Cited by 64Epilepsy research and treatmentPharmacological Effects and Toxicity StudiesDiet and metabolism studies

Lamotrigine can be beneficial in patients with Dravet syndrome

Open access
Dalic, Linda, Mullen, Saul A, Roulet Perez, Eliane, Scheffer, Ingrid·2015·Developmental Medicine & Child Neurology

Abstract

Dravet syndrome, a severe infantile epilepsy syndrome, is typically resistant to anti‐epileptic drugs (AED). Lamotrigine (LTG), an AED that is effective for both focal and generalized seizures, has been reported to aggravate seizures in Dravet syndrome. Therefore, LTG is usually avoided in Dravet syndrome. We describe two adults and a child with Dravet syndrome in whom LTG resulted in decreased seizure duration and frequency. This benefit was highlighted in each patient when LTG was withdrawn after 6 to 15 years, and resulted in an increased frequency of convulsive seizures together with longer seizure duration. A 25‐year‐old male required hospital admission for frequent seizures for the first time in 7 years, 6 weeks after ceasing LTG. Reintroduction of LTG improved seizure control, suggesting that in some patients with Dravet syndrome, LTG may be beneficial.

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Crossref · 10.1111/dmcn.12593

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  • The SCB topiramate can be useful in Dravet syndrome, whereas others, such as lamotrigine and phenytoin, may exacerbate seizures in some patients and be helpful in others.

    “However, the SCB topiramate can be useful in Dravet syndrome 181 , whereas others, such as lamotrigine and phenytoin, may exacerbate seizures in some patients and be helpful in others 208,209 .”

    From Developmental and epileptic encephalopathies (2024) · cites this paper as [208]

    The Abstract reports that lamotrigine has been associated with seizure exacerbation but reduced seizures in the three patients described. It lists phenytoin among drugs that worsen seizures; it does not say phenytoin can help some patients. The topiramate statement has a separate citation and is not assessed here. (LLM, conf=0.88)

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Authors
Dalic, L., Mullen, S. A., Roulet Perez, E., & Scheffer, I.
Affiliations
  • Austin Health (AU)
  • The University of Melbourne (AU)
  • Paediatric Neurology and Neurorehabilitation Unit Centre Hospitalier Universitaire Vaudois Lausanne Switzerland
  • Royal Children's Hospital (AU)
Corresponding author
Scheffer, Ingrid
Venue
Developmental Medicine & Child Neurology
Publisher
Wiley
Published
2014-09-22
Volume
57
Issue
2
Pages
200-202
ISSN
  • 0012-1622 (ISSN-L)
  • 1469-8749
OpenAlex
W2083980682
Cited by
64
References
15
Citations by year
2026: 3 · 2025: 10 · 2024: 3 · 2023: 4 · 2022: 5 · 2021: 7 · 2020: 4 · 2019: 8 · 2018: 9 · 2017: 5 · 2016: 3 · 2015: 2 · 2014: 1
FWCI
2.80
Type
journal article
Language
en
Open access
Locations
  • Developmental Medicine & Child Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • IRIS (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
Funders
  • State Government of Victoria
  • National Health and Medical Research Council
  • National Medical Research Council
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmacological Effects and Toxicity Studies
  • Health Sciences › Medicine › Physiology › Diet and metabolism studies
Keywords
Dravet syndrome, lamotrigine, drug-resistant epilepsy, seizure control, seizure aggravation, antiepileptic drugs, convulsions, infantile epilepsy
MeSH terms
Lamotrigine, Adolescent, Adult, Anticonvulsants, Epilepsies, Myoclonic, Humans, Male, Seizures, Triazines

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