ÁÖÀǷ°áÇÌ °úÀ×ÇൿÀå¾Ö ¾Æµ¿¿¡¼­ Osmotic-Controlled Release Oral Delivery System MethylphenidateÀÇ Ä¡·á¼øÀÀµµ
Treatment Adherence of Osmotic-Controlled Release Oral Delivery System Methylphenidate in Korean Children and Adolescents with Attention-Deficit Hyperactivity Disorder

Journal of the Korean Academy of Child and Adolescent Psychiatry 2014³â 25±Ç 2È£ p.65 ~ p.72

±èºÀ¼®(Kim Bong-Seog) - ÀÎÁ¦´ëÇб³ Àǰú´ëÇÐ »ó°è¹éº´¿ø Á¤½Å°Ç°­ÀÇÇб³½Ç
ÀÌÁ¤¼·(Lee Jung-Sub) - ÀÎÇÏ´ëÇб³ Àǰú´ëÇÐ Á¤½Å°Ç°­ÀÇÇб³½Ç
±èÀÇÁ¤(Kim Eui-Jung) - ÀÌÈ­¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø Á¤½Å°Ç°­ÀÇÇб³½Ç
¼ºÇü¸ð(Sung Hyung-Mo) - CHAÀǰúÇдëÇб³ ±¸¹ÌÂ÷º´¿ø Á¤½Å°Ç°­ÀÇÇб³½Ç
½ÅÀ±¹Ì(Shin Yun-Mi) - ¾ÆÁÖ´ëÇб³ Àǰú´ëÇÐ Á¤½Å°Ç°­ÀÇÇб³½Ç
Ȳ¼ºÇý(Hwang Seong-Hye) - Çؼö¼ÒÁßÇѾÆÀÌÁ¤½Å°úÀÇ¿ø
À¯ÇÑÀÍ(Yoo Han-Ik) - ¼­¿ï³ú°úÇבּ¸¼Ò

Abstract

Objectives£ºThe objective of this study was to evaluate the treatment duration and adherence of osmotic-controlled release oral delivery system (OROS) methylphenidate for treatment of attention-deficit hyperactivity disorder (ADHD).

Methods£º A total of 843 children with ADHD were recruited : 213 children (25.3%) who had previously taken medications for ADHD and 630 drug-naive children (74.7%) were recruited. The dosage was adjusted according to the clinician¡¯s judgment. The primary efficacy endpoint of this study was treatment retention rate, which was estimated at Week 12 and Week 20 using the Kaplan-Meier curve. The Swanson, Nolan and Pelham-IV (SNAP-IV), Clinical Global Impression-Severity (CGI-S), Clinical Global Impression-Improvement, and the side effect rating scale were measured at every visit. Remission rates were presented based on SNAP-IV and CGI-S, respectively.

Results£º The treatment retention rate at 12 weeks and at 20 weeks was 76.2% and 66.8%, respectively. Divided according to 6?8, 9?11, 12?14 and 15?18 years of age, younger children tended to show a statistically higher treatment retention rate (p=.02). Based on SNAP-IV and CGI scores, children with better response to medication showed tendencies of statistically higher treatment retention rate. The most common adverse events included loss of appetite (7.1%) and insomnia (3.3%). There was no serious adverse event related to the treatment, such as death.

Conclusion£º The use of OROS methylphenidate for treatment of ADHD was safe and tolerable for children. In this study, lower age and better treatment response showed a statistically significant relationship with higher treatment adherence. Boys showed a trend of high treatment adherence. The treatment adherence at 20 weeks was satisfactory, however, the treatment adherence after 20 weeks showed a sharp decrease. Therefore, treatment persistence for six months after the beginning of ADHD treatment is important. In addition, the positive role of psycho-education for children and parents is necessary for increasing treatment adherence.

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ADHD, Treatment Adherence, OROS Methylphenidate
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