A patient interface (1) is for aerosol treatment, having a base (2) to surround the patients mouth and nose and engage the skin with a resilient seal, and with a strap (8) to attach to a patients head. There is a support (3) on and across the base for supporting an aerosol delivery head with prongs (4, 5). An enclosed volume is formed in the interface by attachment of a shell (10), which has an extraction port (11) for attachment of an extraction system (20) to extract gas from this volume. An HFNT system includes a patient interface surrounding the nose and mouth and an aerosol delivery apparatus (4, 6), an extraction apparatus (20), and a controller (100) to control delivery of aerosol and/or gas to the interface and to extract gases from a volume enclosed by the interface. Because of the fully sealed volume within the interface there are a wide range of control scenarios possible, using pressure sensing in the volume, bypass valves (201), dynamically-controllable nebulizer (203).

A system and method for performing a bronchoscopy. The system may include a bronchoscope, a multi-fluid conduit apparatus, and a switching apparatus. The bronchoscope may include an insertion tube having a distal end, a control section, and a working channel. The multi-fluid conduit apparatus may include a first conduit section operably coupled to a vacuum source, a second conduit section operably coupled to an oxygen source, and a third conduit section operably coupled to the working channel, each of the first and second conduit sections being fluidly coupled to the third conduit section. The switching apparatus may include a valve apparatus operably coupled to each of the first and second conduit sections and an actuator apparatus operably coupled to the valve apparatus. The actuator apparatus may alter the valve apparatus between: (1) a suction supply state; and (2) an oxygen supply state.

A gas delivery system and method are provided that include a therapeutic gas delivery device, and a high-frequency ventilator delivering a breathing gas to a respiratory circuit. The therapeutic gas delivery system also includes a flow sensor assembly having a single interior chamber. The flow sensor assembly includes a flow sensor connected with the therapeutic gas delivery device and configured to measure a flow rate of the breathing gas. The flow sensor has a sensor gas inlet and a sensor gas outlet. The flow sensor assembly further includes a one-way flow valve disposed downstream of the sensor gas outlet. The one-way flow valve includes a valve gas inlet and a valve gas outlet. Inner diameters of the valve gas inlet and the valve gas outlet are greater than or equal to an inner diameter of at least one of the sensor gas inlet and the sensor gas outlet.

A breathing assistance device with improved pressure characteristics provides a high level of CPAP per unit of supplementary respirable gas consumed while maintaining low CPAP fluctuations throughout the breath cycle utilizing a frustrum-shaped air channel to accelerate air flow. In some embodiments, a manometer is provided for monitoring pressure and/or a pressure relief valve is provided as a safety measure against overpressure delivered to a patient. In some embodiments, the device is disposable for one-time or single patient use.

A medical device measures a pressure of a pressurized breathing gas and includes a pressure sensor arranged at a point of measurement and measures the pressure of a sample gas at a sampling point. The sampling point and the point of measurement are connected by a pressure sampling tube in which a pressure wave of the sample gas can propagate from the sampling point to the point of measurement. The tube has a sampling tube volume and an acoustic impedance. The device further includes a damping arrangement fluidly communicating with the tube. The damping arrangement includes a flow restrictor and a receptor chamber arrangement. The receptor arrangement includes a receptor chamber which receives the pressure wave. The restrictor correlates to the acoustic impedance to prevent acoustic resonance in the tube. The receptor chamber correlates at least to the tube volume to prevent acoustic resonance in the tube.

Several methods of supporting respiratory function of a patient before, during and/or after a medical procedure are disclosed. In certain arrangements, supporting respiratory function while a patient is under general anaesthesia can include providing a high gas flow that is greater than 15 L/min while the patient is under general anaesthesia. In certain arrangements, a method of providing ventilation while a patient is under general anaesthesia involves providing only a gas flow delivered through a nasal interface that is greater than 15 L/min while the patient is under general anaesthesia.

The present invention relates to a respiratory therapy device (1) for the targeted assistance of a secretion removal from the airways of a patient and a method for operating such a respiratory therapy device (1). The respiratory therapy device (1) comprises a flow unit (2) for generating a respiratory airflow for an insufflation and a respiratory airflow for an exsufflation, which comprises a patient interface (3) for connecting the patient and a respiratory air interface and two fans (5, 6) fluidically connected in parallel each having an intake side (15, 16) and a delivery side (25, 26). A first fan (5) is fluidically coupled with its intake side (15) and a second fan (6) is fluidically coupled with its delivery side (26) to a switchable valve unit (7).

A portable system for delivery of humidified high flow nasal cannula therapy includes a portable system housing, a respiratory circuit positioned within the housing comprising an ambient air conduit and an oxygen conduit merging downstream into a blended air conduit, an air pump positioned within the housing and connected to an upstream end of the ambient air conduit, configured to transfer ambient air into the ambient air conduit, an oxygen supply connection element connected to an upstream end of the oxygen conduit and configured to connect to an oxygen supply, a humidification chamber connected to a downstream end of the blended air conduit and an upstream end of an air output conduit, and a humidification chamber seating portion connected to the housing and configured to seat the humidification chamber, where the humidification chamber seating portion comprises a sterilization light source.

A breathing assistance device with improved pressure characteristics is capable of providing a high level of CPAP per unit of supplementary respirable gas consumed while maintaining low CPAP fluctuations throughout the breath cycle. The invention also includes a manometer for monitoring pressure and a safety pressure relief valve as additional safety measures against overpressure delivered to a patient. In some embodiments, the device is disposable for one-time or single patient use.

A pulsed oxygen delivery system is disclosed for a closed breathing environment, which includes a source of gaseous oxygen, a phase dilution type oronasal dispensing mask worn by a user in a closed breathing environment defined by a pressure suit, and a pulse control module for delivering a timed and metered bolus of oxygen from the source of gaseous oxygen to the oronasal dispensing mask upon inhalation by the user.