Stein Michael D, VanNoppen Donnell, Herman Debra S, Anderson Bradley J, Conti Micah, Bailey Genie L
Boston University School of Public Health, Boston, MA 02118, United States of America; Behavioral Medicine and Addictions Research, Butler Hospital, Providence, RI 02906, United States of America.
Behavioral Medicine and Addictions Research, Butler Hospital, Providence, RI 02906, United States of America.
J Subst Abuse Treat. 2022 May;136:108661. doi: 10.1016/j.jsat.2021.108661. Epub 2021 Nov 14.
In the current overdose epidemic, effective treatments for opioid use disorders (OUD), including innovations in medication delivery such as extended-release formulations, have the potential to improve treatment access and reduce treatment discontinuation. This study assessed treatment retention in a primary care-based, extended-release buprenorphine program.
The study recruited individuals (n = 92) who transitioned from sublingual buprenorphine to extended-release buprenorphine (BUP-XR) in 2018-2019. The study defined the primary outcome, treatment retention, as three or more consecutive, monthly BUP-XR injections following the transition to BUP-XR in this retrospective chart review.
Participants' mean age was 38 years old and 67% were male. The average duration of sublingual buprenorphine prior to transition was 17.1 (±28.1) months. Three months after transition, 48% of extended-release buprenorphine patients had discontinued BUP-XR treatment. Persons with chronic pain were more likely, and those who had used heroin in the past month less likely to continue BUP-XR. Mean months on sublingual buprenorphine prior to BUP-XR initiation was 24.3 (±32.5) months for people who received 3+ post-induction injections compared to only 8.9 (±19.5) months for those who did not (p = .009).
Extended-release buprenorphine discontinuation was high in a real-world setting. Retention continues to represent a major obstacle to treatment effectiveness, and programs need interventions with even newer MOUD formulations.
在当前的药物过量流行中,针对阿片类物质使用障碍(OUD)的有效治疗方法,包括如缓释制剂等药物递送方面的创新,有可能改善治疗的可及性并减少治疗中断。本研究评估了在以初级保健为基础的缓释丁丙诺啡项目中的治疗留存率。
该研究招募了在2018 - 2019年从舌下含服丁丙诺啡转为缓释丁丙诺啡(BUP-XR)的个体(n = 92)。在这项回顾性病历审查中,该研究将主要结局即治疗留存率定义为转为BUP-XR后连续三个月或更长时间每月接受BUP-XR注射。
参与者的平均年龄为38岁,67%为男性。转为BUP-XR之前舌下含服丁丙诺啡的平均时长为17.1(±28.1)个月。转为BUP-XR三个月后,48%的缓释丁丙诺啡患者停止了BUP-XR治疗。患有慢性疼痛的人更有可能停药,而在过去一个月内使用过海洛因的人继续接受BUP-XR治疗的可能性较小。开始接受BUP-XR治疗前接受3次及以上诱导后注射的人,舌下含服丁丙诺啡的平均时长为24.3(±32.5)个月,而未接受诱导后注射的人仅为8.9(±19.5)个月(p = 0.009)。
在现实环境中,缓释丁丙诺啡的停药率很高。治疗留存率仍然是治疗效果的主要障碍,项目需要采用更新的药物辅助治疗(MOUD)制剂进行干预。