Abstract: A system includes a wearable device including at least four magnets and a plurality of device electrical connectors, wherein first and second portions of the magnets are positioned to respective first and second sides of a wearable device line of symmetry; and an electrode device including a plurality of magnetic elements and a plurality of electrode electrical connectors, wherein first and second portions of the magnetic elements are positioned to respective first and second sides of an electrode device line of symmetry, wherein a first total magnetic force that is to a first side of the wearable device line of symmetry is sufficiently equal to a second total magnetic force that is to a second wearable device line of symmetry, whereby the first total magnetic force and the second total magnetic force cooperate to retain the device electrical connectors in contact with the electrode electrical connectors.

Abstract: Vagal nerve stimulation devices and methods are provided for treating medical conditions, such as conditions associated with insufficient dopamine and/or endogenous opioids in the brain. A device includes one or more electrodes having a contact surface for contacting an outer skin surface of a patient and an energy source coupled to the electrodes. The energy source generates one or more electrical impulses and transmits the electrical impulses to the electrodes and transcutaneously through the outer skin surface of the patient at or near a vagus nerve. The one or more electrical impulses is sufficient to modulate the vagus nerve and release dopamine and/or endogenous opioids in a brain of the patient.

Abstract: A method, including providing an electrical current to an electrode contact located in a cochlea of a human to evoke a hearing percept, and managing flow of perilymph located inside the cochlea locally to the electrode contact while the current is provided to the electrode contact. In an exemplary embodiment, the management is executed using a seal.

Abstract: Vagal nerve stimulation devices and methods are provided for treating medical conditions, such as conditions associated with insufficient dopamine and/or endogenous opioids in the brain. A device includes one or more electrodes having a contact surface for contacting an outer skin surface of a patient and an energy source coupled to the electrodes. The energy source generates one or more electrical impulses and transmits the electrical impulses to the electrodes and transcutaneously through the outer skin surface of the patient at or near a vagus nerve. The one or more electrical impulses is sufficient to modulate the vagus nerve and release dopamine and/or endogenous opioids in a brain of the patient.

Abstract: Vagal nerve stimulation devices and methods are provided for treating medical conditions, such as conditions associated with insufficient dopamine and/or endogenous opioids in the brain. A device includes one or more electrodes having a contact surface for contacting an outer skin surface of a patient and an energy source coupled to the electrodes. The energy source generates one or more electrical impulses and transmits the electrical impulses to the electrodes and transcutaneously through the outer skin surface of the patient at or near a vagus nerve. The one or more electrical impulses is sufficient to modulate the vagus nerve and release dopamine and/or endogenous opioids in a brain of the patient.

Abstract: Systems and methods of mitigating one or more bodily effects of a shock condition experienced by an animal (including a human, e.g., a patient) are described. One exemplary method includes providing a device for applying non-invasive neurostimulation to the animal's trigeminal nerve. The method also includes applying the non-invasive neurostimulation to the animal's trigeminal nerve, thereby increasing oxygen flow to the animal's brain and/or reducing brain inflammation.

Abstract: Systems and methods for treating cognitive dysfunction and/or depression using transcutaneous auricular neurostimulation therapy may include positioning a wearable neurostimulation device about the ear of the patient, connecting the wearable neurostimulation device, to a pulse generator, and delivering a first series of stimulation pulses to at least one first electrode, the first series being configured to increase monoamine neurotransmitter availability, and delivering a second series of stimulation pulses to at least one second electrode, the second series being configured to upregulate opioid receptor agonists.

Abstract: Devices, systems and methods are disclosed that allow a patient to self-treat a medical condition, such as migraine headache, by electrical noninvasive stimulation of a vagus nerve. The system comprises a stimulator that applies an electrical impulse transcutaneously through an outer skin surface of the patient. The electrical impulse includes pulses having a frequency of about 1 kHz to about 20 kHz. The device housing may transmit data to or from a patient interface device, such as a mobile phone or computer, relating to the stimulation parameters. The interface device in turn may communicate with a database contained within other computers, via a network or the internet.

Abstract: Methods and systems for non-invasive selective control of blood pressure are described. For example, noninvasive stimulation of the auriculotemporal nerve (on the surface of the ear) facilitates a decrease in blood pressure without a corresponding decrease in heart rate or breathing rate, as occurs in stimulation of the cervical vagus and trigeminal nerves. Such a therapy may be particularly beneficial during hypertensive crises or like events where the body naturally decreases heart rate and breathing rate to compensate for an increased blood pressure.

Abstract: Systems and related methods for controlling delivery of a stimulus to a pinna of a subject with a stimulator worn on the pinna are described. A wearable stimulation device includes a mechanical, electrical, or other type of stimulator secured to a pinna of a subject. A personal computing device in communication with the wearable stimulation device controls delivery of stimuli and other aspects of operation of the device. In some aspects recommendations regarding neural stimuli and other stimuli or experiences to be delivered in association with the neural stimuli are provided via a computing system in communication with the personal computing device or the wearable stimulation device.

Abstract: A signal processing arrangement generates electrode stimulation signals to stimulation contacts in a cochlear implant electrode array. A signal filter bank transforms an input sound signal into band pass signals, which each represent an associated frequency band of audio frequencies. A signal processing module processes the band pass signals in a sequence of sampling time frames, wherein for each time frame, the processing includes performing a spectral feature analysis of the band pass signals, and dynamically assigning a stimulation focus pattern to one or more of the band pass signals based on the spectral feature analysis. A stimulation coding module is configured to code the processed band pass signals for each time frame to produce the electrode stimulation signals for delivery by the stimulation contacts to a region of adjacent auditory neural tissues.

Abstract: The invention relates to a device for the punctual stimulation of endings, located in the region of the ears, of nerves leading to brain stem nuclei, and device (1) having a battery-powered therapeutic current generator (3), which is arranged in a housing (2) to be worn in the ear region and is provided with an electronic circuit that forms a low-frequency therapeutic current, and said device also having at least one flexible line (5) proceeding from the therapeutic current generator (3) for connecting to an electrode to be positioned at a nerve ending and having a base electrode (7), which is likewise connected to the therapeutic current generator and by means of which the therapeutic circuit leading across the former electrode is closed, wherein the device (1), at least by means of an external part of said device (1), can be adapted to the shape of the body point of patient intended for the positioning of the device due to a mechanically pliable structure.

Abstract: An apparatus and method for determining stimulation channels for a stimulating device is provided. This method and apparatus may involve computing a set of weights for the plurality of stimulation channels of the stimulating hearing prosthesis. These weights may be determined by determining a transimpedance matrix for the stimulating hearing prosthesis where a diagonal of the transimpedance matrix is determined by extrapolation. A transadmittance matrix may then be computed for this transimpedance matrix. An error may then be computed base on positive off-diagonal terms of the transadmittance matrix. The apparatus and method may determine the weights for the stimulation channels by determining an adjustment to the diagonal of the transimpedance matrix that results in a computed error that does not exceed a specified criterion level.

Abstract: Assessment of neuron excitation is implemented by quantifying the interaction between focused and unfocused stimulation applied to a cochlear array. By applying focused and unfocused stimulation to the electrode array and comparing the difference in the responses to the two types of stimulation the interaction may be determined. The magnitude of the interaction may be related to neural excitation and using this data a neural excitation profile may be determined.

Abstract: The invention relates to a device for applying a transcutaneous electrical stimulation stimulus to the surface of a section of the human ear, which comprises a retaining element which is mountable on or in the ear and a number of electrodes which are arranged on or in an electrode carrier, wherein the device comprises a control apparatus which controls or regulates the generation of a potential difference between the electrodes. In order to permit an improved and safer transcutaneous stimulation the invention proposes that at least three electrodes are arranged on or in the electrode carrier, wherein the at least three electrodes are located in one plane, wherein the position of at least one of the at least three electrodes is adjustable on the electrode carrier and wherein the at least one electrode of which the position is adjustable is mounted such as to be displaceable in a translational manner in the plane. Furthermore, the invention relates a method for the operation of such a device.

Abstract: A cochlear implant system has an implantable portion that includes a stimulator module for producing for the auditory system of a user an electrical stimulation signal representative of an acoustic signal. The implantable portion further includes a battery for supplying power to the stimulator module, a receiver module for receiving an electrical power signal across the skin of a user, and a recharge module that uses the electrical power signal to recharge the battery. The recharge module recharges the battery at less than the maximum recharge rate.

Abstract: A BTE prosthetic device for use in a medical system or prosthesis comprises a connector configured to mechanically attach an auxiliary device of the system to the BTE prosthetic device. The connector is electrically connected to an transceiver of the BTE prosthetic device. The connector operates as an electromagnetic antenna for transmitting and/or receiving signals between the BTE prosthetic and other components of the medical system.

Abstract: An exemplary system includes a sound processor configured to 1) divide an audio signal into a plurality of analysis channels and 2) generate one or more tonality indices each representing a tonality of one of the analysis channels, and an implantable cochlear stimulator communicatively coupled to the sound processor and configured to 1) generate one or more stimulation pulses configured to represent the audio signal in accordance with one or more stimulation parameters, and 2) adjust the one or more stimulation parameters based on at least one of the tonality indices.

Abstract: An implantable electrode array includes an elongated carrier (20) and a plurality of electrodes mounted within the carrier. A actuator adjusts the curvature of the carrier and can be controlled by varying an electric potential applied to the actuator. The actuator is based on an electrochemical cells and may be a conducting polymer based actuator.

Abstract: An electrode assembly including a carrier section, an electrode section(s), and joint section(s). Each electrode section including an electrode contact, and an electrode section body. Each joint section connecting the carrier section to at least one electrode section, and providing each connected electrode section with at least one of pitch, roll, and yaw about a point generally along an axis between the carrier section and the electrode section. The joint section made of material of durometer less the durometer of the carrier section. A fill section can substantially occupying the space between the carrier section and the electrode section that is not occupied by the joint section.

Abstract: A minimally invasive method of introducing an electrode to electrically stimulate one or both vocal cords of a subject includes inserting a hollow needle from outside of the subject's body into a postcricoidal region lateral to a posterior cricoarytenoid muscle and forming an insertion path downwardly towards a cricothyroid joint of the subject. The method also includes introducing the electrode via the hollow needle and positioning the electrode relative to at least one vocal cord muscle of the subject based on the insertion path.

Abstract: Disclosed herein, among other things, is a method for stimulating neural targets in the vicinity of a human ear. According to an embodiment, a device is clipped on a patient ear lobe, the device including a neural stimulation electrode. A neural stimulation signal is applied to the electrode to transcutaneously stimulate neural targets in the vicinity of the ear lobe, according to an embodiment. A physiological parameter is sensed using a sensor connected to the device. According to an embodiment, the neural stimulation signal is adjusted in response to the sensed parameter. The method is used is a variety of treatment regimens, including anti-hypertensive and cardiac improvement therapy.

Abstract: A reference electrode for an inner ear stimulation device is disclosed. The reference electrode is to be implanted and includes a protruding conductor portion and an insulated conducting portion connected to a lead for connection to the device. The protruding conductor portion is shaped so as to present a generally smooth surface without any substantial projections to impede removal in the event that the electrode is withdrawn in the direction of the lead. The smooth profile and lack of an undercut assist in preventing biofilm accumulation and growth. This reduces the risk of post-surgical complications such as infection.

Abstract: Presented herein are coil retention systems for use in implantable medical devices. In certain embodiments, a coil retention system comprises an implantable non-magnetized member having a central aperture and an external magnet also having a central aperture. The external magnet is configured to magnetically couple to the implantable non-magnetized member. In certain embodiments, the external magnet and the implantable non-magnetized member have corresponding annular shapes so as to self-align with one another.

Abstract: The present disclosure relates to methods, devices and systems used for the treatment of medical disorders via stimulation of the superficial elements of the trigeminal nerve. More specifically, cutaneous methods of stimulation of the superficial branches of the trigeminal nerve located extracranially in the face, namely the supraorbital, supratrochlear, infraorbital, auriculotemporal, zygomaticotemporal, zygomaticoorbital, zygomaticofacial, infraorbital, nasal and mentalis nerves also referred to collectively as the superficial trigeminal nerve) are disclosed herein.

Abstract: The invention relates to an electrode arrangement for applying of a transcutaneous electrical stimulation stimulus onto the surface of a section of the human ear, which comprises a holding element to be attached at or in the ear as well as at least one electrode, which electrode is arranged in or at an electrode carrier, wherein the holding element comprises a linear guide in which a supporting rod is arranged linear movable in the direction of a longitudinal axis (L) of the holding element and wherein the electrode carrier is arranged at the supporting rod. To obtain an improved transcutaneous stimulation the invention proposes that the electrode carrier comprises at least one carrier section on which the electrode is arranged, wherein the electrode comprises at least one cylindrical and/or spherical segment shaped and/or conical surface section.

Abstract: Apparatus and methods for converting one type of speech processor unit into another type of speech processor unit.

Abstract: A system and method for a Micro Electro-Mechanical System acoustic sensor, or MEMS acoustic sensor, to be used as an implanted microphone for totally implantable cochlear implants or middle ear implants is presented. The MEMS acoustic sensor comprises a coupler that attaches the sensor to an inner part of the ear, a MEMS acoustic sensor that converts acoustic vibrations into a change in capacitance, and a low-noise interface electronics circuit chip that detects the change in capacitance in the MEMS acoustic sensor, creates an signal representing a portion of the acoustic vibrations, and transmits the signal to one or more other devices, such as a cochlear implant. A method of fabrication enables the MEMS acoustic sensor to be fabricated as a small, less than 1 mm3, light weight, less than 30 mg, device suitable for implantation on a structure of the middle ear.

Abstract: An electrode array which is able to be inserted to a desired depth within the cochlea to provide useful percepts for the recipient which will also preferably not cause damage to the sensitive structures of the cochlea. The electrode array is insertable through an opening in the cochlea and into at least the basal region of the cochlea and comprises an elongate carrier having a proximal end, a distal end, and a plurality of electrodes supported by the carrier at respective spaced locations thereon in a region between the proximal end and the distal end. A stabilising collar extends outwardly from the elongate carrier at or adjacent a proximal end thereof and has an abutment surface adapted to abut a portion of the cochlea surface around the cochleostomy and at least substantially prevent movement of the carrier following completion of insertion of the array into the cochlea.

Abstract: Nanoscale photovoltaic devices fabricated from nanoscale waveguides that receive, propagate, and convert incident light into electrical neural signals, and methods of using these photovoltaic devices for visual perception are disclosed herein. A visual neuroprosthetic device includes an array of nanoscale waveguides each nanoscale waveguide in the array having a photovoltaic material located between an internal conductor and an external conductor, wherein each nanoscale waveguide receives, propagates, and converts incident light into electrical neural signals.

Abstract: A system and method for activating stimulation electrodes in cochlear implant electrode is described. A preprocessor filter bank processes an input acoustic audio signal to generate band pass signals that each represent an associated band of audio frequencies. An information extractor extracts stimulation signal information from the band pass signals based on assigning the band pass signals to corresponding electrode stimulation groups that each contain one or more stimulation electrodes, and generates a set of stimulation event signals for each electrode stimulation group that define electrode stimulation timings and amplitudes. A pulse selector selects a set of electrode stimulation signals from the stimulation event signals based on a pulse weighting function that uses channel-specific weighting factors favoring lower frequencies for activating the stimulation electrodes to stimulate neighboring audio nerve tissue.

Abstract: The invention relates to a hearing aid device for humans with impaired hearing, who have an at least partially functional cochlea and a functional nervous signalling pathway from the cochlea via the auditory nerve to the brain. The hearing aid device contains a receiver, a transducer of the sound or other acoustic signals into electrical current serving as a signal representing a sound, a pulsed irradiation source connected to the transducer for receiving the electrical current and for generating modulated pulsed irradiation in dependence from the electrical current, and preferably one or more optical fibers optically coupled to the exit of the pulsed irradiation source, wherein the optical path for conduction of irradiation within the device ends directly opposite a functional element of the natural vibration transduction pathway, e.g.

Abstract: The electrode arrangement applies a transcutaneous electrical stimulation stimulus to the surface of a section of the human ear. A holding element attaches at or in the ear. At least one electrode is held by an electrode carrier. The holding element has a linear guide on a supporting rod which is linear movable in the direction of a longitudinal axis of the holding element. The electrode carrier is arranged at the supporting rod. To improve the handling of the electrode arrangement latching means are between the linear guide and the supporting rod, so that the supporting rod can be latched relatively to the linear guide along the longitudinal axis in predetermined relative positions. The latching means is a rack shaped contour, which is on the supporting rod and which extends into the direction of the longitudinal axis of the holding element.

Abstract: A detection method for detecting a QRS wave is disclosed. An electrocardiogram (ECG) signal is provided. The ECG signal is enhanced to generate a processed signal. A first crest of the processed signal is determined. Each crest following the first crest is defined as a second crest. The level of each second crest is higher than a first threshold value. The result of defining the second crest is utilized to determine whether the QRS wave has occurred and approached a first crest.

Abstract: A hearing assistance system includes a hearing assistance unit, with an interface for receiving a removable module, and a removable module configured to be retained in the interface.

Abstract: Methods and systems of optimizing sound sensation of a cochlear implant patient include dividing an audio signal into a plurality of analysis channels, generating one or more tonality indices each representing a tonality of one of the analysis channels, generating one or more stimulation pulses configured to represent the audio signal in accordance with one or more stimulation parameters, and adjusting at least one of the stimulation parameters based on at least one of the tonality indices.

Abstract: An implantable sound pickup system. The system comprises an intracochlear acoustic sensor implantable in a recipient's cochlea comprising: an elongate core conductor, and a piezoelectric element disposed on the surface of the core conductor configured to detect pressure waves in the perilymph of the cochlea when the acoustic sensor is at least partially implanted in the cochlea, and to produce electrical signals corresponding to the detected pressure waves.

Abstract: A physiological parameter measuring device (14) is disposed within or near an ear canal of a subject (16) to non-invasively sense at least one physiological parameter of the subject which one physiological parameter is associated with at least one physiological condition of the subject. An analyzing device (48) is operatively coupled to the physiological parameter measuring device (14) to analyze the sensed physiological parameter and detect the physiological condition of the subject (16). Based on the detection and analysis of the physiological condition of the subject (16), a stimulating device (20) stimulates the subject (16) with the physiological parameter measuring device (14) within or near the ear canal of the subject (16) to mitigate the physiological condition of the subject (16).

Abstract: Assessment of neuron excitation is implemented by quantifying the interaction between focused and unfocused stimulation applied to a cochlear array. By applying focused and unfocused stimulation to the electrode array and comparing the difference in the responses to the two types of stimulation the interaction may be determined. The magnitude of the interaction may be related to neural excitation and using this data a neural excitation profile may be determined.

Abstract: Coding of received audio signals and the resulting application of electrical stimuli applied to electrodes used in a cochlear implant system are disclosed together with a method of fitting this new coding strategy. One of the aims is to improve place specific stimulation representing pitch by applying near threshold electrical stimuli with limited and focused excitation fields. A range of stimulation rates and a minimal range of current levels above threshold are used for creation of a dynamic loudness percept for a cochlear implant recipient. Another aim is to disclose a coding scheme based on a model of physiological measures (i.e. refractoriness, adaptation, spread of activation field, spatiotemporal acoustical cochlear activation patterns and spontaneous activity) to estimate the proportions of available excitable auditory neurons close to the electrodes available for stimulation.

Abstract: An adjustable implant electrode system comprises an adjustable implant electrode assembly and an adjustment device for adjusting the adjustable implant electrode assembly to a desired position. The adjustable implant electrode assembly comprises an implant, a plurality of electrodes, and a plurality of magnetic components. The electrodes are disposed in the implant for providing stimulating currents according to a control signal. The magnetic components are combined with the electrodes in one-to-one correspondence. The adjustment device comprises a control unit, an excitation unit, and one or more magnetic units. The control unit is used to select one or more magnetic components to be moved from the magnetic components, and the excitation unit is used to excite the selected one or more magnetic components for the same to generate a magnetic pole, and the magnetic unit is adapted to generate a magnetic field to drive the magnetic pole and accordingly move the implant.

Abstract: There is provided a cochlear implant for improving the hearing ability of a patient suffered from hearing impairment comprising an internal receiving unit implanted into the body, which comprises a receiving part for receiving external signal, an active electrode and a reference electrode, characterized in that the active electrode is constructed with a single electrode wire having different thickness in at least two different regions. The active electrode of the internal receiving unit is inserted into a space formed at between the mastoid bone and the ear canal skin and end of the active electrode is inserted into the scala tympani of the cochlea and directly stimulates spiral ganglion. The cochlear implant provides easier implantation into the body and improved hearing ability at a lower cost.

Abstract: A bimodal hearing prosthesis configured to deliver electrical and acoustic stimulation to a recipient such that a frequency range of a received sound that is represented by the electrical stimulation is perceived simultaneously with the frequency range of the received sound that is represented by the acoustic stimulation.

Abstract: Alternative stimuli, i.e., stimuli other than the constant amplitude stimuli used in prior fitting schemes, are used to set the parameters of a hearing prosthesis, such as a cochlear implant system. The use of such alternative stimuli allows the entire fitting process to be completed in a very short time period, and generally eliminates the need for secondary adjustments. In one preferred embodiment, the alternative stimuli comprise white noise that is internally generated within the speech processor.

Abstract: An implantable fixation structure includes a c-shape bone fixation clip adapted to fit over and attach to a bony bridge element in the middle ear of a patient. A c-shape electrode fixation clip is adapted to fit over and attach to an electrode array element in the middle ear of the patient. A connecting bar has a first end connected to the bone fixation clip and a second end connected to the electrode fixation clip. A coupling clip is connected to the connecting bar between the first end and the second end and adapted to fit over and attach to a cochlear implant element and hold the cochlear implant element in a desired position relative to the middle ear of the patient.

Abstract: A cochlear implant sound processor is powered by a rechargeable battery that is permanently integrated into the sound processor. The sound processor contains an inductive coil that may be tuned to an external charging coil for battery recharging. The electronic circuits and coil of the sound processor are housed in a material transparent to RF signals. The sound processor may be placed in a recharging base station in which the sound processor is positioned in a space surrounded by the inductive charging coil embedded in a material transparent to RF signals. The inductive charging coil sends power to the coil inside the processor and thereby recharges the battery. An alternative embodiment utilizes contacts in the sound processor case and aligned terminals in the recharging base station that allow direct charging of the battery.

Abstract: Methods and systems for modifying the parameters of at least one hearing device for a patient with residual hearing provide needed orchestration of acoustic and electric stimulation of patients wearing such devices.

Abstract: Apparatus and methods for converting one type of speech processor unit into another type of speech processor unit.

Abstract: Methods and systems for modifying the parameters of at least one hearing device for a patient with residual hearing provide needed orchestration of acoustic and electric stimulation of patients wearing such devices.

Abstract: A reference electrode for an inner ear stimulation device is disclosed. The reference electrode is to be implanted and includes a protruding conductor portion and an insulated conducting portion connected to a lead for connection to the device. The protruding conductor portion is shaped so as to present a generally smooth surface without any substantial projections to impede removal in the event that the electrode is withdrawn in the direction of the lead. The smooth profile and lack of an undercut assist in preventing biofilm accumulation and growth. This reduces the risk of post-surgical complications such as infection.