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Dbs leads

Manufactured by Medtronic
Sourced in United States

DBS leads are medical devices used in deep brain stimulation (DBS) procedures. They are thin, flexible wires that are implanted into specific regions of the brain to deliver electrical stimulation. DBS leads are designed to provide targeted, adjustable, and reversible stimulation to help manage certain neurological conditions.

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Lab products found in correlation

3 protocols using dbs leads

1

Invasive Brain Mapping for Intractable Epilepsy

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Human subjects with medically intractable epilepsy undergoing inpatient invasive electrophysiologic mapping of their seizure focus were implanted at Harborview Medical Center (Seattle, WA) with subdural electrocorticographic (ECoG) grids (8 by 8 contacts, 2.3 mm exposed diameter, Ad-tech Medical, Racine, WI, USA). ECoG grid placement was determined solely based on clinical needs without consideration of research benefits. Although the clinical management of each patient was tailored to their specific medical needs, the subjects’ antiepileptic medications generally were weaned or fully discontinued during the period of monitoring until a sufficient quantity of seizures had been captured to adequately localize their seizure focus, following which they resumed taking full doses of their anti-epileptic medications. We conducted all stimulation studies after subjects were back on their anti-epileptic medications, after approximately one week of clinical monitoring.
Human DBS subjects were implanted at University of Washington Medical Center (Seattle, WA) with DBS leads (Medtronic) and subdural ECoG strips (1 by 8 contacts, Ad-tech Medical, Racine, WI, USA).
All patients gave informed consent under protocols approved by the University of Washington Institutional Review Board.
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2

Invasive Brain Mapping for Intractable Epilepsy

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Human subjects with medically intractable epilepsy undergoing inpatient invasive electrophysiologic mapping of their seizure focus were implanted at Harborview Medical Center (Seattle, WA) with subdural electrocorticographic (ECoG) grids (8 by 8 contacts, 2.3 mm exposed diameter, Ad-tech Medical, Racine, WI, USA). ECoG grid placement was determined solely based on clinical needs without consideration of research benefits. Although the clinical management of each patient was tailored to their specific medical needs, the subjects’ antiepileptic medications generally were weaned or fully discontinued during the period of monitoring until a sufficient quantity of seizures had been captured to adequately localize their seizure focus, following which they resumed taking full doses of their anti-epileptic medications. We conducted all stimulation studies after subjects were back on their anti-epileptic medications, after approximately one week of clinical monitoring.
Human DBS subjects were implanted at University of Washington Medical Center (Seattle, WA) with DBS leads (Medtronic) and subdural ECoG strips (1 by 8 contacts, Ad-tech Medical, Racine, WI, USA).
All patients gave informed consent under protocols approved by the University of Washington Institutional Review Board.
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3

Stereotactic Deep Brain Stimulation Protocol

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Frame-based, stereotactic DBS lead implantations were performed under local anesthesia. Targeting was performed using stereotactic computerized tomography (CT) fused to high-resolution gadolinium-enhanced MPRAGE plus FGATIR MR imaging, and deformable three-dimensional atlas matching to facilitate direct patient-specific target and trajectory selection, avoiding cortical and periventricular veins, sulci, and ventricles. Multiple-pass microelectrode mapping was used to verify and refine target selection physiologically. The DBS leads (model 3387, Medtronic, Minneapolis, MN) were implanted at the selected site, and intraoperative macrostimulation via the implanted lead was used as a final confirmation of appropriate lead position. Pulse generators were implanted and the DBS devices were activated 1 month after intracranial lead implantation. Following initial DBS activation, repeated follow-up evaluations were performed during the first 6 months to optimize chronic stimulation parameters and make appropriate medication adjustments. All postoperative adjustments of DBS parameter settings were performed while the participants were in an off-medication state (i.e., medications were held the night before programming sessions).
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