Abstract: A system of treating atelectasis is provided that includes a tracheal tube positioned within an airway of a ventilated patient and an acoustic sensor coupled to the tracheal tube. The system also includes a monitor communicatively coupled to the acoustic sensor. The monitor includes a processor configured to receive a baseline signal from the acoustic sensor. The processor is configured to provide control instructions to adjust a pressure of a gas mixture delivered to the airway through the tracheal tube. The processor is also configured to receive an updated signal from the acoustic sensor after the adjustment and identify a change in airway openness of lungs of the ventilated patient caused by the adjustment of the pressure. Further, identifying the change is based on the baseline signal and the updated signal.

Abstract: Methods for curing early stages of, and preventing upper respiratory infections and applicators therefor are disclosed. One embodiment of the invention comprises using an applicator capable of generating a mist with the same predetermined effective formula concentration and average droplet size but at two flow volume levels. In accordance with the method of the invention, the flow volume is alternated between high and low flow levels as the applicator is used to treat the entire upper respiratory tract in a series of steps.

Abstract: A humidifier tub includes a first side having an air inlet opening configured to receive the pressurized flow of respiratory gas. A second side opposes the first side. An air outlet opening is configured to discharge the pressurized flow of respiratory gas with added humidity. An inlet passage extends from the air inlet opening toward the second side so that the pressurized flow of respiratory gas travels through the inlet passage in a first direction. A guidance structure is located between the first and second sides and positioned so that a traveling direction of the pressurized flow of respiratory gas changes from the first direction to a second direction upon the pressurized flow of respiratory gas engaging the guidance structure. The guidance structure extends downward from a lid. In addition, the first direction is a lateral direction and the second direction is a downward direction.

Abstract: A ventilator with integrated breathing air humidifier has at least two defined air pathways provided in the breathing air humidifier. The breathing air humidifier is installed and fixed on a horizontal surface of the ventilator. The breathing air humidifier comprises at least a top part and a bottom part, a water reservoir being provided in the bottom part, wherein the top part cannot be removed from the bottom part when the unit is in at least one operating mode. The ventilator may have an air humidifier with at least one water reservoir, and at least one filling device for the water reservoir in the breathing air humidifier, wherein the filing device can be operated with one hand and/or opened with one hand.

Abstract: A device for regulating breathing gas delivered to a user, comprising a gas circuit comprising a main line having at least an upstream end intended to be connected to at least one gas source and a downstream end intended to be connected to at least one user station such as a mask, the main line comprising at least one electromechanical control valve configured to regulate the gas pressure between the upstream and the downstream, the circuit comprising a secondary line comprising an upstream end intended to be connected to at least one gas source and a downstream end intended to be connected to the same user station(s), the secondary line comprising at least one auxiliary member for regulating the gas flow, the device comprising a switching system configured to control the flow of gas between the upstream and the downstream of the circuit via the main line or via the secondary line, characterized in that the auxiliary member for regulating the secondary line is a pneumatic pressure regulator.

Abstract: A mask protecting the user and attached or sown to utility and or wear onto the body to prevent general contamination of the user, especially dust, flu, biological, or chemical, control or terminate person to person contamination, stop continue body or utility recontamination and spreading of dust, biological or chemical agents into the body, or utility. The new mask may include a medical or anti bacteria disinfectants, maybe powder, liquid, capsule or other types to control and kill germs, further the new mask have a holder, with plurality of holes, and connectors and or interconnector holding the masks to the body or utilities, like professional garment or uniforms, neck tires, T shirt, shirts, seat, car seat, bed, ear, chin, head, hand, while covering the users, faces, or half faces, particularly, the nose, eyes and the mouth from harm.

Abstract: A patient ventilating (23) and aspirating system (8) is disclosed that has a suction tube (9) and connector (6) for connecting to a catheter mount that has a sealed passageway (15) The catheter mount passageway (15) is sealed with an elastomeric seal (16) including a perforation or slit (17). A connector (12) with a piercing member is associated with the suction tube (9). When the connector is attached to the catheter mount the piercing member (20) pierces the seal (16) such that the suction tube (9) can pass through the connector (6) and catheter mount.

Abstract: The present disclosure pertains to a system and method for monitoring lung disease in a patient that is based on information that is derivable from home therapy devices including a ventilation therapy device and an oxygen saturation monitor such as a pulse oximeter. The measured parameters are used to model shunt fraction and a volume of dead space. Based on changes in gas exchange and results of a nitrogen washout test, a change in gas exchange impairment in the patient is observed and is then used to determine progression of a disease, identify a cause of the impairment, and/or to guide treatment of the patient.

Abstract: A gas-washout vent includes a housing with a first wall with one or more passages through the wall configured to provide fluid communication with a portion of the patient interface system exposed to a therapy pressure. The passages include respective first openings on a first surface of the first wall. The housing at least partially defines a second opening in communication with ambient atmosphere. A diffusing material is located at least partially within the housing to be adjacent the first surface. A surface of the diffusing material facing the first surface is spaced away from the first surface by a gap that extends to provide a fluid communication between all of the first openings and between all of the first openings and the second opening. The housing is configured so that air is prevented from flowing out of the housing at all areas directly opposite each of the first openings.

Abstract: A portable oxygen-air blender including a gas distributor valve, a plurality of venturi valves, and an oxygen monitor. The gas distributor valve selectively routes the flow of oxygen from a compressed gas reservoir into one of several venturi valves to be blended with atmospheric air in a predetermined ratio. The blended oxygen-air mixture may be safely delivered to neonatal patients who require a specific concentration of oxygen to breathe. A monitoring system allows the user to verify concurrently that the patient is receiving the correct blend of oxygen and make adjustments to the patient's treatment.

Abstract: A medication infusion device includes a pre-filled medication container containing sterile liquid medication. The medication infusion device also includes an infusion needle and the infusion needle has a distal end, wherein the distal end of the infusion needle is movable relative to the pre-filled medication container. There is a pierceable elastomeric component arranged at the distal end of the infusion needle to define a sterile environment, and this sterile environment is shared by the pre-filled medication container and the distal end of the infusion needle. The distal end of the infusion needle is embedded in a pierceable elastomeric component in order to keep the infusion needle enclosed in the sterile environment and prevent medication from flowing out of the infusion needle.

Abstract: An embodiment of the present invention provides a mask, ventilation therapy equipment and a method executed based on the ventilation therapy equipment, and belongs to the field of ventilation therapy equipment. The mask comprises a mask body, acquisition units and output units, wherein the acquisition units are arranged on the mask body and are used for acquiring eye movement data of the eyes of a user; the eye movement data comprises action data of the eyes of the user; and the output units are connected with the acquisition units, and are used for outputting the eye movement data. By the mask, a ventilation therapy equipment system and the method executed based on the ventilation therapy equipment system, the operation intention expressed by the user with the eyes can be recognized so as to carry out follow-up control on the ventilation therapy equipment, and the user experience is greatly enhanced.

Abstract: A wearable concentration improvement apparatus to identify trigger events has one or more sensor, a fluid channel for supply of gas from a unit to one or more gas outlets, and head securement to a user's head. The head securement positions the one or more outlets proximate the user's airway. The fluid channel provides gas to the one or more outlets according to identification of a trigger event by the apparatus.

Abstract: A positive airway pressure (PAP) device for supplying a flow of breathable gas to a patient includes a flow generator configured to pressurize a flow of breathable gas and a humidifier configured to receive and humidify the pressurized flow of breathable gas from the flow generator. The PAP device also includes a power source. The flow generator, humidifier and power source are positioned so that heat generated by at least one of the flow generator and the power source is conveyed to water in the humidifier.

Abstract: A supplemental oxygen delivery system is described in which Aerosol is delivered into a housing 10, 20, which sits in the circuit from the supplemental oxygen supply and optional humidifier. The supplemental oxygen passes through this chamber 10, 20 in which the aerosol is located, and collects the aerosol transporting it to a patient via a nasal cannula 3 or a face mask 4. An aerosol generator 9 is mounted to the housing 10, 20 and delivers aerosol into an oxygen stream 13 flowing between an inlet 14 and an outlet 15 of the housing 10. The housing 10 also has a removable plug 16 in the base 17 thereof for draining any liquid that accumulates in the housing 10. There is no disruption of oxygen delivery to patients using nasal cannulas who currently have to use a separate face-mask when receiving nebulized medication.

Abstract: Inhaled medications present a great opportunity for controlled drug delivery for self medicated patients. With this invention most medicinal aerosol generators have the potential for much more controlled dosage and monitoring of doses to the patient than current inhaled medication systems. The pressurized metered dose inhaler has especially great potential for controlled drug delivery being that the aerosol drug formulation is in a permanently sealed container that can use a digital program controlled electromechanical valve on a metered dose inhaler to control drug dose and time of release. An electromechanical inhaler valve actuator can also provide dose control, monitoring, breath activation timing and other important features.

Abstract: New medical circuit components and methods for forming such components are disclosed. These components include microstructures for humidification and/or condensate management. The disclosed microstructures can be incorporated into a variety of components, including tubes (e.g., inspiratory breathing tubes and expiratory breathing tubes and other tubing between various elements of a breathing circuit, such as ventilators, humidifiers, filters, water traps, sample lines, connectors, gas analyzers, and the like), Y-connectors, catheter mounts, humidifiers, and patient interfaces (e.g., masks for covering the nose and face, nasal masks, cannulas, nasal pillows, etc.), floats, probes, and sensors in a variety of medical circuits.

Abstract: There is provided a phototherapy apparatus, in which the therapeutic light is delivered through or in proximity to one or more massage components. The massage component provides mechanical massage to the subject biological tissue and modifies the properties of the subject tissue in thickness, density, etc. to facilitate the absorption of the therapeutic light and enhance the effect of the phototherapy procedure.

Abstract: A vent arrangement for a respiratory pressure therapy device may include one or a plurality of vents configured with a variable aperture for communicating a flow of breathable gas. The vent arrangement may be configured with a cross section profile exposed to the flow of breathable gas communicating through the vent that does not change as the aperture size changes. A vent arrangement may include a plurality of the vents and the aperture size of each vent may be controlled independently or together, and may be controlled according to one or more input signals from one or more sensors. Examples of suitable input signals include flow, pressure, noise, accelerometer outputs, orientation of a patient or presence of any obstructions. A patient interface or an air circuit may include the vent arrangement, or the vent arrangement may be configured to connect with a patient interface or an air circuit.

Abstract: A disposable face mask includes an upper portion of the face mask and a lower portion of the face mask, the upper portion and lower portion of the face masks each adjoin monolithically formed therewith face mask straps defined by perforations in a web of material used to form the face mask and straps, wherein the perforations allow the straps to be partially separated and utilized for securing said face mask to a wearer's face. The disposable face mask may be made by perforating patterns into a web of materials to define the face mask straps and face mask body that are formed monolithically from the web of materials. The face masks may be wound on a roll for dispensing by tearing off from the roll and then separating the straps at the perforations.