Abstract

To study the efficacy of vagus nerve stimulation (VNS) therapy as an adjunctive treatment for intractable epilepsy in patients under 12 years of age, we analyzed 2-year postimplant data of 35 consecutive patients. Of the 35 patients, 18 (51.4%) at 6 months, 18 (51.4%) at 12 months, and 21 (60.1%) at 24 months showed ≥50% reduction in seizure frequency (responders). Although incremental seizure freedom was noted, no patient remained seizure-free throughout the 3 study periods. Partial response (≥50% seizure reduction in 2 or less study periods) was seen in 8 (22.9%) patients. Twelve patients (34.3%) were nonresponders. Out of 29 patients with primary generalized epilepsy, 20 (68.9%) and, out of 6 patients with focal epilepsy, 3 (50%) had ≥50% seizure control in at least one study period. No major complications or side effects requiring discontinuation of VNS therapy were encountered. We conclude that (1) patients with intractable primary generalized epilepsy respond better to VNS therapy, (2) cumulative effect of neuromodulation with improving responder rate to seizure freedom with continuation of VNS therapy is noted, and (3) VNS therapy is safe and is well tolerated in children receiving implant under 12 years of age.

Highlights

  • Neuromodulation therapies are nonpharmacotherapeutic options for patients with drug resistant epilepsy who are not candidates for resective epilepsy surgery

  • One study of 11 patients with tuberous sclerosis had a mean age of 14 years with a range from 2 to 35 years [23]

  • vagus nerve stimulation (VNS) therapy has been approved as adjunctive treatment for drug resistant focal epilepsy in patients >12 years of age [1]

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Summary

Introduction

Neuromodulation therapies are nonpharmacotherapeutic options for patients with drug resistant epilepsy who are not candidates for resective epilepsy surgery. Initial studies with randomized controlled trials reporting on the efficacy of VNS involved rather short followup duration (3 months to 3.5 months) and ≥50% seizure reduction ranged from 23.4% to 39% of the patients [2,3,4,5]. Since 1999, several studies have reported long-term followup ranging from 6 months to 10 years with ≥50% seizure reduction observed in 35% to 63.8% of the patients [6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22]

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