Evidence map›Paper›PMID 31530275›Full record

ArticleBMC medicine2019

The case for a universal hepatitis C vaccine to achieve hepatitis C elimination.

Nick Scott, David P Wilson, Alexander J Thompson, Eleanor Barnes, Manal El-Sayed, Adele Schwartz Benzaken, Heidi E Drummer, Margaret E Hellard

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  7. [Development approaches for vaccines against hepatitis C virus infections].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 8 institutions in 4 countries.

Nick ScottDisease Elimination Program, Burnet Institute, Melbourne, Australia. nick.scott@burnet.edu.au.
David P WilsonDisease Elimination Program, Burnet Institute, Melbourne, Australia.
Alexander J ThompsonDepartment of Medicine, The University of Melbourne, Parkville, Australia.
Eleanor BarnesNuffield Department of Medicine, University of Oxford, Oxford, UK.
Manal El-SayedDepartment of Paediatrics, Ain Shams University, Cairo, Egypt.
Adele Schwartz BenzakenGlobal Medical Director for Aids Health Care Foundation, Brasília, DF, Brazil.
Heidi E DrummerDisease Elimination Program, Burnet Institute, Melbourne, Australia.
Margaret E HellardDisease Elimination Program, Burnet Institute, Melbourne, Australia.
Ain Shams University · EGBurnet Institute · AUHealth Care Foundation · CAMonash University · AUOxford BioMedica (United Kingdom) · GBPeter Doherty Institute · AUSt Vincent's Hospital · AUThe Alfred Hospital · AU

Funding

Medical Research Council MR/K010239/1
6 · The paper itself

Abstract

backgroundThe introduction of highly effective direct-acting antiviral (DAA) therapy for hepatitis C has led to calls to eliminate it as a public health threat through treatment-as-prevention. Recent studies suggest it is possible to develop a vaccine to prevent hepatitis C. Using a mathematical model, we examined the potential impact of a hepatitis C vaccine on the feasibility and cost of achieving the global WHO elimination target of an 80% reduction in incidence by 2030 in the era of DAA treatment.

methodsThe model was calibrated to 167 countries and included two population groups (people who inject drugs (PWID) and the general community), features of the care cascade, and the coverage of health systems to deliver services. Projections were made for 2018-2030.

resultsThe optimal incidence reduction strategy was to implement test and treat programmes among PWID, and in settings with high levels of community transmission undertake screening and treatment of the general population. With a vaccine available, the optimal strategy was to include vaccination within test and treat programmes, in addition to vaccinating adolescents in settings with high levels of community transmission. Of the 167 countries modelled, between 0 and 48 could achieve an 80% reduction in incidence without a vaccine. This increased to 15-113 countries if a 75% efficacious vaccine with a 10-year duration of protection were available. If a vaccination course cost US$200, vaccine use reduced the cost of elimination for 66 countries (40%) by an aggregate of US$7.4 (US$6.6-8.2) billion. For a US$50 per course vaccine, this increased to a US$9.8 (US$8.7-10.8) billion cost reduction across 78 countries (47%).

conclusionsThese findings strongly support the case for hepatitis C vaccine development as an urgent public health need, to ensure hepatitis C elimination is achievable and at substantially reduced costs for a majority of countries.

Indexed as

Disease EradicationModels, TheoreticalVaccinationAntiviral AgentsHepacivirusHepatitis CHepatitis C, ChronicHumansIncidencePublic HealthSubstance Abuse, IntravenousUniversal Health CareVaccination CoverageViral Hepatitis VaccinesAntiviral AgentsViral Hepatitis VaccinesEliminationHepatitis CMathematical modelVaccine

Identifiers

PMID31530275
PMCPMC6749704
OpenAlexW2974887310

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.