Medical therapy of epilepsy: When to initiate treatment and when to combine?

被引:28
作者
Brodie, MJ [1 ]
机构
[1] Univ Glasgow, Western Infirm, Epilepsy Unit, Glasgow G11 6NT, Lanark, Scotland
关键词
epilepsy; treatment; antiepileptic drugs; strategy;
D O I
10.1007/s00415-005-0735-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Most patients reporting more than one well-documented or witnessed seizure require prophylactic antiepileptic (AED) therapy. Those with an underlying brain disorder and/or an abnormal electroencephalogram should probably be treated after their first event. The goal should be maintenance of a normal lifestyle by complete seizure control with no or minimal side-effects. Failure of the first AED due to lack of efficacy implies refractoriness. A policy of consecutive substitutions is unlikely to be an effective strategy. Thus, if the first or second monotherapy improves control but does not produce seizure freedom, an AED with different and perhaps multiple mechanisms of action should be added. Strategies for combining drugs should involve individual assessment of patient-related factors, including seizure type and epilepsy syndrome classifications coupled with an understanding of the pharmacology, side-effects and interaction profile of the AEDs. Reducing the dose of one or more AEDs may help accommodate the introduction of a second or third drug. An orderly approach to the pharmacological management and, when appropriate, surgical investigations for each epilepsy syndrome will optimise the chance of perfect seizure control and help more people achieve safer and more fulfilled lives.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 36 条
[1]   Adjunctive therapy versus alternative monotherapy in patients with partial epilepsy failing on a single drug: a multicentre, randomised, pragmatic controlled trial [J].
Beghi, E ;
Gatti, G ;
Tonini, C ;
Ben-Menachem, E ;
Chadwick, DW ;
Nikanorova, M ;
Gromov, SA ;
Smith, PEM ;
Specchio, LM ;
Perucca, E .
EPILEPSY RESEARCH, 2003, 57 (01) :1-13
[2]   How long does it take for partial epilepsy to become intractable? [J].
Berg, AT ;
Langfitt, J ;
Shinnar, S ;
Vickrey, BG ;
Sperling, MR ;
Walczak, T ;
Bazil, C ;
Pacia, SV ;
Spencer, SS .
NEUROLOGY, 2003, 60 (02) :186-190
[3]   THE RISK OF SEIZURE RECURRENCE FOLLOWING A 1ST UNPROVOKED SEIZURE - A QUANTITATIVE REVIEW [J].
BERG, AT ;
SHINNAR, S .
NEUROLOGY, 1991, 41 (07) :965-972
[4]  
Brodie M.J., 2002, NEUROLOGY S5, V58, P2
[5]   Management of epilepsy in adolescents and adults [J].
Brodie, MJ ;
French, JA .
LANCET, 2000, 356 (9226) :323-329
[6]   Success or failure with antiepileptic drug therapy - Beyond empiricism? [J].
Brodie, MJ ;
Leach, JP .
NEUROLOGY, 2003, 60 (02) :162-163
[7]   Lamotrigine substitution study: Evidence for synergism with sodium valproate? [J].
Brodie, MJ ;
Yuen, AWC .
EPILEPSY RESEARCH, 1997, 26 (03) :423-432
[8]   The Star Systems - Overview and use in determining antiepileptic drug choice [J].
Brodie, MJ ;
Kwan, P .
CNS DRUGS, 2001, 15 (01) :1-12
[9]   Reappraisal of polytherapy in epilepsy: A critical review of drug load and adverse effects [J].
Deckers, CLP ;
Hekster, YA ;
Keyser, A ;
Meinardi, H ;
Renier, WO .
EPILEPSIA, 1997, 38 (05) :570-575
[10]   Selection of antiepileptic drug polytherapy based on mechanisms of action: The evidence reviewed [J].
Deckers, CLP ;
Czuczwar, SJ ;
Hekster, YA ;
Keyser, A ;
Kubova, H ;
Meinardi, H ;
Patsalos, PN ;
Renier, WO ;
Van Rijn, CM .
EPILEPSIA, 2000, 41 (11) :1364-1374