What clinical scores are used to assess cirrhosis severity and what do they measure?

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Clinical Scoring Systems in Cirrhosis: Assessment and Prognostic Value

The most important clinical scoring systems used in cirrhosis are the Child-Turcotte-Pugh (CTP) score, Model for End-Stage Liver Disease (MELD), and Acute-on-Chronic Liver Failure (ACLF) scores, which measure liver function, predict mortality, and guide treatment decisions including transplantation eligibility.

Child-Turcotte-Pugh (CTP) Score

The CTP score is one of the oldest and most widely used scoring systems for cirrhosis assessment:

  • Components: Measures 5 parameters 1:

    • Encephalopathy (grade 1-4)
    • Ascites (absent/slight/moderate)
    • Bilirubin (mg/dL)
    • Albumin (g/dL)
    • Prothrombin time/INR
  • Scoring and Classification:

    • Class A: 5-6 points (90% 5-year survival)
    • Class B: 7-9 points (80% 5-year survival)
    • Class C: 10-15 points (<35% 1-year survival without transplant)
  • Clinical Utility:

    • Risk stratification before procedures
    • Assessment of disease severity
    • Simple bedside calculation
  • Limitations:

    • Includes subjective parameters (encephalopathy, ascites)
    • Not formally validated as a prognostic tool 1
    • Limited discrimination within classes

Model for End-Stage Liver Disease (MELD)

MELD has become the primary tool for liver transplant allocation:

  • Components: Objective laboratory values 1, 2:

    • Serum bilirubin
    • Serum creatinine (capped at 4.0 mg/dL)
    • International Normalized Ratio (INR)
  • Formula: MELD = 3.78 × log(bilirubin mg/dL) + 11.2 × log(INR) + 9.6 × log(creatinine mg/dL) + 6.4 2

  • Mortality Risk by MELD Score 2:

    MELD Score Mortality Risk
    6-9 1.9%
    10-19 6%
    20-29 19.6%
    30-39 52.6%
    40+ 71.3%
  • Clinical Utility:

    • Organ allocation for transplantation
    • Prediction of 3-month mortality
    • Objective assessment without subjective parameters
    • Transplant listing recommended at MELD ≥15 2
  • Limitations:

    • Doesn't account for complications like hepatic encephalopathy
    • May not accurately represent certain conditions (HCC, metabolic disorders) 3

MELD-Na (Sodium-modified MELD)

An important modification of the original MELD score:

  • Components: Adds serum sodium to the original MELD formula
  • Clinical Utility: Better predicts mortality in patients with ascites and hyponatremia
  • Advantage: Accounts for the prognostic significance of hyponatremia in cirrhosis

Acute-on-Chronic Liver Failure (ACLF) Scores

These newer scoring systems assess patients with acute decompensation:

CLIF-C Organ Failure (CLIF-C OF) Score

  • Components: Assesses six organ systems 1:

    • Liver
    • Kidney
    • Brain
    • Coagulation
    • Circulation
    • Respiration
  • Clinical Utility:

    • Diagnosis of ACLF
    • Assessment of ACLF severity
    • Prediction of 28-day mortality
    • Sequential assessment of response to intervention 1

CLIF-C ACLF Score

  • Components: Combines CLIF-C OF with age and white blood cell count
  • Clinical Utility: More accurate prediction of mortality in ACLF patients

NACSELD ACLF Score

  • Components: Assesses four organ systems (brain, kidneys, circulation, respiration) 1
  • Limitation: Underestimates mortality risk compared to CLIF-C criteria 1

Disease-Specific Scores

Maddrey Discriminant Function (mDF)

  • Components: Bilirubin and prothrombin time 1
  • Clinical Utility:
    • Identifies severe alcoholic hepatitis (mDF ≥32)
    • Guides corticosteroid therapy decisions

Glasgow Alcoholic Hepatitis Score (GAHS)

  • Components: Age, bilirubin, blood urea, prothrombin time, and white blood cell count 1
  • Clinical Utility: Identifies patients who benefit from corticosteroid treatment (GAHS ≥9)

ABIC Score

  • Components: Age, bilirubin, INR, and creatinine 1
  • Clinical Utility: Stratifies alcoholic hepatitis patients into low, intermediate, and high risk of death

Clinical Application and Comparative Value

  • Transplant Evaluation: MELD is the primary tool for organ allocation, with a score ≥15 recommended for listing 2

  • ACLF Management: CLIF-C scores are recommended for diagnosis and monitoring of ACLF 1

  • Alcoholic Hepatitis: Multiple specialized scores (Maddrey DF, GAHS, ABIC) provide similar efficacy in predicting short-term survival 1

  • Sequential Assessment: Regular monitoring of scores is essential as they can change over time, particularly in ACLF where sequential assessment at days 3-7 improves prognostic accuracy 1

Practical Considerations

  • Timing of Assessment: Regular reassessment is crucial, especially with clinical deterioration

  • Score Selection: Choose the appropriate score based on clinical context:

    • For transplant evaluation: MELD/MELD-Na
    • For ACLF: CLIF-C OF/ACLF scores
    • For alcoholic hepatitis: Maddrey DF, GAHS, or ABIC
  • Limitations: No single score captures all aspects of cirrhosis; clinical judgment remains essential

  • Mortality Prediction: ACLF-specific scores outperform conventional cirrhosis scores (MELD, CTP) for critically ill patients 1

The appropriate use of these scoring systems enables better risk stratification, treatment decisions, and resource allocation for patients with cirrhosis across the spectrum of disease severity.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Liver Transplantation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Prognostic scores of cirrhosis].

Gastroenterologia y hepatologia, 2008

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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