A respiratory ventilation device—for sending a fan-generated air flow into a duct extending to a respiratory mask—extends between lower (bottom) and upper ends. A ventilation chamber contains the fan and is connected to a humidifier, which has a water-accommodating reservoir and a connecting chamber adjacent the ventilation chamber. An intake opening leads out of the ventilation chamber. An exhaust opening leads into an exhaust channel attachable to the duct. A humidification chamber has the water reservoir. First and second openings are formed between the connecting and humidification chambers. The connecting chamber extends between the humidification and ventilation chambers. A separating wall extends between the connecting and humidification chambers. The first and second openings are made in the separating wall, which is arranged such that the humidification chamber extends between the bottom and the separating wall. The connecting chamber extends between the separating wall and the ventilation chamber.

A patient interface may include a dual chamber cushion assembly having a nasal chamber and an oral chamber. The nasal chamber may be arranged to deliver pressurized breathable gas to a patients nasal passages, and the oral chamber may be arranged to deliver pressurized breathable gas to the patients oral passages. The nasal chamber may be pressurized to a different level than an oral chamber to promote nasal breathing. An air passage may fluidly connect the nasal chamber and the oral chamber so that pressurized breathable gas may flow from the nasal chamber to the oral chamber.

Aspects of the present technology comprise a positioning and stabilising structure to hold a seal-forming structure in a therapeutically effective position on a head of a patient. The seal-forming structure may be constructed and arranged to form a seal with a region of the patients face surrounding an entrance to the patients airways for sealed delivery of a flow of air at a therapeutic pressure of at least 4 cmH2O with respect to ambient air pressure throughout the patients respiratory cycle in use. The positioning and stabilising structure may comprise a front hoop arranged to contact, in use, at least a region of the patients head superior to an otobasion superior of the patients head and a rear strap. The positioning and stabilising structure may comprise an adjustment mechanism for adjustment of the front hoop and the rear strap relative to the patients head, the adjustment mechanism being arranged in a single operation to adjust both the front hoop and rear strap to enable the positioning and stabilising structure to fit different size heads.

A system for delivering a composition containing a nutritional supplement matrix to a user through the oral mucosa, in which the matrix is held under pressure in a canister that has a nozzle with at least one rotating internal member positioned between the canister outlet and the nozzle outlet, in which the rotating member agitates the composition to increase atomization to aid in absorption.

A breathing assistance apparatus has a pressurised gases source featuring a lightweight impeller with a plastic shaft. The impeller is shroudless. The plastic shaft is supported within the stator by a bearing structure. The resilient motor mount couples the stator and the housing and provides compliance and/or damping for the motor.

A blower unit, particularly for an apparatus for assisting respiration, comprises a housing (2), an impeller (1) accommodated in an impeller chamber (3) in the housing (2), and a motor (12), connected to the impeller (1) via a shaft (15), which is accommodated in a motor chamber (13) in the housing (2). The motor (12) is fixed between walls (14, 18) of the motor chamber (13) by means of buffers, with at least one of the buffers being a sealing ring (16) which separates the shaft (15) from a passage for cooling air (33) which, in radial section, extends annularly around the motor (12).

A pressure support system for providing pressure support therapy to a patient, the pressure support device includes an airflow generator structured to generate a flow of breathing gas to the patient, a temperature conditioning unit structured to adjust a temperature of the breathing gas provided to the patient, and a processing unit structured to estimate a core body temperature of the patient for selected times of day based on one or more inputs and to control the temperature conditioning unit to adjust temperature of the breathing provided to the patient at the selected times of day based on the estimated core body temperatures of the patient.

A respiratory therapy device, which may include a flow generator, is provided. The RPT device includes a touch screen display that displays user interface screens to a user and accepts input from users to control parameters and functionality of the RPT device (e.g., a flow generator).

Systems and methods for hypoxia delivery are provided. An apparatus for providing intermittent normoxia and hypoxia intervals includes a breathing component, a normoxia fluid source, a hypoxia fluid source, a valve, and a control system. The valve is configured to disrupt flow from at least one of the normoxia fluid source and the hypoxia fluid source and the control system is configured to cause the at least one valve to switch between delivery of fluid from the normoxia fluid source and the hypoxia fluid source while maintaining positive pressure at the breathing component.

A respiratory device can include an oxygen generator and a ventilator. The oxygen generator can include a first inlet to ambient air, a vacuum or pressure swing oxygen generating system in fluid communication with the first inlet, a first fluid pathway, and a first outlet. The ventilator can include a second inlet to ambient air and a blower in fluid communication with the second inlet to draw ambient air. The ventilator can include a third inlet in fluid communication with the first fluid pathway upstream of the first outlet. The blower can also be in fluid communication with the second inlet to draw at least some of the extracted oxygen. The ventilator can also include a second outlet in fluid communication with the blower to dispense a mixture of the ambient air and the extracted oxygen to the user.