This disclosure relates to a nasal cannula without nostril prongs. The nasal cannula may be used together with an oxygen delivery system, such as a portable oxygen concentrator, or another type of breathing device such as a continuous positive airway pressure (CPAP) machine. In an example, a nasal cannula includes a tube configured to connect to an oxygen supply, and a fitting configured to connect to the tube. The fitting includes a single discharge port having a first section configured to be situated inferior to a first nostril of a user and a second section configured to be situated inferior to a second nostril of the user. Further, the fitting does not include nostril prongs. Because the fitting does not include nostril prongs, patient comfort is dramatically increased relative to prior designs.

The present disclosure describes a ventilator. The ventilator includes tubing configured to receive an input gas and a flow outlet airline in fluid communication with the tubing. The flow outlet airline includes an airline outlet, and the flow outlet airline is configured to supply an output gas to a user via the airline outlet. The ventilator includes an aerosol generator in fluid communication with the flow outlet airline. The aerosol generator is configured to receive an input liquid through an inlet tube and transform the liquid input into an aerosol. The ventilator further includes a breath detection airline including an airline inlet, wherein the airline inlet is separated from the airline outlet of the flow outlet airline, and configured to receive breathing gas from the user during exhalation by the user via the airline inlet. A method of supplying respiratory gas containing an aerosol is disclosed.

A portable medical ventilator using pulse flow from an oxygen concentrator to gain higher oxygen concentration includes a positive pressure source to deliver pressurized air to the patient and a negative pressure source to trigger the oxygen concentrator. A patient circuit attached to a patient interface mask connects the ventilator to the patient. The ventilator includes a controller module that is configured to generate a signal to the negative pressure device to trigger the concentrator to initiate one or more pulses of oxygen from the oxygen concentrator. The oxygen pulses are delivered to the patient interface directly through multi-tube or a multi lumen patient circuit. The oxygen does not mix with air in the ventilator or in the patient circuit and bypasses the leaks in the patient circuit and/or patient interface.

A relay administration device 50 for use in connection to a nitric oxide administration device 20 which supplies NO generated from air, includes an NO densitometer 506, a flowmeter 507 or pressure gauge 504, a control unit 600 which calculates a dosage of NO to be administered to a patient based on an NO concentration measured by the NO densitometer 506 and a value of the flowmeter 507 or the pressure gauge 504, and a two-way valve 505 which is configured to increase a flow rate when the calculated dosage is less than a predetermined value and to decrease the flow rate when the calculated dosage is greater than a predetermined value.

A dynamic oxygen conserver includes a housing and an inhalation sensor coupled to the housing. The sensor has a printed circuit board (PCB) assembly with a first PCB for a breathing side for a user of the dynamic oxygen conserver. A second PCB is coupled to the first PCB. The second PCB is for an atmosphere side opposite the breathing side. In addition, a spacer assembly is coupled between the first and second PCB. The spacer assembly has a metallized diaphragm this is dynamically responsive to breathing by the user of the dynamic oxygen conserver.

Described are methods and devices for therapeutic or medical gas delivery that utilize at least one proportional control valve and at least one binary control valve. The proportional control valve may be in series with the binary control valve to provide a valve combination capable of pulsing therapeutic gas at different flow rates, depending on the setting of the proportional control valve. Alternatively, the proportional control valve and binary control valve may be in parallel flow paths.

A nasal cannula device according to various embodiments can include a flexible tube, an anti-kink device, and an ear protection device. The anti-kink devices may be attached to or integral with the distal end of the flexible tube that connects to a connection adapter, so that the anti-kink device provides support to the flexible tube to prevent kinking of the flexible tube. The ear protection device may be attached to or integral with a portion of the flexible tube that contacts a user's ear. The ear protection device comprises a soft material to mitigate skin irritation of the user's ear.

A ventilator, including an enclosure; a tubing configured to receive an input gas; a flow outlet airline in fluid communication with the tubing, wherein the flow outlet airline includes an airline outlet, and the flow outlet airline is configured to supply an output gas to a user via the airline outlet; a breath detection airline including an airline inlet, wherein the airline inlet is separated from the airline outlet of the flow outlet airline, and the breath detection airline is configured to receive breathing gas from the user during exhalation by the user via the airline inlet; a pressure sensor in direct fluid communication with the breath detection airline, wherein the pressure sensor is configured to measure breathing pressure from the user, and the pressure sensor is configured to generate sensor data indicative of breathing by the user.

The present disclosure relates to an oxygen mask comprising a mask body defining a cavity configured to be positioned, over the mouth and nose of a patient, an oxygen port formed on the upper half of the mask body, an annular aperture formed on the mask body, and at least one vent port formed on the mask body, wherein each vent port is formed on the bottom half of the mask body in a manner that patient’s exhaled gases are directed towards the vent port.

Oxygen concentrator methods and apparatus estimate sieve bed effective capacity. Estimation applies function(s) to a parameter of a measured pressure-time characteristic of the bed, characteristic of a phase of an adsorption cycle of the concentrator at a predetermined motor speed of its compression system. Estimation may involve operating the concentrator at a predetermined bed pressure and measuring a mass flow of gas entering or exiting the bed, and may use the measured mass flow and one or more functions. Estimation may involve a measured bed exhaust mass flow for a purge phase when bed pressure is regulated to maintain a predetermined target pressure using motor speed adjustment. The estimation may apply exhaust mass flow function(s) to the measured exhaust mass flow. Estimation of the effective capacity may involve applying motor speed function(s) to measured motor speed, such as an adjusted one for regulating canister pressure to achieve a target pressure.