Publication

Antiepileptic drug use in women of childbearing age

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Last modified
  • 02/20/2025
Type of Material
Authors
    Kimford J. Meador, Emory UniversityPatricia Penovich, Minnesota Epilepsy GroupGus A. Baker, University of LiverpoolPage B. Pennell, Emory UniversityEdward Bromfield, Harvard–Brigham & Women'sAlison Pack, Columbia UniversityJoyce D. Liporace, Riddle Health CareMaria Sam, Wake Forest UniversityLaura A. Kalayjian, University of Southern California, Los AngelesDavid J Thurman, Emory UniversityEugene Moore, Emory UniversityDavid W. Loring, Emory UniversityDavid W Loring, Emory University
Language
  • English
Date
  • 2009-07
Publisher
  • Elsevier
Publication Version
Copyright Statement
  • © 2009 Elsevier Inc. Published by Elsevier Inc. All rights reserved.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1525-5050
Volume
  • 15
Issue
  • 3
Start Page
  • 339
End Page
  • 343
Grant/Funding Information
  • This study was supported by Grants 2 RO1 NS038455 from the NIH/NINDS, 1 R01050659 from the NIH/NINDS, and RB219738 from the UK Epilepsy Research Foundation.
  • National Institute of Neurological Disorders and Stroke : NINDS
Abstract
  • Research on antiepileptic drug (AED) teratogenesis has demonstrated an increased risk for valproate. The impact of these findings on current AED prescribing patterns for women of childbearing age with epilepsy is uncertain. The Neurodevelopmental Effects of Antiepileptic Drugs (NEAD) Study is an ongoing prospective multicenter observational investigation that enrolled pregnant women with epilepsy on the most common AED monotherapies from October 1999 to February 2004 (carbamazepine, lamotrigine, valproate, and phenytoin). A 2007 survey of AED use in women of childbearing age at eight NEAD centers found a total of 932 women of childbearing age with epilepsy (6% taking no AED, 53% monotherapy, 41% polytherapy). The most common monotherapies were lamotrigine or levetiracetam. Since 2004, prescriptions of carbamazepine, phenytoin, and valproate have decreased, whereas those for levetiracetam have increased. Except for the top two AED monotherapies, there were marked differences in other monotherapies and in polytherapies between U.S. and UK centers. Future investigations are needed to examine reasons for drug choice.
Author Notes
  • Corresponding author. Address: Department of Neurology, Emory University, Woodruff Memorial Research Building, 101 Woodruff Circle, Suite 6000, Mail Stop 1930-001-1AN, Atlanta, GA 30322, USA. Fax: +1 404 727 3157. kimford.meador@emory.edu (K.J. Meador)
Keywords
Research Categories
  • Biology, Neuroscience

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