Theme: Epidemiology & Public Health Research Year: 2022
Enhanced and more timely HCV treatment uptake among people who inject drugs is important for
elimination. We aimed to measure the association between drug dependence (as a potential barrier
to HCV testing/treatment) and timely HCV RNA testing and treatment following HCV notification in
the DAA era in New South Wales (NSW), Australia.
We conducted a cohort study of people who had a first record of HCV notification in the DAA era
(2016-2017). HCV notifications were linked to administrative data sources. HCV RNA testing within
four weeks, and treatment within six months of HCV notification were defined as “timely”. Drug
dependence was defined by receipt of opioid agonist therapy or hospitalization for injecting drug userelated causes. The study population were categorized as those with evidence of recent (2016-2018),
distant (before 2016), or no drug dependence.
Among 5,582 people with an HCV notification, 1,849 (33%), 656 (12%), and 3,077 (55%) had evidence
of recent, distant, and no drug dependence, respectively. Timely HCV RNA testing was undertaken in
40%, 50% and 55%, of those with recent, distant, and no drug dependence, respectively. Among an
estimated 3,925 people with chronic HCV infection, treatment was initiated in 59% (27% timely) of
those with recent, 64% (38% timely) distant, and 61% (39% timely) no drug dependence. Timely HCV
RNA testing and treatment was lower among those with evidence of recent compared to no drug
dependence (adjusted odds ratios 0.63; 95% CI: 0.55, 0.72 and 0.65; 95% CI: 0.55, 0.77, respectively).
More than half of people with recent drug dependence did not receive timely HCV RNA testing. Timely
treatment was less common among those with recent drug dependence. Innovative strategies to
enhance timely diagnosis and treatment including point-of-care technologies, and simplified models
of care are required to optimize HCV elimination efforts.
Disclosure of Interest Statement:
GD reports grants from Gilead, Abbvie, and Merck. JG is a consultant/advisor and has received
grants from Abbvie, Camurus, Cepheid, Gilead Sciences, Hologic, Indivior, and Merck/MSD. All
remaining authors have no potential conflicts to declare.