Remission in Children and Adolescents Diagnosed with Attention-Deficit/Hyperactivity Disorder via an Effective and Tolerable Titration Scheme for Osmotic Release Oral System Methylphenidate

被引:18
作者
Chou, Wen-Jiun [2 ]
Chen, Shin-Jaw [3 ]
Chen, Ying-Sheue [1 ]
Liang, Hsin-Yi [4 ]
Lin, Chih-Chien [5 ]
Tang, Ching-Shu [2 ]
Huang, Yu-Shu [4 ]
Yeh, Chin-Bin [6 ]
Chou, Miao-Chun [2 ]
Lin, Dai-Yueh [1 ]
Hou, Po-Hsun [5 ]
Wu, Yu-Yu [4 ]
Liu, Hung-Jen [1 ]
Huang, Ya-Fen [4 ]
Hwang, Kai-Ling [1 ]
Chan, Chin-Hong [5 ]
Pan, Chia-Ho [1 ]
Chang, Hsueh-Ling [4 ]
Huang, Chi-Fen [4 ]
Hsu, Ju-Wei [1 ]
机构
[1] Natl Yang Ming Univ, Taipei Vet Gen Hosp, Dept Psychiat, Taipei 112, Taiwan
[2] Chang Gung Univ, Chang Gung Mem Hosp, Kaohsiung Med Ctr, Dept Child Psychiat,Coll Med, Kaohsiung, Taiwan
[3] Dr Yins Clin, Tainan, Taiwan
[4] Chang Gung Univ, Chang Gung Mem Hosp, Dept Child Psychiat, Linkou Med Ctr,Coll Med, Tao Yuang, Taiwan
[5] Taichung Vet Gen Hosp, Dept Psychiat, Taichung, Taiwan
[6] Triserv Gen Hosp, Dept Psychiat, Taipei, Taiwan
关键词
DEFICIT HYPERACTIVITY DISORDER; DAILY ATOMOXETINE TREATMENT; FOLLOW-UP; OPEN-LABEL; OROS(R) METHYLPHENIDATE; PSYCHIATRIC-DISORDERS; CONDUCT PROBLEMS; DOSE-RESPONSE; DOUBLE-BLIND; ADHD;
D O I
10.1089/cap.2011.0006
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives: The purpose of this study was to identify the optimal dose of osmotic release oral system methylphenidate (OROS-MPH) using a dosage forced-titration scheme to achieve symptomatic remission in children with attention-deficit/hyperactivity disorder (ADHD). We also evaluated the efficacy and safety of, and patient and parent satisfaction with, the change in therapy from immediate-release methylphenidate (IR-MPH) to OROS-MPH over 10 weeks. Method: We recruited 521 children and adolescents aged 6-18 years with an American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders, 4th ed. (DSM-IV) diagnosis of ADHD, who had received IR-MPH treatments (< 70mg/day) for at least 1 month. The treatment, switched from IR-MPH to OROS-MPH according to a conversion scheme, started with a 6-week forced-titration phase of OROS-MPH to achieve symptomatic remission (defined as a score of 0 or 1 for each of the first 18 ADHD items in the Chinese version of the Swanson, Nolan, and Pelham, Version IV [SNAP-IV]), followed by a 4-week maintenance phase. The global ADHD severity and drug side effects of the participants were evaluated. Parents completed the ratings scales for the ADHD-related symptoms. Patient and parent satisfaction for the OROS-MPH treatment was also assessed. Results: Among the 439 participants with ADHD who completed the trial, 290 participants (66.1%) achieved symptomatic remission. The mean dose of OROS-MPH among participants in remission was 36.7 mg (1.08 mg/kg) per day. Increased efficacy, superior satisfaction, and safety equivalent to that of IR-MPH were demonstrated in intra-individual comparisons from the baseline to the end of study. Determinants for remission included less severe ADHD symptoms (SNAP-IV score < 40), no family history of ADHD, and an appropriate dosage of medication according to the patient's weight. Conclusions: The findings suggest remission as a treatment goal for ADHD therapy by providing an optimal dosage of medication for children and adolescents with ADHD through using an effective and tolerable forced-titration scheme.
引用
收藏
页码:215 / 225
页数:11
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