MELD Score

Model for End-Stage Liver Disease

Predicts short-term mortality in chronic liver disease and is the primary metric for liver transplant organ allocation in UNOS/OPTN and Eurotransplant systems. Includes MELD, MELD-Na and MELD 3.0.

HepatologyLiver TransplantationCirrhosis
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Formulae

MELD (original)

MELD = 9.57 × ln(Creatinine) + 3.78 × ln(Bilirubin) + 11.2 × ln(INR) + 6.43

Minimum value of 1.0 for Cr, Bil and INR. Creatinine capped at 4.0 mg/dL (use 4.0 if on dialysis ≥2×/week). Score capped at 40.

MELD-Na

MELD-Na = MELD − Na − [0.025 × MELD × (140 − Na)] + 140

Sodium clamped between 125 and 137 mEq/L. Score capped at 40. Adopted by UNOS in January 2016.

MELD 3.0

MELD 3.0 = 4.56×ln(Bil) + 0.82×(137−Na) − 0.24×(137−Na)×ln(Bil) + 9.09×ln(INR) + 11.14×ln(Cr) + 1.85×(3.5−Alb) − 1.83×(3.5−Alb)×ln(Cr) + 1.33 (if female) + 7

Creatinine range 1.0–3.0; Albumin range 1.5–3.5; Sodium clamped 125–137. Developed by Kim et al. (2021).

Interpretation

MELD ScoreDisease Severity90-Day MortalityUNOS Status
< 10Low~2%Monitored; transplant unlikely
10–19Moderate~6%Listed; monitored closely
20–29High~20%Active transplant listing
30–39Very high~52%High priority
≥ 40Critical~71%Highest priority (1A/1B)

Mortality estimates from Kamath et al. (2001). Scores updated continuously; organ offers go to highest MELD patient in compatible blood group within region.

Clinical Application

MELD was originally developed to predict 90-day mortality after TIPS placement and was subsequently validated as a general predictor of mortality in end-stage liver disease. It replaced the Child-Pugh score for UNOS organ allocation in February 2002.

  • Transplant listing: MELD ≥15 is the threshold above which transplant survival benefit exceeds waitlist mortality in most centres.
  • MELD-Na: Incorporates hyponatraemia, which independently predicts waitlist mortality. Adopted by UNOS in 2016; preferred over MELD alone for allocation.
  • MELD 3.0: Addresses sex-based disparity in transplant access — women historically receive fewer transplants at equivalent disease severity. Incorporates albumin (a marker of sarcopenia) and corrects for sex. Implemented by OPTN in August 2022.
  • Exceptions: Patients with HCC, HRS-AKI and hepatopulmonary syndrome receive MELD exception points to account for conditions not reflected by standard labs.
  • Surgical risk: Child-Pugh class is still widely used alongside MELD for perioperative risk stratification in cirrhotic patients.

Evidence & Validation

The original MELD score was validated in a cohort of 231 patients undergoing TIPS and subsequently in over 3,500 patients from multiple centres in a seminal Mayo Clinic study. The c-statistic for 90-day mortality was 0.87.

MELD-Na was validated in the UNOS waiting-list dataset by Biggins et al. (2006), demonstrating a c-statistic of 0.87 vs 0.85 for MELD alone. The 2021 MELD 3.0 paper by Kim et al. used 4 validation cohorts (n > 75,000 patient-years) and showed improvement in c-statistic for 90-day waitlist mortality from 0.838 (MELD-Na) to 0.854 (MELD 3.0) in women.

Limitations

  • Does not account for aetiology of liver disease (HCV, ALD, NASH — outcomes differ)
  • Creatinine influenced by muscle mass; women and elderly patients may have falsely low creatinine underestimating severity
  • Does not capture quality of life, encephalopathy, or refractory ascites
  • Serum creatinine varies with lab methodology; harmonisation across centres can differ
  • MELD 3.0 requires albumin, which was historically not in the original MELD formula and adds an extra lab requirement
  • HCC, HRS and other exception conditions require separate scoring adjustments

Key Guidelines

  • AASLD Practice Guidance: Evaluation for liver transplantation (2022)
  • EASL Clinical Practice Guidelines: Liver transplantation (2016)
  • OPTN Policy: Allocation of Livers and Liver-Intestines (implemented MELD 3.0, August 2022)
  • BSG: Guidelines on the management of ascites in cirrhosis (2022)

References

  1. Kamath PS, et al. A model to predict survival in patients with end-stage liver disease. Hepatology. 2001;33(2):464–470.
  2. Biggins SW, et al. Evidence-based incorporation of serum sodium concentration into MELD. Gastroenterology. 2006;130(6):1652–1660.
  3. Kim WR, et al. MELD 3.0: The Model for End-Stage Liver Disease Updated for the 21st Century. Hepatology. 2021;74(4):1913–1922.
  4. Wiesner R, et al. Model for end-stage liver disease (MELD) and allocation of donor livers. Gastroenterology. 2003;124(1):91–96.
  5. OPTN Policy 9: Allocation of Livers and Liver-Intestines. Available at: optn.transplant.hrsa.gov.

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