A comparison of monotherapy with lamotrigine or carbamazepine in patients with newly diagnosed partial epilepsy

被引:96
作者
Nieto-Barrera, M
Brozmanova, M
Capovilla, G
Christe, W
Pedersen, B
Kane, K
O'Neill, F
机构
[1] Glaxo Wellcome Res & Dev Ltd, Neurol & Psychiat Clin Dev, Greenford UB6 0HE, Middx, England
[2] Hosp Virgen Rocio, Seville, Spain
[3] Childrens Hosp, Bratislava, Slovakia
[4] Osp C Poma, Mantua, Italy
[5] Klinikum Ernst Von Bergmann, Potsdam, Germany
[6] Aalborg Hosp, DK-9100 Aalborg, Denmark
关键词
partial epilepsy; lamotrigine; carbamazepine; monotherapy; newly diagnosed;
D O I
10.1016/S0920-1211(01)00271-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Monotherapy with lamotrigine or carbamazepine was evaluated in a multicentre open trial of patients aged 2 years and above with newly diagnosed partial epilepsy. A total of 417 patients were randomised to treatment with lamotrigine, while 201 patients received carbamazepine. Following a dose escalation period of 6 weeks, maintenance therapy (Weeks 7-24) was adjusted according to response. Efficacy was similar with both treatments (65% with lamotrigine, 73% with carbamazepine, P = 0.085). Efficacy was assessed by the proportion of patients seizure free during the last 16 weeks of treatment; all subjects who remained in the study for at least 18 weeks after the week 4 visit were included in the analysis. More patients receiving lamotrigine completed the study (81%), compared with those receiving carbamazepine (77%). This difference was primarily due to discontinuation as a result of adverse events, reported by 34 (8%) of those treated with lamotrigine but 26 (13%) of those treated with carbamazepine. The proportion of patients who experienced adverse events in the lamotrigine group was lower (218 patients. 52%) compared with the carbamazepine group (120 patients, 60%). The proportion of patients with adverse events considered to be drug related was lower in the lamotrigine group (132 patients, 32%) compared with the carbamazepine group (83 patients, 41%). Somnolence was the only adverse event reported at an incidence of greater than 5% and where there was a difference of 5% or more between treatment groups (4% lamotrigine, 11% carbamazepine patients), The small subsets of elderly patients (aged 65 years or over) and paediatric patients (aged 2-12 years) also showed better tolerability to lamotrigine than to carbamazepine. In conclusion, monotherapy with lamotrigine is as effective as carbamazepine in patients with newly diagnosed partial epilepsy. Patients were able to tolerate lamotrigine better than carbamazepine, so more patients receiving lamotrigine were able to remain on therapy. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 155
页数:11
相关论文
共 19 条
[1]
Appleton RE, 1996, ROY SOC MED INT CONG, P103
[2]
DOUBLE-BLIND COMPARISON OF LAMOTRIGINE AND CARBAMAZEPINE IN NEWLY-DIAGNOSED EPILEPSY [J].
BRODIE, MJ ;
RICHENS, A ;
YUEN, AWC .
LANCET, 1995, 345 (8948) :476-479
[3]
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
[4]
Brodie MJ, 1999, EPILEPSIA, V40, P94
[5]
SERUM ANTICONVULSANT CONCENTRATIONS AND THE RISK OF DRUG-INDUCED SKIN ERUPTIONS [J].
CHADWICK, D ;
SHAW, MDM ;
FOY, P ;
RAWLINS, MD ;
TURNBULL, DM .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1984, 47 (06) :642-644
[6]
CHRISTIE W, 1999, EUR J NEUROL S3, V6, P73
[7]
A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children [J].
Duchowny, M ;
Pellock, JM ;
Graf, WD ;
Billard, C ;
Gilman, J ;
Casale, E ;
Womble, G ;
Risner, M ;
Manasco, P .
NEUROLOGY, 1999, 53 (08) :1724-1731
[8]
PRISONS, PRISON SENTENCES AND PUBLIC-ORDER [J].
FAUGERON, C ;
LEBOULAIRE, JM .
REVUE FRANCAISE DE SOCIOLOGIE, 1992, 33 (01) :3-32
[9]
GILLIAM F, 1998, NEUROLOGY, V51, P940
[10]
LAMOTRIGINE - A REVIEW OF ITS PHARMACOLOGICAL PROPERTIES AND CLINICAL EFFICACY IN EPILEPSY [J].
GOA, KL ;
ROSS, SR ;
CHRISP, P .
DRUGS, 1993, 46 (01) :152-176