Abstract: An apparatus for covering a left eye and a right eye of a human, includes: a first eye piece configured for covering a left eye of a human; and a second eye piece configured for covering a right eye of the human; wherein the first eye piece and the second eye piece are configured for preventing transmission of visible light; and wherein at least one of the first eye piece and the second eye piece comprises a region that is transparent for electromagnetic radiation with a wavelength range outside a visible range.

Abstract: An apparatus for covering eyes of a human includes: an eye piece configured for covering one of the eyes of the human; and an eye patch configured for covering the other one of the eyes of the human; wherein the eye piece and the eye patch are configured for preventing transmission of visible light; and wherein the eye piece comprises a region that is transparent for electromagnetic radiation with a wavelength range outside a visible range.

Abstract: An apparatus for testing a directional hearing instrument includes: a first microphone for coupling with an output of the hearing instrument, wherein the first microphone is configured to receive an audio output signal from the hearing instrument; a first speaker for transmission of a first signal having a first frequency component at a first frequency; a second speaker for transmission of a second signal having a second frequency component at a second frequency; and a processing unit configured to determine one or more hearing instrument parameters based on cross spectrum analysis of the first signal and the audio output signal.

Abstract: A filter device for a hearing test probe and a method of manufacturing a filter device are disclosed. The filter device extends along a center axis in a first direction from a first end to a second end. The filter device comprising: a first part having a first filter structure, a second part having a second filter structure, a first channel extending along the center axis. The first part and second part are joined together, and the first filter structure and the second filter structure define a filter element with a first set of filter openings for the first channel.

Abstract: A method and apparatus for determining the impedance of the plurality of channels comprising a plurality of channels having a plurality of first channels and a plurality of second channels, at least one reference channel, a signal generator electrically connected to the plurality of channels, a reference signal generator connected to the reference channel, at least one amplifier connected to each of the plurality of channels and the reference channel and at least one filter connected to an output of the at least one amplifier to filter the output signal from the at least one amplifier. The signal generator is configured to provide a plurality of input signals to the plurality of channels. The reference signal generator provides an input signal to the reference channel.

Abstract: A method and system for sleep stage determination is disclosed comprising: acquiring EEG data from two or more EEG electrodes of an electrode arrangement, wherein the EEG data is divided into one or more epochs; detecting graphoelements from the EEG data for each epoch using a graphoelement detector; calculating a differential entropy from the EEG data for each epoch in an entropy module; and assigning a sleep stage to each epoch based on the calculated differential entropy and the detected graphoelements in a classifier module. This new method and system of sleep staging is potentially suited for, but not limited to, unattended sleep diagnostic scenarios.

Abstract: Automated seizure detection from within an electroencephalogram (EEG) by instrumental means employs novel algorithms within software, using specific measurements of individual waves in trains, rather than any “bulk” process. The acquired signal is filtered, the wave shapes are individually described within a number of parallel runs using a variety of parameters, then criteria (including regularity criteria) are calculated and applied in order to create raw detection results. Finally the raw results are “integrated” for display. As a result, reported seizures closely follow the incidence and duration of seizures detected by trained clinicians. The invention is useful in intensive-care monitoring of EEGs from neonates and in EEG monitoring in general.

Abstract: The described embodiments relate generally to methods, systems and devices for sleep stage determination using frontal electrodes. Certain embodiments relate to a system for sleep stage determination comprising a sensing unit and a processing unit. The sensing unit is positioned over a forehead area of a patient and has first, second and third electrodes for positioning at locations on or adjacent the forehead area for detecting electrical potentials of a human head. The processing unit is coupled to the sensing unit for receiving biological signals corresponding to the detected electrical potentials and processing the biological signals to determine a sleep stage of the patient. The processing of the biological signals is based on a plurality of rules.

Abstract: Embodiments of the invention relate to a wireless physiological monitoring system. The system includes at least one wireless sensor and a monitoring device which are linked to one another of a wireless fashion for measuring physiological signals of a patient. The at least one wireless sensor is located on the patient and may comprise a wireless surface electrode assembly or a wireless needle assembly. The system may also comprise a wireless stimulator synchronized with the wireless sensor for performing certain diagnostic tests, such as nerve conduction velocity tests, for example. The wireless sensor preferably includes active, reference and common conductors. The common conductor can be used to measure the common mode voltage of the patient in the vicinity of the testing, and this voltage can then be subtracted from the measured active and reference voltages.

Abstract: The described embodiments relate generally to methods, systems and devices for sleep stage determination using frontal electrodes. Certain embodiments relate to a system for sleep stage determination comprising a sensing unit and a processing unit. The sensing unit is positioned over a forehead area of a patient and has first, second and third electrodes for positioning at locations on or adjacent the forehead area for detecting electrical potentials of a human head. The processing unit is coupled to the sensing unit for receiving biological signals corresponding to the detected electrical potentials and processing the biological signals to determine a sleep stage of the patient. The processing of the biological signals is based on a plurality of rules.

Abstract: A method and device for automatically assessing loss of hearing sensitivity and compression (recruitment) with user defined frequency resolution by means of extrapolated DPOAE I/O functions and ABRs as well as for automatically fitting hearing aids without any cooperation of the subject tested using a device having a display screen attached to a handheld device generating and collecting otoacoustic emission signals and brain stem response signals into a programmed with a clinical audiogram with fitting parameters for hearing aids calculated on the basis of assessed hearing threshold and compression and identifying the type of hearing required for the individual.

Abstract: The described embodiments relate generally to methods, systems and devices for sleep stage determination using frontal electrodes. Certain embodiments relate to a system for sleep stage determination comprising a sensing unit and a processing unit. The sensing unit is positioned over a forehead area of a patient and has first, second and third electrodes for positioning at locations on or adjacent the forehead area for detecting electrical potentials of a human head. The processing unit is coupled to the sensing unit for receiving biological signals corresponding to the detected electrical potentials and processing the biological signals to determine a sleep stage of the patient. The processing of the biological signals is based on a plurality of rules.

Abstract: A method and device for automatically assessing loss of hearing sensitivity and compression (recruitment) with user defined frequency resolution by means of extrapolated DPOAE I/O functions and ABRs as well as for automatically fitting hearing aids without any cooperation of the subject tested using a device having a display screen attached to a handheld device generating and collecting otoacoustic emission signals and brain stem response signals into a programmed with a clinical audiogram with fitting parameters for hearing aids calculated on the basis of assessed hearing threshold and compression and identifying the type of hearing required for the individual.

Abstract: A method of providing phototherapy to a patient. In some embodiments, the method includes the steps of placing a patient on a rigid support surface of a phototherapy device, the support surface being adapted to support the patient without substantial deformation; transmitting light from a light source through a first portion of the support surface to the patient; and limiting light transmission from the light source through a second portion of the support surface.

Abstract: A phototherapy system having a rigid support surface adapted to support a patient without substantial deformation; a light source disposed so as to transmit light through the support surface; and a mask adapted to permit light transmission from the light source through a first portion of the support surface and to limit light transmission from the light source through a second portion of the support surface.

Abstract: A method and device for automatically assessing loss of hearing sensitivity and compression (recruitment) with user defined frequency resolution by means of extrapolated DPOAE I/O functions and ABRs as well as for automatically fitting hearing aids without any cooperation of the subject tested using a device having a display screen attached to a handheld device generating and collecting otoacoustic emission signals and brain stem response signals into a programmed with a clinical audiogram with fitting parameters for hearing aids calculated on the basis of assessed hearing threshold and compression and identifying the type of hearing required for the individual.

Abstract: A method for diagnosing impairments of a subject's gaze stabilization system is provided. The method includes measuring the subject's static visual acuity to obtain an assessment, setting at least one test parameter based on the assessment, measuring the subject's dynamic visual acuity using the test parameters to obtain a first dynamic measurement and a second dynamic measurement, and determining an impairment of the subject's gaze stabilization system using the assessment and the first and second dynamic measurements.

Abstract: A phototherapy system and device is disclosed, including an array of light sources from at least two distinct spectral light regions. The first spectral light region represents the treatment color, and thus is chosen for its phototherapeutic value. For instance, blue light may be the treatment color for hyperbilirubinemia. The second spectral light region represents the balancing color, and is chosen for its ability to mitigate discomfort that may be caused by viewing the treatment color. When blue is the treatment color, yellow has been found to be an effective balancing color.

Abstract: A noninvasive device and methods for measuring the end-tidal carbon monoxide concentration in a patient's breath, particularly newborn and premature infants. The patient's breath is monitored. An average carbon monoxide concentration is determined based on an average of discrete samples in a given time period. The ratio of the end-tidal portion of the breath flow sample is separately determined, preferably based on monitoring the level of carbon dioxide in the gas sample and identifying the carbon dioxide concentration levels corresponding to the end-tidal portion of the breath sample. The sensed carbon monoxide level is converted to the end-tidal carbon monoxide level by subtracting the ambient carbon monoxide level and dividing the remainder by the ratio of end-tidal breath to breath in the breath sample.