A pulse oximetry system includes a wrist portion configured for placement on a wrist of a subject, the wrist portion having a first component and a second component configured to removably secure to one another. The wrist portion can include emitter(s) and detector(s) operably positioned by the wrist portion. In some implementations, the pulse oximetry system further includes a ring member configured to secure around the subject's finger and operably position emitter(s) and detector(s) and a cable connected to the wrist portion in electrical communication with the emitter(s) and the detector(s) of the ring member and configured to transmit the signal(s) from the detector(s) to the wrist portion. The system includes a battery and hardware processor(s) configured to receive and process signal(s) outputted by the detector(s) to determine physiological parameter(s) of the subject.

A physiological data detection method is provided. The physiological data detection method includes the following steps. Firstly, an ECG signal and a PPG signal are detected. Then, a plurality of RRI values is calculated according to the ECG signal, and a plurality of PPI values is calculated according to the PPG signal. Thereafter, wrong RRI values are excluded according to the RRI values and/or the PPI values. Then, whether an abnormal state occurs or not is determined by using the remaining RRI values. A wearable device therefor is also provided.

A wearable device for healthcare and a method thereof, wherein the device is worn on a finger for measuring the health data of the user, including but not limited to, the heart rate, blood oxygen saturation, etc. The wearing size of the device is adjustable for different sizes of fingers. In one embodiment, the device includes a main body at least partially worn on a digit of a user; at least one physiological sensor attached to the main body for detecting physiological information; and at least two branches coupled to the main body for holding the digit while reducing the movement of the device. At least a part of at least one branch is changeable such that the wearing size of the device is adjustable for different sizes of digits. In another embodiment, at least a part of at least one branch is movable such that the wearing size of the device is adjustable for different sizes of digits.

A surface of a vehicle component can be dynamically deformable surface. The dynamically deformable surface can be configured to undergo deformations to dynamically form a dynamic button or other user interface element on demand. The dynamically deformable surface can include one or more biosensors. When a user engages the dynamic button with a portion of the body, the one or more biosensors can acquire user biodata. The user biodata can be used by the vehicle as input for various purposes. For instance, the vehicle can operate as a health-monitoring and/or comfort monitoring system. As a result of these arrangements, buttons and other user interface elements can appear and disappear depending on the need and/or application, providing a cleaner vehicle cockpit interface and greatly expanding the possibilities of where such buttons can be located at and how many things can be controlled by the driver using physical interfaces.

Methods, systems, and devices for controlling external devices are described. A method may include receiving physiological data associated with a user from a wearable device, and identifying one or more physiological states, physical activities, or both, associated with the user based on the physiological data. Physiological states may include physiological states associated with waking up, falling asleep, anxiety, relaxation, and the like. The method may further include transmitting an instruction to one or more external devices based on the one or more physiological states, physical activities, or both, where the instruction is configured to selectively modify one or more operational parameters associated with the one or more external devices.

Methods, systems, and devices for leveraging data from multiple data sources are described. A method includes receiving physiological data associated with a user from a wearable device and receiving additional data from an external device different from the wearable device, the additional data including at least data associated with characteristics of an environment associated with the user. The method further includes identifying one or more relationships between the collected physiological data and the characteristics of the environment associated with the user, and causing a graphical user interface (GUI) of a user device to display an indication of the one or more relationships, a message associated with the one or more relationships, or both. In some cases, the method includes causing the GUI to display instructions for selectively adjusting the one or more characteristics of the environment associated with the user based on the one or more relationships.

Methods, systems, and devices for temperature analysis are described. The method may include receiving physiological data associated with a user collected via a first set of sensors of a wearable device. The physiological data may include skin temperature data. The method may include receiving surrounding temperature data associated with an environment surrounding the user. The surrounding temperature data may be collected via the first set of sensors, a second set of sensors, or both. The method may additionally include identifying one or more physiological characteristics associated with the user based at least in part on a comparison of the skin temperature data and the surrounding temperature data, and causing a graphical user interface (GUI) of a user device to display an indication of the one or more physiological characteristics, a message or alert associated with the one or more physiological characteristics, or both.

The invention provides a multi-sensor system that uses an algorithm based on adaptive filtering to monitor a patient's respiratory rate. The system features a first sensor selected from the following group: i) an impedance pneumography sensor featuring at least two electrodes and a processing circuit configured to measure an impedance pneumography signal; ii) an ECG sensor featuring at least two electrodes and an ECG processing circuit configured to measure an ECG signal; and iii) a PPG sensor featuring a light source, photodetector, and PPG processing circuit configured to measure a PPG signal. Each of these sensors measures a time-dependent signal which is sensitive to respiratory rate and, during operation, is processed to determine an initial respiratory rate value. An adaptive digital filter is determined from the initial respiratory rate. The system features a second sensor (e.g. a digital 3-axis accelerometer) that attaches to the patient's torso and measures an ACC signal indicating movement of the chest or abdomen that is also sensitive to respiratory rate. This second signal is processed with the adaptive filter to determine a final value for respiratory rate.

A sensor, such as a photoplethysmography sensor, for non-invasively monitoring a characteristic of an organism, such as a vital body sign. The sensor has multiple light sources disposed on a substrate and an array of optical probing channels for conveying light from the light sources to a probed region. Each detector pixel of an array of detector pixels receives light from a respective optical detection channel after interaction with a subregion of the probed region and spatial filtering, and generates a corresponding pixel signal. A processor derives a value of the vital body sign based at least upon the plurality of pixel signals

We disclose an improvement for oximeters, which makes oximeters more reliable when making measurements on patients of darker skin complexion. The device of our invention discloses a re-entrant cavity, inside which some of the tissues of the patient are forced into, by pressing the device of our invention against the skin of the patient. The probing electromagnetic radiation beams (typically deep red and infra-red radiation) are directed to propagate through said re-entrant cavity, inside which some of the outer tissues of the patient are forced, along a path that is approximately parallel to, and just under, the skin of the patient. This probed volume inside said re-entrant cavity contains more arterial and less venous blood, when compared with measurements made by perpendicular beams, that penetrate deep under the skin, which causes that the measurements made by our device are more accurate than many existing oximeters.