In an example, a ventilator includes an outer container containing liquid, an inverted container submerged in the liquid to provide inverted container space between a closed top and an inner container liquid level; gas supply line to supply breathing gas to the inverted container space; and inhalation line having an inlet in the inverted container space to provide breathing gas to patient. The inverted container moves upward from a first elevation when the inverted container space reaches a hydrostatic delivery pressure and volume of the inverted container space increases. The inverted container stops moving upward and the gas supply line stops supplying when the inverted container reaches a second elevation above the first. Based on a breath demand signal or preset timing, the inhalation line opens to permit flow of breathing gas to the patient at the hydrostatic delivery pressure, lowering the inverted container due to lost buoyancy resulting in sinkage.

In an example, a ventilator includes an outer container containing liquid, an inverted container submerged in the liquid to provide inverted container space between a closed top and an inner container liquid level; gas supply line to supply breathing gas to the inverted container space; and inhalation line having an inlet in the inverted container space to provide breathing gas to patient. The inverted container moves upward from a first elevation when the inverted container space reaches a hydrostatic delivery pressure and volume of the inverted container space increases. The inverted container stops moving upward and the gas supply line stops supplying when the inverted container reaches a second elevation above the first. Based on a breath demand signal or preset timing, the inhalation line opens to permit flow of breathing gas to the patient at the hydrostatic delivery pressure, lowering the inverted container due to lost buoyancy resulting in sinkage.

A respiratory humidification system includes a humidifier that is capable of electronic communication with one or more other components of the system thereby permitting transfer of data or control signals between the humidifier and other components of the system. In some systems, a flow generator, such as a ventilator, is provided to supply a flow of breathing gas. The humidifier and the flow generator are capable of electronic communication with one another. In some arrangements, an operating mode or parameter of the humidifier to be set or confirmed by the flow generator, either automatically or manually through a user interface of the flow generator. The humidifier can also utilize data provided by the flow generator or other system component, such as an incubator, to set or confirm an operating mode or parameter of the humidifier. In some arrangements, a user interface of the humidifier can display data from another system component, such as a nebulizer or pulse oximeter.

Various control methods can indirectly determine incorrect connections between components in a respiratory therapy system. For example, incorrect connections can occur between a patient interface, a humidifier and/or a gases source. The methods can indirectly detect if reverse flow conditions or other error conditions exist. A reverse flow condition can occur when gases flows in a direction different from an intended direction of flow. The methods can be implemented at the humidifier side, at the gases source side, or both.

A ventilator system includes a gas flow chamber configured to receive ventilation gas circulating in a ventilation gas pathway of the ventilator and at least one UVC lamp. The UVC lamp is configured to radiate UVC spectrum light into the gas flow chamber to inactivate pathogens in the ventilation gas. A flow sensor is configured to measure a gas flow rate of the ventilation gas and a controller is configured to receive the gas flow rate, determine an intensity based on the gas flow rate, and control power to the UVC lamp based on the intensity.

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.

A respiratory humidification system includes a humidifier that is capable of electronic communication with one or more other components of the system thereby permitting transfer of data or control signals between the humidifier and other components of the system. In some systems, a flow generator, such as a ventilator, is provided to supply a flow of breathing gas. The humidifier and the flow generator are capable of electronic communication with one another. In some arrangements, an operating mode or parameter of the humidifier to be set or confirmed by the flow generator, either automatically or manually through a user interface of the flow generator. The humidifier can also utilize data provided by the flow generator or other system component, such as an incubator, to set or confirm an operating mode or parameter of the humidifier. In some arrangements, a user interface of the humidifier can display data from another system component, such as a nebulizer or pulse oximeter.

An adaptor for a respiratory assistance system delivers aerosols to a patient. The adaptor is lightweight with a small footprint to increase patient comfort. The adaptor has a nozzle and a sealing mechanism to maintain pressure therein regardless of whether the nozzle is inserted into the adaptor. The adaptor is configured to connect to medical tubing and a medicament delivery device.

A suction discharge unit of a suction discharge device includes a first unit and a second unit. The second unit controls the pressure inside the first unit. The first unit includes a storage chamber and a water sealing chamber. The water sealing chamber includes a first chamber communicating with the storage chamber, and a second chamber is sealed from the first chamber by sealing water. A negative pressure control unit is disposed in the second chamber. The negative pressure control unit includes a liquid retaining part retaining a liquid, a control member including control holes, and a support tube supporting the control member. The negative pressure control unit controls the pressure of the first chamber by causing gas to flow from the second chamber into the first chamber via the control holes and the liquid based on the pressure of the second chamber and the pressure of the first chamber.

A cuff pressure stabilizer (100, 200, 300, 500, 600, 800) is provided that includes an inflation lumen proximal port connector (134), which is shaped to form an air-tight seal with an inflation lumen proximal port (15) of a catheter (10) additionally having an inflatable cuff (11) and an inflation lumen (13); a fluid reservoir (120, 524, 624); a liquid column container (118, 518, 618), which is (a) open to the atmosphere (99) at at least one site along the liquid column container, (b) in fluid communication with the fluid reservoir (120, 524, 624), and (c) in communication with the inflation lumen proximal port connector (134) via the fluid reservoir (120, 524, 624); and a liquid (121), which is contained (a) in the fluid reservoir (120, 524, 624), (b) in the liquid column container (118, 518, 618), or (c) partially in the fluid reservoir (120, 524, 624) and partially in the liquid column container (118, 518, 618), and which has a density of between 1.5 and 5 g/cm3 at 4 degrees Celsius at 1 atm.