Pharmacotherapies Research Unit, Drug and Alcohol Services South Australia, South Australia, Australia.
Addiction. 2010 Jan;105(1):146-54. doi: 10.1111/j.1360-0443.2009.02717.x. Epub 2009 Oct 19.
To investigate the safety and efficacy of once-daily supervised oral administration of sustained-release dexamphetamine in people dependent on methamphetamine.
Randomized, double-blind, placebo-controlled trial.
Forty-nine methamphetamine-dependent drug users from Drug and Alcohol Services South Australia (DASSA) clinics.
Participants were assigned randomly to receive up to 110 mg/day sustained-release dexamphetamine (n = 23) or placebo (n = 26) for a maximum of 12 weeks, with gradual reduction of the study medication over an additional 4 weeks. Medication was taken daily under pharmacist supervision.
Primary outcome measures included treatment retention, measures of methamphetamine consumption (self-report and hair analysis), degree of methamphetamine dependence and severity of methamphetamine withdrawal. Hair samples were analysed for methamphetamine using liquid chromatography-mass spectrometry.
Treatment retention was significantly different between groups, with those who received dexamphetamine remaining in treatment for an average of 86.3 days compared with 48.6 days for those receiving placebo (P = 0.014). There were significant reductions in self-reported methamphetamine use between baseline and follow-up within each group (P < 0.0001), with a trend to a greater reduction among the dexamphetamine group (P = 0.086). Based on hair analysis, there was a significant decrease in methamphetamine concentration for both groups (P < 0.0001). At follow-up, degree of methamphetamine dependence was significantly lower in the dexamphetamine group (P = 0.042). Dexamphetamine maintenance was not associated with serious adverse events.
The results of this preliminary study have demonstrated that a maintenance pharmacotherapy programme of daily sustained-release amphetamine dispensing under pharmacist supervision is both feasible and safe. The increased retention in the dexamphetamine group, together with the general decreases in methamphetamine use, degree of dependence and withdrawal symptom severity, provide preliminary evidence that this may be an efficacious treatment option for methamphetamine dependence.
研究每日一次监督口服缓释苯丙胺对甲基苯丙胺依赖者的安全性和有效性。
随机、双盲、安慰剂对照试验。
来自南澳大利亚药物和酒精服务(DASSA)诊所的 49 名甲基苯丙胺依赖吸毒者。
参与者随机分配接受高达 110 毫克/天的缓释苯丙胺(n = 23)或安慰剂(n = 26),最长 12 周,在另外 4 周内逐渐减少研究药物。药物在药剂师的监督下每日服用。
主要结果包括治疗保留率、甲基苯丙胺使用的衡量标准(自我报告和毛发分析)、甲基苯丙胺依赖程度和甲基苯丙胺戒断的严重程度。使用液相色谱-质谱法对毛发样本进行了甲基苯丙胺分析。
两组之间的治疗保留率有显著差异,接受苯丙胺治疗的患者平均治疗时间为 86.3 天,而接受安慰剂的患者为 48.6 天(P = 0.014)。每个组内的自我报告的甲基苯丙胺使用量与基线相比均有显著减少(P < 0.0001),苯丙胺组的减少趋势更为明显(P = 0.086)。基于毛发分析,两组的甲基苯丙胺浓度均显著降低(P < 0.0001)。随访时,苯丙胺组的甲基苯丙胺依赖程度显著降低(P = 0.042)。苯丙胺维持治疗与严重不良事件无关。
这项初步研究的结果表明,在药剂师监督下每天服用缓释苯丙胺的维持药物治疗方案是可行且安全的。苯丙胺组的保留率增加,以及甲基苯丙胺使用量、依赖程度和戒断症状严重程度的普遍下降,初步证明这可能是治疗甲基苯丙胺依赖的有效治疗选择。