Efficacy and tolerability of conversion to monotherapy with lamotrigine compared with valproate and carbamazepine in patients with epilepsy
- PMID: 15256191
- DOI: 10.1016/j.yebeh.2004.04.006
Efficacy and tolerability of conversion to monotherapy with lamotrigine compared with valproate and carbamazepine in patients with epilepsy
Abstract
Objective: This randomized, open-label study was designed to compare the efficacy and tolerability of lamotrigine monotherapy with those of valproate and carbamazepine monotherapy in patients with epilepsy whose seizures were uncontrolled on their prestudy antiepileptic drug monotherapy.
Methods: Patients meeting eligibility criteria were randomized 2:1 to lamotrigine:carbamazepine or lamotrigine:valproate. The treatment phase was divided into a 4-week dose-escalation phase (Weeks 1-4), during which lamotrigine, carbamazepine, or valproate was added to patient's prestudy monotherapy; an 8-week add-on phase (Weeks 5-12), during which patients were stabilized on both the study medication and their prestudy antiepileptic therapy; an 8-week withdrawal phase (Weeks 13-20), during which prestudy antiepileptic therapy could be withdrawn if clinically appropriate; and an 8-week monotherapy phase (Weeks 21-28), during which patients could be treated with study medication as monotherapy.
Results: The numbers of patients randomized to the carbamazepine and valproate arms of the study were 144 (98 lamotrigine, 46 carbamazepine) and 158 (105 lamotrigine, 53 valproate), respectively. Successful monotherapy sustained for at least 7 weeks was achieved in comparable percentages of patients in the lamotrigine group (56%) and the carbamazepine group (54%) and in more patients in the lamotrigine group (49%) than the valproate group (40%). Among monotherapy completers, the percentage of patients with zero seizures during the monotherapy phase was comparable for lamotrigine (41%) and carbamazepine (30%) and significantly higher (P<0.05) with lamotrigine (32%) than with valproate (11%). No differences between treatments were observed with respect to time to treatment failure or time to first seizure. Lamotrigine was also better tolerated than carbamazepine or valproate.
Conclusion: Lamotrigine monotherapy was as effective as and better tolerated than carbamazepine or valproate monotherapy in patients whose seizures were uncontrolled on their prestudy antiepileptic drug monotherapy.
Similar articles
-
Open study evaluating lamotrigine efficacy and safety in add-on treatment and consecutive monotherapy in patients with carbamazepine- or valproate-resistant epilepsy.Seizure. 2000 Oct;9(7):486-92. doi: 10.1053/seiz.2000.0444. Seizure. 2000. PMID: 11034873 Clinical Trial.
-
Lamotrigine monotherapy compared with carbamazepine, phenytoin, or valproate monotherapy in patients with epilepsy.Epilepsy Behav. 2003 Dec;4(6):659-66. doi: 10.1016/j.yebeh.2003.08.033. Epilepsy Behav. 2003. PMID: 14698699 Clinical Trial.
-
A dosing algorithm for converting from valproate monotherapy to lamotrigine monotherapy in patients with epilepsy.Epilepsy Behav. 2005 Feb;6(1):63-70. doi: 10.1016/j.yebeh.2004.11.002. Epilepsy Behav. 2005. PMID: 15652736 Clinical Trial.
-
Use of antiepileptic drugs in the treatment of epilepsy in people with intellectual disability.J Intellect Disabil Res. 1998 Dec;42 Suppl 1:1-15. J Intellect Disabil Res. 1998. PMID: 10030426 Review.
-
The clinical efficacy of lamotrigine as an antiepileptic drug.Neurology. 1994 Nov;44(11 Suppl 8):S29-35. Neurology. 1994. PMID: 7970004 Review.
Cited by
-
The effectiveness of antiepileptic drug treatment in glioma patients: lamotrigine versus lacosamide.J Neurooncol. 2021 Aug;154(1):73-81. doi: 10.1007/s11060-021-03800-z. Epub 2021 Jul 1. J Neurooncol. 2021. PMID: 34196916 Free PMC article.
-
Antiepileptic drug monotherapy for epilepsy: a network meta-analysis of individual participant data.Cochrane Database Syst Rev. 2017 Jun 29;6(6):CD011412. doi: 10.1002/14651858.CD011412.pub2. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2017 Dec 15;12:CD011412. doi: 10.1002/14651858.CD011412.pub3. PMID: 28661008 Free PMC article. Updated.
-
Risk of Valproic Acid-Related Tremor: A Systematic Review and Meta-Analysis.Front Neurol. 2020 Dec 15;11:576579. doi: 10.3389/fneur.2020.576579. eCollection 2020. Front Neurol. 2020. PMID: 33384651 Free PMC article.
-
Antiepileptic drug monotherapy for epilepsy: a network meta-analysis of individual participant data.Cochrane Database Syst Rev. 2017 Dec 15;12(12):CD011412. doi: 10.1002/14651858.CD011412.pub3. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2022 Apr 1;4:CD011412. doi: 10.1002/14651858.CD011412.pub4. PMID: 29243813 Free PMC article. Updated.
-
Structured clinical documentation in the electronic medical record to improve quality and to support practice-based research in epilepsy.Epilepsia. 2017 Jan;58(1):68-76. doi: 10.1111/epi.13607. Epub 2016 Nov 19. Epilepsia. 2017. PMID: 27864833 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical