Evidence map›Paper›PMID 41576312›Full record

ArticleNeurology2026

Safety of Intracranial Neuromodulation in Drug-Resistant Pediatric and Adult Epilepsy.

Cheng-Yen Kuo, Filip Mivalt, Raunak Singh, Ryan Toan Dinh Nguyen, Donnie Keith Starnes, Lily Wong-Kisiel, Nicholas M Gregg, Jamie Joseph Van Gompel, Kai Miller, Gregory A Worrell and 1 more

Abstract read
In one paragraph

Article in Neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Cheng-Yen KuoDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-8406-3660
Filip MivaltDepartments of Neurology, Mayo Clinic, Rochester, MN.
Raunak SinghDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-8659-146X
Ryan Toan Dinh NguyenDepartments of Neurology, Mayo Clinic, Rochester, MN.
Donnie Keith StarnesDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-9111-4243
Lily Wong-KisielDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-5306-0862
Nicholas M GreggDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-6151-043X
Jamie Joseph Van GompelDepartments of Neurosurgery, Mayo Clinic, Rochester, MN.
Kai MillerDepartments of Neurosurgery, Mayo Clinic, Rochester, MN.
Gregory A WorrellDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0003-2916-0553
Brian N LundstromDepartments of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-5310-5549

Funding

Novel Diagnostic Stimulation to Quantify Cortical Excitability and Guide Epilepsy TherapyR01NS129622 · NINDS · MAYO CLINIC ROCHESTER · PI Brian Nils Lundstrom · 2023 to 2026
$1.6M
NINDS NIH HHS R01 NS129622
6 · The paper itself

Abstract

BACKGROUND AND

objectivesIntracranial neuromodulation is an established therapy for drug-resistant epilepsy (DRE) in adults. Improving seizure outcomes and expanding its application to pediatric patients remain priorities. Off-label use of 2-lead and 4-lead devices targeting multiple network nodes, combined with varied stimulation parameters, has emerged in pursuit of better outcomes. Although early findings are promising, the safety of these approaches remains underexplored. This study evaluates adverse event (AE) rates associated with different intracranial neuromodulation devices from a single center.

methodsThis retrospective study from the Mayo Clinic (Rochester, MN) included patients with DRE who underwent intracranial neuromodulation between August 2004 and December 2024. Demographic data, epilepsy characteristics, treatment indications, procedural details, and AEs were extracted from medical records. AEs are undesirable events associated with implantation and use of the device, regardless of causation. Serious AEs were life threatening or resulted in hospitalization, persistent or significant disability, or death. Patients were classified as children (<13 years), adolescents (13-18 years), or adults (≥19 years).

resultsA total of 217 patients (108 male patients, 109 female patients; 14 children, 43 adolescents, 160 adults) were analyzed. Devices included 2-lead deep brain stimulation (DBS) (111 patients), 4-lead DBS (51 patients), and responsive neurostimulation (55 patients). Device-related AEs included stimulation-related paresthesia (7.8%), infections (4.1%), asymptomatic intracranial hemorrhage (ICH) (3.7%), bowstring effect (extension wire tethering that limits neck mobility) (3.2%), operation-related focal weakness (2.3%), wound dehiscence (1.8%), device migration (1.8%), lead malposition (1.4%), lead fracture (1.4%), lead migration (0.5%), extensor wire fracture (0.5%), extrusion (0.5%), and symptomatic ICH (0.5%). While no significant difference in overall AE rates was found between sexes, device explantation was significantly higher in female patients than in male patients (11.9% [13/109] vs 1.9% [2/108], DISCUSSION: Intracranial neuromodulation demonstrated an acceptable safety profile across sexes and age groups. However, children and patients with 4-lead DBS systems were at increased risk of the bowstring effect. These findings highlight the need for tailored device design and surgical strategies to optimize safety, particularly in pediatric populations.

Indexed as

Deep Brain StimulationDrug Resistant EpilepsyAdolescentAdultChildElectrodes, ImplantedFemaleHumansMaleMiddle AgedRetrospective StudiesYoung Adult

Identifiers

PMID41576312
PMCPMC13263061

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.