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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Cannabinoids in attention-deficit/hyperactivity disorder: A randomised-controlled trial
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Cannabinoids in attention-deficit/hyperactivity disorder: A randomised-controlled trial

机译:在注意力缺陷/多动障碍中的大麻素:随机对照试验

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Adults with ADHD describe self-medicating with cannabis, with some reporting a preference for cannabis over ADHD medications. A small number of psychiatrists in the US prescribe cannabis medication for ADHD, despite there being no evidence from randomised controlled studies. The EMA-C trial (Experimental Medicine in ADHD-Cannabinoids) was a pilot randomised placebo-controlled experimental study of a cannabinoid medication, Sativex Oromucosal Spray, in 30 adults with ADHD. The primary outcome was cognitive performance and activity level using the QbTest. Secondary outcomes included ADHD and emotional lability (EL) symptoms. From 17.07.14 to 18.06.15, 30 participants were randomly assigned to the active (n=15) or placebo (n=15) group. For the primary outcome, no significant difference was found in the ITT analysis although the overall pattern of scores was such that the active group usually had scores that were better than the placebo group (Est=-0.17, 95%CI-0.40 to 0.07, p=0.16, n=15/11 active/placebo). For secondary outcomes Sativex was associated with a nominally significant improvement in hyperactivity/impulsivity (p=0.03) and a cognitive measure of inhibition (p=0.05), and a trend towards improvement for inattention (p=0.10) and EL (p=0.11). Per-protocol effects were higher. Results did not meet significance following adjustment for multiple testing. One serious (muscular seizures/spasms) and three mild adverse events occurred in the active group and one serious (cardiovascular problems) adverse event in the placebo group. Adults with ADHD may represent a subgroup of individuals who experience a reduction of symptoms and no cognitive impairments following cannabinoid use. While not definitive, this study provides preliminary evidence supporting the self-medication theory of cannabis use in ADHD and the need for further studies of the endocannabinoid system in ADHD. (C) 2017 Elsevier B.V. and ECNP. All rights reserved.
机译:具有ADHD的成年人描述了与大麻的自我药物,其中一些报告偏好于大麻的ADHD药物。尽管没有随机对照研究没有证据,但美国的一小批精神科医生为ADHD规定了ADHD的大麻药物。 EMA-C试验(ADHD-cannabinoids的实验药物)是一种试点随机安慰剂控制的大麻蛋白用药,SatiTex Oromucasapaals喷雾,30名成人与ADHD。主要结果是使用Qbtest的认知性能和活动水平。二次结果包括ADHD和情绪萎靡(EL)症状。从17.07.14到18.06.15,将30名参与者随机分配给活动(n = 15)或安慰剂(n = 15)组。对于主要结果,但ITT分析中没有发现显着差异,尽管活性组通常具有比安慰剂组更好的分数(EST = -0.17,95%CI-0.40至0.07, p = 0.16,n = 15/11主动/安慰剂)。对于次要的结果,SATITYX与多动/冲击(P = 0.03)的名义上显着改善和抑制的认知措施(p = 0.05),以及疏忽改善的趋势(p = 0.10)和EL(p = 0.11 )。每协议效应较高。结果在多次测试调整后不符合重要性。活跃组中发生严重(肌肉癫痫发作/痉挛)和三种轻微的不良事件,并在安慰剂组中发生严重(心血管问题)不良事件。具有ADHD的成年人可以代表在大麻蛋白使用后经历减少症状和没有认知障碍的个人的子组。虽然不是明确的,但本研究提供了支持在ADHD中的大麻的自我用药理论的初步证据,以及进一步研究ADHD中的内胆碱系统。 (c)2017 Elsevier B.V.和ECNP。版权所有。

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