Evidence map›Paper›PMID 39365581›Full record

ArticleJAMA network open2024

Variation in Opioid Agonist Dosing in Clinical Trials by Race and Ethnicity.

Rachael K Ross, Shodai Inose, Matisyahu Shulman, Edward V Nunes, Lauren C Zalla, A Kathleen Burlew, Kara E Rudolph

Abstract read
In one paragraph

Article in JAMA network open, 2024. 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
–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

5 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Rachael K RossDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York.
Shodai InoseDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York.
Matisyahu ShulmanDepartment of Psychiatry, Columbia University Irving Medical Center, Columbia University, New York, New York.
Edward V NunesDepartment of Psychiatry, Columbia University Irving Medical Center, Columbia University, New York, New York.
Lauren C ZallaDepartment of Epidemiology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland.
A Kathleen BurlewDepartment of Psychology, University of Cincinnati, Cincinnati, Ohio.
Kara E RudolphDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York.

Funding

Design and analysis advances to improve generalizability of clinical trials for treating opioid use disorderR01DA056407 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Kara Elizabeth Rudolph, Elizabeth A. Stuart · 2022 to 2026
$3.1M
The Urban Environment as a Modifiable Social Determinant of Health among People with HIVK99AI181608 · NIAID · JOHNS HOPKINS UNIVERSITY · PI ZALLA, LAUREN C. · 2024 to 2025
$253k
NIAID NIH HHS K99 AI181608NIDA NIH HHS R01 DA056407
6 · The paper itself

Abstract

Importance: Racial and ethnic disparities in access to treatment and quality of treatment for opioid use disorder (OUD) have been identified in usual care settings. In contrast, disparities in treatment quality within clinical trials are relatively unexamined. Objective: To estimate racial and ethnic differences in the dose of opioid agonist treatment for OUD in the first 4 weeks of treatment in clinical trials. Design, Setting, and Participants: This cohort study performed analysis of the methadone and buprenorphine treatment arms of 3 trials conducted by the National Institute on Drug Abuse Clinical Trials Network between May 2006, and January 31, 2017, at multiple Clinical Trials Network sites across the US. Trial participants who were randomized to and initiated buprenorphine or methadone treatment and who identified as Hispanic, non-Hispanic Black, or non-Hispanic White were included in the present study. Data were analyzed from November 1, 2023, to August 5, 2024. Exposure: Combined race and ethnicity as self-classified by the patient at trial enrollment. Main Outcomes and Measures: The maximum daily dose of buprenorphine or methadone received in each week for the first 4 weeks of treatment. The mean dose and the percentage of patients receiving a higher dose (buprenorphine ≥16 mg and methadone ≥60 mg) were compared across race and ethnicity groups. Results: A total of 1748 patients (1263 who initiated buprenorphine and 485 who initiated methadone treatment) were included in the analysis (1168 [66.8%] male; median age, 33 [IQR, 26-45] years). Of these, 138 patients (7.9%) identified as Black, 273 (15.6%) as Hispanic, and 1337 (76.5%) as White. In week 4, Black patients received buprenorphine doses 2.5 (95% CI -4.6 to -0.5) mg lower and methadone doses 16.7 (95% CI, -30.7 to -2.7) mg lower compared with White patients, after standardizing by age and sex. In week 4, the percentage of patients receiving a higher dose of medication (buprenorphine ≥16 mg; methadone ≥60 mg) was 16.9 (95% CI, -31.9 to -1.9) points lower for Black patients compared with White patients. Hispanic and White patients received similar buprenorphine doses; Hispanic patients received lower methadone doses than White patients. Conclusions and Relevance: In this cohort study of data from 3 clinical trials, White patients generally received higher doses of medication than Black patients. Future research is needed to understand the mechanisms of and interventions to reduce disparities in OUD treatment quality and how such disparities impact generalizability of trial results.

Indexed as

Analgesics, OpioidBuprenorphineMethadoneOpiate Substitution TreatmentOpioid-Related DisordersAdultBlack or African AmericanCohort StudiesDose-Response Relationship, DrugEthnicityFemaleHispanic or LatinoHumansMaleMiddle AgedUnited StatesAnalgesics, OpioidBuprenorphineMethadone

Identifiers

PMID39365581
PMCPMC11581645

What OpenQuestion holds

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LicenceCC BY
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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.