Steele Margaret, Weiss Margaret, Swanson James, Wang Jenny, Prinzo Rosanna S, Binder Carin E
Department of Psychiatry, Pediatrics and Family Medicine, University of Western Ontario, London, ON.
Can J Clin Pharmacol. 2006 Winter;13(1):e50-62. Epub 2006 Jan 23.
The thrice daily dosing regimen of immediate release methylphenidate (IR-MPH) for Attention Deficit/Hyperactivity Disorder (ADHD) requires in-school dosing, leading to issues surrounding dispensing and storage of controlled substances by school personnel and concerns over children?s privacy and the embarrassment associated with taking medication in public at school. OROS-methylphenidate (OROS-MPH) is a once-daily controlled-release formulation of methylphenidate (MPH) developed to overcome some of the limitations associated with IR-MPH and first-generation sustained-release formulations. Randomized, controlled trials (RCTs) that focus on treatment efficacy provide the best evidence for demonstrating whether an intervention works, but under ideal conditions one cannot discount the importance of efficacy study results. However, the most useful information to clinicians comes from an effectiveness study design.
To evaluate the effectiveness and tolerability of OROS-MPH versus usual care with IR-MPH in children aged 6 to 12 years with ADHD.
This 8 week, multicentre, open-label study randomized 147 subjects to either once-daily OROS-MPH or usual care with IR-MPH. Subjects were titrated to a clinically effective dose of either study medication over 4 weeks and maintained on that dose for an additional 4 weeks. The SNAP-IV parent-rating scale was used to assess effectiveness.
OROS-MPH showed statistically significant superiority to IR-MPH in remission rate based on the 18 ADHD symptoms (p=0.0002, X2=13.8, df=1) and severity of ADHD and ODD symptoms (p=0.004, F=8.4, df=1,127), as well as on the following secondary assessments: IOWA Conners, Conners Parent Rating Scale (short version), Parent Stress Index, (short version); Visual Analogue Scale for social play; Clinical Global Impression-Severity, Clinical Global Impression-Improvement and Parent Satisfaction with treatment. OROS-MPH and IR-MPH were both well tolerated with a similar side effect profile.
Once-daily OROS-MPH is significantly more effective than usual care with IR-MPH based on multiple outcome measures including remission rate.
用于治疗注意力缺陷多动障碍(ADHD)的速释哌甲酯(IR-MPH)每日三次给药方案需要在学校给药,这引发了学校工作人员在受控物质的配药和储存方面的问题,以及对儿童隐私和在学校当众服药带来的尴尬的担忧。盐酸哌甲酯控释片(OROS-MPH)是一种每日一次的哌甲酯控释制剂,旨在克服与IR-MPH和第一代缓释制剂相关的一些局限性。关注治疗效果的随机对照试验(RCT)为证明一种干预措施是否有效提供了最佳证据,但在理想条件下,人们不能忽视疗效研究结果的重要性。然而,对临床医生最有用的信息来自有效性研究设计。
评估OROS-MPH与IR-MPH常规治疗对6至12岁ADHD儿童的有效性和耐受性。
这项为期8周的多中心开放标签研究将147名受试者随机分为每日一次的OROS-MPH组或IR-MPH常规治疗组。受试者在4周内滴定至两种研究药物的临床有效剂量,并在该剂量下再维持4周。使用SNAP-IV家长评定量表评估有效性。
基于18种ADHD症状(p=0.0002,X2=13.8, df=)、ADHD和对立违抗障碍(ODD)症状的严重程度(p=0.004,F=8.4, df=1,127),以及以下次要评估指标:爱荷华康纳斯量表、康纳斯家长评定量表(简版)、家长压力指数(简版);社交游戏视觉模拟量表;临床总体印象-严重程度、临床总体印象-改善程度以及家长对治疗满意度,OROS-MPH显示出在缓解率方面显著优于IR-MPH。OROS-MPH和IR-MPH耐受性均良好,副作用特征相似。
基于包括缓解率在内的多项结果指标,每日一次的OROS-MPH比IR-MPH常规治疗显著更有效。