Objective: To assess the extent to which adults with epilepsy were optimize
d and individualized on phenytoin monotherapy in the Western Cape, South Af
rica and to estimate the average optimized dose and serum phenytoin concent
ration, and the therapeutic range for this patient group.
Methods: Patients were considered to be optimized on phenytoin if they were
seizure-free or the best compromise was achieved between seizure reduction
and side-effects.
Results: 538 (233 black and 305 coloured) adult people with epilepsy were t
reated at nine epilepsy clinics as outpatients. Of these patients, 332 (226
male and 106 female, 149 black and 183 coloured) were included in the data
analysis as they were considered to have reliable phenytoin levels. Phenyt
oin doses and steady-state serum concentrations were predicted using the Mi
chaelis-Menten equation. Patients attended a clinical pharmacokinetic servi
ce for 7.7 +/- 5.3 (range 1-22) months. The average optimized dose was 305.
8 (range 100-500) mg/day and the average optimized level was 62.7 +/- 23.9
(range 15-133) mu mol/l. Most patients (61.9%) were optimized in the therap
eutic range 40-79 mu mol/l; 21.1% were optimized above and 17% below this r
ange. In 1.6% of patients serum concentrations above 120 mu mol/l were requ
ired. Dosage adjustments were made in 47.0% of patients, increased in 31.9%
and reduced in 15.1%.
Conclusion: These findings indicate that many patients (47%) attending outp
atient clinics were not optimized on phenytoin therapy.