Evidence map›Paper›PMID 26864802›Full record

ArticleHepatology (Baltimore, Md.)2016

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.

Natasha K Martin, Peter Vickerman, Iain F Brew, Joan Williamson, Alec Miners, William L Irving, Sushma Saksena, Sharon J Hutchinson, Sema Mandal, Eamonn O'Moore and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 pooled it
7.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 3 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Is the universal population Hepatitis C virus screening a cost-effective strategy? A systematic review of the economic evidence.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2020
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  9. Modeling the Health Economic Burden of Hepatitis C Virus Infection in Turkey: Cost-Effectiveness of Targeted Screening.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 2 countries.

Natasha K MartinDivision of Global Public Health, University of California San Diego, San Diego, CA.
Peter VickermanSchool of Social and Community Medicine, University of Bristol, Bristol, UK.
Iain F BrewLeeds Community Healthcare NHS Trust, Leeds, UK.
Joan WilliamsonLeeds Community Healthcare NHS Trust, Leeds, UK.
Alec MinersLondon School of Hygiene and Tropical Medicine, London, UK.
William L IrvingUniversity of Nottingham, Nottingham, UK.
Sushma SaksenaCounty Durham and Darlington NHS Trust, Darlington, UK.
Sharon J HutchinsonGlasgow Caledonian University, Glasgow, UK.
Sema MandalPublic Health England, London, UK.
Eamonn O'MoorePublic Health England, London, UK.
Matthew HickmanSchool of Social and Community Medicine, University of Bristol, Bristol, UK.
University of Bristol · GBLeeds Community Healthcare NHS Trust · GBPublic Health England · GBCounty Durham and Darlington NHS Foundation Trust · GBGlasgow Caledonian University · GBLondon School of Hygiene & Tropical Medicine · GBUniversity of Nottingham · GB

Funding

VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUSAN JANET LITTLE · 1994 to 2026
$78.4M
Modeling Structural HIV Determinants in Substance Users and related populationsR01DA037773 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MARTIN, NATASHA, STRATHDEE, STEFFANIE A. · 2015 to 2017
$1.4M
Department of Health PDF-2011-04-049Department of Health RP-DG-0610-10055Medical Research Council G0701627Medical Research Council MR/K023233/1Medical Research Council MR/N005953/1NIAID NIH HHS P30 AI036214NIDA NIH HHS R01 DA037773
6 · The paper itself

Abstract

unlabelledPrisoners 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.

conclusionsIncreased 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).

Indexed as

Models, TheoreticalPrisonersAdolescentAdultAgedAntiviral AgentsCost-Benefit AnalysisHepatitis CHumansMass ScreeningMiddle AgedSustained Virologic ResponseUnited KingdomYoung AdultAntiviral Agents

Identifiers

PMID26864802
PMCPMC4920048
OpenAlexW2395160937

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.