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2
A double-blind, placebo-controlled trial of dexmethylphenidate hydrochloride and d,l-threo-methylphenidate hydrochloride in children with attention-deficit/hyperactivity disorder.一项关于盐酸右哌甲酯和盐酸消旋苏式哌甲酯治疗注意力缺陷/多动障碍儿童的双盲、安慰剂对照试验。
J Am Acad Child Adolesc Psychiatry. 2004 Nov;43(11):1406-14. doi: 10.1097/01.chi.0000138351.98604.92.
3
Efficacy of two once-daily methylphenidate formulations compared across dose levels at different times of the day: preliminary indications from a secondary analysis of the COMACS study data.两种每日一次的哌甲酯制剂在一天中不同时间的不同剂量水平下的疗效比较:来自COMACS研究数据二次分析的初步迹象
BMC Psychiatry. 2004 Sep 30;4:28. doi: 10.1186/1471-244X-4-28.
4
Benzedrine and dexedrine in the treatment of children's behavior disorders.
Pediatrics. 1950 Jan;5(1):24-37.
5
Emergence of tics in children with ADHD: impact of once-daily OROS methylphenidate therapy.
J Child Adolesc Psychopharmacol. 2004 Summer;14(2):185-94. doi: 10.1089/1044546041649138.
6
Stimulant treatment over five years: adherence, effectiveness, and adverse effects.五年兴奋剂治疗:依从性、有效性和不良反应。
J Am Acad Child Adolesc Psychiatry. 2004 May;43(5):559-67. doi: 10.1097/00004583-200405000-00009.
7
Impact of methylphenidate delivery profiles on driving performance of adolescents with attention-deficit/hyperactivity disorder: a pilot study.哌甲酯给药方式对注意力缺陷多动障碍青少年驾驶性能的影响:一项初步研究。
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National Institute of Mental Health Multimodal Treatment Study of ADHD follow-up: 24-month outcomes of treatment strategies for attention-deficit/hyperactivity disorder.美国国立精神卫生研究所多动症多模式治疗研究随访:注意缺陷多动障碍治疗策略的24个月结果
Pediatrics. 2004 Apr;113(4):754-61. doi: 10.1542/peds.113.4.754.
9
A comparison of once-daily extended-release methylphenidate formulations in children with attention-deficit/hyperactivity disorder in the laboratory school (the Comacs Study).实验室学校中患有注意力缺陷/多动障碍儿童使用每日一次缓释哌甲酯制剂的比较(Comacs研究)
Pediatrics. 2004 Mar;113(3 Pt 1):e206-16. doi: 10.1542/peds.113.3.e206.
10
A dose-response study of OROS methylphenidate in children with attention-deficit/hyperactivity disorder.盐酸哌甲酯控释片治疗注意缺陷多动障碍儿童的剂量反应研究。
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注意缺陷/多动障碍:药物治疗

Attention deficit/hyperactivity disorder: pharmacotherapy.

作者信息

Elia Josephine

机构信息

Dr. Elia is from the Department of Child and Adolescent Psychiatry at the Children's Hospital of Philadelphia and the Department of Psychiatry at the University of Pennsylvania in Philadelphia, Pennsylvania.

出版信息

Psychiatry (Edgmont). 2005 Jan;2(1):27-35.

PMID:21179640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3004727/
Abstract

Pharmacotherapy, one of the effective modalities of treatment for attention deficit/hyperactivity disorder (ADHD), was discovered serendipitously and, until recently, consisted primarily of short-acting methylphenidate and dextroamphetamine compounds. The US Food and Drug Administration's (FDA) approval of Concerta in 2000 followed by approval of additional long-acting methylphenidate (Ritalin LA; Metadate CD) and amphetamine formulations (Adderall XR) expanded the repertoire. By providing sustained efficacy for most of the school day, mid-day administration is avoided, privacy is preserved, and adherence to treatment improves. In 2001, an isomer preparation of methylphenidate, Focalin, was approved, and in 2002, Strattera, a selective noradrenergic agent expanded treatment options to non-controlled agents. At this time, stimulant preparations continue to remain the first-line agents due to their unparalleled efficacy and safety record. However, current treatment remains empirical due to lack of scientific data guiding the choice of agent as well as dose.

摘要

药物治疗是治疗注意力缺陷多动障碍(ADHD)的有效方法之一,它是偶然被发现的,直到最近,主要由短效哌甲酯和右旋苯丙胺化合物组成。2000年美国食品药品监督管理局(FDA)批准了康纳达,随后又批准了其他长效哌甲酯(利他林LA;美达新CD)和苯丙胺制剂(安非他明XR),从而扩大了药物种类。通过在学校一天的大部分时间里提供持续疗效,避免了中午用药,保护了隐私,并提高了治疗依从性。2001年,哌甲酯的一种异构体制剂福卡林被批准,2002年,一种选择性去甲肾上腺素能药物择思达将治疗选择扩展到了非管制药物。目前,由于其无与伦比的疗效和安全记录,兴奋剂制剂仍然是一线药物。然而,由于缺乏指导药物选择和剂量的科学数据,目前的治疗仍然是经验性的。