Abstract: A non-invasive ventilation patient interface comprises a fresh gas entry port, an exhaust gas vent port, and a filter media disposed in the exhaust gas vent port. The fresh gas entry port is configured for coupling with a fresh gas supply. The exhaust gas vent port is configured for allowing expulsion of exhaust gas from the patient interface in response to exhalation of a patient. The filter media is configured for filtering contagious from the exhaust gas, diffusing the exhaust gas, and controlling an expulsion flow of the exhaust gas through the exhaust gas vent port.

Abstract: An adapter assembly including a manifold and a valve assembly. The valve assembly includes a seat and a valve body having a circular base and a wall. The wall extends from a trailing side of the base to form a dome-like shape terminating at an end at which a slit is formed, with the wall defining opposing sealing edges at the slit. The seat has an upper circumferential surface and a lower circumferential surface. The upper surface engages a leading side of the base, whereas the lower surface engages a trailing side. At least one of the upper and lower surfaces forms a segment of increased height. Upon final assembly, the valve body is disposed across a passageway of the manifold, with the slit providing a selectively openable path. A force imparted by the segment of increased height flexes the base and biases the sealing edges into engagement.

Abstract: A non-invasive ventilation patient interface comprises a fresh gas entry port, an exhaust gas entry port, and a facial skin interface. Fresh gas entry port is configured for coupling with a fresh gas supply. The exhaust gas vent port is configured for allowing expulsion of exhaust gas from the patient interface. The facial skin interface is configured for eliminating fluid from within the patient interface and for eliminating fluid from facial skin which is covered by the patient interface.

Abstract: Described herein is a mask for delivery of gas, such as oxygen, to a patient and useable in a naso-gastric intubation procedure without disruption of the seal between the mask and the patient's face. The body of the mask includes a fenestration or opening through which the naso-gastric tube may be inserted. The fenestration is preferably shaped to support the tube in a manner that is comfortable for the patient and that eliminates or minimizes the amount of gas lost to the atmosphere outside the mask. In at least some embodiments, the fenestration is closed when a tube is not inserted therethrough so that the mask may be used normally without loss of the gas through the fenestration.

Abstract: A mask for patient ventilation comprises a frame portion, a front portion, a retention strap, and a gas delivery orifice. The frame portion is for surrounding a respiratory opening of a patient. The front portion is coupled with the frame portion and covers the respiratory opening region. The retention strap is for maintaining positive pressure between the frame portion and the patient. The gas delivery orifice is coupled with the frame portion and configured such that the gas delivery orifice is lateral to the front portion.

Abstract: A non-invasive ventilation patient interface comprises a fresh gas entry port, a frame, and a zygomatic facial interface. The fresh gas entry port is configured for coupling with a fresh gas supply. The frame is configured for coupling with a head strap system, wherein the head strap system is configured for supplying a securing force to secure the patient interface in a position over a respiratory opening of a patient. The zygomatic facial interface is coupled with the frame and configured for spreading the securing force away from a nasal bridge of the patient and onto left and right zygomatic arch regions of the patient.

Abstract: A control system for a high frequency oscillating ventilator (HFOV) includes an oscillator controller and a mean airway pressure (MAP) controller. The HFOV includes a reciprocating piston which is adapted to generate positive and negative pressure waves for delivery to a patient airway. The oscillator controller comprises a pair of closed loop control circuits including an oscillator pressure loop and a centering loop which are collectively adapted to regulate frequency and amplitude of piston reciprocations and centering of the piston. The MAP controller comprises a closed loop control circuit that is adapted for regulating MAP at the patient utilizing feedback in the form of patient circuit pressure. Likewise, the oscillator controller utilizes patient circuit pressure as well as piston displacement feedback in order to regulate movement of the piston.

Abstract: A carbon dioxide sensor for use in a respiratory therapy system. The carbon dioxide sensor determines whether a patient interface is fluidly coupled to a patient.

Abstract: A ventilation mask for sealing on a face of a patient comprises a nasal passage opener configured for facilitating in opening the nasal passage of the patient. The nasal passage opener is disposed over a nasal valve of the patient when the ventilation mask is sealed on the face of the patient.

Abstract: In a method for adjusting a ventilation mask, a ventilative state is measured of a ventilation mask that is placed over a respiratory opening of a patient. A sealing portion of the ventilation mask is for establishing a fluid seal between the ventilation mask and the patient. The sealing portion comprises a plurality of bladders. An unintentional leak of the fluid seal is determined based on a measured change of the ventilative state. A bladder of the plurality of bladders is adjusted to seal the unintentional leak.

Abstract: A retainer clip configured to engage a tubing member includes a base portion and a clamp portion which may be formed as a unitary structure. The base portion is generally disc-shaped and has a front side and a back side. The clamp portion is disposed on the base portion and extends upwardly from the front side and includes a spaced pair of clamp fingers which collectively define a slot that opens into a channel. The channel is adapted to frictionally engage the tubing member. The back side includes a layer of adhesive for adhering the retainer clip to the patient such as to the patient's skin. An interface assembly for delivering gas from a gas source to a patient includes a user interface, at least one tubing member extending from the user interface, and at least one of the retainer clips configured to anchor the tubing member to the patient.

Abstract: An integrated nasal mask is adapted for delivering gas to a patient and comprises a mask body and a pair of elongate nostril-engaging stems. The mask body is generally triangularly shaped and includes a nasal opening sized and configured to substantially envelope a patient's nose. The nasal opening opens to a nasal cavity. The nostril-engaging stems extend outwardly from the nasal cavity. Each one of the stems defines a fluid passageway for delivering gas to the patient's nose and for allowing discharge of exhalation gasses during the exhalation phase of the breathing cycle.

Abstract: A device for humidifying respiratory gases. The device includes: a humidification component that holds a water volume; and a heating element that converts received electrical energy to electromagnetic radiation, wherein the electromagnetic radiation is transferred to the water volume, thereby heating the water volume to achieve a heated water volume.

Abstract: To assess regional oxygen uptake and/or perfusion in a patient, a volume of air inhaled by the patient is determined and, according to a method of electrical impedance tomography, a first regional lung volume is measured at a first time point of a breathold procedure. The first regional lung volume is compared to a second regional lung volume at a second time point of the breathold procedure.

Abstract: In a mask for patient ventilation, a frame portion is included for surrounding a respiratory opening of a patient. A retention strap is coupled with the frame portion for maintaining positive pressure between the frame portion and the respiratory opening of the patient. A removable insert is configured to physically attach and detach from the frame portion without requiring removal of the frame or the retention strap from the patient.

Abstract: A metered dose inhaler (MDI) spacer has a body that defines a dose receiving chamber. A proximal end portion coupled between the body and a mouth port through which a metered dose may be inhaled by a user of the MDI spacer. A distal end portion is coupled with the body. A combined one-way and flow rate control valve coupled with the distal end portion is configured for permitting external airflow into and prohibiting internal airflow out of the dose receiving chamber. A collar coupled with the distal end portion is configured for receiving an actuator shaft of a metered dose inhaler and for forming a seal about an aerosol nozzle of the metered dose inhaler such that a metered dose of medication is admissible into the dose receiving chamber via the collar while airflow into and out of the dose receiving chamber via the collar is prohibited.

Abstract: A device for humidifying respiratory gases. The device includes: a humidification component that holds a water volume; and a heating element that converts received electrical energy to electromagnetic radiation, wherein the electromagnetic radiation is transferred to the water volume, thereby heating the water volume to achieve a heated water volume.

Abstract: A resuscitation device comprising a main housing, and an expiratory relief valve.

Abstract: A ventilation mask comprises a corrugated flexible seal, and a plurality of ridges disposed along the corrugated flexible seal. The corrugated flexible seal is configured for establishing a fluid seal between the ventilation mask and a patient, and for allowing facial movements of the patient while maintaining the fluid seal. The plurality of ridges disposed along the corrugated flexible seal is configured for physical contact with the patient.

Abstract: An nCPAP device for assisting patient breathing includes a generator body forming an inlet, a chamber, and first and second flow circuits. The chamber directs pressurized gas from the inlet to the flow circuits. The flow circuits each include a nozzle, a channel, and at least one port. The nozzle emits a jet stream into the channel in a direction of a patient side thereof. The port fluidly connects the channel to ambient, and promotes entrainment of ambient air with the jet stream. In some embodiments, the channel forms a ramp feature directing exhaled air toward the jet stream in an angular fashion. The generator body requires reduced driving pressures to achieve target CPAP levels and reduces total imposed WOB as compared to conventional designs.