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🟢 Hepatitis C Antiviral Treatment (DAA)

This tool gives the HCV direct-acting-antiviral regimen direction by cirrhosis status and pregnancy, with pre-treatment assessment and the SVR12 endpoint.

Clinical takeaway

Protease-inhibitor regimens are contraindicated in decompensated cirrhosis, which is managed by hepatology with SOF/VEL + ribavirin. (original synthesis · not guideline verbatim)

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When to use

Use to choose a pangenotypic regimen in non-cirrhotic/compensated disease, a specialist SOF/VEL + RBV regimen in decompensation, and to defer therapy in pregnancy.

How it works

No cirrhosis/compensated → SOF/VEL 12 weeks or GLE/PIB 8 weeks. Decompensated → protease inhibitors contraindicated, SOF/VEL + RBV 12 weeks. Pregnant → defer. Endpoint SVR12.

Key points

  • Protease-inhibitor regimens are contraindicated in decompensated cirrhosis, which is managed by hepatology with SOF/VEL + ribavirin. (original synthesis · not guideline verbatim)
  • Pre-treatment HBsAg screening prevents HBV reactivation during DAA therapy.
  • Cirrhotic patients continue HCC surveillance even after achieving SVR.

References

Decision support for licensed clinicians only; not a substitute for clinical judgement, diagnosis or local protocols.

Worked calculation

The values below come from this tool's own example placeholders and are computed server-side with the formula shown on this page, so the arithmetic can be checked quickly. It demonstrates how to substitute values only — it is not clinical advice and not a real case.

Cirrhosis statusNo cirrhosis
PregnancyYes

DispositionDefer DAA in pregnancy

  • NoteDAAs are not recommended in pregnancy; antiviral treatment can be given after delivery and the end of breastfeeding. Women of childbearing potential should be screened for pregnancy before treatment and avoid pregnancy during treatment
  • PrincipleAll HCV RNA–positive individuals should receive antiviral treatment at an appropriate time, with the endpoint of SVR12
  • BasisGuideline for the Prevention and Treatment of Hepatitis C (2022 edition)
Cirrhosis statusDecompensated cirrhosis (Child B/C or prior decompensation)
PregnancyNo

Regimen directionSOF/VEL + RBV 12 weeks

  • IndicationAll HCV RNA–positive individuals should receive antiviral treatment (with very few exceptions of very short life expectancy)
  • Recommended regimenDecompensated: protease inhibitors (e.g. glecaprevir/pibrentasvir) contraindicated; use sofosbuvir/velpatasvir + ribavirin for 12 weeks (RBV contraindicated → no combination, extend to 24 weeks)
  • Pre-treatment assessmentLiver disease severity (cirrhosis/decompensation), renal function, quantitative HCV RNA, HBsAg, comorbidities and drug-drug interactions; genotyping may be omitted with a pangenotypic regimen where local 3b prevalence < 5%

Frequently asked questions

What is Hepatitis C Antiviral Treatment (DAA)?
This tool gives the HCV direct-acting-antiviral regimen direction by cirrhosis status and pregnancy, with pre-treatment assessment and the SVR12 endpoint.
How is Hepatitis C Antiviral Treatment (DAA) calculated? What is the core formula?
No cirrhosis/compensated → SOF/VEL 12 weeks or GLE/PIB 8 weeks. Decompensated → protease inhibitors contraindicated, SOF/VEL + RBV 12 weeks. Pregnant → defer. Endpoint SVR12.
When is Hepatitis C Antiviral Treatment (DAA) used?
Use to choose a pangenotypic regimen in non-cirrhotic/compensated disease, a specialist SOF/VEL + RBV regimen in decompensation, and to defer therapy in pregnancy.
What are the key clinical points for Hepatitis C Antiviral Treatment (DAA)?
Protease-inhibitor regimens are contraindicated in decompensated cirrhosis, which is managed by hepatology with SOF/VEL + ribavirin. (original synthesis · not guideline verbatim) Pre-treatment HBsAg screening prevents HBV reactivation during DAA therapy. Cirrhotic patients continue HCC surveillance even after achieving SVR.
What are the limits and cautions when using Hepatitis C Antiviral Treatment (DAA)?
For licensed clinicians and clinical researchers. Interpret results with history, investigations and local protocols; not a diagnosis or prescription, and not a substitute for multidisciplinary decision-making or local guidelines.
How is Hepatitis C Antiviral Treatment (DAA) calculated in practice? Can you show a worked example?
Inputs: Cirrhosis status No cirrhosis, Pregnancy Yes → Result: Disposition Defer DAA in pregnancy(Note: DAAs are not recommended in pregnancy; antiviral treatment can be given after delivery and the end of breastfeeding. Women of childbearing potential should be screened for pregnancy before treatment and avoid pregnancy during treatment, Principle: All HCV RNA–positive individuals should receive antiviral treatment at an appropriate time, with the endpoint of SVR12, Basis: Guideline for the Prevention and Treatment of Hepatitis C (2022 edition)) Inputs: Cirrhosis status Decompensated cirrhosis (Child B/C or prior decompensation), Pregnancy No → Result: Regimen direction SOF/VEL + RBV 12 weeks(Indication: All HCV RNA–positive individuals should receive antiviral treatment (with very few exceptions of very short life expectancy), Recommended regimen: Decompensated: protease inhibitors (e.g. glecaprevir/pibrentasvir) contraindicated; use sofosbuvir/velpatasvir + ribavirin for 12 weeks (RBV contraindicated → no combination, extend to 24 weeks), Pre-treatment assessment: Liver disease severity (cirrhosis/decompensation), renal function, quantitative HCV RNA, HBsAg, comorbidities and drug-drug interactions; genotyping may be omitted with a pangenotypic regimen where local 3b prevalence < 5%)

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