Roh Hyosung, Kim Bongseog
Department of Psychiatry, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Korea.
Soa Chongsonyon Chongsin Uihak. 2021 Jan 1;32(1):10-16. doi: 10.5765/jkacap.200024.
The aim of this study was to compare the compliance, efficacy, and satisfaction associated with methylphenidate and atomoxetine for treating attention-deficit/hyperactivity disorder (ADHD).
The subjects were 44 patients who met the Diagnostic and Statistical Manual of Mental Disorder-5 diagnostic criteria for ADHD and were treated with methylphenidate or atomoxetine. The methylphenidate formulations included immediate release (IR), extended release (ER), and osmotic-controlled release oral delivery system (OROS). Patients and parents reported the average number of days per week the medication was taken. Efficacy was assessed using the ADHD Rating Scale. Satisfaction with medication scale (SAMS)-parent report form and SAMS-self-report form were used to evaluate parents' and patients' satisfaction, respectively.
Patients and parents were more satisfied with methylphenidate than with atomoxetine. There were no significant differences in the compliance with and efficacy of methylphenidate and atomoxetine. Compliance with methylphenidate IR and ER was markedly lower than that with OROS methylphenidate or atomoxetine.
Methylphenidate OROS formulation can be considered a suitable option given its high rates of compliance, satisfaction, and efficacy.
本研究旨在比较哌甲酯和托莫西汀治疗注意力缺陷多动障碍(ADHD)的依从性、疗效和满意度。
研究对象为44例符合《精神疾病诊断与统计手册》第5版ADHD诊断标准并接受哌甲酯或托莫西汀治疗的患者。哌甲酯制剂包括速释(IR)、缓释(ER)和渗透控释口服给药系统(OROS)。患者和家长报告每周服用药物的平均天数。使用ADHD评定量表评估疗效。分别使用药物满意度量表(SAMS)家长报告表和SAMS自我报告表评估家长和患者的满意度。
患者和家长对哌甲酯的满意度高于托莫西汀。哌甲酯和托莫西汀在依从性和疗效方面无显著差异。哌甲酯IR和ER的依从性明显低于OROS哌甲酯或托莫西汀。
鉴于其高依从性、满意度和疗效,OROS哌甲酯制剂可被视为一种合适的选择。