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Society for Developmental and Behavioral Pediatrics Clinical Practice Guideline for the Assessment and Treatment of Children and Adolescents with Complex Attention-Deficit/Hyperactivity Disorder.发育行为儿科学会关于儿童和青少年复杂注意缺陷多动障碍评估和治疗的临床实践指南。
J Dev Behav Pediatr. 2020 Feb/Mar;41 Suppl 2S:S35-S57. doi: 10.1097/DBP.0000000000000770.
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Pharmacokinetics of AR19, an Immediate-Release Amphetamine Sulfate Formulation Designed to Deter Manipulation for Administration Via Nonoral Routes: Bioequivalence to Reference Racemic Amphetamine Sulfate, Dose Proportionality, and Food Effect.AR19 的药代动力学:一种旨在防止通过非口服途径给药的速释硫酸安非他命制剂,与参比消旋硫酸安非他命具有生物等效性、剂量比例和食物效应。
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An update on the pharmacokinetic considerations in the treatment of ADHD with long-acting methylphenidate and amphetamine formulations.长效哌甲酯和苯丙胺制剂治疗 ADHD 的药代动力学考虑因素的最新进展。
Expert Opin Drug Metab Toxicol. 2019 Nov;15(11):937-974. doi: 10.1080/17425255.2019.1675636. Epub 2019 Nov 8.
4
Clinical Practice Guideline for the Diagnosis, Evaluation, and Treatment of Attention-Deficit/Hyperactivity Disorder in Children and Adolescents.儿童和青少年注意缺陷多动障碍的诊断、评估和治疗临床实践指南。
Pediatrics. 2019 Oct;144(4). doi: 10.1542/peds.2019-2528.
5
A Randomized, Double-Blind, Placebo-Controlled Study of HLD200, a Delayed-Release and Extended-Release Methylphenidate, in Children with Attention-Deficit/Hyperactivity Disorder: An Evaluation of Safety and Efficacy Throughout the Day and Across Settings.一项随机、双盲、安慰剂对照研究评估 HLD200(一种控释和缓释哌甲酯)治疗注意缺陷多动障碍儿童的安全性和疗效:全天和跨环境的评估。
J Child Adolesc Psychopharmacol. 2020 Feb;30(1):2-14. doi: 10.1089/cap.2019.0070. Epub 2019 Aug 29.
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Pharmacokinetics of HLD200, a Delayed-Release and Extended-Release Methylphenidate: Evaluation of Dose Proportionality, Food Effect, Multiple-Dose Modeling, and Comparative Bioavailability with Immediate-Release Methylphenidate in Healthy Adults.HLD200的药代动力学,一种缓释和长效释放的哌甲酯:在健康成年人中评价剂量比例、食物影响、多剂量模型以及与速释哌甲酯的比较生物利用度。
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7
A randomized, double-blind, 3-way crossover, analog classroom study of SHP465 mixed amphetamine salts extended-release in adolescents with ADHD.一项关于 SHP465 混合安非他命硫酸盐缓释剂在 ADHD 青少年中应用的随机、双盲、三向交叉、模拟课堂研究。
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Early-Onset Efficacy and Safety Pilot Study of Amphetamine Extended-Release Oral Suspension in the Treatment of Children with Attention-Deficit/Hyperactivity Disorder.苯丙胺缓释口服混悬液治疗儿童注意缺陷多动障碍的早期疗效与安全性初步研究
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Trends in attention-deficit hyperactivity disorder medication use: a retrospective observational study using population-based databases.注意缺陷多动障碍药物使用趋势:一项基于人群数据库的回顾性观察研究
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Comparative efficacy and tolerability of medications for attention-deficit hyperactivity disorder in children, adolescents, and adults: a systematic review and network meta-analysis.儿童、青少年和成人注意力缺陷多动障碍药物治疗的疗效和耐受性比较:一项系统评价和网状Meta分析
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注意力缺陷多动障碍药物的新型制剂:兴奋剂的选择与管理

Novel Formulations of ADHD Medications: Stimulant Selection and Management.

作者信息

Childress Ann C

机构信息

Center for Psychiatry and Behavioral Medicine, Inc., Las Vegas.

出版信息

Focus (Am Psychiatr Publ). 2021 Jan;19(1):31-38. doi: 10.1176/appi.focus.20200032. Epub 2021 Jan 25.

DOI:10.1176/appi.focus.20200032
PMID:34483764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8412159/
Abstract

Attention-deficit hyperactivity disorder (ADHD) is the most commonly diagnosed psychiatric disorder in children and adolescents in the United States. In 2016, approximately 3.8 million U.S. children ages 2 to 17 years with ADHD were being treated with medication. There are approximately 30 different amphetamine (AMPH) and methylphenidate (MPH) formulations on the market. These include immediate-release and extended-release compounds. The extended-release formulations contain various ratios of immediate-release and extended-release components, which determine the pharmacokinetic (PK) profile. For stimulants, the PK and pharmacodynamic (PD) profiles are tightly linked, and the immediate-release and extended-release percentages influence onset and duration of drug effects. Choosing the right stimulant medication for a patient depends on an understanding of the PK/PD profile, the time of day that symptoms are most impairing, the need for morning and evening symptom control and individual patient preferences.

摘要

注意力缺陷多动障碍(ADHD)是美国儿童和青少年中最常被诊断出的精神疾病。2016年,约380万年龄在2至17岁的美国ADHD儿童正在接受药物治疗。市场上大约有30种不同的苯丙胺(AMPH)和哌甲酯(MPH)制剂。这些制剂包括速释和缓释化合物。缓释制剂含有不同比例的速释和缓释成分,这决定了药代动力学(PK)特征。对于兴奋剂而言,PK和药效学(PD)特征紧密相连,速释和缓释的百分比会影响药物作用的起效时间和持续时间。为患者选择合适的兴奋剂药物取决于对PK/PD特征的了解、症状最严重的时间段、早晚症状控制的需求以及患者的个人偏好。