Samantha Young , Janet Raboud , Zoë Dodd , Kora DeBeck , MJ Milloy , Dean Wilson , Kanna Hayashi , Ahmed M. Bayoumi , Nadia Fairbairn
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We used multivariable generalized estimating equations to estimate the relationship between type of opioid exposure – measured using urine drug tests and categorized as: (1) fentanyl-positive, (2) fentanyl-negative opioid-positive, and (3) fentanyl- and opioid-negative, and report of their methadone dose being too low.</div></div><div><h3>Results</h3><div>In total, 1732 observations from 616 participants were included, of which 914 (52.8 %) observations had a fentanyl-positive, 178 (10.3 %) had a fentanyl-negative opioid-positive, and 640 (37.0 %) had a fentanyl- and opioid-negative urine drug test. Compared with those with a fentanyl-positive urine drug test, in the adjusted model those with a fentanyl- and opioid-negative urine drug test were significantly less likely to report their methadone dose as too low (adjusted odds ratio [AOR]=0.57, 95 % CI 0.41–0.81), while there was no significant association among those with a fentanyl-negative opioid-positive urine drug test (AOR=0.92, 95 % CI 0.59–1.43).</div></div><div><h3>Conclusions</h3><div>We found that exposure to non-fentanyl opioids while on methadone was not associated with feeling the dose was too low compared with individuals exposed to fentanyl. 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引用次数: 0
摘要
背景:接触芬太尼的人可能会报告,在普遍接受的治疗范围内,美沙酮的剂量感觉过低。我们检查了自我报告的美沙酮剂量充分性。方法:我们进行了一项回顾性队列研究,使用来自加拿大温哥华2016年12月至2020年3月期间三个社区招募的前瞻性队列研究的数据,研究对象是每天服用至少60mg剂量的美沙酮的个体。我们使用多变量广义估计方程来估计阿片类药物暴露类型之间的关系——通过尿液药物测试来测量,并分类为:(1)芬太尼阳性,(2)芬太尼阴性阿片类药物阳性,(3)芬太尼和阿片类药物阴性,并报告他们的美沙酮剂量过低。结果:共纳入616名参与者的1732项观察结果,其中914项(52.8%)观察结果为芬太尼阳性,178项(10.3%)观察结果为芬太尼阴性阿片类阳性,640项(37.0%)观察结果为芬太尼和阿片类阴性尿检。与芬太尼尿检阳性的患者相比,在调整后的模型中,芬太尼尿检阴性和阿片类药物尿检阴性的患者报告美沙酮剂量过低的可能性显著降低(调整后的优势比[AOR]=0.57, 95% CI 0.41-0.81),而芬太尼尿检阴性的阿片类药物尿检阳性患者报告美沙酮剂量过低的可能性显著降低(AOR=0.92, 95% CI 0.59-1.43)。结论:我们发现,与服用芬太尼的个体相比,服用美沙酮时暴露于非芬太尼类阿片类药物与感觉剂量过低无关。我们的研究结果支持对持续暴露于不受管制的阿片类药物(包括芬太尼)的个体进行适当的美沙酮滴定。
Examining the association between fentanyl use and perceived adequacy of methadone dose: A retrospective cohort study
Background
People exposed to fentanyl may report that the dose of methadone in the commonly accepted therapeutic range feels too low. We examined self-reported methadone dose adequacy.
Methods
We conducted a retrospective cohort study of individuals prescribed methadone at a dose of at least 60 mg daily using data from three community-recruited prospective cohort studies of people who use drugs in Vancouver, Canada from December 2016 through March 2020. We used multivariable generalized estimating equations to estimate the relationship between type of opioid exposure – measured using urine drug tests and categorized as: (1) fentanyl-positive, (2) fentanyl-negative opioid-positive, and (3) fentanyl- and opioid-negative, and report of their methadone dose being too low.
Results
In total, 1732 observations from 616 participants were included, of which 914 (52.8 %) observations had a fentanyl-positive, 178 (10.3 %) had a fentanyl-negative opioid-positive, and 640 (37.0 %) had a fentanyl- and opioid-negative urine drug test. Compared with those with a fentanyl-positive urine drug test, in the adjusted model those with a fentanyl- and opioid-negative urine drug test were significantly less likely to report their methadone dose as too low (adjusted odds ratio [AOR]=0.57, 95 % CI 0.41–0.81), while there was no significant association among those with a fentanyl-negative opioid-positive urine drug test (AOR=0.92, 95 % CI 0.59–1.43).
Conclusions
We found that exposure to non-fentanyl opioids while on methadone was not associated with feeling the dose was too low compared with individuals exposed to fentanyl. Our findings support adequate titration of methadone for individuals with continued exposure to unregulated opioids including fentanyl.
期刊介绍:
Drug and Alcohol Dependence is an international journal devoted to publishing original research, scholarly reviews, commentaries, and policy analyses in the area of drug, alcohol and tobacco use and dependence. Articles range from studies of the chemistry of substances of abuse, their actions at molecular and cellular sites, in vitro and in vivo investigations of their biochemical, pharmacological and behavioural actions, laboratory-based and clinical research in humans, substance abuse treatment and prevention research, and studies employing methods from epidemiology, sociology, and economics.