Abstract: A method for determining a degree of degradation of a user interface worn by an individual during one or more uses of a respiratory therapy system includes receiving data associated with the user interface. The method further includes determining, based at least in part on the received data, a value of at least one degradation indicator associated with the user interface. The method further includes determining the degree of degradation of the user interface based at least in part on the value of the at least one degradation indicator.

Abstract: Methods and systems are disclosed related to determining whether there is a proper fit between a user interface and a face of a user. The methods and systems involve generating seal information associated with a seal region between a face of a user and a current user interface donned on the face of the user. The methods and systems are further related to analyzing the seal information to determine whether a leak exists in the seal region. If the leak exists, the systems and methods include analyzing the seal information to determine a location of the leak within the seal region. The systems and methods further include determining a new user interface to replace the current user interface based on the current user interface and the location of the leak.

Abstract: A method includes receiving physiological data associated with a user during at least a portion of an initial sleep session. The method also includes receiving demographic information associated with the user. The method also includes receiving subjective feedback associated with at least a portion of the initial sleep session from the user. The method also includes determining a profile for the user based at least in part on the physiological data associated with the user, the demographic information associated with the user, and the subjective feedback for the initial sleep session. The method also includes determining a recommended therapy for the user and one or more recommended parameters for the recommended therapy based at least in part on a comparison between the determined profile for the user and profiles associated with a plurality of other users.

Abstract: A system and method to match an interface to the face of a user for respiratory therapy. A facial image of the user is stored. Facial features based on the facial image are determined. A database stores facial profiles based on facial features and a corresponding plurality of interfaces. A database stores operational data of respiratory therapy devices with the plurality of corresponding interfaces. A selection engine is coupled to the databases. The selection engine is operative to select an interface for the user from the plurality of corresponding interfaces based on a desired outcome based on the stored operational data and the facial features. The collected data may also be employed to determine whether the selected interface is correctly fitted to the face of the user.

Abstract: Apparatus and methods provide compliance management tools such as for respiratory pressure therapy. In some versions, a respiratory pressure therapy system may include one or more processors, such as of a data server, configured to communicate with a computing device and/or a respiratory pressure therapy device. The respiratory pressure therapy device may be configured to deliver respiratory pressure therapy to a patient for a session. The computing device may be associated with the patient. The processor(s) may be further configured to compute a therapy quality indicator of the session from usage data relating to the session. The therapy quality indicator may be a number derived from contributions of a plurality of usage variables for the session in the usage data. The processor(s) may be further configured to present, such as by transmitting, the therapy quality indicator to the computing device. The therapy quality indicator may promote patient compliance.

Abstract: A method for determining how using a respiratory therapy system impacts sleep sessions of a user, includes receiving first activity information corresponding to actions of a user occurring prior to a use of the respiratory therapy system by the user. The first activity information includes activity information associated with use of a mobile device by the user prior to the use of the respiratory therapy system. The method also includes receiving second activity information corresponding to actions of the user occurring after the use of the respiratory therapy system. The second activity information includes activity information associated with use of the mobile device by the user after the use of the respiratory therapy system, as well as respiratory information generated by the respiratory therapy system during a sleep session of the user when using the respiratory therapy system.

Abstract: A system and method to collect feedback data from a patient wearing an interface such as a mask when using a respiratory pressure therapy device such as a CPAP device. The system includes a storage device including a facial image of the patient. An interface in communication with the respiratory pressure therapy device collect operational data from when the patient uses the interface. A patient interface collects subjective patient input data from the patient in relation to the patient interface. An analysis module correlates a characteristic of the interface with the facial image data, operational data and subjective patient input data.

Abstract: A system for providing continuous positive air pressure therapy is provided. The system includes a flow generator, a sensor, and a computing device. The computing device is configured to control operation of the flow generator based on sensor data. The computing device is further configured to display, on a display device, one or more questions relating to demographic and/or subjective feedback; responsive to displaying the one or more questions, receive one or more inputs indicating answers to the one or more questions; transmit the answers to a remote processing system; receive, from the remote processing system, settings determined based on the transmitted answers; and adjust control settings of the system based on the received settings.

Abstract: A method includes receiving physiological data associated with a sleep session of a user. The method also includes identifying a triggering event based at least in part on the physiological data. The method also includes generating image data in response to identifying the triggering event, the image data being reproducible as one or more images of at least a portion of the user during the sleep session. The method also includes causing at least a portion of the image data to be communicated to the user subsequent to the sleep session.

Abstract: A method includes receiving electronically data associated with physical or psychological factors of a user, the data being collected from (a) a plurality of smart home devices, (b) a plurality of mobile devices, or (c) both. The physical or psychological factors are based on at least one physical activity of the user. The method further includes identifying, based on the data, an effect on sleep quality of the user, based on which a remedial action is determined for improving sleep quality of the user. The method also includes causing the remedial action to be communicated in electronic form to the user in real-time during the physical activity, and automatically implementing, without input from the user, at least a part of the remedial action via one or more of the devices. The remedial action increases least one of a deep-sleep state and sleep duration of the user.

Abstract: According to some implementations of the present disclosure, a method for determining a remaining useful life of an interface of a respiratory therapy system is disclosed. Acoustic data associated with an acoustic reflection of an acoustic signal is received. The acoustic reflection is indicative of a portion of a structural shape of the interface. The received acoustic data is analyzed to identify a physical feature of the portion of the structural shape of the interface. The physical feature is compared to a reference feature. Based at least in part on the comparison, the remaining useful life of the interface is determined.

Abstract: A method for optimizing sleep for a user of a respiratory therapy system is described herein. The method includes receiving therapy instructions to be implemented using the respiratory therapy system for a sleep session. The therapy instructions include a plurality of prescribed control parameters, each of the plurality of prescribed control parameters having a value or a range of values. The method further includes receiving a desired sleep comfort level for the sleep session, and adjusting one or more of the values or the range of values of the plurality of prescribed control parameters, to one or more adjusted values or range of values based on the desired sleep comfort level. The adjustments to the adjusted values are implemented to aid the user in achieving the desired sleep comfort level.

Abstract: A method of predicting an unintentional leak in a respiratory system during a sleep session includes causing, during the sleep session, pressurized air to be delivered from a respiratory device to a user via a conduit coupled to a user interface. The method also includes receiving historical first data associated with pressurized air delivered from the respiratory device during one or more prior sleep sessions; receiving current first data associated with the pressurized air being delivered from the respiratory device during the sleep session; receiving historical second data associated with the user during one or more prior sleep sessions; and receiving, via one or more second sensors, current second data associated with the user during the current sleep session. The method determines, a likelihood that an unintentional leak in the respiratory system will occur within a predetermined amount of time.

Abstract: Techniques for data security are provided. Face data for a patient is received, where the face data is linked to an identifier of the patient. A suggested medical device is determined by processing the face data using a recommendation model. Therapy data stored in a first data store and equipment data stored in a second data store are identified based on the identifier, where the equipment data indicates an actual medical device that was provided to the patient. The suggested medical device, the therapy data, and the equipment data are associated.

Abstract: A system for providing continuous positive air pressure therapy is provided. The system includes a flow generator, a sensor, and a computing device. The computing device is configured to control operation of the flow generator based on sensor data. The computing device is further configured to display, on a display device, one or more questions relating to demographic and/or subjective feedback; responsive to displaying the one or more questions, receive one or more inputs indicating answers to the one or more questions; transmit the answers to a remote processing system; receive, from the remote processing system, settings determined based on the transmitted answers; and adjust control settings of the system based on the received settings.

Abstract: A mask cushion or a mask assembly therewith provides a comfortable and effective seal for provision of a gas therapy by a respiratory treatment apparatus. The mask cushion may be integrated with or coupled to a mask frame. The mask cushion typically includes an inner cushion component. The mask cushion also includes a patient facial-contact side portion with a chamber and a barrier to form the chamber that may be flexible. The chamber may serve as an outer layer with respect to the inner cushion component. The chamber may be partially or completely filled with a gas, fluid or gel. The inner cushion may be formed with a soft flexible material such as an elastomer or foam, etc. The barrier may be a membrane and may also be soft flexible material.

Abstract: A respiratory therapy system for providing continuous positive air pressure (CPAP) to a patient may include a flow generator for generating a supply of breathable gas, a sensor to measure a physical quantity while the breathable gas is supplied, and a computing device. The computing device may be configured to: receive sensor data that is based on measured physical property of the supply of breathable gas; control the flow generator to adjust a property of the supply of breathable gas; display a question and a plurality of selectable responses; receive a first input selecting one of the selectable responses; and display a coaching response corresponding to the selected response.

Abstract: A system for providing continuous positive air pressure therapy is provided. The system includes a flow generator, a sensor, and a computing device. The computing device is configured to control operation of the flow generator based on sensor data. The computing device is further configured to display, on a display device, one or more questions relating to demographic and/or subjective feedback; responsive to displaying the one or more questions, receive one or more inputs indicating answers to the one or more questions; transmit the answers to a remote processing system; receive, from the remote processing system, settings determined based on the transmitted answers; and adjust control settings of the system based on the received settings.

Abstract: A system includes a respiratory device, a mask, a microphone, a speaker, and a control system. The respiratory device is configured to supply pressurized air. The mask is coupled to the respiratory device and configured to engage a user during a sleep session to aid in directing the supplied pressurized air to the user. The microphone is configured to generate audio data. The speaker is configured to emit sound. The control system is configured to analyze the audio data to determine if noise associated with air leaking from the mask is occurring. Responsive to (i) the analysis resulting in a determination that noise associated with air leaking from the mask is occurring, (ii) the respiratory device determining that air is leaking from the mask, or (iii) both, the speaker is caused to emit the sound to aid in masking the noise associated with the air leaking from the mask.

Abstract: A mouth seal assembly for use with a nasal mask system includes a mouth seal adapted to form a seal with the patient's mouth. The mouth seal is substantially independent from a supply of pressurized air from the nasal mask system. An anti-asphyxia valve may be provided to either the mouth seal over the patient's lips or the nasal mask system. A strap arrangement may support the mouth seal in a desired position on the patient's face in use.