Zonisamide in pediatric epilepsy: Re-view of the Japanese experience

被引:59
作者
Glauser, TA
Pellock, JM
机构
[1] Childrens Hosp, Med Ctr, Dept Neurol, Childrens Comprehens Epilepsy Program, Cincinnati, OH 45229 USA
[2] Virginia Commonwealth Univ, Med Coll Virginia, Comprehens Epilepsy Inst, Div Child Neurol, Richmond, VA 23298 USA
关键词
D O I
10.1177/088307380201700201
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Zonisamide is a novel anticonvulsant that is structurally and mechanistically unique, compared with other antiepilepsy drugs. Available in Japan and South Korea since 1989, it was approved in the United States in the year 2000 as adjunctive therapy for partial seizures in adults. There has been extensive clinical trial and clinical practice experience with zonisamide therapy in Japanese children. Open-label data from pediatric clinical trials conducted in Japan suggest that zonisamide is well tolerated and effective against partial- and generalized-onset seizures in children. Despite this wealth of open-label data, no formal pharmacokinetic studies and only one well-controlled trial of zonisamide's efficacy and safety in Japanese children have been completed to date. No controlled clinical trials of zonisamide in children have been completed in the United States or Europe. Additional controlled trials in children with partial- or generalized-onset seizures, infantile spasms, and Lennox-Gastaut syndrome axe warranted to further delineate zonisamide's broad spectrum of efficacy and tolerability in children.
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页码:87 / 96
页数:10
相关论文
共 65 条
[1]   ETHNIC-DIFFERENCES IN THE PHARMACOKINETICS OF ORAL NIFEDIPINE [J].
AHSAN, CH ;
RENWICK, AG ;
MACKLIN, B ;
CHALLENOR, VF ;
WALLER, DG ;
GEORGE, CF .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1991, 31 (04) :399-403
[2]   Rifampin drastically reduces plasma concentrations and effects of oral midazolam [J].
Backman, JT ;
Olkkola, KT ;
Neuvonen, PJ .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 59 (01) :7-13
[3]  
Blum D E, 1998, Adv Neurol, V76, P57
[4]   An overview of the efficacy and tolerability of new antiepileptic drugs [J].
Chadwick, DW .
EPILEPSIA, 1997, 38 :S59-S62
[5]  
CHADWICK DW, 1996, EPILEPSIA S4, V37, P6
[6]   GENETICALLY-DETERMINED VARIABILITY IN ACETYLATION AND OXIDATION - THERAPEUTIC IMPLICATIONS [J].
CLARK, DWJ .
DRUGS, 1985, 29 (04) :342-375
[7]   METABOLIC POLYMORPHISMS [J].
DALY, AK ;
CHOLERTON, S ;
GREGORY, W ;
IDLE, JR .
PHARMACOLOGY & THERAPEUTICS, 1993, 57 (2-3) :129-160
[8]   AGE-DEPENDENT DOSE-RESPONSE TO GENTAMICIN [J].
ECHEVERRIA, P ;
SIBER, GR ;
PAISLEY, J ;
SMITH, AL ;
SMITH, DH ;
JAFFE, N .
JOURNAL OF PEDIATRICS, 1975, 87 (05) :805-808
[9]  
*EL PHARM, 2000, ZON PACK INS
[10]   New drugs for the treatment of epilepsy [J].
Fraser, AD .
CLINICAL BIOCHEMISTRY, 1996, 29 (02) :97-110