Temporo-Parietal Extraventricular Approach for Deep Brain Stimulation Targeting the Anterior Nucleus of the Thalamus: Institutional Experience

Author:

Parisi Veronica1,Gregg Nicholas M.2,Lundstrom Brian N.2,Alcala-Zermeno Juan Luis23,Worrell Gregory2,Kerezoudis Panagiotis4,Grewal Sanjeet S.5,Brinkmann Benjamin H.2,Middlebrooks Erik H.6,Van Gompel Jamie J.4ORCID

Affiliation:

1. Department of Neurosurgery, AORN “Antonio Cardarelli”, Naples, Italy;

2. Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA;

3. Department of Neurology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA;

4. Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA;

5. Department of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA;

6. Department of Radiology, Mayo Clinic, Jacksonville, Florida, USA

Abstract

BACKGROUND AND OBJECTIVES: The anterior nucleus of the thalamus (ANT) is a common target for deep brain stimulation (DBS) for drug-resistant epilepsy (DRE). However, the surgical approach to the ANT remains challenging because of its unique anatomy. This study aims to summarize our experience with the posterior temporo-parietal extraventricular (TPEV) approach targeting the ANT for DBS in DRE. METHODS: We performed a retrospective analysis of patients with DRE who underwent ANT-DBS using the TPEV approach between January 2011 and February 2021. Subjects with at least 6-month follow-up were eligible. The final lead position and number of active contacts targeting the anteroventral nucleus (AV) of the ANT were assessed using Lead-DBS. Mean seizure frequency reduction percentage and responder rate (≥50% decrease in seizure frequency) were determined. RESULTS: Thirty-one patients (mean age: 32.9 years; 52% female patients) were included. The mean follow-up period was 27.6 months ± 13.9 (29, 16-36). The mean seizure frequency reduction percentage was 65% ± 26 (75, 50-82). Twenty-six of 31 participants (83%) were responders, P < .001. Two subjects (6%) were seizure-free for at least 6 months at the last evaluation. Antiepileptic drugs dose and/or number decreased in 17/31 subjects (55%). The success rate for placing at least 1 contact at AV was 87% (27/31 patients) bilaterally. The number of active contacts at the AV was significantly greater in the responder group, 3.1 ± 1.3 (3, 2-4) vs 1.8 ± 1.1 (2, 1-2.5); P = .041 with a positive correlation between the number of active contacts and seizure reduction percentage; r = 0.445, R2 = 0.198, P = .012. CONCLUSION: The TPEV trajectory is a safe and effective approach to target the ANT for DBS. Future studies are needed to compare the clinical outcomes and target accuracy with the standard approaches.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Surgery

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