Abstract: A multi-camera endoscope includes a the tip section comprising: a front looking camera and a front discrete illuminator to essentially illuminate the field of view of said front looking camera; a right side looking camera and a right discrete illuminator to essentially illuminate the field of view of said right side looking camera; a left side looking camera and a left discrete illuminator to essentially illuminate the field of view of said left side looking camera; and a multi-component cover configured to cover and seal said tip section such as to essentially prevent entry of fluids from the environment of said endoscope to inner parts of said tip section. The tip cover includes removable or repositionable window components which provide access to internal components of the tip for repair or removal, without removing the main tip cover.

Abstract: A cable connection structure includes: a cable having a core and a jacket made of an insulating material to cover the core; and a substrate connected with the cable. The substrate includes: a base material made of an insulating material; an external connection electrode formed on a surface of the base material and connected with the core; and a via provided in the base material and having an end exposed from a mounting surface of the substrate on which the cable is mounted, the via being connected with the external connection electrode. The via is provided at least at one of both ends of a surface of the external connection electrode perpendicular to an axial direction of the cable, on a proximal end side of the cable.

Abstract: The present invention discloses a capsule endoscope and a method to prevent the capsule from being covered by a residue or mucous in a patient's digestive tract. The capsule endoscope comprises an improved surface, preventing a residue or mucous to adhere onto the surface of the capsule, and in the unlikely event that a residue or a mucous is collected by the capsule the improved surface can allow an easy and successful clean before an image is taken.

Abstract: A focus control device includes a processor including hardware, the processor being configured to implement: an area setting process that sets a plurality of areas to a captured image that has been captured by an imaging section, each of the plurality of areas including a plurality of pixels; a direction determination process that determines whether a target in-focus position lies in a NEAR direction or a FAR direction with respect to a reference position with respect to some or all of the plurality of areas set to the captured image to calculate a direction determination result with respect to each of the plurality of areas, the target in-focus position being a target of an in-focus object plane position; and a focus control process that preferentially brings an area among the plurality of areas that is situated away from the imaging section into focus based on the direction determination result.

Abstract: A capsule medical device configured to be introduced into a subject to acquire information about the subject is provided. The capsule medical device includes: a capsule-shaped casing including: a first casing including a hemispherical portion and a cylindrical portion; and a second casing that is a cylindrical casing where an opening edge portion having an opening is positioned at one end, the cylindrical portion of the first casing being fitted on an outer peripheral surface of the second casing on a side of the opening to incorporate an information acquisition member for acquiring information about the subject; and a positioning member including: a first abutment surface configured to abut on an end surface of the second casing on the side of the opening; and a second abutment surface configured to abut on the information acquisition member.

Abstract: An endoscopic system for use a controlled light environment is disclosed. In an implementation, the system may include an endoscope having an image sensor, an emitter, and a control circuit. The control circuit controls a frequency of the emitter in response to signals that correspond to the frequency of the emitter. The image sensor has input and output pads, where a pad count is reduced by not having a dedicated input synchronization clock pad. A frame period is divided into three defined states: a rolling-readout state during which image data is output through the pads, a service-line state during which non-image data is output through the pads, and a configuration state during which instruction data is received by the image sensor through the pads. Signal transitions are encoded within output data from the image sensor and correspond with defined states.

Abstract: An imaging apparatus is adapted for use in an optical instrument having an elongated shaft with a transparent distal end portion. The imaging apparatus includes and image sensor assembly, a first articulating structure, and a second articulating structure mounted on the first articulating structure. First and second lateral side support structures at the lateral sides of the image sensor assembly are each mounted on the second articulating structure so as to position the image sensor assembly in an operating position in the instrument transparent end portion. The connection to the second articulating structure allows an articulation of the image sensor assembly about a lateral articulation axis extending transverse to the longitudinal axis of the shaft distal end portion. This lateral articulation is in addition to the ability of the first articulating structure to rotate about the longitudinal axis of the shaft distal end portion.

Abstract: Embodiments of a hybrid imaging sensor that optimizes a pixel array area on a substrate using a stacking scheme for placement of related circuitry with minimal vertical interconnects between stacked substrates and associated features are disclosed. Embodiments of maximized pixel array size/die size (area optimization) are disclosed, and an optimized imaging sensor providing improved image quality, improved functionality, and improved form factors for specific applications common to the industry of digital imaging are also disclosed.

Abstract: An endoscope system has an illuminator configured to illuminate an object to be observed with normal light, an image processor that generates an observed image from one field/frame worth of image-pixel signals. The image-pixel signals is read from an image sensor provided in the tip portion of a video scope, and the image processor generates a plurality of spectral images in accordance to the emission of a plurality of narrow-band light. Furthermore, the endoscope system has a detector that detects an operator's aiming spot with respect to at least the plurality of spectral images, a determiner that determines a diagnosis object area that contains the detected aiming spot, and a spectral image processor that extracts a diseased portion with spectral characteristics different from those of the other portions, among the plurality of diagnosis object areas that are defined within the plurality of spectral images.

Abstract: Provided is an endoscope light source apparatus including: first and second solid-state light sources that emit first and second light beams, respectively; a third solid-state light source that emits a third light beam that generates white light by being combined with the first and second light beams; an optical member that combines the first, second, and third light beams to generate a combined light; an optical filter that is provided so as to be insertable into/retractable from an optical path of the combined light; and a controller, wherein, in a first excitation-light illumination mode, the controller turns on the first and second solid-state light sources and weakly turns on the third solid-state light source, and, in a second excitation-light illumination mode, turns on the first solid-state light source, turns off the second solid-state light source, and weakly turns on the third solid-state light source.

Abstract: A ventilatory laryngoscope with disposable laryngoscope lens including: a laryngoscope handle and a laryngoscope lens that is connected with an extension arm of the handle; transparent lens protecting cover on the end of the lens cavity; oxygen injecting through-hole on the cover; oxygen supply pipe in seal plug connection with the through-hole, the other end connected with an oxygen source pipe; scrubbing nozzle on the cover, and a drug delivery pipe. The laryngoscope has advantages: during the trachea intubation, ventilation and oxygen supply may be achieved in the body to effectively prevent cerebral anoxia and prolong the safe time limit of the intubation, improve the success rate of cardio-pulmonary resuscitation, and provide a safe and reliable guarantee; improve intubation safety and reduce professional risk; the secreta may be removed from the cover to achieve timely rescue of critically ill patients by collecting clear glottis image and smoothly completing the intubation.

Abstract: The invention relates to an apparatus and a method therewith to quantify visual field in infants. The invention provides a novel solution to the unmet need of detection of defects in the visual field in infants and/or babies and providing an apparatus with a software framework to minimize the errors of recording the readings and increasing their precision and analyzing said results automatically using the software embedded in the system. Said apparatus to quantify visual field in infants comprise of a light projection device onto a dome-shaped hemispherical structure with an infra-red camera along with fixation lights, a means for monitoring responses of the subject during testing, a means for recording and analyzing the readings. Said means to detect and record the eye/head movement in the subject during testing comprises said infra red (IR) camera connected to a device wherein software application is embedded.

Abstract: The present disclosure relates generally to systems and method for testing and determining corrective lens prescription for a patient. In an example embodiment, a method includes using a hand-portable first electronic device, a second electronic device with a computerized screen, and a server to conduct a vision test for a person. The vision test includes determining, an axis prescription, a cylinder prescription, and a sphere prescription for each eye of the person. A corrective lens prescription is provided for the person based, at least in part, on the determined axis, cylinder, and sphere prescription for each eye of the person.

Abstract: Methods and systems for single beam scanning capable of imaging the surface of a spherical body of arbitrary radius of curvature are provided. The spherical imaging methods and systems utilize one or more off-axis parabolic (OAP) mirror to perform a geometrical transformation of the spherical surface to a flat rectilinear imaging coordinate grid such that the single scanning beam maintains a normal incidence across the curved field of view of the spherical body. The imaging methods and systems project the spherical surface to a Cartesian plane and then the remapped surface is rapidly imaged by raster-scanning an illumination beam in the rectangular coordinate such that the OAP mirror produces a rectilinear image of the target. The imaging of the spherical surface is accomplished while maintaining the target, illumination source, and detector in a stationary position. The imaging systems and methods may utilize a single source and a single detector, and may incorporate a THz illumination source.

Abstract: A method of monitoring a patient includes operating each of one or more wireless sensing devices to measure a physiological parameter from a patient and wirelessly transmit a parameter dataset, and receiving the one or more parameter datasets from the one or more wireless sensing devices. The method further includes calculating a patient condition index based on the one or more parameter datasets, wherein the patient condition index is an indicator of stability of the one or more physiological parameters. A measurement interval is then assigned for each wireless sensing device based on the patient condition index, and each wireless sensing device is operated according to the respective measurement interval.

Abstract: A monitoring system using an activity sensor to determine patterns of activity based upon the user activity occurring over time.

Abstract: An apparatus for real time monitoring of a patient is provided and includes a memory element for storing data, a processor that executes instructions associated with the data, an interface that receives sensor data from a sensor that takes measurements from the patient and sends the sensor data according to the sensor's measurement latency, a latency calculator that frequently calculates a latency threshold that varies according to at least a health status of the patient, a timer that continuously monitors the sensor's measurement latency, a comparator that frequently compares the sensor's measurement latency with the calculated latency threshold, and a feedback module that automatically changes the sensor's measurement latency to match with the calculated latency threshold.

Abstract: A method for controlling an optoacoustic imaging system includes the steps of analyzing sinogram data values to identify variations, storing information concerning the variations, generating first and second sinograms, and processing the sinograms to mitigate the effect of the variations. In the analyzing step, sinogram data values are analyzed to identify one or more variations that are related to performance of one or more of the discrete components of the optoacoustic imaging system. The identified variations are then stored. A first sinogram is generated by sampling transducer elements acoustically coupled with a surface of a volume for a predetermined period of time after delivery of a pulse of light having a first wavelength, the first sinogram containing one channel for each of the transducer elements.

Abstract: Methods and apparatuses for 3D imaging (including 3D optical coherence tomography imaging) to measure the shape of orthodontic aligners, teeth, and other oral structures simultaneously, in-vivo or in-vitro. These methods and apparatuses may be used to determine contact locations of aligners with teeth and/or teeth with other teeth with very high precision, including determining the size of gaps where they are not in contact. These measurements may be used design, modify or replace an aligner and/or to verify aligner fit. 3D models of the whole aligner and teeth may be generated.

Abstract: A fluorescence imaging device detects fluorescence in parts of the visible and invisible spectrum, and projects the fluorescence image directly on the human body, as well as on a monitor, with improved sensitivity, video frame rate and depth of focus, and enhanced capabilities of detecting distribution and properties of multiple fluorophores. Direct projection of three-dimensional visible representations of florescence on three-dimensional body areas advantageously permits viewing of it during surgical procedures, including during cancer removal, reconstructive surgery and wound care, etc. A NIR laser and a human visible laser (HVL) are aligned coaxially and scanned over the operating field of view. When the NIR laser passes over the area where the florescent dye is present, it energizes the dye which emits at a shifted NIR frequency detected by a photo diode. The HVL is turned on when emission is detected, providing visual indication of those positions.

Abstract: A wearable device includes a measurement device to measure a physiological parameter adapted to be placed on a wrist or an ear of a user. A plurality of semiconductor light sources such as light emitting diodes generate corresponding output light having an initial light intensity. A receiver includes spatially separated detectors receiving reflected light from the output lights and coupled to analog to digital converters. The receiver is configured to synchronize to the semiconductor source(s). The measurement device improves signal-to-noise ratio of the output signal by increasing light intensity relative to the initial light intensity and by increasing a pulse rate. Further improvement in signal-to-noise ratio is achieved by using change detection, where the receiver compares the signals with light on and with light off.

Abstract: An acoustic wave receiving apparatus is used, which includes: a holding member; a reception transducer array; a liquid vessel to which the reception transducer array is fixed and configured to store an acoustic matching liquid; a liquid supplying unit; a controlling unit configured to control a supplying rate of the acoustic matching liquid; and a scanning unit, wherein the controlling unit is configured to reduce the supply of the acoustic matching liquid into the liquid vessel when the reception transducer array detects an acoustic wave.

Abstract: A temperature probe includes a handle and a shaft extending from the handle. The shaft includes a distal end, a proximal end, and a tip at the distal end. The temperature probe also includes a capacitance sensor disposed on one of the handle and the shaft, the capacitance sensor configured to measure a change in capacitance when positioned proximate a conductor. The temperature probe further includes a temperature sensor disposed on the shaft, the temperature sensor configured to measure a body cavity temperature of a patient.

Abstract: A method for digital thermal monitoring assessment of vascular function comprising a temporary arterial occlusion using a pneumatic cuff positioned on a subject's upper limb, monitoring skin temperature at the fingertip of the occluded limb for a period of time before, during, and after the occlusion, calculating a Zero Reactivity Curve based on variables including start temperature, room temperature, and the slope of temperature decline during the occlusion, and assessing vascular function based on comparing the Zero Reactivity Curve and the observed temperature rebound after the occlusion is removed.

Abstract: A patient monitoring system comprises a data acquisition device that records physiological signals from a patient, the data acquisition device having at least 3 receiving ports, each receiving port configured to connect to a patient connector. The monitoring system further includes a galvanic patient connector that galvanically connects a first receiving port of the patient connector and the patient, and at least a first capacitive patient connector and a second capacitive patient connector. Each capacitive patient connector capacitively couples a respective receiving port of the data acquisition device and the patient.

Abstract: Wrist-worn devices and related methods measure a pulse transit time non-invasively and calculate a blood pressure value using the pulse transit time. A wrist-worn device includes an accelerometer, a photo-lethysmogram (PPG) or a pulse pressure sensor, and a controller. The PPG or the pulse pressure sensor coupled to the wrist-worn device for detecting an arrival of a blood pressure pulse at the user's wrist. The controller is configured to process output signals from the accelerometer to detect when the blood pressure pulse is propagated from the left ventricle of the user's heart, process a signal from the PPG or the pulse pressure sensor to detect when the blood pressure pulse arrives at the wrist, calculate a pulse transit time (PTT) for propagation of the blood pressure pulse from the left ventricle to the wrist, and generate one or more blood pressure values for the user based on the PTT.

Abstract: A method for producing an image representative of the vasculature of a subject using a MRI system includes the acquisition of a signal indicative of a subject' cardiac phase. During each heartbeat of the subject, image slices of a volume covering a region of interest (ROI) within the subject are acquired by applying a volume-selective venous suppression pulse to suppress (a) venous signal for an upper slice in the ROI; (b) venous signal for slices that are upstream for venous flow in the ROI; and (c) background signal from the upstream slices. Next, a slice-selective background suppression pulse is applied to suppress background signal of the upper slice. Following a quiescent time interval, a spectrally selective fat suppression pulse is applied to the entire volume to attenuate signal from background fat signal. Then, a simultaneous multi-slice acquisition of the upper slice and the upstream slices is performed.

Abstract: 3D cine MR angiography systems and methods are disclosed for use during the steady state intravascular distribution phase of ferumoxytol. The 3D cine MRA technique enables improved delineation of cardiac anatomy in pediatric patients undergoing cardiovascular MRI.

Abstract: A biosensor includes: a flexible base, a first sensor includes a first sensor main body; and a second sensor includes a second sensor main body that is detachably installed on the side face of the flexible base installed with the first sensor main body, and is arranged at intervals on the first sensor main body. The second sensor is detachably installed on the flexible base installed with the first sensor, and does not overlap with the first sensor, thereby allowing the second sensor to work together with the first sensor, thereby obtaining different physiological parameters. The second sensor can also be detached from the flexible base and used independently to increase user convenience.

Abstract: A system for monitoring relative nerve health and the presence of neuropraxia is described. The system utilizes the integration of a waveform function of an elicited or monitored nerve response to provide an indication of the strength of a detected signal from a nerve and thus the relative health and integrity of the nerve. In some embodiments motor nerve stimulation innervates muscle and an EMG waveform is obtained in response thereto. The integration under the waveform is expressed and an indexed value indicating a percentage of a certain threshold value. Methods set forth provide a more reliable status of a nerve in real-time and allow action to be taken to reduce neuropraxia or prevent permanent nerve damage.

Abstract: A method and system for determining a patient's risk of ventricular tachycardia are disclosed. The method includes receiving ECG signals from a patient and filtering the collected ECG signals to generate filtered ECG signals. The method further includes identifying a heart vector from the filtered ECG signals, and measuring a velocity of the heart vector movement. A change in curvature of the identified heart vector movement is quantified and a risk of ventricular tachycardia is determined based at least on the measured velocity and the quantified change in curvature of the identified heart vector movement.

Abstract: An electrocardiogram analyzer includes a first acquiring section that acquires a body surface electrocardiogram of a subject, a second acquiring section that acquires an intracardiac electrocardiogram of a ventricle of a heart of the subject, and an analyzing section that performs a frequency analysis on the intracardiac electrocardiogram and includes a range setting section that sets an analysis time range of the frequency analysis in the intracardiac electrocardiogram based on a unit waveform of the body surface electrocardiogram, and a calculating section that, in the analysis time range, performs the frequency analysis on the intracardiac electrocardiogram, and that calculates an index value indicating a ratio of local abnormal ventricular activities in the intracardiac electrocardiogram.

Abstract: A method of atrial focal source detection is provided which includes detecting, via sensors, electro-cardiogram (ECG) signals over time. Each ECG signal is detected via one of the sensors and indicates electrical activity of a heart. The method also includes determining, for each ECG signal, local activation times (LATs) each indicating a time of one of a plurality of atrial activations of a corresponding ECG signal and detecting whether one or more focal source areas of activation in the heart is indicated based on the detected ECG signals and the one or more local LATs. S-waves can be distinguished from non-S-waves by generating models for each atrial activation and classifying atrial activations. Maps can be generated by visually indicating, for each sensor, a level of incidence of the atrial activations occurring before atrial activations of neighboring sensors within a period of time.

Abstract: A system for processing ECG to detect atrial fibrillation includes three software modules. A beat module is executable on a processor to receive a time series of ECG data, identify heart beats, and determine a beat AFIB value based on a timing of each identified heart beat. The beat AFIB value represents a presence or absence of AFIB based on variability in the timing of each identified heart beat. A segment module is executable to receive the time series of ECG data, divide the time series of ECG data into two or more time segments, and determine a segment AFIB value for each time segment. The segment AFIB value indicates a presence or absence of AFIB in the time segment based on whether any of a set of rhythms are identified. The AFIB detection module is executable to determine an AFIB identification value for each time segment based on the beat AFIB value during that time segment and the segment AFIB value for that time segment.

Abstract: A cardiac rhythm management system includes a first implantable device such as a defibrillator and a second implantable device such as a leadless cardiac pacemaker. A programmer is configured to receive and display heart data emanating from the implantable defibrillator and from the leadless cardiac pacemaker. The heart data emanating from the leadless cardiac pacemaker is displayed in temporal alignment with the heart data emanating from the implantable defibrillator.

Abstract: An ECG device comprising limb leads and chest wall leads is described which is also suitable for deriving the hemodynamic activity of the heart and the function of the vessels and, respectively, also for evaluating the fluid equilibrium. This is achieved in that at least part of the electrodes of the multichannel ECG is developed with additional embodiments for physical emissions and measurements, for example, electric current and voltage, pressure, sound vibrations, light, and that an electrode is provided for the current supply and, respectively, the voltage measurement at the upper thorax aperture. Furthermore, an alternating current field is built up between the electrodes or, respectively, the distance between the electrodes is used as an ion conductor.

Abstract: An electronic device for long-term adhesion to a mammal includes a housing with an electronic component. The electronic device may include a first wing and a second wing, each being integrally formed with the housing. An electrode is positioned on a bottom surface of each of the wings, the electrodes electrically connected to the electronic component. An adhesive layer is provided for adhesion to a surface of the mammal. The adhesive layer may cover a portion of the bottom surfaces of the wings but generally does not cover the electrode or a bottom surface of the housing. A method of applying an electronic device to a mammal includes removing first and second adhesive covers from first and second wings of the electronic device to expose an electrode and an adhesive coated on a bottom surface of each wing.

Abstract: An electroencephalogram analysis apparatus includes an electroencephalogram acquisition part and a comparison part. The electroencephalogram acquisition part is configured to acquire a first electroencephalogram measured at a first region on a head of a test subject and a second electroencephalogram measured at a second region positioned behind the first region on the head of the test subject. The comparison part is configured to compare a power of the first electroencephalogram in a specific frequency band with a power of the second encephalogram in the specific frequency band.

Abstract: A pedicle access system including a cannula, a stylet, and a removable T-handle. The pedicle access system may be used to percutaneously approach the pedicle, initiate pilot hole formation, and conduct a stimulation signal to the target site for the purposes of performing a pedicle integrity assessment during the pilot hole formation. To do this, the cannula and stylet are locked in combination and inserted through an operating corridor to the pedicle target site, using the T-handle to facilitate easy movement and positioning of the cannula/stylet combination. A stimulation signal may be applied during pilot hole formation to conduct the pedicle integrity assessment. In a significant aspect, the T-handle may be detached from the cannula/stylet combination to facilitate the use of various surgical tools as necessary.

Abstract: Apparatus for monitoring vital signs of one or more living subjects comprises a monitoring station and at least one sensor in communication with the monitoring station. The sensor comprises an antenna system, an ultra wideband radar system coupled to the antenna system, a signal processor and a communication system. The signal processor is connected to receive a signal from the ultra wideband radar system and configured to extract from the signal information about one or more vital signs of a person or animal in a sensing volume corresponding to the antenna system. The communication system is configured to transmit the information to the monitoring station.

Abstract: A system and method for automating an appropriate voxel prescription in a uniquely definable region of interest (ROI) in a tissue of a patient is provided, such as for purpose of conducting magnetic resonance spectroscopy (MRS) in the ROI. The dimensions and coordinates of a single three dimensional rectilinear volume (voxel) within a single region of interest (ROI) are automatically identified.

Abstract: Systems, methods, and computer-readable media for optimizing an electromagnetic navigation system are provided. Multiple test signals corresponding to multiple combinations of phase offset values of a plurality of frequency components, respectively, are generated. Based on the test signals, a table including peak signal amplitudes associated with the respective test signals is generated. A minimum value of the stored peak signal amplitudes is identified in the table. Based on the table, a determination is made as to which combination of phase offset values is associated with the minimum value of the stored peak signal amplitudes. The determined combination of phase offset values is stored in a memory for use, during an electromagnetic navigation procedure, in generating a signal including the frequency components having the determined combination of phase offset values, respectively.

Abstract: Low profile antennas for ingestible devices, such as ingestible event markers, are provided. Aspects of the ingestible devices of the invention include low profile signal transmission antennas configured such that they are flexible or degrade after use, allowing the antenna and attached components to pass easily through the body. Embodiments of the low profile antennas are configured to emit a detectable signal upon contact with a target physiological site. Also provided are methods of making and using the devices of the invention.

Abstract: The system of the present invention includes a conductive element, an electronic component, and a partial power source in the form of dissimilar materials. Upon contact with a conducting fluid, a voltage potential is created and the power source is completed, which activates the system. The electronic component controls the conductance between the dissimilar materials to produce a unique current signature. The system can also measure the conditions of the environment surrounding the system.

Abstract: Ingestible bio-telemetry communication network and associated systems are described. The communication network can include one or more ingestible bio-telemetry tags; and a reader, wherein each of the one or more ingestible bio-telemetry tags generates an out-link signal comprising, for each bit of data in a frame, a pulse reverse keyed symbol. Multiple ingestible bio-telemetry tags can be managed at the same time by allowing the frequency of the transmit carrier signal to change, or “hop” to different frequencies so as to minimize likelihood of collision. A reader can identify the proper frequency either by a signal from the tags indicated the frequency of the next hop or, when no bi-directional communication is available, by deducing the carrier signal frequency from the start bits of a received frame from the tag and scanning for the shifted carrier signal frequency within a tolerance of the deduced carrier signal frequency.

Abstract: A method for the assessment of the lung parenchyma in a human or an animal is indicated using a series of magnetic resonance (MR) images of the lung parenchyma acquired at different breathing positions in the same human or animal. The method comprises at least the steps of a.) estimating a change of the lung volume VL between the different breathing positions, b.) determining a signal intensity SI({right arrow over (x)}i) in at least one same region or position {right arrow over (x)}i of the lung parenchyma for each of the MR images, and c.) determining at least one respiratory index ?({right arrow over (x)}i) according to the formula ? ? ( x ? i ) = - d ? ( log ? ( SI ? ( x ? i ) ) ) d ? ( log ? ( V L ) ) . ( Fig .

Abstract: An apparatus for producing information indicative of cardiac malfunctions, for example atrial fibrillation, includes a processing system for processing an analysis signal produced by a sensor system responsive to motion including cardiovascular motion. The processing system is configured to form a first indicator quantity indicating degree of concentration of the autocorrelation of the analysis signal to a point corresponding to zero time difference between analysis signal samples whose mutual correlation is expressed by the autocorrelation and a second indicator quantity indicating the spectral entropy of the analysis signal. The processing system is configured to determine an indicator of cardiac malfunction on the basis of at least the first indicator quantity and the second indicator quantity.

Abstract: The present invention relates to a patient off-bed notification system, which includes a pressure-sensitive sensor pad, a signal converter, and a signal transmitter. The pressure-sensitive sensor pad includes an upper conductive layer, a bottom conductive layer, and an insulating layer arranged therebetween, where the upper conductive layer and the bottom conductive layer can generate an electrical signal due to a pressure change. The signal converter is used to receive the electrical signal from the pressure-sensitive sensor pad and perform operational analysis to produce a corresponding patient status signal. The signal transmitter transmits the patient status signal from the signal converter to a server, and the server displays or/and stores corresponding information according to the patient status signal. Thus, patient's statuses in bed can be known at any time, and the harm caused when the patient leaves the bed alone can be minimized, thus effectively improving the work efficiency of caregivers.

Abstract: A swing diagnosis method includes a procedure of calculating levels of a plurality of items including a first item regarding at least one of a backswing and a downswing, and a second item regarding impact on the basis of data regarding a swing, and a procedure of outputting information regarding the levels of the plurality of items.

Abstract: Systems, devices and methods for quantitatively assessing hand function strength and range of motion via various instrumentations are disclosed. In one example embodiment, a hand function diagnostic and therapeutic system includes distal and proximal finger flexion measurement apparatuses used to automate quantitative assessment of hand function based on a combination of strength, range of motion, and time performance metrics.