Pharmacologic Treatment of Intractable Epilepsy in Children: A Syndrome-Based Approach

被引:5
作者
Hussain, Shaun [1 ]
Sankar, Raman [1 ]
机构
[1] Univ Calif Los Angeles, Mattel Childrens Hosp, Ctr Hlth Sci, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
LANDAU-KLEFFNER-SYNDROME; IDIOPATHIC GENERALIZED EPILEPSY; ELECTRICAL STATUS EPILEPTICUS; SEVERE MYOCLONIC EPILEPSY; LENNOX-GASTAUT-SYNDROME; CHANNEL ALPHA-1-SUBUNIT MUTATIONS; LAMOTRIGINE ADJUNCTIVE THERAPY; BENIGN CHILDHOOD EPILEPSY; TYPICAL ABSENCE SEIZURES; NEURONAL SODIUM-CHANNEL;
D O I
10.1016/j.spen.2011.06.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
The successful pharmacologic treatment of intractable childhood epilepsy is predicated upon an accurate classification of the epilepsy syndrome. The selection of an antiepileptic drug is facilitated by the knowledge of syndrome-specific efficacy, the anticipation of potential side effects, and a careful risk-benefit assessment tailored to each patient. As such, the identification of comorbidities and careful monitoring for treatment-emergent adverse events, especially cognitive and behavioral effects, is of utmost importance. Especially in refractory cases, polypharmacy may increase the likelihood of side effects, but carefully chosen combinations can result in synergistic benefit. For most epilepsy syndromes, newer antiepileptic drugs typically yield equivalent efficacy and superior tolerability. Nevertheless, continued research is needed to further contrast the syndrome-specific efficacy and tolerability of available drugs and to foster the development of new agents with superior efficacy and side effect profiles. Semin Pediatr Neurol 18:171-178 (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:171 / 178
页数:8
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