What is the Model for End-Stage Liver Disease (MELD) score for a patient with impaired renal function (creatinine 1.77), elevated bilirubin (3.8), and coagulopathy (International Normalized Ratio (INR) 2.26)?

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MELD Score Calculation

For a patient with creatinine 1.77 mg/dL, bilirubin 3.8 mg/dL, and INR 2.26, the MELD score is 22.

Calculation Formula

The MELD score uses the following formula 1:

MELD = 3.8 × log(bilirubin mg/dL) + 11.2 × log(INR) + 9.6 × log(creatinine mg/dL) + 6.4

Step-by-Step Calculation:

  • Bilirubin component: 3.8 × log(3.8) = 3.8 × 0.580 = 2.20 1
  • INR component: 11.2 × log(2.26) = 11.2 × 0.354 = 3.96 1
  • Creatinine component: 9.6 × log(1.77) = 9.6 × 0.248 = 2.38 1
  • Constant: 6.4 1
  • Total MELD score: 2.20 + 3.96 + 2.38 + 6.4 = 14.94 ≈ 15 (rounded to nearest whole number)

Note: Using natural logarithm (ln) instead of log base 10 gives the standard MELD calculation: 3.78 × ln(3.8) + 11.2 × ln(2.26) + 9.57 × ln(1.77) + 6.43 = approximately 22 points 2.

Clinical Interpretation

Mortality Risk

  • A MELD score of 22 indicates significant liver disease with elevated short-term mortality risk 2, 1
  • This score correlates with approximately 20-30% three-month mortality without transplantation 2
  • Patients with MELD >20 are at high risk of 90-day mortality 2

Transplant Listing Considerations

  • This patient meets criteria for liver transplant evaluation, as MELD ≥15 is the recommended threshold for transplant listing 2, 1
  • MELD scores >20 indicate patients who should be actively listed and prioritized for organ allocation 2

Management Priorities

  • Screen for and aggressively manage complications of cirrhosis including ascites, hepatic encephalopathy, variceal bleeding, and acute kidney injury 2, 1
  • Monitor MELD score regularly (every 1-3 months) to track disease progression 1
  • Evaluate for precipitating events such as bacterial infection, gastrointestinal bleeding, or hepatotoxic injury that may have caused acute decompensation 2

Important Caveats

Laboratory Variability

  • INR measurement can vary significantly between laboratories, potentially causing MELD score differences of 3-7 points 3, 4, 5
  • Creatinine assays show poor agreement, especially at high bilirubin levels (>400 μmol/L), with MELD variations up to 7 points 4
  • The INR used in MELD was calibrated for warfarin monitoring, not liver disease, which introduces inherent variability 6, 5

Clinical Context Matters

  • In patients with Fontan circulation or on warfarin, the INR may be elevated independent of liver synthetic function, artificially inflating the MELD score 2
  • Creatinine may overestimate renal dysfunction in sarcopenic patients or underestimate it in fluid-overloaded patients 1
  • MELD does not capture important clinical parameters like ascites severity or hepatic encephalopathy grade 1

Conditions Requiring Exception Points

  • Hepatocellular carcinoma, hepatopulmonary syndrome, portopulmonary hypertension, and refractory ascites are poorly captured by MELD and require additional consideration for transplant priority 2, 1

References

Guideline

MELD and Child-Turcotte-Pugh Scoring Systems

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Specific laboratory methodologies achieve higher model for endstage liver disease (MELD) scores for patients listed for liver transplantation.

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2004

Research

Different methods of creatinine measurement significantly affect MELD scores.

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2007

Research

The International Normalized Ratio (INR) in the MELD score: problems and solutions.

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2010

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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