Complications and Mortality Rate of Vagus Nerve Stimulation for Drug-Resistant Epilepsy
- PMID: 39099993
- PMCID: PMC11297726
- DOI: 10.7759/cureus.63842
Complications and Mortality Rate of Vagus Nerve Stimulation for Drug-Resistant Epilepsy
Abstract
Objective: The goal of this study is to evaluate the complications and mortality associated with vagus nerve stimulation (VNS).
Methods: We retrospectively reviewed medical records of patients who underwent VNS implantation for the treatment of drug-resistant epilepsy (DRE) between 2000 and 2023. The mean follow-up time was 10.6 years, ranging from three months to 22 years.
Results: In total, 55 adult and pediatric patients received VNS therapy with 117 procedures performed over 23 years. The most common early complications were hoarseness and cough which were reported in eight adult patients (6.8%). Four children with intellectual disability (ID) had infection (3.4%), eight patients had lead breakage (6.8%), and two had device migration (1.7%). Four of all patients (7.3%) demonstrated late complications due to chronic nerve stimulation including vocal cord dysfunction, late-onset severe AV block, and obstructive sleep apnea (OSA). Three patients (5.5%) had VNS deactivated permanently due to complications and/or lack of efficacy. Two patients died from probable sudden unexpected death in epilepsy (SUDEP) with an incidence of 3.4/1000 person-years.
Conclusions: VNS therapy is safe over long-term follow-up but not without risks. Most post-operative complications are minor and transient for adults. Children with ID tend to have infection and device migration. Late-onset cardiac complications and OSA can develop in some patients during VNS therapy and should not be overlooked. The SUDEP rate may decrease with VNS therapy over time.
Keywords: av block; complications; drug-resistant epilepsy; sleep apnea; sudep (sudden unexplained death in epilepsy); vagus nerve stimulation.
Copyright © 2024, Ma et al.
Conflict of interest statement
Human subjects: Consent was obtained or waived by all participants in this study. IRB Committee of Walter Reed National Military Medical Center issued approval WRNMMC-EDO-2023-1129. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: Disclaimer: The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Uniformed Services University of the Health Sciences, Department Health Agency, Department of Defense or the U.S. Government. .
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