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注意缺陷多动障碍:儿科药物治疗的最新进展。

Attention-deficit hyperactivity disorder: recent advances in paediatric pharmacotherapy.

机构信息

Department of Psychiatry, University of Nebraska Medical Center, Omaha, Nebraska 68198-5581, USA.

出版信息

Drugs. 2010;70(1):15-40. doi: 10.2165/11530540-000000000-00000.

Abstract

Throughout this decade, there has been significant research into pharmacotherapies for attention-deficit hyperactivity disorder (ADHD). This article considers the efficacy and safety of five of the more novel long-acting pharmacological treatments recently approved by the FDA for marketing in the US for paediatric ADHD, along with an alpha(2)-adrenoceptor agonist in preparation. Reviewed treatments include the non-stimulant atomoxetine, three novel extended-release (XR) stimulant preparations: dexmethylphenidate, lisdexamfetamine dimesylate and the methylphenidate transdermal system (TDS), and the recently approved XR alpha(2)-adrenoceptor agonist, guanfacine. Dexmethylphenidate XR is a stimulant treatment in a single isomer form, and has an efficacy and tolerability similar to two doses of immediate-release (IR) dexmethylphenidate when taken 4 hours apart, but is dosed at half of the usual d,l-methylphenidate dose. Dexmethylphenidate XR utilizes a beaded bimodal release, with 50% initially released and another 50% released 4 hours later to provide benefit lasting up to 10-12 hours. Lisdexamfetamine was the first stimulant treatment approved as a prodrug, whereby the single isomer d-amfetamine remains pharmacologically inactive until activated by cleaving the lysine. Its efficacy and tolerability are generally consistent with that of XR mixed amfetamine salts, with this activation method and more consistent absorption generally resulting in up to an 11- to 13-hour benefit. The methylphenidate TDS patch utilizes skin absorption to provide predictable and uniform delivery of methylphenidate when worn for 9 hours/day. The efficacy and tolerability of the methylphenidate TDS patch is generally consistent with that of osmotic-controlled release oral system (OROS) methylphenidate, providing benefit for about 11-12 hours. Because of their formulation, lisdexamfetamine and methylphenidate each have an onset of effect at about 2 hours after administration. An adjustable wear time for the methylphenidate TDS patch accommodates related adverse effects, but its disadvantages are frequent skin irritation and the need to remember to take the patch off. Atomoxetine is the first non-stimulant treatment approved by the FDA and employs weight-based dosing up to 1.4 mg/kg/day. Benefit is generally observed within 2-8 weeks of initiation and is considered to have a lesser therapeutic effect than that of stimulants. A recent parallel-group controlled study found that atomoxetine (up to 1.8 mg/kg/day) and OROS methylphenidate both improved ADHD symptoms, although subjects receiving OROS methylphenidate had a significantly better response. Interestingly, treatment-naive children had a similar beneficial response to atomoxetine as those receiving OROS methylphenidate. Subsequent crossover treatment revealed a subgroup of youths who did not respond well to OROS methylphenidate but did respond to atomoxetine. Also identified was a larger than expected subgroup who did not respond well to either active treatment, confirming the need to continue the pursuit of novel treatments. As of September of 2009, guanfacine in XR form is the first alpha(2)-adrenoceptor agonist to gain approval to treat ADHD, approved for the treatment of 6- to 17-year olds. A second alpha(2)-adrenoceptor agonist, clonidine, is in development as a potential XR treatment for paediatric ADHD. IR clonidine has a fast onset and short half-life, with its use historically limited by somnolence. Although early formulations did not improve inattention well, recent evidence suggests that clonidine XR may have potential use as monotherapy or in extending benefit when taken with a stimulant. Guanfacine has a more specific neuronal action and a longer action than that of clonidine. The approved dosing of guanfacine XR 1 to 4 mg daily generally provides symptom benefit lasting 8-14 hours, and up to 24 hours in some children and adolescents receiving a higher dose. Such recent developments and ongoing study of additional potential pharmacological interventions may lead to additional future treatment options for children with ADHD.

摘要

在这十年中,人们对治疗注意缺陷多动障碍(ADHD)的药物疗法进行了大量研究。本文考虑了最近由美国食品和药物管理局(FDA)批准在美国市场上用于治疗小儿 ADHD 的五种较新的长效药理学治疗方法的疗效和安全性,以及一种正在准备中的α2-肾上腺素受体激动剂。 审查的治疗方法包括非兴奋剂阿托西汀、三种新型的延长释放(XR)兴奋剂制剂:右苯丙胺、右苯丙胺二甲硫酸盐和哌甲酯透皮系统(TDS),以及最近批准的 XRα2-肾上腺素受体激动剂胍法辛。右苯丙胺 XR 是一种单异构体形式的兴奋剂治疗方法,其疗效和耐受性与间隔 4 小时服用的两种剂量的即刻释放(IR)右苯丙胺相似,但剂量仅为 d,l-哌甲酯通常剂量的一半。右苯丙胺 XR 利用珠状双模态释放,50%的药物立即释放,另外 50%在 4 小时后释放,从而提供长达 10-12 小时的益处。右苯丙胺是第一种被批准为前体药物的兴奋剂治疗方法,其中单异构体 d-苯丙胺在被赖氨酸裂解激活之前保持药理活性。其疗效和耐受性与 XR 混合苯丙胺盐通常一致,这种激活方法和更一致的吸收通常可提供长达 11-13 小时的益处。哌甲酯 TDS 贴片利用皮肤吸收,当每天佩戴 9 小时时,可提供可预测和均匀的哌甲酯输送。哌甲酯 TDS 贴片的疗效和耐受性通常与控释口服系统(OROS)哌甲酯一致,可提供约 11-12 小时的益处。由于其配方,右苯丙胺和哌甲酯在给药后约 2 小时开始起效。哌甲酯 TDS 贴片的可调佩戴时间可适应相关的不良反应,但它的缺点是皮肤经常刺激和需要记住取下贴片。阿托西汀是 FDA 批准的第一种非兴奋剂治疗方法,采用基于体重的剂量,最高可达 1.4mg/kg/天。在开始治疗后 2-8 周内一般可观察到疗效,被认为比兴奋剂的治疗效果小。最近一项平行组对照研究发现,阿托西汀(最高 1.8mg/kg/天)和 OROS 哌甲酯都改善了 ADHD 症状,尽管接受 OROS 哌甲酯治疗的受试者反应更好。有趣的是,治疗初治的儿童对阿托西汀的有益反应与接受 OROS 哌甲酯的儿童相似。随后的交叉治疗显示,有一组青少年对 OROS 哌甲酯反应不佳,但对阿托西汀有反应。还发现了一个比预期更大的亚组对任何一种活性治疗都反应不佳,这证实了继续寻找新的治疗方法的必要性。截至 2009 年 9 月,XR 形式的胍法辛是第一种获得批准治疗 ADHD 的α2-肾上腺素受体激动剂,批准用于治疗 6-17 岁的儿童。第二种α2-肾上腺素受体激动剂可乐定正在开发为治疗小儿 ADHD 的潜在 XR 治疗方法。IR 可乐定起效快,半衰期短,其使用历史上受到嗜睡的限制。尽管早期制剂对注意力不集中的改善效果不佳,但最近的证据表明,可乐定 XR 可能具有作为单一疗法或与兴奋剂联合使用时延长益处的潜在用途。胍法辛具有比可乐定更特异的神经元作用和更长的作用时间。批准的胍法辛 XR 剂量为每天 1 至 4mg,通常可提供持续 8-14 小时的症状缓解,在一些接受更高剂量的儿童和青少年中,可提供长达 24 小时的缓解。最近的这些发展和对其他潜在药理学干预措施的持续研究可能会为患有 ADHD 的儿童提供更多未来的治疗选择。

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