Stein Michael D, Herman Debra S, Moitra Ethan, Hecht Jacki, Lopez Rosalie, Anderson Bradley J, Brown Richard A
Alpert Medical School of Brown University, Department of Medicine, Providence, RI, USA; Butler Hospital, Providence, RI, USA.
Alpert Medical School of Brown University, Department of Medicine, Providence, RI, USA; Butler Hospital, Providence, RI, USA.
Drug Alcohol Depend. 2015 Feb 1;147:243-50. doi: 10.1016/j.drugalcdep.2014.11.007. Epub 2014 Nov 26.
Buprenorphine opioid agonist treatment (OAT) has established efficacy for treating opioid dependency but early relapse rates are high and are often associated with withdrawal-related or emotional distress.
To determine whether a novel distress tolerance (DT) intervention during buprenorphine initiation decreases opioid relapse, we conducted a preliminary randomized controlled trial with opioid-dependent outpatients. Participants received buprenorphine-naloxone induction and 3-months of maintenance buprenorphine plus seven, 50-min manualized, individual sessions (DT vs. health education (HE) control) over a 28-day period, linked to clinician medication dosing visits, and beginning 2 days prior to buprenorphine induction. Primary outcomes included use of illicit opioids (positive defined as any self-reported use in the prior 28 days or detected by urine toxicology) and treatment drop out.
Among 49 participants, the mean age was 41 years, 65.3% were male. Persons randomized to DT had lower rates of opioid use at all three monthly assessments, and at 3-months, 72% of HE participants were opioid positive compared with 62.5% of DT participants. Rates of dropout were 24% and 25% in the HE and DT arms, respectively.
This distress tolerance treatment produced a small, but not statistically significant reduction in opioid use during the first three months of treatment although no differences were found in drop-out rates between conditions. If replicated in a larger study, DT could offer clinicians a useful behavioral treatment to complement the effects of buprenorphine.
丁丙诺啡阿片类激动剂治疗(OAT)已被证实对治疗阿片类药物依赖有效,但早期复发率较高,且常与戒断相关或情绪困扰有关。
为了确定在开始使用丁丙诺啡期间进行一种新型的痛苦耐受(DT)干预是否能降低阿片类药物复发率,我们对阿片类药物依赖的门诊患者进行了一项初步的随机对照试验。参与者接受丁丙诺啡 - 纳洛酮诱导和为期3个月的丁丙诺啡维持治疗,外加在28天内进行七次、每次50分钟的个体化手册治疗(DT组与健康教育(HE)对照组),与临床医生的药物剂量访视相关联,并在丁丙诺啡诱导前2天开始。主要结局包括非法阿片类药物的使用(阳性定义为在前28天内任何自我报告的使用或通过尿液毒理学检测到)和治疗退出。
在49名参与者中,平均年龄为41岁,65.3%为男性。随机分配到DT组的人在所有三个月的评估中阿片类药物使用率较低,在3个月时,HE组72%的参与者阿片类药物检测呈阳性,而DT组为62.5%。HE组和DT组的退出率分别为24%和25%。
这种痛苦耐受治疗在治疗的前三个月使阿片类药物使用量有小幅下降,但无统计学意义,尽管两组在退出率上没有差异。如果在更大规模的研究中得到重复验证,DT可以为临床医生提供一种有用的行为治疗方法,以补充丁丙诺啡的治疗效果。