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Model for End-stage Liver Disease (MELD) score for predicting 3-month mortality in patients with advanced liver disease.
Clinical decision-support tool for qualified healthcare professionals. Results are not a diagnosis and should not replace professional clinical judgment.
The MELD score estimates 3-month mortality in patients with chronic, noncholestatic liver disease and is used for transplant waitlist prioritization. It is derived from a single set of laboratory values and does not capture all factors relevant to transplant candidacy (e.g., sodium, encephalopathy, ascites, functional status). The dialysis rule and creatinine capping reflect UNOS allocation practice; results should be interpreted by clinicians experienced in hepatology.
Specialty
GastroenterologyCategory
GastroenterologyDifficulty
Basic
Estimated Time
30 seconds
Version
1.0
Last Updated
2026-07
Formula
Keywords
| Classification | Range |
|---|---|
Low Risk | <10 |
Moderate Risk | 10–19 |
High Risk | 20–29 |
Very High Risk | 30–39 |
Extremely High Risk | ≥40 |
Calculates the Model for End-stage Liver Disease (MELD) score to estimate 3-month mortality in adults with chronic liver disease and to guide liver transplant prioritization.
MELD = 3.78 x ln(bilirubin) + 11.2 x ln(INR) + 9.57 x ln(creatinine) + 6.43, with bilirubin and creatinine in mg/dL. Bilirubin, INR, and creatinine are floored at 1.0, creatinine is capped at 4.0 (and set to 4.0 when dialysis was required), and the result is rounded to the nearest integer.
Serum bilirubin in mg/dL, entered into a natural logarithm and floored at 1.0.
Common error: Values below 1.0 are raised to 1.0, so very low bilirubin does not further lower the score.
Serum creatinine in mg/dL; floored at 1.0 and capped at 4.0, or set to 4.0 when on dialysis.
International normalized ratio, entered into a natural logarithm and floored at 1.0.
Yes forces the creatinine term to 4.0, reflecting transplant allocation practice.
MELD <10 indicates low 3-month mortality risk; 10–19 moderate; 20–29 high; 30–39 very high; ≥40 extremely high risk. Higher scores warrant expedited transplant evaluation.
MELD is a well-validated mortality-risk score that estimates 3-month survival in chronic liver disease and historically underpinned liver transplant prioritization in the United States. Current U.S. liver allocation uses the MELD 3.0 model (adopted July 2023), which incorporates albumin, sex, and updated coefficients rather than the classic MELD formula.
A 55-year-old man with decompensated alcoholic cirrhosis is being evaluated for transplant listing. Bilirubin is 2.5 mg/dL, creatinine 1.2 mg/dL, INR 1.5, and he is not on dialysis.
Inputs:
Expected Result: MELD = 3.78×ln(2.5) + 11.2×ln(1.5) + 9.57×ln(1.2) + 6.43 ≈ 16 — moderate 3-month mortality risk (band 10–19).
In the standard MELD calculation, bilirubin, INR, and creatinine are floored at 1.0 before the logarithms are taken, so a very low creatinine cannot lower the score below what a value of 1.0 would produce. Creatinine is also capped at 4.0, and is set to 4.0 when dialysis was required at least twice in the last week.
The classic MELD formula uses bilirubin, INR, and creatinine with fixed coefficients. Current U.S. liver allocation uses the MELD 3.0 model, adopted in July 2023, which incorporates albumin, sex, and updated coefficients. The classic score remains a valid prognostic estimate of 3-month mortality in chronic liver disease, but it is no longer the allocation score.
Creatinine depends on muscle mass, so patients with low muscle mass can have a deceptively low creatinine and therefore a lower MELD than their true severity warrants. The score also omits ascites and hepatic encephalopathy, which carry independent prognostic information, and INR assays vary between laboratories, which affects reproducibility of the score over time.
Disclaimer: This calculator is intended for educational and clinical decision support purposes only. Classic MELD is a prognostic mortality-risk score; current U.S. liver allocation uses the MELD 3.0 model. Transplant decisions must incorporate the full clinical picture and institutional policies.