Abstract: There is provided a hearing assistance system comprising an auditory prosthesis device for neural stimulation of a patient's hearing at one of the patient's ears and a hearing aid for acoustic stimulation of the patient's hearing at the same one or the other one of the patient's ears.

Abstract: An exemplary cochlear electrode array includes a flexible body having a pre-curved spiral shape so as to conform with the curvature of a human cochlea, a plurality of stimulation electrode contacts spaced apart along a first side of the flexible body, a bundle of wires embedded within the flexible body for electrically connecting the electrode contacts to at least one stimulation signal source, at least one inflatable portion extending along at least part of the length of the flexible body, the at least one inflatable portion being adapted to straighten the flexible body, starting from the pre-curved shape, prior to insertion into the cochlea upon being inflated by being filled with gas or liquid, and to allow the flexible body to gradually reassume its pre-curved shape during insertion of the flexible body into the cochlea upon gradual withdrawal of gas or liquid from the at least one inflatable portion.

Abstract: A system for stimulation of a patient's ipsilateral cochlea, having at least two spaced apart patient-worn microphones for providing first and second audio signals from ambient sound; a sound processor for generating an ipsilateral auditory nerve stimulation signal in a plurality of output channels from at least one of the input audio signals; and a stimulation assembly for being implanted within the ipsilateral cochlea and having a plurality of stimulation channels for ipsilateral stimulation of the patient's hearing according to the ipsilateral auditory nerve stimulation signal. The sound processor comprising a DOA unit for determining periodically a main direction of incidence of ambient sound from a sound source by analyzing the first and second audio signals, and a directional information coding unit for coding information concerning the determined main direction of incidence in the ipsilateral auditory nerve stimulation signal in manner to enable the patient to localize the sound source.

Abstract: An at least partially implantable hearing aid has an input transducer (26) for capturing audio signals from ambient sound, an audio signal processing unit (32) for processing the captured audio signals, an actuator (20) for stimulating a patient's hearing, and a driver unit (44) for driving the actuator. The actuator has a rigid housing (64) closed on at least one side by a vibration diaphragm (66) that is driven by a piezoelectric transducer (68, 88). The housing is designed to float in the cochlea in direct contact with the cochlear liquids in order to couple vibration energy from the diaphragm directly into the cochlear liquids.

Abstract: A bone conduction hearing aid system with right and left ear microphone arrangements; right and left ear ambient sound signal processing units, right and left ear bone conduction output transducers for stimulating the user's right and left ear cochlea, respectively; a right and left ear cross-talk compensation filter units for generating right and left ear crosstalk compensation signals, respectively, from the processed audio signals of the respective signal processing unit according to an estimated transcranial transfer function; and means for subtracting the left ear cross-talk compensation signal from the processed audio signals of the right ear signal processing unit to generate the right ear output audio signals, and means for subtracting the right ear cross-talk compensation signal from the processed audio signals of the left ear signal processing unit to generate the left ear output audio signals.

Abstract: A system includes a sound processor included in an electro-acoustic stimulation (“EAS”) device and that directs a cochlear implant to apply electrical stimulation to a patient and a receiver to apply acoustic stimulation to the patient. The system further includes a volume control facility and a selection facility that selectively associates the volume control facility with the electrical stimulation in response to a first user input, selectively associates the volume control facility with the acoustic stimulation in response to a second user input, and selectively associates the volume control facility with both the electrical stimulation and the acoustic stimulation in response to a third user input.

Abstract: An exemplary system includes 1) an electro-acoustic stimulation (“EAS”) subsystem that directs a cochlear implant to apply electrical stimulation to a patient, and directs a receiver to apply acoustic stimulation to the patient; and 2) a volume control subsystem communicatively coupled to the EAS subsystem and that facilitates independent control of a first volume level perceived by the patient when the electrical stimulation is applied and a second volume level perceived by the patient when the acoustic stimulation is applied.

Abstract: An exemplary system includes 1) a first sound processor included in a first auditory prosthesis system associated with a first ear of a patient, the first sound processor including a first volume control facility, and 2) a second sound processor included in a second auditory prosthesis system associated with a second ear of the patient, the second sound processor including a second volume control facility. The first volume control facility adjusts, in response to actuation of the first volume control facility, a first volume level perceived by the patient when electrical stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system. The second volume control facility adjusts, in response to actuation of the second volume control facility, a second volume level perceived by the patient when acoustic stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system.

Abstract: The invention relates to an auditory prosthesis device for neural stimulation of a patient's hearing, comprising means for providing an input audio signal, a sound processor for generating a neural stimulation signal from the input audio signal, an implantable stimulation assembly for stimulation of the patient's hearing according to the neural stimulation signal, and a control unit for controlling the sound processor, the control unit being adapted to control at least one parameter used in the generation of the neural stimulation signal from the input audio signal such that, during an adjustment period, the value of the at least one parameter is automatically changed from a first value to a second value as a function of the time having passed since a reference point in time.

Abstract: An exemplary system includes 1) a first sound processor included in a first auditory prosthesis system associated with a first ear of a patient, the first sound processor including a first volume control facility, and 2) a second sound processor included in a second auditory prosthesis system associated with a second ear of the patient, the second sound processor including a second volume control facility. The first volume control facility adjusts, in response to actuation of the first volume control facility, a first volume level perceived by the patient when electrical stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system. The second volume control facility adjusts, in response to actuation of the second volume control facility, a second volume level perceived by the patient when acoustic stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system.

Abstract: A system includes a sound processor included in an electro-acoustic stimulation (“EAS”) device and that directs a cochlear implant to apply electrical stimulation to a patient and a receiver to apply acoustic stimulation to the patient. The system further includes a volume control facility and a selection facility that selectively associates the volume control facility with the electrical stimulation in response to a first user input, selectively associates the volume control facility with the acoustic stimulation in response to a second user input, and selectively associates the volume control facility with both the electrical stimulation and the acoustic stimulation in response to a third user input.

Abstract: A system includes a cochlear implant electrode arrangement comprising a plurality of stimulation channels; means for dividing an audio signal into a plurality of analysis channels means for establishing an electrode-nerve-interface model of hearing stimulation via the cochlear implant electrode arrangement means for determining a signal level value and a noise level value for each analysis channel by analyzing the respective frequency domain signal; means for determining a noise reduction gain parameter for at least some of the analysis channels as a function of the signal level value and the noise level value of the respective analysis channel means for applying noise reduction to the frequency domain signal according to the noise reduction gain parameters to generate a noise reduced frequency domain signal; and means for generating a stimulation signal for each of the stimulation channels according to the noise reduced frequency domain signal.

Abstract: An exemplary system includes 1) an electro-acoustic stimulation (“EAS”) subsystem that directs a cochlear implant to apply electrical stimulation to a patient, and directs a receiver to apply acoustic stimulation to the patient; and 2) a volume control subsystem communicatively coupled to the EAS subsystem and that facilitates independent control of a first volume level perceived by the patient when the electrical stimulation is applied and a second volume level perceived by the patient when the acoustic stimulation is applied.

Abstract: An exemplary system includes an electro-acoustic stimulation (EAS) subsystem and a volume control subsystem communicatively coupled to the EAS subsystem. The EAS subsystem is configured to direct a cochlear implant to apply electrical stimulation representative of audio content included in a first frequency band to a patient and to direct a receiver to apply acoustic stimulation representative of audio content included in a second frequency band to the patient. The volume control subsystem is configured to facilitate independent control of a volume associated with the electrical stimulation and a volume associated with the acoustic stimulation. Corresponding systems, devices, and methods are also disclosed.

Abstract: An exemplary system includes an electro-acoustic stimulation (EAS) subsystem and a volume control subsystem communicatively coupled to the EAS subsystem. The EAS subsystem is configured to direct a cochlear implant to apply electrical stimulation representative of audio content included in a first frequency band to a patient and to direct a receiver to apply acoustic stimulation representative of audio content included in a second frequency band to the patient. The volume control subsystem is configured to facilitate independent control of a volume associated with the electrical stimulation and a volume associated with the acoustic stimulation. Corresponding systems, devices, and methods are also disclosed.

Abstract: A hearing instrument and a method of operating a hearing instrument are provided. The hearing instrument includes an electro-acoustic or electro-mechanical output transducer. When a low battery status of the hearing instrument is detected, a low power audio signal processing mode is selected to extend a lifetime of a battery. The low power audio signal processing mode includes reducing a gain at predefined frequencies; switching off an audio signal processing function for one or more audio frequencies; switching-off parts of a digital audio processor to reduce a duty cycle; and reducing power consumption of an audio signal preamplifier, an audio signal analog-to-digital converter or an audio signal digital-to-analog converter.

Abstract: A bone conduction hearing aid system with right and left ear microphone arrangements; right and left ear ambient sound signal processing units, right and left ear bone conduction output transducers for stimulating the user's right and left ear cochlea, respectively; a right and left ear cross-talk compensation filter units for generating right and left ear crosstalk compensation signals, respectively, from the processed audio signals of the respective signal processing unit according to an estimated transcranial transfer function; and means for subtracting the left ear cross-talk compensation signal from the processed audio signals of the right ear signal processing unit to generate the right ear output audio signals, and means for subtracting the right ear cross-talk compensation signal from the processed audio signals of the left ear signal processing unit to generate the left ear output audio signals.

Abstract: A method for operating a hearing aid in a hearing aid system where the hearing aid is continuously learnable for the particular user. A sound environment classification system is provided for tracking and defining sound environment classes relevant to the user. In an ongoing learning process, the classes are redefined based on new environments to which the hearing aid is subjected by the user.

Abstract: An at least partially implantable hearing aid has an input transducer (26) for capturing audio signals from ambient sound, an audio signal processing unit (32) for processing the captured audio signals, an actuator (20) for stimulating a patient's hearing, and a driver unit (44) for driving the actuator. The actuator has a rigid housing (64) closed on at least one side by a vibration diaphragm (66) that is driven by a piezoelectric transducer (68, 88). The housing is designed to float in the cochlea in direct contact with the cochlear liquids in order to couple vibration energy from the diaphragm directly into the cochlear liquids.

Abstract: It should be possible to quickly and effectively adjust a hearing aid even in the high-frequency range above 8 kHz. For this purpose it is provided that an open-loop gain measurement is carried out in the upper frequency range and a maximum amplification or a frequency-dependent maximum amplification curve is fixed. This maximum amplification in the high-frequency range should not be exceeded. The hearing aid wearer can then optionally select one of a plurality of amplification curves located there below. In the low-frequency range a conventional amplification adjustment is carried out for example by a prescriptive audiogram-based formula. A hybrid adjustment procedure that is easy to carry out is thereby provided for the entire frequency range.