Ang Joshua, Hajarizadeh Behzad, Tillakeratne Shane, Dore Gregory J, Treloar Carla, Amin Janaki, van Dyk Jodi, Degenhardt Louisa, Applegate Tanya, Dunlop Adrian, Fraser Chris, Conway Brian, Wong Alexander, Fuchs Dennaye, Powis Jeff, Mason Kate, Gane Edward J, Weltman Martin, Read Phillip, Martinello Marianne, Rowe Emily, Baker David A, Wade Alexandra, Matthews Gail, Lafferty Lise, Lloyd Andrew, Grebely Jason, Cunningham Evan B
Kirby Institute, UNSW, Sydney, NSW, Australia.
Centre for Social Research in Health, UNSW, Sydney, 2052, NSW, Australia.
Int J Drug Policy. 2025 Sep;143:104859. doi: 10.1016/j.drugpo.2025.104859. Epub 2025 Jun 18.
Injecting drug use following treatment for hepatitis C virus (HCV) may result in reinfection, potentially reversing individual, and population benefits of HCV treatment. The aim of this study was to evaluate the incidence of HCV reinfection following successful direct acting antiviral (DAA) therapy among people with recent injecting drug use.
This analysis used data from an observational cohort study of people with recent injecting drug use (previous six months) following successful DAA treatment in Australia, Canada, and New Zealand. Participants were either recruited prior to commencing DAA therapy or after a documented sustained virological response (SVR). Participants were assessed three-monthly for HCV reinfection. Reinfection was defined as recurrence of virus distinct from the initial infecting strain or recurrence after confirmed cure at or after 12 weeks post-treatment. Person-time of observation and Cox proportional hazard models were used to calculate reinfection incidence and associated factors.
Among 112 participants who contributed follow-up time at risk of reinfection (113 person-years of follow-up time), the median age was 43 years, 34 % were female, and 86 % reported injecting drug use in the month prior to enrolment. Eleven cases of reinfection were observed for an incidence of 9.7/100 person-years (95 % confidence interval [CI], 5.4-17.4) overall, 11.1/100 person-years (95 % CI, 6.1-20.0) among people who reported injecting drugs during follow-up, and 24.3/100 person-years (95 % CI, 7.8-75.3) among those who reported sharing needles/syringes during follow-up. All cases of HCV reinfection occurred among people reporting injecting drug use during the study.
The relatively high incidence of reinfection seen in this study underscores the importance of targeted harm reduction measures and monitoring for HCV reinfections within the first year following successful treatment among people who inject drugs. Additional research into integrated models of care incorporating harm reduction and supporting reducing risk of reinfection and HCV treatment are needed.
丙型肝炎病毒(HCV)治疗后注射吸毒可能导致再次感染,这有可能逆转个体以及人群从HCV治疗中获得的益处。本研究的目的是评估近期有注射吸毒行为的人群在接受直接抗病毒药物(DAA)治疗成功后的HCV再次感染发生率。
本分析使用了来自澳大利亚、加拿大和新西兰对近期有注射吸毒行为(过去六个月内)的人群在接受DAA治疗成功后进行的一项观察性队列研究的数据。参与者要么在开始DAA治疗前招募,要么在记录到持续病毒学应答(SVR)后招募。对参与者每三个月评估一次HCV再次感染情况。再次感染定义为与初始感染毒株不同的病毒复发,或在治疗后12周及以后确认治愈后复发。使用观察人时和Cox比例风险模型来计算再次感染发生率及相关因素。
在112名有再次感染风险随访时间的参与者中(随访时间共113人年),中位年龄为43岁,34%为女性,86%报告在入组前一个月有注射吸毒行为。观察到11例再次感染病例,总体发生率为9.7/100人年(95%置信区间[CI],5.4 - 17.4),在随访期间报告有注射吸毒行为的人群中发生率为11.1/100人年(95%CI,6.1 - 20.0),在随访期间报告有共用针头/注射器行为的人群中发生率为24.3/100人年(95%CI,7.8 - 75.3)。所有HCV再次感染病例均发生在研究期间报告有注射吸毒行为的人群中。
本研究中观察到的相对较高的再次感染发生率强调了在注射吸毒者成功治疗后的第一年内采取针对性减少伤害措施以及监测HCV再次感染的重要性。需要对纳入减少伤害并支持降低再次感染风险和HCV治疗的综合护理模式进行更多研究。