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AASLD-IDSA 2019/2020 Hepatitis C Guidance: testing and treatment update

This joint AASLD-IDSA guidance covers screening, diagnosis, and direct-acting antiviral (DAA) treatment of chronic hepatitis C virus infection in adults. Its central message is that nearly all HCV-infected patients, including most with cirrhosis and many special populations, can now be treated with short-course, pangenotypic DAA regimens without needing genotype testing in most cases.

AASLD2020 editionSummary
Official guidelineHepatitis C Guidance 2019 Update: American Association for the Study of Liver Diseases-Infectious Diseases Society of America Recommendations for Testing, Managing, and Treating Hepatitis C Virus Infection. AASLD, 2020.
Read the official guideline · Checked for a newer edition on 2026-10-20
We do not reproduce the guideline text — this page is an independent summary.

Who it applies to

Adults and adolescents with confirmed or suspected hepatitis C virus infection evaluated in primary care or specialty settings, including people who inject drugs, those with cirrhosis, HIV coinfection, renal impairment, and prior treatment failures.

Key recommendations

  • One-time HCV screening (antibody testing) is recommended for all adults aged 18 and older at least once, and for all pregnant women during each pregnancy, regardless of perceived risk.
  • Periodic repeat testing is recommended for persons with ongoing risk factors, such as people who inject drugs or men who have sex with men with high-risk behavior.
  • A reactive antibody test should be followed by HCV RNA testing to confirm active (viremic) infection before treatment decisions are made.
  • Pretreatment HCV genotype testing is not required before starting most pangenotypic DAA regimens, simplifying the treatment pathway.
  • Treatment with DAAs is recommended for essentially all patients with chronic HCV infection, except those with short life expectancy that cannot be improved by treatment, liver transplantation, or antiviral therapy.
  • Simplified treatment algorithms using fixed-dose combination pangenotypic regimens (such as sofosbuvir-velpatasvir or glecaprevir-pibrentasvir) for 8 to 12 weeks are endorsed for treatment-naive patients without cirrhosis or with compensated cirrhosis in appropriate settings.
  • People who inject drugs should be offered the same DAA treatment as other populations, since ongoing drug use is not a contraindication to therapy.
  • Patients with decompensated cirrhosis should avoid protease inhibitor-containing regimens and be managed in conjunction with or referred to a liver specialist.
  • Sustained virologic response at 12 weeks after completing treatment (SVR12) confirms cure and should be assessed with HCV RNA testing.
  • Patients with cirrhosis who achieve cure still require ongoing surveillance for hepatocellular carcinoma, as this risk persists after SVR.

What is new in this edition

  • Updated guidance incorporated simplified, genotype-independent treatment algorithms for treatment-naive patients to make prescribing feasible for non-specialist providers.
  • Expanded and reinforced recommendations supporting treatment of people who inject drugs without requiring abstinence.

Practice points for students

  • Universal one-time screening for all adults is now standard, not just risk-based testing.
  • Confirm active infection with HCV RNA before assuming a positive antibody result means current infection.
  • Genotype testing is largely unnecessary before starting modern pangenotypic DAA therapy.
  • Active drug use alone is not a reason to withhold or delay DAA treatment.
  • SVR12 is the test of cure, but cirrhotic patients still need lifelong HCC surveillance even after cure.

Condition

Hepatitis C

Other guidelines on this topic

Independent educational summary written by the WhiteCoat Pro editorial team with AI assistance and checked by a second AI model. It does not reproduce the guideline text, tables or figures, and it is not affiliated with or endorsed by AASLD. It is not medical advice: always read the original guideline before applying it to patients.