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种族和民族差异对阿片类激动剂在临床试验中的剂量的影响。

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

机构信息

Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York.

Department of Psychiatry, Columbia University Irving Medical Center, Columbia University, New York, New York.

出版信息

JAMA Netw Open. 2024 Oct 1;7(10):e2436612. doi: 10.1001/jamanetworkopen.2024.36612.

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.

摘要

重要性

在常规护理环境中,已经确定了在获得阿片类药物使用障碍(OUD)治疗和治疗质量方面存在种族和民族差异。相比之下,临床试验中治疗质量的差异相对较少受到关注。

目的

估计在临床试验中,OUD 治疗的阿片类激动剂治疗的第 4 周内的剂量存在种族和民族差异。

设计、地点和参与者:这项队列研究对美国国立药物滥用临床试验网络在 2006 年 5 月至 2017 年 1 月 31 日期间进行的 3 项试验的美沙酮和丁丙诺啡治疗臂进行了分析,该研究在多个临床试验网络地点进行。在本研究中,纳入了随机分配并开始接受丁丙诺啡或美沙酮治疗且自我认定为西班牙裔、非西班牙裔黑人和非西班牙裔白人的试验参与者。数据分析于 2023 年 11 月 1 日至 2024 年 8 月 5 日进行。

暴露

在试验入组时,患者自我认定的种族和民族的组合。

主要结果和测量

治疗的前 4 周内每周接受的丁丙诺啡或美沙酮的最大日剂量。在种族和民族群体之间比较了每周的平均剂量和接受更高剂量(丁丙诺啡≥16 毫克和美沙酮≥60 毫克)的患者比例。

结果

共有 1748 名患者(1263 名开始接受丁丙诺啡治疗,485 名开始接受美沙酮治疗)纳入分析(1168 名[66.8%]为男性;中位年龄为 33 [IQR,26-45] 岁)。其中,138 名患者(7.9%)为黑人,273 名(15.6%)为西班牙裔,1337 名(76.5%)为白人。在第 4 周,黑人患者接受的丁丙诺啡剂量比白人患者低 2.5 毫克(95%CI,-4.6 至-0.5),接受的美沙酮剂量低 16.7 毫克(95%CI,-30.7 至-2.7),这是在按年龄和性别标准化后得出的结果。在第 4 周,接受更高剂量药物治疗(丁丙诺啡≥16 毫克;美沙酮≥60 毫克)的患者比例,黑人患者比白人患者低 16.9 个百分点(95%CI,-31.9 至-1.9)。西班牙裔和白人患者接受的丁丙诺啡剂量相似;西班牙裔患者接受的美沙酮剂量低于白人患者。

结论和相关性

在这项来自 3 项临床试验的队列研究中,白人患者通常接受的药物剂量高于黑人患者。需要进一步研究以了解 OUD 治疗质量差异的机制和干预措施,以及这些差异如何影响试验结果的普遍性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11581645/d5f4d1235eb2/jamanetwopen-e2436612-g001.jpg

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