Clinical feasibility of immediate overnight switching from slow-release carbamazepine to oxcarbazepine in Korean patients with refractory partial epilepsy
Received 14 January 2010; received in revised form 14 April 2010; accepted 7 May 2010. published online 10 June 2010.
Abstract
We assessed the clinical variables predicting the feasibility of immediate overnight switching from slow-release carbamazepine to oxcarbazepine in Korean patients with refractory partial epilepsy. Thirty patients aged 15 years or older with refractory partial epilepsy, who had been treated with slow-release carbamazepine as monotherapy or in combination therapy, were switched overnight from slow-release carbamazepine (mean dose at switching, 900mg/day) to oxcarbazepine. Of these 30 patients, 29 (96.7%) had been treated with a slow-release formulation of carbamazepine. The proportion of patients with polytherapy was 85.3%. Overall, 9 of 30 (30%) switched patients experienced clinically significant adverse events until 2 weeks after switching, including 2 with seizure aggravation. The only clinical variable related to the failure of overnight switching was the number of seizures at baseline.
aDepartment of Neurology, University of Ulsan, Seoul, Republic of Korea
bDepartment of Neurology, Yonsei University, Seoul, Republic of Korea
cDepartment of Neurology, Hallym Institute of Epilepsy Research, Seoul, Republic of Korea
dDepartment of Neurology, Inje University, Pusan, Republic of Korea
eDepartment of Neurology, Dong-A University, Pusan, Republic of Korea
fDepartment of Neurology, Bong-Seng Memorial Hospital, Pusan, Republic of Korea
Corresponding author at: Department of Neurology, Yonsei University College of Medicine, Severance Hospital, 134 Sinchon-dong, Seodaemun-gu, Seoul 120-752, Republic of Korea. Tel.: +82 2 2228 1600.