Evidence map›Paper›PMID 40580781›Full record

ArticleGeneral hospital psychiatry

Risk of self-harm and overdose after starting buprenorphine for opioid use disorder.

Gregory E Simon, Susan M Shortreed, Eric Johnson, Brian K Ahmedani, Stacy A Sterling, Cynthia I Campbell, Rulin C Hechter, Rebecca A Ziebell, Sujaya Parthasarathy

Abstract readComparative Study
In one paragraph

Article in General hospital psychiatry. 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. Article
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.

Gregory E SimonKaiser Permanente Washington Health Research Institute, Seattle, WA, United States of America. Electronic address: gregory.e.simon@kp.org.
Susan M ShortreedKaiser Permanente Washington Health Research Institute, Seattle, WA, United States of America.
Eric JohnsonKaiser Permanente Washington Health Research Institute, Seattle, WA, United States of America.
Brian K AhmedaniHenry Ford Health Center for Health Services Research, Detroit, MI, United States of America.
Stacy A SterlingKaiser Permanente Northern California Division of Research, Pleasanton, CA, United States of America.
Cynthia I CampbellKaiser Permanente Northern California Division of Research, Pleasanton, CA, United States of America.
Rulin C HechterKaiser Permanente Southern California Department of Research and Evaluation, Pasadena, CA, United States of America.
Rebecca A ZiebellKaiser Permanente Washington Health Research Institute, Seattle, WA, United States of America.
Sujaya ParthasarathyKaiser Permanente Northern California Division of Research, Pleasanton, CA, United States of America.

Funding

Whose Depression Are We Measuring?: Considering the role of place on Black women’s depression outcomesU19MH121738 · NIMH · KAISER FOUNDATION RESEARCH INSTITUTE · PI SIMON, GREGORY E. · 2019 to 2023
$10.6M
NIMH NIH HHS U19 MH121738
6 · The paper itself

Abstract

objectiveCompare risk of intentional self-harm and overdose after visits for opioid use disorder (OUD) followed by starting vs. not starting buprenorphine.

methodsRecords from four health systems identified visits during 1/1/2012-12/31/2019 by health system members aged 13 or older with OUD diagnosis and no recent OUD medication. Following a target-trial emulation approach, visits followed by buprenorphine dispensing within 7 days were matched to unexposed visits. Analyses compared risk of diagnosed self-harm injury or poisoning (primary outcome) as well as opioid-involved poisoning and any injury or poisoning (secondary outcomes) within 90 days.

resultsAmong 183,809 visits by 30,955 patients, 15,508 (8.4 %) had buprenorphine dispensing within 7 days, and 2260 (1.2 %) had self-harm diagnosis within 90 days. Average duration of buprenorphine treatment before interruption was 44.3 days (SD 32.1). In primary intention-to-treat analyses using logistic regression and adjusting for baseline risk of self-harm, starting buprenorphine was not associated with significant difference in self-harm (odds ratio [OR] 1.01, 95 % CI 0.81-1.24) or opioid-involved poisoning (OR 1.09, 95 % CI 0.86-1.38). In secondary as-treated analyses censoring outcomes after treatment change, buprenorphine initiation was associated with no significant difference in hazard of self-harm (Hazard Ratio [HR] 0.74, 95 % CI 0.53-1.02) and with significantly lower hazard of opioid-involved poisoning (HR 0.63, 95 % CI 0.43-0.94).

conclusionsAmong people with OUD, starting buprenorphine was not followed by lower risk of self-harm, likely reflecting frequent discontinuation and high risk of self-harm or overdose shortly after discontinuation. These findings reinforce the need to improve treatment continuity among those starting buprenorphine.

Indexed as

BuprenorphineNarcotic AntagonistsOpiate OverdoseOpiate Substitution TreatmentOpioid-Related DisordersSelf-Injurious BehaviorAdolescentAdultAgedFemaleHumansLogistic ModelsMaleMiddle AgedOdds RatioPatient ComplianceBuprenorphineNarcotic Antagonists

Identifiers

PMID40580781
PMCPMC12239826

What OpenQuestion holds

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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.