Conversion from carbamazepine or oxcarbazepine to topiramate in adolescents and adults with epilepsy

被引:0
|
作者
Kowalik, A. [1 ]
Rimpau, W. [2 ]
Adam, H.
Kuehn, F.
van Oene, J. [3 ]
Schreiner, A. [4 ]
Bogdanow, M. [5 ]
Schaeuble, B. [6 ]
机构
[1] Burgerspital Stuttgart, Abt Neurol, Stuttgart, Germany
[2] Pk Klin Weissensee, Abt Neurol, Berlin, Germany
[3] Janssen Cilag EMEA, Tilburg, Netherlands
[4] Janssen Cilag EMEA, Neuss, Germany
[5] ClinAssess, Leverkusen, Germany
[6] Janssen Cilag GmbH, Therapeut Area CNS, Med & Sci Affairs, Raiffeisenstr 8, D-41470 Neuss, Germany
来源
ZEITSCHRIFT FUR EPILEPTOLOGIE | 2008年 / 21卷 / 02期
关键词
epilepsy; carbamazepine; oxcarbazepine; topiramate; QOLIE-10;
D O I
10.1007/s10309-008-0304-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To explore effectiveness, tolerability and changes in quality of life in patients with epilepsy converting to topiramate (TPM) from carbamazepine (CBZ) or oxcarbazepine (OXC) due to insufficient effectiveness and/or tolerability. Methods A multicenter, openlabel, non-interventional trial was used to examine patients (>= 12 years) with epilepsy, changing to TPM monotherapy from baseline mono-or combination therapy with CBZ or OXC. TPM was added to the existing antiepileptic drug (AED) treatment and started at a dose of 25 mg once daily. The dose was titrated up with 25 mg/d increments, once every 1-2 weeks, until a final dose between 50 and 200 mg/d was reached. On the basis of clinical judgment, the treating physician decided whether the existing AED treatment with CBZ or OXC could then be withdrawn. Type and number of seizures, preferred TPM dose, quality of life (QOLIE10 questionnaire), subjective perception of improvement and adverse events (AE) were documented. Results 140 patients (53.5% women, mean age 47 years) decided to switch to TPM due to insufficient effectiveness (75% of patients) and/or poor tolerability (80%) of the CBZ/OXC treatment. Average duration of follow-up was 24 weeks with an overall discontinuation rate of 19.3%, mainly due to AEs (12.1%). At the study endpoint, the intended shift to TPM monotherapy was achieved in 73% of patients at a median TPM dose of 100 mg/d. A seizure reduction of >= 50% was achieved in 91% of patients in the last scheduled period (weeks 12-26); 62% of patients entering that period remained seizure free. Quality of life at the endpoint improved significantly when compared with baseline for all domains of QOLIE-10 (P < 0.001). Most frequent AEs (reported by 75% of patients) were paresthesia (9.3%), weight loss (7.9%), convulsions (5.7%) and memory disorders (5.0%). Conclusion In patients with epilepsy, previously not satisfactorily treated with CBZ or OXC, conversion to TPM may result in an improvement in seizure control as well as in quality of life.
引用
收藏
页码:69 / 78
页数:10
相关论文
共 50 条
  • [31] Carbamazepine- and oxcarbazepine-induced hyponatremia in people with epilepsy
    Berghuis, Bianca
    van der Palen, Job
    de Haan, Gerrit-Jan
    Lindhout, Dick
    Koeleman, Bobby P. C.
    Sander, Josemir W.
    EPILEPSIA, 2017, 58 (07) : 1227 - 1233
  • [32] Effects of carbamazepine and oxcarbazepine on the reproductive endocrine function in women with epilepsy
    Lofgren, Eeva
    Tapanainen, Juha S.
    Koivunen, Riitta
    Pakarinen, Arto
    Isojarvi, Jouko I. T.
    EPILEPSIA, 2006, 47 (09) : 1441 - 1446
  • [33] Comparison of efficacy of trileptal (oxcarbazepine) and carbamazepine in the treatment of temporal epilepsy
    Sokolov, L. V.
    Kalinin, V. V.
    Zheleznova, E. V.
    Zemiyanaya, A. A.
    Polyansky, D. A.
    Basamygin, A. V.
    ZHURNAL NEVROLOGII I PSIKHIATRII IMENI S S KORSAKOVA, 2008, : 63 - 67
  • [34] Effects of carbamazepine and oxcarbazepine on reproductive endocrine function in women with epilepsy
    Lofgren, E
    Tapanainen, J
    Koivunen, R
    Pakarinen, AJ
    Isojarvi, JIT
    EPILEPSIA, 2005, 46 : 87 - 87
  • [35] Quality of Life in Patients With Epilepsy Taking Carbamazepine or Oxcarbazepine Monotherapy
    Aslan, Kezban
    Bozdemir, Hacer
    Uguz, Sukru
    Seydaoglu, Gulsah
    NEUROSURGERY QUARTERLY, 2011, 21 (04) : 247 - 251
  • [36] Thyroid function in men taking carbamazepine, oxcarbazepine, or valproate for epilepsy
    Isojärvi, JIT
    Turkka, J
    Pakarinen, AJ
    Kotila, M
    Rättyä, J
    Myllylä, VV
    EPILEPSIA, 2001, 42 (07) : 930 - 934
  • [37] Efficacy and tolerability of topiramate in patients with epilepsy previously treated with carbamazepine or oxcarbazepine - Results of an open-label, non-interventional study
    Schreiner, Andreas
    Wettach, Joern-Roland
    Barbara, Schauble
    EPILEPSIA, 2006, 47 : 173 - 173
  • [38] Are there differences in patients switching from phenytoin, valproic acid, carbamazepine or oxcarbazepine to topiramate? Results from a prospective, observational study
    Owega, A.
    Schreiner, A.
    Rettig, K.
    Schauble, B.
    EUROPEAN JOURNAL OF NEUROLOGY, 2007, 14 : 90 - 91
  • [39] Are there differences in patients switching from phenytoin, valproic acid, carbamazepine or oxcarbazepine to topiramate?: Results from a prospective, observational study
    Owega, A.
    Schreiner, A.
    Rettig, K.
    Schauble, B.
    JOURNAL OF NEUROLOGY, 2007, 254 : 128 - 128
  • [40] Are there differences in patients switching from phenytoin, valproic acid, carbamazepine or oxcarbazepine to topiramate?: Results from an prospective, observational study
    Owega, A.
    Schreiner, A.
    Rettig, K.
    Schaeuble, B.
    EPILEPSIA, 2007, 48 : 43 - 44