Clinical Scorecard: Comparison of FibroScan-AST Score and Liver Stiffness in Predicting Liver Complications Following HCV Treatment Success
At a Glance
Category
Detail
Condition
Hepatitis C virus (HCV) infection with advanced fibrosis
Key Mechanisms
Liver stiffness (LS) reflects fibrosis, inflammation, and portal hypertension; FAST score combines LS, AST, and CAP to indicate steatohepatitis and fibrosis progression
Target Population
Patients with HCV infection (with or without HIV coinfection) achieving sustained virological response (SVR) after direct-acting antiviral (DAA) therapy and LS ≥9.5 kPa pretreatment
Care Setting
Infectious diseases units and hepatology clinics with access to vibration-controlled transient elastography (VCTE)
Key Highlights
Liver stiffness (LS) independently predicts liver complications including decompensation and hepatocellular carcinoma (HCC) after SVR.
FAST score ≥0.35 is independently associated with increased risk of liver complications but does not outperform LS alone in predictive capacity.
44% of patients had fatty liver disease (CAP ≥248 dB/m) at SVR, highlighting the role of steatotic liver disease in post-SVR outcomes.
Guideline-Based Recommendations
Diagnosis
Use vibration-controlled transient elastography (VCTE) to measure liver stiffness (LS) and controlled attenuation parameter (CAP) at SVR.
Calculate FAST score incorporating LS, AST, and CAP to assess risk of liver complications.
Diagnose hepatic decompensations clinically and HCC according to American Association for the Study of Liver Diseases criteria.
Management
Continue surveillance for liver complications post-SVR, especially in patients with LS ≥9.5 kPa pretreatment.
Perform biannual HCC screening with alpha-fetoprotein and liver ultrasound in patients with cirrhosis.
Conduct gastroesophageal varices surveillance with endoscopy in patients with LS ≥21 kPa.
Monitoring & Follow-up
Clinical and analytical evaluation every 6 months post-SVR.
Regular VCTE assessments to monitor liver stiffness and steatosis status.
Monitor for liver-related events including hepatic decompensation and HCC.
Risks
Patients with higher LS and FAST scores have increased risk of liver complications despite SVR.
Presence of fatty liver disease may contribute to fibrogenesis and hepatocarcinogenesis post-SVR.
Limited positive predictive value of LS alone necessitates comprehensive risk assessment.
Patient & Prescribing Data
Patients with chronic HCV infection (with or without HIV coinfection) achieving SVR after DAA therapy with advanced fibrosis (LS ≥9.5 kPa).
DAA-based regimens effectively achieve SVR; however, liver stiffness and FAST score remain important for risk stratification of liver complications post-treatment.
Clinical Best Practices
Incorporate LS measurement via VCTE at SVR to stratify risk for liver complications.
Use FAST score as an adjunct to identify patients with steatohepatitis and higher risk but rely primarily on LS for prediction.
Maintain regular surveillance protocols including imaging and laboratory tests for early detection of liver events.
Manage patients with cirrhosis according to established protocols including HCC and varices screening.
by Anaïs Corma-Gómez, Diana Corona-Mata, Jésica Martín-Carmona, María José Galindo, Angela Camacho, Carmen Martín-Sierra, Marina Gallo-Marín, Pilar Rincón, Ignacio Perez-Valero, Margarita Pérez-García, Angela Carrasco-Dorado, Juan A Pineda, Antonio Rivero-Juárez, Antonio Rivero, Luis M Real, Juan Macías, on behalf of the GEHEP-011 Study Group
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