Am. Kanner et al., THE UTILITY OF PLACING SPHENOIDAL ELECTRODES UNDER THE FORAMEN OVALE WITH FLUOROSCOPIC GUIDANCE, Journal of clinical neurophysiology, 12(1), 1995, pp. 72-81
Although sphenoidal electrodes are widely used to detect epileptiform
activity, there is no agreement on an optimal target to which electrod
es should be aimed. The purpose of this study was to determine whether
fluoroscopic guidance is a reliable method for placing electrodes dir
ectly below the foramen ovale and whether such positioning enhances th
eir capacity to detect epileptiform activity when compared to similar
electrodes placed blindly into the infratemporal fossa. We examined th
e surface/sphenoidal EEG recordings of 17 patients with intractable pa
rtial seizures of anterotemporal origin, after fluoroscopically placed
sphenoidal electrodes (FPSE) had been inserted to lie just below the
foramen ovale. A criterion for eligibility was a previous prolonged vi
deo/EEG monitoring with blindly placed sphenoidal electrodes (BPSE) th
at failed to detect seizures with a focal onset, No blindly placed ele
ctrode, for which there was radiographic documentation, reached the fo
ramen ovale. Fluoroscopic guidance assured accurate targeting. FPSE de
tected a unilateral anterotemporal interictal focus in four patients i
n whom BPSE had failed to record any interictal spikes and detected bi
temporal independent interictal foci in one patient in whom BPSE had i
dentified only unilateral spikes. In nine other patients, the spike co
unt obtained with FPSE recordings increased by >100% when compared to
that obtained with BPSE recordings. FPSE recorded seizures with an ant
erotemporal focal onset pattern in 10 patients in whom BPSE had record
ed seizures with a regional, lateralized, or nonlocalized onset patter
n. In nine of these 10 patients, this was adequate to recommend surger
y and avoid invasive monitoring. Fluoroscopic guidance assures accurat
e targeting of the foramen ovale. When compared to BPSE, FPSE resulted
in better detection of interictal and ictal epileptiform activity of
mesial-basal-temporal origin.