Between January 1992 and June 1995, 160 patients were presurgically ev
aluated for medically refractory epilepsy by the Epilepsy Monitoring a
nd Surgery Team at the University Hospital of Gent. All these patients
underwent a comprehensive presurgical evaluation, including extensive
neurological history and examination, video-EEG monitoring of intel i
ctal EEG and habitual seizures, CT and optimum MR. In a large subgroup
of these patients a comprehensive neuropsychological examination and
interictal (18)FDG-PET were pet-formed. After the non-invasive phase o
f the presurgical evaluation, a bilateral carotid angiography and intr
acarotid amytal procedure was planned in 27 patients to establish hemi
spheric language dominance and bilateral memory function. After proper
selection, 14 patients underwent invasive video-EEG monitoring with i
ntracranial implantation of parenchymal and/or subdural electrodes to
further document the area of seizure onset. From the initial group of
160 potential surgical candidates, 40 patients (20 M, 20 F) with mean
age of 31 years (range : 2 months - 55 years) and mean duration of unc
ontrolled seizures of 16 years (range : 2 months-47 years) eventually
underwent a surgical procedure. 30/40 patients were on high dose anti-
epileptic polytherapy. Optimum MR detected structural abnormalities, c
onfined to a limited brain area, in 39 patients. These abnormalities w
ere of space-occupying nature in 21 cases; an atrophic lesion was susp
ected in 17 patients. Structural abnormalities were most frequently lo
cated in the temporal lobe (n = 26) and the frontal lobe (n = 7). Vide
o-EEG monitoring documented complex partial seizures in 32 patients wi
th occasional secondary generalisation in 14. In most of these patient
s, seizures could be subclassified as being of temporal lobe origin ba
sed on clinical and EEG criteria. Two patients had only simple partial
seizures. One patient with Sturge-Weber syndrome and a strictly unila
teral angioma had hemiconvulsions. A mentally retarded patient with Le
nnox-Gastaut syndrome had different types of seizures. After non-invas
ive and invasive exploration, the area of seizure onset could be deter
mined in all patients. Standard or modified temporal lobectomy +/- hip
pocampectomy were the most commonly performed procedures (n = 26). In
5 patients complete lesionectomies were performed for epileptogenic st
ructural lesions in and outside the temporal lobe. In 2 patients only
partial lesionectomies were possible; in 5 patients only biopsies coul
d be performed. Anterior 2/3 callosotomy and hemispherectomy were each
performed in one patient. Postsurgical seizure control, after average
follow-up of 20 months (range : 6-40 months), was excellent in 27 pat
ients who became seizure-free. In these patients antiepileptic therapy
was tapered 2 years after surgery. An additional 4 patients continue
to experience non-disabling simple partial seizures only. Patients in
whom only biopsies ol partial lesionectomies were performed have poor
seizure control. Three patients died as a result of the intrinsic mali
gnancy of their space-occupying lesion. Two patients who are seizure f
ree experienced a moderate postoperative hemiparesis with subtotal rec
overy. Overall quality of life was substantially improved both in pati
ents who became entirely seizure free or who experienced a very signif
icant reduction in seizure frequency. Presurgical evaluation and epile
psy surgery are a labour intensive but rewarding therapeutic alternati
ve for patients with medically refractory epilepsy. Besides providing
therapeutic efficacy, comprehensive presurgical evaluation and epileps
y surgery allow for fruitful clinical neurological research.