Abstract: Various implementations of the present disclosure are directed to systems and methods for leak detection in a respiratory therapy system using acoustic data. According to some implementations, a method includes receiving acoustic data associated with airflow caused by operation of a respiratory therapy system during a sleep session of a user. The method also includes analyzing at least a portion of the acoustic data to determine a value of a parameter associated with the at least a portion of the acoustic data. The method further includes determining an occurrence of a leak during the sleep session in response to the determined value of the parameter satisfying a condition.

Abstract: A system and method detects an occlusion in a respiratory therapy system. The system and method includes determining an acoustic signature for a conduit of a headgear user interface. The determined acoustic signature is analyzed to identify an anomaly in the acoustic signature. In response to the determined acoustic signature being identified as anomalous, a determination is made if the identified anomaly relates to an occlusion of the conduit.

Abstract: A method of detecting rainout in a respiratory therapy system that includes a conduit fluidly coupled to a user interface comprises generating, via at least one microphone, acoustic data representative of noise associated with the respiratory therapy system. The method further comprises analyzing the acoustic data to detect a presence of liquid in the respiratory therapy system. The method further comprises causing an action to be performed, based on the detected presence of the liquid.

Abstract: Systems and methods are disclosed for categorizing and/or characterizing a user interface. The systems and methods include generating acoustic data associated with an acoustic reflection of an acoustic signal, the acoustic reflection being indicative of, at least in part, one or more features of a user interface coupled to a respiratory therapy device via a conduit. The systems and methods further include analyzing the generated acoustic data. The systems and methods further include categorizing and/or characterizing the user interface based, at least in part, on the analyzed acoustic data.

Abstract: The present disclosure relates to a method for identifying a user interface. Flow data associated with air flowing in a respiratory therapy system is received. Acoustic data associated with the respiratory therapy system is received. The received flow data and the received acoustic data are analyzed. Based at least in part on the analysis, a mask type for the user interface is determined.

Abstract: A method includes generating acoustic data representative of at least one or more reflections of an acoustic signal. The one or more reflections are indicative of a length and/or a diameter of a conduit coupled to a respiratory therapy device. The method further includes analyzing the acoustic data to determine the length and/or diameter of the conduit. In some cases, analyzing the acoustic data includes determining a resonant frequency of the conduit, and determining the length of the conduit based at least in part on the resonant frequency. In some cases, analyzing the acoustic data includes comparing the acoustic data to predetermined sets of acoustic data that each correspond to a known length and/or diameter of the conduit, and selecting one of the predetermined sets of acoustic data that best matches the generated acoustic data. The selected set of acoustic data corresponds to the length and/or diameter of the conduit.

Abstract: A method includes generating, by a sensor, physiological data associated with a user during a sleep session. The method also includes processing, by an electronic device including one or more processors, the generated physiological data to distinguish between on-therapy data and off-therapy data. The on-therapy data is the generated physiological data while a respiratory therapy system is coupled to the user and supplies pressurized air to an airway of the user. The off-therapy data is the generated physiological data while the respiratory therapy system is not supplying pressurized air to the airway of the user. The method also includes determining, by the electronic device, a sleep measure based at least in part on the off-therapy data.

Abstract: A method includes receiving first physiological data associated with a user. The method also includes determining a first emotion score associated with the user based at least in part on the first physiological data. The method also includes modifying one or more settings of a respiratory therapy system responsive to determining that the first emotion score satisfies a predetermined condition.

Abstract: A plurality of flow rate values associated with pressurized air directed to an airway of a user of a respiratory therapy system is received. A plurality of pressure values associated with the pressurized air directed to the airway of the user is received. A first time associated with a first breath of the user and a second time associated with a second breath of the user are identified. The plurality of flow rate values is filtered based at least in part on the identified first time and the identified second time. The filtering produces a subset of the plurality of flow rate values. An intentional leak characteristic curve for the respiratory therapy system is determined using at least two of the subset of the plurality of flow rate values and the corresponding pressure values for said at least two of the subset of the plurality of flow rate values.

Abstract: A plurality of flow rate values associated with pressurized air directed to an airway of a user of a respiratory therapy system is received. A plurality of pressure values associated with the pressurized air directed to the airway of the user is received. A first time associated with a first breath of the user and a second time associated with a second breath of the user are identified. The plurality of flow rate values is filtered based at least in part on the identified first time and the identified second time. The filtering produces a subset of the plurality of flow rate values. An intentional leak characteristic curve for the respiratory therapy system is determined using at least two of the subset of the plurality of flow rate values and the corresponding pressure values for the at least two of the subset of the plurality of flow rate values.

Abstract: The present disclosure relates to a method for identifying a user interface. Flow data associated with air flowing in a respiratory therapy system is received. Acoustic data associated with the respiratory therapy system is received. The received flow data and the received acoustic data are analyzed. Based at least in part on the analysis, a mask type for the user interface is determined.

Abstract: Methods and apparatus provide monitoring of coughing and/or a sleep disordered breathing state of a person. One or more sensors may be configured for non-contact active and/or passive sensing. The processor(s) may extract respiratory effort signal(s) from one or more motion signals generated by active non-contact sensing with the sensor(s). The processor(s) may extract one or more energy band signals from an acoustic audio signal generated by passive non-contact sensing with the sensor(s). The processor(s) may assess the energy band signal(s) and/or the respiratory efforts signal(s) to generate intensity signal(s) representing sleep disorder breathing modulation. The processor(s) may classify feature(s) derived from the one or more intensity signals to generate measure(s) of coughing and/or sleep disordered breathing.

Abstract: A method includes emitting an acoustic signal into an airway of a user. The method further includes, detecting an acoustic reflection of the acoustic signal caused by one or more physical features within the airway of the user. The method also includes analyzing acoustic data associated with the acoustic reflection. The method also further includes characterizing an occurrence of the physical obstruction in the airway of the user. The characterization is based, at least in part, on the analyzed acoustic data. The characterization is indicative of an apnea event or a hypopnea event in the user, wherein the apnea event comprises an obstructive apnea event, a central apnea event or a mixed apnea event, and further distinguishes between the occurrence of the obstructive apnea event, the central apnea event, the mixed apnea event or the hypopnea event in the user.

Abstract: A system includes a memory device storing machine-readable instructions and a control system including one or more processors configured to execute the machine-readable instructions to receive initial physiological data associated with a user, determine, based at least in part on initial physiological data, an initial sleepiness level for the user, prompt the user, via an electronic device, to perform a first activity, receive subsequent physiological data associated with the user, determine, based at least in part on the subsequent physiological data, a subsequent sleepiness level for the user, and determine a first activity score based at least in part on the initial sleepiness level and the subsequent sleepiness level, the first activity score being indicative of an effectiveness of the first activity in modifying the sleepiness of the user.

Abstract: A system has an electronic interface, one or more sensors, a memory, and a control system including one or more processors. The processors are configured to execute instructions for activating an edema test, automatically or in response to receiving a user request via the electronic interface. Upon activation, user instructions are provided to locate, via one or more of the sensors, a skin area in the subject for testing. A user is instructed to depress the skin area for causing a temporary indentation. One or more images of the temporary indentation are captured, via one or more of the sensors, over a period of time following the depression of the skin area by the user. The images are analyzed for characteristics of skin bounce-back, which represents rebounding of the skin area after the temporary indentation. An edema result is determined based on the characteristics of the skin bounce-back.

Abstract: A plurality of flow rate values associated with pressurized air directed to an airway of a user of a respiratory therapy system is received. A plurality of pressure values associated with the pressurized air directed to the airway of the user is received. A first time associated with a first breath of the user and a second time associated with a second breath of the user are identified. The plurality of flow rate values is filtered based at least in part on the identified first time and the identified second time. The filtering produces a subset of the plurality of flow rate values. An intentional leak characteristic curve for the respiratory therapy system is determined using at least two of the subset of the plurality of flow rate values and the corresponding pressure values for said at least two of the subset of the plurality of flow rate values.

Abstract: Methods and devices provide physiological movement detection with active sound generation. In some versions, a processor may detect breathing and/or gross body motion. The processor may control producing, via a speaker coupled to the processor, a sound signal in a user's vicinity. The processor may control sensing, via a microphone coupled to the processor, a reflected sound signal. This reflected sound signal is a reflection of the sound signal from the user. The processor may process the reflected sound, such as by a demodulation technique. The processor may detect breathing from the processed reflected sound signal. The sound signal may be produced as a series of tone pairs in a frame of slots or as a phase-continuous repeated waveform having changing frequencies (e.g., triangular or ramp sawtooth). Evaluation of detected movement information may determine sleep states or scoring, fatigue indications, subject recognition, chronic disease monitoring/prediction, and other output parameters.

Abstract: An actuator assist apparatus for use with an actuator has a housing and a piston member slidably disposed in the housing. The piston member divides the interior of the housing into a first fluid chamber and a second fluid chamber. The actuator assist apparatus is configurable between a first, primed, configuration and an activated configuration. A force applicator is configured to store energy when the apparatus is in the primed configuration and release the energy to move the piston member relative to the housing. Movement of the piston member applies a force which assists in urging the actuator towards an extended configuration, thereby reducing the minimum operating pressure of the actuator.

Abstract: An actuator assist apparatus for use with an actuator has a housing and a piston member slidably disposed in the housing. The piston member divides the interior of the housing into a first fluid chamber and a second fluid chamber. The actuator assist apparatus is configurable between a first, primed, configuration and an activated configuration. A force applicator is configured to store energy when the apparatus is in the primed configuration and release the energy to move the piston member relative to the housing. Movement of the piston member applies a force which assists in urging the actuator towards an extended configuration, thereby reducing the minimum operating pressure of the actuator.