Exemplar Hospital Initiation Trial to Enhance Treatment Engagement (EXHIT ENTRE): protocol for CTN-0098 an open-label randomized comparative effectiveness trial of extended-release buprenorphine versus treatment as usual on post-hospital treatment engagement for hospitalized patients with opioid use disorder.

IF 3.7 2区 医学 Q1 SUBSTANCE ABUSE Addiction Science & Clinical Practice Pub Date : 2024-12-02 DOI:10.1186/s13722-024-00510-5
Gavin Bart, Kelly S Barth, Paulette Baukol, Eva Enns, Udi E Ghitza, Jacklyn Harris, Eve Jelstrom, Jane M Liebschutz, Kara M Magane, Delia Voronca, Zoe M Weinstein, P Todd Korthuis
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引用次数: 0

Abstract

Background: Hospitalizations involving opioid use disorder (OUD) are increasing. Addiction consultation services (ACS) initiate medications for opioid use disorder (MOUD) in hospital settings and arrange post-hospital follow-up for ongoing MOUD care. Engagement in MOUD following hospital discharge is hampered by challenges in timely access to MOUD. This protocol describes an open-label randomized comparative effectiveness trial comparing ACS treatment as usual (TAU) to a single injection of a 28-day formulation extended-release buprenorphine (XR-BUP) on MOUD engagement 34-days following hospital discharge.

Methods: Six U.S. hospitals with ACS capable of prescribing all MOUD (i.e., methadone, buprenorphine, and extended-release naltrexone) recruit and randomize hospitalized patients with OUD who have not been on MOUD in the fourteen days prior to hospitalization. TAU may consist of any MOUD other than XR-BUP. Participants randomized to XR-BUP may receive any MOUD throughout their hospital stay and receive a 28-day XR-BUP injection within 72-hours of anticipated hospital discharge. There is no intervention beyond hospital stay. Participants are followed 34-, 90-, and 180-days following hospital discharge. The primary outcome is engagement in any MOUD 34-days following hospital discharge, which we hypothesize will be greater in the XR-BUP group. Randomizing 342 participants (171 per arm) provides 90% power to detect difference in the primary outcome between groups with an odds ratio of 2.1. Safety, secondary, and exploratory outcomes include: adverse events, MOUD engagement on days 90 and 180, opioid positive urine drug tests, self-reported drug use, hospital readmissions and emergency department visits, use of non-opioid drugs, fatal and non-fatal opioid overdose, all-cause mortality, quality of life, and cost-effectiveness. Data are analyzed by intention-to-treat, with pre-planned per-protocol and other secondary analyses that examine gender as an effect modifier, differences between groups, and impact of missingness.

Discussion: Engagement in MOUD care following hospitalization in individuals with OUD is low. This randomized comparative effectiveness trial can inform hospital ACS in medication selection to improve MOUD engagement 34-days following hospital discharge.

Trial registration: NCT04345718.

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加强治疗参与的医院启动试验范例(EXHIT ENTRE): CTN-0098方案一项开放标签随机对照试验,缓释丁丙诺啡与常规治疗对阿片类药物使用障碍住院患者院后治疗参与的影响。
背景:因阿片类药物使用障碍(OUD)住院的人数正在增加。成瘾咨询服务(ACS)在医院环境中启动阿片类药物使用障碍(mod)的药物治疗,并为正在进行的mod护理安排院后随访。由于难以及时获得药物治疗,出院后参与药物治疗受到阻碍。该方案描述了一项开放标签随机比较疗效试验,比较了ACS常规治疗(TAU)和出院后34天单次注射28天配方的丁丙诺啡(XR-BUP)。方法:美国6家能够开具所有mod(即美沙酮、丁丙诺啡和缓释纳曲酮)处方的ACS医院招募并随机分配住院前14天未服用mod的OUD患者。TAU可以由除XR-BUP以外的任何mod组成。随机分配到XR-BUP组的参与者可以在住院期间接受任何mod治疗,并在预期出院后72小时内接受28天XR-BUP注射。住院后没有干预措施。受试者出院后分别随访34天、90天和180天。主要转归是出院后34天任何mod的参与情况,我们假设XR-BUP组的参与情况会更大。随机分配342名参与者(每组171人)提供了90%的能力来检测组间主要结局的差异,优势比为2.1。安全性、继发性和探索性结果包括:不良事件、第90天和180天的mod参与、阿片类药物尿检阳性、自我报告的药物使用、再入院和急诊就诊、非阿片类药物的使用、致死性和非致死性阿片类药物过量、全因死亡率、生活质量和成本效益。数据通过意向治疗、预先计划的协议和其他次要分析来分析,这些分析将性别作为影响因素、组间差异和缺失的影响。讨论:OUD患者住院后参与OUD护理的比例较低。该随机比较效果试验可为医院ACS在药物选择方面提供信息,以提高出院后34天的mod参与度。试验注册:NCT04345718。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Addiction Science & Clinical Practice
Addiction Science & Clinical Practice Psychology-Clinical Psychology
CiteScore
3.90
自引率
10.80%
发文量
64
审稿时长
28 weeks
期刊介绍: Addiction Science & Clinical Practice provides a forum for clinically relevant research and perspectives that contribute to improving the quality of care for people with unhealthy alcohol, tobacco, or other drug use and addictive behaviours across a spectrum of clinical settings. Addiction Science & Clinical Practice accepts articles of clinical relevance related to the prevention and treatment of unhealthy alcohol, tobacco, and other drug use across the spectrum of clinical settings. Topics of interest address issues related to the following: the spectrum of unhealthy use of alcohol, tobacco, and other drugs among the range of affected persons (e.g., not limited by age, race/ethnicity, gender, or sexual orientation); the array of clinical prevention and treatment practices (from health messages, to identification and early intervention, to more extensive interventions including counseling and pharmacotherapy and other management strategies); and identification and management of medical, psychiatric, social, and other health consequences of substance use. Addiction Science & Clinical Practice is particularly interested in articles that address how to improve the quality of care for people with unhealthy substance use and related conditions as described in the (US) Institute of Medicine report, Improving the Quality of Healthcare for Mental Health and Substance Use Conditions (Washington, DC: National Academies Press, 2006). Such articles address the quality of care and of health services. Although the journal also welcomes submissions that address these conditions in addiction speciality-treatment settings, the journal is particularly interested in including articles that address unhealthy use outside these settings, including experience with novel models of care and outcomes, and outcomes of research-practice collaborations. Although Addiction Science & Clinical Practice is generally not an outlet for basic science research, we will accept basic science research manuscripts that have clearly described potential clinical relevance and are accessible to audiences outside a narrow laboratory research field.
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