The present invention relates to an electrically operable resuscitation device comprising a piston/cylinder assembly including a rigid cylinder including at least one gas inlet and at least one gas outlet, a piston to travel in said cylinder, and at least one valve, the or each valve configured to allow gas to be displaced into said cylinder through said at least one gas inlet during at least one of a first stroke direction and second stroke direction of said piston in said cylinder, and for allowing gas to displaced through said at least one gas outlet during an opposite of said at least one of the first stroke direction and second stroke direction of said piston in said cylinder; a motor, selected from one of a stepper motor and feedback motor and stepper motor with feedback and linear motor, operatively connected to said piston to move said piston in said cylinder; a patient interface in ducted fluid connection with said piston/cylinder assembly to receive gas via said at least one gas outlet and to deliver said gas to said patient.

Respiratory systems with a flow generator can provide bubble CPAP therapy by controlling the pressure of a flow of gas delivered to a patient. The controller of the respiratory system can control a motor speed of its flow generator so as to control the pressure of the flow of gas. The controller can also detect presence of bubbling and/or possible leaks in the gas pathway of the system. The respiratory system can include a high flow respiratory system.

A patient interface comprises a support structure and a seal-forming structure. The support structure is arranged to support the sealing portion and is configured to connect to the frame. The sealing portion comprises textile and is attached to the support structure along an outer perimeter of the sealing portion such that in use the sealing portion may be in tension due to reactive stress of the support structure and/or a resilient stretch characteristic of the textile such that the sealing portion exerts a force against the patient's face.

Systems and methods for generating nitric oxide are disclosed. A nitic oxide (NO) generation system includes at least one pair of electrodes configured to generate a product gas containing NO from a flow of a reactant gas; and a controller configured to regulate the amount of nitric oxide in the product gas produced by the at least one pair of electrodes by utilizing duty cycle values of plasma pulses selected from a plurality of discrete duty cycles to produce a target rate of NO production based on an average of discrete production rates associated with each of the plurality of discrete duty cycles.

A ventilator for respiration gas supply, comprising a respiration gas source, a control unit, a memory, a pressure sensor and/or a flow sensor, an exchangeable respiration gas tube, at least one connection stub for the respiration gas tube, a patient interface and a valve. The control unit is set up to use signals from the pressure sensor and/or flow sensor to ascertain the patient's respiration phase and to ascertain the patient's current tidal volume during successive inhalations and exhalations and to compare a first set volume threshold for the tidal volume with the current tidal volume and to determine whether the latter is below the former and if so, to react by driving the respiration gas source to set a second pressure for the respiration gas for inhalation and driving the respiration gas source to set the CPAP pressure for the respiration gas for exhalation.

A modular ventilator according to the present disclosure may include a ventilator core and a ventilator service module. The ventilator core provides the basic functionality necessary for delivering suitably oxygenated air to a patient without most or all typical patient monitoring functions except a basic alarm or safety alert triggered by loss of pressure at the output. Additional patient monitoring functions are embodiment in the removable ventilator service module, which may be powered by its own power source and/or by the power source of the ventilator core when coupled thereto. The ventilator core is configured for low cost manufacture and ease of operation and may be portable so as to be easily deployable in a non-hospital setting. The ventilator core may employ a venture-based O.sub.2 regulator for adjusting the oxygen-air mixture at the output, which may facilitate the manufacture of the ventilator core at lower cost than conventional ventilators.

A diagnostic tool can include a face mask, a casing, a plurality of sensors, and processing circuitry. The face mask can include an air-intake port, a first check valve integrated into the air-intake port, an air-exhaust port, and a second check valve integrated into the air-exhaust port. The casing can be coupled to the face mask having an air-intake chamber coupled to the air-intake port and an air-exhaust chamber coupled to the air-exhaust port. The processing circuitry can be communicatively coupled to the plurality of sensors. The processing circuitry can include computing logic for handling information detected by the plurality of sensors.

A system and method of removing pathogens and particulates in a breathable air supply includes supplying pressurized air from a portable pressurized air source, flowing the pressurized air through a filter media including capturing multiple pathogens and particulate contaminates from the pressurized air, outputting filtered, pressurized air and delivering the filtered, pressurized air to a mask.

A surgical humidification system includes a source of gas flow and a humidifier that receives the gas flow and outputs a humidified gas to a delivery conduit. The delivery conduit has an outlet and a suitable interface, such as a diffuser, is connected to the outlet. The interface can be positioned near or within an open surgical cavity of a patient to supply the humidified gas to the cavity. The system also includes a pressure relief arrangement that operates to relieve pressure from the system above a normal operating pressure. The pressure relief arrangement can be located in a non-sterile portion of the system, such as upstream from the humidifier, for example.

A nasal ventilation mask having one or more attachment ports located adjacent to and overlying an upper lip of a patient when worn.