Evidence map›Paper›PMID 40183345›Full record

ArticleSubstance use & addiction journal2025

Outpatient Initiation of 7-Day Injectable Buprenorphine: A Direct-to-Inject Case Series.

Sarah Rosenwohl-Mack, Leslie W Suen, Alexander A Logan, Damian Peterson, Hannah R Snyder

Registry-linked trialAbstract read
In one paragraph

Article in Substance use & addiction journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07469501 (Improving Buprenorphine Initiation Among Individuals With Opioid Use Disorder Using Fentanyl), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT07469501 phase4not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Improving Buprenorphine Initiation Among Individuals With Opioid Use Disorder Using Fentanyl

TypeinterventionalSponsorUniversity of California, San FranciscoRan2026 to 2027Enrolled50ConditionsOpioid Use Disorder, FentanylArmsInjectable buprenorphine, Sublingual Buprenorphine (SUBOXONE, Zubsolv, or generic tablets)
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Qualitative study of blister pack use during buprenorphine low dose initiation.Journal of the American Pharmacists Association : JAPhA
    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

5 authors.

Sarah Rosenwohl-MackDepartment of Family and Community Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-2885-9605
Leslie W SuenDivision of General Internal Medicine at San Francisco General Hospital, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0003-4786-356X
Alexander A LoganDivision of Hospital Medicine at San Francisco General Hospital, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0003-2233-678X
Damian PetersonSan Francisco Department of Public Health, San Francisco, CA, USA.ORCID 0000-0002-6670-0726
Hannah R SnyderDepartment of Family and Community Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-8120-3824

Funding

Enhancing buprenorphine low dose initiation (COPILOT)K23DA060329 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Leslie W. Suen · 2024 to 2026
$593k
NIDA NIH HHS K23 DA060329
6 · The paper itself

Abstract

backgroundBuprenorphine is an effective treatment for opioid use disorder, but it can be challenging to avoid withdrawal in the process of buprenorphine initiation. After the recent FDA approval of 7-day long-acting injectable buprenorphine, some clinicians have used this formulation to start patients on buprenorphine without a prior sublingual "test dose." Very little is known about the feasibility of this practice in an outpatient setting. CASES: In this case series, we conducted a retrospective chart review of electronic health record data for all patients who were ordered 7-day long-acting injectable buprenorphine for a "direct-to-inject" initiation within a single public health system from January 1, 2024 to November 15, 2024. We excluded patients who received a cumulative dose of 4 mg or more of sublingual buprenorphine in the 24 hours before injection. We reported on chart-documented patient experiences after injection, whether patients returned to care, and retention on buprenorphine at 7- and 30-days post-injection. We identified 21 unique patients who received direct-to-inject buprenorphine in 22 attempts. In 17 (77%) attempts, the patient received no buprenorphine in the preceding 24 hours. In 5 (23%) attempts, patients received some buprenorphine in the preceding 24 hours (<4 mg) and/or had evidence of buprenorphine in a same-day urine drug screen. Patient experiences post-injection fit into 1 of 3 themes: "It felt fine" (n = 6), "I felt unwell but okay" (n = 13), and "It felt very rough" (n = 3). Most attempts resulted in buprenorphine treatment retention at 7 days (n = 17, 77%) and 30 days (n = 16, 73%) after injection. DISCUSSION: Direct-to-inject buprenorphine was generally well tolerated, with excellent retention on buprenorphine at 7- and 30 days post-injection. Further research is needed to evaluate the correlation between preinjection patient characteristics (time since last use, level of withdrawal) and post-injection patient experience of withdrawal.

Indexed as

BuprenorphineNarcotic AntagonistsOpiate Substitution TreatmentOpioid-Related DisordersAdultAmbulatory CareDelayed-Action PreparationsFemaleHumansInjectionsMaleMiddle AgedOutpatientsRetrospective StudiesBuprenorphineDelayed-Action PreparationsNarcotic Antagonistsbuprenorphinefentanylopioid medication-assisted treatmentopioid use disorder

Identifiers

PMID40183345
PMCPMC12353995

What Socratic holds

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Registered trials

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.