Does Oxcarbazepine Warrant Therapeutic Drug Monitoring?

被引:19
作者
Bring, Penny [1 ,2 ]
Ensom, Mary H. H. [1 ,3 ]
机构
[1] Univ British Columbia, Fac Pharmaceut Sci, Vancouver, BC, Canada
[2] Vancouver Gen Hosp, Dept Pharm, Vancouver, BC, Canada
[3] Childrens & Womens Hlth Ctr British Columbia, Dept Pharm, Vancouver, BC V6H 3N1, Canada
关键词
D O I
10.2165/0003088-200847120-00002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oxcarbazepine, the 10-keto analogue of carbamazepine, is approved for the treatment of partial seizures or generalized tonic-clonic seizures. The primary metabolite of oxcarbazepine is monohydroxylated derivative (MHD). This review follows a decision-making algorithm to determine if therapeutic drug monitoring of MHD is warranted. Important factors to take into account include the appropriateness of oxcarbazepine for the therapeutic indication; ability to measure MHD concentrations; existence of a good concentration-response relationship, narrow therapeutic range or unpredictable pharmacokinetic parameters; assessability of the pharmacological response of oxcarbazepine; adequate duration of therapy; and potential influence of MHD concentrations in the clinical decision-making process. Based on the available evidence, therapeutic drug monitoring of MHD is not routinely warranted but may be beneficial in optimizing seizure control at the extremes of age, during pregnancy, in renal insufficiency, or to determine the significance of potential drug interactions or rule out noncompliance.
引用
收藏
页码:767 / 778
页数:12
相关论文
共 66 条
  • [1] Enantioselective HPLC-UV method for determination of eslicarbazepine acetate (BIA 2-093) and its metabolites in human plasma
    Alves, Gilberto
    Figueiredo, Isabel
    Castel-Branco, Margarida
    Loureiro, Ana
    Fortuna, Ana
    Falcao, Amilcar
    Caramona, Margarida
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2007, 21 (11) : 1127 - 1134
  • [2] [Anonymous], US INT PROJ AG SEX R
  • [3] 10-hydroxycarbazepine serum concentration-to-oxcarbazepine dose ratio - Influence of age and concomitant antiepileptic drugs
    Armijo, JA
    Vega-Gil, N
    Shushtarian, M
    Adin, J
    Herranz, JL
    [J]. THERAPEUTIC DRUG MONITORING, 2005, 27 (02) : 199 - 204
  • [4] Extended-release formulations for the treatment of epilepsy
    Bialer, Meir
    [J]. CNS DRUGS, 2007, 21 (09) : 765 - 774
  • [5] A double-blind controlled clinical trial of oxcarbazepine versus phenytoin in adults with previously untreated epilepsy
    Bill, PA
    Vigonius, U
    Pohlmann, H
    Guerreiro, CAM
    Kochen, S
    Saffer, D
    Moore, A
    [J]. EPILEPSY RESEARCH, 1997, 27 (03) : 195 - 204
  • [6] Oxcarbazepine in treatment of childhood epilepsy: A survey of 46 children and adolescents
    Borusiak, P
    Korn-Merker, E
    Holert, N
    Boenigk, HE
    [J]. JOURNAL OF EPILEPSY, 1998, 11 (06): : 355 - 360
  • [7] Liquid chromatography-electrospray mass spectrometry determination of carbamazepine, oxcarbazepine and eight of their metabolites in human plasma
    Breton, H
    Cociglio, M
    Bressolle, F
    Peyriere, H
    Blayac, JP
    Hillaire-Buys, D
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 828 (1-2): : 80 - 90
  • [8] Primary care: Epilepsy.
    Browne, TR
    Holmes, GL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (15) : 1145 - 1151
  • [9] Simultaneous analysis of six antiepileptic drugs and two selected metabolites in human plasma by liquid chromatography after solid-phase extraction
    Bugamelli, F
    Sabbioni, C
    Mandrioli, R
    Kenndler, E
    Albani, F
    Raggi, MA
    [J]. ANALYTICA CHIMICA ACTA, 2002, 472 (1-2) : 1 - 10
  • [10] Oxcarbazepine concentrations during pregnancy: A retrospective study in patients with epilepsy
    Christensen, Jakob
    Sabers, Anne
    Sidenius, Per
    [J]. NEUROLOGY, 2006, 67 (08) : 1497 - 1499