The Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.
Liver Int. 2024 Nov;44(11):2996-3007. doi: 10.1111/liv.16074. Epub 2024 Aug 27.
Hepatitis C virus (HCV) burden is higher among people in prison given high prevalence of injecting drug use. This study evaluated direct-acting antiviral (DAA) treatment outcome in prisons.
The Surveillance and Treatment of Prisoners with hepatitis C (SToP-C) study enrolled individuals incarcerated in four Australian prisons (2017-2019). Participants with detectable HCV RNA were offered sofosbuvir-velpatasvir for 12 weeks. Sustained virological response (SVR) was assessed in intention-to-treat (ITT; participants commencing treatment and due for SVR assessment before study close) and per-protocol (PP; participants with documented treatment completion and SVR assessment) populations.
Among 799 participants with HCV, 324 (41%) commenced treatment (94% male; median age, 32 years; median duration of incarceration, 9 months). In ITT population (n = 310), 201 had documented treatment completion (65% [95% CI: 59-70]), and 137 achieved SVR (ITT-SVR: 44% [95% CI: 39-50]). In PP population (n = 143), 137 achieved SVR (PP-SVR: 96% [95% CI: 91-98]). Six participants had quantifiable HCV RNA at SVR assessment from treatment failure (n = 2) or reinfection (n = 4). Release or inter-prison transfer was common reasons for no documented treatment completion (n = 106/109 [97%]) and no SVR assessment (n = 57/58 [98%]). In ITT analysis, longer incarceration was associated with increased SVR (adjusted OR per month 1.03 [95% CI: 1.01-1.04]).
Among participants who completed DAA treatment and were assessed for SVR, treatment outcome was consistent with non-prison clinical studies. However, most individuals did not complete treatment or lacked study-documented treatment outcome due to release or transfer. Strategies to accommodate dynamic prisoner populations are required to ensure continuity of HCV care, including treatment completion and post-treatment care.
由于注射吸毒的高流行率,监狱中的人感染丙型肝炎病毒(HCV)的负担更高。本研究评估了直接作用抗病毒(DAA)治疗在监狱中的效果。
监狱中丙型肝炎病毒的监测和治疗(SToP-C)研究纳入了 4 所澳大利亚监狱中的囚犯(2017-2019 年)。检测到 HCV RNA 的参与者接受了索磷布韦-维帕他韦治疗 12 周。在意向治疗(ITT;开始治疗且研究结束前应进行 SVR 评估的参与者)和按方案(PP;有记录的治疗完成和 SVR 评估的参与者)人群中评估持续病毒学应答(SVR)。
在 799 名 HCV 患者中,有 324 名(41%)开始治疗(94%为男性;中位年龄 32 岁;中位监禁时间 9 个月)。在 ITT 人群(n=310)中,有 201 名记录了治疗完成(65%[95%CI:59-70%]),有 137 名达到 SVR(ITT-SVR:44%[95%CI:39-50%])。在 PP 人群(n=143)中,有 137 名达到 SVR(PP-SVR:96%[95%CI:91-98%])。6 名参与者在 SVR 评估时出现可量化的 HCV RNA,原因是治疗失败(n=2)或再感染(n=4)。释放或监狱之间的转移是记录的治疗完成(n=106/109 [97%])和 SVR 评估(n=57/58 [98%])缺失的常见原因。在 ITT 分析中,监禁时间延长与 SVR 增加相关(校正后的每月 OR 为 1.03[95%CI:1.01-1.04])。
在完成 DAA 治疗并接受 SVR 评估的参与者中,治疗结果与非监狱临床研究一致。然而,由于释放或转移,大多数人没有完成治疗或缺乏研究记录的治疗结果。需要制定策略来容纳不断变化的囚犯群体,以确保 HCV 护理的连续性,包括治疗完成和治疗后护理。