Abstract: A patient interface device includes a bladder assembly having a headgear bladder member, a nose bridge bladder member, and a connecting tube member provided between the headgear bladder member and the nose bridge bladder member. The headgear bladder member is in sealed fluid communication with the nose bridge bladder member through the connecting tube member, and is filled with a fluid medium. The bladder assembly is structured such that the nose bridge bladder member will be inflated as a pressure on the headgear bladder member increases and such that the nose bridge bladder member will be deflated as the pressure on headgear bladder member decreases. Inflation of the nose bridge bladder member causes the top of a cushion member to move toward the patient's nose bridge, and deflation of the nose bridge bladder member causes the top of the cushion member to move away from the patient's nose bridge.

Abstract: A mask assembly includes a mask with an inflatable bladder. The internal pressure of the inflatable bladder can be set to be higher than the delivered therapeutic pressure. The pressure offset may be constant, or it may vary over the range of therapeutic pressures. Thus, the force necessary to maintain a contact seal between the mask and the patient can be reduced, thereby providing a system that is more comfortable to the patient, which increases patient compliance.

Abstract: A nebulizer with a negative pressure structure includes a nebulization body, a carrying cavity, a nebulizing element and a negative pressure generating element. The carrying cavity is provided for carrying a nebulized liquid and has a through hole. The nebulizing element is installed at the through hole and includes a piezoelectric driving unit and a nebulizing plate disposed on a side of the piezoelectric driving unit. The negative pressure generating element is formed on the carrying cavity and provided for changing the volume of the carrying cavity or removing air from the carrying cavity to reduce the air pressure in the carrying cavity, so as to nebulize a liquid of low surface tension or high viscosity effectively.

Abstract: A mask for delivery of respiratory therapy to a patient may include one or more of the following improvements: rigidizer provided to headgear strap, locking clip/clip receptacle headgear connection, keyed headgear buckles, lotion dispenser on frame, rotatable prongs to adjust orientation, alignment indicators provided to prong, cushion and/or frame, chin flap with bellows arrangement, vent holes positioned away from gas entry port, and vent holes to direct washout gas at an angle.

Abstract: An aerosol inhalation device assembly for diagnostic and therapeutic use for deep lung alveolar aerosol targeted drug delivery includes a nebulizer for generating an aerosol containing droplets of a liquid. The nebulizer has a pressurized gas inlet and a nebulizer outlet. An inhalation chamber is in fluid communication with the nebulizer outlet. The inhalation chamber is defined by at least one sidewall. An inhalation mouthpiece assembly is in fluid communication with the inhalation chamber and extends outwardly from the at least one sidewall of the inhalation chamber. A filter assembly is in fluid communication with the inhalation chamber. The filter assembly includes a filter medium. An exit port is in direct fluid communication with the filter assembly. A method of using the nebulizer is also provided.

Abstract: A method and apparatus for automatically controlling partial pressure of oxygen in the breathing loop of a rebreather diving system. A diver may adjustably select a control parameter to maintain partial pressure of oxygen at a setpoint that varies with ambient pressure and is within a range between a maximum safe partial pressure of oxygen at depth and a minimum safe partial pressure of oxygen for the purpose of biasing the performance of the rebreather either towards minimizing gas venting from the rebreather breathing loop or minimizing decompression time. A method and apparatus for managing and monitoring the use of dive resources in comparison with a target dive time specified by the diver, calculating and indicating remaining dive time based on dive resource values and calculating and indicating dive resource values required to meet preselected dive resource end values and dive requirements.

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: A mask assembly for use as part of an apparatus for supplying a flow of respiratory gases to a user is disclosed. The mask assembly includes a mask body having an inlet through which said flow of respiratory gases are provided to the interior of said mask body. A mask seal assembly comprising a seal of flexible material and a clip of rigid material is attached to the body. The seal has a first side and a second side. The first side of the seal is shaped to approximately match the contours of a user's face and in use substantially seal against a user's face. The second side is attached to the clip. The clip provides an interface extending substantially the full perimeter or periphery of the mask seal assembly for releasably attaching the mask seal assembly to the mask body. The clip comprises a bridging portion spanning outwards from the perimeter or periphery of the mask body to space at least a portion of the second side of the seal outwards from the perimeter or periphery of the mask body.

Abstract: An apparatus, method and system for delivering CO2 into an inspiratory gas stream to formulate a blended respiratory gas in a manner that continuously maintains a target CO2 concentration in a volume of the inspired respiratory gas, for example, over the course of a breath or a volumetrically definable part thereof or a series of partial or full breaths.

Abstract: An endotracheal tube for mechanically ventilating patients is disclosed. The endotracheal tube comprises a distal end for insertion into the patient's airway, past the vocal chords, through the subglottal region, and into the patient's lung; and a proximal end for connection to a mechanical ventilator. The endotracheal tube further comprises a cuff at the distal end of the endotracheal tube to be located in the subglottal region of the patient below the vocal chords, an inflating lumen for inflating the cuff, and a suction lumen having a suction inlet port leading from the outer surface of the endotracheal tube, and to be located in the subglottal region, for evacuating secretions and/or rinsing fluid from the subglottal region during the mechanical ventilation of the patient.

Abstract: The present invention provides a system and method for supplying, generating, conserving, and managing oxygen that is ideally suited for use on-board an aircraft for supply of breathable oxygen to passengers and flight crew. The system includes several components that together optimize oxygen utilization while reducing costs from maintenance and added weight of traditional pressurized gaseous cylinders. Components of the system include a pressurized cylinder of oxygen enriched gas or a chemical oxygen generator for rapid use in emergency situations, an on-board oxygen generator (OBOG) of the ceramic oxygen generator (COG) type incorporating solid electrolyte oxygen separation (SEOS) technology, a controller, a pulsed oxygen supplier, a crew/passenger breathing mask, and one or more sensors including sensors that detect inhale/exhale phases and communicate with the controller so that flow of oxygen may be regulated for conservation and to adapt to physiological needs.

Abstract: A uterine contractile device includes a series of perforated tubes, a sealing balloon, and an additional connecting tube to deliver a vacuum force inside the lumen of a postpartum uterus. The uterine contractile device may be used after child birth to facilitate contraction of a woman's uterus. By facilitating contraction of the uterus, a medical professional may achieve immediate and sustained hemostasis of the mother.

Abstract: A nebulizer dispenser has a T-piece, a body sealingly coupled to the T-piece and configured to contain a liquid medication, and a breathing piece sealingly coupled to the T-piece. The dispenser also has a ball-and-socket joint coupled between the T-piece and either the breathing piece or the body. The ball-and-socket joint allows relative rotational motion of the T-piece in a pitch axis, a yaw axis, and a roll axis.

Abstract: An active inhaler for delivery of an inhalation formulation has an overall flow resistance of at least 60,000 Pa1/2 s/m3 for ambient air drawn into a mouthpiece of the inhaler. This flow resistance when air and the aerosol are sucked via the mouthpiece is produced by the sizing of at least on air supply opening and/or an insert within the mouthpiece.

Abstract: The invention concerns a breathing assistance apparatus having a source of Nitric Oxide in fluid communication with a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: A dose indicator device for a pressurized metered dose inhaler comprises an inner wheel, annular outer wheel, actuator and housing; the inner wheel comprising primary indexing teeth and a flexible drive arm; the outer wheel comprising secondary indexing teeth on an outer face of the outer wheel; the inner wheel and outer wheel located at least partially within the housing such that the inner wheel and outer wheel are rotatable about a common longitudinal axis of rotation; the actuator movable in a plane perpendicular to the axis of rotation to engage the primary indexing teeth to rotate the inner wheel; the housing being fixed relative to the axis of rotation and comprising a deflector; the deflector configured such that, on rotation of the inner wheel, the drive arm is intermittently deflected and brought into contact with the secondary indexing teeth to rotate the outer wheel about the axis of rotation.

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: The system and method of the present application predicts if there is sufficient CO2 absorbent capacity for the next anesthesia case. If insufficient, the canister can be preemptively replaced when no patient is connected to the breathing system. Such prediction also allows clinicians to determine if the CO2 canister has to be changed during the present case or to wait until the end of the case. In the latter, the clinician may buy time by increasing the fresh gas flow rate to reduce the amount of patient CO2 gases recirculated. A predictive estimation of CO2 breakthrough allows more time to prepare for an orderly CO2 canister replacement during a quiet period in the anesthesia care.

Abstract: A patient interface device includes a patient sealing assembly adapted to communicate a flow of breathing gas within an airway of a patient, a fluid coupling conduit fluidly coupled to the patient sealing assembly, the fluid coupling conduit being structured to receive the flow of breathing gas and communicate the flow of breathing gas to the patient sealing assembly, and a headgear component structured to secure the patient interface device to the patient's head, the headgear component including a strap member having a generally C-shaped connector member. The generally C-shaped connector member is structured to at least partially wrap around and be releasably received and held by or within a receiving feature provided on one of: (i) the fluid coupling conduit, and (ii) an extension member extending outwardly from the patient sealing assembly.

Abstract: A patient interface system for delivering a gas to a patient includes a patient interface device that includes at least one inhalation valve and at least one exhalation valve. The system also includes a venturi device that has at least one port for connection to a gas source. The venturi device has at least one primary air entrainment window and at least one secondary air entrainment window which is downstream of the at least one primary air entrainment window. The inhalation valve is disposed between: (1) the main body and (2) the primary and secondary air entrainment windows of the venturi device. At least one of the primary air entrainment window and secondary air entrainment window includes a means for closing the respective window, thereby changing a degree at which the respective window is open and changing a flow rate of the air flowing through the respective window.