Model projections on the impact of HCV treatment in the prevention of HCV transmission among people who inject drugs in Europe

. 2018 Mar ; 68 (3) : 402-411. [epub] 20180108

Jazyk angličtina Země Nizozemsko Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid29080808

Grantová podpora
P30 AI036214 NIAID NIH HHS - United States
R01 DA037773 NIDA NIH HHS - United States
RP-DG-0610-10055 Department of Health - United Kingdom

Odkazy

PubMed 29080808
PubMed Central PMC5841161
DOI 10.1016/j.jhep.2017.10.010
PII: S0168-8278(17)32387-5
Knihovny.cz E-zdroje

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).

Aix Marseille Univ INSERM IRD SESSTIM Sciences Economiques and Sociales de la Santé and Traitement de l'Information Médicale Marseille France; ORS PACA Observatoire Régional de la Santé Provence Alpes Côte d'Azur Marseille France

Department of Medicine Huddinge Division of Infectious Diseases Karolinska Institutet Karolinska University Hospital Stockholm Sweden

Division of Global Public Health University of California San Diego San Diego CA USA; Population Health Sciences Bristol Medical School University of Bristol Bristol UK

French Institute for Public Health Surveillance St Maurice France; CERMES3 Paris France

Glasgow Caledonian University Glasgow Scotland UK; Health Protection Scotland Glasgow Scotland UK

Health Protection Scotland Glasgow Scotland UK

HealthNorth Bremen Germany; University of Hamburg Hamburg Germany

National Institute for Health and Welfare Helsinki Finland

National Monitoring Centre for Drugs and Drug Addiction Prague Czech Republic; Charles University and General University Hospital Prague Prague Czech Republic; National Institute of Mental Health Klecany Czech Republic

Odense University Hospital Odense Denmark

Population Health Sciences Bristol Medical School University of Bristol Bristol UK

Public Health Service of Amsterdam Amsterdam The Netherlands

Public Health Service of Amsterdam Amsterdam The Netherlands; Academic Medical Centre University of Amsterdam Amsterdam The Netherlands

Public Health Service of Amsterdam Amsterdam The Netherlands; University Medical Center Utrecht Utrecht The Netherlands

Robert Koch Institute Berlin Germany

University of Dundee Dundee Scotland UK

University of Hamburg Hamburg Germany

University of Ljubljana Ljubljana Slovenia; University Medical Centre Ljubljana Ljubljana Slovenia

University of Oslo Oslo Norway

University of Oslo Oslo Norway; Akershus University Hospital Lørenskog Norway

Ziekenhuis Oost Limburg Genk Belgium; Hasselt University Diepenbeek Belgium; University Hospital Leuven Leuven Belgium

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Williams R, et al. Addressing liver disease in the UK: a blueprint for attaining excellence in health care and reducing premature mortality from lifestyle issues of excess consumption of alcohol, obesity, and viral hepatitis. Lancet. 2014;384(9958):1953–97. PubMed

Nelson PK, et al. Global epidemiology of hepatitis B and hepatitis C in people who inject drugs: results of systematic reviews. Lancet. 2011;378(9791):571–583. PubMed PMC

Ly KN, et al. The increasing burden of mortality from viral hepatitis in the United States between 1999 and 2007. Annals of internal medicine. 2012;156(4):271–278. PubMed

Cowie B, Allard N, MacLachlan J. O86 EUROPEAN RESPONSES IN FOCUS: COMPARING VIRAL HEPATITIS AND HIV RELATED DEATHS IN EUROPE 1990–2010 IN THE GLOBAL BURDEN OF DISEASE STUDY 2010. Journal of Hepatology. 2014;1(60):S35–S36.

ECDC and EMCDDA. Prevention and control of infectious diseases among people who inject drugs. Stockholm: ECDC; 2011. pp. 4–5.

European Monitoring Centre for Drugs and Drug Addition. EMCDDA Insights. Vol. 23. Luxembourg: Publications Office of the European Union; 2016. Hepatitis C among drug users in Europe: epidemiology, treatment and prevention.

Turner KM, et al. The impact of needle and syringe provision and opiate substitution therapy on the incidence of hepatitis C virus in injecting drug users: pooling of UK evidence. Addiction. 2011;106(11):1978–1988. PubMed

Van Den Berg C, et al. Full participation in harm reduction programmes is associated with decreased risk for human immunodeficiency virus and hepatitis C virus: evidence from the Amsterdam Cohort Studies among drug users. Addiction. 2007;102(9):1454–1462. PubMed PMC

Vickerman P, et al. Can needle and syringe programmes and opiate substitution therapy achieve substantial reductions in hepatitis C virus prevalence? Model projections for different epidemic settings. Addiction. 2012;107(11):1984–1995. PubMed

Martin NK, et al. Combination interventions to prevent HCV transmission among people who inject drugs: modeling the impact of antiviral treatment, needle and syringe programs, and opiate substitution therapy. Clin Infect Dis. 2013;57(Suppl 2):S39–S45. PubMed PMC

Martin NK, et al. Can antiviral therapy for hepatitis C reduce the prevalence of HCV among injecting drug user populations? A modeling analysis of its prevention utility. J Hepatol. 2011;54(6):1137–1144. PubMed

Martin NK, et al. HCV treatment for prevention among people who inject drugs: modeling treatment scale-up in the age of direct-acting antivirals. Hepatology. 2013;58(5):1598–1609. PubMed PMC

Wedemeyer H, et al. Strategies to manage hepatitis C virus (HCV) disease burden. J Viral Hepat. 2014;21(Suppl 1):60–89. PubMed

De Vos A, Kretzschmar M. Benefits of hepatitis C virus treatment: A balance of preventing onward transmission and re-infection. Mathematical biosciences. 2014;258:11–18. PubMed

de Vos AS, et al. Decline in incidence of HIV and hepatitis C virus infection among injecting drug users in Amsterdam; evidence for harm reduction? Addiction. 2013;108(6):1070–81. PubMed

Dore GJ, Feld JJ. Hepatitis C virus therapeutic development: in pursuit of “perfectovir”. Clinical Infectious Diseases. 2015;60(12):1829–1836. PubMed

Everson G, et al. Safety and efficacy of treatment with the interferon-free ribavirin-free combination of sofosbuvir+ GS-5816 for 12 weeks in treatment naive patients with genotype 1-6 HCV infection. 49th European Association for the Study of the Liver International Liver Congress (EASL 2014) 2014

Martin NK, et al. Hepatitis C virus treatment for prevention among people who inject drugs: Modeling treatment scale-up in the age of direct-acting antivirals. Hepatology. 2013;58(5):1598–609. PubMed PMC

European Association for the Study of the, L. EASL recommendations on treatment of hepatitis C 2014. J Hepatol. 2014;61(2):373–95. PubMed

European Association for the Study of the Liver. Electronic address, e.e.e. EASL Recommendations on Treatment of Hepatitis C 2015. J Hepatol. 2015;63(1):199–236. PubMed

Leidner AJ, et al. Cost-effectiveness of hepatitis C treatment for patients in early stages of liver disease. Hepatology. 2015;61(6):1860–9. PubMed PMC

Martin NK, et al. How should HCV treatment be prioritized in the direct-acting antiviral era? An economic evaluation including population prevention benefits. Journal of hepatology. 2016 PubMed PMC

Martin NK, et al. Combination Interventions to Prevent HCV Transmission Among People Who Inject Drugs: Modeling the Impact of Antiviral Treatment, Needle and Syringe Programs, and Opiate Substitution Therapy. Clinical Infectious Diseases. 2013;57:S39–S45. PubMed PMC

Vickerman P, et al. The more you look, the more you find: effects of hepatitis C virus testing interval on reinfection incidence and clearance and implications for future vaccine study design. The Journal of infectious diseases. 2012;205(9):1342–1350. PubMed PMC

Martin NK, et al. Can antiviral therapy for hepatitis C reduce the prevalence of HCV among injecting drug user populations? A modeling analysis of its prevention utility. J Hepatol. 2011;54(6):1137–44. PubMed

Martin NK, Vickerman P, Hickman M. Mathematical modelling of hepatitis C treatment for injecting drug users. J Theor Biol. 2011;274(1):58–66. PubMed

Zábranský T, Mravčík V, Chomynová P. Overal mortality of drug users in the Czech Republic. 1st. ResAd/EMCDDA; 2009.

Zabransky T, et al. Hepatitis C virus infection among injecting drug users in the Czech Republic–prevalence and associated factors. European addiction research. 2006;12(3):151–160. PubMed

ŠVŮGEROVÁ H. Spotřeba injekčního materiálu klienty pražských harm reduction služeb v závislosti na vzorcích užívání (Consumption of material for injection clients of Prague harm reduction services depending on use patterns) Mgr, Univerzita Karlova v Praze, 1 lékařská fakulta, obor adiktologie (MADI) 2015

Briggs A, Claxton K, Sculpher M. Decision Modelling for Health Economic Evaluation. In: Gray A, Briggs A, editors. Handbooks in Health Economic Evaluation Series. Oxford: Oxford University Press; 2006.

ECDC, editor. European Centre for Disease Prevention and Control. Hepatitis C surveillance in Europe - 2013. Stockholm: 2015.

Jones HE, et al. Recapture or precapture? Fallibility of standard capture-recapture methods in the presence of referrals between sources. American journal of epidemiology. 2014:kwu056. PubMed PMC

Palmateer NE, et al. Rapid decline in HCV incidence among people who inject drugs associated with national scale-up in coverage of a combination of harm reduction interventions. PLoS One. 2014;9(8):e104515. PubMed PMC

Martin NK, et al. Combination interventions to prevent HCV transmission among people who inject drugs: modeling the impact of antiviral treatment, needle and syringe programs, and opiate substitution therapy. Clin Infect Dis. 2013;57(Suppl 2):S39–45. PubMed PMC

Grebely J, et al. Efficacy and safety of ledipasvir/sofosbuvir with and without ribavirin in patients with chronic HCV genotype 1 infection receiving opioid substitution therapy: Analysis of Phase 3 ION trials. Clinical Infectious Diseases. 2016:ciw580. PubMed

Dore GJ, et al. Elbasvir–Grazoprevir to Treat Hepatitis C Virus Infection in Persons Receiving Opioid Agonist TherapyA Randomized TrialElbasvir–Grazoprevir in Persons With HCV Receiving OAT. Annals of internal medicine. 2016;165(9):625–634. PubMed

Sacks-Davis R, et al. Many hepatitis C reinfections that spontaneously clear may be undetected: Markov-chain Monte Carlo analysis of observational study data. Journal of The Royal Society Interface. 2015;12(104):20141197. PubMed PMC

Mehta SH, et al. Protection against persistence of hepatitis C. The Lancet. 2002;359(9316):1478–1483. PubMed

Grebely J, et al. Hepatitis C virus clearance, reinfection, and persistence, with insights from studies of injecting drug users: towards a vaccine. The Lancet Infectious Diseases. 2012;12(5):408–414. PubMed PMC

Micallef J, et al. High incidence of hepatitis C virus reinfection within a cohort of injecting drug users. Journal of viral hepatitis. 2007;14(6):413–418. PubMed

Aitken CK, et al. High incidence of hepatitis C virus reinfection in a cohort of injecting drug users. Hepatology. 2008;48(6):1746–1752. PubMed

Simmons B, et al. Risk of late relapse or reinfection with hepatitis C virus after achieving a sustained virological response: a systematic review and meta-analysis. Clinical Infectious Diseases. 2016:civ948. PubMed PMC

Alavi M, et al. Injecting risk behaviours following treatment for hepatitis C virus infection among people who inject drugs: The Australian Trial in Acute Hepatitis C. International Journal of Drug Policy. 2015;26(10):976–983. PubMed PMC

Duberg AS, et al. The future disease burden of hepatitis C virus infection in Sweden and the impact of different treatment strategies. Scandinavian Journal of Gastroenterology. 2015;50(2):233–244. PubMed

Razavi H, et al. The present and future disease burden of hepatitis C virus (HCV) infection with today’s treatment paradigm. J Viral Hepat. 2014;21(Suppl 1):34–59. PubMed

Harris R, et al. Increased uptake and new therapies are needed to avert rising hepatitis C-related end stage liver disease in England: modelling the predicted impact of treatment under different scenario. J Hepatol. 2014 doi: http://dx.doi.org/10.1016/j.jhep.2014.05.008. PubMed DOI

Mullhaupt B, et al. Modeling the Health and Economic Burden of Hepatitis C Virus in Switzerland. Plos One. 2015;10(6):13. PubMed PMC

Innes H, et al. Strategies for the treatment of Hepatitis C in an era of interferon-free therapies: what public health outcomes do we value most? Gut. 2015;64(11):1800–9. PubMed

Martin NK, et al. HCV treatment rates and sustained viral response among people who inject drugs in seven UK sites: real world results and modelling of treatment impact. J Viral Hepat. 2015;22(4):399. PubMed PMC

Mravčík V, et al. In: Výroční zpráva o stavu ve věcech drog v České republice v roce 2013 [Annual Report on Drug Situation 2013 – Czech Republic] MRAVČÍK V, editor. Praha: Úřad vlády České republiky; 2014.

D A, editor. Reitox National Focal Point. Report on the drug situation 2013 of the republic of Slovenia. 2013.

Razavi H, et al. The present and future disease burden of hepatitis C virus (HCV) infection with today’s treatment paradigm. Journal of viral hepatitis. 2014;21(s1):34–59. PubMed

van Santen DK, et al. Cost-Effectiveness of Hepatitis C Treatment for People Who Inject Drugs and the Impact of the Type of Epidemic; Extrapolating from Amsterdam, the Netherlands. PloS one. 2016;11(10):e0163488. PubMed PMC

Micallef JM, Kaldor JM, Dore GJ. Spontaneous viral clearance following acute hepatitis C infection: a systematic review of longitudinal studies. Journal of Viral Hepatitis. 2006;13(1):34–41. PubMed

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