McGill University, Department of Family Medicine, Montreal, QC, Canada; Centre de recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.
Centre de recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.
Int J Drug Policy. 2019 Oct;72:69-76. doi: 10.1016/j.drugpo.2019.04.002. Epub 2019 Apr 19.
Multiple barriers for accessing hepatitis C virus (HCV) treatment were identified during the interferon-based (IFN) treatment era for people who inject drugs (PWID). Whether these barriers persist since the introduction of IFN-free direct-acting antiviral (DAA) agents in Canada remains to be documented. This study examined temporal trends in HCV treatment initiation and associated factors during the transition from INF-based to all-oral DAA regimens.
The study population was drawn from a prospective cohort of PWID in Montreal, Canada. At three-month/one-year intervals between 2011 and 2017, participants with chronic HCV infection completed an interviewer-administered questionnaire on socio-demographic characteristics, drug use and health service utilisation, including HCV treatment. Time-updated Cox multivariate regression models, stratified by DAA + INF (2011-2013) and all-oral DAA (2014-2017) availability periods, were conducted to examine associations between time to HCV treatment initiation and associated barriers and facilitators.
Of 308 participants (85% male, median age 42 [IQR: 33, 50]), 80 (26%) initiated HCV treatment during 915 person-years (PY). Incidence rates increased from 1.6 /100 PY (95%CI:0.9-2.6) in 2011 to 12.7 (10.6-15.1) in 2017 (p-trend = 0.0012). In multivariate analyses, visiting a primary care physician (2011-2013: aHR = 3.63[1.21-10.9]; 2014-2017: 2.52[1.10-5.77]) and frequent injection (0.23[0.05-0.99] and 0.49[0.24-0.99]) were consistently associated with treatment initiation. Participants aged >40 (2.27[1.24-4.13]), receiving opioid agonist therapy (OAT) (2.17[1.19-3.94]), and reporting prior HCV treatment (3.00[1.75-5.15]) were more likely to initiate treatment in the all-oral DAA period.
Treatment initiation increased between 2011 and 2017, but still remains low among PWID. Primary care visiting was a key facilitator regardless of the period, while engagement in OAT and health services, indicated by prior HCV treatment, increased the likelihood of treatment initiation in the DAA era. These findings suggest that access to health services is essential but not enough to scale up treatment in this population.
在为吸毒者(PWID)提供基于干扰素(IFN)的治疗时代,已经确定了许多获得丙型肝炎病毒(HCV)治疗的障碍。自加拿大引入无干扰素直接作用抗病毒(DAA)药物以来,这些障碍是否仍然存在,仍有待记录。本研究检查了从基于 IFN 向全口服 DAA 方案过渡期间 HCV 治疗开始和相关因素的时间趋势。
研究人群来自加拿大蒙特利尔的一个前瞻性吸毒者队列。在 2011 年至 2017 年期间,每三个月/一年,患有慢性 HCV 感染的参与者完成了一份由访谈者管理的问卷,内容包括社会人口统计学特征、药物使用和卫生服务利用情况,包括 HCV 治疗。在 DAA+IFN(2011-2013 年)和全口服 DAA(2014-2017 年)可用期间,采用时间更新的 Cox 多变量回归模型,对 HCV 治疗开始时间与相关障碍和促进因素之间的关系进行了分析。
在 308 名参与者(85%为男性,中位年龄 42[IQR:33,50])中,80 名(26%)在 915 人年(PY)内接受了 HCV 治疗。发病率从 2011 年的 1.6/100 PY(95%CI:0.9-2.6)增加到 2017 年的 12.7(10.6-15.1)(p趋势=0.0012)。在多变量分析中,就诊于初级保健医生(2011-2013 年:aHR=3.63[1.21-10.9];2014-2017 年:2.52[1.10-5.77])和频繁注射(0.23[0.05-0.99]和 0.49[0.24-0.99])与治疗开始始终相关。年龄>40 岁(2.27[1.24-4.13])、接受阿片类药物替代治疗(OAT)(2.17[1.19-3.94])和报告既往 HCV 治疗(3.00[1.75-5.15])的参与者更有可能在全口服 DAA 期间开始治疗。
2011 年至 2017 年间,治疗开始率有所增加,但在吸毒者中仍处于较低水平。初级保健就诊是一个关键的促进因素,无论在哪个时期都是如此,而接受 OAT 和卫生服务,表明之前接受过 HCV 治疗,增加了 DAA 时代治疗开始的可能性。这些发现表明,获得卫生服务是必要的,但不足以在该人群中扩大治疗规模。