Methods and systems for non-contact monitoring of a patient to determine respiratory parameters such as respiration rate, tidal volume, minute volume, oxygen saturation, and other parameters such as motion or activity. The systems and methods receive a first, video signal from the patient and from that extract a distance or depth signal from the relevant area to calculate the parameter(s) from the depth signal. The systems and methods also receive a second, light intensity signal from an IR feature projected onto the patient, and from that calculate the parameter(s) from the light intensity signal. The parameter(s) from the two signals can be combined or compared to provide a qualified output parameter.

Embodiments described herein relate to an analyte monitoring device having a user interface with a display and a plurality of actuators. The display is configured to render a plurality of display screens, including a home screen and an alert screen. The home screen is divided into a plurality of simultaneously displayed panels, with a first panel displays a rate of change of continuously monitored analyte levels in interstitial fluid, a second panel simultaneously displays a current analyte level and an analyte trend indicator, and a third panel displays status information of a plurality of components of the device. When an alarm condition is detected, the display renders the alert screen in place of the home screen, the alert screen displaying information corresponding to the detected alarm condition. Furthermore, the actuators are configured to affect further output of the analyte monitoring device corresponding to the detected condition.

The present embodiments provide systems and methods for, among others, tracking sensor insertion locations in a continuous analyte monitoring system. Data gathered from sensor sessions can be used in different ways, such as providing a user with a suggested rotation of insertion locations, correlating data from a given sensor session with sensor accuracy and/or sensor session length, and providing a user with a suggested next insertion location based upon past sensor accuracy and/or sensor session length at that location.

A method of providing a quantitative volumetric assessment of organ health or a quantitative map of an organ. The method comprises obtaining a volumetric map of organ health comprising information defining a state of tissue health across at least part of an organ, receiving an input defining at least one organ section, determining an assessment organ volume based at least partly on the at least one defined organ section, calculating an organ-viability measure for the assessment organ volume based at least partly on information within the volumetric map defining the state of tissue health across the organ volume, and outputting an indication of the organ-viability measure.

Improved graphical user and digital interfaces for analyte monitoring systems are provided. For example, disclosed herein are various embodiments of GUIs including Time-in-Ranges, Analyte Level/Trend Alert, and sensor usage interfaces. In addition, various embodiments of digital interfaces are described, including methods for data backfilling, expired or failed sensor transmissions, merging data from multiple devices in an analyte monitoring system, transitioning a previously activated analyte sensor to a new reader device, and autonomous sensor system alarms, among other embodiments.

The present disclosure is directed to a method and device to determine the hemoglobin value of a mammal. The device includes a plurality of light emitting diodes, one or more sensors and a processor.

An application user is granted access to one or more applications that provide the user with information and assistance. Altitude and/or motion data is collected from one or more devices associated with the user, and the device altitude and/or motion data is utilized to identify physical activities being performed by the user. The device altitude and/or motion data is further analyzed to determine physical activity count data, physical activity speed, velocity, and/or acceleration data, and physical activity length data. The physical activity data is then analyzed to identify and monitor changes or anomalies in the physical and/or psychological state of the user using baseline physical activity data. Upon identification of changes or anomalies in the user's physical and/or psychological state, one or more actions are taken to assist the user.

Various methods and systems are provided for a set of devices for an imaging system. In one example, the set of devices includes a first device configured to obtain a first set of image data and a second device configured to obtain a second set of image data along at least one dimension. The first and second sets of data may be compiled to generate a field-of-view (FOV) preview.

A pain-monitoring device and method according to an embodiment of the present disclosure is a pain-monitoring device for obtaining information related to a pain of a user and providing a service of monitoring the pain of the user, includes: an input unit sensing pain-related input of the user; a display unit outputting pain-related information; and a control unit controlling the input unit and the display unit, in which the input unit includes: a touch input unit sensing touch input of the user; and a pressure measurement unit measuring pressure input of the user, and the control unit creates user-input pain information in accordance with the sensed pressure input and touch input.

A cognitive training platform comprises at least one processor that is configured to: obtain a cognitive response function for a user that represents a cognitive state, or change in cognitive state, as a function of one or more stimulus parameters of a stimulus to which the user is exposed; expose the user to a first stimulus that is characterized by respective first values of the one or more stimulus parameters; determine, based on at least one sensor measurement, first cognitive performance values indicative of a response to the first stimulus; determine, using the cognitive response function, respective second values of the one or more stimulus parameters that will result in at least one improved cognitive performance value relative to the first cognitive performance values; and expose the user to a second stimulus that is characterized by the respective second values of the one or more stimulus parameters.