Handheld carboxy therapy applicators are disclosed. In one implementation, a handheld carboxy therapy applicator includes a heater module, a humidification module, and a hypodermic needle. The heater module is configured to receive a flow of gas and to warm gas within the flow of gas. The humidification module is in fluid communication, such as in a serial connection, with the heater module. The humidification module is configured to receive the flow of gas from the heater module and to humidify the gas within the flow of gas. The hypodermic needle is in serial connection with the humidification module. The hypodermic needle is configured to receive the flow of gas from the humidification module and to inject the flow of gas into a tissue of a patient.

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

An apparatus for humidifying a flow of pressurised, breathable air includes varying a first pressure of the flow of breathable gas to vary a level of thermal engagement between the conductive portion of the reservoir and the heater plate, varying a height of the variable portion varies a level of thermal engagement between the conductive portion of the reservoir and the heater plate, use of a humidifier reservoir base component with a maximum water capacity substantially equal to the predetermined maximum volume of water of the humidifier reservoir or the use of intersecting inlet and outlet axes.

An aerosol delivery system has a nebulizer and a humidifier providing a gas flow to the nebulizer. A controller varies humidity level of the gas flow to the nebulizer so that if the nebulizer is not operating it has about 100% humidity and it is operating the value is less to allow for the humidification effect of the nebulizer. The control may be achieved by dynamically varying proportions of flow through a dry branch and a humidification branch.

An interchangeable mouthpiece for an inhalator, in particular for an electronic cigarette product, a conventional cigarette product or a medical inhaler, comprises a housing which forms an interior space and has an air inlet opening and an air outlet opening, an adapter by means of which the mouthpiece is connectable to a mouth-side end of the inhalator so that the air inlet opening is flow-coupled to the inhalator in a connected state, and a data acquisition device which at least comprises a sensor, a data memory, a processor and an energy storage unit, with a flow channel being formed in the interior of the housing as a result of a separation and flow-connecting the air inlet opening to the air outlet opening, and with the data acquisition device being configured to store, in the data memory, a data record comprising at least an operational parameter depending on a fluidic condition within the flow channel.

A method for providing respiratory support to a patient includes intubating the patient with an invasive patient interface having a sealable member operable to form a sealing engagement with the patient's airway. While the patient is intubated, the sealable member is operated to form a non-sealing arrangement of the invasive patient interface within the patient's airway and a flow of respiratory gas is provided to the patient via the invasive patient interface. This respiratory support is provided during absence of spontaneous breathing.

The present disclosure provides for a flow therapy apparatus that can implement one or more closed loop control systems to control the flow of gases of a flow therapy apparatus. The flow therapy apparatus can monitor blood oxygen saturation (SpO2) of a patient and control the fraction of oxygen delivered to the patient (FdO2). The flow therapy apparatus can automatically adjust the FdO2 in order to achieve a targeted SpO2 value for the patient.

A humidifier includes a water supply and a nebulizer bank having a plurality of ultrasonic nebulizers, where each of the plurality of ultrasonic nebulizers is in fluid communication with the water supply and is structurally configured for breaking up water in liquid form into aerosol droplets for humidifying a volume. The humidifier may further include a controller in communication with each of the plurality of ultrasonic nebulizers to selectively activate each of the plurality of ultrasonic nebulizers independently from one another, where the controller is configured to stage activation of one or more of the plurality of ultrasonic nebulizers while accounting for at least one of: (i) a time from startup to a production of an aerosol droplet for each ultrasonic nebulizer; (ii) a threshold power consumption for the humidifier; (iii) a temperature of a component of the humidifier; and (iv) a predetermined humidity of the volume.

The invention relates to a respiratory system comprising a first patient interface for delivery of a first flow of gases to a patient, a second patient interface for delivery of a second flow of gases to the patient, and a device and/or sensing arrangement that is configure to facilitate a switching of the system between a first respiratory mode where the device allowing delivery of the first flow of gases to an outlet of the first patient interface when the second patient interface is absent from the patient, and a second respiratory mode where the device reducing or stopping delivery of the first flow of gases to the outlet of the first patient interface when the second patient interface is located together with the first patient interface upon the patient.

A respiratory therapy system configured to deliver gases to a patient can have a non-sealed gas flow generating arrangement configured to deliver a high flow of positive gas to an airway of a patient and a negative flow of gas away from an airway of the patient. The positive and negative flows of gas can be generated simultaneously. The flow of positive and negative gases reduces exhaled gases in anatomical dead spaces of the patient.