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Soletra

Manufactured by Medtronic
Sourced in United States

The Soletra is a lab equipment product designed for use in clinical and research settings. It serves as a general-purpose power supply capable of providing a stable and adjustable electrical current. The core function of the Soletra is to deliver consistent and reliable power to a variety of laboratory instruments and equipment.

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7 protocols using soletra

1

Bilateral GPi DBS for Parkinson's Rigidity

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Quadripolar DBS electrodes (Medtronic, Minneapolis, MN) were implanted bilaterally in the posteroventral part of the GPi under general anesthesia in a single operating session. All dopaminergic medication had been withdrawn the day before, and patients were briefly woken during the procedure to test the clinical effect of stimulation on rigidity. The ventral contact was kept above the optical tract, as evidenced by the induction of visual flashes by stimulation. There was no Intraoperative microelectrode recording during the procedure.
The pulse generators (Soletra, Medtronic) were implanted 2-3 days later. The exact location of the two selected electrode contacts (one on the left and one on the right) was determined using stereotactic coordinates derived from a 3D CT scan performed a few days after surgery. The stimulation parameters were set and adjusted during appointments with the consultant and regular follow-up hospitalizations, based solely on clinical efficacy criteria.
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2

Epidural Motor Cortex Stimulation Protocol

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The surgical procedure was performed with patients under total intravenous anesthesia: a quadripolar electrode strip (model Resume; Medtronic Inc, Minneapolis, Minnesota) was epidurally placed over M1 (through a burr hole over, contralateral to the most affected body side in three patients and bilaterally in remaining patients) and connected to a Soletra or Kinetra (Medtronic Inc) implantable pulse generator (IPG) located in the subclavian region. In all patients, contacts were oriented along the craniocaudal axis of the precentral gyrus: contact 3 was 2 to 3 cm from midline, contact 0 was 4 cm more lateral (Figure 1). Implantation site was preoperatively defined (using magnetic resonance imaging and neuronavigation) and verified by means of motor-evoked potentials and by identifying N20-P20 phase reversal of somatosensory evoked potentials obtained from contralateral median nerve stimulation [22 (link)]. Patients postoperatively underwent a computed tomography scan to confirm that the electrode paddle was correctly placed and to rule out surgical complications.
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3

Mood Response to STN DBS in PD

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Thirty-eight participants with PD and bilateral STN-DBS were recruited from the Washington University in St. Louis Movement Disorders Center. Six of these participants previously participated in a different study that measured mood response to STN DBS [11 (link)]. Participants were informed of all relevant risks and provided signed consent forms in accordance with the Declaration of Helsinki; the study was approved by the Washington University in St. Louis Human Research Protection Office. Subjects were included based on clinically definite diagnosis of PD [20 (link)–22 (link)], previously implanted bilateral STN-DBS electrodes and an absence of neurological deficits including dementia, head injury or stroke. Details regarding the specific surgical technique used to implant DBS electrodes and the programming paradigm can be found elsewhere [23 (link)]. Soletra or Activa (Medtronic Inc.) pulse generators were used in all participants. DBS implants were previously optimized for motor benefit using monopolar stimulation prior to recruitment into the study.
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4

Deep Brain Stimulation Targeting in Movement Disorders

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The globus pallidus internus (GPi), subthalamic nucleus (STN) and ventral intermediate nucleus (VIM) were selected as the location of surgery, which was decided by a multiple‐member disciplinary team. The locations were determined by using T2 weighted magnetic resonance imaging (MRI) (1.5 T; General Electric Healthcare) and confirmed with intraoperative macrostimulation. Quadripolar DBS electrodes (model 3387 for STN and GPi and 3389 for VIM; Medtronic) were implanted under local anesthesia, and motor function and adverse effects were strictly monitored during macrostimulation. The detailed location of GPi and STN target were mentioned in our previous study.14 VIM target planning started with standard stereotactic coordinates relative to the posterior commissure (PC) on the anterior–posterior commissure (AC‐PC)‐aligned MRI: 10.5‐11 mm lateral to the wall of the third ventricle, 6‐7 mm anterior, and 0 mm dorsal. Patients remained in our hospital for three nights using a 3625 external stimulator for trial stimulation. Permanent IPGs were implanted only after temporary stimulation showed preliminary efficacy. The IPG (Soletra, 37603 or 37612RC; Medtronic) was then implanted subclavicularly under general anesthesia. Postoperative MRI or CT was performed for each patient to confirm the location of the electrodes.
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5

Battery Life of Medtronic IPGs

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We compared the battery lifespan of four different types of IPGs manufactured by one single company (Medtronic, USA).
The older generation of IPGs analyzed includes the Kinetra®, a 8-contact neurostimulator for two DBS-leads, and the Soletra®, a 4-contact neurostimulator for one DBS-lead. The newer generation of IPGs analyzed includes the Activa® PC, a programmable 2-lead 16-contact neurostimulator, and Activa® SC, a single lead 8-contact stimulator.
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6

Stereotactic Deep Brain Stimulation for Dystonia

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Surgery was performed under isofluorane general anesthesia, in view of the young age of the children. Stereotactic MRI was performed pre-operatively under anesthesia with a Leksell G Frame in place to determine co-ordinates targeted in the postero-latero-ventral GPi. Bilateral electrodes were implanted in each case. The electrodes used are all Medtronic 3389 circumferential electrodes: contacts 0.5 mm apart and 1.5 mm in length. Final electrode placement was confirmed by post-operative stereotactic CT scan, under the same general anesthetic, fused with the intra-operative in-frame pre-surgical MRI. The pulse generator was then inserted (Soletra and Kinetra until 2008, and Activa RC pulse generators thereafter, Medtronic, Minneapolis, MN, USA).
Accuracy of electrode placement within our service has been studied previously (22 (link)). Mean Euclidean distance between final electrode tip position and target position was 2.2 mm with no difference in accuracy between isolated genetic/idiopathic and acquired dystonia cases. No correlation was found between outcome at 1 year and Euclidian distance between target and actual position (22 (link)).
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7

Stereotactic Deep Brain Stimulation for Dystonia

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Surgery was performed under isofluorane general anesthesia, in view of the young age of the children. Stereotactic MRI was performed pre-operatively under anesthesia with a Leksell G Frame in place to determine co-ordinates targeted in the postero-latero-ventral GPi. Bilateral electrodes were implanted in each case. The electrodes used are all Medtronic 3389 circumferential electrodes: contacts 0.5 mm apart and 1.5 mm in length. Final electrode placement was confirmed by post-operative stereotactic CT scan, under the same general anesthetic, fused with the intra-operative in-frame pre-surgical MRI. The pulse generator was then inserted (Soletra and Kinetra until 2008, and Activa RC pulse generators thereafter, Medtronic, Minneapolis, MN, USA).
Accuracy of electrode placement within our service has been studied previously (22 (link)). Mean Euclidean distance between final electrode tip position and target position was 2.2 mm with no difference in accuracy between isolated genetic/idiopathic and acquired dystonia cases. No correlation was found between outcome at 1 year and Euclidian distance between target and actual position (22 (link)).
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