Evidence map›Paper›PMID 29080808›Full record

ArticleJournal of hepatology2018

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

Hannah Fraser, Natasha K Martin, Henrikki Brummer-Korvenkontio, Patrizia Carrieri, Olav Dalgard, John Dillon, David Goldberg, Sharon Hutchinson, Marie Jauffret-Roustide, Martin Kåberg and 13 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 3 pooled it
11.1field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 3 syntheses or guidelines pooled it, 134 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 17 institutions in 12 countries.

Hannah FraserPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK. Electronic address: hannah.fraser@bristol.ac.uk.
Natasha K MartinDivision of Global Public Health, University of California, San Diego, San Diego, CA, USA; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Henrikki Brummer-KorvenkontioNational Institute for Health and Welfare, Helsinki, Finland.
Patrizia CarrieriAix Marseille Univ, INSERM, IRD, SESSTIM, Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, Marseille, France; ORS PACA, Observatoire Régional de la Santé Provence-Alpes-Côte d'Azur, Marseille, France.
Olav DalgardUniversity of Oslo, Oslo, Norway; Akershus University Hospital, Lørenskog, Norway.
John DillonUniversity of Dundee, Dundee, Scotland, UK.
David GoldbergHealth Protection Scotland, Glasgow, Scotland, UK.
Sharon HutchinsonGlasgow Caledonian University, Glasgow, Scotland, UK; Health Protection Scotland, Glasgow, Scotland, UK.
Marie Jauffret-RoustideFrench Institute for Public Health Surveillance, St. Maurice, France; CERMES3 (Inserm U988/UMR CNRS 8211/EHESS/Paris Descartes University), Paris, France.
Martin KåbergDepartment of Medicine, Huddinge, Division of Infectious Diseases, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Amy A MatserPublic Health Service of Amsterdam, Amsterdam, The Netherlands; University Medical Center Utrecht, Utrecht, The Netherlands.
Mojca MatičičUniversity of Ljubljana, Ljubljana, Slovenia; University Medical Centre Ljubljana, Ljubljana, Slovenia.
Havard MidgardUniversity of Oslo, Oslo, Norway.
Viktor MravcikNational Monitoring Centre for Drugs and Drug Addiction, Prague, Czech Republic; Charles University and General University Hospital in Prague, Prague, Czech Republic; National Institute of Mental Health, Klecany, Czech Republic.
Anne ØvrehusOdense University Hospital, Odense, Denmark.
Maria PrinsPublic Health Service of Amsterdam, Amsterdam, The Netherlands; Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
Jens ReimerHealthNorth, Bremen, Germany; University of Hamburg, Hamburg, Germany.
Geert RobaeysZiekenhuis Oost-Limburg, Genk, Belgium; Hasselt University, Diepenbeek, Belgium; University Hospital Leuven, Leuven, Belgium.
Bernd SchulteUniversity of Hamburg, Hamburg, Germany.
Daniela K van SantenPublic Health Service of Amsterdam, Amsterdam, The Netherlands.
Ruth ZimmermannRobert Koch Institute, Berlin, Germany.
Peter VickermanPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Matthew HickmanPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
University of Bristol · GBGGD Amsterdam · NLUniversität Hamburg · DEAkershus University Hospital · NOCharles University · CZÉcole des hautes études en sciences sociales · FRFinnish Institute for Health and Welfare · FIGlasgow Caledonian University · GBHasselt University · BEHealth Protection Scotland · GBInstitut de Recherche pour le Développement · FRKarolinska University Hospital · SEOdense University Hospital · DKRobert Koch Institute · DEUniversity of Dundee · GBUniversity of Ljubljana · SIUniversity of Oslo · NO

Funding

VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Maile Ann Young Karris · 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 RP-DG-0610-10055NIAID NIH HHS P30 AI036214NIDA NIH HHS R01 DA037773
6 · The paper itself

Abstract

BACKGROUND &

aimsPrevention 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.

methodsWe 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.

resultsAt 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%.

conclusionsThe 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).

Indexed as

Hepatitis C, ChronicSubstance Abuse, IntravenousAntiviral AgentsDisease Transmission, InfectiousEuropeHumansIncidenceModels, TheoreticalNeedle-Exchange ProgramsNeeds AssessmentOpiate Substitution TreatmentPrevalenceAntiviral AgentsDirect-acting antiviralsHepatitis COpioid substitution therapyPWID

Identifiers

PMID29080808
PMCPMC5841161
OpenAlexW2765561710

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.