Lamotrigine monotherapy compared with carbamazepine, phenytoin, or valproate monotherapy in patients with epilepsy

被引:45
作者
Kaminow, L [1 ]
Schimschock, JR
Hammer, AE
Vuong, A
机构
[1] Maine Neurol, Scarborough, ME USA
[2] GlaxoSmithKline, Res Triangle Pk, NC USA
关键词
lamotrigine; epilepsy; valproate; carbamazepine; monotherapy;
D O I
10.1016/j.yebeh.2003.08.033
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
03 [法学]; 0303 [社会学]; 030303 [人类学]; 04 [教育学]; 0402 [心理学];
摘要
Objective. This open-label study evaluated the efficacy and tolerability of lamotrigine monotherapy compared with monotherapy with conventional antiepileptic drugs in patients converting from previous monotherapy because of inadequate seizure control or unacceptable side effects. Methods. This study was conducted in 26 neurology clinics and epilepsy centers throughout the United States. The study enrolled 115 patients with epilepsy converting from previous monotherapy because of inadequate seizure control or unacceptable side effects. Patients were randomized 1: 1 to receive 24 weeks of lamotrigine monotherapy or monotherapy with a conventional antiepileptic drug (carbamazepine, phenytoin, or valproate based on physician's choice). Patients were converted during an less than or equal to8-week Escalation/Taper Phase from their prestudy antiepileptic drug (carbamazepine, phenytoin, or valproate) to lamotrigine via a protocol-specified dosing algorithm or to conventional therapy via standard dosing guidelines. After monotherapy was achieved, patients continued in the study for a 24-week Maintenance Phase. Results. More lamotrigine patients (65%) than conventional therapy patients (57%) completed the 24-week Maintenance Phase (primary efficacy endpoint). The mean time to withdrawal from the study was 175 days (SD = 83.1) for lamotrigine patients compared with 156 days (SD = 80.7) for conventional therapy patients. Adverse events, the most common reason for discontinuing the Maintenance Phase, accounted for 16% of withdrawals among lamotrigine patients compared with 26% of withdrawals among conventional therapy patients. The mean reduction in seizure frequency was 53% (SD = 55.1) for patients using lamotrigine compared with 32% (SD = 149.9) for patients using conventional therapy. Humanistic measures including investigator global assessment, the patient self-assessment, and QOLIE-31 scores show that lamotrigine monotherapy was perceived by both physicians and patients to have benefits over monotherapy with conventional antiepileptic drugs. Conclusions. Converting from monotherapy with a less effective or poorly tolerated conventional antiepileptic drug to monotherapy with lamotrigine is associated with better clinical and humanistic outcomes than converting to an alternative conventional antiepileptic drug. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:659 / 666
页数:8
相关论文
共 25 条
[1]
[2]
DOUBLE-BLIND CROSSOVER TRIAL OF LAMOTRIGINE (LAMICTAL) AS ADD-ON THERAPY IN INTRACTABLE EPILEPSY [J].
BINNIE, CD ;
DEBETS, RMC ;
ENGELSMAN, M ;
MEIJER, JWA ;
MEINARDI, H ;
OVERWEG, J ;
PECK, AW ;
VANWIERINGEN, A ;
YUEN, WC .
EPILEPSY RESEARCH, 1989, 4 (03) :222-229
[3]
Weight change associated with valproate and lamotrigine monotherapy in patients with epilepsy [J].
Biton, V ;
Mirza, W ;
Montouris, G ;
Vuong, A ;
Hammer, AE ;
Barrett, PS .
NEUROLOGY, 2001, 56 (02) :172-177
[4]
Controlled trial of lamotrigine (Lamictal(R)) for treatment-resistant partial seizures [J].
Boas, J ;
Dam, M ;
Friis, ML ;
Kristensen, O ;
Pedersen, B ;
Gallagher, J .
ACTA NEUROLOGICA SCANDINAVICA, 1996, 94 (04) :247-252
[5]
DOUBLE-BLIND COMPARISON OF LAMOTRIGINE AND CARBAMAZEPINE IN NEWLY-DIAGNOSED EPILEPSY [J].
BRODIE, MJ ;
RICHENS, A ;
YUEN, AWC .
LANCET, 1995, 345 (8948) :476-479
[6]
Multicentre, double-blind, randomised comparison between lamotrigine and carbamazepine in elderly patients with newly diagnosed epilepsy [J].
Brodie, MJ ;
Overstall, PW ;
Giorgi, L .
EPILEPSY RESEARCH, 1999, 37 (01) :81-87
[7]
Development and cross-cultural translations of a 31-item quality of life in epilepsy inventory [J].
Cramer, JA ;
Perrine, K ;
Devinsky, O ;
Bryant-Comstock, L ;
Meador, T ;
Hermann, B .
EPILEPSIA, 1998, 39 (01) :81-88
[8]
CONTROLLED TRIAL OF LAMOTRIGINE (LAMICTAL) FOR REFRACTORY PARTIAL SEIZURES [J].
JAWAD, S ;
RICHENS, A ;
GOODWIN, G ;
YUEN, WC .
EPILEPSIA, 1989, 30 (03) :356-363
[9]
The Expert Consensus Guideline Series Treatment of Epilepsy [J].
Karceski, Steven ;
Morrell, Martha ;
Carpenter, Daniel .
EPILEPSY & BEHAVIOR, 2001, 2 (06) :A1-A50
[10]
*LAMICTAL, 2003, TABL PRESCR INF