Abstract: An ophthalmic lens having an electronic system is described herein for monitoring the medical condition of the wearer using at least one sensor and at least one problem template. In a further embodiment, the problem template includes a pattern and/or a threshold. In at least one embodiment, the lens works in conjunction with a second lens and/or an external device to monitor for a medical condition or to perform a test protocol of the wearer. Examples of the at least one sensor include an eyelid position sensor system, an eye movement sensor system, a biosensor, a bioimpedance sensor, a temperature sensor, and a pulse oximeter.

Abstract: A head mounted compact goggle based video oculography system comprises: a goggle base surrounding the subject's eyes; an angled hot mirror; at least one digital camera attached to the goggle base along the top side of the goggle base taking images of at least one of the subject's eyes via a hot mirror reflection; an integral display for selectively displaying visual stimulus to the subject through the hot mirror and attached to the goggle base along the rear side of the goggle base; a controller coupled to the display generating each visual stimulus for each neuro-otologic test to be displayed to the subject via the display and coupled to each digital camera and receiving and storing data signals there from, the controller configured to calculate eye related data from the digital camera images during each neuro-otologic test, and configured to display the eye related data to users.

Abstract: Systems for determining an individual's current focal distance by measuring parameters associated with binocular vision focusing using one or two contact lenses are provided. In an aspect, a system includes a first contact lens and a second contact lens respectively configured to be worn over first and second eyes of an individual. The first contact lens and the second contact lens respectively include first and second circuits configured to respectively generate first data related to the first eye and second data related to the second eye for determining the current focal distance.

Abstract: Certain embodiments pertain to pupil ptychography methods and systems.

Abstract: A data processing method performed by a computer for determining breathing signal data which represents a breathing cycle of a patient, comprising the steps of: acquiring image data representing a sequence of training thermal images of at least a part of the surface of the patient's body over time, the sequence covering at least one half breathing cycle and being captured by a thermographic camera; and tracking at least one tracked point in the image data over the sequence of training thermal images to find a trajectory of the tracked point as the breathing signal data, wherein the tracked point is a point on the surface of the patient's body.

Abstract: A noninvasive method for monitoring the blood pressure and arterial compliance of a patient based on measurements of a flow velocity and a pulse wave velocity is described. An embodiment uses a photoplethysmograph and includes a method to monitor the dynamic behavior of the arterial blood flow, coupled with a hemodynamic mathematical model of the arterial blood flow motion in a fully nonlinear vessel. A derived mathematical model creates the patient specific dependence of a blood pressure versus PWV and blood velocity, which allows continuous monitoring of arterial blood pressure.

Abstract: An electronic device includes a camera, an ambient light sensor, and a proximity sensor. The electronic device uses one or more of the camera and the proximity sensor to emit light into a body part of a user touching a surface of the electronic device and one or more of the camera, the ambient light sensor, and the proximity sensor to receive at least part of the emitted light reflected by the body part of the user. The electronic device computes health data of the user based upon sensor data regarding the received light. In some implementations, the electronic device may also include one or more electrical contacts that contact one or more body parts of the user. In such implementations, the health data may be further computed based on the an electrical measurement obtained using the electrical contacts.

Abstract: Provided is a highly reliable technique for the evaluation of ischemic conditions. A preferred embodiment is a nuclear medicine measurement protocol in which the administration of a radiopharmaceutical agent and radiation measurement are performed twice at rest and under stress. In the nuclear medicine measurement protocol, radiation collection is performed without radiopharmaceutical agent administration before the second radiopharmaceutical agent administration, and the result is used to correct the nuclear medicine measurement result after the second radiopharmaceutical agent administration.

Abstract: Haemodynamic parameters such as the amplitude and phase of a pulse wave passing through a region of interest can be obtained from a video image of the exposed skin of a patient by processing of the reflectance photoplethysmographic signal using signal averaging. The region of interest is defined and a reflectance photoplethysmographic signal obtained by finding the mean pixel intensity across the region of interest for each video frame. Signal averaging is performed on the resulting pulsatile waveform by detecting peaks in the waveform, selecting those parts of the waveform which lie within a window centred on the peaks, and summing the selected parts of the waveform to find an average pulse waveform. The region of interest is then divided into sub-regions and an average pulse waveform for the video sequence is found for each of the sub-regions in the same way.

Abstract: An apparatus comprising at least one light source, at least one photodetector, a first layer of optical material configured to embed the at least one light source, and a second layer of optical material configured to embed the at least one photodetector. The first and second layer of optical material are configured to guide light from the at least one light source and to prevent the light from the at least one light source directly reaching the at least on photodetector, and the second layer of optical material is configured to guide light towards the at least one photodetector.

Abstract: An intelligent health strap. A detection and analysis method comprises: acquiring multiple groups of pulse data collected by multiple pulse sensors (11); and according to the multiple groups of pulse data, using a calculation method for analysis to obtain physical sign information (12). An intelligent health wrist strap and an intelligent health ankle strap having multiple pulse sensors are used for performing pulse monitoring and analysis, displaying multiple types of pulse physical sign information, and transmitting data to an external device, so that a user can conveniently monitor changes of individual physiological status, and the intelligent health wrist strap and the intelligent health ankle strap can provide massage and health-care for wrists and ankles.

Abstract: A hermetically sealed biocompatible pressure sensor module configured for implant at a desired site at which a pressure is to be measured. Anodic bonding of the pressure module package components which have similar thermal coefficients of expansion provides low stress bonding and maintains long term reliability, dependability and accuracy. The pressure sensor module includes a pressure sensitive membrane which is in direct contact with the environment at which a pressure is to be measured. The pressure sensor module forms a part of a pressure measuring system which uses a telemetry link between the pressure sensor module and an external controller for data transmission and transfer. Operating power for the pressure sensor module is provided by the external controller and an internal rechargeable energy storage component. Accordingly, the pressure measuring system provides a dual stage power and data transfer capability for use with an implantable system.

Abstract: Described embodiments include a catheter, which includes a plurality of splines at a distal end of the catheter, and a plurality of helical conducting elements disposed on the splines. Other embodiments are also described.

Abstract: Intracardiac electrograms are recorded using a multi-electrode catheter and respective annotations established. Within a time window a pattern comprising a monotonically increasing local activation time sequence from a set of electrograms from neighboring electrodes is detected. The set is reordered and displayed for the operator.

Abstract: A method for detecting a position of a signal source in a living body includes: arranging three electrodes on a surface of the living body and alternately connecting a first external resistance and a second external resistance in parallel between the electrodes and a ground potential; measuring first voltages Vi (i=1, 2, 3) generated at the respective electrodes when the first external resistance is connected in parallel between the electrodes and the ground potential, and second voltages Vi (i=1, 2, 3) generated at the respective electrodes when the second external resistance is connected in parallel between the electrodes and the ground potential; and calculating three ratios Vi/V?i (i=1, 2, 3) from the first and second voltages Vi and V?i, and detecting the position of the signal source in the living body based on the three ratios Vi/V?i (i=1, 2, 3).

Abstract: There are disclosed systems and methods for seizure diagnosis by video electroencephalography (Video-EEG). There is disclosed a fully automated, portable, point-of-care diagnostic video EEG device. In an embodiment, the device includes a tracker configured for placement on a patient. The tracker has a set of sensors disposed thereon. An EEG headset is configured for detecting electrical activities of a brain of the patient. The EEG headset is configured for communicating the electrical activities of the brain of the patient. A telescoping stand provides built-in sensors. A mobile computing device is in communication with the built-in sensors and in communication with the EEG headset. A set of wheels provides controlled movement of the telescoping stand. Other embodiments are also disclosed.

Abstract: System for registering a coordinate system associated with a pre-acquired model of an object with a reference coordinate system. The system includes a portable unit which includes a display, a tracking system for tracking the portable unit and a processor. The processor is coupled with the portable unit and with the tracking system. The processor determines the position and orientation of the portable unit. The processor further determines the position of at least one marker located on the object according to at least one of, a tracked pointer and respective position related information. The processor further displays registration related information on the display. At least one of the registration related information and the display location of the registration related information are related to the position and orientation of the portable unit. The position of the at least one marker, in the coordinate system associated with the pre-acquired model, is predetermined.

Abstract: In order to provide a static magnetic field homogeneity adjustment method capable of reducing an arrangement amount of magnetic pieces and achieving desired magnetic field homogeneity with high accuracy in magnetic field homogeneity adjustment, there is provided a static magnetic field homogeneity adjustment method in an imaging space of computing positions of a plurality of magnetic pieces separated from the imaging space through shimming computation with respect to a static magnetic field in the imaging space generated by a magnetic field generation device, and disposing the plurality of magnetic pieces at the positions obtained through the shimming computation, the method including an adjustment step of imposing restriction that a polarity of a magnetic field distribution generated in the imaging space by the magnetic pieces disposed at the positions is either positive or negative during the shimming computation, and adjusting the static magnetic field homogeneity.

Abstract: The present invention relates to a cabling arrangement and a coil apparatus for use in an MPI apparatus to increase the sensitivity of the apparatus. The cabling arrangement comprises a first AC terminal (320), a second AC terminal (330), wherein said first and second AC terminals are configured for coupling an AC voltage between them, a first internal terminal (301), a second internal terminal (302), wherein said first and second internal terminals are configured for coupling a DC voltage between them, a first subset of one or more first conductors (401) coupled between the first internal terminal and the second AC terminal, and a second subset of one or more second conductors (402) coupled between the second internal terminal and the second AC terminal, wherein said first and second conductors are arranged to form a coil (125, 126, 127; 601, 602, 603, 604) to generate a magnetic field in a zone of interest.

Abstract: A device for measuring an electrical impedance of biologic tissue may include electrodes configured to contact the biologic tissue and generate a differential voltage thereon. The device may include a first circuit coupled to the electrodes and configured to force an oscillating input signal therethrough, and a differential amplitude modulation (AM) demodulator coupled to the plurality of electrodes. The differential AM demodulator may be configured to demodulate the differential voltage, and generate a base-band signal representative of the demodulated differential voltage. The device may further include an output circuit downstream from the differential AM demodulator and may be configured to generate an output signal representative of the electrical impedance as a function of the base-band signal.

Abstract: A system for selecting a calibration includes a data structure (138) including non-transitory computer readable storage media having a plurality of calibration entries stored therein and indexed to position and/or orientation criteria for a field generator. The field generator is configured for placement in an environment for sensor tracking. A calibration selection module (140) is configured to determine a position and/or orientation of the field generator and, based on the position and/or orientation, determine, using the data structure, corresponding calibration information stored in the data structure. The calibration information is optimized based upon the position and/or orientation of the field generator.

Abstract: A position detection system includes: a cylindrical detection coil configured to detect a magnetic field generated by a magnetic field generation unit; and a calculation unit configured to calculate at least one of a position and a direction of the magnetic field generation unit based on the magnetic field detected by the detection coil. A relationship between a diameter Ds and a length Ls in a winding direction, of the detection coil, satisfies Formula (1), and each of coefficients G1, G2, and G3 in Formula (1) is respectively given by each of Formulae (2), (3) and (4). ? G 1 ? ( L S D S ) 2 + G 2 ? ( L S D S ) + G 3 ? ? 0.2 ( 1 ) G 1 = - 1.73 ? 10 - 5 ? D S 2 + 7.36 ? 10 - 3 ? D S - 4.71 ? 10 - 2 ( 2 ) G 2 = 3.74 ? 10 - 5 ? D S 2 - 1.54 ? 10 - 3 ? D S + 1.16 ? 10 - 2 ( 3 ) G 3 = - 8.96 ? 10 - 5 ? D S 2 - 1.74 ? 10 - 3 ? D S + 1.

Abstract: Systems, methods, and software products analyze foot strikes. A runner profile defining characteristics of a user and a shoe type of the shoes is received. Shoe characteristics are retrieved based upon the shoe type. A model of shoe wear is configured based upon both the runner profile and the shoe characteristics. Sensor data indicative of movement of a runner's foot is received from a foot strike monitor configured with the shoes and processed through the model to determine a user's expected lifetime for the shoes. The user's expected lifetime is indicated to the user.

Abstract: The disclosed embodiments relate to the design of a system that identifies a person. During operation, the system receives channel state information (CSI) for a set of orthogonal frequency division modulation (OFDM) subcarriers while the person moves in a region that includes two or more nodes that use the set of OFDM subcarriers to communicate with one another. Next, the system analyzes the CSI to obtain an analysis result. The system then determines the identity of the person based on the analysis result.

Abstract: A monitoring system comprises a floor covering with a sheet-type pressure sensor and a sensor control unit. The latter includes an ADC for providing a digital raw signal, a microcontroller configured to carry out data extraction by signal processing of the digital raw signal and generating a digital processed signal having a lower digital bandwidth than the digital raw signal, and a communications module connected to or integrated within the microcontroller so as to receive the digital processed signal. The communications module is configured to establish data communication with one or more database servers and to transmit the extracted data to the one or more database servers.

Abstract: In an embodiment, an apparatus (42) that provides advice on nutritional and caloric intake requirements for a child based on the child's current growth phase activity behavior and status corresponding to the child's current body mass index, the nutritional requirements determined in terms of a ratio of nutrient components that are tailored to the growth phase of the child.

Abstract: A method for transmitting activity information from a wearable medical device (101) to a patient monitoring system (105), wherein the method comprises generating an activity data packet, wherein the activity data packet comprises at least a first activity field indicative of a recent activity and a second activity field indicative of a past activity, and transmitting the activity data packet from the wearable medical device (101) to the patient monitoring system (105).

Abstract: A motion capture system includes a motion sensor having a flexible body and a fiber bragg gratings (FBG) sensor inserted into the body, a fixture configured to fix the motion sensor to a human body of a user, a light source configured to irradiate light to the motion sensor, and a measurer configured to analyze a reflected light output from the motion sensor, wherein the FBG sensor includes an optical fiber extending along a longitudinal direction of the body and a sensing unit formed in a partial region of the optical fiber and having a plurality of gratings, and wherein a change of a wavelength spectrum of the reflected light, caused by the change of an interval of the gratings due to a motion of the user, is detected to measure a motion state of the user.

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: A method for performing an assay to determine the presence or concentration of an analyte contained in a sample of body fluid by using a device comprising at least one analyte quantification member and a sensor associated therewith, the method includes: applying a first sample to the analyte quantification member; and detecting the presence or absence of an adequate sample volume; wherein upon detection of the absence of an adequate sample volume, initiating a finite timed period, and signaling the user to introduce a second sample of body fluid to the analyte quantification member. Associated arrangements and devices are also disclosed.

Abstract: Methods and apparatus for providing multi-stage signal amplification in a medical telemetry system are provided.

Abstract: A catheter system includes a catheter with an elongate catheter body, a catheter tip coupled to a distal end of the catheter body, and at least one light-emitting element configured to emit light to excite flavin adenine dinucleotide (FAD) molecules. The catheter system further including at least one light sensor configured to sense a light emitted by the excited FAD molecules.

Abstract: The present application discloses a novel algorithm to convert medical hyperspectral images (MHSI) into RGB (RedBlueGreen) images in different medical conditions by making use of the three spectral bands (Red, Green and Blue) of the MHSI and mapping them into Red, Green and Blue components for visualization of hyperspectral images.

Abstract: A device and a method to measure the concentrations of oxygenated and deoxygenated hemoglobin in tissue around a tumor via near-infrared (NIR) spectroscopy with a photonic mixer device (PMD) is described.

Abstract: The invention relates to a medical sensor system (10) for detecting a feature (12), such as an analyte, in a human or animal body. The system (10) includes at least one sensor (14; 34) having a reservoir (18) with a cap (16) designed as a controllable organic membrane (20), wherein (for example) application of a voltage of a particular magnitude, or application of a voltage for a particular time, effects a change in the permeability of the membrane (20).

Abstract: The invention is directed to methods and devices for efficient separation of plasma irons whole blood which are suitable for point of care use in resource poor environments, in some embodiments, elements of such devices comprise (a) a sample collection receptacle (SCR) with at least one port, the sample collection receptacle capable of holding a predetermined volume of a sample of undiluted whole blood drawn through a port; (b) a filter chamber having an inlet and an outlet, and containing at least one filter capable of separating plasma from blood cells as sample passes from an inlet side to an outlet side of the at least one filter whenever the filter chamber is placed in Quid communication with a port of the sample collection receptacle; and (c) a manually driven pump operationally associated with the SCR and filter chamber for (i) drawing a predetermined volume of sample into ore SCR by a first user action and (ii) driving the predetermined volume at a substantially constant linear flow under a pressure n

Abstract: A blood separation device adapted to receive a blood sample having a whole blood portion and a plasma portion is disclosed. The blood separation device includes a housing defining a first chamber, a second chamber, and a separation member disposed therebetween. The blood separation device also includes an actuator, wherein actuation of the actuator draws the blood sample into the first chamber and the separation member is adapted to allow the plasma portion to pass through the separation member to the second chamber. The blood separation device matches the plasma chamber volume, the blood chamber volume, and the applied single pressure source so that the correct trans-membrane pressure and shear rate is obtained.

Abstract: A system and a method for assessing a condition in a subject. Phones from speech of the subject are recognized, one or more prosodic or speech-excitation-source features of the phones are extracted, and an assessment of a condition of the subject, is generated based on a correlation between the features of the phones and the condition.

Abstract: Described embodiments include an apparatus that includes an expandable structure, configured for insertion into a body of a subject, and a plurality of conducting elements coupled to the expandable structure. Each of the conducting elements comprises a respective coil and has an insulated portion that is electrically insulated from tissue of the subject, and an uninsulated portion configured to exchange signals with the tissue, while in contact with the tissue. Other embodiments are also described.

Abstract: In some examples, processing circuitry of a medical device system determines, for each of a plurality of patient parameters, a difference metric for a current period based on a value of a patient parameter determined for the current period and a value of the patient parameter determined for an immediately preceding period, and determines a score for the current period based on a sum of the difference metrics for at least some of the plurality of patient parameters. The processing circuitry determines a threshold for the current period based on scores determined for N periods that precede the current period, compares the score for the current period to the threshold, and determines whether to generate an alert indicating that an acute cardiac event of the patient, e.g., ventricular tachyarrhythmia, is predicted, and/or deliver a therapy configured to prevent the acute cardiac event, based on the comparison.

Abstract: An injection device adapted to be worn on the body of a patient. The device includes an injector containing an agent for treating hypoglycaemia. A control assembly including a signal receiver is configured to receive signals from a glucose sensor, the control assembly being electrically coupled to an alarm and configured to activate the alarm upon a signal received in the signal receiver being indicative of hypoglycaemia, the control assembly being configured to cause the injector to administer through a needle a dose of the agent to the patient after a predetermined period of time of the signal receiver receiving the signal indicative of hypoglycaemia, the control assembly having a manually activated switch that when activated prior to the expiration of the predetermined period of time causes the control assembly to abort the injection of the agent.

Abstract: The following invention is a device for measuring the force applied by the residual limb of an amputee to the distal region of a socket. The device has an upper surface with a “force sensor measuring region” that maintains a central location on the upper surface of the DFMD. The DFMD is affixed to the inside surface of the distal most area of the socket and maintains a permanent location of the “force sensor measuring region” of the device. Regardless of physical characteristics or changes to the socket, liner, socks, proper or improper placement of the limb into the socket, the consistent location of the “force sensor measuring region” on the DFMD provides congruent force data as it relates to the force applied by the socket to the distal area of the residual limb. The data collected by the DFMD is processed and modified by a software algorithm into meaningful data for the user and/or medical professional.

Abstract: A system and method for allowing any surgeon, including those surgeons who perform a fewer number of a replacement procedure as compared to a more experienced surgeon who performs a greater number of procedures, to provide an improved likelihood of a favorable outcome approaching, if not exceeding, a likelihood of a favorable outcome as performed by a very experienced surgeon with the replacement procedure. Force sensing is included to aid in quantifying installation of an implant, particularly a cup into a pelvic bone.

Abstract: A mobile system for measuring opticokinetic nystagmus in a subject includes a display screen to provide an opticokinetic stimulus and an imaging system to record eye movement data of the subject. The mobile system is configured to compare the stimulus and the recorded eye movement data to provide objective vision acuity testing.

Abstract: An automatic configuration system for an operator console wherein one or more operators control and monitor physical facilities, operations or physically dispersed services. The system includes wearable personal identification devices worn by the operators and a control unit for communicating with the wearable personal identification devices in order to detect the presence of one or more operators within a defined control room area. Each personal identification device includes a sensor unit for monitoring operator data, and is adapted to communicate the operator data to the control unit, which is adapted to configure the operator console based on the operator data.

Abstract: A mobile electronic device 1 includes a plurality of sensors, a detector that detects a biological reaction by one of the sensors, and at least one controller 10 that performs control to change a detection cycle of other sensors according to whether the biological reaction is detected.

Abstract: Sensors mounted on a textile include at least one of electrically conductive textile electrodes; single or multiple optically coupled infrared and red emitter and photodiode or photo transistor; and thin film or Resistive Temperature Detector (RTD). Textile electrodes, electrical connections, and electrical functionalization use at least one of nanoparticles, nanostructures, and mesostructures. Conductive thread, for electrical connections, may include a fiber core made from conductive materials such as but not limited to metals, alloys, and graphine structures, and a sheath of insulating materials such as but not limited to nylon, polyester, and cotton.

Abstract: A non-invasive sensor unit, such as a glove or pad, is adapted to be placed over the chest of an injured person who may be in need of CPR and/or AED. The sensor unit includes a plurality of electrodes for detecting one or more ECG voltages of the person. A controller processes the ECG voltages and displays them on a display, thereby enabling the user to assess whether CPR and/or AED is needed. The sensor unit is adapted to continue to provide ECG data while the user is applying chest compressions to the person. The sensor unit may include accelerometers for reducing artifacts from the ECG voltages that arise from the movement of the user while applying chest compressions. The electrodes are, in some embodiments, capacitive sensors that enable ECG voltages to be detected without requiring direct contact with the skin of the person.

Abstract: A moisture-sensitive device is provided that includes a dissolvable conductive material. Exposure of the dissolvable conductive material to urine or some other fluid causes the dissolvable conductive material to dissolve, increasing an effective resistance of the dissolvable conductive material. This change in resistance can be detected to determine the presence of an aqueous fluid. In response to such detection, a transmitter can then provide a wireless transmission indicative of the presence of the fluid. This moisture-sensitive device can be provided in a diaper and transmissions produced by the device can be detected using a smart phone or other device and used to indicate to a user that the diaper has been soiled.

Abstract: Disclosed is a wearable device which includes a tape-like fabric body, at least one electrically conductive unit, at least one electric signal detection unit, and a data transmission unit. The electric signal detection unit and the data transmission unit are arranged on two opposite surfaces of the tape-like fabric body, and are electrically connected to each other by the electrically conductive unit. The electric signal detection unit includes a sensing portion and a connection portion, wherein the sensing portion is configured to come in contact with a body surface of a living body to detect its physiological signals, and the connection portion is configured to transmit the physiological signals to the data transmission unit. At least one of the tape-like fabric body and the sensing portion includes a heat accumulating fiber for blocking heat dissipated from the body surface of the living body to increase detection efficiency.