Division of Psychiatry, Department of Clinical Neuroscience, Karolinska Institutet, 17176 Stockholm, Sweden.
Drug Alcohol Depend. 2010 Apr 1;108(1-2):130-3. doi: 10.1016/j.drugalcdep.2009.11.006. Epub 2009 Dec 16.
The efficacy of stimulant treatment in patients with substance use disorders and comorbid attention deficit hyperactivity disorder (ADHD) has been tested for cocaine and alcohol dependence but so far no studies have been conducted in amphetamine dependent individuals. The present trial was a pilot study aiming to test the feasibility of treating amphetamine dependent patients with comorbid ADHD with central stimulant medication. The study was a double-blind, placebo controlled trial with parallel groups design comparing the efficacy of a fixed dose (72mg) of OROS methylphenidate (MPH) with placebo (PL) in reducing ADHD symptoms in currently abstinent adults with amphetamine dependence and ADHD. Twenty-four treatment seeking patients who met the DSM IV criteria for amphetamine dependence and ADHD were randomized to MPH/PL. The trial was conducted at an outpatient facility with twice weekly visits, measuring ADHD symptoms and drug use. Patients rated their ADHD symptoms on a weekly basis and provided supervised urine specimens for drug toxicology twice weekly. All patients participated in weekly sessions of a skills training programme. Both the groups significantly reduced their self-rated ADHD symptoms during the 12-week treatment but there was no difference between the two treatment arms. Drug use, both measured by urine toxicology and self-report did not differ between the groups. No difference was found between the two groups with regards to craving for amphetamine or in retention in treatment. Larger studies with higher doses combined with individual dosage and longer follow-up periods are warranted.
兴奋剂治疗对伴有注意缺陷多动障碍(ADHD)共病的物质使用障碍患者的疗效已经在可卡因和酒精依赖患者中进行了测试,但迄今为止,尚未在安非他命依赖个体中进行研究。本试验是一项旨在测试用中枢兴奋剂药物治疗伴有 ADHD 的安非他命依赖患者的可行性的试点研究。该研究是一项双盲、安慰剂对照的平行组设计试验,比较了固定剂量(72mg)奥昔布宁控释片(MPH)与安慰剂(PL)在减少目前戒断的伴有 ADHD 的安非他命依赖成年人的 ADHD 症状方面的疗效。24 名符合 DSM-IV 安非他命依赖和 ADHD 标准的治疗寻求者被随机分配到 MPH/PL 组。该试验在一个门诊设施中进行,每周两次就诊,测量 ADHD 症状和药物使用情况。患者每周对自己的 ADHD 症状进行评分,并每周两次提供监督尿液样本进行药物毒理学检测。所有患者都参加了每周一次的技能培训课程。两组患者在 12 周的治疗期间均显著降低了自我报告的 ADHD 症状,但两组之间无差异。两组的药物使用情况,无论是通过尿液毒理学还是自我报告,均无差异。两组在对安非他命的渴望或治疗保留方面均无差异。需要更大规模的研究,使用更高的剂量,结合个体剂量和更长的随访时间。