4.4 Article

Vagus nerve stimulation for drug-resistant epilepsy induced by tuberous sclerosis complex

Journal

EPILEPSY & BEHAVIOR
Volume 126, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yebeh.2021.108431

Keywords

Vagus nerve stimulation; Tuberous sclerosis complex; Drug-resistant epilepsy; Neuropsychological evaluation; Depression

Funding

  1. Major Program of the National Natural Science Foundation of China [81790654, 81790650, 81790651, 11932003]
  2. Capital's Funds for Health Improvement and Research [2020-4-8012]

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This study shows that Vagus Nerve Stimulation (VNS) is a safe and effective treatment for drug-resistant epilepsy (DRE) induced by tuberous sclerosis complex (TSC), and it may improve cognitive and emotional states in patients. Further investigations are needed to validate the results.
Objective: This study investigated the dynamic and long-term efficacy of vagus nerve stimulation (VNS) in patients with drug-resistant epilepsy (DRE) induced by tuberous sclerosis complex (TSC). In addition, the impact of VNS on cognition and emotion after a one-year follow-up was evaluated. Methods: A total of 17 patients diagnosed with DRE induced by TSC were retrospectively recruited between 2008 and 2019. Dynamic changes in seizure frequency were observed in the responders (>50% reduction of seizure frequency at last follow-up) and non-responders. Clinical characteristics and seizure outcomes were comprehensively analyzed to determine factors associated with seizure outcomes. The Wechsler intelligence scale was applied in a subgroup of six pediatric patients, whereas the Self-rating Anxiety Scale (SAS) and Self-rating Depression Scale (SDS) were assessed in a subgroup of nine patients to determine the impact of VNS therapy on cognitive performance and emotional state. Results: The follow-up duration for the 17 patients who underwent VNS treatment ranged from 0.5 to 10 years (mean +/- SD: 4.1 +/- 3.2 years). Monthly seizures decreased significantly from three months to four years post-treatment (p < 0.05). At the last follow-up, 70.6% of the patients achieved at least a 50% reduction in seizure frequency, and three patients were completely seizure free. Comparatively, non-responder patients experienced deterioration of seizure frequency after the first year. Notably, after one-year follow-up the mean standard score of full-scale intelligence quotient increased from 67.33 to 69.5 (p = 0.078) while the mean, standard score of SDS decreased from 49.22 to 45.67 (p = 0.003) compared to preoperative neuropsychological evaluation results. Conclusion: VNS is a safe and effective treatment for patients with DRE caused by TSC. Although early outcomes were encouraging, a follow-up of at least one-year was required to predict long-term outcomes in patients receiving VNS treatment. Moreover, VNS may improve depressive mood in patients with DRE caused by TSC. Further investigations are needed to validate the present results. (c) 2021 Elsevier Inc. All rights reserved.

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