Sugama Michiko, Ishizaki Asayo
Oji Clinic, Division of Medicine, The Association of Remedial Teaching for People with Developmental Handicaps, Tokyo.
No To Hattatsu. 2009 Nov;41(6):436-41.
We switched medication from conventional immediate-release preparations of methylphenidate to extended-release tablets (an osmotic release oral system) in 165 of 181 cases with attention deficit/hyperactivity disorder (AD/HD), in accordance with the revised indications for these tablets. We investigated the types of developmental disorders, doses of the drug, efficacy, adverse effects, concomitant medication, other relevant problems, and so on, prior to switching the medications. The most common types of developmental disorders were AD/HD with symptoms of pervasive developmental disorder (PDD) and PDD with symptoms of AD/HD. The efficacy evaluation revealed that the extended release tablets had efficacy equivalent to or greater than that of the immediate release preparation. The efficacy rate was 82.7% in our patients. However, cases with difficulty ingesting the tablets, requiring small doses, and those over 18 years of age still seen in the pediatrics department, remained as problematic issues which require further consideration.
根据这些缓释片修订后的适应症,我们在181例注意力缺陷/多动障碍(AD/HD)患者中的165例中,将药物从常规速释哌甲酯制剂换成了缓释片(渗透泵控释口服系统)。在换药前,我们调查了发育障碍类型、药物剂量、疗效、不良反应、合并用药及其他相关问题等。最常见的发育障碍类型是伴有广泛性发育障碍(PDD)症状的AD/HD以及伴有AD/HD症状的PDD。疗效评估显示,缓释片的疗效等同于或优于速释制剂。我们患者中的有效率为82.7%。然而,存在片剂吞咽困难、需要小剂量用药的病例,以及18岁以上仍在儿科就诊的患者,仍是需要进一步考虑的问题。