Epidemiology
Epilepsy
is one of the most common of the serious neurological disorders. Genetic,
congenital, and developmental conditions are mostly associated with
it among younger patients; tumors are more likely over age 40; head
trauma and central nervous system infections may occur at any age. The
prevalence of active epilepsy is roughly in the range 5–10 per
1000 people. Up to 5% of people experience non febrile seizures at some
point in life; epilepsy's lifetime prevalence is relatively high because
most patients either stop having seizures or (less commonly) die of
it. Epilepsy's approximate annual incidence rate is 40–70 per
100,000 in industrialized countries and 100–190 per 100,000 in
resource-poor countries; socioeconomically deprived people are at higher
risk. In industrialized countries the incidence rate decreased in children
but increased among the elderly during the three decades prior to 2003,
for reasons not fully understood.
Beyond
symptoms of the underlying diseases that can cause certain epilepsies,
people with epilepsy are at risk for death from four main problems:
status epilepticus (most often associated with anticonvulsant noncompliance),
suicide associated with depression, trauma from seizures, and sudden
unexpected death in epilepsy (SUDEP) Those at highest risk for epilepsy-related
deaths usually have underlying neurological impairment or poorly controlled
seizures; those with more benign epilepsy syndromes have little risk
for epilepsy-related death.
Certain
diseases also seem to occur in higher than expected rates in people
with epilepsy, and the risk of these "comorbities" often varies
with the epilepsy syndrome. These diseases include depression and anxiety
disorders, migraine and other headaches, infertility and low sexual
libido. Attention-deficit/hyperactivity disorder (ADHD) affects three
to five times more children with epilepsy than children in the general
population. Epilepsy is prevalent in autism.