Evidence map›Paper›PMID 41520431›Full record

ArticleAddictive behaviors2026

Risk of opioid overdose during buprenorphine treatment for opioid use disorder in the fentanyl era.

Laura C Chambers, Benjamin D Hallowell, Andrew R Zullo, McClaren Rodriguez, Marzan A Khan, Justin Berk, Rachel Gaither, Macy Daly, Rachel S Wightman, Francesca L Beaudoin

Abstract read
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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5 · Who and what money

Authors and funding

10 authors.

Laura C ChambersDepartment of Epidemiology, Brown University, Providence, RI, USA. Electronic address: laura_chambers@brown.edu.
Benjamin D HallowellSubstance Use Epidemiology Program, Rhode Island Department of Health, Providence, RI, USA.
Andrew R ZulloDepartment of Epidemiology, Brown University, Providence, RI, USA.
McClaren RodriguezSubstance Use Epidemiology Program, Rhode Island Department of Health, Providence, RI, USA.
Marzan A KhanDepartment of Health Services, Policy, and Practice, Brown University, Providence, RI, USA.
Justin BerkDepartment of Medicine, Alpert Medical School of Brown University, Providence, RI, USA.
Rachel GaitherDepartment of Epidemiology, Brown University, Providence, RI, USA.
Macy DalyResearch, Data Evaluation, and Compliance Unit, Rhode Island Department of Behavioral Healthcare, Developmental Disabilities, and Hospitals, Cranston, RI, USA.
Rachel S WightmanDepartment of Emergency Medicine, Alpert Medical School of Brown University, Providence, RI, USA.
Francesca L BeaudoinDepartment of Epidemiology, Brown University, Providence, RI, USA; Department of Emergency Medicine, Alpert Medical School of Brown University, Providence, RI, USA.

Funding

Injectable Extended-Release Buprenorphine (XR-B) in a Correctional Setting: A Pilot Randomized Controlled TrialK23DA055695 · NIDA · RHODE ISLAND HOSPITAL · PI Justin Berk · 2022 to 2026
$1.0M
Identifying optimal buprenorphine dosing for OUD treatment and prevention of overdoseUH3DA056880 · NIDA · BROWN UNIVERSITY · PI Francesca Beaudoin, Rachel Wightman · 2025 to 2026
$1.0M
Identifying optimal buprenorphine dosing for OUD treatment and prevention of overdoseUG3DA056880 · NIDA · BROWN UNIVERSITY · PI BEAUDOIN, FRANCESCA, WIGHTMAN, RACHEL · 2022 to 2022
$425k
NIDA NIH HHS K23 DA055695NIDA NIH HHS UG3 DA056880NIDA NIH HHS UH3 DA056880
6 · The paper itself

Abstract

backgroundFor patients who use fentanyl, higher than currently recommended maintenance doses of buprenorphine treatment for opioid use disorder (OUD) may be needed to prevent cravings and withdrawal, but some clinicians and regulators are concerned that higher doses may increase overdose risk. We evaluated buprenorphine effectiveness for overdose prevention in the fentanyl era.

methodsWe conducted a retrospective cohort study of Rhode Island residents initiating buprenorphine for OUD (October 2016‒September 2022) using statewide administrative data. On each of 365 follow-up days, patients were classified as having an active buprenorphine prescription (yes/no) and a non-fatal or fatal opioid overdose (yes/no). Follow-up was discontinued if patients died or initiated methadone or naltrexone. Generalized estimating equations compared opioid overdose risk for days with versus without an active buprenorphine prescription, controlling for potential confounders and clustering by patient.

resultsAmong 8,676 patients initiating buprenorphine, most were aged 25-44 years (56.0 %) and male (61.3 %). In the 365 days following initiation, 52.6 % of person-days were covered by an active buprenorphine prescription, 1,069 patients (12.3 %) had follow-up discontinued due to methadone initiation, and 411 patients (4.7 %) experienced 545 opioid overdoses. Opioid overdose risk was 61 % lower for days with versus without an active buprenorphine prescription (adjusted risk ratio = 0.39, 95 % confidence interval = 0.31-0.49). Daily doses prescribed on days with and without an opioid overdose event were similar (P = 0.261).

conclusionsBuprenorphine remains effective for overdose prevention in the fentanyl era among patients who remain in treatment. There was no evidence that higher doses were associated with greater overdose risk.

Indexed as

Analgesics, OpioidBuprenorphineDrug OverdoseFentanylNarcotic AntagonistsOpiate OverdoseOpiate Substitution TreatmentOpioid-Related DisordersAdultFemaleHumansMaleMiddle AgedRetrospective StudiesRhode IslandAnalgesics, OpioidBuprenorphineFentanylNarcotic AntagonistsBuprenorphineFentanylMedications for opioid use disorderOpioid overdoseOpioid use disorderOverdose

Identifiers

PMID41520431
PMCPMC12937454

What OpenQuestion holds

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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.