Cognitive outcome of antiepileptic treatment with levetiracetam versus carbamazepine monotherapy: A non-interventional surveillance trial

被引:47
作者
Helmstaedter, Christoph [1 ]
Witt, Jun-Alexander [1 ]
机构
[1] Univ Bonn, Univ Clin Epileptol Bonn, D-53105 Bonn, Germany
关键词
Levetiracetam; Carbamazepine; Monotherapy; Cognition; Neuropsychology; Quality of life; Cognitive outcome; Memory; Executive functions; Epilepsy; REFRACTORY PARTIAL SEIZURES; IDIOPATHIC GENERALIZED EPILEPSY; QUALITY-OF-LIFE; ADD-ON THERAPY; DOUBLE-BLIND; TERM TREATMENT; DRUGS; MULTICENTER; IMPROVEMENT; ATTENTION;
D O I
10.1016/j.yebeh.2010.02.011
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
010107 [宗教学]; 030301 [社会学]; 070906 [古生物学及地层学(含古人类学)];
摘要
This open-label, non-interventional, controlled surveillance study evaluated the cognitive outcome of patients administered levetiracetam (LEV) or carbamazepine (CBZ) monotherapy as primary treatment or as substitution for previous treatment. Executive functions, verbal memory, and subjective ratings were assessed before and 6 months after initiation of LEV or CBZ monotherapy. Analyses included 498 patients: 370 received LEV (63% pretreated), and 128 CBZ (34% pretreated). Mostly because of the substitution condition, the seizure freedom rate was slightly higher with LEV as opposed to CBZ (78% vs 69%). Almost all cognitive measures improved with LEV but not with CBZ, and repeated-measures MANOVA did not indicate seizure control or pretreatment as decisive with respect to cognitive change. With LEV, executive functions improved in 15% and deteriorated in 5% of patients; the opposite pattern was seen under CBZ (improvement with LEV OR = 2.3, deterioration with CBZ OR = 3.4). The findings suggest a mild but definitely superior cognitive outcome with LEV as opposed to CBZ monotherapy. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:74 / 80
页数:7
相关论文
共 33 条
[1]
Newer antiepileptic drugs and cognitive issues [J].
Aldenkamp, AP ;
De Krom, M ;
Reijs, R .
EPILEPSIA, 2003, 44 :21-29
[2]
Efficacy and tolerability of levetiracetam 3000 mg/d in patients with refractory partial seizures: A multicenter, double-blind, responder-selected study evaluating monotherapy [J].
Ben-Menachem, E ;
Falter, T .
EPILEPSIA, 2000, 41 (10) :1276-1283
[3]
Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy [J].
Berkovic, S. F. ;
Knowlton, R. C. ;
Leroy, R. F. ;
Schiemann, J. ;
Falter, U. .
NEUROLOGY, 2007, 69 (18) :1751-1760
[4]
Comparison of levetiracetam and controlled-release carbamazepine in newly diagnosed epilepsy [J].
Brodie, M. J. ;
Perucca, E. ;
Ryvlin, P. ;
Ben-Menachem, E. ;
Meencke, H. -J. .
NEUROLOGY, 2007, 68 (06) :402-408
[5]
Levetiracetam for partial seizures - Results of a double-blind, randomized clinical trial [J].
Cereghino, JJ ;
Biton, V ;
Abou-Khalil, B ;
Dreifuss, F ;
Gauer, LJ ;
Leppik, I .
NEUROLOGY, 2000, 55 (02) :236-242
[6]
Neuropsychological and psychiatric impact of add-on titration of pregabalin versus levetiracetam: A comparative short-term study [J].
Ciesielski, Anne-Sophie ;
Samson, Severine ;
Steinhoff, Bernhard J. .
EPILEPSY & BEHAVIOR, 2006, 9 (03) :424-431
[7]
Maintenance of improvement in health-related quality of life during long-term treatment with levetiracetam [J].
Cramer, JA ;
Van Hammée, G .
EPILEPSY & BEHAVIOR, 2003, 4 (02) :118-123
[8]
Folker Henrik, 2008, Ugeskr Laeger, V170, P830
[9]
A systematic review of the safety profile of levetiracetam: a new antiepileptic drug [J].
French, J ;
Edrich, P ;
Cramer, JA .
EPILEPSY RESEARCH, 2001, 47 (1-2) :77-90
[10]
When antiepileptic drugs aggravate epilepsy [J].
Genton, P .
BRAIN & DEVELOPMENT, 2000, 22 (02) :75-80