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3389 electrode

Manufactured by Medtronic
Sourced in United States

The 3389 electrodes are a type of lab equipment used for recording electrical signals. They are designed to interface with various measurement devices and systems. The electrodes provide a means to capture and transmit electrical data for analysis and monitoring purposes.

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7 protocols using 3389 electrode

1

Postoperative Imaging of Implanted Electrodes

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After the Medtronic 3,389 electrodes were permanently implanted, both awake and asleep groups received intravenous propofol general anesthesia again. Impulse generator (IPG) was implanted in the right subclavian subcutaneous package and connected to extended electrodes on the same day. Patients were sent to neurosurgery intensive care unit (ICU) for tracheal extubation and recovery after surgery. Within 24 h after the operation, brain computed tomography (CT) scanning was performed for each patient to exclude intracranial complications and preliminarily evaluate the position of the electrodes (Figure 1B). About 1 week after surgery, postoperative 1.5 T MRI brain imaging was scanned for evaluating the final position of the electrodes by image fusion.
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2

Deep Brain Stimulation Targeting Procedures

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The DBS procedure was conducted using standard means. Electrodes were implanted under local anaesthetic using a stereotactic frame affixed to the patient’s head (Cosman–Roberts–Wells (CRW) frame). With the frame in place, each patient was scanned using CT, which was subsequently fused with a pre-procedural MRI scan for treatment targeting. The DBS electrodes were placed dorso-ventrally down the ALIC to the target site. The target site was 1 mm posterior to the posterior edge of the AC, 4–5 mm lateral to the midline and 2.5–3 mm below the AC–posterior commissure line. This site corresponds to the BNST at the posterior border of the nucleus accumbens, lateral and dorsal to the anterior regions of the hypothalamus. The patients were implanted using Medtronic 3389 electrodes with 1.5 mm contacts and 0.5 mm spacing.
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3

Deep Brain Stimulation for Mood Regulation

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Implantation of DBS leads was performed according to standard stereotactic procedures using frame‐based magnetic resonance imaging (MRI) for target determination, under local anesthesia. Participants underwent bilateral implantation of quadripolar 3389 electrodes (Medtronic, Minnesota, USA), spaced 0.5 mm apart and 1.5 mm long (Fig. 2). The surgical target (of the electrode tip) was the NAc as identified on MRI. Stereotactic atlases place this 7 mm lateral to the midline, 3 mm anterior to the anterior border of the anterior commissure, and 4 mm inferior to the intercommissural line. The two ventral contacts were targeted in the center of the NAc (E0, E1, E8, E9). Intra‐operative test stimulation was conducted to assess mood and behavior. The electrodes were connected via subcutaneous extensions to Activa PC, or RC stimulator (Medtronic, Minnesota, USA) placed in the infraclavicular pocket, under general anesthesia. Post‐operative computed tomography (CT) fused with pre‐operative MRI verified the position of the implanted electrodes. DBS was switched on 2 days following the surgery.
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4

Advanced Parkinson's Disease STN-DBS

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Patients eligible for inclusion were adults (≥18 years) with advanced PD (persistent motor fluctuations, intractable tremors or medication-induced side effects despite optimal pharmaceutical therapy) who positively responded to levodopa and who underwent awake bilateral STN-DBS surgery using Medtronic 3389 electrodes. Patients had complete preinsertion, postinsertion, and follow-up UPDRS 3.0 or MDS-UPDRS III scores of the same electrode trajectory. Patients were excluded if other neurological or psychiatric conditions were present, if the surgical intervention was a revision of an in situ DBS system, if microrecordings were performed, if more than one electrode insertion attempt per hemisphere was performed, and if concomitant medication was given during the surgery. All patients were assessed by a panel of neurosurgeons, movement disorder neurologists, and neuropsychologists prior to their STN-DBS surgery.
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5

Stereotactic Targeting of Anterior Nucleus

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The details of our implantation procedure have been reported previously. 49 In brief, with patients under anesthesia, a Leksell (Elekta) frame was placed, and stereotactic MR images were obtained. Using a Schaltenbrand and Wahren atlas overlay and anatomical guidance, we targeted the anterior nucleus by initially using coordinates from Hodaie et al., and modifying as necessary. 22 Medtronic 3389 electrodes were then implanted in the anterior nucleus and intraoperative fluoroscopy was used to ensure their accurate placement. Five of the 6 patients had additional bilateral leads placed in the hippocampus (n = 4) and centromedian nucleus (n = 1). Electrode locations were confirmed with a CT scan and the patient was taken back to the operating theater. The leads were then tunneled and connected to lead extensions, which were then connected to a battery placed in the standard subclavicular pocket. 22, 49
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6

Unilateral Deep Brain Stimulation for Parkinson's Disease

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A 68-year-old man who had been diagnosed with PD for 11 years was unilaterally implanted with a Medtronic 3389 electrode in the left GP and a Medtronic Activa PC + S sensing pulse generator (Afshar et al., 2013 (link)). His OFF-meds MDS-Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) III motor score (Goetz et al., 2008 (link)) was 50 and freezing of gait questionnaire (Nieuwboer et al., 2009 (link)) score was 13. His levodopa daily equivalent dosage was 1,025 mg (Tomlinson et al., 2010 (link)). He gave informed consent and the protocol was approved by the University of Minnesota Institutional Review Board.
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7

Unilateral Deep Brain Stimulation for Parkinson's Disease

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A 68-year-old man who had been diagnosed with PD for 11 years was unilaterally implanted with a Medtronic 3389 electrode in the left GP and a Medtronic Activa PC + S sensing pulse generator (Afshar et al., 2013 (link)). His OFF-meds MDS-Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) III motor score (Goetz et al., 2008 (link)) was 50 and freezing of gait questionnaire (Nieuwboer et al., 2009 (link)) score was 13. His levodopa daily equivalent dosage was 1,025 mg (Tomlinson et al., 2010 (link)). He gave informed consent and the protocol was approved by the University of Minnesota Institutional Review Board.
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