Evidence map›Paper›PMID 32321570›Full record

ArticleAddiction science & clinical practice2020

Health and economic outcomes of treatment with extended-release naltrexone among pre-release prisoners with opioid use disorder (HOPPER): protocol for an evaluation of two randomized effectiveness trials.

Sean M Murphy, Philip J Jeng, Sabrina A Poole, Ali Jalali, Frank J Vocci, Michael S Gordon, George E Woody, Daniel Polsky

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Addiction science & clinical practice, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Sustained-release naltrexone for opioid dependence.The Cochrane database of systematic reviews · 2025
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Informing evidence-based medicine for opioid use disorder using pharmacoeconomic studies.Expert review of pharmacoeconomics & outcomes research · 2024
    Review
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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

8 authors at 4 institutions in 1 country.

Sean M MurphyDepartment of Population Health Sciences, Weill Cornell Medical College, 425 East 61st Street, Suite 301, New York, NY, 10065, USA. smm2010@med.cornell.edu.ORCID 0000-0001-9104-0670
Philip J JengDepartment of Population Health Sciences, Weill Cornell Medical College, 425 East 61st Street, Suite 301, New York, NY, 10065, USA.
Sabrina A PooleDepartment of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Ali JalaliDepartment of Population Health Sciences, Weill Cornell Medical College, 425 East 61st Street, Suite 301, New York, NY, 10065, USA.
Frank J VocciFriends Research Institute, Baltimore, MD, USA.
Michael S GordonFriends Research Institute, Baltimore, MD, USA.
George E WoodyDepartment of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Daniel PolskyDepartment of Health Policy and Management, Bloomberg School of Public Health, Carey Business School, Johns Hopkins University, Baltimore, MD, USA.
Cornell University · USFriends Research Institute · USUniversity of Pennsylvania · USJohns Hopkins University · US

Funding

Penn Mental Health AIDS Research CenterP30MH097488 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Karine Dube, Kelly L Jordan-Sciutto · 2013 to 2026
$23.5M
Utilization of health services after engagement with opioid use disorder (OUD) treatment provider by individuals with and without post-traumatic stress disorderP30DA040500 · NIDA · WEILL MEDICAL COLL OF CORNELL UNIV · PI Yuhua Bao · 2015 to 2026
$20.7M
Long-acting naltrexone for pre-release prisoners: A randomized trial of mobile treatmentR01DA040636 · NIDA · FRIENDS RESEARCH INSTITUTE, INC. · PI GORDON, MICHAEL SCOTT · 2016 to 2021
$3.1M
Health and Economic Outcomes of Treatment with Extended-Release Naltrexone Among Pre-Release Prisoners with Opioid Use DisorderR01DA046721 · NIDA · WEILL MEDICAL COLL OF CORNELL UNIV · PI MURPHY, SEAN M. · 2019 to 2022
$1.6M
NIDA NIH HHS P30 DA040500NIDA NIH HHS R01 DA040636NIDA NIH HHS R01DA040636NIDA NIH HHS R01 DA046721NIDA NIH HHS R01DA046721NIMH NIH HHS P30 MH097488
6 · The paper itself

Abstract

backgroundPersons with an opioid use disorder (OUD) who were incarcerated face many challenges to remaining abstinent; concomitantly, opioid-overdose is the leading cause of death among this population, with the initial weeks following release proving especially fatal. Extended-release naltrexone (XR-NTX) is the most widely-accepted, evidence-based OUD pharmacotherapy in criminal justice settings, and ensures approximately 30 days of protection from opioid overdose. The high cost of XR-NTX serves as a barrier to uptake by many prison/jail systems; however, the cost of the medication should not be viewed in isolation. Prison/jail healthcare budgets are ultimately determined by policymakers, and the benefits/cost-offsets associated with effective OUD treatment will directly and indirectly affect their overall budgets, and society as a whole.

methodsThis protocol describes a study funded by the National Institute of Drug Abuse (NIDA) to: evaluate changes in healthcare utilization, health-related quality-of-life, and other resources associated with different strategies of XR-NTX delivery to persons with OUD being released from incarceration; and estimate the relative "value" of each strategy. Data from two ongoing, publicly-funded, randomized-controlled trials will be used to evaluate these questions. In Study A, (XR-NTX Before vs. After Reentry), participants are randomized to receive their first XR-NTX dose before release, or at a nearby program post-release. In Study B, (enhanced XR-NTX vs. XR-NTX), both arms receive XR-NTX prior to release; the enhanced arm receives mobile medical (place of residence) XR-NTX treatment post-release, and the XR-NTX arm receives referral to a community treatment program post-release. The economic data collection instruments required to evaluate outcomes of interest were incorporated into both studies from baseline. Moreover, because the same instruments are being used in both trials on comparable populations, we have the opportunity to not only assess differences in outcomes between study arms within each trial, but also to merge the data sets and test for differences across trials. DISCUSSION: Initiating XR-NTX for OUD prior to release from incarceration may improve patient health and well-being, while also producing downstream cost-offsets. This study offers the unique opportunity to assess the effectiveness and cost-effectiveness of multiple strategies, according to different stakeholder perspectives.

Indexed as

Delayed-Action PreparationsNaltrexoneNarcotic AntagonistsOpioid-Related DisordersPatient Acceptance of Health CarePrisonersCost-Benefit AnalysisFemaleHumansInjections, IntramuscularMalePrisonsQuality of LifeRandomized Controlled Trials as TopicTreatment OutcomeDelayed-Action PreparationsNaltrexoneNarcotic AntagonistsCost-effectivenessExtended-release naltrexoneHealthcare utilizationHealth-related quality-of-lifeJustice involved personsOpioid use disorder

Identifiers

PMID32321570
PMCPMC7178627
OpenAlexW3018648194

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.