Hepatitis C Treatment Pathway
Test → treat → cure. Any Australian GP or nurse practitioner can prescribe pan-genotypic direct-acting antivirals (DAAs) for hepatitis C — no genotype required, no specialist sign-off needed for uncomplicated cases. This tool walks the workflow and suggests the regimen.
⚠ Use clinical judgement. This tool assumes treatment-naive, uncomplicated chronic HCV. Cirrhosis, prior DAA treatment failure, decompensated liver disease, pregnancy, significant drug interactions, and HBV/HIV co-infection all change the pathway — these need specialist or REACH-C input. Always run a drug-interaction check before prescribing (sofosbuvir and the protease inhibitors interact with several common medicines).
Step-by-step pathway
The two first-line regimens
Both are pan-genotypic — genotype testing is no longer required for PBS. Either is suitable first-line for treatment-naive patients.
Glecaprevir / pibrentasvir (Maviret)
3 tablets once daily with food. 8 weeks treatment-naive (with or without compensated cirrhosis). No renal dose adjustment. Contraindicated in decompensated cirrhosis (Child–Pugh B/C) — it's a protease inhibitor. Common SE: headache, fatigue, nausea.
Sofosbuvir / velpatasvir (Epclusa)
1 tablet once daily. 12 weeks (with or without cirrhosis). No renal dose adjustment. Safe in decompensated cirrhosis (preferred when decompensation present, usually with specialist input). Consider adding ribavirin in genotype-3 with compensated cirrhosis. Common SE: headache, fatigue, nausea.
Salvage (NS5A-experienced / prior DAA failure): sofosbuvir/velpatasvir/voxilaprevir (Vosevi) for 12 weeks — usually specialist-directed.
Pre-treatment work-up (one round of bloods)
- HCV RNA (quantitative) — confirms current infection. Genotype NOT required for PBS.
- FBC, LFTs, U&E, INR — baseline; needed for APRI / FIB-4.
- Cirrhosis assessment — FibroScan, or APRI / FIB-4 from FBC + LFTs. If you can't assess fibrosis promptly, start treatment anyway (don't delay) — but flag for fibrosis assessment.
- HBV serology (HBsAg, anti-HBc, anti-HBs) — HBV reactivation risk during DAA therapy; check before or within 4 weeks of starting.
- HIV serology — co-infection alters management.
- Pregnancy test if relevant — ribavirin is teratogenic; DAAs not recommended in pregnancy.
- Drug interaction check — review all concomitant medicines (statins, amiodarone, anticonvulsants, PPIs with some regimens, St John's Wort).
Confirming cure — SVR12
SVR12 = sustained virological response. Check HCV RNA at least 12 weeks after completing treatment. Undetectable RNA = cure (≥95% with pan-genotypic DAAs in primary care). Document the cure, counsel that cure does not confer immunity (re-infection is possible with ongoing risk), and offer harm-reduction. If RNA is still detectable → treatment failure; refer for resistance testing and salvage (Vosevi).
When to involve a specialist or REACH-C
Any GP can treat uncomplicated HCV. Seek specialist or
REACH-C input for:
- Cirrhosis (especially decompensated — Child–Pugh B/C)
- Prior DAA treatment failure
- HBV or HIV co-infection
- Significant renal impairment or complex drug interactions
- Pregnancy, or current/planned pregnancy
- Hepatocellular carcinoma, or current/prior
- You are not experienced in HCV treatment (consensus statement: practitioners not experienced should consult an experienced specialist before initiating)
REACH-C provides specialist approval, typically within 24 hours, via an online form — a time-efficient option for GPs newer to HCV treatment.
ashm.org.au/resources/reach-c
Clinical support
Australian Centre for Disease Control HepLink
Free clinical and patient support line, Mon–Fri 9am–5pm.
1800 437 222 (1800 HEP ABC)
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