Evidence map›Paper›PMID 41481976›Full record

Observational studyThe International journal on drug policy2026

Hepatitis C treatment in a jail setting: A retrospective cohort analysis of low-barrier initiation of direct acting antivirals.

Justin Berk, Matthew J Akiyama, Nicole Schachman, Reed Junkin, Aprotim Bhowmik, Deborah Davis, Saengnapha Williams, Josiah Rich, Matthew Murphy

Abstract readObservational Study
In one paragraph

Observational study in The International journal on drug policy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Justin BerkUniversity Warren Alpert Medical School Providence, RI, United States. Electronic address: justin_berk@brown.edu.
Matthew J AkiyamaUniversity Warren Alpert Medical School Providence, RI, United States.
Nicole SchachmanUniversity Warren Alpert Medical School Providence, RI, United States.
Reed JunkinUniversity Warren Alpert Medical School Providence, RI, United States.
Aprotim BhowmikUniversity Warren Alpert Medical School Providence, RI, United States.
Deborah DavisUniversity Warren Alpert Medical School Providence, RI, United States.
Saengnapha WilliamsUniversity Warren Alpert Medical School Providence, RI, United States.
Josiah RichUniversity Warren Alpert Medical School Providence, RI, United States.
Matthew MurphyUniversity Warren Alpert Medical School Providence, RI, United States.

Funding

Injectable Extended-Release Buprenorphine (XR-B) in a Correctional Setting: A Pilot Randomized Controlled TrialK23DA055695 · NIDA · RHODE ISLAND HOSPITAL · PI Justin Berk · 2022 to 2026
$1.0M
An intervention to improve HIV pre-exposure prophylaxis initiation, adherence and linkage to care for recently incarcerated men who inject drugs.K23DA054003 · NIDA · RHODE ISLAND HOSPITAL · PI Matthew Murphy · 2022 to 2026
$977k
Implementing a Low-Threshold Hepatitis C Treatment in a Jail SettingR34DA061732 · NIDA · RHODE ISLAND HOSPITAL · PI Justin Berk · 2024 to 2026
$723k
NIDA NIH HHS K23 DA054003NIDA NIH HHS K23 DA055695NIDA NIH HHS L30 DA052067NIDA NIH HHS R34 DA061732
6 · The paper itself

Abstract

introductionA significant proportion of individuals with hepatitis C virus (HCV) experience incarceration. Jails house individuals who are pre-trial or for short sentences and represent a critical setting to expand HCV treatment access. Low-barrier treatment models may help overcome implementation barriers to initiating treatment in jail settings. In 2021, the Rhode Island Department of Corrections began implementing low-barrier HCV treatment including take-home medications for those released before completing therapy in both a jail (pre-trial) and prison (sentenced) setting. This study aimed to evaluate response to therapy for HCV infection between individuals who initiated treatment in jail versus those who initiated in prison.

methodsThis study was an observational cohort of people receiving low-barrier HCV treatment initiation between January 2021 and September 2023 at the Rhode Island Department of Corrections. Logistic regression compared individuals who initiated therapy in jail to those initiating in prison. The primary outcome sustained virological response 12 weeks after treatment completion (SVR12).

resultsOf 160 individuals who initiated treatment during incarceration, 84 initiated in jail and 76 in prison. SVR12 was similar between individuals who initiated HCV treatment in jail (85%) and those who initiated in prison (86%). There was no statistical difference in likelihood of SVR12 between those initiating in a jail versus a prison in unadjusted bivariate analysis or an adjusted model. Individuals completing treatment in-facility were more likely to achieve SVR12.

conclusionJail-based HCV treatment initiation is feasible. However, individuals released with medication face challenges in linkage to care. Improved discharge planning and community linkage are critical to post-release treatment success.

Indexed as

Antiviral AgentsHepatitis CJailsPrisonersPrisonsAdultFemaleHumansMaleMiddle AgedRetrospective StudiesRhode IslandSustained Virologic ResponseAntiviral AgentsCriminal justiceDirect-acting antiviralsHepatitis cIncarcerationSubstance use disorder

Identifiers

PMID41481976
PMCPMC13048350

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.