A connector is provided for coupling with an invasive patient interface for providing respiratory support to a patient. The connector comprises a connector body having: (i) an inlet port couplable with a flow source providing a flow of respiratory gas; (ii) a gases exit port; and (iii) a device port couplable with the invasive patient interface. The connector also has a lumen having a first end and a second end. The connector body defines a gas flow path between the inlet port and both the device port and the lumen first end and the lumen second end is disposed outside the device port. The lumen provides improved CO2 clearance. Some embodiments provide for gas sampling and/or variable expiratory resistance.

A portable display unit 3000, 3500, 4000 for a breathing assistance apparatus, the portable display unit comprising: a display unit housing 3001, 3501, 4000; a screen 3051, 3551, 4051; and a tethering component for tethering the portable display unit 3000, 3500, 4000 with abase unit 50 of the breathing assistance apparatus.

Described is a respiratory humidifying device comprising: a moisture exchanger positioned in a respiratory system having an inspiration and expiration respiratory cycle, the moisture exchanger positioned such that airflow occurring in the inspiration and expiration respiratory cycle is in contact with the moisture exchanger, the moisture exchanger being temperature-responsive and having a critical solution temperature; a heater; and a controller controlling a supply of power to the heater such that: the heater causes the moisture exchanger temperature to rise to or above a first target temperature by about a first target point in the respiratory cycle; and the moisture exchanger temperature falls to or is below a second target temperature by about a second target point in the respiratory cycle, wherein the first target temperature is above the second target temperature, and wherein during inspiration moisture is added to the incoming air and during expiration the moisture exchanger extracts moisture from the air.

A device for administering oxygen therapy to a patient comprises a gas intake valve; a primary flow path connecting the gas intake valve to a gas output connector, the primary flow path comprising a flow controller configured to adjust a first flow rate through the primary flow path, wherein the flow controller is in electronic communication with a processor and memory; at least one physiological sensor communicatively coupled to the processor performing a method comprising: receiving a target oxygen saturation level; receiving at least one measured physiological parameter from the at least one physiological sensor; analyzing the at least one measured physiological parameter to determine a predicted oxygen saturation level of a patient for a first time window; and adjusting the first flow rate with the flow controller to bring the predicted oxygen saturation level within a threshold value of the target oxygen saturation level.

An improved system and method of determining a low water and/or water-out condition in a humidifier chamber of a respiratory or surgical humidifier system can use a specific frequency band to detect changes in a temperature of a heater plate. The temperature changes can correlate to the specific heat capacity value of the humidifier chamber. The low water and/or water-out detection process can be performed without having to determine the gases flow rate and/or can be run continuously. A heater plate assembly of the system can include a compliant insulation sheet to improve thermal coupling between the heating element and the top heating plate of the heater plate assembly, thereby improving the low water and/or water-out detection process.

Several methods of supporting respiratory function of a patient before, during and/or after a medical procedure are disclosed. In certain arrangements, supporting respiratory function while a patient is under general anaesthesia can include providing a high gas flow a high gas flow that is greater than 15 L/min while the patient is under general anaesthesia. In certain arrangements, a method of providing ventilation while a patient is under general anaesthesia involves providing only a gas flow delivered through a nasal interface that is greater than 15 L/min while the patient is under general anaesthesia.

The invention relates to a method of determining water level in a humidifier chamber that is part of a humidified gases delivery apparatus and system. The method comprising the steps of delivering power to a heater plate, varying the power delivered to the heater plate, measuring the rate of change of temperature and determining the level of water based on the heating characteristics of the volume of water within the chamber, in particular determining the level of water within the chamber based on the rate of change of temperature and the supplied power.

Improved respiratory treatment systems are described e.g. for treatment of respiratory diseases and provision of respiratory therapy, together with components therefor. In one form, the technology relates to a positioning and stabilizing structure which includes a first headgear tube, a second headgear tube and a flow regulator. A flow regulator is provided to adjust the proportion of flow of respiratory gas to the first headgear tube and the second headgear tube. In another form, the technology relates to a patient interface configured to adjust the proportion of the supply of breathable gas that flows from a first flow path to a patient's first naris and from a second flow path to the patient's second naris. In yet a further form, the technology relates to improves conduits for respiratory treatment systems.

An example sensing and secretion bypass apparatus and an associated method of manufacturing. The sensing and secretion bypass apparatus may include an air flow sensor. The sensing and secretion bypass apparatus may further include an adapter including a chamber having a first end configured to receive an air flow and a second end connected to the air flow sensor. The air flow may include secretions. The sensing and secretion bypass apparatus may further include an elevated member disposed within the chamber proximate the second end and configured to prevent the secretions from entering the air flow sensor. The sensing and secretion bypass apparatus may further include a disposal housing in fluid communication with the chamber of the adapter and configured to collect the secretions received via the first end of the chamber.

The invention relates to a breathing assistance apparatus that may be configured to reduce the risk of damage to electronics within the apparatus as a result of liquid leaks within the apparatus or impacts to the apparatus. In other forms, the apparatus may be configured to allow for easy assembly and/or safe operation.