Abstract: A gas delivery conduit adapted for fluidly connecting to a respiratory gases delivery system in a high flow therapy system. In one embodiment, a nasal cannula includes a base portion defining a first therapeutic gas passageway, a nozzle disposed adjacent the base portion and defining a second therapeutic gas passageway, the first passageway being in gaseous communication with the second passageway and a conduit configured to facilitate sensing that has an inlet side that is independent of and axially spaced apart from an outlet side of the nozzle. The conduit inlet side can extend beyond the nozzle outlet side of the nasal cannula. Additionally, the nasal cannula has a feature adapted to prevent one of the conduit and the nozzle from creating a seal with a user's rare and a feature adapted to prevent one of the conduit and the nozzle from creating a seal with a user's nare.

Abstract: A patient interface for treating sleep disorder breathing includes a textile tube that also provides support for the seal forming structure. The textile tube includes an inner and outer layer that are joined along seams to form an air chamber or passageway. The textile tube can be pre-shaped so that the textile tube resiliently returns to a pre-determined shape prior to the introduction of pressurized air.

Abstract: A resuscitation bag (bag valve mask resuscitator or BVM or BVMR) or other similar ventilation device (for example: anesthesia bag) includes a structure that allows a selectable, and repeatable volume be delivered to patients. The reservoir of the BVMR is formed from elastic, gastight material in the form of an elongated hollow body, with an essentially circular cross section. A range of motion control (ROMC) structure controls, or selectively limits the range of motion or collapse of the elastic bag to limit or control the volume expelled from the bag to the patient.

Abstract: Distinctly keyed male-female couplers are pneumatically connected to medical ventilator by distinct lines carrying pulsatile gas or sensory signals. Ventilator-mounted female coupler has entranceway cavity and larger receiving cavity delimited by catch edge. Male fence-forming longitudinal winglets extend from sealing plate carry terminal end convexities which latch onto catch edge. Winglets move inward due to larger fence circumference than entranceway and seat on catch. Winglets placed in tension due to locking length less than entranceway span, then convert force into sealing compressive force between sealing plate and female tube end. Conjoining male tube bayoneted and sheathed by projecting female tube, resulting in another gas seal. Two compressive seals formed between male distal port and pneumatic line. Extending male key(s) on winglet insertable into matching female slots. Convexities block insertion of non-matching couplers set due to interference by convexities on female on entranceway edges.

Abstract: One aspect of the disclosure includes a respiratory valve apparatus. The respiratory valve apparatus may include: a housing having an inner chamber, an endotracheal tube connection port, a ventilator connection port, and a resuscitation bag connection port; and a piston assembly positioned within the inner chamber and including a piston having a first passageway and a second passageway through the piston, wherein the first passageway provides a first flow pathway between the endotracheal tube connection port and the ventilator or connection port when the piston is in a first position, and wherein the second passageway provides a second flow pathway between the endotracheal tube connection port and the resuscitation bag connection port when in a second position.

Abstract: A patient interface for delivering breathable gas to a patient includes a sealing portion adapted to form a seal with the patient and a support portion to which the sealing portion is mounted. A first headgear chord is connected to a first side of the support portion, and a second headgear chord connected to a second side of the support portion. Headgear is adapted to connect to the first and second headgear chords to secure the support portion to a head of the patient. At least one adjustment device on the support portion is adapted to selectively move the first and second headgear chords to tighten or loosen the headgear.

Abstract: A head-mountable flow generator is configured to deliver a flow of breathable gas at a continuously positive pressure with respect to ambient air pressure to a patient interface in communication with an entrance to a patient's airways including at least an entrance of the patient's nares, while the patient is sleeping, to ameliorate sleep disordered breathing. The flow generator includes a motor, an impeller assembly and housing that encases the motor and the impeller assembly. The housing is configured to be mounted on the patient's head and comprises an inlet to receive the flow of breathable gas and a pair of opposing outlets to deliver the flow of breathable gas. In addition, the impeller assembly is configured to pressurize the flow of breathable gas received from the inlet, and the housing is configured to convey the pressurized flow of breathable gas through both outlets.

Abstract: A respiratory flow therapy apparatus including a sensor module can measure a flow rate of gases or gases concentration provided to a patient. The sensor module can be located after a blower and/or mixer. The sensor module can include at least an ultrasonic transmitter, a receiver, a temperature sensor, a pressure sensor, a humidity sensor and/or a flow rate sensor. The receivers can be immersed in the gases flow path. The receivers can cancel delays in the transmitters and improve accuracy of measurements of characteristics of the gases flow. The receivers can allow for detection of a fault condition in a blower motor of the apparatus.

Abstract: A flexible positive airway pressure (PAP) mask body, frame, and cushion are described. The mask body includes prongs that insert through and act upon apertures of the mask frame to connect the mask frame to the mask body. An airtight seal may be created between the mask body and the mask frame by a ball and socket connector, of the mask frame, having an elongated portion that extends through and has an outer perimeter commensurate with an aperture located in the mask body. The mask body may be configured with elongated portions that extend from the mask body chamber and to ends of eye sockets of the user. Headgear may couple to end portions of the mask frame corresponding to the elongated portions of the mask body. When pulling pressure by the headgear, additional contact is created between elongated portions of the mask cushion and the user's face.

Abstract: A gas delivery conduit adapted for fluidly connecting to a respiratory gases delivery system in a high flow therapy system, the gas delivery conduit includes a first connector adapted for connecting to the respiratory gases delivery system, a second connector adapted for connecting to a fitting of a patient interface, tubing fluidly connecting the first connector to the second connector where the first connector has a gas inlet adapted to receive the supplied respiratory gas, one of electrical contacts and temperature contacts integrated into the first connector. The gas delivery conduit further can include a sensing conduit integrated into the gas delivery conduit, where the first connector of the gas delivery conduit is adapted to allow the user to couple the first connector with the respiratory gases delivery system in a single motion.

Abstract: Provided are a humidification device and a humidification system, the humidification device includes a desorption structure, where the desorption structure includes a first housing, a heating layer and a desorption metal organic framework (MOF) portion; the first housing is provided with an air inlet and an air outlet; the heating layer is arranged in an inner side of the first housing; the desorption MOF portion is arranged inside the first housing and attached to the heating layer, where a temperature of the desorption MOF portion is adjusted based on a temperature of the heating layer, and the desorption MOF portion is of a preset moisture. The humidification device provided by the present disclosure can realize precise control on the humidity of the air, and have the properties of ease of use, high capacity, portability and low cost.

Abstract: A respiratory mask connector and a respiratory mask. The respiratory mask connector is configured to connect a frame to a connection pipe. The respiratory mask connector has a connection face and a spherical face, the connection face being configured to be connected to the frame, and the spherical face being configured to be in ball-socket connection with a pipe head of the connection pipe. The connection face and the spherical face are respectively configured as either the outer wall surface of the respiratory mask connector or the inner wall surface of the respiratory mask connector. The respiratory mask connector can be used for a respiratory mask.

Abstract: In one embodiment, a nasal cannula is shaped to fit within a user's nares, where the nasal cannula includes at least one prong allowing high flow delivery of humidified gases and creates positive airway pressure in the patient's airway. The prongs have angled ends such that, in use, gases flowing through the prongs are directed to the user's nasal passages. The nasal cannula body is partially swivelling and preferably has a ball joint connector. In another embodiment the nasal cannula may have at least one flared end prong that preferably seals within a patient's nare.

Abstract: The present invention generally relates to systems and method for delivery of therapeutic gas to patients in need thereof using enhanced breathing circuit gas (BCG) flow measurement. At least some of these enhanced BCG flow measurements can be used to address some surprising phenomena that may, at times, occur when wild stream blending therapeutic gas into breathing gas that a patient receives from a breathing circuit affiliated with a ventilator. Utilizing at least some of these enhanced BCG flow measurements the dose of therapeutic gas wild stream blended into breathing gas that the patient receives from a ventilator can at least be more accurate and/or over delivery of therapeutic gas into the breathing gas can be avoided and/or reduced.

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 patient interface structure for delivery of respiratory therapy to a patient includes a cushion assembly that has an elastomeric piece with a mouth seal portion configured to seal around the patient's mouth and a nasal seal portion configured to seal against at least an underside of the patient's nose. The cushion assembly also has a cushion clip attached to the elastomeric piece and forms at least part of a plenum chamber with the elastomeric piece. The cushion clip is more rigid than the elastomeric piece. A front plate that is more rigid than the elastomeric piece and has a plurality of headgear attachment points is attachable to the cushion clip by way of a snap fit connection. A gas passage extends along a surface of the front plate and includes an inlet opening configured to connect to an air delivery tube or a connector for an air delivery tube.

Abstract: A positive air pressure delivery device includes a housing having an inhalation inlet, an inhalation outlet, and an interior cavity in fluid communication with the inhalation inlet and outlet. A pressurized fluid inlet includes an outlet orifice in fluid communication with the interior cavity between the inhalation inlet and outlet. A sound reducer baffle has a convex dome surface positioned downstream of and facing the outlet orifice in a spaced apart relationship therewith. One embodiment of the housings includes a body, an end cap and a baffle insert. In various embodiments, the positive air pressure delivery device may be used in combination with other therapy devices, including an OPEP and pressure indicator. A kit and method of using the device are also provided.

Abstract: A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient, the system including a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the pressurized respiratory gas is controlled by a microprocessor.

Abstract: An ultraviolet disinfecting cartridge system utilizes an ultraviolet disinfecting cartridge particularly adapted for coupling with a face mask that covers the nose and mouth or to the inhale and exhale tubing of a patient ventilator. The ultraviolet disinfecting cartridge includes multiple UV light emitters that emit UVGI light into the flow channel of the cartridge to neutralize or destroy pathogens. A plurality of baffles may be configured in the flow channel to create a serpentine airflow to increase pathogen exposure time to UV light. A photocatalyst material such as titanium oxide may be configured within the flow channel that is activated by UV light to increase disinfection. An ionizer may be configured proximal to the inlet to produce charged particles that provide disinfection. Any ozone produced may be mitigated by a catalytic converter to a safe level. Inlet and outlet filters may be detachably attachable to the ultraviolet disinfecting cartridge.

Abstract: A mask assembly can include a mask seal. In some configurations, the mask assembly can be configured to be fully positioned lower than a bridge of a nose of a face of a user and to provide an exposed bridge of the nose of the user. The mask seal can comprise a nasal region comprising at least one nasal opening, a first paddle on a first side of the nasal region and a second paddle on a second side of the nasal region. The first paddle is configured to contact one side of the nose of the user and the second paddle is configured to contact the other side of the nose of the user.