A system for determining muscle activation comprises a set of electrode adherable to a skin of a subject, and a processor in communication with the electrodes. The processor has a circuit configured for receiving locations of the electrodes and electrical signals detected by the electrodes, analyzing the signals to identify a section of an active muscle, identifying locations of at least a segment of active muscles and activation patterns of the active muscles based on the identified section, and constructing a displayable map of the locations and the activation patterns, wherein patterns corresponding to different active muscles are distinguishable on the map.

A patient monitoring device configured to monitor cardiac activity and sleep stage information of a patient is provided. The device includes a plurality of electrodes to acquire electrocardiogram (ECG) signals from the patient, at least one motion sensor configured to generate a motion signal based upon movement of the patient, and at least one processor. The processor is configured derive motion parameters from the motion signal, derive ECG parameters from the ECG signals, determine whether the patient is in an immobilized sleep stage or a non-immobilized sleep stage based upon the motion parameters and the ECG parameters, adjust one or more cardiac arrhythmia detection parameters such that the device operates in a first monitoring and treatment mode when the patient is in an immobilized sleep stage, and monitor the patient for the cardiac arrhythmia using the first monitoring and treatment mode.

A monitoring unit which is configured to monitor a patient during an operation of a high-frequency surgery device, wherein the high-frequency surgery device is configured to separate and/or coagulate biological tissue by means of high-frequency electrical energy, wherein the monitoring unit has: measuring electrodes which are disposed in a periphery of the patient, and an evaluation and control unit which is configured to impress a predetermined measuring alternating voltage or a predetermined measuring alternating current on the measuring electrodes, and to monitor an impedance decreasing between the measuring electrodes and to monitor a time curve of the impedance and/or to monitor a temporal change thereof

Provided is a method for controlling a mask apparatus. The method for controlling the mask apparatus includes measuring a current pressure value with respect to a mask by using a pressure sensor, comparing each of a preset atmospheric pressure maximum estimation and a preset and a preset atmospheric pressure minimum estimation to the current pressure value; updating the atmospheric pressure maximum estimation and the atmospheric pressure minimum estimation according to the comparison result, and controlling a voice output of a speaker based on a difference between the updated atmospheric pressure maximum estimation and the updated atmospheric pressure minimum estimation.

A health monitoring urinalysis system that monitors several health indicators from human urine is provided. The system includes a temperature sensor and several electrochemical sensors that are installed in a urine collection basin, such as, a toilet or a urinal and may automatically collect urine information after each use. The system collects data during the routine and normal use of a urine collection basin. The system includes a control and measurement unit that may be installed outside the urine collection basin. The control and measurement unit receives sensor measurements and transmits the measurements to one or more remote electronic devices. The remote electronic devices and/or the processor of the control and measurement unit perform data analysis, provide diagnostic, and generate health alerts. The system performs recurrent health monitoring after the urine collection basin is used and may detect abnormal conditions at early stages, in addition to a routine urine test.

A drug overdose detection apparatus that is configured to measure the blood oxygen level of a user and upon detection in a drop thereof provide administration of a substance to counteract the drug overdose. The present invention includes a housing that is configured to be worn by a user has an interior volume. Disposed in the interior volume of the housing is a substance administration assembly wherein the substance administration assembly includes a syringe member, a plunger member and a plunger driver. A motor is operably coupled to the plunger driver and facilitates movement thereof. A spring needle assembly is operably coupled to the substance administration assembly and includes a spring biased needle that is operable to inject into a patient so as to inject the substance. The present invention further includes an audio alarm and transceiver configured to provide alerts and transmit signals.

A vitals monitoring handcuff apparatus comprising a housing structure that is adapted to be coupled with a set of handcuffs and to contain a plurality of modules and units; a first module that is located within the housing structure and adapted to measure a wearer's heartrate via a sensor; a second module that is located within the housing structure and is adapted to measure the wearer's respiration rate via a sensor; a controller unit that is located within the housing structure, is configured to relay instructional programs to the modules and units which causes the modules and units to operate, and the controller unit receives data from the modules and inputs that data into associated algorithms that produce corresponding output signals; a communication unit that is located within the housing structure and receives the output signals from the controller unit and is adapted to relay the output signals to a user; and a rechargeable power unit located within the housing structure that is accessed by a port on an exterior of the housing structure, provides power to the vitals monitoring handcuff apparatus's other modules and units, and having a receiver which connects with an exterior power source via the port.

Techniques related to temporary setpoint values are disclosed. The techniques may involve causing operation of a fluid delivery device in a closed-loop mode for automatically delivering fluid based on a difference between a first setpoint value and an analyte concentration value during operation of the fluid delivery device in the closed-loop mode. Additionally, the techniques may involve obtaining a second setpoint value. The second setpoint value may be a temporary setpoint value to be used for a period of time to regulate fluid delivery, and the second setpoint value may be greater than the first setpoint value. The techniques may further involve causing operation of the fluid delivery device for automatically reducing fluid delivery for the period of time based on the second setpoint value.

Described are systems for beds that can include sensors for sensing physical phenomena in an environment surrounding a bed, a display for outputting information about the environment, the bed, and a sleeper, and a controller communicably coupled to the sensors. The controller can receive the sensed physical phenomena from the sensors, analyze the physical phenomena to determine at least one of environmental, sleep, and health metrics of a sleeper in the bed, and determine, based on at least one of the environmental, sleep, and health metrics of the sleeper, control signals to modify the environment surrounding the bed. The controller can also output, at the display, the environmental, sleep, and health metrics of the sleeper. The controller can also transmit the control signals to a second controller in order to engage a home automation device. The physical phenomena can include ambient sound, ambient light, ambient CO2 concentration, and/or ambient temperature.

A wearable fall prevention device and method including at least one gyroscope, an actuator, a pressure applicator, and a controller. The at least one gyroscope is configured to detect and signal to a controller when a user's movement and/or orientation surpasses a specified threshold. The controller receives the signal from the at least one gyroscope and generates an actuation signal received by the at least one actuator, activating the at least one pressure applicator. The at least one pressure applicator is adapted to come into contact with the user's neck and vagus nerves at a specified pressure. When the at least one gyroscope detects a user has dropped below the specified threshold, the at least one gyroscope sends a signal to the controller, generating an actuation signal that deactivates the at least one actuator and disengages the at least one pressure applicator from the user's neck and vagus nerves.