Outcomes of treatment for hepatitis C in prisoners using a nurse-led, statewide model of care.


Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
05 2019
Historique:
received: 22 07 2018
revised: 26 11 2018
accepted: 07 01 2019
pubmed: 18 1 2019
medline: 25 11 2020
entrez: 18 1 2019
Statut: ppublish

Résumé

Treatment programs for people who inject drugs (PWID), including prisoners, are important for achieving hepatitis C elimination targets. There are multiple barriers to treatment of hepatitis C in prisons, including access to specialist physicians, testing and antiviral therapy, short prison sentences, and frequent inter-prison transfer. We aimed to assess the effectiveness of a nurse-led model of care for the treatment of prisoners with hepatitis C. A statewide program for assessment and management of hepatitis C was developed in Victoria, Australia to improve access to care for prisoners. This nurse-led model of care is supported by telemedicine to provide decentralized care within all prisons in the state. We prospectively evaluated the feasibility and efficacy of this nurse-led model of care for hepatitis C within the 14 adult prisons over a 13-month period. The primary endpoint was sustained virological response at post-treatment week 12 (SVR12) using per protocol analysis. There were 416 prisoners included in the analysis. The median age was 41 years, 90% were male, 50% had genotype 3 and 44% genotype 1 hepatitis C and 21% had cirrhosis. Injecting drug use was reported by 68% in the month prior to prison entry, 54% were receiving opioid substitution therapy, and 86% reported never previously engaging with specialist HCV care. Treatment duration was 8 weeks in 24%, 12 weeks in 59%, and 24 weeks in 17% of treatment courses. The SVR12 rate was 96% (301/313) per protocol. Inter-prison transfer occurred during 26% of treatment courses but was not associated with lower SVR12 rates. No treatment-related serious adverse events occurred. Hepatitis C treatment using a decentralized, nurse-led model of care is highly effective and can reach large numbers of prisoners. Large scale prison treatment programs should be considered to support hepatitis C elimination efforts. There is a high burden of hepatitis C infection among prisoners worldwide. Prisoners who continue to inject drugs are also at risk of developing new infections. For this reason, the prison setting provides an opportunity to treat those people at greatest risk of infection and to stop transmission to others. We developed a new method of providing hepatitis C treatment to prisoners, in which nurses rather than doctors assessed prisoners locally at each prison site. Treatment was safe and most prisoners were cured. Such programs will contribute greatly to achieving the World Health Organization's hepatitis C elimination goals.

Sections du résumé

BACKGROUND & AIMS
Treatment programs for people who inject drugs (PWID), including prisoners, are important for achieving hepatitis C elimination targets. There are multiple barriers to treatment of hepatitis C in prisons, including access to specialist physicians, testing and antiviral therapy, short prison sentences, and frequent inter-prison transfer. We aimed to assess the effectiveness of a nurse-led model of care for the treatment of prisoners with hepatitis C.
METHODS
A statewide program for assessment and management of hepatitis C was developed in Victoria, Australia to improve access to care for prisoners. This nurse-led model of care is supported by telemedicine to provide decentralized care within all prisons in the state. We prospectively evaluated the feasibility and efficacy of this nurse-led model of care for hepatitis C within the 14 adult prisons over a 13-month period. The primary endpoint was sustained virological response at post-treatment week 12 (SVR12) using per protocol analysis.
RESULTS
There were 416 prisoners included in the analysis. The median age was 41 years, 90% were male, 50% had genotype 3 and 44% genotype 1 hepatitis C and 21% had cirrhosis. Injecting drug use was reported by 68% in the month prior to prison entry, 54% were receiving opioid substitution therapy, and 86% reported never previously engaging with specialist HCV care. Treatment duration was 8 weeks in 24%, 12 weeks in 59%, and 24 weeks in 17% of treatment courses. The SVR12 rate was 96% (301/313) per protocol. Inter-prison transfer occurred during 26% of treatment courses but was not associated with lower SVR12 rates. No treatment-related serious adverse events occurred.
CONCLUSION
Hepatitis C treatment using a decentralized, nurse-led model of care is highly effective and can reach large numbers of prisoners. Large scale prison treatment programs should be considered to support hepatitis C elimination efforts.
LAY SUMMARY
There is a high burden of hepatitis C infection among prisoners worldwide. Prisoners who continue to inject drugs are also at risk of developing new infections. For this reason, the prison setting provides an opportunity to treat those people at greatest risk of infection and to stop transmission to others. We developed a new method of providing hepatitis C treatment to prisoners, in which nurses rather than doctors assessed prisoners locally at each prison site. Treatment was safe and most prisoners were cured. Such programs will contribute greatly to achieving the World Health Organization's hepatitis C elimination goals.

Identifiants

pubmed: 30654067
pii: S0168-8278(19)30024-8
doi: 10.1016/j.jhep.2019.01.012
pii:
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

839-846

Informations de copyright

Crown Copyright © 2019. Published by Elsevier B.V. All rights reserved.

Auteurs

Timothy Papaluca (T)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia.

Lucy McDonald (L)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia.

Anne Craigie (A)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia.

Annabelle Gibson (A)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia.

Paul Desmond (P)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia.

Darren Wong (D)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia.

Rebecca Winter (R)

Burnet Institute, Melbourne, Australia.

Nick Scott (N)

Burnet Institute, Melbourne, Australia; Department of Epidemiology and Preventative Medicine, Monash University, Australia.

Jessica Howell (J)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia; Burnet Institute, Melbourne, Australia.

Joseph Doyle (J)

Burnet Institute, Melbourne, Australia; Department of Infectious Diseases, The Alfred and Monash University, Melbourne Australia.

Alisa Pedrana (A)

Burnet Institute, Melbourne, Australia.

Andrew Lloyd (A)

Kirby Institute, University of New South Wales, Australia.

Mark Stoove (M)

Burnet Institute, Melbourne, Australia; Department of Epidemiology and Preventative Medicine, Monash University, Australia.

Margaret Hellard (M)

Burnet Institute, Melbourne, Australia; Department of Epidemiology and Preventative Medicine, Monash University, Australia.

David Iser (D)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia; Department of Infectious Diseases, The Alfred and Monash University, Melbourne Australia.

Alexander Thompson (A)

Department of Gastroenterology, St Vincent's Hospital and the University of Melbourne, Australia. Electronic address: alexander.THOMPSON@svha.org.au.

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Classifications MeSH