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首页> 外文期刊>Child and adolescent mental health >Early identification of stimulant treatment responders, partial responders and non-responders using objective measures in children and adolescents with hyperkinetic disorder
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Early identification of stimulant treatment responders, partial responders and non-responders using objective measures in children and adolescents with hyperkinetic disorder

机译:使用客观测量方法早期识别兴奋性治疗反应者,部分反应者和非反应者,用于多动症儿童和青少年

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摘要

Background: The aim of this study was to evaluate stimulant medication response following a single dose of methylphenidate (MPH) in children and young people with hyperkinetic disorder using infrared motion analysis combined with a continuous performance task (QbTest system) as objective measures. The hypothesis was put forward that a moderate testdose of stimulant medication could determine a robust treatment response, partial response and non-response in relation to activity, attention and impulse control measures. Methods: The study included 44 children and young people between the ages of 7-18 years with a diagnosis of hyperkinetic disorder (F90 & F90.1). A single dose-protocol incorporated the time course effects of both immediate release MPH and extended-release MPH (Concerta XL, Equasym XL) to determine comparable peak efficacy periods post intake. Results: A robust treatment response with objective measures reverting to the population mean was found in 37 participants (84%). Three participants (7%) demonstrated a partial response to MPH and four participants (9%) were determined as non-responders due to deteriorating activity measures together with no improvements in attention and impulse control measures. Conclusion: Objective measures provide early into prescribing the opportunity to measure treatment response and monitor adverse reactions to stimulant medication. Most treatment responders demonstrated an effective response to MPH on a moderate testdose facilitating a swift and more optimal titration process.
机译:背景:本研究的目的是使用红外运动分析结合连续执行任务(QbTest系统)作为客观指标,评估单剂量哌醋甲酯(MPH)对运动亢进症儿童和青少年的兴奋性药物反应。提出了这样的假设:适量的兴奋剂药物可以在活动,注意力和冲动控制措施方面确定强有力的治疗反应,部分反应和无反应。方法:该研究包括44名年龄在7-18岁之间的儿童和青少年,他们被诊断为运动过度障碍(F90和F90.1)。单一剂量方案结合了立即释放MPH和延长释放MPH(Concerta XL,Equasym XL)的时程效应,以确定摄入后可比较的峰值疗效期。结果:在37名参与者(84%)中发现了强有力的治疗反应,客观指标恢复了人群平均值。三名参与者(7%)表现出对MPH的部分反应,四名参与者(9%)由于活动措施恶化且注意力和冲动控制措施未得到改善而被确定为无反应者。结论:客观的措施为早期规定了衡量治疗反应和监测对兴奋药物不良反应的机会。大多数治疗反应者在中等剂量下表现出对MPH的有效反应,从而促进了更快,更理想的滴定过程。

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