Abstract: The invention also provides an integrated system that combines an ablation system used in the electrophysiology (EP) lab with a novel, body-worn monitor and data-management software system. The body-worn monitor differs from conventional monitors in that it measures stroke volume (SV) and cardiac output (CO) in addition to heart rate (HR) and ECG waveforms. The combined system collects numerical and waveform data from patients before, during, and after an EP procedure, thereby providing a robust data set that can be used for a variety of analytics and reporting purposes. The body-worn monitor can be applied to the patient immediately after the EP procedure, e.g. while they are recovering in a hospital. Once applied, the body-worn monitor measures data in real-time, and transmits them to both an EMR and a software application running on a mobile device, such as a smartphone, tablet, or personal digital assistant.

Abstract: The invention also provides an integrated system that combines an ablation system used in the electrophysiology (EP) lab with a novel, body-worn monitor and data-management software system. The body-worn monitor differs from conventional monitors in that it measures stroke volume (SV) and cardiac output (CO) in addition to heart rate (HR) and ECG waveforms. The combined system collects numerical and waveform data from patients before, during, and after an EP procedure, thereby providing a robust data set that can be used for a variety of analytics and reporting purposes. The body-worn monitor can be applied to the patient immediately after the EP procedure, e.g. while they are recovering in a hospital. Once applied, the body-worn monitor measures data in real-time, and transmits them to both an EMR and a software application running on a mobile device, such as a smartphone, tablet, or personal digital assistant.

Abstract: The invention also provides an integrated system that combines an ablation system used in the electrophysiology (EP) lab with a novel, body-worn monitor and data-management software system. The body-worn monitor differs from conventional monitors in that it measures stroke volume (SV) and cardiac output (CO) in addition to heart rate (HR) and ECG waveforms. The combined system collects numerical and waveform data from patients before, during, and after an EP procedure, thereby providing a robust data set that can be used for a variety of analytics and reporting purposes. The body-worn monitor can be applied to the patient immediately after the EP procedure, e.g. while they are recovering in a hospital. Once applied, the body-worn monitor measures data in real-time, and transmits them to both an EMR and a software application running on a mobile device, such as a smartphone, tablet, or personal digital assistant.

Abstract: The invention also provides an integrated system that combines an ablation system used in the electrophysiology (EP) lab with a novel, body-worn monitor and data-management software system. The body-worn monitor differs from conventional monitors in that it measures stroke volume (SV) and cardiac output (CO) in addition to heart rate (HR) and ECG waveforms. The combined system collects numerical and waveform data from patients before, during, and after an EP procedure, thereby providing a robust data set that can be used for a variety of analytics and reporting purposes. The body-worn monitor can be applied to the patient immediately after the EP procedure, e.g. while they are recovering in a hospital. Once applied, the body-worn monitor measures data in real-time, and transmits them to both an EMR and a software application running on a mobile device, such as a smartphone, tablet, or personal digital assistant.

Abstract: Provided is a method of sensing a radio wave in diagnostic imaging of breast cancer, including arranging a plurality of transmitting and receiving antennas along a periphery of a breast, transmitting a radio wave signal from at least one first antenna among the plurality of transmitting and receiving antennas, receiving a scattered wave signal for the radio wave signal from the remaining antennas, other than the first antenna, among the plurality of transmitting and receiving antennas, and rotating the plurality of transmitting and receiving antennas by a predetermined angle.

Abstract: An apparatus includes a baseboard, a grid, a first marker, and a second marker. The grid has a plurality of cells integrally formed with the baseboard. The first marker is integrally formed with the baseboard and intersects the grid at a first angle with respect to a reference line. The second marker is integrally formed with the baseboard and intersects the grid at a second angle with respect to the reference line. The first angle and the second angle are vertically opposite. The grid, the first marker, and the second marker are made of materials having luminescence characteristics that are different than an x-ray characteristic of a material of the baseboard.

Abstract: A photoacoustic imaging apparatus performs imaging of an optical absorber. The photoacoustic imaging apparatus includes a light source, a detector configured to detect an acoustic wave generated from the optical absorber that has absorbed energy of light emitted from the light source, and a signal processing unit configured to form an image of the optical absorber. The signal processing unit stores information indicating whether a rate of change in pressure of the acoustic wave detected by the detector is positive or negative before performing a waveform process on the acoustic wave.

Abstract: In an MRI magnet structure for use with a radiation beam source as an assembly, magnet coils of varying diameters are concentrically arranged along a magnetic axis, the magnetic coils not sharing a common inner or outer radius. Mechanical support is provided to retain the magnetic coils in necessary relative fixed positions. The patient bore tube is provided through the assembly and defines a patient bore axis in an essentially horizontal direction such that the magnetic axis is inclined to the patient bore axis by an angle of 30°-60°. At least one radiation therapy beam access cavity provides access in a straight line for a radiation therapy beam to reach a treatment region within the magnet structure.

Abstract: The invention relates to a device and a method for quantifying a variation of oxygenation in a tissue by using a magnetic resonance imaging technique. The variation of oxygenation in a tissue can be quantified from a measured variation of a proton longitudinal relaxation rate ?R1 and from calibration data. The method of the invention is characterized in that the variation of proton longitudinal relaxation rate ?R1 that is used is a variation of proton longitudinal relaxation rate of lipids rather than a variation of proton longitudinal relaxation rate of water molecules.

Abstract: A medical imaging system comprises an image data acquisition module to acquire imaging data and a motion detection module to acquire motion information. A reconstruction module reconstructs image datasets from the imaging data and with use of the motion information to correct for motion. The motion detection module is provided with a shape-sensing photonic fibre system to provide a photonic output representative of the spatial shape of the photonic fibre and an arithmetic unit to compute the motion information on the basis of the photonic output.

Abstract: A system and method for tracking catheter electrode locations with the body of a patient during an MRI scan sequence includes mitigation logic configured to identify one or more impedance measurements that were taken during potentially noise-inducing conditions (i.e., magnet gradients, RF pulses), and were thus subject to corruption by noise. The mitigation logic is configured to replace the potentially corrupt impedance measurements with previously-obtained impedance measurements taken from an immediately preceding acquisition cycle (e.g., from a previous time-slice).

Abstract: Apparatus associated with improved magnetic resonance imaging (MRI) guided needle biopsy procedures (e.g., breast needle biopsy) are described. One example apparatus includes a support structure configured to support a patient in a face-down prone position where a breast of the patient is positioned in a first free hanging pre-imaging position. The example apparatus includes an immobilization structure configured to reposition the breast into an immobilized position suitable for MRI and for medical instrument access. The immobilization structure may include a biopsy plate, a pressure plate, and MRI coils. The MRI coils are configured to be repositioned from a first position associated with the free hanging pre-imaging position to a second position associated with the immobilized position to facilitate improving the signal to noise ratio associated with signal received from the breast through the MRI coils. The biopsy plate is removable without removing either of the MRI coils.

Abstract: In MR imaging in a suite of rooms including a diagnostic room and a second surgical room, the magnet includes a diagnostic table separable from a docking station of the magnet and the second room includes a second surgical table. An imaging control computer controls operation of the imaging system and a movement control computer controls operation of the magnet moving system and the patient support table. During imaging in the surgical room, the diagnostic table is separated and docked at a secondary docking station while an emulating computer system cooperate with the imaging control computer system by emulating outputs from the disconnected diagnostic table for controlling operation of the imaging system.

Abstract: A docking-station useful for providing a neonate predefined, continuous, stabilized and non-interrupted life-support environmental conditions, comprising of: (i) a neonate incubator, having at least one first opening and a life support system, and (ii) an imaging-device, having a scanning chamber with at least one second opening. The docking-station is configured such that said neonate incubator first opening and said scanning chamber second opening are juxtapose-able so as to reversibly hermetically communicate; thereby providing said neonate predefined, continuous, stabilized, non-interrupted life-support environmental conditions during the entire process of scanning.

Abstract: Alignment of imaging modalities is disclosed. Orientation of an ultrasound imaging probe can be determined. A fluoroscopic imaging device can be aligned with respect to the orientation of the ultrasound imaging probe and a medical device can be implanted based on images obtained from the ultrasound imaging probe and the fluoroscopic imaging device.

Abstract: The present invention involves a surgical hardware and software monitoring system and method allows for surgical planning while the patient is available for surgery, for example while the patient is being prepared for surgery so that the system may model the surgical site. In one embodiment, the model may be used to track contemplated surgical procedures and warn the physician regarding possible boundary violations that would indicate an inappropriate location in a surgical procedure. In another embodiment, the monitoring system may track the movement of instruments during the procedure and in reference to the model to enhance observation of the procedure.

Abstract: Provided are an ultrasound system and method for providing a guide line corresponding to a pathway through which a needle is introduced or inserted. The ultrasound system includes an ultrasound data acquisition unit that transmits an ultrasound signal to a living body into which the needle is inserted, receives an ultrasound echo signal reflected from the living body, and acquires ultrasound data corresponding to each of a plurality of ultrasound images, and a processor that generates the plurality of ultrasound images by using the ultrasound data, creates a mask image for detecting a position and an angle at which the needle is introduced, detects the position and angle by using the mask image, and sets a guide line of the needle on the ultrasound image by using the position and angle.

Abstract: A nuclear medicine diagnostic apparatus includes a support unit for supporting an inspection object from front, an opening for receiving a breast of the inspection object supported by the support unit, a detector ring opposed to the inspection object across a supporting surface of the support unit for detecting radiation generated from the breast, a chest mat provided around the opening formed in the support unit for supporting the chest of the inspection object, and an outer mat provided outward of the chest mat for supporting the inspection object. The chest mat is formed of a material having a greater sagging rate than the outer mat.

Abstract: An image of an object is synergistically reconstructed using two or multiple imaging modalities. A first reconstructed image, showing structural information of the object is produced using a first imaging modality. The first reconstructed image is segmented, and known optical properties of the object are then mapped to the first reconstructed image. Optical signal emissions from the object are detected and registered with the first reconstructed image. A second reconstructed image volume is then produced using a second imaging modality, based on the mapped optical properties after registration between the first image and the data from the second modality. The second reconstructed image depicts some optical property, such as a bioluminescent source distribution, or optical properties, such as, attenuation and scattering properties, of the object.

Abstract: Systems and methods automatically locate optical surfaces of an eye and automatically generate surface models of the optical surfaces. A method includes OCT scanning of an eye. Returning portions of a sample beam are processed to locate a point on the optical surface and first locations on the optical surface within a first radial distance of the point. A first surface model of the optical surface is generated based on the location of the point and the first locations. Returning portions of the sample beam are processed so as to detect second locations on the optical surface beyond the first radial distance and within a second radial distance from the point. A second surface model of the optical surface is generated based on the location of the point on the optical surface and the first and second locations on the optical surface.

Abstract: Apparatuses and methods for performing a procedure on a uterine cavity of a patient are disclosed. The methods can include visualizing the uterine cavity, biopsying a tissue with a biopsy device, and ejecting fluid from the biopsying device into the uterine cavity. The apparatuses can have a sealable acorn tip, a handle, a repositioning clip, a distal indicia, proximal indicia, and a fluid reservoir. The biopsying device can be configured to biopsy and eject fluid under the control of a single hand of a user of the device.

Abstract: Systems and methods for detecting circulatory anomalies such as, for example, right-to-left cardiac and pulmonary shunts. A fluorescing indicator is injected into the bloodstream of a subject. An optical sensor is used to transcutaneously excite the indicator into fluorescence and to transcutaneously detect the fluorescence, and a relative concentration of the indicator is determined as a function of time. An indicator dilution curve is generated from the relative concentration readings, the curve shape is analyzed for the indication of a shunt and, if a shunt is detected, a ratiometric area under the curve analysis is performed and combined with a calculated cardiac output value to provide a shunt conductance value. A Valsalva maneuver may be performed as a part of the method. System embodiments may include a controller/monitor that monitors, times, cues and/or analyzes various steps of a shunt detection test.

Abstract: An ultrasound catheter system can be configured to provide therapeutic ultrasound and imaging. An ultrasound catheter system can comprise a catheter having a distal portion. In several embodiments, a first ultrasonic element can be disposed in the distal portion of the catheter and can be configured to emit a first ultrasonic energy to enhance delivery of a therapeutic compound. In some embodiments, a second ultrasonic element can be disposed in the distal portion of the catheter and can be configured to convert a second ultrasonic energy that is reflected from an imaging site into an electrical signal.

Abstract: A medical data acquisition and display system utilizing separate data signals to transmit both high-resolution data and low-latency synchronization data acquired from patient sensors utilizing different wireless protocols. The low-latency stream of data transmitted over a radio frequency transmission as a timing-pulse in real-time. This high-resolution data includes detailed sensor readings from the patient and also includes digital markers (i.e., the timing-pulse) identifying the temporal location of the high-resolution data relative to imaging data that is simultaneously acquired from a patient. The high-resolution data can be electrocardiogram (ECG) data. The timing pulse can be based on the physiological QRS complex within the ECG data. The imaging data can be echocardiogram imagery of a heart that generated the ECG data.

Abstract: An ultrasound diagnosis apparatus includes a control panel through which a command for manipulation of the ultrasound diagnosis apparatus is input, a keyboard configured to input, and a controller configured to determine whether or not an input time of text is reached and to control movement of the keyboard such that the keyboard extends outward.

Abstract: An apparatus and method for a vector interpolation of an ultrasound image are provided. The apparatus includes a probe, beam former, demodulator and interpolation processor. The probe converts an electric signal into an ultrasound signal, transmits the ultrasound signal to an object, and converts a reflected ultrasound signal from the object into a reflected electric signal. The beam former forms a receive-focused signal based on the electric signal converted from the reflected ultrasound signal by the probe. The demodulator demodulates the receive-focused signal for forming I data corresponding to in-phase components and Q data corresponding to quadrature-phase components. And the interpolation processor performs a vector interpolation with 1:M weighting (M is a natural number) between different complex-valued signals, based on the I data and the Q data.

Abstract: Systems and methods for producing three-dimensional ultrasound images are disclosed herein. In one embodiment, ultrasound image data are acquired in discrete time increments at one or more positions relative to a subject. The image data is time stamped relative to an offset to a reference point. The image data is synchronized relative to the reference point and combined to form a loop of three dimensional images.

Abstract: An ultrasound imaging system and method includes performing a gesture with a probe and detecting the gesture based on data from a motion sensing system in the probe. The motion sensing system includes at least one sensor selected from the group of an accelerometer, a gyro sensor and a magnetic sensor. The ultrasound imaging system and method also includes performing a control operation based on the detected gesture.

Abstract: A portable ultrasound imaging system includes a scan head coupled by a cable to a portable battery-powered data processor and display unit. The scan head enclosure houses an array of ultrasonic transducers and the circuitry associated therewith, including pulse synchronizer circuitry used in the transmit mode for transmission of ultrasonic pulses and beam forming circuitry used in the receive mode to dynamically focus reflected ultrasonic signals returning from the region of interest being imaged.

Abstract: An ultrasound element includes a silicon substrate, a lower electrode layer that has a plurality of lower electrode sections, and a plurality of lower wiring sections, and is connected to a lower electrode terminal to which a drive signal and a bias signal are applied, a lower insulating layer, an upper insulating layer in which a plurality of cavities smaller than the respective lower electrode sections are formed, an upper electrode layer that has a plurality of upper electrode sections that are disposed to face the respective lower electrode sections via the respective cavities, and are smaller than the lower electrode sections and larger than the cavities, and a plurality of upper wiring sections, and is connected to an upper electrode terminal at a ground potential that detects a capacitance signal, and a protection layer.

Abstract: A laser diagnostic system includes multiple lasers providing incident light on a sample, the light modulated and cooperatively phased to stimulate red emissions from the sample; and a detector coupled to a spectrum analyzer, to detect both the incident light and the red emissions from the sample, and to provide a signal indicating detection of a pathology in the sample.

Abstract: An imaging system is provided that includes a pulsed light source providing pulsed light and is applicable to both microscopes and endoscopes. One or more optical elements with certain dispersive properties are positioned to receive the pulsed light and apply selective dispersive properties to shift the focal plane according to the user and to produce two photon (2p) wide field uniform illumination and 2p wide field structured illumination for the purpose of improving the optical axial resolution and rejection of background signal. An imaging element receives the signal arising from the 2p wide field uniform illumination and 2p wide field structured illumination and produces a respective 3D resolved image of a sample.

Abstract: An apparatus for turbid sample measurement comprising a plurality of light sources for illuminating a turbid sample target area with non-spatial structured light, a projection system for illuminating the turbid sample target area with spatial structured light, a sensor for collecting light from the turbid sample target area, and a processor to analyze the data captured by the sensor to yield scattering and absorption coefficients of the turbid sample. A method comprises illuminating the sample with spatial structured light, collecting light reflected from the sample at a number of wavelengths, illuminating the sample with non-spatial structured light, collecting light reflected from the sample at a number of wavelengths, and combining the measurements of the collected light to obtain the optical properties of the sample and/or the concentration of absorbing or fluorescent molecules. The wavelengths of the spatial and non-spatial light sources are preferably different.

Abstract: Methods for preventing or treating motor-related neurological conditions include using ocular light therapy in connection with a conventional therapy for a motor-related neurological condition, such as a drug regimen, to adjust levels of melatonin and/or dopamine in the body of a subject. The ocular light therapy may include elevated levels of blue-green light or green light (e.g., light within a wavelength range of 460 nm to 570 nm, 490 nm to 570 nm, about 520 nm to 570 nm, etc.). The ocular light therapy may also include reduced levels of amber, orange and/or red light. Methods for diagnosing motor-related neurological conditions include use of ocular light therapy to cause a subject to temporarily exhibit one or more symptoms of any motor-related neurological condition to which the subject is predisposed, or which the subject may already be experiencing. A temporary increase in such symptoms may be effected by ocular administration of light including increased amounts of amber, orange and/or red light.

Abstract: A biological sensing apparatus comprises an excitation source configured to induce waves in a biological target, and an optical waveguide interferometer configured to sense the induced waves in the biological target. The optical waveguide interferometer comprises a probe segment having a probe segment end, and an adjustable coupler configured to permit setting a gap between the probe segment end and the biological target. A controller is coupled to the adjustable coupler and configured to set the gap between the probe segment end and the biological target.

Abstract: Methods and apparatus are provided for assessing endothelial function in a mammal. The methods involve applying to the artery a substantially constant external pressure, where the pressure is provided via a cuff adjacent to and/or around a region of the mammal's body; determining, over the course of one or more cardiac cycles, changes in pressure in the cuff resulting from cardiac activity of the mammal to establish a baseline value for a parameter related to endothelial function in the mammal; applying a stimulus to the mammal; determining, over the course of one or more cardiac cycles, changes in pressure in the cuff resulting from cardiac activity of the mammal to establish a stimulus-effected value for a parameter related to endothelial function in the mammal; wherein differences in the baseline value and the stimulus-effected value provide a measure of endothelial function in the mammal.

Abstract: A motion/vibration sensor includes a transmit/receive antenna unit, an oscillation unit and a frequency-mixing unit. The transmit/receive antenna unit receives an output signal from the oscillation unit and transmits a detection signal toward at least one object. The detection signal is reflected by the object as a reflected detection signal and received by the transmit/receive antenna unit. The oscillation unit receives the reflected detection signal from the transmit/receive antenna unit for self-injection locking; and the frequency-mixing unit receives the reflected detection signal from the transmit/receive antenna unit for frequency demodulation. The frequency-mixing unit mixes and demodulates the reflected detection signal from the transmit/receive antenna unit with the output signal from the oscillation unit into a baseband output signal which represents a motion/vibration information.

Abstract: A medical device monitors a level of fluid accumulation, e.g., pulmonary edema, and one or more respiratory parameters of the patient to detect worsening heart failure. The medical device may use intrathoracic impedance measurements to monitor both the fluid accumulation and the one or more respiratory parameters. Respiration rate and volume, also referred to as the tidal volume, are examples of respiratory parameters. The medical device examines the one or more respiratory parameters after determining that the fluid accumulation indicates worsening heart failure. In this manner, the medical device uses the one or more respiratory parameters to confirm a determination of worsening heart failure that was made based on the fluid accumulation.

Abstract: A neuromodulation system includes a first therapy element adapted for positioning within a superior vena cava, and a second therapy element adapted for positioning within a pulmonary artery. The first therapy element is carried on a first elongate flexible shaft, and the second therapy element is carried on a second elongate flexible shaft. One of the first and second shafts is slidably received within a lumen of the other of the first and second shafts—so that the second therapy element may be advanced within the body relative to the first therapy element. A stimulator is configured to energize the first therapy element within the first blood vessel to deliver therapy to a first nerve fiber disposed external to the superior vena cava and to energize the second therapy element within the pulmonary artery to deliver sympathetic therapy to a second nerve fiber disposed external to the pulmonary artery.

Abstract: Techniques associated with a wearable device structure with enhanced motion detection by a motion sensor are described, including a band configured to be worn, a nodule coupled to the band, the nodule including a structure configured to enhance detection of movement of an adjacent skin surface, the structure having an articulator configured to rotate in a plurality of planes, and a sensor coupled to the structure and configured to detect rotational motion.

Abstract: Techniques associated with amplifying orientation changes for enhanced motion detection by a motion sensor are described, including structures configured to enhance detection of motion, the structure having an articulator configured to amplify a motion and a pin configured to apply a force on a pivot point on the articulator, a motion sensor coupled to the structure and configured to detect motion of the structure, and circuitry configured to translate data associated with rotational motion of the articulator into a movement of an adjacent surface. In some embodiments, a method includes coupling a motion sensor to a skin surface using an articulator, the articulator configured to rotate in multiple planes, detecting rotational motion of the articulator using the motion sensor, and deriving data associated with movement on the skin surface.

Abstract: Embodiments relate generally to electrical and electronic hardware, computer software, wired and wireless network communications, and wearable computing devices for sensing health and wellness-related information. More specifically, disclosed is a physiological sensor using, for example, acoustic signal energy to determine physiological characteristics, such as a heart rate, the physiological sensor being disposed in a wearable device (or carried device). In one embodiment, a physiological signal generator is disposed substantially in a wearable housing. At least a portion of a skin surface microphone (“SSM”) including a piezoelectric sensor is configured to receive acoustic signals. The wearable housing is configured to position the SSM to receive an acoustic signal originating from human tissue. The physiological signal generator is configured to receive a piezoelectric signal based on an acoustic signal, and to generate a physiological signal including data representing a heartbeat or heart rate.

Abstract: Embodiments relate generally to electrical and electronic hardware, computer software, wired and wireless network communications, and wearable computing devices for sensing health and wellness-related physiological characteristics. More specifically, disclosed is a physiological sensor using, for example, acoustic signal energy to determine physiological characteristics in one mode, such as a heart rate, the physiological sensor being disposed in a wearable device (or carried device), and generating data communication signals using acoustic signal energy in another mode. The physiological sensor also can be configured to receive data communication signals. In at least one embodiment, an apparatus includes one or more multimodal physiological sensors configured to receive physiological signals in a first mode and at least generate data communication signals in a second mode.

Abstract: The present invention includes a system and method for detecting a pulse. The system includes a sound sensor unit device having a self-adhesive material and a sensor body with a sound chamber, a power source, a MEMS microphone and a transmitting device. The sensor unit wirelessly sends a first signal to a remote unit adapted to receive the first signal.

Abstract: A system for in-place visualization of sensed data is provided. The system includes a formable sheet comprising a display and sensors embedded within the sheet underneath the display. The display will display information relating to sensed data on a portion of the display corresponding to locations of the sensors located underneath the display. As a result, the display displays the information above or directly above the sensors that output data.

Abstract: The invention also provides an integrated system that combines an ablation system used in the electrophysiology (EP) lab with a novel, body-worn monitor and data-management software system. The body-worn monitor differs from conventional monitors in that it measures stroke volume (SV) and cardiac output (CO) in addition to heart rate (HR) and ECG waveforms. The combined system collects numerical and waveform data from patients before, during, and after an EP procedure, thereby providing a robust data set that can be used for a variety of analytics and reporting purposes. The body-worn monitor can be applied to the patient immediately after the EP procedure, e.g. while they are recovering in a hospital. Once applied, the body-worn monitor measures data in real-time, and transmits them to both an EMR and a software application running on a mobile device, such as a smartphone, tablet, or personal digital assistant.

Abstract: Apparatuses and methods for extracting, de-noising, and analyzing electrocardiogram signals. Any of the apparatuses described herein may be implemented as a (or as part of a) computerized system. For example, described herein are apparatuses and methods of using them or performing the methods, for extracting and/or de-noising ECG signals from a starting signal. Also described herein are apparatuses and methods for analyzing an ECG signal, for example, to generate one or more indicators or markers of cardiac fitness, including in particular indicators of atrial fibrillation. Described herein are apparatuses and method for determining if a patient is experiencing a cardiac event, such as an arrhythmia.

Abstract: A monitoring apparatus (50) monitors heart activity by sensing one or more signals accessible at an outer skin surface of a person (100). The monitoring apparatus (50) includes one or more electrodes for contacting onto the outer skin surface of the person (100), a signal processing arrangement (108) for processing one or more signals provided from the one or more electrodes to generate corresponding processed signals, and a display arrangement (106) for receiving the processed signals to generate presentation information from which a heart beat rate of the person (100) is discernible. The signal processing arrangement includes a detector for detecting signal artefacts arising from one or more electronic devices coupled to the person (100) and for removing an influence of the signal artefacts from the processed signals, such that the processed signals provide a more accurate indication of the heart beat rate.

Abstract: An impairment detection device includes a body and a housing removably secured to the body that together resemble a beverage container. A breath analyzer is located within the housing or body and includes a chemical sensor that is configured to detect a chemical impairment level of a user, such as resulting from the use of drugs and/or alcohol. The housing is configured to be removably secured to the body to enable a user to quickly attach and remove the housing from the body. The combination of the housing and body provides a disguise for the impairment detection device because it resembles an actual beverage container. A mouthpiece extends from the housing and is in communication with the chemical sensor for receiving a user breath sample. The housing includes a user interface that is operably associated with the breath analyzer.

Abstract: Described herein are passive nasal respiratory devices, in particular, passive nasal respiratory devices configured to achieve positive end-expiratory pressure (PEEP) in a subject wearing the device. PEEP devices may have a threshold pressure for opening during expiration. These devices may include a flap valve that opens on inhalation nested with a spring valve that opens when exhalation pressure exceeds a predetermined threshold. The device may be configured to be comfortably worn by a sleeping subject.