Division on Substance Abuse, New York State Psychiatric Institute, Department of Psychiatry, and College of Physicians and Surgeons, Columbia University, 1051 Riverside Dr, Unit 120, New York, NY 10032, USA.
Pain. 2013 Aug;154(8):1442-8. doi: 10.1016/j.pain.2013.05.004. Epub 2013 May 7.
Few studies have examined abuse of prescription opioids among individuals with chronic pain under buprenorphine/naloxone (Bup/Nx) maintenance. The current 7-week inpatient study assessed oral oxycodone self-administration by patients with chronic pain who had a history of opioid abuse. Participants (n=25) were transitioned from their preadmission prescribed opioid to Bup/Nx. All of the participants were tested under each of the sublingual Bup/Nx maintenance doses (2/0.5, 8/2 or 16/4 mg) in random order. During each maintenance period, participants could self-administer oxycodone orally (0, 10, 20, 40 or 60 mg prescription opioids) or receive money during laboratory sessions. Drug choice (percentage) was the primary dependent variable. Subjective ratings of clinical pain and withdrawal symptoms also were measured. Mann-Whitney tests compared percentage of drug choice for each active oxycodone dose to placebo. Logistic regression analyses identified correlates of oxycodone preference, defined as 60% or greater choice of oxycodone compared to money. Pain was significantly reduced while participants were maintained on Bup/Nx compared to preadmission ratings. No differences in percentage drug choice were observed between the active oxycodone doses and placebo under each Bup/Nx maintenance dose. However, factors associated with oxycodone preference were lower Bup/Nx maintenance dose, more withdrawal symptoms and more pain. These data suggest that Bup/Nx was effective in reducing pain and supplemental oxycodone use. Importantly, adequate management of pain and withdrawal symptoms by Bup/Nx may reduce oxycodone preference in this population.
很少有研究检查过在丁丙诺啡/纳洛酮(Bup/Nx)维持治疗下慢性疼痛患者处方类阿片类药物滥用的情况。目前这项为期 7 周的住院研究评估了有阿片类药物滥用史的慢性疼痛患者口服羟考酮的自我给药情况。参与者(n=25)从他们入院前的处方类阿片药物转为 Bup/Nx。所有参与者都以随机顺序接受了每种舌下 Bup/Nx 维持剂量(2/0.5、8/2 或 16/4 mg)的测试。在每个维持期内,参与者可以口服(0、10、20、40 或 60 mg 处方类阿片药物)自我给药羟考酮,或在实验室期间获得金钱。药物选择(百分比)是主要的因变量。还测量了临床疼痛和戒断症状的主观评分。Mann-Whitney 检验比较了每个活性羟考酮剂量与安慰剂的药物选择百分比。逻辑回归分析确定了羟考酮偏好的相关因素,定义为与金钱相比,羟考酮的选择超过 60%。与入院前的评分相比,参与者在 Bup/Nx 维持治疗时疼痛明显减轻。在每个 Bup/Nx 维持剂量下,与安慰剂相比,活性羟考酮剂量之间没有观察到药物选择百分比的差异。然而,与羟考酮偏好相关的因素是 Bup/Nx 维持剂量较低、戒断症状更多和疼痛更严重。这些数据表明 Bup/Nx 有效减轻疼痛并减少补充使用羟考酮。重要的是,通过 Bup/Nx 充分管理疼痛和戒断症状可能会减少该人群对羟考酮的偏好。