Evidence map›Paper›PMID 35149614›Full record

ArticleJournal of addiction medicine

Rapid Overlap Initiation Protocol Using Low Dose Buprenorphine for Opioid Use Disorder Treatment in an Outpatient Setting: A Case Series.

Leslie W Suen, Trevor G Lee, Michael Silva, Paulette Walton, Phillip O Coffin, Michelle Geier, Christine S Soran

Open access · greenAbstract read
In one paragraph

Article in Journal of addiction medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  11. Qualitative study of blister pack use during buprenorphine low dose initiation.Journal of the American Pharmacists Association : JAPhA
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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

7 authors at 2 institutions in 2 countries.

Leslie W SuenFrom the National Clinician Scholars Program, Philip R. Lee Institute for Health Policy, University of California, San Francisco, CA (LWS); San Francisco Veterans Affairs Medical Center, San Francisco, CA (LWS); San Francisco Department of Public Health, San Francisco, CA (TGL, PC, MG); Division of Substance Abuse and Addiction Medicine, San Francisco General Hospital, University of California, San Francisco, CA (MS, PW, CSS); Division of General Internal Medicine, San Francisco General Hospital, University of California, San Francisco, CA (CSS).
Trevor G Lee
Michael Silva
Paulette Walton
Phillip O Coffin
Michelle Geier
Christine S Soran
Centre de Santé et de Services Sociaux Cavendish · CASan Francisco General Hospital · US

Funding

Midcareer K24 Award for Mentoring and Patient-Oriented ResearchK24DA042720 · NIDA · SAN FRANCISCO DEPARTMENT OF PUBLIC HEALTH · PI PHILLIP O COFFIN · 2016 to 2026
$1.6M
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 DA060329NIDA NIH HHS K24 DA042720
6 · The paper itself

Abstract

objectivesFear and risk of precipitated withdrawal are barriers for initiating buprenorphine in individuals with opioid use disorder, particularly among those using fentanyl. A buprenorphine rapid overlap initiation (ROI) protocol (also knownas "rapidmicro-dosing") utilizing small, escalating doses of buprenorphine can overcome this barrier, reaching therapeutic doses in 3 to 4 days. We sought to demonstrate the feasibility of implementing a buprenorphine ROI protocol for buprenorphine initiation in the outpatient setting.

methodsWe conducted a retrospective chart review of patients prescribed an outpatient ROI protocol at the Office-based Buprenorphine Induction Clinic from October to December 2020. The ROI protocol utilizes divided doses of sublingual buprenorphine tablets and blister packaging for easier dosing. Patients were not required to stop other opioid use and were advised to follow up on day 4 of initiation.

resultsTwelve patients were included, of whom eleven (92%) were using fentanyl at intake. Eleven patients picked up their prescription. Seven patients returned for follow-up (58%), and all 7 completed the ROI protocol. One patient reported any withdrawal symptoms, which were mild. At 30 days, 7 patients (58%) were retained in care, and 5 (42%) were still receiving buprenorphine treatment, 4 (33%) of whom had been abstinent from nonprescribed opioid use for ≥2 weeks.

conclusionsThe ROI protocol was successful in initiating buprenorphine treatment for patients in our outpatient clinic, many of whom were using fentanyl. The ROI protocol may offer a safe alternative to traditional buprenorphine initiation and warrants further study.

Indexed as

BuprenorphineOpioid-Related DisordersSubstance Withdrawal SyndromeAnalgesics, OpioidFentanylHumansOpiate Substitution TreatmentOutpatientsRetrospective StudiesTabletsAnalgesics, OpioidBuprenorphineFentanylTablets

Identifiers

PMID35149614
PMCPMC11006272
OpenAlexW4211252681

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.