ICF Alliance for Public Health in Ukraine, 9th Floor, Building 10A, 5 Dilova (Dymytrova) Str., Kyiv 03150, Ukraine; Johns Hopkins Bloomberg School of Public Health, Department of Health, Behavior and Society, 624 N Broadway, Baltimore, MD 21205, USA.
ICF Alliance for Public Health in Ukraine, 9th Floor, Building 10A, 5 Dilova (Dymytrova) Str., Kyiv 03150, Ukraine.
Int J Drug Policy. 2017 Sep;47:187-195. doi: 10.1016/j.drugpo.2017.07.023. Epub 2017 Aug 12.
HCV prevalence estimates among people who inject drugs (PWID) in Ukraine is high (60-90%), yet barriers to HCV treatment and care remain substantial including limited access to direct acting antiviral (DAA) medications. A feasibility scale-up project implemented HCV treatment in community-based settings to improve access to DAA treatment for key populations in this context.
Using program-level data and verified medical records, we describe the development, implementation processes and outcomes for HCV treatment for PWID and other risks groups. Most participants (76%) received a combination of sofosbuvir, pegylated interferon, and ribavirin for 12 weeks. Treatment enrollment started in June 2015; the first two waves are reported. Data on demographics, HIV characteristics, HCV genotype and RNA levels, including sustained virologic response (SVR) were obtained from verified medical records. We used logistic regression to examine the independent correlates of achieving a SVR.
The project was implemented in 19 healthcare institutions from 16 regions of Ukraine, mainly within AIDS specialty centers. Our analytical sample included 1126 participants who were mostly men (73%) and the majority were HIV co-infected (79%). Treatment retention was 97.7%; the proportions of participants who achieved SVR for the overall sample and for those with complete data (N=1029) were 86.2% (95% CI 84.08-88.19%) and 94.3% (95% CI 92.8-95.7%) respectively. The analysis of data restricted to only those with SVR data available showed that PWID who were currently injecting had comparable SVR rates (89.2%, 95% CI 81.5-94.5%) to PWID not injecting (94.4%, 95% CI 92.4-96.1), PWID on methadone (94.4%, 95%CI 92.4-96.1), and 'other' risk groups (95.2%, 95% CI 91.3-97.7). Independent factors associated with achieving a SVR were female sex (AOR: 3.44, 95% CI 1.45-8.14), HCV genotype 3 (AOR: 4.57, 95% CI 1.97-10.59) compared to genotype 1. SVR rates in PWID actively injecting did not differ significantly from any other group.
Both patient-level and structural factors influence HCV treatment scale-up in Ukraine, but patient-level outcomes confirm high levels of achieving SVR in PWID, irrespective of injection and treatment status.
乌克兰注射吸毒人群(PWID)中的丙型肝炎病毒(HCV)流行率很高(60-90%),但 HCV 治疗和护理的障碍仍然很大,包括获得直接作用抗病毒药物(DAA)的机会有限。一个可行性扩大项目在社区环境中实施 HCV 治疗,以改善这一背景下关键人群获得 DAA 治疗的机会。
使用项目层面的数据和经过验证的医疗记录,我们描述了为 PWID 和其他风险群体进行 HCV 治疗的开发、实施过程和结果。大多数参与者(76%)接受了为期 12 周的索非布韦、聚乙二醇干扰素和利巴韦林联合治疗。治疗登记于 2015 年 6 月开始,报告了前两波。从经过验证的医疗记录中获得人口统计学、HIV 特征、HCV 基因型和 RNA 水平的数据,包括持续病毒学应答(SVR)。我们使用逻辑回归来检验达到 SVR 的独立相关因素。
该项目在乌克兰 16 个地区的 19 家医疗机构实施,主要在艾滋病专科中心内开展。我们的分析样本包括 1126 名参与者,他们主要是男性(73%),大多数人 HIV 合并感染(79%)。治疗保留率为 97.7%;总体样本和具有完整数据(N=1029)的参与者中达到 SVR 的比例分别为 86.2%(95%CI 84.08-88.19%)和 94.3%(95%CI 92.8-95.7%)。仅对具有 SVR 数据的参与者进行数据分析显示,目前正在注射的 PWID 的 SVR 率(89.2%,95%CI 81.5-94.5%)与未注射的 PWID(94.4%,95%CI 92.4-96.1%)、美沙酮治疗的 PWID(94.4%,95%CI 92.4-96.1%)和“其他”风险群体(95.2%,95%CI 91.3-97.7%)相当。与达到 SVR 相关的独立因素包括女性(AOR:3.44,95%CI 1.45-8.14),与基因型 1 相比,HCV 基因型 3(AOR:4.57,95%CI 1.97-10.59)。目前正在积极注射的 PWID 的 SVR 率与任何其他群体没有显著差异。
在乌克兰,患者层面和结构因素都影响 HCV 治疗的扩大,但患者层面的结果证实,PWID 达到 SVR 的水平很高,无论其注射和治疗状况如何。