The article, “The FASTER-BUP Study, Extended-Release Injectable Buprenorphine for the Treatment of Opioid Use Disorder Among Individuals at High Risk of Overdose: Protocol for an Observational Prospective Study,” has been published in SAj.
In this commentary, the authors state that North America is facing an unprecedented public health emergency of opioid-related morbidity and mortality. The mortality benefits of oral medication treatment for opioid use disorder (MOUD), such as methadone or buprenorphine, are well documented. However, barriers to access and long-term engagement have prevented maximizing their benefits. Long-acting injectable buprenorphine formulations were developed to address some of the challenges associated with oral MOUD. The “Pilot study to assess the feasibility, efficacy, and safety of extended-release injectable buprenorphine for the treatment of opioid use disorder among individuals at high risk of overdose” (FASTER-BUP) was developed to explore this treatment option in populations at high risk of overdose in a real-world Canadian setting. FASTER-BUP is a 24-week observational prospective study evaluating the feasibility and clinical utility of extended-release injectable buprenorphine (XR-BUP) for the treatment of opioid use disorder (OUD) among 40 adults at high risk of overdose (ie, lifetime history of overdose or a positive urine drug test (UDT) for fentanyl within 30 days prior to screening) in Vancouver, BC. The primary outcome is retention in treatment and secondary outcomes include: use of unregulated opioids, safety, overdose events, treatment satisfaction, changes in drug-related problems, changes in quality of life, opioid cravings, health service utilization, and criminal activity. FASTER-BUP is the first study to explore XR-BUP among individuals at high risk of overdose in a real-world Canadian setting. This commentary provides a brief narrative about the study thus far and presents insights on key adaptations to the study protocol, including those adopted to mitigate recruitment challenges.
In the AUTHORS’ OWN WORDS, they relate the importance of their work:
“Despite its demonstrable efficacy, XR-BUP remains an understudied and underutilized tool with limited programs existing in Canada. In 2018, Health Canada approved one formulation of XR-BUP (ie, SublocadeTM). The approval of this medication expanded treatment options for individuals with OUD, particularly those for whom medication adherence may pose a challenge. However, there remains a lack of research exploring XR-BUP in real-world Canadian settings and in populations, such as individuals at high risk of overdose, who may benefit most from this treatment. The FASTER-BUP study aims to address this research gap and this narrative provides insight into key adaptations to the study protocol in the hope that it informs future studies.”
“FASTER-BUP is among the first to explore XR-BUP among individuals at high risk of overdose in the Canadian context. Adaptable study materials and partnering with AMCT permitted critical shifts to the study protocol, thus resulting in increased recruitment efforts and study enrollment. This study will generate important preliminary data which will support the development of a larger effectiveness clinical trial evaluating XR-BUP in real-world settings. Ultimately, findings from this study will inform interventions to address Canada’s worsening opioid epidemic.”