Lima Viviane D, Rozada Ignacio, Grebely Jason, Hull Mark, Lourenco Lillian, Nosyk Bohdan, Krajden Mel, Yoshida Eric, Wood Evan, Montaner Julio S G
British Columbia Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
The Kirby Institute, University of New South Wales Australia, Sydney, NSW, Australia.
PLoS One. 2015 Dec 3;10(12):e0143836. doi: 10.1371/journal.pone.0143836. eCollection 2015.
Widely access to interferon-free direct-acting antiviral regimens (IFN-free DAA) is poised to dramatically change the impact of the HCV epidemic among people who inject drugs (PWID). We evaluated the long-term effect of increasing HCV testing, treatment and engagement into harm-reduction activities, focused on active PWID, on the HCV epidemic in British Columbia (BC), Canada.
We built a compartmental model of HCV disease transmission stratified by disease progression, transmission risk, and fibrosis level. We explored the effect of: (1) Increasing treatment rates from 8 to 20, 40 and 80 per 1000 infected PWID/year; (2) Increasing treatment eligibility based on fibrosis level; (3) Maximizing the effect of testing by performing it immediately upon ending the acute phase; (4) Increasing access to harm-reduction activities to reduce the risk of re-infection; (5) Different HCV antiviral regimens on the Control Reproduction Number Rc. We assessed the impact of these interventions on incidence, prevalence and mortality from 2016 to 2030.
Of all HCV antiviral regimens, only IFN-free DAAs offered a high chance of disease elimination (i.e. Rc < 1), but it would be necessary to substantially increase the current low testing and treatment rates. Assuming a treatment rate of 80 per 1000 infected PWID per year, coupled with a high testing rate, the incidence rate, at the end of 2030, could decrease from 92.9 per 1000 susceptible PWID per year (Status Quo) to 82.8 (by treating only PWID with fibrosis level F2 and higher) or to 65.5 (by treating PWID regardless of fibrosis level). If PWID also had access to increased harm-reduction activities, the incidence rate further decreased to 53.1 per 1000 susceptible PWID per year. We also obtained significant decreases in prevalence and mortality at the end of 2030.
The combination of increased access to HCV testing, highly efficacious antiviral treatment and harm-reduction programs can substantially decrease the burden of the HCV epidemic among PWID. However, unless we increase the current levels of treatment and testing, the HCV epidemic among PWID in BC, and in other parts of the world with similar epidemiological background, will remain a substantial public health concern for many years.
广泛使用无干扰素直接抗病毒方案(IFN 无 DAA)有望显著改变丙型肝炎病毒(HCV)流行对注射吸毒者(PWID)的影响。我们评估了增加 HCV 检测、治疗以及参与减少伤害活动(重点针对活跃的 PWID)对加拿大不列颠哥伦比亚省(BC)HCV 流行的长期影响。
我们构建了一个按疾病进展、传播风险和纤维化水平分层的 HCV 疾病传播 compartmental 模型。我们探讨了以下因素的影响:(1)将治疗率从每 1000 名受感染 PWID/年 8 例提高到 20 例、40 例和 80 例;(2)根据纤维化水平提高治疗资格;(3)通过在急性期结束后立即进行检测来最大化检测效果;(4)增加获得减少伤害活动的机会以降低再次感染风险;(5)不同的 HCV 抗病毒方案对控制繁殖数 Rc 的影响。我们评估了这些干预措施对 2016 年至 2030 年发病率、患病率和死亡率的影响。
在所有 HCV 抗病毒方案中,只有 IFN 无 DAA 提供了高疾病消除几率(即 Rc < 1),但有必要大幅提高当前较低的检测和治疗率。假设每年每 1000 名受感染 PWID 的治疗率为 80 例,再加上高检测率,到 2030 年底,发病率可能从每年每 1000 名易感 PWID 92.9 例(现状)降至 82.8 例(仅治疗纤维化水平为 F2 及更高的 PWID)或降至 65.5 例(无论纤维化水平如何均治疗 PWID)。如果 PWID 还能获得更多减少伤害活动的机会,发病率将进一步降至每年每 1000 名易感 PWID 53.1 例。我们还在 2030 年底获得了患病率和死亡率的显著下降。
增加 HCV 检测机会、高效抗病毒治疗和减少伤害计划相结合,可以大幅降低 PWID 中 HCV 流行的负担。然而,除非我们提高当前的治疗和检测水平,BC 省以及世界其他具有类似流行病学背景地区的 PWID 中的 HCV 流行在未来许多年仍将是一个重大的公共卫生问题。