Evidence map›Paper›PMID 41798714›Full record

ArticleCurrent addiction reports2025

Medications for OUD: Extended-Release Naltrexone.

A Benjamin Srivastava

Abstract read
In one paragraph

Article in Current addiction reports, 2025. 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. Review
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

1 author.

A Benjamin SrivastavaDivision on Substance Use Disorders, Department of Psychiatry, Columbia University Irving Medical Center, New York, USA.

Funding

Neural mechanisms of anxiety during early and protracted abstinence in alcohol use disorderK23AA030355 · NIAAA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI A B Srivastava · 2024 to 2026
$583k
NIAAA NIH HHS K23 AA030355
6 · The paper itself

Abstract

Purpose of Review: Opioid use disorder (OUD) is a chronic, relapsing illness associated with significant morbidity and mortality. Extended-release naltrexone (XR-NTX) is an evidence-based pharmacotherapeutic agent for the treatment of OUD. This review aims at reviewing the extant literature support XR-NTX, its limitations, and providing directions for future research. Recent Findings: XR-NTX has been shown to be comparable to treatment with buprenorphine in head-to-head randomized controlled trials. XR-NTX has demonstrated clinical efficacy in several vulnerable populations with OUD including adolescents, criminal justice offenders, and patients infected with human immunodeficiency virus (HIV). XR-NTX has demonstrated efficacy for other substance use disorders including alcohol use disorder (AUD) and, when combined with bupropion, methamphetamine use disorder. Challenges to treatment include managing opioid withdrawal symptoms during XR-NTX induction as well relapse and overdose upon treatment discontinuation. Summary: XR-NTX is a first-line pharmacotherapeutic option when treating opioid use disorder with demonstrated efficacy; challenges include supporting the patient during withdrawal to facilitate successful induction and encouraging compliance to mitigate risks of relapse and overdose.

Indexed as

AntagonistExtended-releaseNaltrexoneOpioid use disorderRelapse prevention

Identifiers

PMID41798714
PMCPMC12962592

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.