Timely Hepatitis C RNA Testing and Treatment in the Era of Direct-Acting Antiviral Therapy among People with Hepatitis C in New South Wales, Australia

Viruses. 2022 Jul 8;14(7):1496. doi: 10.3390/v14071496.

Abstract

This study aimed to identify the factors associated with timely (within four weeks) HCV RNA testing and timely (within six months) DAA initiation following HCV notification in the DAA era. We conducted a cohort study of people with an HCV notification in NSW, Australia. Notifications of positive HCV serology were linked to administrative datasets. Weights were applied to account for spontaneous clearance. Logistic regression analyses were performed. Among 5582 people with an HCV notification during 2016-2017, 3867 (69%) were tested for HCV RNA, including 2770 (50%) who received timely testing. Among an estimated 3925 people with chronic HCV infection, 2372 (60%) initiated DAA therapy, including 1370 (35%) who received timely treatment. Factors associated with timely HCV RNA testing included age (≥30 years), female sex, non-Aboriginal ethnicity, country of birth being Australia, and no history of drug dependence. Factors associated with timely treatment were age (≥30 years), male sex, non-Aboriginal ethnicity, country of birth being Australia, no history of drug dependence, and HCV/HIV co-infection. In the DAA era, 50% of people with an HCV notification did not receive timely HCV RNA testing. Most people with an HCV infection received therapy; however, DAA initiation was delayed among many.

Keywords: HCV RNA testing; data linkage; direct acting antiviral therapy; hepatitis C virus; treatment uptake.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use
  • Australia / epidemiology
  • Cohort Studies
  • Female
  • HIV Infections* / drug therapy
  • Hepacivirus / genetics
  • Hepatitis C* / diagnosis
  • Hepatitis C* / drug therapy
  • Hepatitis C* / epidemiology
  • Hepatitis C, Chronic* / diagnosis
  • Hepatitis C, Chronic* / drug therapy
  • Hepatitis C, Chronic* / epidemiology
  • Humans
  • Male
  • New South Wales / epidemiology
  • RNA

Substances

  • Antiviral Agents
  • RNA

Grants and funding

The Kirby Institute is funded by the Australian Government Department of Health, under the agreement ID number 2-D3X513. This publication is part of the Bloodborne viruses and sexually transmissible infections Research, Strategic Interventions and Evaluation (BRISE) program, funded by the New South Wales Ministry of Health. J.G. is supported by an Australian National Health and Medical Research Council (NHMRC) Investigator Grant (1176131). G.J.D. is supported through a National Health and Medical Research Council (NHMRC) Investigator Grant (2008276). M.T.Y. is supported by a PhD Scientia Scholarship from UNSW Sydney.