Propagation of interictal discharges in temporal lobe epilepsy: Correlation of spatiotemporal mapping with intracranial foramen ovale electrode recordings

2006 ◽  
Vol 117 (12) ◽  
pp. 2615-2626 ◽  
Author(s):  
D ZUMSTEG ◽  
A FRIEDMAN ◽  
H WIESER ◽  
R WENNBERG
2018 ◽  
Vol 129 ◽  
pp. e146
Author(s):  
Jason B. Richards ◽  
Lina Barker ◽  
Aatif M. Husain ◽  
Matthew Luedke ◽  
Saurabh R. Sinha ◽  
...  

2008 ◽  
Vol 62 (suppl_5) ◽  
pp. ONS481-ONS489 ◽  
Author(s):  
Martin Ortler ◽  
Gerlig Widmann ◽  
Eugen Trinka ◽  
Thomas Fiegele ◽  
Wilhelm Eisner ◽  
...  

Abstract Objective: Semi-invasive foramen ovale electrodes (FOEs) are used as an alternative to invasive recording techniques in the presurgical evaluation of patients with temporal lobe epilepsy. To maximize patient safety and interventional success, frameless stereotactic FOE placement by use of a variation of an upper jaw fixation device with an external fiducial frame, in combination with an aiming device and standard navigation software, was evaluated by the Innsbruck Epilepsy Surgery Program. Methods: Patients were immobilized noninvasively with the Vogele-Bale-Hohner headholder (Medical Intelligence GmbH, Schwabmünchen, Germany) to plan computed tomography and surgery. Frameless stereotactic cannulation of the foramen and intracranial electrode placement were achieved with the help of an aiming device mounted to the base plate of the headholder. Ease of applicability, safety, and results obtained with foramen ovale recording were investigated. Results: Twenty-six FOEs were placed in 13 patients under general anesthesia. The foramen ovale was successfully cannulated in all patients. One patient reported transient painful mastication after the procedure as a complication attributable to use of the Vogele-Bale-Hohner mouthpiece. In one patient, a persistent slight buccal hypesthesia was present 3 months after the procedure. To pass the foramen, slight adjustments in the needle position had to be made in 10 sides (38.4%). To place the intracranial electrodes, adjustments were necessary six times (23.7%). An entirely new path had to be planned once (3.8%). Seizure recording provided conclusive information in all patients (100%). Outcome in operated patients was Engel Class Ia in six patients, Class IId in one patient, Class IIb in one patient, and Class IVa in one patient (minimum follow-up, 6 mo). Conclusion: The Vogele-Bale-Hohner headholder combined with an external registration frame eliminates the need for invasive head clamp fixation. FOE placement can be planned “offline” and performed under general anesthesia later. This can be valuable in patients with distorted anatomy and/or small foramina or in patients not able to undergo the procedure under sedation. Results are satisfactory with regard to patient safety, patient comfort, predictability, and reproducibility. FOEs supported further treatment decisions in all patients.


Epilepsia ◽  
2014 ◽  
Vol 55 (5) ◽  
pp. 713-724 ◽  
Author(s):  
Sameer A. Sheth ◽  
Joshua P. Aronson ◽  
Mouhsin M. Shafi ◽  
H. Wesley Phillips ◽  
Naymee Velez-Ruiz ◽  
...  

2002 ◽  
Vol 87 (1) ◽  
pp. 634-639 ◽  
Author(s):  
Margherita D'Antuono ◽  
Ruba Benini ◽  
Giuseppe Biagini ◽  
Giovanna D'Arcangelo ◽  
Michaela Barbarosie ◽  
...  

In mouse brain slices that contain reciprocally connected hippocampus and entorhinal cortex (EC) networks, CA3 outputs control the EC propensity to generate experimentally induced ictal-like discharges resembling electrographic seizures. Neuronal damage in limbic areas, such as CA3 and dentate hilus, occurs in patients with temporal lobe epilepsy and in animal models (e.g., pilocarpine- or kainate-treated rodents) mimicking this epileptic disorder. Hence, hippocampal damage in epileptic mice may lead to decreased CA3 output function that in turn would allow EC networks to generate ictal-like events. Here we tested this hypothesis and found that CA3-driven interictal discharges induced by 4-aminopyridine (4AP, 50 μM) in hippocampus-EC slices from mice injected with pilocarpine 13–22 days earlier have a lower frequency than in age-matched control slices. Moreover, EC-driven ictal-like discharges in pilocarpine-treated slices occur throughout the experiment (≤6 h) and spread to the CA1/subicular area via the temporoammonic path; in contrast, they disappear in control slices within 2 h of 4AP application and propagate via the trisynaptic hippocampal circuit. Thus, different network interactions within the hippocampus-EC loop characterize control and pilocarpine-treated slices maintained in vitro. We propose that these functional changes, which are presumably caused by seizure-induced cell damage, lead to seizures in vivo. This process is facilitated by a decreased control of EC excitability by hippocampal outputs and possibly sustained by the reverberant activity between EC and CA1/subiculum networks that are excited via the temporoammonic path.


Author(s):  
Ancor Sanz-García ◽  
Lorena Vega-Zelaya ◽  
Jesús Pastor ◽  
Cristina V. Torres ◽  
Rafael G. Sola ◽  
...  

Epilepsia ◽  
2006 ◽  
Vol 47 (8) ◽  
pp. 1300-1307 ◽  
Author(s):  
Tonicarlo R. Velasco ◽  
Americo C. Sakamoto ◽  
Veriano Alexandre ◽  
Roger Walz ◽  
Charles L. Dalmagro ◽  
...  

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