35 results about "Peripheral nerve stimulation" patented technology

Systems, devices, and methods for stimulating peripheral nerves in the fingers or hand to treat tremor are described. For example, a wearable ring device for delivering electrical stimulation to sensory nerves in a patient's finger can include an annular ring having a plurality of electrodes and a detachable unit having a power source and a pulse generator.

Methods and systems for providing peripheral nerve stimulation are disclosed. Stimulation is delivered to a trunk of the nerve using electrodes configured at different circumferential locations about the nerve. Action potentials evoked by the stimulation within branches of the nerve are measured to map neural element within the trunk to the branches. The mapping can inform the selection of stimulation parameters that provide a therapeutic benefit and / or avoid unwanted side effects.

A Peripheral Nerve Stimulation (PNS) system and method are disclosed. The system includes a headset with ear hooks and electrodes for placement on the mastoid processes. A stimulation device connected to the headset via lead wires delivers a pulsed electrical current to the electrodes. The device communicates with a computing device equipped with a mobile application that controls the stimulation characteristics. The mobile application allows users to adjust settings, monitor progress, and access treatment sessions. The system also includes snap ports for electrode attachment, self-adhesive hydrogel electrodes, and current control mechanisms using a digital potentiometer and waveform generator. The method includes pre- and post-session anxiety rating, personalized treatment based on user inputs, and tracking of physiological biomarkers. The application supports multiple operating systems, secure cloud data storage, and enables data sharing with healthcare providers. The invention provides a comprehensive, customizable, safe solution for managing anxiety and insomnia.

The application provides a peripheral nerve precise regulation method and system based on a multi-channel flexible electrode, and is applied to the technical field of data processing. The physiological parameter information of a target user is processed based on a target peripheral nerve stimulation model to generate a muscle contraction characteristic comprehensive index, wherein the muscle contraction characteristic comprehensive index includes a muscle contraction amplitude, a contraction frequency, and the contraction frequency is clearly distinguished according to fast muscle, slow muscle and different movement modes. The training purpose information and the muscle contraction characteristic comprehensive index of the target user are processed based on the target peripheral nerve stimulation model to generate a preliminarily adjusted muscle contraction signal. The preliminarily adjusted muscle contraction signal is processed based on the physiological characteristic information of a target organ to generate a secondarily adjusted muscle contraction signal. The secondarily adjusted muscle contraction signal is processed based on the movement intensity interval information of the target organ to generate a target peripheral nerve stimulation signal.

A peripheral nerve stimulator can be used to stimulate a peripheral nerve to treat essential tremor, Parkinsonian tremor, and other forms of tremor. The stimulator can have electrodes that are placed circumferentially around the patient's wrist or arm. Specific nerves in the wrist or arm can be targeted by appropriate spacing of the electrodes. Positioning the electrodes on generally opposing sides of the target nerve can result in improved stimulation of the nerve. The stimulation pattern may alternate between the nerves. Improved stimulation algorithms can incorporate tremor feedback, external data, predictive adaptation, and long-term monitoring data.

The invention provides a peripheral nerve stimulation system. The peripheral nerve stimulation system comprises a stimulation front end, a release part, a wire and a base, the stimulation front end and the release part are used for being implanted into a body, and the stimulation front end is used for being connected with a target nerve; the base is used for being arranged outside a body; the two ends of the wire are connected with the base and the stimulation front end respectively. The base is configured to send stimulation energy to the stimulation front end through the wire; wherein the stimulation front end is configured to be degradable, and the release part is configured to drive the wire to be released and separated from the stimulation front end when receiving release energy from the base; after the lead is disengaged from the stimulation front end, the lead is configured to be removed from the body. By means of the configuration, the precision and effectiveness of intraoperative electrical stimulation treatment and the convenience of percutaneous electrical stimulation treatment are achieved at the same time, and a secondary operation can be omitted after treatment is completed.

Obstructive sleep apnea from blockage of the upper airway can result in significant daytime drowsiness, with many long-term co-morbidities associated with this disorder such as such as hypertension. A common cause of obstructive sleep apnea is the complete concentric collapse of the soft pallet or retrusion of the genioglossus muscle into the upper airway obstructing breathing. The latter can be due to exhaustion of the muscle due to heightened activation during wake periods, or a greater number of type II muscle fibers can contribute to muscle fatigue. It could also be neurological, whereby the hypoglossal nerve which controls most the upper airway muscles fails to innervate the genioglossus sufficiently to prevent backward movement and pharyngeal block. Described herein is an intelligent personalized closed loop neuromodulation system and methods to prevent backwards movement of the genioglossus muscle through stimulation of certain branches of the hypoglossal nerve and muscle motor points, by using muscle feedback from electromyogram sensors to provide optimal stimulus. Alternative embodiments to treat neuropathic pain and urinary dysfunction are enclosed.

Apparatus and methods for managing pain uses a single composite modulation / stimulation signal with variable characteristics to achieve the same results as separate varying electromagnetic signals, including spinal cord stimulation or peripheral nerve stimulation.

The application discloses a kind of for peripheral nerve stimulation optical genetic system, the system includes: light stimulation module, terminal control module and host computer;The light stimulation module includes μLED and the lead wire connected with the positive and negative electrode of μLED, the light stimulation module is implanted in the site required to stimulate, for regulating the neuron activity of the site;The terminal control module includes terminal circuit board and battery, the terminal circuit board is connected with the lead wire, the battery is detachably connected with the terminal circuit board, the terminal control module is fixed on experimental body, for controlling μLED;The host computer is established wireless communication with the terminal control module, for inputting light stimulation parameter and acting on the experimental body, and receiving the working state information of μLED.It is convenient to use the optical genetic system in the application, not limited by the behavior of experimental body, meet the experimental demand, improve the operability of optical genetic system.

Systems and methods of the present disclosure are directed to systems and methods for treating cognitive dysfunction in a subject in need thereof. The system can include a light source and a speaker. A visual neural stimulation system provides, via the light source, visual stimulation having a first value of a first parameter. An auditory neural stimulation system provides, via the speaker, audio stimulation having a second value of the second parameter. A stimuli orchestration component selects, for a first time interval, one of the visual stimulation or the audio stimulation to vary based on a policy, selects, for the first time interval, the other of the visual stimulation or the audio stimulation to keep constant based on the policy, and provides causes the one of the visual neural stimulation system or the auditory neural stimulation system to vary the one of the visual stimulation or the audio stimulation.

An electrode array for peripheral nerve stimulation, in particular for auricular punctual stimulation of the vagus nerve, including a planar carrier and a plurality of needle-shaped electrodes protruding from the carrier and at least one electrical terminal, which is electrically conductively connected to the electrodes or to a subgroup of electrodes, for electrical connection to a stimulation device, the electrodes having a maximum length of 0.6 mm, preferably 0.4 mm

A method or actions performed by a processor of a system includes displaying a representation of multiple tracts, fibers, nerve bundles, modulation targets, or symptoms, and a representation of electrodes of a cuff lead; in response to selection of at least one of the electrodes, displaying an indication of which tracts, fibers, or nerve bundles can be activated or which modulation targets or symptoms can be affected, using the at least one selected electrode; in response to selection of one of the tracts, fibers, nerve bundles, modulation targets, or symptoms, displaying an indication of at least one of the electrodes for activating the selected tract, fiber, or nerve bundle or for affecting the selected modulation target or symptom; and, optionally, programming a stimulator to stimulate the nerve using the at least one selected electrode or the at least one indicated electrode.

A system and method for treating patients with symptoms of restless legs syndrome (RLS) and periodic limb movement disorder (PLMD) using high-frequency stimulation by applying high-frequency pulsed electrical stimulation therapy signals to the peroneal nerve or its branches, where the therapy signals exceed the motor threshold of muscles stimulated by the peroneal nerve or its branches. Surface electromyography (sEMG) responses to the nerve stimulation can be used to assess patient responsiveness to the nerve stimulation or to assess nerve stimulation efficacy, for example, to compare various nerve stimulation parameter settings and select between such settings to address or balance one or more goals. The sEMG responses can be obtained with the muscle at rest or during muscle activation.

This invention discloses a system and method for treating patients with symptoms of restless legs syndrome (RLS) or periodic limb movement disorder (PLMD) using high-frequency stimulation by applying a high-frequency pulsed electrical stimulation therapeutic signal to the peroneal nerve or its branches, wherein the therapeutic signal is above the motor threshold of the muscles innervated by the peroneal nerve or its branches. Surface EMG (sEMG) responses to nerve stimulation can be used to assess a patient's response to nerve stimulation or to evaluate the efficacy of nerve stimulation, such as comparing various nerve stimulation parameter settings and selecting between these settings to achieve or balance one or more goals. The sEMG response can be obtained during muscle rest or during muscle activation.

The present invention provides a peripheral nerve stimulation system, comprising: a stimulation portion, a release portion, wires, and a base. The stimulation portion and the release portion are configured to be implanted into a body, and the stimulation portion is configured to be connected to a target nerve; the base is configured to be arranged outside the body; two ends of each wire are respectively connected to the base and the stimulation portion; the base is configured to deliver stimulation energy to the stimulation portion through the wires; the stimulation portion is configured to be degradable; the release portion is configured to drive the wires to be detached from the stimulation portion when receiving release energy from the base; and once the wires have been detached from the stimulation portion, the wires are configured to be removed from the body. By means of such a configuration, both the precision and efficacy of intraoperative electrical stimulation treatment and the convenience of percutaneous electrical stimulation treatment are achieved, and the need for a second surgery can be eliminated upon the completion of treatment.

A system for stimulating a nerve includes a control module and a cuff lead with electrodes. The control module includes stimulation circuitry, a memory, and a processor configured to direct the stimulation circuitry to deliver a macroburst to the cuff lead for stimulation using the electrodes. The macroburst includes multiple microbursts. Each microburst includes pulses arranged in a temporal sequence. Each pulse has a pulse width of no more than 100 μs and a total amplitude of no more than 100 μA. A system for mapping a nerve can include a processor for directing the control module to deliver stimulation pulses according to at least one nerve mapping paradigm that includes a temporal sequence of pulses: associating stimulation effects with the electrodes of the cuff lead based on the temporal sequence: and mapping the electrodes to one or more axons, fascicles, nerve fibers, tracts of the nerve, or peripheral organs.

Provided is a peripheral nerve stimulation system comprising: a device for electrically stimulating a peripheral nerve and measuring an evoked compound action potential (ECAP) from the peripheral nerve; a control unit for receiving feedback of the ECAP measured after stimulating the peripheral nerve and determining a threshold value of the ECAP; and a stimulation determination unit for determining, according to the threshold value, a stimulation intensity of an electrode that stimulates the peripheral nerve.

Methods and systems for providing peripheral nerve stimulation are disclosed. Stimulation is delivered to a trunk of the nerve using electrodes configured at different circumferential locations about the nerve. Action potentials evoked by the stimulation within branches of the nerve are measured to map neural element within the trunk to the branches. The mapping can inform the selection of stimulation parameters that provide a therapeutic benefit and / or avoid unwanted side effects.

Systems and methods of the present disclosure are directed to systems and methods for treating cognitive dysfunction in a subject in need thereof. The system can include a light source and a speaker. A visual neural stimulation system provides, via the light source, visual stimulation having a first value of a first parameter. An auditory neural stimulation system provides, via the speaker, audio stimulation having a second value of the second parameter. A stimuli orchestration component selects, for a first time interval, one of the visual stimulation or the audio stimulation to vary based on a policy, selects, for the first time interval, the other of the visual stimulation or the audio stimulation to keep constant based on the policy, and provides causes the one of the visual neural stimulation system or the auditory neural stimulation system to vary the one of the visual stimulation or the audio stimulation.

Embodiments pertain to methods of optimizing peripheral nerve stimulation in a subject by stimulating a peripheral nerve of the subject, where the stimulation includes modulating an intensity and frequency of the stimulation; and receiving sensory feedback from the subject after the stimulation. Additional embodiments pertain to systems and computing devices for optimizing peripheral nerve stimulation in a subject in accordance with the methods of the present disclosure.

A method or actions performed by a processor of a system includes displaying a representation of multiple tracts, fibers, nerve bundles, modulation targets, or symptoms, and a representation of electrodes of a cuff lead; in response to selection of at least one of the electrodes, displaying an indication of which tracts, fibers, or nen e bundles can be activated or which modulation targets or symptoms can be affected, using the at least one selected electrode; in response to selection of one of the tracts, fibers, nerve bundles, modulation targets, or symptoms, displaying an indication of at least one of the electrodes for activating the selected tract, fiber, or nerve bundle or for affecting the selected modulation target or symptom; and, optionally, programming a stimulator to stimulate the nerve using the at least one selected electrode or the at least one indicated electrode.

The present disclosure is directed to systems for providing occipital nerve stimulation (ONS), peripheral nerve stimulation (PNS), and / or spinal cord stimulation (SCS). Methods of delivery are also provided. Stimulator lead bodies as disclosed herein can include features designed to prevent lead migration and retention in tissue. Delivery systems are also provided to deliver these stimulator lead bodies. The delivery systems can include features to test placement of the stimulation lead bodies during delivery to ensure accurate placement of the electrode.

Obstructive sleep apnea, causing daytime drowsiness and comorbidities like hypertension, often stems from soft palate collapse or genioglossus muscle retrusion. This can be due to muscle exhaustion (heightened activation, more type II fibers) or insufficient hypoglossal nerve innervation. Described herein is an intelligent personalized closed loop neuromodulation system and methods to prevent backwards movement of the genioglossus muscle through stimulation of certain branches of the hypoglossal nerve and muscle motor points, by using muscle feedback from electromyogram sensors to provide optimal stimulus. Alternative embodiments to treat neuropathic pain and urinary dysfunction are enclosed.

A magnetic resonance imaging system, and a magnetic resonance imaging method are provided. The method includes: acquiring a scanning sequence for a magnetic resonance imaging system, the scanning sequence including a gradient pulse; and determining a first-type segment of the scanning sequence, in which a peripheral nerve stimulation score exceeds a threshold, maintaining a slew rate of a gradient pulse of the first-type segment, and reducing an absolute value of an amplitude of the gradient pulse of the first-type segment.

The invention relates to multi-modal stimulation for treating tremor. A peripheral nerve stimulator is provided that stimulates the peripheral nerve to treat idiopathic tremor and other dyskinesia as well as overactive bladder, cardiac dysfunction, and neurotransmitter dysfunction. The peripheral nerve stimulator may be a non-invasive surface stimulator that provides multi-modal optimized therapy. The stimulation may be vibratory, electromechanical, thermal, radiant, electrical, magnetic, electromagnetic, optical, mechanical, chemical, thermal, ultrasonic, radio frequency (RF), acoustic, infrared, ultraviolet, X-ray, and / or microwave. Stimulation may be delivered using an open loop system and / or a closed loop system with feedback. Stimulation may be for one site or several sites.

Systems and methods of the present disclosure are directed to systems and methods for treating cognitive dysfunction in a subject in need thereof. The system can include a light source and a speaker. A visual neural stimulation system provides, via the light source, visual stimulation having a first value of a first parameter. An auditory neural stimulation system provides, via the speaker, audio stimulation having a second value of the second parameter. A stimuli orchestration component selects, for a first time interval, one of the visual stimulation or the audio stimulation to vary based on a policy, selects, for the first time interval, the other of the visual stimulation or the audio stimulation to keep constant based on the policy, and provides causes the one of the visual neural stimulation system or the auditory neural stimulation system to vary the one of the visual stimulation or the audio stimulation.

The application discloses an electrode implantation tool, wherein the distal end of the electrode is provided with a fixing component, the implantation tool comprises an outer sheath and an inner sheath, the inner sheath comprises an inner sheath tube and a first handle, the outer sheath comprises an outer sheath tube and a second handle, the inner sheath tube can be inserted into the outer sheath tube, the first handle is fixed in the second handle, the inner diameter of the inner sheath tube is smaller than the outer diameter of the fixing component, the inner diameter of the outer sheath tube is larger than the outer diameter of the fixing component, and the other part of the electrode except the fixing component can be inserted into the inner sheath tube. The implantation tool provided by the application has a very small diameter and is suitable for conveying a full-implant peripheral electrode or a percutaneous implant electrode for peripheral nerve stimulation treatment with a small diameter, and is matched with the fixing structure at the distal end of the electrode, so that the electrode can be conveyed into the body and firmly combined and fixed with the human body tissue.

A peripheral nerve stimulation control system, the system comprising: an implantable device configured to electrically stimulate a peripheral nerve and measure evoked compound action potential (ECAP) from the peripheral nerve; a controller configured to receive feedback of the evoked compound action potential (ECAP) measured after stimulation of the peripheral nerve and determine a threshold value of the evoked compound action potential (ECAP); and a stimulation determiner configured to determine a stimulation intensity for stimulating the peripheral nerve according to the threshold value is provided.

The utility model provides a peripheral nerve stimulation system. The peripheral nerve stimulation system comprises a stimulation front end, a release part, a wire and a base, the stimulation front end and the release part are used for being implanted into a body, and the stimulation front end is used for being connected with a target nerve; the base is used for being arranged outside a body; the two ends of the wire are connected with the base and the stimulation front end respectively. The base is configured to send stimulation energy to the stimulation front end through the wire; wherein the stimulation front end is configured to be degradable, and the release part is configured to drive the wire to be released and separated from the stimulation front end when receiving release energy from the base; after the lead is disengaged from the stimulation front end, the lead is configured to be removed from the body. By means of the configuration, the precision and effectiveness of intraoperative electrical stimulation treatment and the convenience of percutaneous electrical stimulation treatment are achieved at the same time, and a secondary operation can be omitted after treatment is completed.