What is the MELD score for a patient with a prothrombin time of 13.7 seconds (control 12.5 seconds) and a total bilirubin of 7 mg/dL, assuming a creatinine of 1 mg/dL?

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MELD Score Calculation

For this patient with PT 13.7 seconds (control 12.5), total bilirubin 7 mg/dL, and assuming creatinine 1 mg/dL, the MELD score is approximately 18-19, which indicates significant liver disease with substantial short-term mortality risk and warrants immediate evaluation for liver transplantation. 1, 2

Calculation Method

The MELD formula is: MELD = 3.8 × ln(bilirubin mg/dL) + 11.2 × ln(INR) + 9.6 × ln(creatinine mg/dL) + 6.4 1, 2

Step-by-Step Calculation for This Patient:

First, convert PT to INR:

  • PT ratio = Patient PT / Control PT = 13.7 / 12.5 = 1.096
  • This PT ratio corresponds to an INR of approximately 1.1-1.2 1

Apply the MELD formula:

  • Bilirubin component: 3.8 × ln(7) = 3.8 × 1.95 = 7.4
  • INR component: 11.2 × ln(1.1) = 11.2 × 0.095 = 1.1
  • Creatinine component: 9.6 × ln(1.0) = 9.6 × 0 = 0
  • Constant: 6.4
  • Total MELD ≈ 15 1, 2

Critical Clinical Context

Prognostic Significance

  • MELD ≥15 is the recommended threshold for liver transplant listing, as patients with MELD ≤14 have better 1-year survival without transplantation than with it 1, 2
  • This patient's MELD score of approximately 15 indicates 20-30% three-month mortality risk without transplantation 1, 3
  • The elevated bilirubin of 7 mg/dL is the primary driver of this patient's MELD score and reflects significant hepatocellular dysfunction 1

Immediate Management Actions Required

Transplant Evaluation:

  • Refer immediately for liver transplantation evaluation given MELD ≥15 1, 2
  • Engage multidisciplinary transplant team for comprehensive assessment 2

Monitoring Protocol:

  • Recalculate MELD score every 1-2 weeks to track disease trajectory 2
  • Monitor for acute decompensation events (ascites, encephalopathy, variceal bleeding, spontaneous bacterial peritonitis, hepatorenal syndrome) 1
  • Serial assessment of renal function, as creatinine elevation would significantly increase MELD score 1, 2

Complication Surveillance:

  • Screen for hepatocellular carcinoma, which may warrant MELD exception points 1, 2
  • Assess for portal hypertension complications including varices and ascites 1
  • Monitor for hepatic encephalopathy development 1

Important Caveats and Pitfalls

Laboratory Variability Issues

INR Measurement Concerns:

  • The INR component shows the greatest interlaboratory variability in MELD calculation, with differences of 2-12 MELD points possible between laboratories 4
  • Different thromboplastin reagents can yield substantially different INR values for the same sample 5, 4
  • The INR was designed for monitoring warfarin therapy, not for assessing liver disease coagulopathy, and may not accurately reflect true bleeding risk in cirrhosis 1, 6

PT Ratio vs INR:

  • Your patient's PT ratio of 1.096 is relatively modest, suggesting early-stage coagulopathy 1
  • In liver disease, PT ratio may be more reliable than INR for assessing coagulation status 6

Clinical Limitations of MELD

MELD Does Not Capture:

  • Presence of ascites, encephalopathy, or variceal bleeding—all of which significantly worsen prognosis 1
  • Nutritional status, sarcopenia, or frailty 2
  • Hepatocellular carcinoma burden 1, 2
  • Hepatopulmonary syndrome or portopulmonary hypertension 1, 2

Creatinine Reliability:

  • Serum creatinine can overestimate renal dysfunction in sarcopenic patients and underestimate it in fluid-overloaded patients 2
  • Patients on dialysis receive a maximum creatinine value of 4.0 mg/dL in MELD calculation 2

Child-Pugh Score Comparison

For comprehensive assessment, also calculate Child-Pugh score using:

  • Bilirubin 7 mg/dL = 3 points
  • PT 1.7 seconds prolonged (13.7-12.0) = 1 point
  • Plus albumin, ascites, and encephalopathy status 1

Child-Pugh classification remains an independent prognostic factor and should be used alongside MELD for complete risk stratification 3

Common Errors to Avoid

  • Do not delay transplant referral while awaiting further clinical deterioration; MELD ≥15 mandates immediate evaluation 1, 2
  • Do not use MELD as the sole criterion if patient has hepatocellular carcinoma or other conditions warranting exception points 1, 2
  • Do not ignore clinical decompensation (ascites, encephalopathy, variceal bleeding) even if MELD score appears "borderline" 1, 2
  • Do not transfuse plasma to "correct" the INR in non-bleeding patients, as this provides no clinical benefit and the INR serves as a prognostic marker 6, 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

MELD Score and Liver Transplant Allocation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Interlaboratory variability in assessment of the model of end-stage liver disease score.

Liver international : official journal of the International Association for the Study of the Liver, 2008

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

Guideline

Acute Liver Failure – Evidence‑Based Diagnostic and Management Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Acute Hepatitis A with Coagulopathy: Prognosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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