Stereo-electroencephalography (SEEG) in children surgically cured of their epilepsy

Delphine Taussig1, Axel Lebas2, Mathilde Chipaux1

  • 1Service de neurochirurgie pédiatrique, fondation Rothschild, 25-29, rue Manin, 75940 Paris cedex 19, France.

Insights

Stereoelectroencephalography (SEEG) in children is safe and effective for identifying the epileptogenic zone, leading to successful surgical outcomes. Younger children appear to have less complex epileptic networks, suggesting tailored surgical approaches.

Area of Science:

  • Pediatric Neurology
  • Neurosurgery
  • Epileptology

Background:

  • Stereoelectroencephalography (SEEG) is an invasive neurophysiological method used to precisely localize the epileptogenic zone in refractory epilepsy.
  • Its safety and efficacy in pediatric populations require detailed investigation.

Purpose of the Study:

  • To analyze SEEG data in children who achieved surgical cure.
  • To evaluate the safety and outcomes of SEEG in pediatric epilepsy surgery.
  • To compare SEEG findings and surgical outcomes between younger (<5 years) and older (≥5 years) children.

Main Methods:

  • Retrospective analysis of 48 children who underwent SEEG and subsequent epilepsy surgery with at least one-year follow-up.
  • Detailed review of demographic, surgical, and SEEG recording data.
  • Comparison between two age groups: <5 years (Group 1) and ≥5 years (Group 2).

Main Results:

  • SEEG was well-tolerated with minimal complications (one case of asymptomatic intracerebral bleeding).
  • Auras were significantly more frequent in older children (Group 2).
  • SEEG enabled tailored resections, including multilobar and infralobar procedures; interictal abnormalities were less frequent in younger children (Group 1).

Conclusions:

  • SEEG in children demonstrates low morbidity and facilitates successful epilepsy surgery.
  • The epileptic network may be less complex in younger children, warranting further quantitative analysis.
  • SEEG is a valuable tool for guiding surgical resection in pediatric epilepsy.
Abstract

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