a cause, or recommend a drug. Physician adjudication is required.

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Fibrosis risk by non-invasive tests

  1. ✓ Low

    FIB-4 <1.3 (<2.0 from 65), stiffness <8 kPa

  2. ✓ Indeterminate

    Needs a second-line test

  3. ● High

    FIB-4 >2.67, stiffness ≥12 kPa or ELF ≥9.8

Liver tests and imaging
Patient
Sex

A standard US drink is about 14 g.

Cardiometabolic criteria
Other liver disease and context
Cirrhosis, decompensation and trends

Live result · computed in your browser

Priority

Advanced fibrosis likely

LV-FIB-05

A high-risk non-invasive result (or known cirrhosis) needs specialist evaluation. Confirmation of stage belongs to hepatology.

Detected clinical pattern

Alcohol-Related Liver Disease Predominant

Alcohol intake is above the MetALD range. The pattern is classified as alcohol-related liver disease.

  • Alcohol: Alcohol 90 g/day · ALD range
  • Fibrosis risk: Fibrosis risk · high

Calculations

FIB-4
3.2

Lower cutoff 1.3; high above 2.67.

Recommended next steps

For physician consideration. Urgent review always comes first.

  1. 1Consider referral to hepatology.AASLD 2023.
Evidence and rule trace · 6 rules

LV-ALC-01Alcohol intake category

Inputs: alcohol 90 g/day (male)

Alcohol-related liver disease predominant.

LV-CALC-01Derived value

Inputs: age 49 · AST 80 · ALT 52 · platelets 170

FIB-4 = 3.2

LV-FIB-01FIB-4 and its stratum

Inputs: FIB-4 3.2 · cutoff 1.3

High risk of advanced fibrosis.

LV-04ALT above the AASLD upper limit

Inputs: ALT 52 U/L (limit 33 for male)

ALT above the sex-specific upper limit.

LV-FIB-05Advanced fibrosis likely

Inputs: FIB-4 3.2

High-risk fibrosis result.

LV-REF-01Hepatology referral to consider

Inputs: advanced fibrosis likely

Referral to hepatology is reasonable to consider.

Evidence

  • EV-AASLD-2023 · Rinella ME, Neuschwander-Tetri BA, Siddiqui MS, et al. AASLD Practice Guidance on the clinical assessment and management of nonalcoholic fatty liver disease. Hepatology. 2023;77(5):1797-1835.
  • EV-DELPHI-2023 · Rinella ME, Lazarus JV, Ratziu V, et al. A multisociety Delphi consensus statement on new fatty liver disease nomenclature. Hepatology. 2023;78(6):1966-1986.
  • EV-MCPHERSON-2017 · McPherson S, Hardy T, Dufour JF, et al. Age as a confounding factor for the accurate non-invasive diagnosis of advanced NAFLD fibrosis. Am J Gastroenterol. 2017;112(5):740-751.

Physician adjudication required. Clinical decision support for physician review. This output classifies steatotic liver disease under the 2023 nomenclature and stratifies fibrosis risk. It does not stage fibrosis by itself, diagnose a cause, or recommend a drug. Physician adjudication is required.

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