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左乙拉西坦在癫痫儿科患者中的临床药代动力学监测。

Levetiracetam Clinical Pharmacokinetic Monitoring in Pediatric Patients with Epilepsy.

机构信息

Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, BC, Canada.

Pharmacy Department (0B7), Children's and Women's Health Centre of British Columbia, 4500 Oak Street, Vancouver, BC, V6H 3N1, Canada.

出版信息

Clin Pharmacokinet. 2017 Nov;56(11):1267-1285. doi: 10.1007/s40262-017-0537-1.

Abstract

Levetiracetam is a broad-spectrum antiepileptic drug (AED) with a unique mechanism of action. Older AEDs can cause serious short- and long-term adverse drug reactions and complications, rendering them undesirable to use in pediatric patients. Characteristics that make levetiracetam a near-ideal AED include its broad spectrum of activity, good tolerability profile, and minimal drug-drug interactions. Clinical pharmacokinetic monitoring (CPM) is often recommended in pediatric patients for certain AEDs due to large interindividual pharmacokinetic differences and unpredictable drug disposition. Our objective was to determine whether monitoring levetiracetam concentrations is warranted for pediatric patients with epilepsy, using a previously published 9-step decision-making algorithm. A literature search of the MEDLINE (1946-August 2016), EMBASE (1974-August 2016), CENTRAL, and Google Scholar databases was performed to identify relevant English-language articles and answer the questions posed in the algorithm for levetiracetam CPM in pediatric epilepsies. Additional articles were identified from a manual bibliographic review of the relevant literature. We found that levetiracetam CPM met some criteria of the algorithm: levetiracetam is an appropriate adjunctive or monotherapy for pediatric patients with either focal or generalized seizures; it is readily measurable in plasma, with an appropriate degree of sensitivity, accuracy, and precision; it exhibits interindividual variation in pharmacokinetics; often, its pharmacologic effect cannot be easily measured; and the duration of therapy is expected to be long-term. However, important criteria not met include the following: there is no clear evidence for a concentration-response relationship for efficacy or toxicity; the proposed therapeutic range of 12-46 μg/mL is not well-defined and is generally considered as wide. Thus, clinical decision making is unlikely to be affected as a result of routine levetiracetam CPM. In general, routine CPM of levetiracetam cannot be recommended for pediatric patients with epilepsy. However, CPM may be beneficial in select cases, such as patients in whom noncompliance is suspected, those who have severe overdoses, those switching between product brands, or patients for whom an 'individual therapeutic concentration' is documented. Nonetheless, in the majority of pediatric patients with epilepsy, measurement of levetiracetam concentrations is not expected to yield a therapeutic benefit. Thus, clinical assessment and judgment, without measuring drug concentrations, remain the monitoring strategy of choice for levetiracetam therapy.

摘要

左乙拉西坦是一种广谱抗癫痫药物(AED),具有独特的作用机制。较老的 AED 可引起严重的短期和长期药物不良反应和并发症,因此在儿科患者中不希望使用。使左乙拉西坦成为近乎理想的 AED 的特征包括其广泛的活性、良好的耐受性和最小的药物相互作用。由于个体间药代动力学差异大且药物处置不可预测,对于某些 AED,临床药代动力学监测(CPM)通常在儿科患者中推荐。我们的目的是使用以前发表的 9 步决策算法来确定监测癫痫儿科患者左乙拉西坦浓度是否合理。对 MEDLINE(1946 年-2016 年 8 月)、EMBASE(1974 年-2016 年 8 月)、CENTRAL 和 Google Scholar 数据库进行文献检索,以确定相关的英文文章,并回答算法中提出的用于儿科癫痫左乙拉西坦 CPM 的问题。从相关文献的手动文献复习中确定了其他文章。我们发现,左乙拉西坦 CPM 符合该算法的某些标准:左乙拉西坦是局灶性或全身性发作的儿科患者的合适辅助治疗或单药治疗;它可以在血浆中轻松测量,具有适当的灵敏度、准确性和精密度;它在药代动力学方面存在个体间差异;通常,其药理作用难以测量;并且治疗期预计为长期。然而,未满足的重要标准包括以下内容:对于疗效或毒性,没有明确的浓度-反应关系证据;建议的治疗范围为 12-46μg/mL 定义不明确,通常被认为很宽。因此,常规左乙拉西坦 CPM 不太可能影响临床决策。一般来说,不建议对癫痫儿科患者常规进行左乙拉西坦 CPM。然而,CPM 在某些情况下可能是有益的,例如怀疑不遵守治疗方案、严重过量、在产品品牌之间转换或记录了“个体治疗浓度”的患者。尽管如此,在大多数癫痫儿科患者中,测量左乙拉西坦浓度预计不会带来治疗益处。因此,不测量药物浓度的临床评估和判断仍然是左乙拉西坦治疗的首选监测策略。

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