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Review
. 2022 Feb 23:13:796846.
doi: 10.3389/fneur.2022.796846. eCollection 2022.

Deep Brain Stimulation for Refractory Temporal Lobe Epilepsy. Current Status and Future Trends

Affiliations
Review

Deep Brain Stimulation for Refractory Temporal Lobe Epilepsy. Current Status and Future Trends

Francisco Velasco et al. Front Neurol. .

Abstract

A comparative analysis of the targets for deep brain stimulation (DBS) to treat refractory temporal lobe epilepsy and the rationale for its use is presented, with an emphasis on the latency to obtain the significant antiepileptic effect and the long-term seizure control. The analysis includes consideration of surgical techniques currently used to optimize antiseizure effects and decrease surgical risks. Seizure control is similar for programed DBS and DBS responsive to abnormal cortical or subcortical electroencephalogram (EEG) activity. There is no difference in the long-term seizure control between programmed and responsive and intermittent or continuous DBS. However, intermittent programed DBS may have a significant antiseizure effect starting in the first month when applied to a non-sclerotic tissue such as the parahippocampal cortex. DBS induces no neuropsychological deterioration.

Keywords: GABAergic antiepileptic mechanisms; deep brain stimulation; hippocampal sclerosis; neuropsychological evaluation; para-hippocampal cortex; refractory mesial temporal lobe epilepsy; subiculum.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Percentage decrease of seizures from baseline along the 18th month follow-up of the 3 groups studied: Blue line H-DBS, Black line S-DBS and Red line PHC-DBS. * Indicates the significance of seizure reduction p < 0.05 for PHC-DBS occurring since the first month on DBS.
Figure 2
Figure 2
Diagram of a coronal section of the temporal lobe that illustrates the size and location of the studied targets: in blue the hippocampus including dentate gyrus (DG) and Ammon fields C1–C3; subiculum (S); para-hippocampal cortex (PH). Notice the Hippocampus (DG+ CA1-3) and Subiculum (S) are smaller and closer to the Sylvian vessels.

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