Evidence map›Paper›PMID 36075154›Full record

ArticleDrug and alcohol dependence2022

Buprenorphine & methadone dosing strategies to reduce risk of relapse in the treatment of opioid use disorder.

Kara E Rudolph, Nicholas T Williams, Alicia T Singham Goodwin, Matisyahu Shulman, Marc Fishman, Iván Díaz, Sean Luo, John Rotrosen, Edward V Nunes

Open access · greenAbstract read
In one paragraph

Article in Drug and alcohol dependence, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 6 institutions in 1 country.

Kara E RudolphDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA. Electronic address: kr2854@cumc.columbia.edu.
Nicholas T WilliamsDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
Alicia T Singham GoodwinDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
Matisyahu ShulmanDepartment of Psychiatry, School of Medicine, Columbia University, and New York State Psychiatric Institute, New York, NY, USA.
Marc FishmanDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, and Maryland Treatment Centers, Baltimore, MD, USA.
Iván DíazDivision of Biostatistics, Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
Sean LuoDepartment of Psychiatry, School of Medicine, Columbia University, and New York State Psychiatric Institute, New York, NY, USA.
John RotrosenDepartment of Psychiatry, New York University Grossman School of Medicine, New York, NY, USA.
Edward V NunesDepartment of Psychiatry, School of Medicine, Columbia University, and New York State Psychiatric Institute, New York, NY, USA.
Columbia University · USJohns Hopkins University · USNew York Psychoanalytic Society and Institute · USNew York State Psychiatric InstituteNew York University · USWeill Cornell Medicine · US

Funding

Role of disability and pain in opioid overdose: mechanism and risk mitigationR01DA053243 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Kara Elizabeth Rudolph · 2022 to 2026
$3.1M
Mechanisms linking neighborhood poverty to problematic adolescent drug useR00DA042127 · NIDA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RUDOLPH, KARA ELIZABETH · 2018 to 2021
$889k
NIDA NIH HHS R00 DA042127NIDA NIH HHS R01 DA053243
6 · The paper itself

Abstract

backgroundAlthough there is consensus that having a "high-enough" dose of buprenorphine (BUP-NX) or methadone is important for reducing relapse to opioid use, there is debate about what this dose is and how it should be attained. We estimated the extent to which different dosing strategies would affect risk of relapse over 12 weeks of treatment, separately for BUP-NX and methadone.

methodsThis was a secondary analysis of three comparative effectiveness trials. We examined four dosing strategies: 1) increasing dose in response to participant-specific opioid use, 2) increasing dose weekly until some minimum dose (16 mg BUP, 100 mg methadone) was reached, 3) increasing dose weekly until some minimum and increasing dose in response to opioid use thereafter (referred to as the "hybrid strategy"), and 4) keeping dose constant after the first 2 weeks of treatment. We used a longitudinal sequentially doubly robust estimator to estimate contrasts between dosing strategies on risk of relapse.

resultsFor BUP-NX, increasing dose following the hybrid strategy resulted in the lowest risk of relapse. For methadone, holding dose constant resulted in greatest risk of relapse; the other three strategies performed similarly. For example, the hybrid strategy reduced week 12 relapse risk by 13 % (RR: 0.87, 95 %CI: 0.83-0.95) and by 20 % (RR: 0.80, 95 %CI: 0.71-0.90) for BUP-NX and methadone respectively, as compared to holding dose constant.

conclusionsDoses should be targeted toward minimum thresholds and, in the case of BUP-NX, raised when patients continue to use opioids.

Indexed as

BuprenorphineOpioid-Related DisordersAnalgesics, OpioidBuprenorphine, Naloxone Drug CombinationHumansMethadoneNarcotic AntagonistsOpiate Substitution TreatmentRecurrenceAnalgesics, OpioidBuprenorphineBuprenorphine, Naloxone Drug CombinationMethadoneNarcotic AntagonistsAdaptive treatmentBuprenorphineDynamic dosingDynamic treatmentMethadoneOpioid use disorderPersonalized medicine

Identifiers

PMID36075154
PMCPMC9741946
OpenAlexW4293581565

What OpenQuestion holds

Textmetadata
LicenceTDM
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.