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Brain-responsive neurostimulation in patients with medically intractable seizures arising from eloquent and other neocortical areas.
Jobst, Barbara C; Kapur, Ritu; Barkley, Gregory L; Bazil, Carl W; Berg, Michel J; Bergey, Gregory K; Boggs, Jane G; Cash, Sydney S; Cole, Andrew J; Duchowny, Michael S; Duckrow, Robert B; Edwards, Jonathan C; Eisenschenk, Stephan; Fessler, A James; Fountain, Nathan B; Geller, Eric B; Goldman, Alica M; Goodman, Robert R; Gross, Robert E; Gwinn, Ryder P; Heck, Christianne; Herekar, Aamr A; Hirsch, Lawrence J; King-Stephens, David; Labar, Douglas R; Marsh, W R; Meador, Kimford J; Miller, Ian; Mizrahi, Eli M; Murro, Anthony M; Nair, Dileep R; Noe, Katherine H; Olejniczak, Piotr W; Park, Yong D; Rutecki, Paul; Salanova, Vicenta; Sheth, Raj D; Skidmore, Christopher; Smith, Michael C; Spencer, David C; Srinivasan, Shraddha; Tatum, William; Van Ness, Paul; Vossler, David G; Wharen, Robert E; Worrell, Gregory A; Yoshor, Daniel; Zimmerman, Richard S; Skarpaas, Tara L; Morrell, Martha J.
Afiliação
  • Jobst BC; Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, U.S.A.
  • Kapur R; NeuroPace, Inc., Mountain View, California, U.S.A.
  • Barkley GL; Henry Ford Hospital, Detroit, Michigan, U.S.A.
  • Bazil CW; Columbia University Medical Center, New York, New York, U.S.A.
  • Berg MJ; University of Rochester Medical Center, Rochester, New York, U.S.A.
  • Bergey GK; Johns Hopkins Medicine, Baltimore, Maryland, U.S.A.
  • Boggs JG; Wake Forest University Health Sciences, Winston-Salem, North Carolina, U.S.A.
  • Cash SS; Massachusetts General Hospital, Boston, Massachusetts, U.S.A.
  • Cole AJ; Massachusetts General Hospital, Boston, Massachusetts, U.S.A.
  • Duchowny MS; Miami Children's Hospital / Nicklaus Children's Hospital, Miami, Florida, U.S.A.
  • Duckrow RB; Yale University School of Medicine, New Haven, Connecticut, U.S.A.
  • Edwards JC; Medical University of South Carolina, Charleston, South Carolina, U.S.A.
  • Eisenschenk S; University of Florida, Gainesville, Florida, U.S.A.
  • Fessler AJ; University of Rochester Medical Center, Rochester, New York, U.S.A.
  • Fountain NB; University of Virginia School of Medicine, Charlottesville, Virginia, U.S.A.
  • Geller EB; Institute of Neurology and Neurosurgery at Saint Barnabas, Livingston, New Jersey, U.S.A.
  • Goldman AM; Baylor College of Medicine, Houston, Texas, U.S.A.
  • Goodman RR; Saint Luke's Hospital, New York, New York, U.S.A.
  • Gross RE; Emory University School of Medicine, Atlanta, Georgia, U.S.A.
  • Gwinn RP; Swedish Neuroscience Institute, Seattle, Washington, U.S.A.
  • Heck C; Keck School of Medicine of USC, Los Angeles, California, U.S.A.
  • Herekar AA; Via Christi Epilepsy Center, Wichita, Kansas, U.S.A.
  • Hirsch LJ; Yale University School of Medicine, New Haven, Connecticut, U.S.A.
  • King-Stephens D; California Pacific Medical Center, San Francisco, California, U.S.A.
  • Labar DR; Weill Cornell Medical College, New York, New York, U.S.A.
  • Marsh WR; Mayo Clinic Minnesota, Rochester, Minnesota, U.S.A.
  • Meador KJ; Stanford University, Stanford, California, U.S.A.
  • Miller I; Miami Children's Hospital / Nicklaus Children's Hospital, Miami, Florida, U.S.A.
  • Mizrahi EM; Baylor College of Medicine, Houston, Texas, U.S.A.
  • Murro AM; Augusta University, Augusta, Georgia, U.S.A.
  • Nair DR; Cleveland Clinic Foundation, Cleveland, Ohio, U.S.A.
  • Noe KH; Mayo Clinic Arizona, Scottsdale, Arizona, U.S.A.
  • Olejniczak PW; Louisiana State University, New Orleans, Louisiana, U.S.A.
  • Park YD; Augusta University, Augusta, Georgia, U.S.A.
  • Rutecki P; University of Wisconsin Hospital and Clinics, Madison, Wisconsin, U.S.A.
  • Salanova V; Indiana University School of Medicine, Indianapolis, Indiana, U.S.A.
  • Sheth RD; Nemours Foundation, Jacksonville, Florida, U.S.A.
  • Skidmore C; Thomas Jefferson University, Philadelphia, Pennsylvania, U.S.A.
  • Smith MC; Rush University Medical Center, Chicago, Illinois, U.S.A.
  • Spencer DC; Oregon Health & Science University, Portland, Oregon, U.S.A.
  • Srinivasan S; Columbia University Medical Center, New York, New York, U.S.A.
  • Tatum W; Mayo Clinic's Campus in Florida, Jacksonville, Florida, U.S.A.
  • Van Ness P; Baylor College of Medicine, Houston, Texas, U.S.A.
  • Vossler DG; Valley Neuroscience Institute, Renton, Washington, U.S.A.
  • Wharen RE; Mayo Clinic's Campus in Florida, Jacksonville, Florida, U.S.A.
  • Worrell GA; Mayo Clinic Minnesota, Rochester, Minnesota, U.S.A.
  • Yoshor D; Baylor College of Medicine, Houston, Texas, U.S.A.
  • Zimmerman RS; Mayo Clinic Arizona, Scottsdale, Arizona, U.S.A.
  • Skarpaas TL; NeuroPace, Inc., Mountain View, California, U.S.A.
  • Morrell MJ; NeuroPace, Inc., Mountain View, California, U.S.A.
Epilepsia ; 58(6): 1005-1014, 2017 06.
Article em En | MEDLINE | ID: mdl-28387951
ABSTRACT

OBJECTIVE:

Evaluate the seizure-reduction response and safety of brain-responsive stimulation in adults with medically intractable partial-onset seizures of neocortical origin.

METHODS:

Patients with partial seizures of neocortical origin were identified from prospective clinical trials of a brain-responsive neurostimulator (RNS System, NeuroPace). The seizure reduction over years 2-6 postimplantation was calculated by assessing the seizure frequency compared to a preimplantation baseline. Safety was assessed based on reported adverse events. Additional analyses considered safety and seizure reduction according to lobe and functional area (e.g., eloquent cortex) of seizure onset.

RESULTS:

There were 126 patients with seizures of neocortical onset. The average follow-up was 6.1 implant years. The median percent seizure reduction was 70% in patients with frontal and parietal seizure onsets, 58% in those with temporal neocortical onsets, and 51% in those with multilobar onsets (last observation carried forward [LOCF] analysis). Twenty-six percent of patients experienced at least one seizure-free period of 6 months or longer and 14% experienced at least one seizure-free period of 1 year or longer. Patients with lesions on magnetic resonance imaging (MRI; 77% reduction, LOCF) and those with normal MRI findings (45% reduction, LOCF) benefitted, although the treatment response was more robust in patients with an MRI lesion (p = 0.02, generalized estimating equation [GEE]). There were no differences in the seizure reduction in patients with and without prior epilepsy surgery or vagus nerve stimulation. Stimulation parameters used for treatment did not cause acute or chronic neurologic deficits, even in eloquent cortical areas. The rates of infection (0.017 per patient implant year) and perioperative hemorrhage (0.8%) were not greater than with other neurostimulation devices.

SIGNIFICANCE:

Brain-responsive stimulation represents a safe and effective treatment option for patients with medically intractable epilepsy, including adults with seizures of neocortical onset, and those with onsets from eloquent cortex.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Cerebral / Terapia por Estimulação Elétrica / Neocórtex / Estimulação Encefálica Profunda / Eletroencefalografia / Epilepsia Resistente a Medicamentos Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Epilepsia Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Cerebral / Terapia por Estimulação Elétrica / Neocórtex / Estimulação Encefálica Profunda / Eletroencefalografia / Epilepsia Resistente a Medicamentos Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Epilepsia Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos