Disparities in Uptake of Direct-acting Antiviral Therapy for Hepatitis C Among People Who Inject Drugs in a Canadian Setting
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Background & Aims: Despite the high burden of hepatitis C virus (HCV) infection among people who inject drugs (PWID), uptake of interferon-based therapies has been extremely low. Increasing availability of direct-acting antiviral (DAA)-based therapies offers the possibility of rapid treatment expansion with the goal of controlling the HCV epidemic. We evaluated DAA-based treatment uptake among HCV-positive PWID in Vancouver after introduction of DAAs in the government drug formulary.
Methods: Using data from three cohorts of PWID in Vancouver, Canada, we investigated factors associated with DAA-therapies uptake among participants with HCV between April 2015 and November 2017.
Results: Of the 915 HCV-positive PWID, 611 (66.8%) were recent PWID and 369 (40.3%) had HIV coinfection. During the study period, 146 (16.0%) initiated DAA-therapies, a rate of 6.0 per 100 person-year, with higher initiation rates among non-recent PWID and an increasing trend over time. In multivariable analysis, HIV coinfection (Adjusted Odds Ratio [AOR] = 2.29, 95% Confidence Interval [CI]: 1.55-3.40), white race (AOR = 1.56, 95% CI: 1.05-2.35), and engagement in HCV care (AOR = 1.94, 95% CI: 1.31-2.90) were positively associated with DAA-therapies uptake, while high-risk drinking (AOR = 0.47, 95% CI: 0.23-0.88) and daily crack use were negatively associated (AOR = 0.41, 95% CI: 0.17-0.85). Among recent PWID, engagement in opioid agonist therapy emerged as an independent correlate of DAA uptake.
Conclusions: Despite increases in HCV treatment uptake among PWID after the introduction of DAAs in our setting, disparities in access remain. Social-structural and behavioural barriers to HCV care should be addressed for the success of any HCV elimination strategy.
Estadt A, Kline D, Miller W, Feinberg J, Hurt C, Mixson L Harm Reduct J. 2024; 21(1):214.
PMID: 39614319 PMC: 11606200. DOI: 10.1186/s12954-024-01131-6.
Malme K, Stene-Johansen K, Klundby I, Backe O, Foshaug T, Greve M Viruses. 2024; 16(6).
PMID: 38932151 PMC: 11209464. DOI: 10.3390/v16060858.
Burton M, Voluse A, Patel A Addict Sci Clin Pract. 2024; 19(1):51.
PMID: 38918869 PMC: 11197191. DOI: 10.1186/s13722-024-00480-8.
Gagne M, Tetu I, Gregoire J, Moisan J Int J Nurs Stud Adv. 2024; 3:100029.
PMID: 38746734 PMC: 11080331. DOI: 10.1016/j.ijnsa.2021.100029.
Kimball S, Reynoso M, McKnight C, Des Jarlais D PLoS One. 2024; 19(4):e0302471.
PMID: 38669250 PMC: 11051606. DOI: 10.1371/journal.pone.0302471.