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.

A personal airway humidification apparatus includes means for generating a heated air laden with gaseous (molecular) water. The personal airway humidification apparatus further includes an accumulator coupled to the generating means for retaining a volume of the gaseous water-laden heated air prior to being delivered by natural breathing to a user and a delivery tube coupled to the accumulator. The delivery tube has a sufficiently large diameter bore to enable the user's natural breathing to draw the gaseous water-laden heated air from the accumulator and through the delivery tube. The personal airway humidification apparatus also includes a one-way valve coupled to the delivery tube for venting exhalations of the user to atmosphere and preventing the exhalations from being exhaled back into the delivery tube and an interface device by which the gaseous water-laden heated air enters the user's mouth from the delivery tube.

A new innovative and unique solution to minimize the problems of mouth leakage using a CPAP machine is disclosed. A mouthpiece module is specifically designed to solve the problem of mouth leakage which compromises the therapeutic effect of CPAP treatment. The mouthpiece module comprises a flexible absorbent material which partially wraps around the lips and is secured to the back of the head by straps or an elastic band. In one embodiment, the mouthpiece is detachable from a securement strap.

An airway assist device (AAD) is provided. The device includes an upper AAD component and a lower AAD component. The upper AAD component includes and upper tooth guide connected to an upper plate having a pair of depending legs. The upper AAD component further includes an upper force receiving plate. The AAD also includes a lower AAD component. The lower AAD component includes a lower tooth guide connected to a lower plate. The lower AAD component further includes a lower force receiving plate. The upper and lower AAD components are connected in a way that allows relative longitudinal movement between the two components between a neutral position and a plurality of extended positions. A ratchet mechanism inhibits movement of the lower plate from any extended position toward the neutral position. The ratchet mechanism may be manually disengaged to allow the lower AAD component to return to the neutral position. An oxygen delivery housing may be connected to the upper plate to distribute oxygen.

A saliva collector comprises a reservoir, a bubble barrier, and a membrane, where the bubble barrier and membrane are arranged in tandem on a flow path from an inlet to an outlet on the reservoir. Air aspirated from a patient's oral cavity enters the reservoir through the inlet, passes through the bubble barrier to remove foam and bubbles, passes through the membrane to remove entrained liquid saliva, and passes out through the outlet.

A system for introducing vibrational waves into a body of a subject to treat sleep disorders is provided. The system includes a bed frame having a first vibration contact and a second vibration contact. The first vibration contact is in mechanical communication with a first location of the body of the subject, and the second vibration contact is in mechanical communication with a second location of the body of the subject. A first vibration source is connected to the first vibration contact and configured to cause a first vibration of the first vibration contact. A second vibration source is connected to the second vibration contact and configured to cause a second vibration of the second vibration contact. The location or orientation of the first vibration contact and the second vibration contact are configured such that the first vibration combines with the second vibration to generate a super-imposed vibration.

A respiratory assembly is provided. The assembly includes at least one post having a nasal engaging portion on about a first end thereof for delivering treatment gases to the nasal cavity of a patient. A pair of tubes capable of receiving gas from a hose or fluid source are selectively engaged with the pair of posts for delivering treatment gases from the inlet through the receptacle and into the nasal cavity of the patient. A splitter may be positioned between the hose or fluid source and the pair of tubes. Ball and socket joints may provide enhanced flexibility of the assembly while in use.

A respiratory acoustic device is provided that is easy to operate and transport. The device delivers vibrations artificially to the lungs and airways to fluidize mucus adhering to the airways and promote its discharge. A respiratory acoustic device 1 is provided with a housing 10, and a mouthpiece 20 that is in communication with the housing 10. The housing 10 has a reflecting end 12 for reflecting air that has been blown in from the mouthpiece 20 and an open end 13 through which air that has been blown in from the mouthpiece 20 can escape. If a sudden exhalation such as a cough is blown into the housing 10 through the mouthpiece 20, the device causes the noise due to said exhalation to resonate with the oral and lower airway cavities, and vibrate the user's lungs and airways with the low frequency acoustic shock waves generated therein.

A system for introducing vibrational waves into a body of a subject to treat sleep disorders is provided. The system includes a bed frame having a first vibration contact and a second vibration contact. The first vibration contact is in mechanical communication with a first location of the body of the subject, and the second vibration contact is in mechanical communication with a second location of the body of the subject. A first vibration source is connected to the first vibration contact and configured to cause a first vibration of the first vibration contact. A second vibration source is connected to the second vibration contact and configured to cause a second vibration of the second vibration contact. The location or orientation of the first vibration contact and the second vibration contact are configured such that the first vibration combines with the second vibration to generate a super-imposed vibration.

A method and system of responding to adverse environmental conditions local to a user of an oxygen concentrator is disclosed. Physiological data of the user is collected. Operational data of the oxygen concentrator is collected during operation of the oxygen concentrator. Environment data local to the oxygen concentrator is collected. Based on the collected environmental data, it is determined whether adverse environmental conditions exist local to the oxygen concentrator. The collected physiological, operational, and environmental data are analyzed to determine a responsive action to the determined adverse environmental conditions. The responsive action is communicated to the user.