Observational Study
Copyright ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Hepatol. Dec 27, 2020; 12(12): 1314-1325
Published online Dec 27, 2020. doi: 10.4254/wjh.v12.i12.1314
HIPPOCRATES® project: A proof of concept of a collaborative program for hepatitis C virus micro-elimination in a prison setting
Rui Gaspar, Rodrigo Liberal, Jorge Tavares, Rui Morgado, Guilherme Macedo
Rui Gaspar, Guilherme Macedo, Department of Gastroenterology, Centro Hospitalar de São João, Porto 4200, Portugal
Rodrigo Liberal, Department of Gastroenterology and Hepatology, Centro Hospitalar de São João, Porto 4200, Portugal
Jorge Tavares, Rui Morgado, Estabelecimento Prisional do Porto, Porto 4200, Portugal
Author contributions: Gaspar R and Liberal R were responsible for the study design, acquisition and interpretation of data, drafting the manuscript, and statistical analysis; Tavares J and Morgado M were responsible for the study design; Macedo G was responsible for creating the project, study design, acquisition and interpretation of data and critical revision of the manuscript for important intellectual content.
Institutional review board statement: All procedures performed were in accordance and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards and ethical approval was obtained from Centro Hospitalar São João.
Informed consent statement: Informed consent was obtained from all individual participants included in the study.
Conflict-of-interest statement: The authors declare no conflict of interest.
Data sharing statement: No additional data are available.
STROBE statement: The authors have read the STROBE Statement—checklist of items, and the manuscript was prepared and revised according to the STROBE Statement—checklist of items.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Rui Gaspar, MD, Doctor, Department of Gastroenterology, Centro Hospitalar de São João, Porto 4200, Portugal. ruilopesgaspar@gmail.com
Received: May 25, 2020
Peer-review started: May 25, 2020
First decision: June 4, 2020
Revised: August 13, 2020
Accepted: November 4, 2020
Article in press: November 4, 2020
Published online: December 27, 2020
Abstract
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

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

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

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

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.

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

Core Tip: Hepatitis C is a curable infectious disease with high cure rates reaching almost 100% with the use of direct-acting antiviral agents. The World Health Organization defined the aim of achieving hepatitis C virus elimination by 2030. In the first phase, patients identified with hepatitis C virus infection were treated. Although, to achieve this ambitious goal, we had to reach difficult to access groups, such as persons who inject drugs (PWID) and prisoners. We developed a strategy where a medical team (2-3 doctors) from the hospital went to prison and was responsible for the outpatient clinics, liver elastography, and giving the medication on-site, increasing access to care by avoiding any need to move the patients outside the prison. This was so successful, reaching 99% of sustained virological response in a difficult to treat cohort, that a national program was created implementing our strategy. Therefore, in Portugal, every prisoner has access to treatment inside the prison.