What is the recommended treatment for Hepatitis C (Hep C)?

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Last updated: July 16, 2025View editorial policy

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Recommended Treatment for Hepatitis C

The recommended treatment for chronic hepatitis C is a direct-acting antiviral (DAA) regimen, specifically either sofosbuvir/velpatasvir or glecaprevir/pibrentasvir for 8 weeks in most patients without cirrhosis. 1

First-line Treatment Options

Pangenotypic Regimens (Preferred)

  • Sofosbuvir/velpatasvir: 400mg/100mg once daily for 8 weeks (without cirrhosis) or 12 weeks (with compensated cirrhosis)
  • Glecaprevir/pibrentasvir: 300mg/120mg once daily (three 100mg/40mg tablets) for 8 weeks (without cirrhosis) or 12 weeks (with compensated cirrhosis)

These pangenotypic regimens are effective against all HCV genotypes (1-6), eliminating the need for genotype testing in many cases 1.

Treatment Duration

Treatment duration depends on several factors:

  • Without cirrhosis: 8 weeks for most treatment-naïve patients
  • With compensated cirrhosis (Child-Pugh A): 8-12 weeks depending on regimen
  • With decompensated cirrhosis (Child-Pugh B/C): 12 weeks (sofosbuvir/velpatasvir with ribavirin)
  • Treatment-experienced patients: Duration varies from 8-16 weeks based on prior treatment history and HCV genotype 1, 2

Special Populations

Recently Acquired Hepatitis C

  • Treat with sofosbuvir/velpatasvir or glecaprevir/pibrentasvir for 8 weeks 1
  • SVR should be assessed at 12 and 24 weeks post-treatment due to possibility of late relapses 1

Decompensated Cirrhosis

  • Sofosbuvir/velpatasvir with ribavirin is preferred
  • Protease inhibitors (glecaprevir, etc.) are contraindicated in Child-Pugh B/C cirrhosis 1

Renal Impairment

  • Glecaprevir/pibrentasvir is preferred for severe renal impairment (eGFR <30 ml/min)
  • Sofosbuvir is not recommended in patients with eGFR <30 ml/min 1

Pre-treatment Assessment

  1. HBV co-infection screening: Test all patients for HBsAg and anti-HBc before starting treatment 2
  2. Fibrosis assessment: Determine stage of liver fibrosis (F0-F4)
  3. Medication review: Check for potential drug-drug interactions
  4. Baseline laboratory tests: Complete blood count, liver function tests, renal function

Monitoring During Treatment

  • Minimal monitoring required for most patients due to high safety profile of DAAs 1
  • HCV RNA or HCV core antigen at week 12 post-treatment (SVR12) to confirm cure 1
  • Monitor for drug-drug interactions throughout treatment 1
  • ALT monitoring at weeks 4,8, and 12 of therapy 1
  • More frequent monitoring for patients with decompensated cirrhosis or on ribavirin

Treatment Success Rates

Modern DAA regimens achieve sustained virological response (SVR) rates exceeding 95% in most patient populations 3, including historically difficult-to-treat groups:

  • Genotype 1 infection (previously hardest to treat)
  • Patients with cirrhosis
  • Prior treatment failures

Common Pitfalls and Caveats

  1. HBV reactivation: Test all patients for HBV before starting treatment; monitor HBV/HCV co-infected patients for hepatitis flares 2

  2. Drug interactions: Review all medications (including over-the-counter and recreational drugs) before starting treatment 1

  3. Treatment discontinuation: Stop treatment immediately for severe adverse events or ALT flares >10 times upper limit of normal 1

  4. Post-treatment monitoring: Patients with advanced fibrosis (F3) or cirrhosis (F4) require continued HCC surveillance every 6 months indefinitely, even after achieving SVR 1

  5. Ribavirin dose adjustment: In patients with decompensated cirrhosis receiving ribavirin, reduce dose if hemoglobin drops below 10 g/dl; stop if below 8.5 g/dl 1

The introduction of DAAs has revolutionized hepatitis C treatment, making it a highly curable infection with short treatment durations and minimal side effects compared to older interferon-based regimens 3, 4.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Direct-acting antivirals: the endgame for hepatitis C?

Current opinion in virology, 2017

Research

Direct-acting antivirals for the treatment of hepatitis C virus infection: optimizing current IFN-free treatment and future perspectives.

Liver international : official journal of the International Association for the Study of the Liver, 2016

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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