Child-Pugh Score in Decompensated Chronic Liver Disease
The Child-Pugh score is essential for classifying your patient's liver disease severity and predicting survival—with decompensated disease (ascites present), this patient likely falls into Child-Pugh class B or C, indicating significantly reduced survival compared to compensated cirrhosis and necessitating evaluation for liver transplantation. 1
Primary Clinical Significance
The Child-Pugh score stratifies patients into three prognostic classes based on five parameters: 1
- Class A (5-6 points): Compensated cirrhosis with median survival exceeding 12 years 1
- Class B (7-9 points): Decompensated cirrhosis with 7-year survival of 68% 1
- Class C (10-15 points): Severely decompensated cirrhosis with 7-year survival of only 25% 1
Your patient with ascites, elevated direct bilirubin, and portal hypertension is by definition decompensated (Class B or C), with median survival reduced to only 1.8 years compared to >12 years for compensated disease. 1
Score Components and Calculation
The score incorporates five variables, each scored 1-3 points: 1
- Bilirubin: <2 mg/dL (1 point), 2-3 mg/dL (2 points), >3 mg/dL (3 points)
- Albumin: >3.5 g/dL (1 point), 2.8-3.5 g/dL (2 points), <2.8 g/dL (3 points)
- INR/PT: INR <1.7 (1 point), 1.7-2.2 (2 points), >2.2 (3 points)
- Ascites: None (1 point), slight/controlled (2 points), moderate/refractory (3 points)
- Encephalopathy: None (1 point), grade 1-2 (2 points), grade 3-4 (3 points)
Prognostic Implications for Your Patient
The presence of ascites as a decompensating event carries specific prognostic weight: 2
- Ascites is the most common first decompensating event (occurring in 30-40% of compensated patients) 1
- Grade 2 ascites with MELD ≥15 indicates 28% risk of further decompensation at 1 year 2
- Grade 3 ascites carries high mortality across all MELD strata (14-20% at 1 year) 2
- Refractory ascites independently predicts mortality with a relative risk of 4.78 3
Clinical Decision-Making Algorithm
Use the Child-Pugh score to guide the following management decisions: 1
Surgical candidacy: Only Child-Pugh A patients with no portal hypertension are optimal candidates for hepatic resection; Child-Pugh B may be considered only in highly selected cases with normal liver function tests and absent clinical portal hypertension 1
Transplant evaluation: Child-Pugh B/C patients require immediate transplant evaluation, as these classes indicate decompensated disease with poor prognosis 1
Medication dosing: Child-Pugh classification guides anticoagulation decisions and drug dosing adjustments in patients requiring therapy for conditions like atrial fibrillation 1
Advantages and Limitations
The Child-Pugh score offers practical bedside utility: 1
- Simple calculation requiring only routine laboratory values and clinical assessment
- Includes clinical parameters (ascites, encephalopathy) that reflect real functional impairment
- Remains effective for prognostic assessment with accuracy comparable to MELD (AUROC 0.796-0.882 for 6-month mortality) 4
Critical limitations to recognize: 1
- Does not assess clinically significant portal hypertension (HVPG ≥10 mmHg), which independently predicts variceal development and decompensation 1
- Subjective components (ascites grading, encephalopathy assessment) introduce variability
- Does not include renal function, which is an established prognostic marker 1
Complementary Assessment
The Child-Pugh score should be supplemented with: 1
- MELD score for transplant prioritization (uses bilirubin, creatinine, INR) and may be superior for long-term outcome prediction 5, 4
- Direct assessment of portal hypertension through imaging findings (splenomegaly, varices, collaterals) or HVPG measurement 1
- Evaluation for complications including hepatorenal syndrome, spontaneous bacterial peritonitis, and hepatic encephalopathy 2
For your specific patient with decompensated disease, both Child-Pugh and MELD scores should be calculated, with MELD-Na potentially offering the highest accuracy for predicting 6-month mortality in decompensated cirrhosis (AUROC 0.833). 4