How to assess for decompensated Hepatitis C (Hep C)?

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Assessment of Decompensated Hepatitis C

Decompensated hepatitis C is defined by a Child-Turcotte-Pugh (CTP) score ≥7, which includes clinical evidence of ascites, hepatic encephalopathy, total bilirubin >2.0 mg/dL, albumin <3.5 g/dL, or INR ≥1.7. 1

Calculate the Child-Turcotte-Pugh Score

The CTP score is the primary tool to differentiate compensated (CTP class A) from decompensated cirrhosis (CTP class B or C). 1

Required laboratory parameters:

  • Total bilirubin (>2.0 mg/dL indicates decompensation) 1
  • Serum albumin (<3.5 g/dL indicates decompensation) 1
  • INR (≥1.7 indicates decompensation) 1

Required clinical assessments:

  • Ascites (presence indicates decompensation) 1
  • Hepatic encephalopathy (presence indicates decompensation) 1

A CTP score ≥7 or any history of prior decompensation confirms decompensated cirrhosis. 1

Clinical Evaluation for Decompensation Events

Assess for the four cardinal manifestations of decompensation:

  • Ascites is the most frequent first decompensation event (occurring in 44.9-47.2% of patients), and should be evaluated clinically and confirmed with ultrasound imaging to detect subclinical ascites 1, 2
  • Upper gastrointestinal bleeding from varices (occurs in 15.7-23.6% as first decompensation) requires assessment for esophageal and gastric varices via endoscopy 2, 3
  • Spontaneous bacterial peritonitis (occurs in 18.0-20.2% as first decompensation) should be suspected in patients with ascites and fever, abdominal pain, or altered mental status 2
  • Hepatic encephalopathy (occurs in 7.9-11.2% as first decompensation) requires clinical grading and assessment 2

Imaging Assessment

Ultrasound of the liver within the prior 6 months is mandatory to:

  • Evaluate for hepatocellular carcinoma (HCC) 1
  • Detect subclinical ascites 1
  • Assess for liver nodularity and splenomegaly as clinical evidence of cirrhosis 1

Laboratory Panel for Decompensation Assessment

Complete blood count (CBC):

  • Platelet count <150,000/mm³ suggests cirrhosis and portal hypertension 1, 4
  • Platelet count ≤140,000/mm³ has 83% sensitivity and 85% specificity for detecting cirrhosis 4

Hepatic function panel:

  • AST/ALT ratio ≥1 suggests cirrhosis (39% sensitivity, 92% specificity) 4
  • Elevated bilirubin >2.0 mg/dL indicates decompensation 1
  • Albumin <3.5 g/dL indicates decompensation 1

Coagulation studies:

  • INR ≥1.7 indicates decompensation 1
  • Prolonged prothrombin time is an early indicator of cirrhosis and portal hypertension 5

Additional markers:

  • Globulin/albumin ratio ≥1 suggests cirrhosis (43% sensitivity, 98% specificity) 4

Endoscopic Evaluation

Upper endoscopy is essential to:

  • Screen for esophageal and gastric varices, as their presence independently correlates with survival 2
  • Assess variceal size, as large esophageal varices predict failure to recompensate (adjusted hazard ratio 0.4) and portal hypertension progression (adjusted hazard ratio 2.9) 3

Prognostic Assessment

Key predictors of poor outcomes in decompensated HCV cirrhosis:

  • Presence of esophageal and gastric varices independently correlates with survival 2
  • Elevated bilirubin independently correlates with worse survival 2
  • Low bilirubin, low INR, and absence of large varices predict recompensation after antiviral therapy 3

Common Pitfalls to Avoid

Do not rely solely on transaminase levels (ALT/AST), as approximately 50% of patients with chronic viral hepatitis can have normal transaminase values despite ongoing liver disease, and routine liver tests correlate poorly with necroinflammatory and fibrosis scores. 6, 5

Do not skip ultrasound imaging, as subclinical ascites may be present without obvious clinical signs and HCC surveillance is critical in cirrhotic patients. 1

Recognize that decompensation can occur with any single criterion met (ascites, encephalopathy, bilirubin >2.0, albumin <3.5, or INR ≥1.7), not just a cumulative CTP score ≥7. 1

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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