Abstract: A method for treating a human subject having unilateral vocal cord paralysis includes sensing electrical activity of a dysfunctional muscle of the subject, generating at least one stimulation parameter, using a processor, based on the sensed electrical activity, and stimulating the dysfunctional muscle, using a stimulating electrode, based on the at least one stimulation parameter. A stimulation system is also provided.

Abstract: A stimulation system and method for treating to a human subject having spasmodic dysphonia includes a sensing electrode configured to detect voice activity of a vocalizing muscle of the subject and to generate a first signal, and a processor configured to receive the first signal from the sensing electrode and to generate at least one stimulation parameter based on the first signal. The system further includes a mechanical actuator configured to receive the stimulation parameter from the processor and to activate a glottic closure reflex of the subject in response to the stimulation parameter and a stimulating electrode configured to receive the stimulation parameter from the processor and stimulate the recurrent laryngeal nerve or the vagus nerve of the subject based on the stimulation parameter.

Abstract: An electrode for use with a cochlear implant system includes an electrode array with at least one electrode contact, and an electrode lead adjacent to the electrode array. The electrode lead has a flexible region configured to allow the electrode lead to bend and has an attachment mechanism with an internal portion positioned within the electrode lead and an external portion configured to be bent and secured to bone. A method of securing the electrode to bone is also disclosed.

Abstract: Methods and systems for monitoring, preventing and/or treating upper airway disorders such as apnea, dysphagia, reflux and/or snoring are described. The methods and systems monitor the upper airway disorders by processing one or more neural signals obtained from one or more upper airway afferents. Upper airway disorders are prevented and/or treated by delivering one or more stimulations to one or more reflex-related afferents, efferents, muscles, and sensory receptors to manipulate the threshold and/or trigger an upper airway reflex including, but not limited to a swallow reflex and/or a negative-pressure reflex.

Abstract: Arrangements are described for generating electrode stimulation signals for stimulation contacts in implanted electrode arrays of a bilateral hearing implant system having electrode arrays on both the left- and right-sides. Left-side and right-side audio input signals are processed to generate corresponding left-side and right-side band pass signals, which each represent an associated band of audio frequencies in the audio input signal. Frequency-specific interaural time delays (ITDs) are estimated for the band pass signals, and the estimated ITDs are used to adjust interaural level differences (ILDs) in the band pass signals. The adjusted band pass signals then are used to generate left-side and right-side electrode stimulation signals for the stimulation contacts in the corresponding left-side and right-side electrode arrays.

Abstract: A hearing aid system with a positioning tool is disclosed. The hearing aid system has a hearing aid, an adhesive interconnection unit and a positioning tool. The interconnection unit can be connected to both the hearing aid and the positioning tool. The positioning tool facilitates a correct positioning of the interconnection unit on the hairless skin area behind the outer ear and ensures that neither the hearing aid nor the interconnection unit touches the skin of the outer ear. The hearing aid position can be fine-tuned by turning it in relation to the interconnection unit.

Abstract: A method is described for an auditory prosthesis system to generate electrical stimulation signals to stimulation contacts on an outer surface of an implanted electrode array. An input audio signal having a prominent sensed frequency is pre-processed to produce multiple representative frequency band signals. Each of the frequency band signals is then processed to generate corresponding electric stimulation signals for the stimulation contacts. Each of the electric stimulation signals has an associated stimulation frequency, and for at least one of the electric stimulation signals, the stimulation frequency is varied to maintain an integer ratio between the stimulation frequency and the prominent sensed frequency of the input audio signal.

Abstract: A system, method, and computer product for adjusting dynamic range of electrical stimulation associated with a cochlear prosthesis system is provided. The cochlear prosthesis system includes an electrode array for stimulating the acoustic nerve. Present electrode impedance values are determined for an electrode in the array. At least one stimulation parameter for the electrode is adjusted based, at least in part, on the present electrode impedance values, such that hearing sensation is not influenced due to a change between the present electrode impedance values and previous electrode impedance values.

Abstract: A method of developing a respiration pacing signal includes detecting respiration and movement activity in an implanted patient and developing corresponding respiration and movement signals. A respiration pacing signal is synchronized with the detected respiration activity and delivered to respiration neural tissue of the implanted patient to promote breathing of the implanted patient. A plurality of respiration sensing modes are used that reflect activity of the movement signal over time to optimize system power consumption over time, including: i. an active respiration mode when the movement signal is either actively changing or remains unchanged for a brief period less than some reduced activity period, wherein the respiration signal is measured continuously, and ii. a plurality of reduced activity respiration modes when the movement signal has remained unchanged for the reduced activity period, wherein the respiration signal is measured only during a limited respiration sampling period.

Abstract: A method of measuring electrically evoked auditory brainstem responses of a patient or animal body is provided. The method includes surgically implanting an auditory prosthesis having an electrode array, the electrode array positioned either intracochlear or substantially proximate a brainstem of the body. At least one electrode is stimulated in the electrode array. Electrically evoked auditory brainstem responses resulting from said stimulation are recorded using, at least in part, an electrode in the electrode array as a negative electrode, and a positive electrode positioned substantially proximate the vertex of the head of the body.

Abstract: An arrangement is described for a hearing implant system. An implantable housing has an outer surface configured to lie under and parallel to the skin of the implanted patient. An implant magnet arrangement is located within the implantable housing and has multiple local magnetic sections with different independent local magnetic fields that are combined together to form a net magnetic field with at least two-fold symmetry and zero net magnetic dipole moment, wherein the magnetic fields are oriented parallel to the outer surface of the implant housing.

Abstract: A method of sensing vibrations in the middle ear is presented. The method includes implanting a transducer in the middle ear. The transducer measures vibration, within a predetermined frequency range, of at least one component of the middle ear. The transducer has a resonance frequency within the predetermined frequency range, and further has a limited frequency response in a portion of the frequency range. The implanting includes operatively coupling the implant to the at least one component of the middle ear such that the limited frequency response of the transducer is complimentary to, and compensated by, the frequency characteristics of the at least one component of the middle ear.

Abstract: A cochlear implant includes an active base section with a front surface configured to lie against an inner modiolar wall of the scala tympani. Electrode contacts are on the front surface configured to face the inner modiolar wall to deliver electrode stimulation signals to nearby modiolar neural tissue. A passive apex section has a front surface without electrode contacts configured to lie against an outer lateral wall of the scala tympani. A U-shape transition bend section is at an apical end of the active base section bending in a reverse direction and transitioning into a basal end of the passive apex section such that the back surface of an apical tip of the passive apex section lies adjacent to a back surface of a basal end of the active base section at an electrode opening in the cochlea when the electrode is implanted in the patient.

Abstract: A method of activating at least two electrodes in a multichannel electrode array using channel specific sampling sequences is presented. A channel specific sampling sequence is defined for each electrode, the sequence having a particular duration, pulse amplitude distribution, and number of pulses. A weighting factor is applied to the channel specific sampling sequence. Each electrode in the multichannel electrode array is then simultaneously activated using sign-correlated pulses, the sign-correlated pulses based on parameters of spatial channel interaction reflecting geometric overlapping of electrical fields from each electrode, non-linear compression, and each electrode's weighted channel specific sampling sequence.

Abstract: A method is described for adjusting hearing implant operating parameters for electrode contacts in an implantable electrode array to minimize tinnitus in an implanted patient. A channel tinnitus masking stimulation level is measured for each electrode contact at which maximum tinnitus masking occurs, Ytin,n. A channel threshold stimulation level also is measured for each electrode contact that represents a lowest detectable stimulation level, Tmeas,n. And a channel maximum stimulation level is measured for each electrode contact that represents a maximum comfortable stimulation level, MCLmeas,n. Channel threshold stimulation level Tn and channel maximum stimulation level MCLn are then adjusted for each electrode contact as a function of the channel tinnitus masking stimulation level Ytin,n and tinnitus masking stimulation levels for adjacent electrode contacts, Ytin,adj.

Abstract: An implantable drug delivery system includes a middle ear section with a proximal end fixed to a tympanic membrane of a patient, and a distal end that penetrates through a fluid-tight sealed opening into the inner ear. An inner ear section has a proximal end that is connected to the distal end of the middle ear guide member at the sealed opening, and a closed distal end terminating the inner ear holding member some predetermined distance within the cochlea. A hollow interior of the inner ear section is configured for containing a replaceable pharmaceutical agent, and an outer surface is configured to release the pharmaceutical agent from the hollow interior into the inner ear of the patient. The middle ear section and the inner ear section are configured to cooperate for replacing the pharmaceutical agent through the proximal end of the middle ear section to the inner ear section.

Abstract: A respiration implant system for a patient with impaired breathing includes one or more temperature sensors configured for placement into an inner wall tissue along an airway passage of the patient and configured to measure temperature in the inner wall tissue in order to produce a temperature signal based on the measured temperature. The system further includes a pacing processor configured to receive the temperature signal from the temperature sensor and to generate a respiration pacing signal based on the temperature signal that is synchronized with a breathing cycle of the patient and a stimulating electrode configured to deliver the respiration pacing signal from the pacing processor to respiration neural tissue of the patient to facilitate breathing in the patient. The respiration implant system may be used as a laryngeal pacemaker system.

Abstract: An arrangement is described for generating electrode stimulation signals to electrode contacts in an implanted cochlear implant electrode array. A signal processor processes an input sound signal to generate stimulation timing signals for signal channels associated with the electrode contacts. A pulse generator produces the electrode stimulation signals for each electrode contact based on the stimulation timing signals. A pulse adapter controls a signal format of the pulse generator in response to a somatic response input signal reflecting presence or absence of an undesired somatic response to the electrode stimulation signals. The signal format is an initial signal format based on biphasic stimulation pulses when the somatic response input signal reflects absence of the undesired somatic response, and an adapted signal form based on triphasic stimulation pulses when the somatic response input signal reflects presence of the undesired somatic response.

Abstract: An implantable magnetic transducer arrangement is described for a hearing implant in a recipient patient. An implant housing hermetically encapsulates an interior housing volume and is fixedly attached to skull bone beneath the skin of the patient. A magnetic transducer is located within the housing volume and includes multiple pie-shaped permanent magnets wherein adjacent magnets have different direction magnetic polarities, and one or more suspension elements that resiliently couple adjacent magnets to allow their relative movement. The magnetic transducer is operatively coupled to an external magnetic drive component above the skin of the patient to form an oscillating system that develops a mechanical stimulation signal to the implant housing for delivery by bone conduction of the skull bone as an audio signal to the cochlea of the patient.

Abstract: Arrangements are described for fitting a cochlear implant system to an implanted patient. A test stimulation sequence is delivered to the implanted patient which is based on a concatenated sequence of time shifted envelopes of sinusoidal amplitude modulated (SAM) signals that have a carrier frequency fc modulated by a jittered modulation frequency fm+?, where ? is a frequency jitter component selected from a jitter range of [??1,+?1]. Patient responses to the test stimulation sequence are simultaneously measured including an auditory steady-state response (ASSR) measurement signal and a psychophysical pitch discrimination response. The time shifted envelopes are adapted to avoid measurement artifacts in the ASSR measurement signal around the modulation frequency fm.