Abstract: A patient interface cushion and specifically a patient interface cushion with fabric, configured to supply pressurized breathing gas to the nasal and oral airways of a user. The patient interface cushion includes a rigid part, configured to support the elastic part, featuring a first opening and a second opening; The elastic part, configured to provide an attachment surface for the fabric part, featuring a third opening in communication with the second opening and a fourth opening allowing the user's nose and mouth to enter the internal cavity of the elastic part. The fabric part, configured to form a sealing area between the lower lip area and the nasal bridge area, featuring a first surface partially connected to the elastic part, a second surface sealing at least a portion of the user's face, and also having an inner edge and an outer edge.

Abstract: A patient interface assembly with optimized connection methods and improved air-tightness. The patient interface assembly forms a complete channel to deliver positive pressure air when connected with an air supply tube and a ventilator. The patient interface assembly includes a patient interface pad, a frame, an elbow assembly, and a quick-release connector. The patient interface pad is fixedly connected to one end of the elbow assembly. The frame is positioned between the elbow assembly and the patient interface pad. The other end of the elbow assembly is connected to the quick-release connector. By reducing the connection steps between parts, the air-tightness of the patient interface assembly is enhanced, and the patient interface assembly is adaptable to various types of frames.

Abstract: Positive airway pressure (“PAP”) systems and methods are provided which supply a patient with a range of pressures for treatment when the patient is determined to be asleep, and an awake pressure for use when the patient is determined to be awake, the awake pressure configured for the comfort of the patient. The awake pressure is configured to be lower than the lower bound of the pressure range and can be a therapeutic or sub-therapeutic pressure. The PAP systems and methods disclosed herein advantageously allow for the pressure range to be tailored for effective treatment of sleep disordered breathing while allowing the awake pressure to be set for the comfort of the patient. This can advantageously increase both the efficacy of the treatment of SDB and patient compliance with the treatment.

Abstract: The breathing assistance apparatus of the present invention includes a manifold that is provided with or retrofittable to gases supply and humidifying devices. The manifold allows gases from an oxygen concentrator to be combined with the flow through a gases supply and humidifying device, most usually air. The combined output of oxygen and other breathing gases (air) is then humidified. The breathing assistance apparatus and manifold of the present invention provides a safe method to add oxygen to the input air stream of a gases supply and humidifying device and reduces the amount of accumulation of oxygen within the gases supply device, reducing fire risk should sparking occur within the device.

Abstract: An inhalation system including a fluid transfer member, a valve member, a cartridge assembly, and a mouthpiece, and a method of use thereof are provided. The valve member connects to an open end of the fluid transfer member. The cartridge assembly, positioned within the valve member, includes a substance holder and an absorbent member accommodated within a cartridge for containing and absorbing an inhaling substance. When the valve member connects to a vaporizer, the vaporizer heats the absorbent member to vaporize and release an inhaling fluid into the fluid transfer member. When the valve member connects to the mouthpiece, the valve member receives and transfers the inhaling fluid vapor from the fluid transfer member to a user's mouth via the mouthpiece. The locking mouthpiece assembly allows authentication of the user prior to releasing the inhaling fluid to the user's mouth.

Abstract: A respiratory treatment device includes a housing enclosing a chamber, a chamber inlet configured to receive a flow of air into the chamber, a first chamber outlet configured to permit the flow of air to exit the chamber, and a second chamber outlet configured to permit the flow of air to exit the chamber. A vane mounted within the chamber is configured to rotate between a first position where the flow of air is directed to exit the chamber through the first chamber outlet, and a second position where the flow of air is directed to exit the chamber through the second chamber outlet. A blocking member disposed on the vane is moveable relative to the chamber inlet between a closed position where the flow of air through the chamber inlet is restricted, and an open position where the flow of air through the chamber inlet is less restricted.

Abstract: A ventilator system includes a ventilator and a host. The ventilator comprises a ventilation drive configured to drive ventilation gas from a gas source to a patient and a patient interface section configured to guide inspiratory gas along an inspiratory path from the ventilation drive to a patient connection, and guide expiratory gas along an expiratory path from the patient connection out of the ventilator. The patient interface section is configured to releasably connect to the ventilation drive. The ventilator is configured to removably connect to the host such that at least one of the inspiratory path and the expiratory path are diverted through the host when the ventilator is removably connected to the host.

Abstract: A clear, soft and malleable plastic constructed face mask is provided that has an elastic strap that is used to secure the mask onto a patient's face. The mask comprises of a malleable aluminium strip on the top for easy molding of the mask around the patient's nose; a front opening covered with a paper filter; and two side openings covered with a paper filter. The mask provides supplemental oxygen through connection to a Y-shaped respiratory/ventilator circuit or standard oxygen tubing. The mask also allows the patient to breathe comfortably without a supplemental oxygen source. It has ribbed tubing for gas sampling. The mask allows a health care employee to visualize breathing on the clear plastic material. The mask provides filtration of aerosolized contaminants.

Abstract: A nostril-shielding nasal mask includes a body including a top portion provided with an arcuate anterior section and arcuate posterior section engaged therewith, a hinge attached to the top portion, a bottom portion attached to the hinge and including a apertures aligned with the nostrils of the user, a scented and/or odor neutralizing air filter removably inserted into the bottom portion, and fasteners attached to the top portion and the bottom portion wherein the fasteners are configured to maintain the top portion and the bottom portion directly abutted against the nose bridge of the user and the nostrils of the user. The fasteners maintain the bottom portion at a first raised, non-operating position and a second lowered, operating position. The arcuate anterior section is engaged with the bottom portion when the bottom portion is disposed at the second lowered, operating position.

Abstract: Disclosed are an apparatus and a method for monitoring the disconnection of a patient interface system during the ventilation, in which values which are indicative for the time curve of the respiratory gas flow are established and subjected to data evaluation, and wherein an alarm is triggered on the basis of the data evaluation if at least one value which is indicative for the time curve of the respiratory gas flow deviates from a specific limit value for a specific period of time.

Abstract: A patient interface system for delivery of a supply of air at positive pressure to the entrance of a patient's airways for treatment of sleep disordered breathing includes an air delivery tube connected to a flexible portion of a plenum; a vent structure having sufficient rigidity to support its own weight under gravity and/or not to block or fold under tube movement or tube drag; and a patient interface structure. The patient interface structure includes a seal forming structure arranged on a top portion of the plenum; and a seal positioning and stabilizing structure connected to a flexible portion of the plenum. The seal-forming structure is substantially decoupled from a tube drag force.

Abstract: Described is a method of stimulating airways of a mammal comprising: cyclically occluding a nasal air stream at a frequency rate between 50 Hz to 650 Hz. Also described is an apparatus for stimulating airways of a mammal, comprising: a fluid connection to each of a first and second naris of the mammal; and an occluding device configured to cyclically occlude a nasal air stream within each fluid connection at a frequency rate between 100 Hz to 650 Hz.

Abstract: A nasal breathing and ventilation device, includes ventilation tubes. One end of each ventilation tube is provided with a nasal dilator. Each nasal dilator includes a nasal dilator channel and a plurality of dilator rings. One end of each nasal dilator channel is provided with a through hole. Each nasal dilator is supported and fixed in the nasal cavity by means of the dilator rings thereof, and is not easy to fall out. The end of each nasal dilator channel away from the through hole is in communication with each ventilation tube. The tube wall at the end of each ventilation tube close to the nasal dilator is provided with ventilation holes. The end of each ventilation tube away from the nasal dilator is connected to a ventilator, and the ventilator conveys air into the nasal cavity at a certain pressure.

Abstract: A respiratory mask can include one or a plurality of force sensors configured to detect a force imparted to a user's skin. Output from the one or more sensors can be represented in a way useful to the patient or healthcare provider for adjusting the mask to achieve a desired fitment. A representation of the detected forces can be displayed on a separate display device or on the mask.

Abstract: Systems and methods for a manually operable volume-adjustable ventilation device. In some embodiments, the device includes a reservoir with an inlet mechanism, an outlet mechanism, and a volume adjuster configured to move a volume adjustment limit of the reservoir and change an expressed maximum volume of the reservoir. The reservoir may have a body comprising a plurality of movable walls defining an enclosed volume. The walls of the reservoir may be movable such that movement expresses the volume adjustment limit of the reservoir. In addition, the walls may be operably connected by movable structures such that two adjacent walls are be configured to rotate around substantially orthogonal axes with respect to each other when the reservoir moves from an uncompressed to a compressed state. Methods of ventilating a patient that involve the manually operable volume-adjustable ventilation device are also disclosed.

Abstract: A patient interface for use in delivering a flow of a breathing gas to an airway of a patient includes a body that defines a cavity therein that is structured to receive the flow of breathing gas. A first aperture defined in the body is positioned and structured to communicate the flow of breathing gas from the cavity to an airway of the patient. A second aperture defined in the body is sized and configured to provide a pathway between the cavity and an ambient environment in which the body is disposed. The patient interface further includes a restrictor element that is selectively coupled to the body. The restrictor element includes a blocking portion that obstructs at least a portion of the second aperture.

Abstract: The breathing assistance apparatus of the present invention includes a manifold that is provided with or retrofittable to gases supply and humidifying devices. The manifold allows gases from an oxygen concentrator to be combined with the flow through a gases supply and humidifying device, most usually air. The combined output of oxygen and other breathing gases (air) is then humidified. The breathing assistance apparatus and manifold of the present invention provides a safe method to add oxygen to the input air stream of a gases supply and humidifying device and reduces the amount of accumulation of oxygen within the gases supply device, reducing fire risk should sparking occur within the device.

Abstract: A nasal delivery device for and method of delivering substance to the middle meatus in a nasal cavity of a subject in the treatment of a condition, in particular an inflammatory or infectious condition, thereof, the delivery device comprising: a nosepiece unit (17) including a nosepiece (20) for fitting to a nostril of a subject and a nozzle (25) through which substance is in use delivered to the respective nasal cavity; and a delivery unit (29) for delivering substance through the nozzle of the nosepiece; wherein the delivery device is configured to provide for deposition of a significant fraction of the delivered dose on, around and in the vicinity of the middle meatus.

Abstract: Method and apparatus varies the oxygen concentration level of air delivered to a person for treatment on training purposes. The apparatus includes a display device for displaying current physiological data as well as data from previous sessions for comparison purpose. The oxygen level is precisely controlled by a central processing unit in response to input data from the person.

Abstract: A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patient's face surrounding the entrance to the patient's airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.