Evidence map›Paper›PMID 37936544›Full record

ArticleJournal of viral hepatitis2024

Incidence of hepatitis C virus infection in the prison setting: The SToP-C study.

Behzad Hajarizadeh, Joanne M Carson, Marianne Byrne, Jason Grebely, Evan Cunningham, Janaki Amin, Peter Vickerman, Natasha K Martin, Carla Treloar, Marianne Martinello and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of viral hepatitis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

13 authors at 5 institutions in 4 countries.

Behzad HajarizadehThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0003-2212-2028
Joanne M CarsonThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0001-8043-0200
Marianne ByrneThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.
Jason GrebelyThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0002-1833-2017
Evan CunninghamThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0002-8048-3473
Janaki AminFaculty of Medicine and Health Sciences, Macquarie University, Sydney, New South Wales, Australia.ORCID 0000-0003-2161-9366
Peter VickermanPopulation Health Sciences, University of Bristol, Bristol, UK.ORCID 0000-0002-8291-5890
Natasha K MartinDivision of Infectious Diseases & Global Public Health, University of California San Diego, San Diego, California, USA.ORCID 0000-0001-8344-1810
Carla TreloarCentre for Social Research in Health, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0002-8230-0386
Marianne MartinelloThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0001-9444-0186
Andrew R LloydThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0001-6277-8887
Gregory J DoreThe Kirby Institute, University of New Soth Wales (UNSW), Sydney, New South Wales, Australia.ORCID 0000-0002-4741-2622
SToP-C study group
UNSW Sydney · AUKnowledge Centre for Agriculture · DKMacquarie University · AUUniversity of Bristol · GBUniversity of California System · US

Funding

Gilead SciencesNational Health and Medical Research Council
6 · The paper itself

Abstract

People in prison are at high risk of HCV given high injecting drug use prevalence. This study evaluated HCV incidence and associated injecting drug use characteristics in prison. The SToP-C study enrolled people incarcerated in four Australian prisons. Participants were tested for HCV at enrolment and then every 3-6 months (October-2014 to November-2019). Participants eligible for this analysis included those at-risk of HCV primary infection (anti-HCV negative) or re-infection (anti-HCV positive, HCV RNA negative) with follow-up assessment. A total of 1643 eligible participants were included in analyses (82% male; median age 33 years; 30% injected drugs in prison; 1818 person-years of follow-up). Overall HCV incidence was 6.11/100 person-years (95%CI: 5.07-7.35), with higher rate of re-infection (9.34/100 person-years; 95%CI: 7.15-12.19) than primary infection (4.60/100 person-years; 95%CI: 3.56-5.96). In total population (n = 1643), HCV risk was significantly higher among participants injecting drugs in prison [vs. no injecting; adjusted hazard ratio (aHR): 10.55, 95%CI: 5.88-18.92), and those who were released and re-incarcerated during follow-up (vs. remained incarcerated; aHR: 1.60, 95%CI: 1.03-2.49). Among participants who injected recently (during past month, n = 321), HCV risk was reduced among those receiving high-dosage opioid agonist therapy (OAT), i.e. methadone ≥60 mg/day or buprenorphine ≥16 mg/day, (vs. no OAT, aHR: 0.11, 95%CI: 0.02-0.80) and increased among those sharing needles/syringes without consistent use of disinfectant to clean injecting equipment (vs. no sharing, HR: 4.60, 95%CI: 1.35-15.66). This study demonstrated high HCV transmission risk in prison, particularly among people injecting drugs. High-dosage OAT was protective, but improved OAT coverage and needle/syringe programmes to reduce sharing injecting equipment are required.

Indexed as

Hepatitis CSubstance Abuse, IntravenousAdultAustraliaFemaleHepacivirusHumansIncidenceMalePrisonsReinfectioncohort studycorrectional facilitiesHCVintravenous substance abuseopiate substitution treatment

Identifiers

PMID37936544
PMCPMC10952254
OpenAlexW4388496988

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.