多媒体成瘾严重程度指数(ASI-MV)对寻求治疗的个体滥用他苯他酮及给药途径的评价

S. Vosburg, Jared Beaumont, S. T. Dailey-Govoni, S. Butler, Jody L. Green
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Objective The purpose of the present study was to further characterize the abuse liability of tapentadol extended-release (ER) by evaluating the prevalence of past 30-day tapentadol ER abuse and reported routes of administration as compared with ER opioids with Food and Drug Administration (FDA) abuse-deterrent labeling (“ADF opioids”) and ER opioids without FDA abuse-deterrent labeling (“non-ADF opioids”). Methods Data were collected from January 2014 through December 2017 from 776 centers located in 43 states throughout the United States using the Addiction Severity Index–Multimedia Version (ASI-MV), an instrument that is integral to the National Addictions Vigilance Intervention and Prevention Program (NAVIPPRO, Inflexxion, an IBH Company, Costa Mesa, CA, USA). Results Tapentadol ER had lower rates of past 30-day abuse than ADF ER and non-ADF ER opioid comparators, both at a population level and when adjusted for drug utilization. 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引用次数: 9

摘要

Tapentadol是一种结合mu阿片受体激动作用和去甲肾上腺素再摄取抑制作用来提供镇痛的分子,与完整的mu阿片受体激动剂相比,其胃肠道副作用的发生率可能更低。他他多作为一种活性药物成分的上市后监测一直显示出低水平的滥用和转移。目的本研究的目的是通过评估过去30天内他他多缓释(ER)与美国食品药品监督管理局(FDA)有滥用威慑标签的ER类阿片(“ADF阿片”)和没有FDA滥用威慑标签的ER类阿片(“非ADF阿片”)的滥用发生率和报告的给药途径,进一步表征他他多缓释(ER)的滥用责任。方法从2014年1月至2017年12月,使用成瘾严重程度指数多媒体版本(ASI-MV)从位于美国43个州的776个中心收集数据,该工具是国家成瘾警戒干预和预防计划(NAVIPPRO, inflexion, IBH公司,美国加利福尼亚州科斯塔梅萨)不可或缺的一部分。结果在人群水平和药物使用调整后,他他多ER在过去30天的滥用率低于ADF ER和非ADF ER阿片类药物比较组。他他多ER主要是口服滥用,尽管它也通过其他给药途径滥用。通过其他给药途径滥用他他多ER的累积率低于ADF和非ADF阿片类药物比较者,尽管报告的他他多ER使用样本量小导致的大置信区间限制了可靠的结论。总之,与ADF组和非ADF组相比,他他多ER组在30天内的滥用率和通过其他给药途径(特别是鼻吸和吸烟)的使用率都较低。
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Evaluation of Abuse and Route of Administration of Extended-Release Tapentadol Among Treatment-Seeking Individuals, as Captured by the Addiction Severity Index–Multimedia Version (ASI-MV)
Abstract Background Tapentadol is a molecule incorporating mu opioid receptor agonism and norepinephrine reuptake inhibition to provide analgesia, with the potential for a lower incidence of gastrointestinal side effects than full mu opioid agonists. Postmarketing surveillance of tapentadol as an active pharmaceutical ingredient has consistently revealed low levels of abuse and diversion. Objective The purpose of the present study was to further characterize the abuse liability of tapentadol extended-release (ER) by evaluating the prevalence of past 30-day tapentadol ER abuse and reported routes of administration as compared with ER opioids with Food and Drug Administration (FDA) abuse-deterrent labeling (“ADF opioids”) and ER opioids without FDA abuse-deterrent labeling (“non-ADF opioids”). Methods Data were collected from January 2014 through December 2017 from 776 centers located in 43 states throughout the United States using the Addiction Severity Index–Multimedia Version (ASI-MV), an instrument that is integral to the National Addictions Vigilance Intervention and Prevention Program (NAVIPPRO, Inflexxion, an IBH Company, Costa Mesa, CA, USA). Results Tapentadol ER had lower rates of past 30-day abuse than ADF ER and non-ADF ER opioid comparators, both at a population level and when adjusted for drug utilization. Tapentadol ER was primarily abused orally, although it was also abused through alternate routes of administration. Cumulative rates of tapentadol ER abuse by alternative routes of administration were lower than both ADF and non-ADF ER opioid comparators, although large confidence intervals resulting from the small sample size of reported tapentadol ER use limit firm conclusions. Conclusions In summary, tapentadol ER was found to have lower rates of both past 30-day abuse and use via alternate routes of administration, specifically snorting and smoking, than ADF and non-ADF ER comparators.
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