Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Department of Family and Community Medicine, University of Toronto, Toronto, Ontario, Canada.
JAMA Netw Open. 2022 Sep 1;5(9):e2234168. doi: 10.1001/jamanetworkopen.2022.34168.
Retention in buprenorphine therapy is associated with a lower risk of opioid overdose. Nevertheless, many patients discontinue treatment, and there is limited evidence to guide buprenorphine tapering.
To understand what prescribing characteristics are associated with opioid overdose following buprenorphine taper.
DESIGN, SETTING, AND PARTICIPANTS: This is a population-based, retrospective, cohort study of adults who were maintained on buprenorphine for at least 60 days and underwent a buprenorphine taper. The study was conducted in the Canadian province of Ontario, using linked administrative health data. New buprenorphine treatment episodes were accrued between January 1, 2013, and January 1, 2019, and the maximum follow-up was April 30, 2020. Data analysis was performed from December 2020 to August 2022.
The primary exposure of interest was time to taper initiation (≤1 year vs >1 year). Secondary exposures included mean rate of taper, percentage days during which the dose was decreasing, and taper duration.
The primary outcome measure was time to fatal or nonfatal opioid overdose within 18 months following treatment discontinuation.
Among 5774 individuals, the median (IQR) age at index date was 34 (28-44) years, and 3462 individuals (60.0%) were male. Time to taper initiation longer than 1 year vs 1 year or less (6.73 vs 10.35 overdoses per 100 person-years; adjusted hazard ratio [aHR], 0.69; 95% CI, 0.48-0.997), a lower mean rate of taper (≤2 mg per month, 6.95 overdoses per 100 person-years; >2 to ≤4 mg per month, 11.48 overdoses per 100 person-years; >4 mg per month, 17.27 overdoses per 100 person-years; ≤2 mg per month vs >4 mg per month, aHR, 0.65; 95% CI, 0.46-0.91; >2 to ≤4 mg per month vs >4 mg per month, aHR, 0.69; 95% CI, 0.51-0.93), and dose decreases in 1.75% or less of days vs more than 3.50% of days during the taper period (5.87 vs 13.87 overdoses per 100 person-years; aHR, 0.64; 95% CI, 0.43-0.93) were associated with reduced risk of opioid overdose; however, taper duration was not.
In this retrospective cohort study, buprenorphine tapers undertaken after at least 1 year of therapy, a slower rate of taper, and a lower percentage of days during which the dose was decreasing were associated with a significantly lower risk of opioid overdose, regardless of taper duration. These findings underscore the importance of a carefully planned taper and could contribute to reduction in opioid-related overdose death.
接受丁丙诺啡治疗的患者,其阿片类药物过量的风险较低。尽管如此,仍有许多患者停止治疗,且目前缺乏指导丁丙诺啡减量的证据。
了解丁丙诺啡减量后阿片类药物过量的相关特征。
设计、地点和参与者:这是一项基于人群的回顾性队列研究,研究对象为至少接受丁丙诺啡治疗 60 天并进行丁丙诺啡减量的成年人。研究在加拿大安大略省进行,使用了关联的行政健康数据。2013 年 1 月 1 日至 2019 年 1 月 1 日期间,新的丁丙诺啡治疗开始,最长随访时间为 2020 年 4 月 30 日。数据分析于 2020 年 12 月至 2022 年 8 月进行。
主要暴露因素为开始减量的时间(≤1 年或>1 年)。次要暴露因素包括平均减量率、剂量减少天数的百分比以及减量持续时间。
主要结局指标是停药后 18 个月内致命或非致命阿片类药物过量的时间。
在 5774 名患者中,指数日期的中位(IQR)年龄为 34(28-44)岁,3462 名患者(60.0%)为男性。与 1 年或以下相比,开始减量的时间超过 1 年(6.73 与 10.35 例每 100 人年的阿片类药物过量;调整后的危险比[aHR],0.69;95%CI,0.48-0.997)、平均减量率较低(≤2mg/月,6.95 例每 100 人年的阿片类药物过量;>2 至≤4mg/月,11.48 例每 100 人年的阿片类药物过量;>4mg/月,17.27 例每 100 人年的阿片类药物过量;≤2mg/月与>4mg/月相比,aHR,0.65;95%CI,0.46-0.91;>2 至≤4mg/月与>4mg/月相比,aHR,0.69;95%CI,0.51-0.93)以及在减量期间剂量减少 1.75%或更少的天数与 3.50%或更多的天数(5.87 与 13.87 例每 100 人年的阿片类药物过量;aHR,0.64;95%CI,0.43-0.93)与阿片类药物过量风险降低相关;然而,减量持续时间无差异。
在这项回顾性队列研究中,接受至少 1 年治疗后开始减量、减量速度较慢以及剂量减少天数比例较低与阿片类药物过量的风险显著降低相关,无论减量持续时间如何。这些发现强调了精心计划减量的重要性,并可能有助于减少与阿片类药物相关的过量死亡。