Centre for Advancing Health Outcomes, Vancouver, British Columbia, Canada.
Faculty of Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
BMJ Open. 2024 Apr 29;14(4):e083453. doi: 10.1136/bmjopen-2023-083453.
Opioid agonist treatment (OAT) tapering involves a gradual reduction in daily medication dose to ultimately reach a state of opioid abstinence. Due to the high risk of relapse and overdose after tapering, this practice is not recommended by clinical guidelines, however, clients may still request to taper off medication. The ideal time to initiate an OAT taper is not known. However, ethically, taper plans should acknowledge clients' preferences and autonomy but apply principles of shared informed decision-making regarding safety and efficacy. Linked population-level data capturing real-world tapering practices provide a valuable opportunity to improve existing evidence on when to contemplate starting an OAT taper. Our objective is to determine the comparative effectiveness of alternative times from OAT initiation at which a taper can be initiated, with a primary outcome of taper completion, as observed in clinical practice in British Columbia (BC), Canada.
We propose a population-level retrospective observational study with a linkage of eight provincial health administrative databases in BC, Canada (01 January 2010 to 17 March 2020). Our primary outcomes include taper completion and all-cause mortality during treatment. We propose a 'per-protocol' target trial to compare different durations to taper initiation on the likelihood of taper completion. A range of sensitivity analyses will be used to assess the heterogeneity and robustness of the results including assessment of effectiveness and safety.
The protocol, cohort creation and analysis plan have been classified and approved as a quality improvement initiative by Providence Health Care Research Ethics Board and the Simon Fraser University Office of Research Ethics. Results will be disseminated to local advocacy groups and decision-makers, national and international clinical guideline developers, presented at international conferences and published in peer-reviewed journals electronically and in print.
阿片类激动剂治疗(OAT)逐渐减量包括逐渐减少每日用药剂量,最终达到阿片类药物戒断状态。由于逐渐减量后复发和过量的风险很高,因此临床指南不建议这样做,但是患者仍可能要求减少药物剂量。开始 OAT 逐渐减量的理想时间尚不清楚。然而,从伦理上讲,逐渐减量计划应承认患者的偏好和自主权,但应应用关于安全性和有效性的共同知情决策原则。捕捉真实世界逐渐减量实践的关联人群水平数据为改善有关何时考虑开始 OAT 逐渐减量的现有证据提供了宝贵机会。我们的目标是确定从 OAT 开始到可以开始逐渐减量的替代时间的比较效果,以临床实践中在不列颠哥伦比亚省(BC)加拿大观察到的逐渐减量完成作为主要结局。
我们提出了一项人群水平回顾性观察研究,将加拿大不列颠哥伦比亚省的八个省级卫生行政数据库进行了链接(2010 年 1 月 1 日至 2020 年 3 月 17 日)。我们的主要结局包括治疗期间逐渐减量完成和全因死亡率。我们提出了一个“按方案”目标试验,以比较不同的逐渐减量开始时间对逐渐减量完成的可能性。将使用一系列敏感性分析来评估结果的异质性和稳健性,包括评估有效性和安全性。
该方案、队列创建和分析计划已被普罗维登斯健康保健研究伦理委员会和西蒙弗雷泽大学研究伦理办公室归类和批准为质量改进计划。结果将传播给当地宣传团体和决策者、国家和国际临床指南制定者,并在国际会议上进行演示,以及在线和印刷版发表在同行评议期刊上。