Abstract: Provided is an object information acquiring apparatus including: a light source; a controller that controls irradiation of light from the light source; a detector that receives an acoustic wave generated from an object onto which light from the light source is irradiated; a processor that generates characteristic information inside the object using the acoustic wave received by the detector; and an acquirer that acquires the shape of the object, wherein the controller controls an irradiation area when light is irradiated from the light source onto the object, based on the shape of the object acquired by the acquirer.

Abstract: A measuring device (10) has at least one sensor (16, 18), which can be applied to the skin surface (12) of a patient for detecting a measured value with the sensor (16, 18). The device (10) has two contact surfaces (20, 22) on an underside (24), which is intended for being in contact with the skin surface (12) of the patient. A current detecting (32, 34), detects a measuring current (30) resulting from a particular effective electric resistance between the contact surfaces (20, 22). A method for operating such a measuring device (10) and a system with such a measuring device (10) are also provided.

Abstract: A head mounted system (HMS) configured to collect facial expressions of the user wearing the HMS. The HMS includes a frame and at least four cameras coupled to the frame. First and second cameras capture the user's right and left eyebrows, and third and fourth cameras capture the right and left sides of the user's upper lip. An optional computer utilizes the images captured by the cameras to detect facial expressions, microexpressions, and/or to improve the user's emotional awareness.

Abstract: Methods and systems are described for detecting the likelihood of an aortic coarctation in an infant using photoplethysmographic pulse signals obtained from the hand and foot of the infant.

Abstract: A system for generating physiological signals using a cloth capacitive sensor, includes a cloth, at least one conductive area arranged on the cloth, a signal circuit; a capacitive sensor formed between the cloth and a human body; a resistor R, a capacitor C, an inductor L, an operational amplifier, a diode, a Schmitt trigger, CMOS, a transistor, or an IC that forms a charge or discharge circuit, connected with the cloth capacitive sensor to change a signal range of frequency, cycle, voltage or current; wherein when a force, pressure, tensile force, torsion or tension is applied between the human body and the cloth, the capacitance changes, the circuit sends a signal, and the system receives the change in capacitance between the conductive cloth and the human body; wherein the change is represented by a frequency, cycle, voltage or current change.

Abstract: A step-on device records the patient's EKG, Respiratory signal, PPG, and weight, giving health care personnel the ability to monitor patient health trends. The device sends the data to a central server via a smartphone or via WiFi. Health care personnel may view the data and trends on an online website or app.

Abstract: A patient monitoring system may receive a physiological signal such as a photoplethysmograph (PPG) signal that exhibits frequency and amplitude modulation based on respiration. A phase locked loop may generate a frequency demodulated signal and an amplitude demodulated signal from the PPG signal. An autocorrelation sequence may be generated for each of the frequency demodulated signal and the amplitude demodulated signal. The autocorrelation sequences may be combined and respiration information may be determined based on the combined autocorrelation sequence.

Abstract: Systems and methods are disclosed for moving a tabletop of a workstation based on biometric input associated with a user, the method being performed by a controller that is configured to send control signals to actuators to move the tabletop. One method includes: accessing a user profile associated with a user device; determining parameters for moving the tabletop, based on the user profile, for eliciting desired biometric inputs from the workstation user at one or more times during the movement of the tabletop; and repeating one or more iterations of: moving the tabletop based on the parameters, by sending control signals to the actuators of the tabletop; receiving, into a data storage device, actual biometric inputs from the workstation user; comparing the received actual biometric inputs with the desired biometric inputs; and if the parameters do not elicit the desired biometric inputs, adjusting the parameters.

Abstract: Systems, devices disclosed provide example methods comprising determining that a triggering event has occurred based on statuses for a set of physiological parameters associated with the patient, the physiological parameters indicative of the patient engaging in a patient initiated physical activity, generating a trigger output signal in response to the determination that the triggering event has occurred, wirelessly transmitting the trigger output signal to a pressure sensing device implanted in a vessel of the patient, triggering, based on receiving the trigger output signal, the pressure sensing device to sense a cardiovascular pressure of the patient; and transmitting, by the pressure sensing device, a wireless signal comprising data corresponding to the sensed cardiovascular pressure of the patient.

Abstract: A blood pressure measurement method uses a pulse wave measurement unit (20) for measuring the pulse wave of a subject using an FBG sensor (10), and a blood pressure value calculation unit (30) for calculating a blood pressure value from waveform date of the measured pulse wave. The blood pressure calculation unit (30) uses a calibration model representing the correlation between measured waveform date of a previously measured pulse wave, and a measured blood pressure value measured by an automatic blood pressure gauge at each measurement point in time of the measured waveform date to estimate the blood pressure value of the subject from the measured waveform date of the pulse wave. It is possible to realize an easy-to-use blood pressure measurement method capable of estimating the blood pressure value with accuracy required for the automatic blood pressure gauge and continuously measuring the blood pressure.

Abstract: [Problem] To provide a finger arterial dilatability testing method, finger arterial dilatability testing device, and finger arterial dilatability testing program with which it is possible to simply test for early signs of arteriosclerosis using the small vessels of the finger arteries.

Abstract: The systems, devices, and methods presented herein use a heart pump to obtain measurements of cardiovascular function. The heart pumps described herein can operate in parallel with and unload the heart. The system can quantify the functioning of the native heart by measuring certain parameters/signals such as pressure or motor current, then calculate and display one or more metrics of cardiovascular function. These metrics, such as left ventricular end diastolic pressure (LVEDP), left ventricular pressure, and contractility, provide valuable information to a user regarding a patient's state of heart function and recovery.

Abstract: A system for detecting blood pressure based on imaging photoplethysmography (iPPG) includes a first inward-facing head-mounted camera to capture images of a first region of interest located on the face below the eyes and above the lips (IMROI1) of a user, and a second inward-facing head-mounted camera to capture images of a second region of interest comprising a portion of a temple and/or forehead (IMROI2) of the user. The system further includes a computer to calculate a blood pressure value for the user based on first and second photoplethysmographic signals recognizable in IMROI1 and IMROI2.

Abstract: PPG sensor emits light at at least three wavelengths (Y1-Y3) and detects the reflected light. The PPG sensor comprises a motion correction unit (130) for correcting motion artefacts from the detected light signals by subtracting the output signal of the detected light at the second wavelength (Y2) from an average of an output signal of the detected light at the first and third wavelength (Y1, Y3). The three wavelengths (Y1-Y3) are arranged around 550 nm. The second wavelength (Y2) is arranged equal distantly between the first and third wavelength.

Abstract: Systems and methods are described for the compositing together of model-linked vascular data from a plurality of sources, including at least one 2-D angiography image, for display in a frame of reference of the at least one angiography image. In some embodiments, a linking model comprises a data structure configured to link locations of angiographic images to corresponding elements of non-image vascular parameter data. The linking data structure is traversed to obtain a mapping to the frame of reference of one or more of the angiographic images.

Abstract: A method for non-invasive assessment of intracranial pressure includes providing an image recording device, recording at least one image of a retina part of an eye of a person using said image recording device, identifying, in said at least one image, at least one artery and at least one vein associated with said artery, determining, in said image, a first characteristic diameter value for said identified artery, determining, in said image, a second characteristic diameter value for said identified vein, calculating an arteriovenous ratio, A/V ratio, based on said first and second characteristic diameter values, and comparing said arteriovenous ratio with a threshold value to estimate intracranial pressure.

Abstract: A system for recording, processing, and monitoring biosignals is provided, the system being configured to suspend data acquisition whenever an electric surgical tool or other generator of high frequency interference is in use. Such a system may protect the hardware of the system and reduce or eliminate the acquisition of distorted signals. The system of some embodiments includes an amplifier system configured to detect the presence of high frequency interference. Related methods are also disclosed.

Abstract: The present invention is directed to a physiological recording device and, more particularly, to a physiological recording device that can be used without skin preparation or the use of electrolytic gels. The invention is further directed to an encouragement ring which stabilizes and helps situate the physiological recording device on a subject's skin to help provide a better electrical signal, increase surface area, and reduce and minimize noise and artifacts during the process of recording or monitoring a physiological signal. The invention is still further directed to surface features on a surface of the physiological recording device with a size and shape that will not substantially bend or break, which limits the depth of application of the recording device, and/or anchors the recording device during normal application. The invention is even further directed to a method for manufacturing a physiological recording device, and minimizing cost of manufacture.

Abstract: According to at least one aspect, a wearable medical device is provided. The wearable medical device may include a sensing electrode to sense an electrocardiogram signal of a patient, a therapy electrode to provide treatment to the patient, a garment to be worn about a torso of the patient and receive the sensing electrode and the therapy electrode, and a controller operatively coupled to the sensing electrode and the therapy electrode. The controller may be configured to determine a current location of the wearable medical device based on a previous position of the medical device and at least a speed and a direction of movement of the wearable medical device.

Abstract: A mapping catheter including an elongate catheter body extending from a proximal end to a distal end, a handle connected to the proximal end of the catheter body, an electrode array connected to the distal end, a deployment shaft, and an irrigation system. The catheter body includes at least one lumen. The irrigation system includes a manifold and a thin, polymeric irrigation tube. The manifold is disposed within the handle and is connectable to a source of irrigation fluid. The irrigation tube is connected to the manifold and extends around the deployment shaft from the manifold to the distal end of the catheter through the catheter body lumen. The irrigation tube forms an annular lumen between an inner surface of the irrigation tube and an outer surface of the deployment shaft. The annular lumen is configured to carry irrigation fluid from the manifold to the array.

Abstract: The invention discloses a method, a system, a computer program and a device for determining the surface charge and/or dipole densities on heart walls. Using the foregoing, a table of dipole densities ?(P?, t) and/or a table of surface charge densities ?(P?, t) of a given heart chamber can be generated.

Abstract: A method is disclosed for displaying patient ECG data. The method includes receiving ECG data including an ECG waveform; receiving analyzed ECG data including arrhythmic events; generating an indicia of the detected arrhythmic event; and displaying the indicia of the detected arrhythmic event in relation to the ECG waveform at a position associated with a time of the detected arrhythmic event. A system for displaying patient ECG data is also disclosed.

Abstract: An example method includes performing amplitude-based detection to determine location of R-peaks for a plurality of electrograms. The method also includes performing wavelet-based detection to determine location of R-peaks for the plurality of electrograms. The method also includes adjusting the location of the R-peaks determined by the wavelet-based detection of R-peaks based on the location of R-peaks determined by the amplitude-based detection of R-peaks. The method also includes storing, in memory, R-peak location data to specify R-peak locations for the plurality of electrograms based on the adjusting.

Abstract: In order to provide an electrode equipped with an insulating wall having excellent patterning properties as well as excellent biocompatibility, there is provided an electrode including, on a substrate, an electrode element; and an insulating wall formed around the electrode element, constituted of a polysiloxane compound (component A) having, per molecule, two or more functional groups selected from the group consisting of a (meth)acryloyl group, a styrenic vinyl group, a vinyl ester group, a maleic acid ester group and a maleimide group, and formed from a polymer obtained by reaction of the functional groups.

Abstract: The disclosure relates to a sensor, a system, and a holder arrangement for biosignal activity measurement. One example embodiment includes a sensor module for brain activity measurement. The sensor module includes a main electrode base. The sensor module also includes a plurality of pins protruding from the main electrode base. The plurality of pins is arranged such that, when applied on a subject, the pins make contact with skin of the subject or are in close proximity with the skin of the subject. The main electrode base comprises electronic circuitry for near infrared spectroscopy (NIRS) measurements and electronic circuitry for electroencephalography (EEG) measurements, both connected to the plurality of pins. The plurality of pins includes electrically conductive pins. The plurality of pins also includes at least one source waveguide pin configured for light emitting purposes or at least one detector waveguide pin configured for light detection purposes.

Abstract: Electrodes for a bio-impedance measuring device or a body composition monitor, the electrodes being integral with or being attached to a surface of at least one device belonging to a group of electronic and/or non-electronic devices used in the preparation of a dialysis treatment or during dialysis, in particular during peritoneal dialysis, the group preferably consisting of organizers of a continuous ambulatory peritoneal dialysis system (CAPD), automated peritoneal dialysis devices, automated peritoneal dialysis-cyclers (APD-Cycler), bioelectrical impedance analyzers (BIA), body composition monitors (BCM), hand-held electrodes holders for the electrodes, and dialysis apparatuses. Devices and methods used during dialysis are also described.

Abstract: An apparatus for measuring complex electrical admittance and/or complex electrical impedance in animal or human patients includes a first electrode and at least a second electrode which are adapted to be disposed in the patient. The apparatus includes a housing adapted to be disposed in the patient. The housing has disposed in it a stimulator in electrical communication with at least the first electrode to stimulate the first electrode with either current or voltage, a sensor in electrical communication with at least the second electrode to sense a response from the second electrode based on the stimulation of the first electrode, and a signal processor in electrical communication with the sensor to determine the complex electrical admittance or impedance of the patient.

Abstract: A method comprises identifying linked anatomical structures in stored images of a patient anatomy and modeling a structure of linkage elements. Each linkage element corresponds to one of the linked anatomical structures. The method also includes modeling a portion of the patient anatomy as a plurality of search slabs and assigning each of the linkage elements to one of the plurality of search slabs. The method also includes receiving tracking data corresponding to a sensed instrument portion. The tracking data includes position information and orientation information for the sensed instrument portion. The method also includes identifying one of the plurality of search slabs which includes the position information for the sensed instrument portion and matching the sensed instrument portion to a matched linkage element from among the linkage elements assigned to the identified one of the plurality of search slabs.

Abstract: A system employs an interventional tool (30), ultrasound imaging system and a multi-planar reformatting module (40). The interventional tool (30) has one or more image tracking points (31). The ultrasound imaging system includes an ultrasound probe (20) operable for generating an ultrasound volume image (22) of a portion or an entirety of the interventional tool (30) within an anatomical region. The multi-planar reformatting imaging module (40) generates two or more multi- planar reformatting images (41) of the interventional tool (30) within the anatomical region. A generation of the two multi-planar reformatting images (41) includes an identification of each image tracking point (31) within the ultrasound volume image (22), and a utilization of each identified image tracking point (31) as an origin of the multi-planar reformatting images (41).

Abstract: An endotracheal tube positioning device includes a first Hall sensor, a second Hall sensor spaced a predetermined distance from the first Hall sensor, a converter, and an integrated circuit board electrically connecting the first Hall sensor and the second Hall sensor to the converter, wherein a position range is established for the device based on a symmetry of voltage readings provided from the first and second Hall sensors to the converter. An endotracheal tube positioning system includes an endotracheal tube having a magnet provided toward a distal tip end, an endotracheal tube positioning device having a first Hall sensor and a second Hall sensor, the positioning device configured to adhere to a skin surface, and a monitor for receiving data based on voltage values provided by the first and second Hall sensors, the data indicating a position of the magnet relative to the adhered position of the positioning device.

Abstract: A system for detecting the location of an endoscopic device inside a patients' body comprises an endoscope assembly with an insertion tube having a set of codes indicative of an insertion depth and a rotational direction of the endoscopic device and a detector to detect the set of codes and calculate the location information. The images captured by the endoscopic device are automatically tagged with corresponding location information. Optionally, the endoscope assembly further comprises a system for generating three dimensional images and videos without increasing the number of cameras. Optionally, the endoscope assembly further comprises a system having a plurality of sensor devices for generating a real time image map of an endoscopic tip portion traversing a lumen. Optionally, the endoscope assembly further comprises a special garment for colonoscopy patients to preserve the modesty of the patients and to protect a physician from spraying fecal matter.

Abstract: A spine measurement system comprising a camera, an encoded collar, and a remote station. A rod is shaped having one or more bends to modify a curvature of a spine. The encoded collar is coupled to the rod. The encoded collar includes a plurality of markings where each marking represents a rod position. The rod and encoded collar are in a field of view of the camera. The camera takes a number of images as the rod rotates at least 360 degrees. The remote station measures the 2D images to produce quantitative measurements that yield a 3D model of the rod shape. The remote station can use the 3D rod shape to determine metrics that relate to how the rod shapes the spine. For example, a Cobb angle can be calculated from the rod shape to determine if the rod yields the desired spine outcome.

Abstract: Systems and methods for detecting onset, presence, and progression of particular states, including intoxication, include observing eye movements of a subject and correlating the observed movements to known baseline neurophysiological indicators of intoxication. A detection system may record eye movement data from a user, compare the eye movement data to a data model comprising threshold eye movement data samples, and from the comparison make a determination whether or not intoxication or impairment is present. The detection system may alert the user to take corrective action if onset or presence of a dangerous condition is detected. The eye movements detected include saccadic and intersaccadic parameters such as intersaccadic drift velocity. Measurements may be collected in situ with a field testing device. An interactive application may be provided on a user device to provoke the desired eye movements during recording.

Abstract: A medical device includes a housing and an electrode arrangement coupled to the housing and configured to sense an electrical physiologic signal from a patient. The device also includes detection circuitry coupled to the electrode arrangement and configured to obtain a cardiac signal component and a non-cardiac signal component from the physiological signal. A processor is coupled to the detection circuitry. The processor is configured to detect patient activity using at least the non-cardiac signal component and discriminate between voluntary and involuntary activity of the patient based on a comparison of temporally aligned cardiac and non-cardiac signal components.

Abstract: A method implemented in a system which comprises a lightweight personal wearable monitoring device, supplied by a battery, comprising an accelerometer, a processing unit, a display, a remote server, said method comprising the steps: /a/ collecting, from a plurality of individuals caused to practice various physical activities from a set of predefined activities, acceleration data from sensing devices placed on each of said individuals, /b/ defining N small data-size specific metrics, computed from acceleration signals, which allow to define a global activity classifier, /c/ acquiring, at a first monitoring device worn by a first user, acceleration signals from the accelerometer of the first monitoring device, /d/ calculating, at the first monitoring device, over each lapsed time unit T1, specific metrics values from the sensed signals, to form a series of specific metrics values, /e/ send them to the processing unit, /f/ allocate an activity type for each time unit together with corresponding specific metric

Abstract: A thermal tag for activity monitoring. The thermal tag includes a base layer having a plurality of metal lines to provide a conductive path, and a pattern layer having one or more infrared emitting features positioned over portions of the conductive path, wherein at least one infrared emitting feature couples to the conductive path to emit a predetermined infrared pattern in accordance with nearby activity.

Abstract: An inserter assembly for continuous glucose monitoring with medication delivery capability where the assembly has a deployment button containing a needle deployment mechanism having a sharp held in a pre-release position, a housing body in which the deployment button is movably received within a top end of the housing body, the housing body having a sensor deployment assembly containing a lumen and a sensor disposed within the lumen and extending out of the lumen to a circuit board that is part of the sensor deployment assembly, the sensor deployment assembly matingly connected to the sharp where the sharp extends beyond the sensor deployment assembly and contains the sensor not fixedly attached to the sharp, and a sensor housing releasably received within a lower end of the housing body, the sharp extending into a sensor deployment assembly recess within the sensor housing and directly above a sensor opening in a bottom of the sensor housing.

Abstract: Disclosed herein is an analyte sensing biointerface that comprises a sensing electrode incorporated within a non-conductive matrix comprising a plurality of passageways extending through the matrix to the sensing electrode. Also disclosed herein are methods of manufacturing a sensing biointerface and methods of detecting an analyte within tissue of a host using an analyte sensing biointerface.

Abstract: A concentration correction system includes an infrared detector and components that produce an aggregate emission of infrared radiation. A mirror assembly includes a mirror and is changeable between a correcting configuration and a measuring configuration. In the correcting configuration, the mirror produces a mirror signal incident on the detector. The mirror assembly also obstructs external body infrared radiation from reaching the detector. In the measuring configuration, the mirror assembly allows the external body infrared radiation onto the detector. A concentration correction method includes receiving external body infrared radiation and simultaneously receiving a first portion of the aggregate emission. A measurement value indicative of concentration is recorded from the detector. A second portion of the aggregate emission reflected with the mirror and produces a mirror signal incident on the detector.

Abstract: The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Abstract: The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Abstract: A system and method for contactless blood pressure determination. The method includes: receiving a captured image sequence; determining, using a trained hemoglobin concentration (HC) changes machine learning model, bit values from a set of bitplanes in the captured image sequence that represent the HC changes of the subject; determining a blood flow data signal; extracting one or more domain knowledge signals associated with the determination of blood pressure; building a trained blood pressure machine learning model with a blood pressure training set, the blood pressure training set including the blood flow data signal of the one or more predetermined ROIs and the one or more domain knowledge signals; determining, using the blood pressure machine learning model trained with a blood pressure training set, an estimation of blood pressure; and outputting the determination of blood pressure.

Abstract: An electrode structure is provided that includes an electrode base having topography located on a surface of the electrode base structure. A biological functionalization layer is located on one or more exposed surfaces of at least the topography of the electrode. A sacrificial layer is located on the biological functionalization layer and is present at least in the physical space located between the individual features of the topography of the electrode.

Abstract: A device for the extraction of blood or a blood compound is provided that includes a tube, a piston assembly, a handle assembly that can be clipped to the piston assembly, and a perforable sealing element that prevents the flow of fluid from a sealed interior space of the tube towards a longitudinal interior cavity of the handle assembly located adjacent to a separable area of the handle assembly. In use, the handle assembly is pushed to the bottom of the tube, causing the handle assembly to be clipped to the piston assembly, the handle assembly and the piston assembly are then moved rearwards forming a vacuum in the space, the piston assembly is clipped to an end cap of the tube and the gripping portion of the handle assembly is separated, obtaining a vacuum container with a perforable closure.

Abstract: This document describes automated nursing assessments. Automation of the nursing assessment involves a nursing-assessment device that makes determinations of a person's mood, physical state, psychosocial state, and neurological state. To determine a mood and physical state of a person, video of the person is captured while the person is positioned in front of an everyday object, such as a mirror. The captured video is then processed according to human condition recognition techniques, which produces indications of the person's mood and physical state, such as whether the person is happy, sad, healthy, sick, vital signs, and so on. In addition to mood and physical state, the person's psychosocial and neurological state are also determined. To do so, questions are asked of the person. These questions are determined from a plurality of psychosocial and neurological state assessment questions, which include queries regarding how the person feels, what the person has been doing, and so on.

Abstract: Embodiments of the invention relate to correlation of physiological data from two or more sources in real-time. As data is gathered from one or more remote physiological sensors, evaluation of associated physiological data takes place in real-time. The sensor data is correlated with other forms of data including objective physiological data, subjective physiological data, cognitive data, and/or quantitative input for multi-variate data analytics to assess and correlate the data. Alerts are generated, applications are activated, and windows are created to support the correlation and associated communication.

Abstract: The present invention relates to a method for detecting a personality consciousness code of an individual, comprising: a) storing reference voice characteristics of different persons that represent acoustic information as expressed by human voice in a form of a time to frequency component relation; b) classifying the acoustic information into 12 different personality consciousness codes by using support vector machine that analyzes said acoustic information; c) receiving data indicative of a sound energy generated by the voice of said individual; d) performing spectral analysis of said received sound energy in order to obtain voice characteristics from an electronic representation of said sound energy; and e) comparing said obtained voice characteristics with the reference voice characteristics and determining the personality consciousness code of said individual by using the support vector machines, and using the obtained voice characteristics to determine the level of consciousness.

Abstract: An on aircraft computer system records and analyzes biometric data to identify indicia of impaired performance, such as pilot fatigue, attention tunneling, or cognitive overload. Such impairment is identified by alterations in pilot gaze or eye movement, head movement, facial parameters, eye lid position, heart rate, breathing, or brain wave patterns. Appropriate corrective action is applied based on the type of impaired performance identified, including altering a level of automation, contacting a ground dispatcher or ground pilot, or contacting a co-pilot or other crew member. Biometric data is continuously logged and correlated with data from other avionics systems to refine formulas relating biometric data to states of alertness and crew rest procedures.

Abstract: An imaging apparatus with improved detection accuracy of the state of a subject is provided. An imaging apparatus comprises: an imaging optical system configured to form an optical image of a face of a subject in a vehicle; an image sensor configured to capture the formed optical image and generate a captured image; and an image processor configured to determine a state of the subject based on the captured image, wherein the imaging apparatus satisfies F?0.0003 f2/p, where F is an F value of the imaging optical system, f is a focal length of the imaging optical system, and p is a pixel pitch of the image sensor.

Abstract: A system is provided for collecting and logging the frequency of flatulence of a person in a selected time period as well as the duration of each occurrence of flatulence. The log entries provide determination of the body cells signaling of the person indicative of the person's health condition whereby underlying diseases may be detected and treated in their early stage.