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Responsive Neurostimulation in Drug-Resistant Pediatric Epilepsy: Findings From the Epilepsy Surgery Subgroup of the Pediatric Epilepsy Research Consortium.
Singh, Rani K; Eschbach, Krista; Samanta, Debopam; Perry, M Scott; Liu, Gang; Alexander, Allyson L; Wong-Kisiel, Lily; Ostendorf, Adam; Tatachar, Priyamvada; Reddy, Shilpa B; McCormack, Michael J; Manuel, Chad M; Gonzalez-Giraldo, Ernesto; Numis, Adam L; Wolf, Steven; Karia, Samir; Karakas, Cemal; Olaya, Joffre; Shrey, Daniel; Auguste, Kurtis I; Depositario-Cabacar, Dewi.
Afiliación
  • Singh RK; Department of Pediatrics, Atrium Health-Levine Children's Hospital, Charlotte, North Carolina; Department of Pediatrics, Wake Forest School of Medicine, Winston-Salem, North Carolina. Electronic address: Rani.Singh@atriumhealth.org.
  • Eschbach K; Section of Neurology, Department of Pediatrics, University of Colorado School of Medicine, Children's Hospital Colorado, Aurora, Colorado.
  • Samanta D; Child Neurology Section, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Alaska.
  • Perry MS; Jane and John Justin Institute for Mind Health, Neurosciences Center, Cook Children's Medical Center, Ft Worth, Texas.
  • Liu G; Department of Pediatrics, Atrium Health-Levine Children's Hospital, Charlotte, North Carolina.
  • Alexander AL; Department of Neurosurgery, School of Medicine, Anschutz Medical Campus, University of Colorado, Aurora, Colorado; Division of Pediatric Neurosurgery, Children's Hospital Colorado, Aurora, Colorado.
  • Wong-Kisiel L; Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Ostendorf A; Division of Neurology, Department of Pediatrics, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
  • Tatachar P; Ann and Robert H Lurie Children's Hospital of Chicago, Chicago, Illinois.
  • Reddy SB; Department of Pediatrics, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee.
  • McCormack MJ; Department of Pediatrics, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Manuel CM; Department of Pediatrics, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Gonzalez-Giraldo E; Department of Neurology, University of California, San Francisco, San Francisco, California.
  • Numis AL; Department of Neurology, University of California, San Francisco, San Francisco, California.
  • Wolf S; Department of Pediatrics, Boston Children's Health Physicians, New York, New York.
  • Karia S; Division of Child Neurology, University of Louisville School of Medicine, Louisville, Kentucky.
  • Karakas C; Division of Child Neurology, University of Louisville School of Medicine, Louisville, Kentucky.
  • Olaya J; Department of Neurosurgery, Children's Hospital Orange County, Orange, California.
  • Shrey D; Department of Neurosciences, Children's Hospital Orange County, Orange, California.
  • Auguste KI; Department of Neurosurgery, University of California, San Francisco, San Francisco, California.
  • Depositario-Cabacar D; Department of Neurology, Children's National Medical Center, Washington, District of Columbia.
Pediatr Neurol ; 143: 106-112, 2023 06.
Article en En | MEDLINE | ID: mdl-37084698
ABSTRACT

BACKGROUND:

Responsive neurostimulation (RNS), a closed-loop intracranial electrical stimulation system, is a palliative surgical option for patients with drug-resistant epilepsy (DRE). RNS is approved by the US Food and Drug Administration for patients aged ≥18 years with pharmacoresistant partial seizures. The published experience of RNS in children is limited.

METHODS:

This is a combined prospective and retrospective study of patients aged ≤18 years undergoing RNS placement. Patients were identified from the multicenter Pediatric Epilepsy Research Consortium Surgery Registry from January 2018 to December 2021, and additional data relevant to this study were retrospectively collected and analyzed.

RESULTS:

Fifty-six patients received RNS during the study period. The mean age at implantation was 14.9 years; the mean duration of epilepsy, 8.1 years; and the mean number of previously trialed antiseizure medications, 4.2. Five patients (9%) previously trialed dietary therapy, and 19 patients (34%) underwent prior surgery. Most patients (70%) underwent invasive electroencephalography evaluation before RNS implantation. Complications occurred in three patients (5.3%) including malpositioned leads or transient weakness. Follow-up (mean 11.7 months) was available for 55 patients (one lost), and four were seizure-free with RNS off. Outcome analysis of stimulation efficacy was available for 51 patients 33 patients (65%) were responders (≥50% reduction in seizure frequency), including five patients (10%) who were seizure free at follow-up.

CONCLUSIONS:

For young patients with focal DRE who are not candidates for surgical resection, neuromodulation should be considered. Although RNS is off-label for patients aged <18 years, this multicenter study suggests that it is a safe and effective palliative option for children with focal DRE.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Epilepsia / Epilepsia Refractaria Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Epilepsia / Epilepsia Refractaria Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2023 Tipo del documento: Article