Evidence map›Paper›PMID 32289189›Full record

ReviewAddiction (Abingdon, England)2020

Global opioid agonist treatment: a review of clinical practices by country.

Harry Jin, Brandon D L Marshall, Louisa Degenhardt, John Strang, Matt Hickman, David A Fiellin, Robert Ali, Julie Bruneau, Sarah Larney

Abstract readReview
In one paragraph

Review in Addiction (Abingdon, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 4 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

42 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Sustained-release naltrexone for opioid dependence.The Cochrane database of systematic reviews · 2025
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Harry JinDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.ORCID 0000-0002-6347-2617
Brandon D L MarshallNDARC, University of NSW, Sydney, New South Wales, Australia.ORCID 0000-0002-0134-7052
Louisa DegenhardtNational Addiction Centre, Institute of Psychiatry, Psychology and Neuroscience, London, UK.ORCID 0000-0002-8513-2218
John StrangSouth London and Maudsley NHS Foundation Trust, Maudsley Hospital, London, UK.ORCID 0000-0002-5413-2725
Matt HickmanPopulation Health Sciences, Bristol Medical School, University of Bristol, UK.ORCID 0000-0001-9864-459X
David A FiellinYale Schools of Medicine and Public Health, New Haven, CT, USA.
Robert AliSchool of Medicine, University of Adelaide, Adelaide, Australia.
Julie BruneauDepartment of Family and Emergency Medicine, Université de Montréal, Québec, Canada.ORCID 0000-0002-3484-6456
Sarah LarneyCentre Hospitalier de l'Université de Montréal Research Center, Quebec, Canada.ORCID 0000-0002-5602-4963

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Project 4: Neonatal Abstinence Syndrome (NAS): Fetus to First YearsP20GM125507 · NIGMS · RHODE ISLAND HOSPITAL · PI Brandon David Lewis Marshall · 2018 to 2026
$23.4M
Department of Health RP-PG-0616-20008Medical Research Council MR/N00616X/1NCATS NIH HHS UL1 TR001863NIDA NIH HHS R01DA1104470NIGMS NIH HHS P20 GM125507
6 · The paper itself

Abstract

aimsWe assessed how opioid agonist treatment (OAT) for opioid use disorder (OUD), specifically methadone and buprenorphine, including buprenorphine-naloxone, is delivered in routine clinical practice, with a focus on factors that affect access to and delivery of these services. The aims of this review were to summarize eligibility criteria for entry to OAT, doses in routine clinical practice, access to and eligibility for unsupervised dosing and urine drug screening practices in OAT programs globally.

methodsWe completed searches of PubMed, Embase, and grey literature databases for cross-sectional or observational cohort studies of OAT using either methadone or buprenorphine. Dose data extracted from eligible studies were compared with guidelines provided by WHO.

resultsWe found 140 reports from 41 countries that contained data for at least one of the relevant indicators. A diagnosis of opioid dependence or opioid use disorder was the most common eligibility requirement for OAT (13 or 17 countries). Reported mean or median doses for methadone ranged from 16-131 mg whereas range for buprenorphine was 2.5-19 mg. Access to unsupervised dosing under some conditions was reported in 18 of 27 countries. Frequency of regular urine drug screenings (UDS) ranged from several times a week to eight times per year (methadone) or as clinically indicated.

conclusionsOpioid agonist treatment practices, including doses prescribed, vary greatly both within and across countries. Of particular concern is the persistence of lower dose prescribing practices, in which patients may be prescribed doses below those proven to yield significant clinical benefits.

Indexed as

Analgesics, OpioidBuprenorphineBuprenorphine, Naloxone Drug CombinationHumansMethadoneNarcotic AntagonistsOpiate Substitution TreatmentOpioid-Related DisordersAnalgesics, OpioidBuprenorphineBuprenorphine, Naloxone Drug CombinationMethadoneNarcotic AntagonistsBuprenorphineclinical practicedosing, methadoneopioid agonist treatmentopioid use disorder

Identifiers

PMID32289189
PMCPMC7554123

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.