A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome

Epilepsia. 2011 Jan;52(1):175-8. doi: 10.1111/j.1528-1167.2010.02885.x. Epub 2011 Jan 4.

Abstract

Dravet syndrome is a severe epileptic encephalopathy starting in the first year of life. Mutations in SCN1A can be identified in the majority of patients, and epileptic seizures in the setting of fever are a clinical hallmark. Fever is also commonly seen after vaccinations and provocation of epileptic seizures by vaccinations in patients with Dravet syndrome has been reported, but not systematically assessed. In a retrospective evaluation of 70 patients with Dravet syndrome and SCN1A mutations, seizures following vaccinations were reported in 27%. In 58% of these patients vaccination-related seizures represented the first clinical manifestation. The majority of seizures occurred after DPT vaccinations and within 72 h after vaccination. Two-thirds of events occurred in the context of fever. Our findings highlight seizures after vaccinations as a common feature in Dravet syndrome and emphasize the need for preventive measures for seizures triggered by vaccination or fever in these children.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Diphtheria-Tetanus-Pertussis Vaccine / adverse effects
  • Epilepsies, Myoclonic / complications
  • Epilepsies, Myoclonic / epidemiology*
  • Epilepsies, Myoclonic / genetics
  • Humans
  • Incidence
  • Infant
  • Mutation / genetics
  • NAV1.1 Voltage-Gated Sodium Channel
  • Nerve Tissue Proteins / genetics
  • Retrospective Studies
  • Seizures / epidemiology*
  • Seizures / etiology
  • Seizures / genetics
  • Sodium Channels / genetics
  • Syndrome
  • Vaccination / adverse effects*
  • Young Adult

Substances

  • Diphtheria-Tetanus-Pertussis Vaccine
  • NAV1.1 Voltage-Gated Sodium Channel
  • Nerve Tissue Proteins
  • SCN1A protein, human
  • Sodium Channels