A physiological monitoring device is provided and includes a physiological sensing device, a first PPG sensor, a vital signs detector, and a PPG controller. The physiological sensing device senses at least one physiological feature of a subject to generate at least one sensing signal. The first PPG sensor senses pulses of a blood vessel of the subject to generate a first PPG signal when the first PPG sensor is activated. The vital signs detector obtains vital signs data according to the at least one sensing signal. The PPG controller detects whether a specific event is happening to the subject according to the vital signs data. In response to detecting that the specific event is happening to the subject, the PPG controller activates the first PPG sensor. The physiological monitoring apparatus obtains a blood oxygen level of the subject according to the first PPG signal.

A noninvasive method and system for sleep apnea detection is disclosed. The method includes the following steps: acquiring vital sign signals of a sleeping user; performing structured processing on the vital sign signals of the user to remove invalid signals to obtain a set of valid vital sign signals; extracting multi-dimensional morphological features from a sleep respiratory signal and performing feature training on an initial model of a classifier by means of the multi-dimensional morphological features so as to obtain a sleep breathing detection model; and inputting the set of valid vital sign signals into the sleep breathing detection model and performing signal processing to obtain predicted probability of the user suffering from sleep apnea. As a result, data relating to the probability of a user suffering from sleep apnea can be more accurately obtained, thereby facilitating the determination of whether a sleep apnea event occurs during sleep.

Supplying therapeutic gas based on inhalation duration. At least some of the example embodiments are methods including: sensing a current inhalation of the patient; providing a flow of therapeutic gas to the patient based on the sensing; and ceasing the flow of therapeutic gas to the patient based on a value indicative of previous inhalation duration.

Systems and methods for assessing compliance with position therapy. In an embodiment, position therapy is provided to a user while the user is wearing a position therapy device. The position therapy comprises, by the device, collecting positional data, determining positions of the user over a time period based on the positional data, and, when it is determined that the user is in a target position, providing feedback to the user to influence the user to change to a non-target position. In addition, the device stores a duration of use in its memory. The duration of use indicates a duration that the user has used the wearable position therapy device in each of one or more positions. An assessment of the user's compliance with the position therapy is then provided based, at least in part, on the duration of use.

In a respiratory apparatus for treatment of sleep apnea and other disorders associated with an obstruction of a patient's airway and which uses an airflow signal, an obstruction index is generated which detects the flattening of the inspiratory portion of the airflow. The obstruction index is used to differentiate normal and obstructed breathing. The obstruction index is based upon different weighting factors applied to sections of the airflow signal thereby improving sensitivity to various types of respiration obstructions.

Oral appliances, and systems and methods, which include oral appliances are described herein. An example oral appliance device for treatment of a sleep disorder or condition in a subject can include an upper portion configured to receive at least one maxillary tooth of the subject, and a lower portion configured to receive at least one mandibular tooth of the subject. The upper and lower portions are engageable such that the portions maintain a restricted orientation relative to each other when engaged, and the engaged restricted orientation is configured to maintain the mandible of the subject in a predetermined clinically beneficial orientation relative to the maxilla.

Provided is an electronic device to monitor a user's biological measurements, where a sensor is configured to acquire a first signal from a user, and a diagnostic processor is configured to pre-process the first signal to generate a second signal, segment the second signal to form signal segments, determine at least one event location for each of the signal segments, match adjacent signal segments for feature alignment, and provide a third signal using results of the feature alignment.

Devices, systems and methods of neurostimulation for treating obstructive sleep apnea.

A method of providing a sleep apnea nerve stimulation therapy to a subject may include detecting a respiratory waveform of the subject with a sensor. The sensor may be configured for coupling to the subject. The respiratory waveform may include a plurality of respiratory cycles each corresponding to at least one of a breath and an attempted breath of the subject. The method may also include identifying a breathing pattern within the respiratory waveform over a period of time. The breathing pattern may include a repeating pattern of a plurality of respiratory cycles followed by at least one respiratory cycle corresponding to a disordered breathing event. The method may also include generating a series of stimulation pulses with an implantable nerve stimulator configured for coupling to a hypoglossal nerve of the subject. The series of stimulation pulses may be coordinated with the breathing pattern.

The present technology relates to systems and/or methods for enabling a respiratory device to be configured when a clinician or healthcare professional is remote from the respiratory device. One form provides a method of configuring a respiratory device, the respiratory device comprising a processor configured to control operation of the respiratory device in accordance with a plurality of operating parameters. The method comprises determining a combination of settings for the device from an identifier sent to the device, the identifier corresponding to the combination of settings, and configuring the respiratory device accordingly. Another form provides a method of verifying the configuration of the respiratory device by outputting an identifier corresponding to the combination of settings for the device, and determining the settings from the identifier.