AI Article Synopsis

  • Antiseizure medications (ASMs) are essential for managing epilepsy and have seen new developments that enhance treatment options not only for epilepsy but also for psychiatric and pain disorders.
  • Understanding the pharmacodynamics (how drugs affect the body) and pharmacokinetics (how the body processes drugs), as well as how ASMs interact with other medications, is vital for effective treatment and monitoring.
  • The review highlights advancements in technology for analyzing drug levels and suggests future strategies, including genetic testing and monitoring biomarkers, to create personalized treatment plans for patients using ASMs.

Article Abstract

Antiseizure medications (ASMs) are the cornerstone of treatment for patients with epilepsy. Several new ASMs have recently been introduced to the market, making it possible to better tailor the treatment of epilepsy, as well as other indications (psychiatry and pain disorders). For this group of drugs there are numerous pharmacological challenges, and updated knowledge on their pharmacodynamic and pharmacokinetic properties is, therefore, crucial for an optimal treatment outcome. This review focuses on educational approaches to the following learning outcomes as described by the International League Against Epilepsy (ILAE): To demonstrate knowledge of pharmacokinetics and pharmacodynamics, drug interactions with ASMs and with concomitant medications, and appropriate monitoring of ASM serum levels (therapeutic drug monitoring, TDM). Basic principles in pharmacology, pharmacokinetic variability, and clinically relevant approaches to manage drug interactions are discussed. Furthermore, recent improvements in analytical technology and sampling are described. Future directions point to the combined implementation of TDM with genetic panels for proper diagnosis, pharmacogenetic tests where relevant, and the use of biochemical markers that will all contribute to personalized treatment. These approaches are clinically relevant for an optimal treatment outcome with ASMs in various patient groups.

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Source
http://dx.doi.org/10.1002/epd2.20069DOI Listing

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