Abstract: A ventilator, or a breathing assistance apparatus, is disclosed to ventilate patients who may have breathing difficulties, said device comprising a inspiratory pressure control duct configured to be immersed in a first body of fluid; a positive end-expiratory pressure control duct configured to be immersed in a second body of fluid; at least one valve connected to the peak inspiratory pressure control duct and to the positive end-expiratory pressure control duct, and at least one controller communicably connected to the valve to control rate of cycling of the valve, thereby controlling number of breaths per minute, and to control the duration of peak inspiratory pressure also known as inspiratory time.

Abstract: A mask system includes a cushion for a mask that seals at its upper extent in a region of the nose that is generally above the tip of the nose or pronasale, and extends across a portion of the cartilaginous framework, alar or flares of the patient's nose, e.g., not extending over or across the nasal bone of the patient's nose.

Abstract: An embodiment of the disclosure provides a universal sealing apparatus for one or more cannulas. The apparatus includes a first portion, a second portion, and a third portion. The first and second portions are configured to removably adhere directly or indirectly to a nose. The third portion is coupled to the first and second portions. The third portion removably couples to one or more cannulas and places a force upon a base of flared portions of the one or more cannulas when the first and second portions are adhered to the nose. The force maintains a fluid seal of the one or more cannulas within one or more respective nostrils of the nose.

Abstract: A connection assembly for a respiratory therapy system, comprising: an outlet assembly, said outlet assembly including an outlet housing and a swivelling disc located on said outlet housing, said outlet housing and said swivelling disc defining, at least in part, a recess; an outlet connector located at an end of a tube portion, said outlet connector including an electrical connector; and a cable having a first end to connect to the electrical connector and a second end to connect to at least one electrical component of the respiratory therapy system, said cable having a slack portion, wherein said outlet connector and said swivelling disc are rotatable in unison between a first position and a second position, and wherein the slack portion of the cable extends from the recess and wraps around the swivelling disc as the swivelling disc is rotated from the first position to the second position.

Abstract: A humidifier that can easily control temperature and humidity in an independent manner, irrespective of a flow rate of medical gas to be supplied, is provided. The humidifier is connected to a respiratory assistance device configured to regulate or assist ventilation of a user. The humidifier is configured to add moisture to gas fed from a gas source in the form of fine particles or water vapor. The humidifier includes a liquid container configured to contain liquid containing at least water, a mist-droplet generation unit configured to generate mist droplets being fine particles of the liquid, and a water retaining member configured to hold at least a part of the mist droplets.

Abstract: A facemask includes integrated actuating modules having sensors and other mechanisms. The facemask has one or more sockets into which various modules may be inserted. The facemask itself or the modules may include air filters and check valves to regulate airflow along or through the various modules. The modules may detect various substances either in the ambient air or the air exhaled by the wearer. The facemask also includes modules for measuring pulmonary and/or cardiovascular exertion, lung capacity and other physiological metrics. Other modules may provide supplements, vitamins or other substances such as tobacco smoke or vapor from vaporizers to the wearer. The modules may include microcontrollers in wireless communication with software applications on electronic devices so that the facemask may also serve as a cellular phone.

Abstract: A breathing assistance apparatus has a main body. A humidification compartment is defined within the main body and is adapted to receive a humidification chamber. A flow generator is positioned within the main body. The flow generator and the humidification compartment are fluidly connected and a liquid containment compartment is interposed between the flow generator and the humidification compartment. The liquid containment compartment is fluidly connected to both the flow generator and the humidification compartment.

Abstract: Disclosed is a mask bead for a patient interface that comprises a contact area, a nose bridge area having a width (B1), side areas, a base area, and a bearing area on a patient. The bearing area extends from the side areas, the base area and the nose bridge area to a central opening is being designed as a sealing lip which frames the central opening. The mask bead further has a maximum width (B2), the ratio B1 to B2 being one to three or greater.

Abstract: In some implementations, a system may receive, from a differential pressure sensor, a differential pressure measurement associated with a differential pressure across an air filter within an airway of a manual ventilator. The system may determine, based on the differential pressure measurement, an air flow rate through the airway. The system may determine timing of a compression cycle of the manual ventilator. The system may determine, based on the timing, a flow threshold associated with a desired breathing cycle. The system may determine a difference between the flow threshold and the air flow rate. The system may provide, via a display associated with the manual ventilator, a representation associated with the difference to indicate whether a compression parameter of the compression cycle is to be adjusted.

Abstract: An air/oxygen blender, optionally with an associated oxygen analyzer, is provided with an exhaust valve in fluid communication with one or more of a proportioning valve and a gas outlet which periodically opens to vent gas therefrom. The exhaust valve is preferably an electrically actuated valve, most preferably a solenoid valve, controlled by a control unit which periodically opens the exhaust valve. In another embodiment, an oxygen analyzer is provided with an exhaust valve in fluid communication with an oxygen sensing chamber. Preferably, the control unit controls the frequency of exhaust valve opening and the time period of exhaust valve opening. A method of prevention of contamination of a lower pressure source air or source oxygen connected to an air/oxygen blender is accomplished by periodically venting of gas from the exhaust valve.

Abstract: A modular powered air purifying respirator (PAPR) is provided including one or more of a first inlet configured to receive an ambient gas; a gas filter in fluid communication with the first inlet and configured to filter the ambient gas; a blower configured to boost at least one of a flow rate or a pressure of the ambient gas entering and/or exiting the gas filter; a second and independent inlet configured to receive a non-ambient gas; a first outlet configured to selectively provide a breathing gas to a user from the ambient gas or the non-ambient gas; and/or a controller and switching device configured to select the source of the breathing gas between the first inlet and the second inlet. Embodiments may also include a power source for the blower.

Abstract: In a method for performing an inhalation a reservoir is filed with a medication fluid or a medication container is connected to a designated connecting piece, a nebulizer unit is connected to a control unit and a mouthpiece, the nebulizer unit is activated, the medication fluid is atomized into a fine particulate aerosol which is emitted into an aerosol chamber formed by the nebulizer unit and the mouthpiece, and an inhalation is performed by a user. A pressure within the aerosol chamber and/or a flow rate through the aerosol chamber is measured using the control unit. The nebulizer is activated with each breath on occurrence of at least one activation criterion detected using the control unit. The nebulizer unit is deactivated with fulfillment of at least one stop criterion.

Abstract: A facemask includes a facemask body, a plurality of electrical contacts and a control circuit. The facemask body has an end including an opening and a skin contact perimeter extending along a periphery of the opening, with the skin contact perimeter configured to sealingly engage with a user's face. Each electrical contact is disposed at a respective region of the skin contact perimeter, and each electrical contact is configured to sense when the respective region of the skin contact perimeter is sealingly engaged with a user's face. The control circuit is disposed on the facemask body, and the control circuit is configured to receive a signal from each electrical contact when the respective region of the skin contact perimeter is sealingly engaged with a user's face and to initiate output of an audible stimulus and/or a visual stimulus in response to receiving a concurrent signal from all of the plurality of electrical contacts.

Abstract: A thermal heat therapy massage roller which includes a cylindrical roller core with interior structural supports, a heating element, a pliable thermally-conductive foam roller body, which is battery operated and due to its thermal capabilities is effective in relieving painful muscle or connective tissue conditions and provides a comfortable thermal option as an exercise, stretching, and core strengthening apparatus.

Abstract: A system for adjusting extrinsic positive end expiratory pressure during an expiratory phase of a ventilator is provided. The system includes a computer system that comprises one or more physical processors programmed with computer program instructions which, when executed cause the computer system to: determine a respiratory reactance from airway flow information of the patient and airway pressure information of the patient, the airway flow information and airway pressure information of the patient being obtained from one or more sensors, and adjust the extrinsic positive end expiratory pressure during the expiratory phase of the ventilator such that the determined respiratory reactance falls within a defined respiratory reactance range.

Abstract: A wearable inhalation delivery device comprising a wearable member that is securable to a wearer's head; and an inhalation delivery device carried by the wearable member and configured to deliver fluid to the wearer's air passages upon inhalation.

Abstract: The present invention provides a drug delivery system that includes a housing configured to contain one or more dispensers. Each dispenser includes an activation mechanism, a nozzle configured to direct the medicament to a predetermined area in the nasal passageway. The nozzles may be configured to create a spray pattern that is about 50-degrees to direct the delivery of a medicament to the sphenopalatine ganglion.

Abstract: A device (400) for delivering medication to a user includes a circular or elliptical body (410) that includes a mouthpiece (420), a flexible strip (401) of medication, a lever (424), and a mouthpiece cover (491), where the mouthpiece cover is rotatable about the body. An electronics module (120) includes a communication circuit (134), a power supply (126), a sensor system (128), and a switch. The lever is configured to actuate the switch when the lever is moved from a closed position to an open position. The lever is further configured to advance a dose of medication on the flexible strip when moved from the closed position to the open position. The switch switches the electronics module from an off state to an active state when the lever is actuated for a first time by a user. The electronics module is configured to not return to the off state thereafter.

Abstract: A respiratory mask can be used to provide therapy to patients who also require a nasogastric (NG) tube. The mask seal can include a path that is designed to deform around an NG tube or other without lifting the mask away from a patient's face. The deforming path can help to minimize gaps that form between the patient's face and the mask seal as a result of the tube, thus reducing leaks and improving the efficacy of the treatment.

Abstract: A walking assistance apparatus includes a knee fastener, a heel fastener, a first wire and a second wire connected to the knee fastener and the heel fastener, a first motor connected to the first wire, a second motor connected to the second wire, and a control circuit that controls the first motor and the second motor. The first wire is connected to a first position included in a right-half region of the heel fastener. The second wire is connected to a second position included in a left-half region of the heel fastener. The control circuit acquires gait information of the user, and, based on the gait information, the control circuit controls the first motor to reduce a length of the first wire and the second motor to reduce a length of the second wire at a predetermined timing.