TY - JOUR
T1 - Model projections on the impact of HCV treatment in the prevention of HCV transmission among people who inject drugs in Europe"
AU - Fraser, Hannah
AU - Martin, Natasha K.
AU - Brummer-Korvenkontio, Henrikki
AU - Carrieri, Patrizia
AU - Dalgard, Olav
AU - Dillon, John
AU - Goldberg, David
AU - Hutchinson, Sharon
AU - Jauffret-Roustide, Marie
AU - Kåberg, Martin
AU - Matser, Amy A.
AU - Matičič, Mojca
AU - Midgard, Havard
AU - Mravcik, Viktor
AU - Øvrehus, Anne
AU - Prins, Maria
AU - Reimer, Jens
AU - Robaeys, Geert
AU - Schulte, Bernd
AU - van Santen, Daniela K.
AU - Zimmermann, Ruth
AU - Vickerman, Peter
AU - Hickman, Matthew
N1 - The study was funded by European Commission Drug Prevention and Information Programme (DIPP) [JUST/2013/DPIP/AG/4812]. In addition we acknowledge support from the National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Evaluation of Interventions at the University of Bristol in partnership with Public Health England. NM, PV, and MH were supported by the National Institute for Drug Abuse [grant number R01 DA037773-01A1]. NM was additionally supported by the University of California San Diego Center for AIDS Research(CFAR)), a National Institute of Health (NIH) funded program [grant number P30 AI036214] The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, the Department of Health or Public Health England. VM: institutional support no. PRVOUK-P03/LF1/9 and the project Nr. LO1611 with a financial support from the MEYS under the NPU I program.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Background & Aims: Prevention of hepatitis C virus (HCV) transmission among people who inject drugs (PWID) is critical for eliminating HCV in Europe. We estimated the impact of current and scaled-up HCV treatment with and without scaling up opioid substitution therapy (OST) and needle and syringe programmes (NSPs) across Europe over the next 10 years. Methods: We collected data on PWID HCV treatment rates, PWID prevalence, HCV prevalence, OST, and NSP coverage from 11 European settings. We parameterised an HCV transmission model to setting-specific data that project chronic HCV prevalence and incidence among PWID. Results: At baseline, chronic HCV prevalence varied from <25% (Slovenia/Czech Republic) to >55% (Finland/Sweden), and <2% (Amsterdam/Hamburg/Norway/Denmark/Sweden) to 5% (Slovenia/Czech Republic) of chronically infected PWID were treated annually. The current treatment rates using new direct-acting antivirals (DAAs) may achieve observable reductions in chronic prevalence (38–63%) in 10 years in Czech Republic, Slovenia, and Amsterdam. Doubling the HCV treatment rates will reduce prevalence in other sites (12–24%; Belgium/Denmark/Hamburg/Norway/Scotland), but is unlikely to reduce prevalence in Sweden and Finland. Scaling-up OST and NSP to 80% coverage with current treatment rates using DAAs could achieve observable reductions in HCV prevalence (18–79%) in all sites. Using DAAs, Slovenia and Amsterdam are projected to reduce incidence to 2 per 100 person years or less in 10 years. Moderate to substantial increases in the current treatment rates are required to achieve the same impact elsewhere, from 1.4 to 3 times (Czech Republic and France), 5–17 times (France, Scotland, Hamburg, Norway, Denmark, Belgium, and Sweden), to 200 times (Finland). Scaling-up OST and NSP coverage to 80% in all sites reduces treatment scale-up needed by 20–80%. Conclusions: The scale-up of HCV treatment and other interventions is needed in most settings to minimise HCV transmission among PWID in Europe. Lay summary: Measuring the amount of HCV in the population of PWID is uncertain. To reduce HCV infection to minimal levels in Europe will require scale-up of both HCV treatment and other interventions that reduce injecting risk (especially OST and provision of sterile injecting equipment).
AB - Background & Aims: Prevention of hepatitis C virus (HCV) transmission among people who inject drugs (PWID) is critical for eliminating HCV in Europe. We estimated the impact of current and scaled-up HCV treatment with and without scaling up opioid substitution therapy (OST) and needle and syringe programmes (NSPs) across Europe over the next 10 years. Methods: We collected data on PWID HCV treatment rates, PWID prevalence, HCV prevalence, OST, and NSP coverage from 11 European settings. We parameterised an HCV transmission model to setting-specific data that project chronic HCV prevalence and incidence among PWID. Results: At baseline, chronic HCV prevalence varied from <25% (Slovenia/Czech Republic) to >55% (Finland/Sweden), and <2% (Amsterdam/Hamburg/Norway/Denmark/Sweden) to 5% (Slovenia/Czech Republic) of chronically infected PWID were treated annually. The current treatment rates using new direct-acting antivirals (DAAs) may achieve observable reductions in chronic prevalence (38–63%) in 10 years in Czech Republic, Slovenia, and Amsterdam. Doubling the HCV treatment rates will reduce prevalence in other sites (12–24%; Belgium/Denmark/Hamburg/Norway/Scotland), but is unlikely to reduce prevalence in Sweden and Finland. Scaling-up OST and NSP to 80% coverage with current treatment rates using DAAs could achieve observable reductions in HCV prevalence (18–79%) in all sites. Using DAAs, Slovenia and Amsterdam are projected to reduce incidence to 2 per 100 person years or less in 10 years. Moderate to substantial increases in the current treatment rates are required to achieve the same impact elsewhere, from 1.4 to 3 times (Czech Republic and France), 5–17 times (France, Scotland, Hamburg, Norway, Denmark, Belgium, and Sweden), to 200 times (Finland). Scaling-up OST and NSP coverage to 80% in all sites reduces treatment scale-up needed by 20–80%. Conclusions: The scale-up of HCV treatment and other interventions is needed in most settings to minimise HCV transmission among PWID in Europe. Lay summary: Measuring the amount of HCV in the population of PWID is uncertain. To reduce HCV infection to minimal levels in Europe will require scale-up of both HCV treatment and other interventions that reduce injecting risk (especially OST and provision of sterile injecting equipment).
KW - Direct-acting antivirals
KW - Hepatitis C
KW - Opioid substitution therapy
KW - PWID
UR - http://www.scopus.com/inward/record.url?scp=85040817518&partnerID=8YFLogxK
U2 - 10.1016/j.jhep.2017.10.010
DO - 10.1016/j.jhep.2017.10.010
M3 - Article
C2 - 29080808
SN - 0168-8278
VL - 68
SP - 402
EP - 411
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 3
ER -