Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?

被引:31
|
作者
Lima, Viviane D. [1 ]
Rozada, Ignacio [1 ]
Grebely, Jason [2 ]
Hull, Mark [1 ]
Lourenco, Lillian [1 ]
Nosyk, Bohdan [1 ]
Krajden, Mel [3 ]
Yoshida, Eric [4 ]
Wood, Evan [1 ]
Montaner, Julio S. G. [1 ]
机构
[1] British Columbia Ctr Excellence HIV AIDS, Vancouver, BC, Canada
[2] Univ New South Wales Australia, Kirby Inst, Sydney, NSW, Australia
[3] British Columbia Ctr Dis Control, Publ Hlth Microbiol & Reference Lab, Vancouver, BC, Canada
[4] Univ British Columbia, Fac Med, Dept Med, Div Gastroenterol, Vancouver, BC, Canada
来源
PLOS ONE | 2015年 / 10卷 / 12期
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
HEPATITIS-C-VIRUS; OPIATE SUBSTITUTION THERAPY; INFECTION; COHORT; USERS; HIV; COINFECTION; METAANALYSIS; MANAGEMENT; CIRRHOSIS;
D O I
10.1371/journal.pone.0143836
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background 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. Methods 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 R-c. We assessed the impact of these interventions on incidence, prevalence and mortality from 2016 to 2030. Results Of all HCV antiviral regimens, only IFN-free DAAs offered a high chance of disease elimination (i.e. R-c < 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 F-2 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. Conclusions 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.
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页数:19
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