A water reservoir for use with a respiratory pressure therapy (RPT) device includes a water reservoir base configured to hold a volume of water to be used for humidification of pressurized breathable air, the water reservoir base including a conductor plate constructed from a heat conducting material; a water reservoir lid connected to the water reservoir base, wherein the water reservoir lid and the water reservoir base are connected via a pair of joints positioned proximate a first end of the water reservoir; a retainer configured to secure the water reservoir to the water reservoir dock; a latch that secures the water reservoir lid and the water reservoir base, the latch being positioned on the water reservoir proximate a second end that is opposite to the first end; and a water reservoir inlet and a water reservoir outlet positioned on a common side of the water reservoir so as to face a common direction.

A system for enhancing secretion removal from an airway of a subject by applying a negative pressure to the airway of the subject just prior to an exsufflation is provided. The negative pressure is applied just after the subject has inhaled under his own power and/or just after generator mechanical insufflation by the system. The negative pressure applied just after inhalation/insufflation and just prior to exsufflation temporarily reduces the cross-sectional area of the airway of the subject. A reduced cross-sectional area User of the airway increases the velocity of air through the airway during a subsequent exsufflation, which results in enhanced secretion clearance. In some embodiments, the system includes one or more of a pressure generator, a subject interface, one or more sensors, a user control interface, one or more processors, and/or other components.

A patient transfer device is configured for use with at least one host device which is capable of providing respiratory support to a patient. The patient transfer device includes an inspiratory port and an expiratory port which are configured to pneumatically connect to the host. An inspiratory connection is pneumatically connected to the inspiratory port and an expiratory connection is pneumatically connected to the expiratory port. An inspiratory valve is coupled between the inspiratory port and the inspiratory connection and expiratory valve is coupled between the expiratory port and the expiratory connection. The inspiratory valve and the expiratory valve are operable between first configurations that permit flow there though and second configurations that occlude flow through the valves. The inspiratory valve and the expiratory valve are configured to operate in the second configuration when the patient transfer device is disconnected from the at least one host device.

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.

A patient interface for delivering breathable gas to a patient includes a sealing portion including a nose tip engagement portion adapted to form a seal with the patient's nose tip, an upper lip engagement portion adapted to form a seal with the patient's upper lip and/or base of the patient's nares, and nostril engagement flaps adapted to form a seal with the patient's nares. The nose tip engagement portion, the upper lip engagement portion, and the nostril engagement flaps are all structured to extend or curve outwardly from a supporting wall defining an air path.

The invention relates to a method for anaesthetizing animals before slaughter, by the anesthetic action of gases or gas mixtures, operated in batch mode, in which the live animals, preferably put together in one or more cages, are placed in a lock chamber for treatment where the animals are brought into contact with anesthetic gas, following a cycle comprising several steps characterized by different contents of anesthetic gas, characterized in that at least one of the steps is carried out using gas recovered from the lock chamber and stored in at least one capacity (2, No. 1, No. 2 etc.) for temporary storage having a variable volume.

The present disclosure pertains to a pressure support system configured to adjust a pressurized flow of breathable gas delivered to a subject. The system is configured to simplify adjustments to humidity and/or temperature control and/or pressure support therapy that enhance the comfort level of the subject during therapy. The system is configured to generate output signals and/or determine various parameters related to the pressurized flow of breathable gas. The system is configured to receive feedback from the subject related to a comfort level of the subject during therapy and automatically adjust the pressurized flow of breathable gas and/or the predetermined therapy regime, provide feedback to the subject, and/or prompt the subject to make manual adjustments based on the output signals, the determined parameters, the feedback, and/or other information.

There is described a ventilator for providing breathable air to a patient. The ventilator includes an airbag defining a longitudinal axis, having a first end, a second end, and a foldable wall extending from the first end to the second end, and being movable from a decompressed state to a compressed state by moving the first end along the longitudinal axis relative to the second end. The wall has fold lines formed therein such that, during movement of the airbag from the decompressed state to the compressed state, the wall is folded along the fold lines. The fold lines define at least one polygonal surface portion of the wall. The ventilator further includes an actuator for driving compression and decompression of the airbag, and a controller for controlling the actuator.

A patient interface for sealed delivery of a flow of air to ameliorate sleep disordered breathing may include: a seal-forming structure to form a pneumatic seal with the entrance to the patient's airways; a positioning and stabilising structure to maintain the seal-forming structure in sealing contact with an area surrounding the entrance to the patient's airways; a plenum chamber pressurised at a pressure above ambient pressure in use; a connection port for the delivery of the flow of breathable gas into the patient interface; and a device positioned within a breathing chamber defined, at least in part, by the seal-forming structure and the plenum chamber, wherein the device divides the breathing chamber into a posterior chamber and an anterior chamber, and wherein the device comprises a plurality of apertures such that turbulence of the air in the posterior chamber is less than turbulence in the air in the anterior chamber.

Improved respiratory treatment systems are described e.g. for treatment of respiratory diseases and provision of respiratory therapy, together with components therefor. In one form, the technology relates to a positioning and stabilizing structure which includes a first headgear tube, a second headgear tube and a flow regulator. A flow regulator is provided to adjust the proportion of flow of respiratory gas to the first headgear tube and the second headgear tube. In another form, the technology relates to a patient interface configured to adjust the proportion of the supply of breathable gas that flows from a first flow path to a patient's first naris and from a second flow path to the patient's second naris. In yet a further form, the technology relates to improves conduits for respiratory treatment systems.