A ventilator, comprising: a manual resuscitator; a motor; a compression plate that is mechanically coupled to the motor, wherein operation of the motor causes the compression plate to periodically compress the manual resuscitator against a resuscitator plate; and one or more operational parameter adjustment controls, wherein operation of the motor is adjusted in response to a value of a particular operational parameter being changed using the one or more operational parameter adjustment controls.

An oxygen production system (100) may include a main control module (120) and a molecular sieve module (140). The molecular sieve module (140) may include a molecular sieve and a molecular sieve information unit. The molecular sieve information unit may be configured to store information of the molecular sieve. The main control module (120) may be configured to read, write and/or update the information of the molecular sieve stored in the molecular sieve information unit. When reading, in response to at least part of the information of the molecular sieve exceeding a preset range, the main control module (120) may control the oxygen production system (100) to perform a corresponding operation. The oxygen production system (100) may occupy small space, have good performance and a high oxygen production efficiency, and enable a user to obtain a more user-friendly experience.

A system for reducing airway obstructions of a patient may include a ventilator, a control unit, a gas delivery circuit with a proximal end in fluid communication with the ventilator and a distal end in fluid communication with a nasal interface, and a nasal interface. The nasal interface may include at least one jet nozzle, and at least one spontaneous respiration sensor in communication with the control unit for detecting a respiration effort pattern and a need for supporting airway patency. The system may be open to ambient. The control unit may determine more than one gas output velocities. The more than one gas output velocities may be synchronized with different parts of a spontaneous breath effort cycle, and a gas output velocity may be determined by a need for supporting airway patency.

A vapor provision system includes a cartridge part (cartomizer) including a vaporizer for generating a vapor from a vapor precursor material for inhalation by a user; and a device part (control unit) comprising a power supply, such as a battery, for supplying power to the vaporizer across an electrical interface established between the cartridge part and the device part when the cartridge part is coupled to the device part for use. The electrical interface is provided by sprung pins in one of the cartridge part and the device part and a circuit board with contact pads in the other of the cartridge part and the device part. The sprung pins and contact pads are arranged in cooperative alignment so that respective ones of the sprung pins are in biased contact with corresponding ones of contact pads when the cartridge part is coupled to the device part for use.

An electronic aerosol provision system includes an airflow sensor operable to measure an airflow parameter, a profile recall unit operable to recall one or more inhalation airflow profiles, a comparison processing unit operable to compare a measured airflow parameter with at least a first inhalation airflow profile while providing aerosol to a user, and a feedback unit operable to provide feedback to the user responsive to the difference between a compared measured airflow parameter and inhalation airflow profile.

Methods and systems for delivering a pharmaceutical gas to a patient. The methods and systems provide a known desired quantity of the pharmaceutical gas to the patient independent of the respiratory pattern of the patient over a plurality of breaths every n.sup.th breath, where n is greater than or equal to 1. The pharmaceutical gases include CO and NO, both of which are provided as a concentration in a carrier gas. The gas control system determines the delivery of the pharmaceutical gas to the patient to result in the known desired quantity (e.g. in molecules, milligrams or other quantified units) of the pharmaceutical gas being delivered. Upon completion of that known desired quantity of pharmaceutical gas over a plurality of breaths, the system can either terminate, continue, activate and alarm, etc.

The present invention includes a device for hypoxia training including a breathable gas source; a mask in fluid communication with the breathable gas source; a mask-state detector that uses one or more criteria to determine if the mask is being worn by a subject, wherein the mask-state detector is capable of communicating an indication of a mask-off state or a mask-on state; a flowmeter in fluid communication with the mask and coupled to the mask-state detector; and a pressure regulator in fluid communication with the mask and with the breathable gas source, and coupled to the mask-state detector, wherein the pressure regulator sets a first pressure at the mask when the mask-state detector communicates an indication of a mask-off state or a second pressure at the mask when the mask-state detector communicates an indication of a mask-on state.

Portable oxygen concentrator elements are described including integrated sensor/accumulator assemblies, new muffler designs, and improved airflow and internal gas connectivity. The result of the elements is an extremely compact, light reliable portable oxygen concentrator that is easy to assemble and relatively inexpensive.

Systems and methods are provided for monitoring the sedation level of patients. Images may be captured of a patient and regions of interest identified. Changes to image properties or to one or more regions of interest may be analyzed to generate physiological parameters for the patient. Physiological parameters may include information related to the patient's breathing behavior and/or activity. Physiological parameters may be used to determine a sedation level of the patient. If it is determined that the patient is over- or under-sedated, appropriate action may be taken, such as displaying an indication, activating an alarm, and/or causing an amount of sedative to be administered to the patient.

Systems and methods for estimating a leak flow in a breathing assistance system including a ventilation device connected to a patient are provided. Data of a flow waveform indicating the flow of gas between the ventilation device and the patient is accessed. A specific portion of the flow waveform is identified, and a linear regression of the identified portion of the flow waveform is performed to determine an estimated leak flow in the breathing assistance system.