Therapeutic drug monitoring of antiepileptic drugs: current status and future prospects. (3rd March 2020)

• Record Type: Journal Article
• Authors: Johannessen Landmark, Cecilie; Johannessen, Svein I.; Patsalos, Philip N.
• Is Part Of: Expert opinion on drug metabolism and toxicology. Volume 16:Number 3(2020)
• Page Start: 227
• Page End: 238
• Publication Date: 2020-03-03
• Subjects: Antiepileptic drugs -- epilepsy -- drug interactions -- pharmacokinetic variability -- therapeutic drug monitoring; Drugs -- Toxicology -- Periodicals; Drugs -- Metabolism -- Periodicals; 615.7
• DOI: 10.1080/17425255.2020.1724956
• Languages: English
• ISSNs: 1742-5255

Abstract

ABSTRACT: Introduction : Antiepileptic drugs (AEDs) are the cornerstone of treatment of patients with epilepsy, and there are presently 27 licensed AEDs making AEDs among the most common medications for which therapeutic drug monitoring (TDM) is performed. The aim of this review is to provide an overview of the current evidence of the use and implementation of AED TDM in patients with epilepsy and other non-epilepsy conditions. Areas covered : The pharmacokinetic variability of AEDs is extensive, resulting in pronounced variability in serum concentrations between patients. TDM may thus be useful to individualize the treatment of patients with epilepsy and also in non-epilepsy conditions. Indications for TDM include settings where pharmacokinetic variability is anticipated (e.g. in children, the elderly, during pregnancy, and patients prescribed polytherapy resulting in drug interactions) and drug adherence. TDM contributes to provide a quality assurance of the treatment. Patient management is, therefore, best guided by the determination of individual therapeutic concentrations. Expert opinion : Because of pharmacokinetic variability is prevalent among AEDs, TDM allows a bespoke approach to epilepsy care allowing dose adjustments based on measured drug concentrations so as to optimize clinical outcome. Future advances include the use of additional markers of toxicity and genetic variability so as to further aid individualization and optimize AED treatment.