Adjunctive lamotrigine for partial seizures in patients aged 1 to 24 months

被引:27
作者
Pina-Garza, J. E. [1 ]
Levisohn, P. [2 ]
Gucuyener, K. [3 ]
Mikati, M. A. [4 ]
Warnock, C. R. [5 ]
Conklin, H. S. [5 ]
Messenheimer, J. [5 ]
机构
[1] Vanderbilt Univ, Nashville, TN USA
[2] Childrens Hosp, Denver, CO 80218 USA
[3] Gazi Univ, Ankara, Turkey
[4] Amer Univ Beirut, Med Ctr, Beirut, Lebanon
[5] GlaxoSmithKline Inc, Neurosci Med Dev Ctr, Res Triangle Pk, NC USA
关键词
D O I
10.1212/01.wnl.0000285493.08622.35
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: This randomized, double-blind, placebo-controlled trial was conducted to assess the efficacy and tolerability of adjunctive lamotrigine for the treatment of partial seizures in infants aged 1 to 24 months. Methods: The study used a responder-enriched design in which all patients received adjunctive lamotrigine during an open-label phase (n = 177; maximum maintenance dose 5.1 mg/kg/day for those on non-enzyme-inducing antiepileptic drugs [AEDs] or valproate and 15.6 mg/kg/day for those on enzyme-inducing AEDs). Patients meeting response criteria were randomly assigned to double-blind treatment for up to 8 weeks with continued lamotrigine (n = 19) or to withdrawal from lamotrigine (placebo; n = 19) while background AEDs were maintained. Results: The proportion of treatment failures (patients who met escape criteria or withdrew before completing the double-blind phase) was lower with lamotrigine (58%) than with placebo (84%). This finding was not significant in the primary analysis (two-sided chi(2) test [primary endpoint]). A post hoc sensitivity analysis of the primary endpoint was also performed (p = 0.045 by one-sided, mid-p corrected Fisher exact test). The median time to meet escape criteria was longer with lamotrigine (42 days) than with placebo (22 days) (p = 0.059). During the last 28 days of the open-label phase, 53% of the patients had a >= 50% reduction in frequency of partial seizures with lamotrigine. Additional reduction in partial seizure frequency was observed during the double-blind phase compared with the last 4 weeks of the open-label phase among those randomly assigned to lamotrigine (32% with a >= 25% reduction) but not those randomly assigned to placebo (5% with a >= 25% reduction). Lamotrigine was well tolerated, with an adverse event profile comparable to that observed in older pediatric patients. Conclusion: Lamotrigine was well tolerated, and the data indicate that it may be efficacious in the treatment of partial seizures in infants aged 1 to 24 months.
引用
收藏
页码:2099 / 2108
页数:10
相关论文
共 23 条
[1]   CLINICAL TRIAL DESIGN AVOIDING UNDUE PLACEBO TREATMENT [J].
AMERY, W ;
DONY, J .
JOURNAL OF CLINICAL PHARMACOLOGY, 1975, 15 (10) :674-679
[2]   ON ALLEGED GAINS IN POWER FROM LOWER P-VALUES [J].
BARNARD, GA .
STATISTICS IN MEDICINE, 1989, 8 (12) :1469-1477
[3]   Long-term safety and efficacy of lamotrigine (Lamictal(R)) in paediatric patients with epilepsy [J].
Besag, FMC ;
Dulac, O ;
Alving, J ;
Mullens, EL .
SEIZURE, 1997, 6 (01) :51-56
[4]   Lamotrigine: A review of its use in childhood epilepsy [J].
Culy C.R. ;
Goa K.L. .
Paediatric Drugs, 2000, 2 (4) :299-330
[5]   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
[6]   Lamictal (lamotrigine) monotherapy for typical absence seizures in children [J].
Frank, LM ;
Enlow, T ;
Holmes, GL ;
Manasco, P ;
Concannon, S ;
Chen, C ;
Womble, G ;
Casale, EJ .
EPILEPSIA, 1999, 40 (07) :973-979
[7]  
Fridericia LS., 1920, Acta Med Scand, V53, P469, DOI DOI 10.1111/J.0954-6820.1920.TB18266.X
[8]   INCIDENCE OF EPILEPSY AND UNPROVOKED SEIZURES IN ROCHESTER, MINNESOTA - 1935-1984 [J].
HAUSER, WA ;
ANNEGERS, JF ;
KURLAND, LT .
EPILEPSIA, 1993, 34 (03) :453-468
[9]  
HAUSER WA, 1995, NEUROSURG CLIN N AM, V6, P419
[10]   A QUASI-EXACT TEST FOR COMPARING 2 BINOMIAL PROPORTIONS [J].
HIRJI, KF ;
TAN, SJ ;
ELASHOFF, RM .
STATISTICS IN MEDICINE, 1991, 10 (07) :1137-1153