Epilepsy in young people: 23 year follow up of the British national child development study

BMJ. 1998 Jan 31;316(7128):339-42. doi: 10.1136/bmj.316.7128.339.

Abstract

Objective: To estimate the incidence and prevalence of epilepsy during childhood and early adult life in England, Scotland, and Wales.

Design: Prospective study of 17,414 children born in England, Scotland, and Wales between 3 and 9 March 1958, followed up at 7, 11, 16, and 23 years of age, with a review of those with epilepsy at age 28.

Subjects: People with epilepsy developing at or before age 23.

Main outcome measures: The age specific incidence, cumulative incidence, and prevalence of epilepsy.

Results: 124 young people had a confirmed diagnosis of epilepsy during their first 23 years (cumulative incidence 8.4 per 1000; 95% confidence interval 6.8 to 10.0). 6 had died by age 23.46 (37%) had neurological impairment or another major health problem in addition to epilepsy. The prevalence of active epilepsy at age 23 was 6.3 per 1000 (4.9 to 7.7).

Conclusions: A wide variety of seizure disorders is included under the term epilepsy. A third of cases had generalised seizures. In only a quarter was the onset of seizures attributed to a specific cause. Children with additional health problems were more likely to continue to have seizures in early adult life than those with epilepsy alone. 1 in 8 were prescribed drug treatment for 6 years or more after their last seizure. All deaths occurred in young adults over the age of 16.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Child
  • Child Development
  • Child, Preschool
  • Cohort Studies
  • England / epidemiology
  • Epilepsy / drug therapy
  • Epilepsy / epidemiology*
  • Epilepsy / mortality
  • Follow-Up Studies
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Prevalence
  • Prospective Studies
  • Scotland / epidemiology
  • Wales / epidemiology