Evidence map›Paper›PMID 28236511›Full record

Trial reportJournal of substance abuse treatment2018

Do patient characteristics moderate the effect of extended-release naltrexone (XR-NTX) for opioid use disorder?

Peter D Friedmann, Donna Wilson, Edward V Nunes, Randall Hoskinson, Joshua D Lee, Michael Gordon, Sean M Murphy, Richard J Bonnie, Donna T Chen, Tamara Y Boney and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of substance abuse treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
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  6. Quality of life measures in treatment for active substance misuse: a scoping review.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2025
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  8. Observational
  9. 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

11 authors at 8 institutions in 1 country.

Peter D FriedmannOffice of Research, Department of Medicine, University of Massachusetts-Baystate and Baystate Health, Springfield, MA, United States. Electronic address: Peter.friedmannmd@baystatehealth.org.
Donna WilsonOffice of Research, Department of Medicine, University of Massachusetts-Baystate and Baystate Health, Springfield, MA, United States.
Edward V NunesNew York State Psychiatric Institute, Columbia University Medical Center, New York, NY, United States.
Randall HoskinsonOffice of Research, Department of Medicine, University of Massachusetts-Baystate and Baystate Health, Springfield, MA, United States.
Joshua D LeeDepartment of Population Health, New York University School of Medicine, New York, United States.
Michael GordonFriends Research Institute, Baltimore, MD, United States.
Sean M MurphyDepartment of Health Policy and Administration, Washington State University, Spokane, WA, United States.
Richard J BonnieUniversity of Virginia School of Law, Charlottesville, VA, United States.
Donna T ChenCenter for Biomedical Ethics and Humanities, Departments of Public Health Sciences and Psychiatry and Neurobehavioral Sciences, University of Virginia School of Medicine, Charlottesville, VA, United States.
Tamara Y BoneyTreatment Research Institute, University of Pennsylvania, Philadelphia, PA, United States.
Charles P O'BrienTreatment Research Institute, University of Pennsylvania, Philadelphia, PA, United States.
Baystate Health · USUniversity of Virginia · USColumbia University Irving Medical Center · USFriends Research Institute · USNew York University · USTreatment Research Institute · USUniversity of Pennsylvania · USWashington State University Spokane · US

Funding

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 KATHRYN E MCCOLLISTER · 2015 to 2026
$20.7M
Treatment Study Using Depot Naltrexone(1/6)Philadelphia Coord/Data Mgmt SiteR01DA024553 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI O'BRIEN, CHARLES P · 2008 to 2013
$3.0M
Treatment Study Using Depot Naltrexone (3/6) NY/Bellevue Protocol Treatment SiteR01DA024555 · NIDA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LEE, JOSHUA D · 2008 to 2014
$2.0M
Treatment Study Using Depot Naltrexone(2/6)Rhode Island Protocol Treatment SiteR01DA024549 · NIDA · RHODE ISLAND HOSPITAL · PI FRIEDMANN, PETER D · 2008 to 2014
$1.9M
Treatment Studies Using Depot Naltrexone (4/6) Columbia Protocol Treatment SiteR01DA024554 · NIDA · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI NUNES, EDWARD V. · 2008 to 2014
$1.8M
Drug Abuse Treatment Development and Research MentoringK24DA022412 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI NUNES, EDWARD V. · 2007 to 2016
$1.7M
Treatment Study Using Depot Naltrexone(5/6)Baltimore Protocol Treatment SiteR01DA024550 · NIDA · FRIENDS RESEARCH INSTITUTE, INC. · PI KINLOCK, TIMOTHY W · 2008 to 2014
$1.5M
NIDA NIH HHS K24 DA022412NIDA NIH HHS P30 DA040500NIDA NIH HHS R01 DA024549NIDA NIH HHS R01 DA024550NIDA NIH HHS R01 DA024553NIDA NIH HHS R01 DA024554NIDA NIH HHS R01 DA024555
6 · The paper itself

Abstract

backgroundExtended release naltrexone (XR-NTX) injected intramuscularly monthly has been shown to reduce relapse in persons with opioid use disorder. Baseline factors, including patients' demographics, comorbidities and lifestyle, may help identify patients who will benefit most or least from XR-NTX treatment.

methodsPotential moderators of XR-NTX's effect were examined in the largest North American randomized open-label effectiveness trial of XR-NTX. Relapse status (Yes/No) at 6-month follow-up was regressed on treatment group (XR-NTX, N=153; or Treatment-as-Usual [TAU], N=155), baseline covariates, and their two-way interaction to identify moderator effects. Baseline covariates included age, gender, summary scores for depression, suicidal thoughts, drug abuse risk, substance use, medical, psychiatric and employment status, socialization, legal and family/social issues, history of abuse and quality of life measures.

resultsAlcohol use to intoxication in the 30days before randomization was a significant moderator: during the treatment phase, those who reported being recently intoxicated before randomization to XR-NTX relapsed to opioids at a rate (56%) similar to TAU (58%), while those without alcohol intoxication in the prior 30days had a lower rate of opioid relapse (41% vs. 65%, respectively, P<0.04).

conclusionsXR-NTX appeared to work equally well across subgroups with diverse demographic, addiction, mental health and environmental characteristics, with the possible exception of working better among those without recent alcohol intoxication. These findings should be reassuring to practitioners increasingly using XR-NTX as medical addiction therapy in diverse and often vulnerable populations.

Indexed as

Secondary PreventionAdultAlcoholic IntoxicationDelayed-Action PreparationsFemaleHumansInjections, IntramuscularMaleNaltrexoneNarcotic AntagonistsOpioid-Related DisordersQuality of LifeTime FactorsDelayed-Action PreparationsNaltrexoneNarcotic Antagonists

Identifiers

PMID28236511
PMCPMC5565721
OpenAlexW2589886115

What OpenQuestion holds

Textmetadata
LicenceTDM
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.