Seizure: European Journal of Epilepsy
Volume 19, Issue 6 , Pages 356-358, July 2010

Clinical feasibility of immediate overnight switching from slow-release carbamazepine to oxcarbazepine in Korean patients with refractory partial epilepsy

  • Sang-Ahm Lee

      Affiliations

    • Department of Neurology, University of Ulsan, Seoul, Republic of Korea
  • ,
  • Kyoung Heo

      Affiliations

    • Department of Neurology, Yonsei University, Seoul, Republic of Korea
  • ,
  • Won-Joo Kim

      Affiliations

    • Department of Neurology, Yonsei University, Seoul, Republic of Korea
  • ,
  • Hong-Ki Song

      Affiliations

    • Department of Neurology, Hallym Institute of Epilepsy Research, Seoul, Republic of Korea
  • ,
  • Sung-Eun Kim

      Affiliations

    • Department of Neurology, Inje University, Pusan, Republic of Korea
  • ,
  • Sang-Ho Kim

      Affiliations

    • Department of Neurology, Dong-A University, Pusan, Republic of Korea
  • ,
  • Soon-Kee No

      Affiliations

    • Department of Neurology, Bong-Seng Memorial Hospital, Pusan, Republic of Korea
  • ,
  • Byung-In Lee

      Affiliations

    • Department of Neurology, Yonsei University, Seoul, Republic of Korea
    • Corresponding Author InformationCorresponding 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.

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.

Abbreviations: OXC, oxcarbazepine, AED, antiepileptic drug, CBZ, carbamazepine

Keywords: Carbamazepine, Oxcarbazepine, Switching, Partial epilepsy

 

PII: S1059-1311(10)00106-8

doi:10.1016/j.seizure.2010.05.002

Seizure: European Journal of Epilepsy
Volume 19, Issue 6 , Pages 356-358, July 2010