A patient interface, including a mask assembly and a headgear assembly, provides improved facial sealing and improved ease of use. The mask assembly includes an inflating or ballooning seal. The seal can be secured between two portions of a snap-fit exoskeleton. The headgear assembly connects to the mask assembly with flexible straps during course fitting and with more rigid straps following course fitting. The straps include holes that fit over a tapering post on the mask assembly.

A heat and moisture exchanger (HME) for engaging a patient’s nose while retrofit into a plenum chamber of a patient interface. The HME includes a frame configured to couple to a ridge of the patient’s nose, and a cradle coupled to the frame. The cradle is configured to be positioned proximate to the patient’s nares. The HME also includes an HME material coupled to the cradle. The HME material is configured to retain moisture exhaled by the patient. Air is configured to pass through the HME material when entering and exiting the patient’s nares. The HME engages and is secured to the patient’s nose independently of any other structure.

A pump arrangement is provided for a breast pump system having a pump motor assembly and a damping arrangement, providing a coupling between an outer surface of the pump motor assembly and an inner surface of a housing for the pump arrangement. A set of one or more limbs extends outwardly from a frame. For example, cushions are formed by a pair of radially extending limbs and a connecting piece connecting to the pair of limbs. This arrangement provides positioning within the housing as well as damping.

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 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 nasal mask having a seal housing and a flexible nasal seal connected or connectable to the seal housing to define a mask cavity. The nasal seal extends between a face-contacting side and an outer side. The nasal seal has a contacting surface having an edge that defines a nose-receiving opening into the mask cavity and which is configured to seal about the user's nose. The nasal seal also has an under-nose support fixedly connected into the seal and which is configured to extend within the mask cavity and having a contact surface that is oriented to contact at least a portion of the under-nose surface of the user.

A method for delivering a substance into an airway of a user via a respiratory system comprises receiving the substance within a receptacle; receiving physiological data; determining one or more sleep-related parameters based on the physiological data; and modifying the delivery of the substance into the airway of the user based at least in part on the one or more sleep-related parameters. The respiratory system includes a respiratory device configured to supply pressurized air to the airway of the user via a conduit and a user interface. The respiratory device, the user interface, and the conduit form an air pathway. The respiratory device is configured to include or engage the receptacle such that an outlet of the receptacle is in direct or indirect fluid communication with the air pathway.

Described herein is a respiratory care apparatus capable of performing multitude of therapy for secretion management and breath assistance therapy. The respiratory care apparatus comprises an electromechanical air router assembly (EARA) and an interfacing assembly. The EARA includes independent first and second pressure generating sources for assisted inhalation/insufflation and assisted exhalation/exsufflation process. The interfacing assembly includes a patient interface port and a patient interface tube. The and negative pressure at the patient interface port for assisted inhalation/insufflation and assisted exhalation/exsufflation processes respectively. The assisted inhalation/insufflation and assisted exhalation/exsufflation processes are carried out independently through separate conduits/passages to reduce contamination and infection. Further, the respiratory care apparatus comprises a garment which oscillates due to alternate positive and negative pressure generation and provides therapy to the patient.