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West ÁõÈıº¿¡¼­ TopiramateÀÇ È¿°ú Efficacy of Topiramate in West Syndrome

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ÀÌÀαÔ, ±è¼º±¸, À̶õ, ±Ç¿µ¼¼, ÀÌÁ¾È­, äÁ¾Èñ, ±è±âÁß, Ȳ¿ë½Â,
¼Ò¼Ó »ó¼¼Á¤º¸
ÀÌÀαԠ( Lee In-Kyu ) 
ÀÎÇÏ´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç

±è¼º±¸ ( Kim Sung-Koo ) 
À»Áö´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
À̶õ ( Lee Ran ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
±Ç¿µ¼¼ ( Kwon Young-Se ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
ÀÌÁ¾È­ ( Lee Jong-Hwa ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
äÁ¾Èñ ( Chae Jong-Hee ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
±è±âÁß ( Kim Ki-Joong ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç
Ȳ¿ë½Â ( Hwang Yong-Seung ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ ¼Ò¾Æ°úÇб³½Ç

Abstract


Purpose: The treatment of West syndrome is difficult since current antiepileptic drugs are rarely effective. The objective of this study is to evaluate the clinical efficacy of topiramate as add-on therapy in the refractory West Syndrome.
Methods: Nineteen children with refractory infantile spasms were included in this study. Topiramate was given as an initial dose of 25 mg per day in addition to the current antiepileptic drug (s). Dosage was increased by 25 mg every week until spasms were controlled, the maximal tolerable dose was reached, or the maximal dose of 25 mg/kg/day was achieved.

Results: Five (26.3%) subjects became seizure free and 7 (36.8%) achieved seizure frequency reduction more than 50%. No significant side effect of topiramate was noted.

Conclusion: Topiramate could be a promising therapy in the treatment of refractory West syndrome.

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West ÁõÈıº
Topiramate; West syndrome; Topiramate

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KoreaMed
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