Evidence map›Paper›PMID 41547690›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

Evaluation of the outcomes of vagal nerve stimulation in children with drug-refractory epilepsy in South Africa.

Edmund Kibuuka, Denis Mutyaba, John Ouma, Jason Labuschagne

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Edmund KibuukaDepartment of Neurosurgery, University of the Witwatersrand, Johannesburg, South Africa.
Denis MutyabaDepartment of Neurosurgery, University of the Witwatersrand, Johannesburg, South Africa.
John OumaDepartment of Neurosurgery, University of the Witwatersrand, Johannesburg, South Africa.
Jason LabuschagneDepartment of Neurosurgery, University of the Witwatersrand, Johannesburg, South Africa. Jason.labuschagne@icloud.com.ORCID http://orcid.org/0000-0002-6567-0131

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate the clinical outcomes of vagal nerve stimulation (VNS) in children with drug refractory epilepsy (DRE) in a Sub-Saharan setting.

methodsWe retrospectively reviewed the data of 93 paediatric patients with DRE who underwent VNS insertion between January 2008 and December 2022. Patient demographics, aetiology of epilepsy and seizure data were analyzed. Seizure outcomes were measured using the Engel, McHugh, and Hague scores. Statistical analysis was performed using the Chi-square test, T-tests, and Spearman's correlation.

resultsOf the 93 patients who underwent VNS implantation 60% achieved a seizure reduction of at least 50%. Demographic factors associated with improved seizure control included age at implantation (p < 0.001) and shorter duration from first reported seizure to implantation (p < 0.001). The mean time to response was 6.9 months. The McHugh scale showed a significant association between the length of follow up and VNS response. Adverse effects of VNS insertion were limited. Our outcome data and complication rates were in line with previous studies from the developed world. Challenges unique to our population included delay from diagnosis to referral; on average, there was a 5-year period from diagnosis of DRE to referral to our center. In addition to the large population and our extensive geographic referral pattern, we identified that a key factor in delayed referral to our center was due to a poor awareness, amongst both caregivers and referring clinicians of VNS as a treatment option for DRE.

conclusionVNS is a safe and effective adjunctive treatment for children with DRE in the Sub-Saharan population, with results comparable to centers in the developed world. In our cohort of patients, the McHugh scale appeared to be a more sensitive tool for assessing and tracking VNS response.

Indexed as

Drug Resistant EpilepsyVagus Nerve StimulationAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesSouth AfricaTreatment OutcomeLMICNeuromodulationVagal nerve stimulation

Identifiers

PMID41547690
PMCPMC12812073

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