EMBED 进展报告:以用户为中心的临床决策支持实用性试验,用于实施由急诊科发起的丁丙诺啡治疗阿片类药物使用障碍。

Journal of psychiatry and brain science Pub Date : 2020-01-01 Epub Date: 2020-02-21 DOI:10.20900/jpbs.20200003
Edward R Melnick, Bidisha Nath, Osama M Ahmed, Cynthia Brandt, David Chartash, James D Dziura, Erik P Hess, Wesley C Holland, Jason A Hoppe, Molly M Jeffery, Liliya Katsovich, Fangyong Li, Charles C Lu, Kaitlin Maciejewski, Matthew Maleska, Jodi A Mao, Shara Martel, Sean Michael, Hyung Paek, Mehul D Patel, Timothy F Platts-Mills, Haseena Rajeevan, Jessica M Ray, Rachel M Skains, William E Soares, Ashley Deutsch, Yauheni Solad, Gail D'Onofrio
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引用次数: 0

摘要

丁丙诺啡(BUP)可以安全有效地减少阿片类药物使用障碍(OUD)患者的渴求、用药过量和死亡率。然而,急诊室启动 BUP 的速度一直很慢,部分原因是医生认为这种做法过于复杂且具有破坏性。我们报告了正在进行的 EMBED(急诊科启动丁丙诺啡治疗阿片类药物使用障碍)项目的进展情况。该项目是一项为期五年的合作项目,涉及五个医疗保健系统,目标是开发、整合、研究和推广以用户为中心的临床决策支持(CDS),以促进在常规急诊护理中采用由急诊科(ED)启动的丁丙诺啡/纳洛酮(BUP)。该项目即将进入第三年,已经完成了多个里程碑式的目标,包括:(1) 以用户为中心设计 CDS 原型;(2) 将 CDS 集成到自动化电子病历 (EHR) 工作流程中;(3) 数据协调,包括推导和验证基于 EHR 的可计算表型、(4) 满足所有伦理和法规要求,获得豁免知情同意;(5) 在单个地点进行干预试点测试;(6) 在 5 个医疗系统的 20 个急诊室开展为期 18 个月的平行分组随机实用试验。在单个急诊室进行干预试点测试后,由急诊室发起的 BUP 和纳洛酮处方率有所提高,采用这种做法的医生人数也翻了一番。正在进行的多中心实用性试验将评估该干预措施的有效性、可扩展性和可推广性,目标是将 OUD 的急诊治疗模式转变为早期识别和治疗:试验注册:Clinicaltrials.gov # NCT03658642。
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Progress Report on EMBED: A Pragmatic Trial of User-Centered Clinical Decision Support to Implement EMergency Department-Initiated BuprenorphinE for Opioid Use Disorder.

Buprenorphine (BUP) can safely and effectively reduce craving, overdose, and mortality rates in people with opioid use disorder (OUD). However, adoption of ED-initiation of BUP has been slow partly due to physician perception this practice is too complex and disruptive. We report progress of the ongoing EMBED (EMergency department-initiated BuprenorphinE for opioid use Disorder) project. This project is a five-year collaboration across five healthcare systems with the goal to develop, integrate, study, and disseminate user-centered Clinical Decision Support (CDS) to promote the adoption of Emergency Department (ED)-initiation of buprenorphine/naloxone (BUP) into routine emergency care. Soon to enter its third year, the project has already completed multiple milestones to achieve its goals including (1) user-centered design of the CDS prototype, (2) integration of the CDS into an automated electronic health record (EHR) workflow, (3) data coordination including derivation and validation of an EHR-based computable phenotype, (4) meeting all ethical and regulatory requirements to achieve a waiver of informed consent, (5) pilot testing of the intervention at a single site, and (6) launching a parallel group-randomized 18-month pragmatic trial in 20 EDs across 5 healthcare systems. Pilot testing of the intervention in a single ED was associated with increased rates of ED-initiated BUP and naloxone prescribing and a doubling of the number of unique physicians adopting the practice. The ongoing multi-center pragmatic trial will assess the intervention's effectiveness, scalability, and generalizability with a goal to shift the emergency care paradigm for OUD towards early identification and treatment.

Trial registration: Clinicaltrials.gov # NCT03658642.

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