How is the Model for End-Stage Liver Disease (MELD) score calculated for liver cirrhosis?

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Last updated: July 14, 2025View editorial policy

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Calculation of MELD Score for Liver Cirrhosis

The Model for End-Stage Liver Disease (MELD) score is calculated using the formula: MELD = 3.78 × ln[serum bilirubin (mg/dL)] + 11.2 × ln[INR] + 9.57 × ln[serum creatinine (mg/dL)] + 6.43.

Components of the MELD Score

The MELD score incorporates three objective laboratory values:

  1. Serum bilirubin (mg/dL) - measures liver's ability to excrete bile
  2. International Normalized Ratio (INR) - measures liver's synthetic function
  3. Serum creatinine (mg/dL) - measures kidney function

Important Calculation Rules

  • The formula uses the natural logarithm (ln) of each laboratory value
  • Laboratory values less than 1.0 are set to 1.0 to avoid negative values
  • Serum creatinine is capped at 4.0 mg/dL
  • For patients who received dialysis twice within the last week, creatinine is automatically set to 4.0 mg/dL
  • The final score is rounded to the nearest whole number
  • The score ranges from 6 (less ill) to 40 (gravely ill)

Clinical Significance and Interpretation

The MELD score was originally developed to assess short-term prognosis in patients undergoing transjugular intrahepatic portosystemic shunts (TIPS) 1. It has since become the standard tool for:

  • Prioritizing patients on liver transplantation waiting lists
  • Predicting 3-month mortality in patients with end-stage liver disease
  • Risk-stratifying cirrhotic patients before surgical procedures

MELD score correlates with mortality risk as follows:

  • Score <10: 1.9% 3-month mortality
  • Score 10-19: 6% 3-month mortality
  • Score 20-29: 19.6% 3-month mortality
  • Score 30-39: 52.6% 3-month mortality
  • Score ≥40: 71.3% 3-month mortality

Advantages Over Other Scoring Systems

The MELD score offers several advantages over the Child-Turcotte-Pugh (CTP) score:

  • Uses only objective laboratory parameters
  • Provides a continuous scale rather than categorical classification
  • Includes assessment of renal function, which is a critical prognostic factor
  • Better predicts short-term mortality in patients with cirrhosis

Clinical Applications Beyond Transplantation

The MELD score is valuable for:

  • Predicting perioperative mortality in cirrhotic patients undergoing non-transplant surgery 2
  • Assessing prognosis in alcoholic hepatitis when MELD ≥18 indicates poor prognosis 1
  • Evaluating candidacy for hepatic resection in cirrhotic patients with hepatocellular carcinoma 3

Limitations and Pitfalls

  • May underestimate mortality in patients with acute-on-chronic liver failure due to extrahepatic organ failures 1
  • Does not account for complications of portal hypertension (varices, ascites) 1
  • May disadvantage patients with viral cirrhosis compared to alcoholic cirrhosis at the same MELD score 4
  • Serum creatinine can be an unreliable marker of renal dysfunction in cirrhotic patients 1

Modified Versions

Several variations have been developed to improve prognostic accuracy:

  1. MELD-Na: Incorporates serum sodium to account for hyponatremia
  2. MELD-lactate (MELD-LA): Adds serum lactate, which improves prediction of in-hospital mortality 1
  3. Delta MELD: Evaluates the change in MELD score over time

When to Refer for Liver Transplantation

According to AASLD guidelines, patients with cirrhosis should be referred for transplantation when:

  • MELD score >10 with evidence of hepatic dysfunction
  • CTP score >7
  • First major complication (ascites, variceal bleeding, or hepatic encephalopathy) 1

Remember that sequential assessment of MELD scores over time provides better prognostic information than a single measurement, particularly in patients with acute-on-chronic liver failure 1.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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