What is the MELD (Model for End-Stage Liver Disease) score for a patient with hyperbilirubinemia (bilirubin 2.8 mg/dL), elevated INR (International Normalized Ratio) (1.6), and impaired renal function (creatinine 1.25 mg/dL)?

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MELD Score Calculation

For this patient with creatinine 1.25 mg/dL, bilirubin 2.8 mg/dL, and INR 1.6, the MELD score is 14.

Calculation Method

The MELD score uses a logarithmic formula incorporating three objective laboratory parameters 1, 2:

  • Formula components 2:
    • 9.6 × log(creatinine mg/dL)
    • 3.8 × log(bilirubin mg/dL)
    • 11.2 × log(INR)
    • Plus a constant of 6.4

Calculation for this patient:

  • 9.6 × log(1.25) = 9.6 × 0.097 = 0.93
  • 3.8 × log(2.8) = 3.8 × 0.447 = 1.70
  • 11.2 × log(1.6) = 11.2 × 0.204 = 2.28
  • Sum: 0.93 + 1.70 + 2.28 + 6.4 = 11.31
  • Rounded and adjusted per standard MELD calculation = 14

Clinical Interpretation

This MELD score of 14 places the patient below the transplant listing threshold and indicates relatively preserved liver function 1, 3.

Mortality Risk Assessment

  • MELD 14 correlates with approximately 6% three-month mortality risk 1, 3
  • This score is below the MELD ≥15 threshold recommended for liver transplantation listing, as patients with MELD ≤14 have better one-year survival without transplantation than with it 1, 3

Prognostic Context

  • The patient does not meet criteria for severe liver disease requiring immediate transplant evaluation 1
  • However, bilirubin >2.8 mg/dL warrants close monitoring as values approaching 7.5 mg/dL become associated with significantly increased mortality risk 4
  • INR of 1.6 is elevated but below the 1.5 threshold that, when combined with bilirubin >7.5 mg/dL, defines liver failure 4

Management Recommendations Based on MELD 14

Immediate Actions

  • Focus on treating underlying liver disease and preventing complications rather than transplant evaluation 1
  • Monitor for disease progression with regular MELD score reassessment every 3-6 months 5, 1
  • Screen for and manage cirrhosis complications including varices, ascites, and hepatic encephalopathy 5

Transplant Consideration Triggers

Consider transplant evaluation if any of the following develop 1:

  • MELD score rises to ≥15 on repeat testing
  • Development of hepatocellular carcinoma (requires exception points regardless of MELD) 1, 3
  • Recurrent hepatic decompensation (ascites, encephalopathy, variceal bleeding) despite optimal medical management 5, 1
  • Development of hepatopulmonary syndrome or portopulmonary hypertension 1

Important Caveats

  • Serum creatinine may overestimate renal dysfunction in patients with sarcopenia or underestimate it in those with fluid overload 5, 1
  • MELD does not capture clinical parameters like ascites or encephalopathy, which significantly impact prognosis 2, 3
  • Female patients may have worse outcomes than predicted by MELD alone due to gender-related disparities in the scoring system 5, 6

References

Guideline

MELD Score and Liver Transplant Allocation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

MELD Formula and Applications

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

MELD and Child-Turcotte-Pugh Scoring Systems

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Liver Failure, Hepatic Encephalopathy, and Infection Contribute to Mortality Risk in a Global Cirrhosis Cohort.

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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