Abstract: Systems and methods implement a status assessment of a respiratory device with sound evaluation. In some versions, the system may include a motor operated pressure generator to generate airflow through an air circuit to a patient interface. The system may include a transducer producing a signal representing sound of the generator in the circuit. The system may include a controller, such as with a processor, for generator control. The system, such as with the controller, computes a sound representation in the frequency domain. The system applies, to the frequency domain representation, any one or more of an integer-multiple function, non-integer-multiple function, a statistical correlation function and resonant frequency function, such as of a fundamental frequency attributable to motor operation. The system may derive a noise vector with data from the function(s). The system may classify the vector to obtain a status indicator of the generator and generate indicator related output.

Abstract: A patient interface is configured to deliver a pressurized flow of respiratory gas to a patient's airways. The patient interface includes a cradle base configured to cradle the patients nose in use. Two protrusions extend from the cradle base and are configured to be inserted into the patients nares in use. Each of the protrusions have formed therein an opening configured to allow a continuous flow of air therethrough. In addition, a plenum base forms a plenum chamber together with the cradle base. The cradle base is configured so that movement of the cradle base is decoupled from the plenum base.

Abstract: Systems, methods, and/or apparatuses for acclimatizing a user to positive airway pressure (PAP) therapy are provided. Generally, a sub-therapeutic treatment pressure is provided initially. It may be ramped up to a full treatment pressure over the course of one or more therapy sessions. The pressure level may be ramped up based on, for example, sleep state, sleep phase, patient compliance with types of treatment (e.g. bilevel vs. CPAP, etc.), clinician input (either at the site, remotely, via pre-programmed smartcards, etc.), etc. Such techniques may be used alone or in combination.

Abstract: A respiratory apparatus includes components to permit different operations of the apparatus with different power supplies. For example, a respiratory therapy apparatus for controlling a respiratory therapy may include a power input circuit to receive a first power or a second power. The first power may be provided by a connectable low-power power supply and the second power by a connectable high-power power supply. A controller of the respiratory apparatus coupled to the power input circuit may be configured to detect one of the power supplies, and based on the detection, selectively activate one of a first mode of operation and a second mode of operation. The first mode of operation may be a non-therapy mode with the first power such as for a data setup or data transfer with the respiratory therapy apparatus and the second mode of operation may be a therapy mode with the second power.

Abstract: A water reservoir for an apparatus for humidifying a flow of breathable gas includes a reservoir base including a cavity structured to hold a volume of liquid and a conductive portion provided to the base. The conductive portion is adapted to thermally engage with a heater plate to allow thermal transfer of heat from the heater plate to the volume of liquid. The conductive portion includes a thin film comprising a non-metallic material, and the thin film includes a wall thickness less than about 1 mm.

Abstract: A patient interface for treating sleep disorder breathing includes a headgear tube that provides support for the seal forming structure. The headgear tube includes a patient-contacting portion and a non-patient contacting portion that are joined along seams to form a gas passageway. The headgear tube may comprise a textile material and/or a foam material. Portions of the headgear tube may be imparted with greater rigidity than other portions.

Abstract: A respiratory pressure therapy (RPT) device is disclosed for treatment of respiratory-related disorders. The RPT device includes a pressure generator, a pneumatic block, a chassis and a device outlet for delivering a supply of flow of gas to a patient interface. The RPT device also comprises an integrated humidifier including a water reservoir. An RPT device is also disclosed that includes a wireless data communication interface integrated with the housing and configured to connect to another device or a network.

Abstract: A patient interface system includes a nasal seal of flexible material to communicate with at least one airway of the patient, and a primary headgear from which the nasal seal is suspended, said primary headgear having at least one aperture though which at least a portion of the nasal seal is inserted with the primary headgear wrapping about at least one portion of the nasal seal in a sling-like fashion.

Abstract: A patient interface assembly is configured to deliver pressurized respiratory gas to a patient's airways. The patient interface assembly includes a cushion configured to sealingly engage the patient's face, a plenum base supporting the cushion, and a positioning and stabilizing structure configured to support the cushion and the plenum base on the patient's face. The positioning and stabilizing structure includes a stiffened portion. The patient interface assembly further includes a removable sleeve. The stiffened portion of the positioning and stabilizing structure is inserted into the removable sleeve. The removable sleeve is configured to be secured to the stiffened portion of the positioning and stabilizing structure by inserting a projection into a side cutout, and the stiffened portion of the positioning and stabilizing structure is prevented from sliding out of the removable sleeve when the projection is received within the side cutout.

Abstract: A patient interface is configured to deliver a pressurized flow of respiratory gas to a patient's airways. The patient interface includes a cushion and shell assembly with a cushion portion mounted on a shell portion that is more rigid than the cushion portion. The cushion portion is configured to sealingly engage the patient's face and has a vent opening. The shell portion includes a plurality of headgear connectors. The patient interface further includes a gas washout vent assembly configured to be positioned within the vent opening of the cushion portion. The gas washout vent assembly includes a main body configured to be secured to the cushion portion, a porous body, and an outer cover with a plurality of openings. The main body at least partially houses the porous body and the outer cover.

Abstract: Systems slow breathing with positive pressure therapy. In embodiments, a current interim breathing rate target is set, and periodically magnitude of a variable pressure waveform scaled to the current interim breathing rate target is increased if breathing rate is greater than the interim rate target to lengthen breath duration. The magnitude of the pressure increase may be a function of the difference between the interim rate target and the breathing rate. The interim rate target may be reduced in response to slowing breathing rate. The waveform cycles, inhalation to exhalation, when airflow decreases to a cycle threshold. Different interim rate targets have different cycle threshold functions that allow easier cycling as the interim rate targets decrease. Similarly, the waveform triggers, exhalation to inhalation, when airflow increases to a trigger threshold. Different interim rate targets have different trigger threshold functions that allow easier triggering as the interim rate targets decrease.

Abstract: A humidifier includes a heating element including a porous structure of electrically resistive and thermally conductive material configured to substantially vaporise liquid that is passed through the porous structure. The porous structure has a liquid inlet and a vapour outlet. The humidifier further includes an outer housing surrounding at least a portion of the porous structure for containing the liquid and vapour within the porous structure. The porous structure includes a first electrical connector and a second electrical connector, the first and second connectors being configured for receiving electrical power and applying a voltage across the porous structure to generate heat.

Abstract: A humidifier includes a humidifier tub including an air inlet and an air outlet. The air outlet may have an exit port positioned in a plane disposed below the air inlet. A base plate is provided to the bottom of the humidifier tub. The base plate and humidifier tub define a water chamber adapted to receive a volume of water. The humidifier tub may include a guidance structure adapted to direct air entering the humidifier tub via the air inlet to swirl downwardly and around within the humidifier tub reaching the water surface before exiting the exit port. The tub may include a structure to prevent the inadvertent entry of water from the tub to the flow generator.

Abstract: A conduit for delivering a supply of gas under a positive pressure includes a conduit wall having a first conduit end and a second conduit end. The first conduit end is adapted to be attached to the supply of gas. The conduit wall is deformable between (a) an open condition in which the conduit wall defines a conduit passage along which the supply of gas can travel between the first conduit end to the second conduit end, and (b) a collapsed condition in which the conduit wall substantially collapses the conduit passage.

Abstract: A method of acclimatizing a patient to provide continuous positive airway pressure (CPAP) therapy, including operating a device for treating sleep disordered breathing (SDB). The device provides continuous positive airway pressure to the patient during sleep via a mask configured to provide a seal with respect to airways of the patient. The method comprises applying full therapeutic pressure during a first session, monitoring a mask pressure during application of the full therapeutic pressure, calculating a difference between the full therapeutic pressure and the mask pressure, comparing the difference to a threshold representing an acceptable level of leak, generating a first signal in response to said comparing, and in response to said first signal indicating a fault in the seal, decreasing an applied pressure to below the full therapeutic pressure during the first session in order to improve the seal of the mask against the patient's face.

Abstract: One form of the present technology includes a sealing structure to seal against a user's face around the user's airways. The sealing structure includes a flap or membrane that extends inward towards the user's airways and includes a structure that prevents an inner boundary of the flap or membrane from being blown outwards (e.g., folded backwards upon itself) due to internal pressurization.

Abstract: A positive airway pressure device includes a blower and a base. A blower outlet passage is connected to the blower and has a central tubular portion and a flexible sealing portion surrounding an outer circumferential surface of the central tubular portion. The base receives a tub with a heat conducting base plate, an internal air passage configured to receive the pressurized flow of respiratory gas from the blower outlet passage, and a pair of tub flanges extending laterally from respective side walls of the tub. Each tub flange has a horizontal portion and a tapered portion. The base further includes a floor with a heater plate a pair of base flanges. Each base flange extends laterally inward from a respective one of the side walls and engages a respective tub flange as the tub is inserted into the base with the tapered portions of the tub flanges being received first.

Abstract: A cushion assembly for a patient interface including an elastomeric seal-forming structure that is shaped to be bisected by a sagittal plane having a line that is tangent to the elastomeric seal-forming structure at a superior tangent point and at an inferior tangent point. A saddle-shaped superior region of the elastomeric seal-forming structure straddles the sagittal plane and includes the superior tangent point. The elastomeric seal-forming structure transitions in a cylinder-shaped superior region from the saddle-shaped region to a dome-shaped superior region offset from the sagittal plane. In addition, an elastomeric wall thickness of the elastomeric seal-forming structure is greater in the cylinder-shaped superior region than in the saddle-shaped superior region and the dome-shaped superior region.