Ling et al.'s 'Sustained-release methylphenidate in a randomized trial of treatment of methamphetamine use disorder'.
Ling et al.'s 'Sustained-release methylphenidate in a randomized trial of treatment of methamphetamine use disorder'.
复制标题
Ling 等人的“缓释哌甲酯用于治疗甲基苯丙胺使用障碍的随机试验”。
DOI:
10.1111/add.12885
复制
发表时间:
2015
期刊:
影响因子:
--
通讯作者:
Nunes,EdwardV
中科院分区:
文献类型:
--
作者:
Levin,FrancesR;Mariani,JohnJ;Bisaga,Adam;Nunes,EdwardV
Ling et al.[1] evaluated the efficacy of methylphenidate sustained-release (MPH-SR) as a treatment for methamphetamine use disorder. The primary outcome measure, self-reported days of methamphetamine use in the last 30 days of the 10-week trial, was not significantly different between active medication and placebo, although several of the secondary outcomes of methamphetamine use showed a beneficial effect of MPH-SR. The takeaway message might be that the results are equivocal, and stimulant medications are not so promising for treating stimulant use disorders [2]. However, we believe that the MPH-SR dose employed in the study, 54mg/day, was modest, and may not have been high enough to produce an optimal effect. The existing evidence supports the effectiveness of higher stimulant doses for stimulant use disorders.Another study found that an MPH dose of 54mg/day was effective among amphetaminedependent patients [3]. Higher doses of MPH are often used to treat attention deficit hyperactive disorder (ADHD), and various studies have shown this to be well tolerated [4–6]. Notably, in one study when a substantially higher dose of MPH-SR was administered (up to 180 mg) to amphetamine-dependent individuals, MPH-SR was superior to placebo in reducing the proportion of amphetamine-positive urines [7]. The same research group did not observe a beneficial effect when lower dosing was used [5]. This is consistent with clinical trials in cocaine-dependent patients in whom higher doses of amphetamine were more likely to elicit cocaine abstinence than lower doses or placebo [8, 9]. Adequate dosage has been found to be essential for effectiveness of other agonist-replacement strategies for substance use disorders, such as methadone or buprenorphine maintenance.