Bring Penny, Ensom Mary H H
University of British Columbia, Vancouver, British Columbia, Canada.
Clin Pharmacokinet. 2008;47(12):767-78. doi: 10.2165/0003088-200847120-00002.
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.
奥卡西平是卡马西平的10-酮类似物,已被批准用于治疗部分性癫痫发作或全身性强直阵挛性癫痫发作。奥卡西平的主要代谢产物是单羟基化衍生物(MHD)。本综述遵循一种决策算法来确定是否有必要对MHD进行治疗药物监测。需要考虑的重要因素包括奥卡西平对治疗指征的适用性;测量MHD浓度的能力;是否存在良好的浓度-反应关系、狭窄的治疗范围或不可预测的药代动力学参数;奥卡西平药理反应的可评估性;足够的治疗持续时间;以及MHD浓度在临床决策过程中的潜在影响。根据现有证据,对MHD进行治疗药物监测并非常规必要,但在优化极端年龄、孕期、肾功能不全时的癫痫控制,或确定潜在药物相互作用的意义或排除不依从性方面可能有益。