Evidence map›Paper›PMID 42227316›Full record

Observational studyAddiction (Abingdon, England)2026

Comparative effectiveness of alternative times to opioid agonist treatment taper initiation on taper completion and all-cause mortality among people with opioid use disorder: A retrospective population-based target trial emulation study in British Columbia, Canada, 2010-2020.

Ruyu Yan, Jeong Eun Min, Megan Kurz, Shaun R Seaman, Paxton Bach, Sander Greenland, Paul Gustafson, Mohammad Ehsanul Karim, Lawrence McCandless, Robert William Platt and 4 more

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in Addiction (Abingdon, England), 2026. 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. Observational
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

14 authors.

Ruyu YanCentre for Advancing Health Outcomes, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0009-0009-2756-4205
Jeong Eun MinCentre for Advancing Health Outcomes, Vancouver, British Columbia, Canada.
Megan KurzCentre for Advancing Health Outcomes, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0009-0001-8589-2006
Shaun R SeamanMedical Research Council (MRC) Biostatistics Unit, University of Cambridge, Cambridge, UK.
Paxton BachBritish Columbia Centre on Substance Use (BCCSU), Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0002-2413-9133
Sander GreenlandDepartment of Epidemiology and Department of Statistics, The University of California, Los Angeles, Los Angeles, California, USA.
Paul GustafsonDepartment of Statistics, University of British Columbia, Vancouver, British Columbia, Canada.
Mohammad Ehsanul KarimCentre for Advancing Health Outcomes, Vancouver, British Columbia, Canada.
Lawrence McCandlessFaculty of Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
Robert William PlattDepartments of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Quebec, Canada.
Uwe SiebertCenter for Health Decision Science and Departments of Epidemiology and Health Policy and Management, Harvard University T.H. Chan School of Public Health, Boston, MA, USA.
María Eugenia SocíasBritish Columbia Centre on Substance Use (BCCSU), Vancouver, British Columbia, Canada.
Hui XieFaculty of Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
Bohdan NosykCentre for Advancing Health Outcomes, Vancouver, British Columbia, Canada.

Funding

DAT-Emulating target trials with big data to strengthen the evidence base for the clinical management of opioid use disorderR01DA050629 · NIDA · SIMON FRASER UNIVERSITY · PI NOSYK, BOHDAN · 2021 to 2025
$2.4M
Health Canada Substance Use and Addictions Program 1819-HQ-000036National Institutes of Health/National Institute on Drug Abuse R01-DA050629NIDA NIH HHS R01 DA050629
6 · The paper itself

Abstract

BACKGROUND AND

aimsOpioid use disorder (OUD) treatment guidelines worldwide recommend opioid agonist treatment (OAT) as a long-term, potentially indefinite treatment for managing OUD. However, many individuals express a strong interest in eventually tapering fully off treatment. Current clinical practice guidelines offer relatively limited guidance or evidence on the appropriate timing to initiate a taper. We aimed to determine the safety and comparative effectiveness of different times from completion of OAT induction at which tapering could be considered to maximize the likelihood of taper completion and minimize the risk of mortality.

designPopulation-based retrospective observational study and target trial emulation based on nine linked administrative health databases.

settingBritish Columbia, Canada, from 1 January 2010 to 17 March 2020.

participantsIndividuals (identified via linkage of nine provincial health administrative databases) completing OAT induction with methadone or buprenorphine/naloxone who were ≥18 years of age with no known pregnancy, no history of cancer or palliative care and not currently incarcerated. We executed both incident-user (no OAT experiences) and prevalent-new-user (no OAT within the past month) analyses. INTERVENTION AND COMPARATOR: The time between completed OAT induction and taper initiation: <3 months, 3-6 months, 6-12 months, compared with 12-48 months. MEASUREMENTS: The primary outcomes were completed taper (reaching a final daily dose of ≤5 mg/day for methadone, or ≤2 mg/0.5 mg/day for buprenorphine/naloxone) and all-cause mortality. A clone-censor-weight approach was used to adjust for informative censoring and balance baseline characteristics between the groups. Logistic regression and pooled logistic regression models were used to estimate odds ratios (ORs) for completed taper and hazard ratios (HRs) for all-cause mortality, respectively, each with 95% compatibility ('confidence') intervals.

findingsWe included 17 726 incident users (buprenorphine/naloxone: 36.9%) and 49 515 treatment episodes (buprenorphine/naloxone: 31.2%) from 31 231 prevalent new users who completed induction in the analyses. Among prevalent new users, beginning tapering within 3 months, between 3 and 6 months and between 6 and 12 months of completing induction was associated with an increased likelihood of completed taper [methadone: <3 months: adjusted odds ratio (aOR) = 3.09, 95% compatibility interval (95% CI) = 2.58-3.68; buprenorphine/naloxone: <3 months: aOR = 6.90, 95% CI = 5.19-9.16] but a higher risk of mortality [methadone: <3 months: adjusted hazard ratio (aHR) = 1.18, 95% CI = 1.12-1.25; buprenorphine/naloxone: <3 months: aHR = 1.12, 95% CI = 1.05-1.19], compared with initiating a taper between 12 and 48 months. Similar results were found among incident users.

conclusionsAlthough initiating early tapering off opioid agonist treatment may be associated with a greater likelihood of taper completion, this practice also increases the risk of mortality.

Indexed as

Analgesics, OpioidBuprenorphine, Naloxone Drug CombinationDrug TaperingOpiate Substitution TreatmentOpioid-Related DisordersAdultBritish ColumbiaBuprenorphineCause of DeathFemaleHumansMaleMethadoneMiddle AgedNarcotic AntagonistsRetrospective StudiesAnalgesics, OpioidBuprenorphineBuprenorphine, Naloxone Drug CombinationMethadoneNarcotic Antagonistsbuprenorphine/naloxoneclone–censor–weight approachcomparative effectivenessmethadoneopioid agonist treatmentopioid use disordertaper initiationtarget trial

Identifiers

PMID42227316
PMCPMC13578844

What Socratic holds

Textmetadata
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 Socratic graph.