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