Effect of vaccinations on seizure risk and disease course in Dravet syndrome

  • Nienke E. Verbeek*
  • , Nicoline A. T. van der Maas
  • , Anja C. M. Sonsma
  • , Elly Ippel
  • , Patricia E. Vermeer-de Bondt
  • , Eveline Hagebeuk
  • , Floor E. Jansen
  • , Huibert H. Geesink
  • , Kees P. Braun
  • , Anton de Louw
  • , Paul B. Augustijn
  • , Rinze F. Neuteboom
  • , Jolanda H. Schieving
  • , Hans Stroink
  • , R. Jeroen Vermeulen
  • , Joost Nicolai
  • , Oebele F. Brouwer
  • , Marjan Van Kempen
  • , Carolien G F de Kovel
  • , Jeanet M. Kemmeren
  • Bobby P. C. Koeleman, Nine V. Knoers, Dick Lindhout, W. Boudewijn Gunning, Eva H. Brilstra
*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Objective:

To study the effect of vaccination-associated seizure onset on disease course and estimate the risk of subsequent seizures after infant pertussis combination and measles, mumps, and rubella (MMR) vaccinations in Dravet syndrome (DS).

Methods:

We retrospectively analyzed data from hospital medical files, child health clinics, and the vaccination register for children with DS and pathogenic SCN1A mutations. Seizures within 24 hours after infant whole-cell, acellular, or nonpertussis combination vaccination or within 5 to 12 days after MMR vaccination were defined as "vaccination-associated." Risks of vaccination-associated seizures for the different vaccines were analyzed in univariable and in multivariable logistic regression for pertussis combination vaccines and by a self-controlled case series analysis using parental seizure registries for MMR vaccines. Disease courses of children with and without vaccination-associated seizure onset were compared.

Results:

Children who had DS (n = 77) with and without vaccination-associated seizure onset (21% and 79%, respectively) differed in age at first seizure (median 3.7 vs 6.1 months, p <0.001) but not in age at first nonvaccination-associated seizure, age at first report of developmental delay, or cognitive outcome. The risk of subsequent vaccination-associated seizures was significantly lower for acellular pertussis (9%; odds ratio 0.18, 95% confidence interval [CI] 0.05-0.71) and nonpertussis (8%; odds ratio 0.11, 95% CI 0.02-0.59) than whole-cell pertussis (37%; reference) vaccines. Self-controlled case series analysis showed an increased incidence rate ratio of seizures of 2.3 (95% CI 1.5-3.4) within the risk period of 5 to 12 days following MMR vaccination.

Conclusions:

Our results suggest that vaccination-associated earlier seizure onset does not alter disease course in DS, while the risk of subsequent vaccination-associated seizures is probably vaccine-specific.

Original languageEnglish
Pages (from-to)596-603
Number of pages8
JournalNeurology
Volume85
Issue number7
DOIs
Publication statusPublished - 18 Aug 2015

Keywords

  • WHOLE-CELL PERTUSSIS
  • ACELLULAR PERTUSSIS
  • FEBRILE SEIZURES
  • CONTROLLED-TRIAL
  • VACCINE
  • EPILEPSY
  • SCN1A
  • MEASLES
  • MUMPS
  • ENCEPHALOPATHY

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