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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 ong...

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Detalles Bibliográficos
Autores principales: Melnick, Edward R., Nath, Bidisha, Ahmed, Osama M., Brandt, Cynthia, Chartash, David, Dziura, James D., Hess, Erik P., Holland, Wesley C., Hoppe, Jason A., Jeffery, Molly M., Katsovich, Liliya, Li, Fangyong, Lu, Charles C., Maciejewski, Kaitlin, Maleska, Matthew, Mao, Jodi A., Martel, Shara, Michael, Sean, Paek, Hyung, Patel, Mehul D., Platts-Mills, Timothy F., Rajeevan, Haseena, Ray, Jessica M., Skains, Rachel M., Soares, William E., Deutsch, Ashley, Solad, Yauheni, D’Onofrio, Gail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164817/
https://www.ncbi.nlm.nih.gov/pubmed/32309637
http://dx.doi.org/10.20900/jpbs.20200003
Descripción
Sumario: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.