Prison-based interventions are key to achieving HCV elimination among people who inject drugs in New South Wales, Australia: A modelling study.


Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
03 2023
Historique:
revised: 07 09 2022
received: 20 06 2022
accepted: 25 10 2022
pubmed: 29 10 2022
medline: 25 2 2023
entrez: 28 10 2022
Statut: ppublish

Résumé

People who inject drugs (PWID) experience high incarceration rates which are associated with increased hepatitis C virus (HCV) transmission risk. We assess the importance of prison-based interventions for achieving HCV elimination among PWID in New South Wales (NSW), Australia. A model of incarceration and HCV transmission among PWID was calibrated in a Bayesian framework to epidemiological and incarceration data from NSW, incorporating elevated HCV acquisition risk among recently released PWID. We projected the contribution of differences in transmission risk during/following incarceration to HCV transmission over 2020-2029. We estimated the past and potential future impact of prison-based opioid agonist therapy (OAT; ~33% coverage) and HCV treatment (1500 treatments in 2019 with 32.9%-83.3% among PWID) on HCV transmission. We estimated the time until HCV incidence reduces by 80% (WHO elimination target) compared to 2016 levels with or without prison-based interventions. Over 2020-2029, incarceration will contribute 23.0% (17.9-30.5) of new HCV infections. If prison-based interventions had not been implemented since 2010, HCV incidence in 2020 would have been 29.7% (95% credibility interval: 22.4-36.1) higher. If current prison and community HCV treatment rates continue, there is an 98.8% probability that elimination targets will be achieved by 2030, with this decreasing to 10.1% without current prison-based interventions. Existing prison-based interventions in NSW are critical components of strategies to reduce HCV incidence among PWID. Prison-based interventions are likely to be pivotal for achieving HCV elimination targets among PWID by 2030.

Sections du résumé

BACKGROUND & AIMS
People who inject drugs (PWID) experience high incarceration rates which are associated with increased hepatitis C virus (HCV) transmission risk. We assess the importance of prison-based interventions for achieving HCV elimination among PWID in New South Wales (NSW), Australia.
METHODS
A model of incarceration and HCV transmission among PWID was calibrated in a Bayesian framework to epidemiological and incarceration data from NSW, incorporating elevated HCV acquisition risk among recently released PWID. We projected the contribution of differences in transmission risk during/following incarceration to HCV transmission over 2020-2029. We estimated the past and potential future impact of prison-based opioid agonist therapy (OAT; ~33% coverage) and HCV treatment (1500 treatments in 2019 with 32.9%-83.3% among PWID) on HCV transmission. We estimated the time until HCV incidence reduces by 80% (WHO elimination target) compared to 2016 levels with or without prison-based interventions.
RESULTS
Over 2020-2029, incarceration will contribute 23.0% (17.9-30.5) of new HCV infections. If prison-based interventions had not been implemented since 2010, HCV incidence in 2020 would have been 29.7% (95% credibility interval: 22.4-36.1) higher. If current prison and community HCV treatment rates continue, there is an 98.8% probability that elimination targets will be achieved by 2030, with this decreasing to 10.1% without current prison-based interventions.
CONCLUSIONS
Existing prison-based interventions in NSW are critical components of strategies to reduce HCV incidence among PWID. Prison-based interventions are likely to be pivotal for achieving HCV elimination targets among PWID by 2030.

Identifiants

pubmed: 36305315
doi: 10.1111/liv.15469
pmc: PMC10308445
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

569-579

Subventions

Organisme : Medical Research Council
ID : MR/N00616X/1
Pays : United Kingdom

Informations de copyright

© 2022 The Authors. Liver International published by John Wiley & Sons Ltd.

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Auteurs

Jack Stone (J)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.

Aaron G Lim (AG)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.

Gregory J Dore (GJ)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Annick Borquez (A)

Division of Infectious Diseases and Global Public Health, University of California, San Diego, California, USA.

Louise Geddes (L)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Richard Gray (R)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Jason Grebely (J)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Bezhad Hajarizadeh (B)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Jenny Iversen (J)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Lisa Maher (L)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Heather Valerio (H)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Natasha K Martin (NK)

Division of Infectious Diseases and Global Public Health, University of California, San Diego, California, USA.

Matthew Hickman (M)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
NIHR Health Protection Research Unit in Behavioural Science and Evaluation at University of Bristol, Bristol, UK.

Andrew R Lloyd (AR)

The Kirby Institute, UNSW Sydney, New South Wales, Sydney, Australia.

Peter Vickerman (P)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
NIHR Health Protection Research Unit in Behavioural Science and Evaluation at University of Bristol, Bristol, UK.

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