Abstract: Techniques for suppressing noise in an environment of a magnetic resonance (MR) imaging system having at least one primary coil and at least one auxiliary sensor. The techniques involve estimating a transform, that, when applied to noise received by the at least one auxiliary sensor, provides an estimate of noise received by the at least one primary coil. The transform is estimated from data obtained by the at least one primary coil and the least one auxiliary sensor, with the data being weighted prior to estimation to remove or suppress data in regions with a high signal to noise ratio. In turn, the estimated transform may be applied to noise measured by the at least one auxiliary sensor during imaging of a patient, to estimate and suppress noise present in the MR signals received by the at least one primary coil during imaging.

Abstract: A system for medical data acquisition comprising a plurality of scanners and a plurality of infrastructure units to operate the scanners, wherein the system is designed to use at least one of the infrastructure units as a common infrastructure unit to operate at least two of the scanners. Also, a method to control this system.

Abstract: An embodiment of the present invention provides a scanning control system for a magnetic resonance imaging system, comprising: a first 3D camera, configured to capture a three-dimensional image of a scan subject located on a scanning table of the magnetic resonance imaging system; a processing device, configured to identify body position information of the scan subject based on the three-dimensional image; and a control device, configured to set scanning parameters related to a body position based on the body position information.

Abstract: A flexible catheter includes an elongated body, and a sensor. The elongated body has proximal and distal end portions and defines a working channel therethrough. The sensor is disposed in the distal end portion of the elongated body and is adapted for detecting the position of a distal end of the elongated body within the anatomy of a patient. The sensor is formed from a wire that forms a first layer of wraps about the distal end portion of the elongated body and that includes first and second leads that form a twisted pair proximal to the first layer of wraps. The twisted pair of the first and second leads extends to the proximal end portion of the elongated body.

Abstract: A system for extending the visual capabilities and working channel of a bronchoscope including a probe having optic and/or tracking capabilities at a distal tip thereof and capable of being advanced through the working channel of a standard bronchoscope. The probe also includes a working channel through which various diagnostic and treatment tools may be advanced.

Abstract: A method of operating a positioning system by registering a first coordinate system of a first positioning system in a second coordinate system of a second positioning system includes determining an interpolation function configured to register the first, non-orthonormal coordinate system in the second, orthonormal coordinate system. Fiducial pairs are collected by the respective positioning systems, each of which contain a respective coordinate in the respective coordinate system, both of which refer to the same physical point in three dimensional space. Establishing a working interpolation function involves an analysis of the fiducial pairs using a thin-plate spline algorithm. The method further includes repeatedly obtaining a first coordinate in the first coordinate system and determining a corresponding second coordinate in the second coordinate system in accordance with the interpolation function.

Abstract: An exemplary tissue detection and location identification apparatus can include, for example, a first electrically conductive layer at least partially (e.g., circumferentially) surrounding a lumen, an insulating layer at least partially (e.g., circumferentially) surrounding the first electrically conductive layer, and a second electrically conductive layer circumferentially surrounding the insulating layer, where the insulating layer can electrically isolate the first electrically conductive layer from the second electrically conductive layer. A further insulating layer can be included which can at least partially surrounding the second electrically conductive layer.

Abstract: Various embodiments of an apparatus, methods, systems and computer program products described herein are directed to a Voice Analysis Engine. According to various embodiments, the Voice Analysis Engine receives first streaming prompt data from a computing device. The Voice Analysis Engine analyzes the first streaming prompt data to provide feedback to the user of the computing device. Upon determining the first streaming prompt data satisfies one or more criteria, the Voice Analysis Engine receives second streaming prompt data from the computing device. The Voice Analysis Engine analyzes the streaming prompt data to predict a respiratory state of the user of the computing device.

Abstract: Cough is a common experience and the most frequent reason why an individual seeks a visit to a physician. The prevalence of cough is about 10+% of the population. Cough is a manifestation of many aerodigestive tract disorders and especially consequential for serious lower airway diseases such as respiratory infections, chronic obstructive pulmonary disease (COPD) and asthma because increased coughing leads to emergency room visits and hospitalization. There is a need for methods to oversee coughing frequency in certain patients. Traditionally, all automated cough monitors have used cough sound as the signal for the measurement of cough. In the present invention movements of the diaphragm muscle, recorded by a motion sensor placed above the xiphoid process, are used for counting coughs. A device for such recordings is described and data were collected.

Abstract: The present disclosure relates to a throwaway device to check and measure respiratory flow rates. The device 100 incorporates a first deflector 104, a blade 108 and a second deflector 106 enclosed inside a housing 102. The first deflector 104 configured at a front end of the housing 102 to facilitate inflow of air inside the housing 102. The second deflector 106 is configured at the rear end of the housing 102 to facilitate outflow of air. The blade 108 is having two conical ends 110 at two opposite edges. The blade 108 positioned between the first deflector 104 and the second deflector 106 which is configured to rotate about a rotational axis A-A?. A mouth piece 112 is removable attached at the front end of the housing 102. The blade, housing and the two deflectors are made of different plastic materials using multiple sessions of injection molding process.

Abstract: Disclosed is a gait start intention detection device for detecting a walker's gait start intention, including a plurality of left foot sole sensor units and a plurality of right foot sole sensor units to measure ground reaction force signals generated from foot soles while walking, and a calculation unit to receive and calculate the left ground reaction force signal and the right ground reaction force signal, wherein the calculation unit calculates a center of pressure (COP) location in a walking direction and a direction perpendicular to the walking direction using data of the ground reaction force signal measured from each sensor unit, and detects the walkers gait start intention when a ground reaction force of a swing foot heel of the walker increases, and at the same time, the COP location moves to a rear side of the walker.

Abstract: The invention relates to a method, software, and device 300 used to determine a size or size range 260 for an aperture in the interatrial septum of a heart. The invention relates to software 200 with a learning model 310 which helps a clinician select a surgical shunt size for a patient, monitoring the patient post operatively, and for making shunt modification recommendations, based on specific and aggregate patient data.

Abstract: A body motion determination system for determining whether a body motion of a subject (S) on a bed (BD) presents or not, includes a load detector (11, 12, 13, 14) configured to detect a load of the subject on the bed; a non-negative-valued average calculating unit (313) configured to calculate a non-negative-valued average of a detection value of the load detector; and a threshold value setting unit (315) configured to set a threshold value to be used in determining whether the body motion of the subject presents or not, based on the non-negative-valued average calculated in a resting period in which the subject merely performs a respiration.

Abstract: Smart apparel for monitoring athletics and associated systems and methods are disclosed. An example apparatus includes a data interface to access first motion data and second motion data generated by the smart apparel, the first motion data associated with a first joint on a body and the second motion data associated with a second joint on the body; a motion data fuser to fuse the first motion data and the second motion data; an analytics determiner to process the fused first and second motion data to identify a progression of a motion based activity; and a display organizer to generate a graphical display representing the progression of the motion based activity.

Abstract: A bed apparatus capable of detecting a state of a user. The bed apparatus includes a bedboard that supports a user, a bed frame that is attached to the bedboard, an acceleration sensor attached to the bedboard, and a controller that detects a state of the user based on a result of detection of the acceleration sensor. The acceleration sensor can detect accelerations in at least two axial directions and is attached to a surface of the bedboard such that two acceleration detection axes of the acceleration sensor are parallel to the surface of the bedboard.

Abstract: The present application relates generally to computer software, mobile electronics, wireless communication links, and wearable monitoring systems. More specifically, techniques, systems, sensors, circuitry, algorithms and methods for wearable monitoring devices and associated exercise apparatus are described. A garment borne sensor system may acquire data on a user's performance during exercise, for example. The data may be analyzed in real time and feedback may be provided to the user based on the analysis. Analysis may be used to alter behavior of the user and/or an apparatus the user is engaged with during an activity, such as exercise, conditioning, therapy, etc. A piece of exercise equipment may be instrumented and in communication with the sensor system or other system and may be controlled in real time to adjust its settings to affect the user during the exercise routine. Communication between the sensor system and other systems may be wireless.

Abstract: This disclosure relates generally to a system and method for shoulder proprioceptive analysis of the person. The present disclosure monitors the shoulder joint motion by quantitative measure of range of motion (ROM) and kinesthesia of shoulder using a smart watch, thereby assessing the limit of active motion and the ability to passively reposition the arm in space. The present disclosure estimates the ROM, velocity, quality of joint movement, direction of hand movement using the sensor data captured by the smart watch. Further, the present disclosure provides a performance metrics of the shoulder function by comparing the shoulder motion before and after a prosthesis procedure. The present disclosure implements a rule engine-based approach classifying the shoulder/arm movement which includes flexion, extension, abduction, and adduction, internal and external rotation.

Abstract: The invention relates to a porous optical fiber for the detection of an analyte in a fluid by optical probing. The optical fiber has a first end and a second end opposite to the first end, as seen in a longitudinal direction, and a circumferential surface delimiting the optical fiber in radial directions perpendicular to the longitudinal direction. The optical fiber comprises a core adapted for supporting at least one optical mode propagating in the longitudinal direction, the core having a circumferential interface delimiting the core in the radial directions. The optical fiber further comprises pores penetrating from an opening at the circumferential surface through the circumferential interface into the core of the optical fiber, wherein a cross-sectional dimension of the openings is dimensioned so as to prevent a particulate fraction of the fluid from entering the pores, while allowing the analyte to enter the pores.

Abstract: A wearable device for biofluid analysis includes a set of sensing electrodes, and the set of sensing electrodes includes a working electrode which includes: (1) abase electrode including a sensing surface; (2) capture probes immobilized on the sensing surface; and (3) a protective layer e disposed on the sensing surface and including a redox couple within the protective layer.

Abstract: A system for transdermal alcohol sensing to be worn near a skin surface of a user, including: an alcohol sensor; a microporous membrane; a housing coupled to the alcohol sensor and the membrane, defining a volume between the alcohol sensor and a first membrane side, and fluidly isolating the volume from a second membrane side opposing the first membrane side; an electronics subsystem electrically coupled to the alcohol sensor, operable to power and receive signals from the alcohol sensor; and a fastener operable to position the second membrane side proximal the skin surface.

Abstract: Systems, methods, and apparatuses for reducing error between calculated analyte levels and impractical analyte measurements using practical analyte measurements as reference measurements for calibration. Reducing the error may include converting a practical reference analyte measurement into an estimated impractical analyte level, updating a conversion function using the estimated impractical analyte level, and using the updated conversion function to calculate an analyte level. In some embodiments, the practical reference analyte measurement may be a capillary blood analyte measurement, and the estimated impractical analyte level may be an estimated venous blood analyte level. In some embodiments, the updated conversion function may minimize the error between analyte levels calculated using the updated conversion function and estimated venous blood analyte levels.

Abstract: Recommendations based on continuous glucose monitoring (CGM) are described. Given the number of people that wear CGM systems and because CGM systems produce measurements continuously, a platform that provides a CGM system may have an enormous amount of data. This amount of data is practically, if not actually, impossible for humans to process. In implementations, a CGM platform includes a data analytics platform that obtains glucose measurements provided by a CGM system and also obtains additional data associated with a user. The data analytics platform processes these measurements and the additional data to predict a health indicator by using models. This prediction serves as a basis for generating a recommendation, such as a message recommending the user take action or adopt a behavior to mitigate a predicted negative health condition.

Abstract: Recommendations based on continuous glucose monitoring (CGM) are described. Given the number of people that wear CGM systems and because CGM systems produce measurements continuously, a platform that provides a CGM system may have an enormous amount of data. This amount of data is practically, if not actually, impossible for humans to process. In implementations, a CGM platform includes a data analytics platform that obtains glucose measurements provided by a CGM system and also obtains additional data associated with a user. The data analytics platform processes these measurements and the additional data to predict a health indicator by using models. This prediction serves as a basis for generating a recommendation, such as a message recommending the user take action or adopt a behavior to mitigate a predicted negative health condition.

Abstract: Disclosed are an apparatus and a method for measuring a blood glucose level. In the blood glucose level measurement apparatus and method, the apparatus coupled to a patch with a microneedle formed in at least one area and configured to calculate a blood glucose level of a body fluid extracted from a user may calculate the blood glucose level by analyzing a reflected light beam reflected from the patch with a microneedle formed in a second area and correct the calculated blood glucose level of the user by analyzing data obtained by measuring a reflected light beam from a first area from which the body fluid is not extracted so as to measure a precise blood glucose level with an error being reduced in consideration of environmental factors influencing measurement.

Abstract: A body fluid leakage detection aqueous composition, for use e.g. in intraoperative pancreatic fluid leakage detection. The composition comprises a gelling agent, increasing the viscosity of the composition, and buffering species, the composition thereby being buffered. The gelling agent is cross-linked ?-glucan microspheres. Further, the composition comprises a pH-indicator. The pH of the composition is at least 0.1 pH units lower, or higher, than a pKa of the pH-indicator.

Abstract: Systems and methods are described, and one method includes determining a fetal blood oxygenation level, including: activating at least one light source with at least two distinct wavelengths of light on an abdomen of a pregnant mammal to direct light into a maternal abdomen toward a fetus; receiving a set of mixed signals from a set of photodetectors positioned at different locations on the maternal abdomen from reflected light that traverses maternal tissue or maternal tissue and fetal tissue; determining the fetal blood oxygenation level by performing computations on a composite fetal signal produced from the mixed signals; and ensuring a skin temperature of the maternal abdomen does not rise to unsafe levels due to activating the at least one light source.

Abstract: Provided is an oxygen saturation-based assessment method, the method includes: obtaining an elevation and oxygen saturation corresponding to a user to be assessed, determining an assessment result corresponding to the user to be assessed based on the elevation and the oxygen saturation. The assessment method can timely assess the adaptability of the user to be assessed, which can prevent the occurrence of plateau reactions and plateau disease in advance and provide exercise guidance. And an oxygen saturation-based assessment device, smart wearable device and storage medium are provided further.

Abstract: A method of determining the perceptual load of a human brain. The perceptual load is induced by a predetermined task carried out by the human. The method includes the steps of: measuring with a functional near-infrared spectroscopy (fNIRS) sensor device a metabolic activity of the human brain while the task is carried out and determining the perceptual load as a function of a measured change in metabolic activity. The invention further relates to a method of determining the level of stimulus perception corresponding systems.

Abstract: A biological fluid collection device (10) that produces a stabilized biological sample with head-to-tail uniformity through the capturing of a high concentration front and subsequent redistribution of the high concentration front throughout a biological fluid is disclosed. The biological fluid collection device includes an inline mixer (16) used for head-to-tail mixing of a concentrated flow front. The mixing is achieved via a two-stage process. First, a front fraction of the flow is captured within a centered mixing chamber (30) via capillary assisted flow action. Second, the captured front volume is then slowly released throughout a small exit hole (36) and recombined with the rest of the flow volume that was diverted around the centered mixer chamber.

Abstract: An evaluation apparatus comprising: a display screen; a gaze point detection unit that detects a position of a gaze point of a subject who observes the display screen; a display control unit that performs display operation including first display operation of displaying question information that is a question for the subject on the display screen, second display operation of displaying a guidance target object that guides the gaze point of the subject to a target position on the display screen, and third display operation of displaying, at positions that do not overlap with the target position on a same circumference of a circle centered at the target position, a plurality of answer target objects that are answers for the question on the display screen after the second display operation.

Abstract: An evaluation apparatus includes a display screen that displays an image; a gaze point detection unit that detects a position of a gaze point of a subject who observes the display screen, a display control unit that performs instruction display operation of displaying, on the display screen, a task target object to be gazed at by the subject and instruction information for instructing the subject to solve a task related to the task target object, a region setting unit that sets, on the display screen, a task region corresponding to the task target object and an instruction region corresponding to the instruction information, and a determination unit that determines whether the gaze point is present in the task region and the instruction region during an instruction display period in which the instruction display operation is performed on the basis of positional data of the gaze point.

Abstract: A control device, system, and method for a vehicle to determine a driver's comfort level, configured to receive a first sensor output of a first physiological sensor measuring at least one first physiological feature of the driver, and receive a second sensor output of a second physiological sensor measuring at least one second physiological feature of the driver, create at least one reference data set by recording the first sensor output over a first predetermined reference time period and recording the second sensor output over a second predetermined reference time period being different than the first predetermined reference time period, determine at least one reference index for the comfort level of the driver based on the reference data set, and determine a comfort level index value of the driver, the index value determined as a function of the reference index and the current first and/or second sensor output.

Abstract: A device, system, and method for mapping myocardial tissue, such as epicardial tissue on the right ventricle. A system for mapping myocardial tissue may include a mapping device having a distal portion that includes a distal assembly sized and configured to be positioned within the pericardial space. The distal assembly may include an expandable shell, at least one inflatable or expandable element within the expandable shell, and a mapping electrode assembly. Inflation or expansion of the at least one inflatable or expandable element, and therefore expansion of the expandable shell, within the pericardial space may provide sufficient force of the mapping electrodes against the myocardial tissue being mapped. The system may also include a delivery sheath with a retention element for controllably retracting the device within the sheath during delivery and removal of the device from the pericardial space.

Abstract: A method includes providing a first electrode and a second electrode, receiving a first plurality of signals from the first electrode during a first period of time, and receiving a second plurality of signals from the second electrode during a second period of time. The method also includes receiving a pooled signal comprising a third plurality of signals from the first electrode and a fourth plurality of signals from the second electrode and isolating, from the pooled signal, one or more of the third plurality of signals and one or more of the fourth plurality of signals.

Abstract: A system for estimating physical parameter(s) of a medium having electrolyte(s), including at least one working electrode; one counter electrode; a current generator delivering to the electrodes electric current pulses; a computer-readable memory including a predefined analytic model of an electric potential, between the working and counter electrodes, as a function of time, receiving as inputs the current and current pulse duration and including the physical parameter to be estimated; an acquisition unit including a signal amplifier for acquiring and amplifying an electric potential recorded by the electrodes; a processor including a stimulation module controlling the current generator to deliver a biphasic charge-balanced current during a stimulation duration; an acquisition module acquiring an electric potential variation during the stimulation duration; and a calculation module receiving the acquired electric potential variation, fitting the acquired electric potential variation using the predefined analy

Abstract: Methods, computer program products, and systems for testing of multisensory integration of a user are provided as well as their association with cognitive and motor outcomes. In various embodiments, the method includes providing a first plurality of signals to the user from a first signaling modality. A second plurality of signals are provided to the user from a second signaling modality. Indications are received at a response sensor from the user in response to each of the first and second plurality of signals. Reaction times between each of the first and second plurality of signals and the respective indication are determined. An observed curve is generated based on the reaction times. A differential curve is determined from the observed curve and a predicted curve. An area under at least a portion of the differential curve is determined. When the area is above a predetermined threshold, an indication that the user has satisfactory integrated sensory information is provided.

Abstract: Methods for screening, diagnosing, or predicting presence, progression, or treatment effects of a cognitive dysfunction such as dementia based on an analysis of drawing behavior changes by a pre-trained Naïve Bayes method are provided. The methods include steps of obtaining drawing data of at least one image created by a test subject on a digital device and obtaining personal data of the test subject; reconstructing the at least one image based on the drawing data obtained; converting the drawing data to drawing features comprising a plurality of motion features and a plurality of geometric features; and determining probability that the test subject has a cognitive dysfunction based on the drawing features and the personal data by a pre-trained Naïve Bayes method with a greedy variable selection.

Abstract: A wearable sensor for measuring a parameter of human skin is described and includes a flexible body comprising sensor components formed on, adjacent or within the flexible body and configured to generate a first signal indicative of the parameter of human skin; microfabricated processing circuitry formed within the flexible body, coupled to the sensor components and configured to process the first signal to produce a second signal; and an antenna, formed on, adjacent or within the flexible body, the antenna being coupled to the processing circuitry and configured to transmit the second signal to an external device.

Abstract: A monitor device (4) for a wound dressing system the device comprising a processor; a memory; a first interface connected to the processor and the memory, configured for collecting wound data from a wound dressing (2), the wound data comprising wound data from different sensor points of the wound dressing; and a second interface. The processor configured to: obtain parameter data based on the wound data; and determine an operating state of the wound dressing based on the parameter data, wherein the operating state is indicative of a degree of wetting of the wound dressing.

Abstract: Joint analysis probe (100). The probe (100) includes a frame (102). The probe (100) also includes a microphone (106) embedded into the frame (102) and configured to measure sounds (108) from a joint (162) of a subject (160) in a non-contact manner. The probe (100) also includes a raised rim (104) around the microphone (106) configured and positioned to be in contact with the subject (160) when the microphone (106) measures the sounds (108) from the joint (162), whereby the raised rim (104) attenuates an ambient noise (110) captured by the microphone (106).

Abstract: A method of providing workout training for a user of an activity tracking system includes displaying a plurality of training plan options to the user on a screen of a personal electronic device, and then receiving a selected training plan option from the user. Selected workout day options are received from the user and the system generates a training schedule for the user based on the selected training plan and the selected workout day options. One or more reminders identify the type of workout for the scheduled day and an option to accept or reject the workout. When the user selects the option to accept the workout, the workout goal associated with the scheduled workout is displayed. The method further includes determining progress toward the workout goal based on the received workout data, and displaying an indicator of progress toward the workout goal on the screen during the workout.

Abstract: Exemplary embodiments described in this disclosure are generally directed to systems and methods for detecting alertness of a driver of a vehicle. In one exemplary method, a driver alertness detection system determines whether a driver of a vehicle is susceptible to lagophthalmos. If the driver is susceptible to lagophthalmos, the driver alertness detection system may evaluate an alertness state of the driver by disregarding an eyelid status of the driver and monitoring biometrics of the driver such as, a heart rate and/or a breathing pattern. Alternatively, the driver alertness detection system may evaluate an alertness state of the driver by placing a higher priority on the biometrics of the driver than on the eyelid status. However, if the driver is not susceptible to lagophthalmos, the driver alertness detection system evaluates the alertness state by placing a higher priority on the eyelid status than on the biometrics of the driver.

Abstract: In a described embodiment, a method of sleep stage detection is disclosed. The method comprises receiving a first vital sign feature 701a including a plurality of first feature values v1-v11 corresponding to respective ones of a plurality of epochs; and performing a first logistic regression operation 701a? to calculate a first indication value 702a for each intermediate one of the epochs based on the corresponding first feature value v6 and those of preceding v1-v5 and succeeding v7-v11 ones of the epochs, the first indication value 702a being descriptive of a sleep stage of the corresponding intermediate epoch. A method of creating a model for logistic regression, a method of extracting a heart rate variability feature, a method of creating a model for extracting a heart rate variability feature, a method of deriving a medical dosage, a method of assessing a responsiveness to a medical dosage, a computer-readable medium, a computing device and a wearable device are also disclosed.

Abstract: A diagnostic assistance method for a disease based on an endoscopic image of a digestive organ with use of a convolutional neural network (CNN). A diagnostic assistance method for a disease based on an endoscopic image of a digestive organ with a CNN trains the CNN using a first endoscopic image of the digestive organ and at least one final diagnosis result on positivity or negativity to the disease in the digestive organ, a past disease, a severity level, and information corresponding to a site where an image is captured, the final diagnosis result corresponding to the first endoscopic image, and the trained CNN outputs at least one of a probability of the positivity and/or the negativity to the disease, a probability of the past disease, a severity level of the disease, an invasion depth of the disease, and a probability corresponding to the site where the image is captured.

Abstract: The present disclosure provides a method of assessing periorbital puffiness in a subject by determining if the subject exhibits pseudoherniation of one or more upper eyelid fat pads and/or one or more of the lower eyelid fat pads, determining if the subject exhibits one or more conditions selected from the group consisting of: edema of the fat pad, edema along the soft tissue of the upper and/or lower eyelids, malar mounds due to edema, malar edema, and mild festoons aggravated by edema, and scoring the periorbital puffiness from both determinations.

Abstract: In various embodiments, an electronic device may include: a light receiver including light receiving circuitry, a light emitter including light emitting circuitry, a partition wall disposed between the light receiver and the light emitter configured to block light emitted by the light emitter from being directly incident on the light receiver, a film disposed above one surface of the light receiver, and a processor. The film may include a transmission region configured to transmit light of all wavelength bands and a selective blocking region configured to absorb light of a specific wavelength band. The processor may be configured to analyze light incident on the light receiver through the film.

Abstract: A method, a structure, and a computer system for a modular sensing unit. The structure comprises a sensor module, a power cable ribbon, and a component module, wherein the component module is in communication with and detachable from the sensor module via the power cable ribbon.

Abstract: An oral measurement apparatus that extends in a longitudinal direction and includes a sensor, a processor, and a temperature information obtaining section. The sensor is disposed at a first end of the oral measurement apparatus in the longitudinal direction and obtains analog information inside a mouth. The processor is disposed closer to the sensor with respect to a central portion of the oral measurement apparatus in the longitudinal direction. The processor converts the analog information obtained by the sensor into digital information and outputs the digital information as a processing result. The temperature information obtaining section obtains temperature information indicating a temperature of the processor and outputs the temperature information.

Abstract: An insertable physiological monitor injector tool is provided. An elongated handle includes a recess formed along a longitudinal axis and has an opening on a distal end. An insertion tube has a hollow elongated shape that is movably positioned within the elongated handle, in the recess. A stationary arbor is affixed on a proximal end to a proximal end of the elongated handle and extends through the insertion tube when the insertion tube is in a retracted position. A tab is affixed to the insertion tube, wherein the tab can lock the insertion tube in an extended position.

Abstract: A system and a method for predicting kinesthetic outcomes from observed position, posture, behavior or activity of an individual 1602, 1702. The system uses kinesthetic activity sensors 102, 104 each collecting one or more of audio, video, or physiological signals and capturing the activity of the individual or an ambient environment of the individual. These signals are delivered into a computer system 106 implementing a learning routine 108 which constructs one or more personalized kinetic state models 1510 of positional states for the individual and transitions between the positional states, and further develops one or more customized multi-dimensional prediction models 1500 for the individual and uses the multidimensional prediction models to predict behaviors, activities and/or positional changes likely to occur in the future, and provides notice of predicted unsafe or undesired outcomes.