Is increased hepatitis C virus case‐finding combined with current or 8‐week to 12‐week direct‐acting antiviral therapy cost‐effective in UK prisons? A prevention benefit analysis

Prisoners have a high prevalence of hepatitis C virus (HCV), but case‐finding may not have been cost‐effective because treatment often exceeded average prison stay combined with a lack of continuity of care. We assessed the cost‐effectiveness of increased HCV case‐finding and treatment in UK prisons using short‐course therapies. A dynamic HCV transmission model assesses the cost‐effectiveness of doubling HCV case‐finding (achieved through introducing opt‐out HCV testing in UK pilot prisons) and increasing treatment in UK prisons compared to status quo voluntary risk‐based testing (6% prison entrants/year), using currently recommended therapies (8‐24 weeks) or interferon (IFN)‐free direct‐acting antivirals (DAAs; 8‐12 weeks, 95% sustained virological response, £3300/week). Costs (British pounds, £) and health utilities (quality‐adjusted life years) were used to calculate mean incremental cost‐effectiveness ratios (ICERs). We assumed 56% referral and 2.5%/25% of referred people who inject drugs (PWID)/ex‐PWID treated within 2 months of diagnosis in prison. PWID and ex‐PWID or non‐PWID are in prison an average 4 and 8 months, respectively. Doubling prison testing rates with existing treatments produces a mean ICER of £19,850/quality‐adjusted life years gained compared to current testing/treatment and is 45% likely to be cost‐effective under a £20,000 willingness‐to‐pay threshold. Switching to 8‐week to 12‐week IFN‐free DAAs in prisons could increase cost‐effectiveness (ICER £15,090/quality‐adjusted life years gained). Excluding prevention benefit decreases cost‐effectiveness. If >10% referred PWID are treated in prison (2.5% base case), either treatment could be highly cost‐effective (ICER<£13,000). HCV case‐finding and IFN‐free DAAs could be highly cost‐effective if DAA cost is 10% lower or with 8 weeks' duration. Conclusions: Increased HCV testing in UK prisons (such as through opt‐out testing) is borderline cost‐effective compared to status quo voluntary risk‐based testing under a £20,000 willingness to pay with current treatments but likely to be cost‐effective if short‐course IFN‐free DAAs are used and could be highly cost‐effective if PWID treatment rates were increased. (Hepatology 2016;63:1796‐1808)

[1]  P. Thokala,et al.  Ledipasvir-Sofosbuvir for Treating Chronic Hepatitis C: A NICE Single Technology Appraisal—An Evidence Review Group Perspective , 2016, PharmacoEconomics.

[2]  J. Grefenstette,et al.  Prevention of Hepatitis C by Screening and Treatment in U.S. Prisons , 2016, Annals of Internal Medicine.

[3]  W. Irving,et al.  Clinical Care Pathways for Patients With Hepatitis C: Reducing Critical Barriers to Effective Treatment , 2016, Open forum infectious diseases.

[4]  M. Hellard,et al.  A longitudinal study of hepatitis C virus testing and infection status notification on behaviour change in people who inject drugs , 2015, Journal of Epidemiology & Community Health.

[5]  G. Dore,et al.  Hepatitis C virus therapeutic development: in pursuit of "perfectovir". , 2015, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[6]  C. Humphreys,et al.  An audit of hepatitis C service provision in a representative sample of prisons in England. , 2015, Journal of public health.

[7]  Karl Claxton,et al.  Methods for the estimation of the National Institute for Health and Care Excellence cost-effectiveness threshold. , 2015, Health technology assessment.

[8]  H. Dvory‐Sobol,et al.  Sofosbuvir with peginterferon-ribavirin for 12 weeks in previously treated patients with hepatitis C genotype 2 or 3 and cirrhosis , 2015, Hepatology.

[9]  Tara L. Kieffer,et al.  Successful treatment with telaprevir‐based regimens for chronic hepatitis C results in significant improvements to serum markers of liver fibrosis , 2015, Journal of viral hepatitis.

[10]  H. Innes,et al.  Strategies for the treatment of Hepatitis C in an era of interferon-free therapies: what public health outcomes do we value most? , 2014, Gut.

[11]  D. De Angelis,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 , 2014, Journal of viral hepatitis.

[12]  M. Hickman,et al.  A stepped wedge cluster randomized control trial of dried blood spot testing to improve the uptake of hepatitis C antibody testing within UK prisons , 2014, European journal of public health.

[13]  Robert Herring,et al.  Ledipasvir and sofosbuvir for 8 or 12 weeks for chronic HCV without cirrhosis. , 2014, The New England journal of medicine.

[14]  Stefan Zeuzem,et al.  Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection. , 2014, The New England journal of medicine.

[15]  M. Abrahamowicz,et al.  Sustained drug use changes after hepatitis C screening and counseling among recently infected persons who inject drugs: a longitudinal study. , 2014, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[16]  Jon Sussex,et al.  Critique of CHE Research Paper 81: Methods for the Estimation of the NICE Cost Effectiveness Threshold , 2013 .

[17]  Christine Katlama,et al.  Slow regression of liver fibrosis presumed by repeated biomarkers after virological cure in patients with chronic hepatitis C. , 2013, Journal of hepatology.

[18]  J. Rich,et al.  Incidence and prevalence of hepatitis C in prisons and other closed settings: Results of a systematic review and meta‐analysis , 2013, Hepatology.

[19]  P. Vickerman,et al.  Cost-effectiveness of HCV case-finding for people who inject drugs via dried blood spot testing in specialist addiction services and prisons , 2013, BMJ Open.

[20]  Bryce D. Smith,et al.  Eradication of Hepatitis C Virus Infection and the Development of Hepatocellular Carcinoma , 2013, Annals of Internal Medicine.

[21]  S. Hutchinson,et al.  Decrease in health-related quality of life associated with awareness of hepatitis C virus infection among people who inject drugs in Scotland. , 2013, Journal of hepatology.

[22]  M. Manns,et al.  Association between sustained virological response and all-cause mortality among patients with chronic hepatitis C and advanced hepatic fibrosis. , 2012, JAMA.

[23]  Ross J. Harris,et al.  Hepatitis C prevalence in England remains low and varies by ethnicity: an updated evidence synthesis. , 2012, European journal of public health.

[24]  P. Vickerman,et al.  Cost‐effectiveness of hepatitis C virus antiviral treatment for injection drug user populations , 2012, Hepatology.

[25]  P. Vickerman,et al.  P53 The cost-effectiveness of HCV antiviral treatment for injecting drug user populations , 2011, Gut.

[26]  J. Shepherd,et al.  Peginterferon alfa and ribavirin for chronic hepatitis C in patients eligible for shortened treatment, re-treatment or in HCV/HIV co-infection: a systematic review and economic evaluation. , 2011, Health technology assessment.

[27]  P. Marcellin,et al.  Efficacy and safety of peginterferon alfa‐2a (40KD) plus ribavirin in hepatitis C patients with advanced fibrosis and cirrhosis , 2010, Hepatology.

[28]  D. De Angelis,et al.  An evidence synthesis approach to estimating Hepatitis C Prevalence in England and Wales , 2009, Statistical methods in medical research.

[29]  W. Edmunds,et al.  The cost‐effectiveness of screening and treatment for hepatitis C in prisons in England and Wales: a cost‐utility analysis , 2008, Journal of viral hepatitis.

[30]  G. Dore,et al.  Estimation of stage‐specific fibrosis progression rates in chronic hepatitis C virus infection: A meta‐analysis and meta‐regression , 2008, Hepatology.

[31]  B. Bacon,et al.  Peginterferon alfa-2a and ribavirin for 16 or 24 weeks in HCV genotype 2 or 3. , 2007, The New England journal of medicine.

[32]  N. Waugh,et al.  Interferon alfa (pegylated and non-pegylated) and ribavirin for the treatment of mild chronic hepatitis C : a systematic review and economic evaluation , 2007 .

[33]  U Siebert,et al.  The cost-effectiveness of testing for hepatitis C in former injecting drug users. , 2006, Health technology assessment.

[34]  Jennifer A. Roberts,et al.  Health benefits of antiviral therapy for mild chronic hepatitis C: randomised controlled trial and economic evaluation. , 2006, Health technology assessment.

[35]  J. Hippisley-Cox,et al.  Clinical pathways for patients with newly diagnosed hepatitis C – What actually happens , 2006, Journal of viral hepatitis.

[36]  J. Kaldor,et al.  Spontaneous viral clearance following acute hepatitis C infection: a systematic review of longitudinal studies , 2006, Journal of viral hepatitis.

[37]  N. Waugh,et al.  Pegylated interferon alpha-2a and -2b in combination with ribavirin in the treatment of chronic hepatitis C: a systematic review and economic evaluation. , 2004, Health technology assessment.

[38]  P. Royle,et al.  Screening for Hepatitis C in injecting drug users: a cost utility analysis. , 2004, Journal of public health.

[39]  Paul Kind,et al.  UK population norms for EQ-5D , 1999 .

[40]  W. Alexander,et al.  European Association for the Study of the Liver , 1968 .

[41]  M. Hellard,et al.  Does informing people who inject drugs of their hepatitis C status influence their injecting behaviour? Analysis of the Networks II study. , 2014, The International journal on drug policy.

[42]  D. Luo,et al.  A randomized controlled clinical study of lower-dose peginterferon alfa-2b in combination with ribavirin in the treatment of chronic hepatitis C , 2006 .