Lanier Ryan K, Umbricht Annie, Harrison Joseph A, Nuwayser Elie S, Bigelow George E
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Psychopharmacology (Berl). 2008 Jun;198(2):149-58. doi: 10.1007/s00213-008-1105-z. Epub 2008 Mar 9.
Managed withdrawal (i.e., detoxification) from opioid dependence is a widespread clinical procedure that is a necessary step for those pursuing abstinence. Buprenorphine is one effective detoxification treatment, however, consensus regarding effective detoxification procedures is lacking.
This study evaluated the efficacy of a buprenorphine transdermal formulation (i.e., patch) in suppressing opioid withdrawal, its safety and tolerability, and its biodelivery when applied for 7 days.
Physically dependent opioid (heroin) users (n = 12) completed a 10-day opioid detoxification in a residential research unit. Each received a single patch application that remained in place for 7 days. Blood samples were drawn prior to patch application and once daily thereafter. Assessments, four times daily, included: the amount of rescue medications ordered to treat withdrawal discomfort; self-report and observer ratings of opioid withdrawal and agonist effects; and vital sign measures.
Overall, the patch appeared safe and well-tolerated. Buprenorphine plasma levels peaked 48 h after patch application at 0.59 ng/ml. Indices of withdrawal (self-reports, observer ratings, rescue medication) were significantly reduced within 24 h of patch application, continued to decline thereafter, and did not reappear following patch removal.
This study confirms that transdermal buprenorphine is safe and clinically effective, and suggests that a 7-day application may provide an effective and comfortable means of detoxification. This patch formulation would appear to be a useful opioid detoxification treatment by reducing compliance concerns, and administering buprenorphine in a formulation less likely to be diverted to illicit use.
从阿片类药物依赖中进行有管理的戒断(即脱毒)是一种广泛应用的临床程序,对于追求戒除的人来说是必要步骤。丁丙诺啡是一种有效的脱毒治疗方法,然而,对于有效的脱毒程序缺乏共识。
本研究评估了丁丙诺啡透皮制剂(即贴片)在抑制阿片类药物戒断方面的疗效、安全性和耐受性,以及应用7天时的生物递送情况。
身体依赖阿片类药物(海洛因)的使用者(n = 12)在住院研究单元完成了为期10天的阿片类药物脱毒。每人接受一次贴片应用,贴片持续贴7天。在贴片应用前和之后每天采集血样。每天进行四次评估,包括:为治疗戒断不适而订购的急救药物数量;阿片类药物戒断和激动剂效应的自我报告和观察者评分;以及生命体征测量。
总体而言,贴片似乎安全且耐受性良好。丁丙诺啡血浆水平在贴片应用后48小时达到峰值,为0.59 ng/ml。戒断指标(自我报告、观察者评分、急救药物)在贴片应用后24小时内显著降低,此后继续下降,贴片去除后未再次出现。
本研究证实透皮丁丙诺啡安全且临床有效,并表明7天的应用可能提供一种有效且舒适的脱毒方法。这种贴片制剂似乎是一种有用的阿片类药物脱毒治疗方法,可减少对依从性的担忧,并以一种不太可能被转用于非法用途的制剂形式给药丁丙诺啡。