Evidence map›Paper›PMID 41874507›Full record

ArticleJAMA network open2026

Slow-Release Oral Morphine vs Methadone for Opioid Use Disorder in the Fentanyl Era.

M Eugenia Socias, Jingxin Lei, Vivienne Zhou, Rohan Anand, Zishan Cui, Stephanie Penta, Marc Larochelle, Sara Lodi, Nadia Fairbairn

Abstract readComparative Study
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

M Eugenia SociasBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Jingxin LeiBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Vivienne ZhouBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Rohan AnandBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Zishan CuiBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Stephanie PentaBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.
Marc LarochelleSection of General Internal Medicine, Department of Medicine, Boston Medical Center and Boston University School of Medicine, Boston, Massachusetts.
Sara LodiDepartment of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Nadia FairbairnBritish Columbia Centre on Substance Use, Vancouver, British Columbia, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Slow-release oral morphine (SROM) is approved for the treatment of opioid use disorder (OUD) in several European countries and has been used off label in Canada since 2017. However, the evidence base to support its use is limited and predates the fentanyl era. Objective: To compare the discontinuation rates and mortality risks of SROM vs methadone for the treatment of OUD. Design, Setting, and Participants: This comparative effectiveness study with a target trial emulation approach used data from observational linked health administrative databases in the Vancouver Coastal Health Authority (VCHA) region in British Columbia, Canada, between July 1, 2017, and June 30, 2024. Participants were adults aged 19 to 65 years with OUD. Exposures: New prescription of SROM or methadone for OUD (ie, no dispensation of medications for OUD in the 7 days prior) within VCHA clinical services. Main Outcomes and Measures: Estimated 12-month risk of treatment discontinuation (≥7 days without medication dispensation) and all-cause mortality, as well as treatment adherence (proportion of days covered [PDC]) over 12 months of follow-up. Both intention-to-treat (ITT) and per-protocol (PP; restricted to episodes where SROM or methadone was dispensed within 4 days of the prescription) analyses were conducted. Results: A total of 3254 unique individuals (median age, 37 [IQR, 30-46] years; 2088 [64.2%] male) contributed to 4059 person-trials (2737 [67.4%] methadone, 1322 [32.6%] SROM) for the ITT analysis, and 1992 unique individuals contributed to 2276 person-trials (1653 [72.6%] methadone, 623 [27.4%] SROM) for the PP analysis. In ITT analyses, the standardized cumulative incidence of discontinuation at 12 months was 99.3% (95% CI, 99.0%-99.5%) and 97.9% (95% CI, 97.5%-98.2%) in the SROM and methadone arms, respectively (adjusted risk difference [ARD], 1.4 percentage points [pp]; 95% CI, 1.0-1.9 pp). PDC was also lower in the SROM group (adjusted risk ratio, 0.89; 95% CI, 0.87-0.91), while mortality risk was similar between arms (ARD, 1.1 pp; 95% CI, -1.3 to 4.1 pp). Of 121 total deaths, only 2 (1.7%) occurred when people were receiving MOUD. PP analyses yielded similar results. Conclusions and Relevance: In this comparative effectiveness study of adults with OUD in a Canadian setting, treatment discontinuation was common. Compared with methadone, SROM was associated with a slightly higher risk of treatment discontinuation and lower adherence but similar mortality risk. The findings suggest either medication may be appropriate if measures are in place to support retention.

Indexed as

Analgesics, OpioidMethadoneMorphineOpiate Substitution TreatmentOpioid-Related DisordersAdministration, OralAdultAgedBritish ColumbiaDelayed-Action PreparationsFemaleFentanylHumansMaleMiddle AgedAnalgesics, OpioidDelayed-Action PreparationsFentanylMethadoneMorphine

Identifiers

PMID41874507
PMCPMC13014207

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.