Seizures are extremely common in the elderly, with an annual incidence reac
hing 100 per 100 000 people aged over 60 years. Most are precipitated by ac
ute symptomatic illnesses such as stroke or systemic disease. Chronic neuro
logical diseases such as Alzheimer's disease may also cause seizure. The ae
tiology of seizures in many patients is unknown. Seizures may be situationa
l and subside quickly, but the prevalence of chronic seizures - epilepsy -
is as high as 1% in the elderly. The majority of seizures are of partial on
set, especially complex partial. Complex partial seizures at this age may b
e very subtle and hard to diagnose. Generalised-onset seizures also occur,
perhaps as a result of diffuse changes with aging or degenerative disease o
r to a combination of genetic and environmental factors.
The prognosis for complete seizure control in this population is relatively
favourable. Physiological and disease-related changes with aging result in
complex pharmacokinetics. Most changes lend to a need for gentler drug tre
atment with cautious initiation of drugs at lower dosages. Consideration mu
st be given to renal and hepatic function. protein binding and drug interac
tions. Determinations of free (unbound) drug concentrations are helpful for
highly protein bound drugs. The dosages of newer drugs excreted renally mu
st be adjusted based on creatinine clearance. The dosage of most drugs is d
etermined empirically by careful observation of seizure control and adverse
effects. Carbamazepine, valproic acid (sodium valproate). gabapentin and l
amotrigine have certain theoretical advantages, hut comparative trials of a
nticonvulsants in the elderly are needed. The ideal drug for older patients
would be effective, without neurological toxicity. with low protein bindin
g, a nonparticipant in drug interactions and amenable to once daily adminis
tration.