Abstract: Disclosed is a device for non-invasively sampling interstitial fluid including one or more analytes from dermis to the skin surface by employing the magneto-hydrodynamic effect and/or reverse iontophoresis. According to a preferable embodiment the device includes a first frame including a first electrode and a second frame including a second electrode, power source and preferably also a first magnet. The first frame is connected to the second frame by a formable connector adapted to provide mechanical connection between the first frame and the second frame and electrical connection between the power source and the first electrode. The direction of the magnetic field and the direction of the electric current produced by the magnet and the power source is such that the Lorenz force drives the fluid from the dermis towards the skin surface.

Abstract: A method of fetal ultrasound monitoring includes detecting contact of a first ultrasound transducer to a mother's abdomen based on input from a contact sensor in the first ultrasound transducer. A first transducer identifier is received from the first ultrasound transducer, and then the first transducer identifier is correlated with a first transducer label. A first heart rate is measured based on output of an ultrasound device in the first ultrasound transducer, and a heart rate indicator is displayed accordingly. A position of the first ultrasound transducer is identified in a two-dimensional plane, and the first transducer label is displayed on an abdomen image based on the first position.

Abstract: Aspects of the present invention disclose a method for audio-visual interaction of a user and implant device to resolve a voice command of the user. The method includes one or more processors determining a health-related issue of a user that corresponds to a voice command of the user. The method further includes identifying an implanted device of the user that relates to the health-related issue. The method further includes collecting sensor data of the implanted device, wherein the sensor data includes one or more conditions of the implanted device and operating environment of the implanted device in the body of the user. The method further includes generating an audio-visual response corresponding to the health-related issue of the user.

Abstract: The disclosed non-invasive blood pressure systems and methods measure a patient's blood pressure without restricting blood flow. Other sensors, such as physiological sensors, sensors that sense data about the NIBP system components, and/or environment sensors sense data that is combined with the NIBP signal. The combined NIBP and sensor signals are used to measure a patient's non-invasive blood pressure.

Abstract: A characteristic of a blood product in a blood product container is determined. Using a smartphone, an image is acquired of a blood bag or tubing of the blood product container disposed in front of the smartphone. The image is processed using a processing circuit of the smartphone or a remote computer in wireless communication with the smartphone. The processing identifies a characteristic of the blood product from the image. A visual notification is generated on a display of the smartphone of the identified characteristic of the blood product.

Abstract: Embodiments of the present disclosure include detecting a concurrent occurrence of a decrease in monitored analyte level and a corresponding decrease in monitored on-skin temperature, confirming a presence of an impending hypoglycemic condition, and asserting a notification corresponding to the confirmed impending hypoglycemic condition. Devices, methods, systems and kits incorporating the same are also provided.

Abstract: One embodiment provides a method, including: obtaining EEG data from one or more single channel EEG sensor worn by a user; classifying, using a processor, the EEG data as one of nominal and abnormal; and providing an indication associated with a classification of the EEG data. Other embodiments are described and claimed.

Abstract: A phototherapy device for delivering light emitted by a light source to an infant. The phototherapy device includes two or more light pads configured to be optically connected to a light source via a connector. Light emitted by the light source is received by the connector and propagated through the connector to the light pads. The phototherapy device also includes a flexible garment configured to maintain the position of the pads on a front and back of an infant.

Abstract: Described herein are methods of making and using and apparatus for wirelessly communicating data and providing power, particularly from a location exterior to a body and to an implantable device disposed within a body with tissue. The described embodiments provide apparatus and methods for efficiently transfer data and power between an external transceiver and an (implanted) biomedical device. The method is to modulate power carrier, which wirelessly powers the device, using an asynchronous modulation scheme, such as amplitude shift keying (ASK) modulation, with minimal modulation depth in order to not disrupt the power flow. The digital data is encoded in the pulse width, eliminating the need for synchronization to the power carrier signal and further minimizing the power consumption necessary for data transfer. Additionally, a reverse backscatter method for obtaining data from the implant is described that has flexible, low power operation.

Abstract: A bio-signal measuring device includes a signal detector detecting a bio-signal; a signal converter converting the bio-signal into a bio-digital signal; a memory; a communicator communicating with an external device; and a processor configured to operate in a first operation mode for storing the bio-digital signal in the memory or a second operation mode for transmitting the bio-digital signal to the external device.

Abstract: An apparatus and method for collecting a predetermined amount of blood or other fluid using an automated sampling system is provided.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: The present disclosure extends to methods, systems, apparatus, and computer program products related to a cable-based measuring system. The cable-based measuring system includes a cable, comprising an inner cable member configured to move linearly within an outer cable housing. The measuring system also includes a measuring device configured to generate measurement information regarding movement of the inner cable member relative to the outer cable housing using one or more encoders. A computer system receives the measurement information from the measuring device. The measurement information indicates length as a function of time, and represents three orthogonal dimensional measurements of a three-dimensional object. Based on the measurement information, the computer system identifies a length of each dimensional measurement, including a length, a width, and a height of the three-dimensional object.

Abstract: Methods and devices for tying management of an implantable medical device to the activities of a primary care physician are described, including access control, simplified parameter optimization, support for tuning a device in response to the effects of other treatments in parallel, and support for helping a primary physician and a patient work together to tune device configuration to the activity and performance needs of the patient. In some embodiments, a medical device is self-configuring in a device parameter domain, based on inputs provided in a patient performance domain. The self-configuring of the medical device is based, for example, on an automatically applied transformation of inputs derived from patient performance domain observations into changes in the configuration of the medical device which affect technical parameters of its operation.

Abstract: The present disclosure allows remote monitoring of measurements in clinical trials. Clinical trial participant data units received from a client device are accessed. The clinical trial participant data units are set to include a clinical trial diary entry from a clinical trial diary application in the client device and clinical trial measurement samples corresponding to the clinical trial diary entry from a measurement device connected to the client device via a short-range wireless connection. If it is determined that such a data unit lacks any collected clinical trial measurement samples, a wireless connection log is searched for a corresponding connectivity issue entry. If such an entry is found, it is determined that a potential connectivity issue exists and a connectivity correction action is triggered. Otherwise, it is determined that a potential compliance issue exists and a compliance correction action is triggered.

Abstract: Electrochemical impedance spectroscopy (EIS) may be used in conjunction with continuous glucose monitoring (CGM) to enable identification of valid and reliable sensor data, as well implementation of Smart Calibration algorithms.

Abstract: The invention provides a body-worn monitor featuring a processing system that receives a digital data stream from an ECG system. A cable houses the ECG system at one terminal end, and plugs into the processing system, which is worn on the patient's wrist like a conventional wristwatch. The ECG system features: i) a connecting portion connected to multiple electrodes worn by the patient; ii) a differential amplifier that receives electrical signals from each electrode and process them to generate an analog ECG waveform; iii) an analog-to-digital converter that converts the analog ECG waveform into a digital ECG waveform; and iv) a transceiver that transmits a digital data stream representing the digital ECG waveform (or information calculated from the waveform) through the cable and to the processing system. Different ECG systems, typically featuring three, five, or twelve electrodes, can be interchanged with one another.

Abstract: A continuous glucose monitoring (CGM) device may include a wearable portion having a sensor configured to produce glucose signals from interstitial fluid, a processor, a memory and transmitter circuitry. The memory may include a pre-determined gain function based on a point-of-interest glucose signal and glucose signals measured prior to the point-of-interest glucose signal. The memory may also include computer program code stored therein that, when executed by the processor, causes the CGM device to (a) measure and store a plurality of glucose signals using the sensor and memory; (b) for a presently-measured glucose signal, employ the plurality of previously-measured glucose signals stored in the memory and the pre-determined gain function to compute a compensated glucose value; and (c) communicate the compensated glucose value to a user of the CGM device. Numerous other embodiments are provided.

Abstract: A system level scheme for networking of implantable devices, electronic patch devices/sensors coupled to the body; and wearable sensors/devices with cellular telephone/mobile devices, peripheral devices and remote servers.

Abstract: The present invention relates to an intraocular pressure measuring and/or monitoring device (1) comprising a contact lens (10) presenting an inner surface (101) and an outer surface (102), and a pressure sensor (2) united with said contact lens (10) and located such that it is applied against an eye (8) of a user for sensing the intraocular pressure (IOP) of said eye (8) when said contact lens (10) is worn by said user, characterized in that said contact lens (10) comprises a soft portion (11) and a rigid portion (12), said rigid portion (12) being adapted to at least partially rigidify a central portion of the inner surface (101) of said contact lens (10) so as to maintain said rigidified inner surface (101) with a curvature radius adapted to flatten at least a portion of the eye surface in contact with the pressure sensor (2) so as to reach a pressure equilibrium around the pressure sensor (2) when said contact lens (10) is worn by said user.

Abstract: A wearable electronic device, for example a smart watch, has an optical sensor module disposed near a side of the device meant to face the wearer. The device also includes a wireless charging module. The optical sensor and wireless charging modules are at least partially integrated together via a flexible printed circuit board (“FPCB”) which is connected to both modules. The wireless charging module surrounds the FPCB of the optical sensor module, thus allowing a reduction in thickness of the wearable device and further allowing simplification in a process of assembly of the device.

Abstract: Methods, devices, systems, and kits are provided that buffer the time spaced glucose signals in a memory, and when a request for real time glucose level information is detected, transmit the buffered glucose signals and real time monitored glucose level information to a remotely located device, process a subset of the received glucose signals to identify a predetermined number of consecutive glucose data points indicating an adverse condition such as an impending hypoglycemic condition, confirm the adverse condition based on comparison of the predetermined number of consecutive glucose data points to a stored glucose data profile associated with the adverse condition, where confirming the adverse condition includes generating a notification signal when the impending hypoglycemic condition is confirmed, and activate a radio frequency (RF) communication module to wirelessly transmit the generated notification signal to the remotely located device only when the notification signal is generated.

Abstract: Athletic performance sensing and/or tracking systems include components for measuring or sensing athletic performance data and/or for storing and/or displaying desired information associated with the athletic performance to the user (or others). Such systems can allow users a wide variety of options in creating workouts, selecting and presenting media content during the athletic performance, etc., e.g., to help keep users entertained and motivated. In some instances, user feedback may be used, optionally in combination with objective data relating to a workout, to control features of the workout routine, to control the music or other media content selected and/or presented, and/or to control features of future workout routines and/or the presented media content.

Abstract: Systems, computer-implemented methods, and tangible non-transitory computer-readable media are provided for performing contact tracing using acoustic communications. For example, a computer-implemented method may include allocating an acoustic token for broadcasting via an audio communication channel, obtaining information associated with the acoustic token received from a first device of a first user based on the broadcasting of the acoustic token where the first user is associated with a disease, determining whether the information associated with the acoustic token from the first device relates to information associated with the acoustic token received from a second device of a second user, and providing information that indicates whether the second user was exposed to the disease based on whether the information associated with the acoustic token from the first device relates to the information associated with the acoustic token from the second device.

Abstract: A biometric information measurement system and method are disclosed. A biometric information measurement system according to an embodiment of the present invention may comprise an implant device that is inserted into the human body so as to measure biometric information and an external device that transmits a signal to the implantable device while sweeping a frequency.

Abstract: Improved methods and systems for personal medical monitoring are disclosed. The monitoring yields status information pertaining to persons being monitored. Notifications, recommendations and/or actions can be initiated by examination or analysis of the status information. The status information can include health, position (location) and other information.

Abstract: A wearable article includes: an annular casing that surrounds a space into which a body of a user is to be inserted; a light-emitting element that is provided in the casing, the light-emitting element emitting light towards the space; an imaging element that is provided in the casing, the imaging element capturing and obtaining an image of the space when the light-emitting element emits light; and an authentication circuit that authenticates the user based on a vein pattern obtained in advance and the image.

Abstract: Disclosed herein is a system for facilitating stress adaption in a workstation. Accordingly, the system may include microphones disposed on the workstation. Further, the one or more microphones may be configured for generating first sound signals of first sounds associated with an environment of the workstation. Further, the system may include a processing device communicatively coupled with the microphones. Further, the processing device may be configured for analyzing the first sound signals, determining first sound characteristics of the first sounds, determining second sound characteristics of second sounds, and generating second sound signals for the one or more second sounds. Further, the system may include acoustic devices disposed on the workstation. Further, the acoustic devices may be communicatively coupled with the processing device. Further, the acoustic devices may be configured for emitting the second sounds based on the second sound signals.

Abstract: A cochlear implant system is disclosed. The system includes a power management unit that is configured to determine a stimulation power consumption of the implantable unit for providing the plurality of stimulation pulses of the stimulation frame to the auditory nerve fibers of the recipient. The determine of the stimulation power consumption of the implantable unit may be based on the plurality of stimulation pulses determined by the external unit, and more specifically, determined by a sound processor arranged within the external unit and/or the implantable unit. The plurality of stimulation pulses may be communicated to the power management unit. Furthermore, the power management unit may be configured to determine a power consumption stage of the implantable unit.

Abstract: To better understand the impact of glycemic events, some entities have begun examining the relationship between the blood glucose level and another physiological parameter. However, this relationship can be difficult to understand. Introduced here are computer programs and associated computer-implemented techniques for discovering glycemic events in a series of data values representative of blood glucose measurements and then altering the measurement schedule of a sensor capable of generating measurements in a dimension other than blood glucose based on the glycemic events. By altering the measurement schedule of the sensor, a diabetes management platform can better understand how, if at all, dimensions other than blood glucose are related to the glycemic health state of a subject whose blood glucose level is being monitored.

Abstract: Provided is a wireless 12-lead or multiple unipolar-lead electrocardiograph system without cable connection between a measurement electrode and device body. The present invention includes a measurement electrode that acquires an electrocardiographic signal of a subject, a Wilson terminal that is connected to the measurement electrode and forms an indifferent electrode, and an electrocardiograph body that generates an electrocardiogram. The measurement electrode has active measurement electrodes that wirelessly communicate with the electrocardiograph body, and passive measurement electrodes that are connected to the active measurement electrodes, and the Wilson terminal. The electrocardiograph body generates the electrocardiogram on the basis of a lead signal sent by the active measurement electrodes.

Abstract: Embodiments presented herein are generally directed to techniques that provide a medical device component with the ability to communicate in both the near-field and far-field via a single antenna arrangement. More specifically, a medical device component includes an electronics circuit, a coil driver, an antenna arrangement, and an isolation circuit. The isolation circuit operates to extract far-field signals received at the antenna arrangement and provide these signals to the electronics circuit. The electronics circuit is protected from near-field signals received at the antenna arrangement via the isolation circuit.

Abstract: A wearable, open and adjustable MRI head coil system having an assembly of support members, panels, or portions defining one or more access openings. The support members, panels, or portions can support, house, or otherwise include radiofrequency receiver antennae or imaging coils such that the assembly is positionable or wearable by a patient for MRI scanning. The radiofrequency receiver antennae or imaging coils, and other devices can be simultaneously in contact with a patient's head, thereby enabling use during diagnostic, therapeutic, surgical, or other interventional procedures.

Abstract: A head-mounted display device for interface with a blood processing machine using a disposable component having tubing and a blood component receptacle includes a frame configured to be mounted on a person's head and configured to hold a lens in front of an eye of the person. The display device includes a display, a wireless transceiver configured to communicate with a network, and a processing circuit. The processing circuit is coupled to the frame, the display and the wireless transceiver and receives instructions for training the person how to use the blood processing machine. The processing circuit overlays indicators, text, highlighting and/or icons on the blood processing machine as seen from a field of view of the person based on the instructions to train the person in using the blood processing machine.

Abstract: The number n of times of chewing is counted by chewing number of times calculation means (13b2) based on a change in the distance l from a photoreflector (50), which is received together with time t by measurement value receiving means (13b1). To vary hardness h of a bag (30) to a stage that can be sensed, according to the number n of times of chewing, a required air pressure is set according to the current number n of times, based on a hardness/air pressure correspondence recording unit (13g) in which stages that have a significant difference therebetween and are stored in association with the number n of times of chewing are recorded. To realize the set air pressure inside the bag (30), the amount of sucking performed using a vacuum pump 20 is controlled by air pressure control means (13b4).

Abstract: An implantable sensor system using one or more sensor implants comprised of micro-electrical mechanical system (MEMS) sensors for the accurate and continuous measurement of physiological hemodynamic signals such as diastolic and systolic blood pressure. Sensor implants are configured to be subcutaneously injected to a placement site adjacent a blood vessel. In some embodiments, sensors comprise micromachined ultrasonic transducers.

Abstract: Techniques for data processing and control for a glucose monitoring system are provided, including obtaining a first sensitivity of a glucose sensor; obtaining a second sensitivity of the glucose sensor; comparing a difference between the first sensitivity and the second sensitivity to a predetermined range of values; if the difference is outside the predetermined range of the values, causing a calibration routine for the glucose sensor to be performed; and if the difference is within the predetermined range of values determining a composite sensitivity for a current calibration of the glucose sensor based on the first sensitivity and the second sensitivity and calculating the glucose level based on the current calibration of the glucose sensor.

Abstract: A prehospital telemedicine system comprises a physiologic monitor; an electronic patient care reporting system (ePCR) system; and a point-of-care blood analyzer communicatively coupled to the physiologic monitor and the ePCR system. The point-of-care blood analyzer is configured to perform an analysis of a blood sample based on an indication of a need for a specific blood analysis provided by one of the physiologic monitor and the ePCR system, and to automatically transmit a result of the analysis to a remote data receiving system. The indication of a need for a specific blood analysis may be based upon any one of the following: vital signs data obtained for a patient by the physiologic monitor; and/or current documentation or past medical history captured on or available through the ePCR system.

Abstract: An auscultation device includes an electrocardiogram (ECG) device, a sound receiver device, a synchronization device and a processor. The ECG device is configured to receive an ECG signal. The sound receiver device is configured to receive a heart sound signal. The synchronization device is configured to transmit a synchronization signal to the ECG device and the sound receiver device, so that the ECG device starts to receive the ECG signal and the sound receiver device starts to receive the heart sound signal in time synchronization. Moreover, the processor is configured to generate an ECG according to the ECG signal, generate a heart sound diagram according to the heart sound signal, and generate a synchronization timing diagram according to the ECG and the heart sound diagram.

Abstract: Systems, devices, and methods are disclosed for wireless communication of analyte data. In embodiments, a method of using a diabetes management partner interface to configure an analyte sensor system for wireless communication with a plurality of partner devices is provided. The method includes the analyte sensor system receiving authorization to provide one of the partner devices with access to a set of configuration parameters via the diabetes management partner interface. The set of configuration parameters is stored in a memory of the analyte sensor system. The method also includes, responsive to input received from the one partner device via the diabetes management partner interface, the analyte sensor system setting or causing a modification to the set of configuration parameters, according to a system requirement of the one partner device.

Abstract: Devices, systems and methods for monitoring glycemic levels in a patient, by calculate a plurality of blood glucose values from a plurality of blood samples taken, calculating a quantile of the blood glucose values taken over a period of days; and creating a Lorenz plot for the blood glucose values in the quantile.

Abstract: A wireless hub includes a vehicle power connector that can draw power from a vehicle battery on a vehicle, a first wireless transmission circuit that can send or receive data with base stations in a long-range wireless network, a second wireless transmission circuit that can provide a short-range wireless network and to transfer data to and from electronic devices, and a network processor that can process data in the first wireless transmission circuit and the second wireless transmission circuit. The wireless hub has an antenna array for millimeter wave communications.

Abstract: According to the techniques herein, one or more sensors coupled to an aligner are used to sense one or more physical qualities of the aligner to determine whether the physical qualities indicate that the aligner material has relaxed and has, e.g., reduced the force systems applied to teeth and/or that the teeth movement for the stage has slowed down. The sensors may provide a signal that represents whether or not the physical qualities fall below a threshold value. A treatment plan may be modified if needed. These techniques have the potential to make treatment plans faster and more effective by speeding up some stages while making sure some, perhaps other, stages are implemented only after the teeth are near the appropriate position.

Abstract: According to some embodiments of the present disclosure, a device and method for determining an allowable amount of blood glucose (bG) of a patient is disclosed. The method further includes receiving a current bG measurement, determining a target bG value, and determining a correction delta bG value based on one or more advice history records. The method includes determining a correction meal rise value and determining a maximum allowed bG value based on the target bG value, the correction delta bG value, and the correction meal rise value. The method includes setting the allowable amount of bG value equal to the maximum allowed bG value when the current bG measurement is greater than the target bG value and determining the allowable amount of bG value using the target bG value and the correction delta bG value when the current bG measurement is less than the target bG value.

Abstract: A system and method for automatically matching a sensor device attached to an animal with an ID tag attached to the animal, wherein a reader device, located in or alongside a passage of an animal enclosure, transmits a signal toward the animal in the passage that triggers the ID tag to transmit ID information, and a monitoring device in communication with the reader device receives the ID information from the reader device, receives sensor device information from the sensor device including a sensor device identity, and determines that the ID tag and the sensor device are attached to a same animal based on time information associated with the ID information and the sensor device information.

Abstract: Devices and methods are described for providing continuous measurement of an analyte concentration. In some embodiments, the device has a sensing mechanism and a sensing membrane that includes at least one surface-active group-containing polymer and that is located over the sensing mechanism. The sensing membrane may have a bioprotective layer configured to substantially block the effect and/or influence of non-constant noise-causing species.

Abstract: Methods and systems for secure data analysis include determining that analysis provider access rules and data provider access rules are compatible. Analysis software is received from an analysis provider and a dataset is received from a data provider. The analysis software is executed on the dataset to generate an analysis output, with access to data in the dataset being constrained by the analysis provider access rules and the data provider access rules. An output of the analysis is sent to the analysis provider.

Abstract: A system and method for automatically matching a sensor device attached to an animal with an ID tag attached to the animal, wherein a handheld reader device triggers transmission of sensor device information from the sensor device and triggers transmission of ID information from the ID tag, and a monitoring device, in communication with the handheld reader device, is configured to determine and record that the ID tag and the sensor device are attached to a same animal based on time information associated with both the ID information transmitted from the ID tag and the sensor device information transmitted from the sensor device.

Abstract: A sensor for evaluating tissue of a subject is provided. The sensor includes a flexible spine disposable on the subject, a flexible member that includes first and second flexible member portions accommodated within the flexible spine, a light source, a detector and a rigid member. The light source is attached to the first flexible member portion and is configured to emit light toward the tissue. The detector is attached to the second flexible member portion and is configured to receive the light having reflected off the tissue. The rigid member is coupled with the first and second flexible member portions. In response to a curvature of the flexible spine, the rigid member moves the first and second flexible member portions along the flexible spine to adjust a distance between the light source and the detector.

Abstract: Systems, devices, methods, and computer readable media are provided for distributing data with multi-tiered encoding. For example, a system for transmission of data streams to endpoints is provided that includes: encoders, each encoder configured to encode a data stream according to at least one encoding parameter; virtual transmitters organized into groups based on at least one transmission characteristic; each group of virtual transmitters configured to receive encoded data from an associated one of the encoders; each virtual transmitter of the plurality of virtual transmitters configured to transmit the encoded data to an associated one of the plurality of endpoints; and at least one controller configured to monitor transmission characteristics of the plurality of virtual transmitters and to adjust membership of the virtual transmitters in the plurality of groups based on the monitored transmission characteristics.