The efficacy of valproate-lamotrigine comedication in refractory complex partial seizures: Evidence for a pharmacodynamic interaction

Citation
F. Pisani et al., The efficacy of valproate-lamotrigine comedication in refractory complex partial seizures: Evidence for a pharmacodynamic interaction, EPILEPSIA, 40(8), 1999, pp. 1141-1146
Citations number
25
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EPILEPSIA
ISSN journal
00139580 → ACNP
Volume
40
Issue
8
Year of publication
1999
Pages
1141 - 1146
Database
ISI
SICI code
0013-9580(199908)40:8<1141:TEOVCI>2.0.ZU;2-3
Abstract
Purpose: To assess the comparative therapeutic value of valproate (VPA), la motrigine (LTG), and their combination in patients with complex partial sei zures resistant to other established antiepileptic drugs (AEDs). Methods: After a 3-month prospective baseline, 20 adults with refractory co mplex partial seizures not exposed previously to VPA and LTG were scheduled to receive three consecutive add-on treatments with VPA, LTG, or their com bination, according to an open, response-conditional, crossover design. Eac h period consisted of a 6- to 12-week dose optimization followed by 3-month evaluation at stabilized serum drug levels. Only patients not responding t o one phase proceeded to the next. Results: A >50% reduction in seizure frequency was observed in three of 20 patients given VPA and in four of 17 patients given LTG. Of the remaining 1 3 patients, four became seizure free, and an additional four experienced se izure reductions of 62-78% when VPA and LTC were given in combination. Mild tremor was observed in three patients receiving VPA and in all patients ta king the VPA-LTG combination. In patients responding to combination therapy , optimized dosages and peak serum levels of both VPA and LTG were lower th an those during separate administration. Conclusions: A considerable proportion of patients who failed to respond to VPA and LTG separately improved when the two drugs were combined, although serum levels of both agents were lower during combination therapy. Despite methodologic limitations in the nonrandomized treatment sequence, these fi ndings suggest that VPA and LTG exhibit a favorable pharmacodynamic interac tion in patients with refractory partial epilepsy. The dosage of both drugs , however, may need to be reduced to minimize the risk of intolerable side effects.