Evidence map›Paper›PMID 39888117›Full record

SynthesisAddiction (Abingdon, England)2025

Extended-release pharmacotherapies for substance use disorders in incarcerated populations: A systematic review.

Amelia Woods, Catherine Foley, Katherine M Conigrave, Winifred Asare-Doku, Anthony Shakeshaft, Stella Settumba-Stolk, Michael Farrell, Michael Doyle

Abstract readSystematic Review
In one paragraph

Synthesis in Addiction (Abingdon, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
–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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. 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

8 authors.

Amelia WoodsNational Drug and Alcohol Research Centre (NDARC), University of New South Wales, Randwick, Australia.ORCID https://orcid.org/0000-0003-1757-023X
Catherine FoleyDrug Health Service, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.ORCID https://orcid.org/0000-0003-0916-0724
Katherine M ConigraveDrug Health Service, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.ORCID https://orcid.org/0000-0002-6428-1441
Winifred Asare-DokuNational Drug and Alcohol Research Centre (NDARC), University of New South Wales, Randwick, Australia.ORCID https://orcid.org/0000-0002-9907-3511
Anthony ShakeshaftNational Drug and Alcohol Research Centre (NDARC), University of New South Wales, Randwick, Australia.ORCID https://orcid.org/0000-0002-5472-0930
Stella Settumba-StolkNational Drug and Alcohol Research Centre (NDARC), University of New South Wales, Randwick, Australia.ORCID https://orcid.org/0000-0001-8514-7770
Michael FarrellNational Drug and Alcohol Research Centre (NDARC), University of New South Wales, Randwick, Australia.ORCID https://orcid.org/0000-0001-7008-8130
Michael DoyleCentral Clinical School, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW, Australia.ORCID https://orcid.org/0000-0003-2083-8575

Funding

National Drug and Alcohol Research Centre
6 · The paper itself

Abstract

BACKGROUND AND

aimsSubstance use (SU) is prevalent among individuals in the criminal justice system (CJS). However, there is often poor access to treatment. We aimed to assess the effectiveness of two medications, extended-release naltrexone (XR-NTX) and extended-release buprenorphine (XR-BUP) for the prison population.

methodsWe searched Scopus, OVID/Embase, PubMed/Medline, ProQuest, EBSCO, Cochrane Library and Australian Criminology Database for original articles published from 1 January 2002 to 31 December 2022. INCLUSION CRITERIA: 18+, substance use disorder; XR treatment; recent incarceration. We extracted study, participants, treatment characteristics and outcome variables. We conducted risk of bias assessments using the RoB-2, ROBINS-I, JBI tools and Evers et al.

resultsWe identified 25 papers (16 studies) examining 3403 participants. Sixteen papers (9 studies) focused on XR-NTX, eight (7 studies) on XR-BUP and one on both. Eighteen papers (11 studies) were from the US, with the remainder from Norway, Australia, UK, Canada and Germany. There were eight RCTs (10 papers), four secondary observational analyses, four cohort studies, four economic analyses, two case series and one qualitative paper. Most studies had small-moderate samples, with varying retention and follow-up periods. Among RCTs, two XR-NTX studies for opioid use found no difference in retention vs treatment as usual and placebo, while one reported improved retention for XR-NTX implant vs methadone. One RCT showed mixed retention results for XR-NTX vs placebo in alcohol use. One XR-BUP study showed improved or equivalent treatment retention (depending on measures) vs sublingual buprenorphine. There was no difference in overdoses. SU for XR-NTX was challenging to assess due to differing definitions, measures and comparators. XR-BUP yielded mixed SU results, with one indicating a greater effect and another no difference from comparators.

conclusionsThere is no clear evidence for the effectiveness of extended release naltrexone and buprenorphine among individuals in the criminal justice system compared with shorter acting formulations. But there is growing evidence for the effectiveness of extended release buprenorphine in reducing opioid use and improving treatment retention in that population, with potential cost offsets from initial medication expenses.

Indexed as

BuprenorphineNaltrexoneNarcotic AntagonistsOpiate Substitution TreatmentPrisonersSubstance-Related DisordersDelayed-Action PreparationsHumansOpioid-Related DisordersBuprenorphineDelayed-Action PreparationsNaltrexoneNarcotic Antagonistsaddiction treatment in prisonsextended‐release pharmacotherapyincarcerated populationsmedication‐assisted treatmentprisoner rehabilitationprison health servicessubstance abuse treatmentsubstance use disorders

Identifiers

PMID39888117
PMCPMC11986285

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.