HIPPOCRATES

Direct-acting antiviral agents Hepatitis C infection Micro-elimination Prison setting Treatment

Journal

World journal of hepatology
ISSN: 1948-5182
Titre abrégé: World J Hepatol
Pays: United States
ID NLM: 101532469

Informations de publication

Date de publication:
27 Dec 2020
Historique:
received: 25 05 2020
revised: 13 08 2020
accepted: 04 11 2020
entrez: 14 1 2021
pubmed: 15 1 2021
medline: 15 1 2021
Statut: ppublish

Résumé

In the last few years we have witnessed a revolution in the treatment of hepatitis C virus (HCV) infection. With the introduction of direct-acting antiviral agents (DAAs), sustained virological response (SVR) is achieved in more than 95% of the patients. The focus is now being turned to the global targets set by the World Health Organization, with the aim of achieving HCV elimination by 2030. Prison inmates constitute one of the high-risk groups, and receive treatment less frequently due to several barriers in access to health care. To describe the management and follow-up of a cohort of HCV monoinfected patients treated with DAA in the prison setting, where tertial referral liver center specialists locally provide, on-site assessment and treatment for the prisoners. A prospective observational study was conducted from April 2017 to March 2020, which included all HCV monoinfected prison inmates in the largest Northern Portugal prison. Demographic, clinical, and laboratory data, as well as transient elastography measurements, were collected onsite by the medical team and prospectively recorded. Patients were treated with DAA according to international guidelines. The primary endpoint was SVR at post-treatment week 12. There were 98 monoinfected HCV male inmates (mean age, 42.7 ± 8.6 years) included in the analysis. Injecting drugs or tattooing were reported in 74.5%, with 38.8% of the latter being done in prison. Alcohol consumption of more than 30 g/d was referred in 69.4%. The most prevalent genotype was 1a (54.1%), followed by 3 (27.6%), 4 (9.2%) and 1b (6.1%). Pretreatment fibrosis degree was mild-to-moderate (F0-F2) in 77.6% and severe in 22.4% (F3-F4). Treatment regimens chosen were: 45.9% elbasvir/grazoprevir, 29.6% sofosbuvir/velpatasvir, and 12.2% sofosbuvir/ledispavir and glecaprevir/pibrentasvir. No major adverse events were observed. SVR at post-treatment week 12 was 99%. In a population considered to be both hard-to-access and a cornerstone for HCV elimination, the onsite evaluation and treatment of HCV-infected prisoners, achieved an exceptional highly effective success rate. This type of collaborative program should be considered to be expanded, to support hepatitis C elimination efforts.

Sections du résumé

BACKGROUND BACKGROUND
In the last few years we have witnessed a revolution in the treatment of hepatitis C virus (HCV) infection. With the introduction of direct-acting antiviral agents (DAAs), sustained virological response (SVR) is achieved in more than 95% of the patients. The focus is now being turned to the global targets set by the World Health Organization, with the aim of achieving HCV elimination by 2030. Prison inmates constitute one of the high-risk groups, and receive treatment less frequently due to several barriers in access to health care.
AIM OBJECTIVE
To describe the management and follow-up of a cohort of HCV monoinfected patients treated with DAA in the prison setting, where tertial referral liver center specialists locally provide, on-site assessment and treatment for the prisoners.
METHODS METHODS
A prospective observational study was conducted from April 2017 to March 2020, which included all HCV monoinfected prison inmates in the largest Northern Portugal prison. Demographic, clinical, and laboratory data, as well as transient elastography measurements, were collected onsite by the medical team and prospectively recorded. Patients were treated with DAA according to international guidelines. The primary endpoint was SVR at post-treatment week 12.
RESULTS RESULTS
There were 98 monoinfected HCV male inmates (mean age, 42.7 ± 8.6 years) included in the analysis. Injecting drugs or tattooing were reported in 74.5%, with 38.8% of the latter being done in prison. Alcohol consumption of more than 30 g/d was referred in 69.4%. The most prevalent genotype was 1a (54.1%), followed by 3 (27.6%), 4 (9.2%) and 1b (6.1%). Pretreatment fibrosis degree was mild-to-moderate (F0-F2) in 77.6% and severe in 22.4% (F3-F4). Treatment regimens chosen were: 45.9% elbasvir/grazoprevir, 29.6% sofosbuvir/velpatasvir, and 12.2% sofosbuvir/ledispavir and glecaprevir/pibrentasvir. No major adverse events were observed. SVR at post-treatment week 12 was 99%.
CONCLUSION CONCLUSIONS
In a population considered to be both hard-to-access and a cornerstone for HCV elimination, the onsite evaluation and treatment of HCV-infected prisoners, achieved an exceptional highly effective success rate. This type of collaborative program should be considered to be expanded, to support hepatitis C elimination efforts.

Identifiants

pubmed: 33442457
doi: 10.4254/wjh.v12.i12.1314
pmc: PMC7772731
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1314-1325

Informations de copyright

©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: The authors declare no conflict of interest.

Références

J Hepatol. 2018 Aug;69(2):461-511
pubmed: 29650333
J Hepatol. 2018 Aug;69(2):406-460
pubmed: 29653741
Hepatology. 1996 Aug;24(2):289-93
pubmed: 8690394
Int J Drug Policy. 2020 Apr 8;:102738
pubmed: 32278651
Infection. 2017 Apr;45(2):131-138
pubmed: 28025726
J Viral Hepat. 2018 Sep;25(9):1066-1077
pubmed: 29624813
Ann Intern Med. 2014 Mar 4;160(5):293-300
pubmed: 24737271
J Viral Hepat. 2018 Nov;25(11):1260-1269
pubmed: 29851232
BMC Public Health. 2019 May 10;19(Suppl 3):466
pubmed: 32326938
Clin Infect Dis. 2018 Jul 18;67(3):460-463
pubmed: 29538639
Ann Epidemiol. 2018 Apr;28(4):231-235
pubmed: 29576049
Harm Reduct J. 2018 May 9;15(1):24
pubmed: 29739400
CMAJ Open. 2019 Dec 3;7(4):E674-E679
pubmed: 31796509
Hepatology. 2013 Mar;57(3):944-52
pubmed: 23111904
Harm Reduct J. 2018 May 11;15(1):25
pubmed: 29751763
J Viral Hepat. 2020 Oct;27(10):987-995
pubmed: 32449969
Public Health Rep. 2017 Jan/Feb;132(1):41-47
pubmed: 28005477
Lancet Gastroenterol Hepatol. 2017 May;2(5):325-336
pubmed: 28397696
Dig Liver Dis. 2020 May;52(5):541-546
pubmed: 32234417
Hepatology. 2013 Apr;57(4):1333-42
pubmed: 23172780

Auteurs

Rui Gaspar (R)

Department of Gastroenterology, Centro Hospitalar de São João, Porto 4200, Portugal. ruilopesgaspar@gmail.com.

Rodrigo Liberal (R)

Department of Gastroenterology and Hepatology, Centro Hospitalar de São João, Porto 4200, Portugal.

Jorge Tavares (J)

Estabelecimento Prisional do Porto, Porto 4200, Portugal.

Rui Morgado (R)

Estabelecimento Prisional do Porto, Porto 4200, Portugal.

Guilherme Macedo (G)

Department of Gastroenterology, Centro Hospitalar de São João, Porto 4200, Portugal.

Classifications MeSH