Abstract: A system may include a first device and a second device. The second device may be configured to execute an application and validate that the application is able to cause the second device to (i) communicate with the first device and (ii) communicate with a user of the second device. The second device may be configured to (a) check one or more settings of the second device and/or (b) convey a request for data to the first device and determine whether the second device receives the requested data. The second device may be configured to cause the second device to display a message requesting confirmation that the second device displayed the message and determine whether the second device receives the requested confirmation that the second device displayed the message.

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

Abstract: A sensing chip attached to a bandage monitors the healing process of a wound by detecting growth factors, thrombin and fibrinogen. The complementary metal-oxide semiconductor includes a functionalized working electrode, functionalized counter electrode and functionalized reference electrode. The healing progress is stimulated by generating oxygen in the wound.

Abstract: Introduced here is a digital pill comprised of a capsule, an ingestible sensor, and a slot antenna. The ingestible sensor can be configured to generate a signal indicative of a characteristic of the living body in which the digital pill is located. Biometric data can be stored, at least temporarily, in a memory in the form of signal values. For example, the slot antenna may transmit biometric data to a computing device across a network on a periodic basis (e.g., every 5 minutes, 15 minutes, 60 minutes, etc.). Alternatively, the slot antenna may stream biometric data to a computing device across the network in real time.

Abstract: Systems for applying a transcutaneous monitor to a person can include a telescoping assembly, a sensor, and a base with adhesive to couple the sensor to skin. The sensor can be located within the telescoping assembly while the base protrudes from a distal end of the system. The system can be configured to couple the sensor to the base by compressing the telescoping assembly.

Abstract: A system for non-invasive examination of a user's blood environment parameters that includes having a plurality of user-input sensors operably configured to measure a partial pressure of O2 and CO2 in a user's blood, a temperature of the user, and a hemoglobin content in the user's blood, an external electronic display unit, and a computing unit with a communication interface and communicatively coupled to the external electronic display unit and the least four user-input sensors, the computing unit operably configured to cause a user's blood environment parameters to display on the external electronic display unit through use of a mathematical software application resident thereon and employing a model of the user's internal environment based on a mathematical expression of an equation for hemoglobin buffer and utilizing the data from the user-input sensors.

Abstract: Analyte monitoring systems, devices, and methods associated with analyte monitoring devices, and devices incorporating the same are provided. Various graphical user interfaces (GUI) and navigation flows are provided for performing various features, activities, functions, etc., associated with the analyte monitoring device or system. Intuitive navigation is provided to enhance the interpretation of analyte measurements.

Abstract: A pressure compensating non-invasive blood-component measuring device has electrically insulated parallel electrodes mounted on a dielectric membrane (106). A main circuit board (201) provides electrical connections to the electrodes and has an orifice (402) to allow flexing. A housing supports the main circuit board, with a second orifice to facilitate the application of a finger onto the insulated electrodes. A bottom circuit board (401) supports a force sensor (408) and fixing elements (313, 314) secure the bottom circuit board to the top circuit board, such that the bottom circuit board does not contact the housing directly. An intermediate board (316) is guided but not restrained by the fixing elements, and is arranged to apply force onto said force sensor.

Abstract: A sensor inserter for a physiological characteristic sensor includes a housing that defines a track system that extends from a bottom of the housing toward a top of the housing. The sensor inserter includes a striker assembly movable relative to the housing between a first state, a second, cocked state and a third, disposal state. The striker assembly is movable from the second, cocked state to the third, disposal state to couple the physiological characteristic sensor to an anatomy. The striker assembly includes a lock beam that engages with the track system as the striker assembly moves between the first state, the second, cocked state and the third, disposal state. In the third, disposal state the lock beam inhibits movement of the striker assembly from the third, disposal state to the first state.

Abstract: The present disclosure relates to a method and system for processing a photoplethysmogram (PPG) signal to improve accuracy of measurement of physiological parameters of a subject. The method may include removing a baseline drift from the PPG signal; obtaining a drift removed signal; filtering the drift removed signal; obtaining a filtered signal; performing motion artifact correction on the filtered signal; and obtaining a corrected signal.

Abstract: A computer-implemented method for analyzing glucose monitoring data comprising: receiving first glucose monitoring data indicative of a glucose level at a measurement time, the first glucose monitoring signals detected in one or more glucose measurement time periods over a first monitoring time period of a continuous glucose monitoring, determining at least one first range event selected from the following group: a normal glucose level event, a hyperglycaemia event, or a hypoglycaemia event; determining how often the first range event is determined for the first monitoring time period; providing a first minimum total, measurement time period, the first minimum total measurement time period being shorter in time than the first monitoring time period; generating first display data representing, for the at least one first range event, the number of first range events in a graphical representation, if the one or more glucose measurement time periods sum up to at least a first minimum total measurement time period

Abstract: Systems for applying a transcutaneous monitor to a person can include a telescoping assembly, a sensor, and a base with adhesive to couple the sensor to skin. The sensor can be located within the telescoping assembly while the base protrudes from a distal end of the system. The system can be configured to couple the sensor to the base by compressing the telescoping assembly.

Abstract: The present invention relates to an integrated sleep diagnosis and treatment device, and more particularly to an integrated apnea diagnosis and treatment device. The present invention additionally relates to method of sleep diagnosis and treatment.

Abstract: A method for generating a filtered EMG signal includes obtaining a combined signal, wherein the combined signal comprises an ECG signal and an EMG signal. A first high pass filter is applied to the combined signal and an ECG model signal is generated, based on the high pass filtered combined signal. The method further includes, generating a partially filtered EMG signal by subtracting the ECG model from the high pass filtered combined signal. A second high pass filter is then applied to the partially filtered EMG signal to generate a second EMG signal and to the ECG model signal to generate a second ECG model signal. A filtered EMG signal is generated based on the second EMG signal and the second ECG model by way of a gating technique.

Abstract: An information processing apparatus of the invention is configured to: determine whether or not first biological information of a measurement subject meets a first condition, the first biological information being measured in a first period; determine, when the first biological information meets the first condition, whether or not a number of times, by which the first biological information meets the first condition with respect to the measurement subject, exceeds a first value; select a first message when the first value is not exceeded; select a second message when the first value is exceeded.

Abstract: Disclosed herein are devices, systems, and methods for updating alarm limits applied in monitoring one or more medical parameters of a subject. The devices, systems, and methods obtain a measurement of ambient pressure at a defined time point (‘t1’) and compare the measurement of ambient pressure at the defined time point (‘t1’) to a reference ambient pressure. If a difference between the measured ambient pressure values at t1 and the reference ambient pressure is at or above a predetermined threshold, the alarm limits are updated to correspond with the ambient pressure at t1 or a user is alerted to update the alarm limits.

Abstract: Provided is a configuration capable of executing a detection test for a comfort level including the quality of sleep, which is measurable at home without requiring the measurement of brain waves or electrocardiogram. The respiratory waveform of a subject during sleep is continuously measured and recorded from the respiratory gas flow, etc., and is window-Fourier transformed at each measurement time to generate a frequency spectrum, and a bandwidth including a respiratory frequency is extracted. The index indicating the regularity of the respiratory period of the subject is also calculated at each time point during the sleep, and the time-dependency of this index during the sleep is represented as a graph. A medical device includes a sleep evaluation system equipped with a control means for performing control so that a sleep cycle repeated at a cycle of about 90 minutes is clearly observed if the comfort level including the quality of sleep of the subject is favorable.

Abstract: A method of detecting an improvement in a seizure condition of a patient includes identifying a first EEG synchronization of the seizure condition of the patient; applying a therapy configured to improve the seizure condition of the patient; and identifying a second EEG synchronization of the seizure condition of the patient subsequent to application of the therapy, wherein an improvement of the seizure condition of the patient is demonstrated by a reduced EEG synchronization of the patient such that the second EEG synchronization is less than the first EEG synchronization.

Abstract: A blood pressure monitor of the present invention includes a cuff to be wrapped around a measurement site. The blood pressure monitor includes a unit including, as elements for blood pressure measurement, a pump, a valve, a pressure sensor, and an inner pipe connecting the pump, valve, and pressure sensor such that fluid can pass therethrough. The blood pressure monitor includes a connecting pipe connecting the cuff and the inner pipe in the unit such that fluid can pass therethrough. The blood pressure monitor includes a self failure diagnosis unit configured to determine whether or not there is a failure in a fluid system including the pump, the valve, the pressure sensor, the inner pipe, the connecting pipe, and the cuff, in a state in which the cuff is empty-wrapped into a cylindrical shape and the capacity of the cuff is restricted.

Abstract: Analyte monitoring systems, devices, and methods associated with analyte monitoring devices, and devices incorporating the same are provided. Various graphical user interfaces (GUI) and navigation flows are provided for performing various features, activities, functions, etc., associated with the analyte monitoring device or system. Intuitive navigation is provided to enhance the interpretation of analyte measurements.