A ventilator includes a ventilation body, the ventilation body includes a ventilation cavity and an air inlet end and an air outlet end communicating with the ventilation cavity, the ventilation body further includes an annular shell configured to form the ventilation cavity, the annular shell is formed with an annular cavity inside, an air inlet and an air outlet communicating with the annular cavity are disposed on the annular shell, the air outlet is communicated with the annular cavity and the ventilation cavity, the air outlet has a slit shape extending along a circumferential direction of the annular shell and is disposed to be capable to guide gas flows out towards the air outlet end. The ventilator may greatly increase the ventilation volume and the gas pressure, by using the ventilation body as mentioned above.

A personal respiratory isolation system (PRIS) provides a personal, negative pressure environment for a patient or user that reduces contamination and spread of pathogens exhaled by the patient into the environment. The PRIS includes an enclosure to receive the patient's head (such as a hood and a drape) and a negative pressure source which draws ambient air into the interior of the enclosure and draws air within the enclosure's interior (including the exhalations of the patient, including any contaminants and/or pathogens) out of the enclosure via a fluid port into a container for biohazard processing or disposal. The PRIS may allow positive air pressure therapeutic treatments to be delivered to the patient within the negative pressure environment, and the PRIS may maintain a constant pressure within the interior of the enclosure. The PRIS may include a transparent, hinged face shield for ease of patient observation and/or access.

A liquid ventilation system includes a reservoir holding a perfluorochemical (“PFC”) fluid, and a suction pump connected to the reservoir to reduce pressure within the reservoir. A sensor is configured to measure an intra-lung pressure. An appliance is configured to be disposed within a patient. The appliance carries an injector to supply the PFC fluid through the appliance. An extraction valve is disposed on an extraction line between the appliance and the reservoir. The extraction valve is arrangeable between a first position enabling fluid communication from the appliance to the reservoir and a second position disabling fluid communication from the appliance to the reservoir.

An automated mechanical ventilator may include a positive pressure source that periodically delivers periodic positive pressure ventilations to a patient when a pressure within the patient's airway is greater than a predetermined threshold. The ventilator may include an inspiratory lumen coupled with the positive pressure source. The ventilator may include an inlet valve interfaced with the inspiratory lumen. The inlet valve may open with each positive pressure ventilation. The ventilator may include an expiratory lumen. The ventilator may include a pressure sensor in fluid communication with the expiratory lumen that senses the pressure within the patient's airway. The ventilator may include an outlet valve interfaced with the expiratory lumen. The ventilator may include a controller that opens the first valve without delivering a positive pressure ventilation when the pressure measured by the pressure sensor is less than the predetermined threshold.

A method for determining that a patient interface component comprising a vent has been replaced between therapy sessions of treatment of sleep disordered breathing, the method comprising: acquiring or receiving first vent flow rate data representing one or more estimated first vent flow rates of gas through a first vent of a patient interface in use during a first therapy session; acquiring or receiving second vent flow rate data representing one or more estimated second vent flow rates of gas through a second vent of a patient interface in use during a second therapy session after the first therapy session; and identifying, by comparison of the second vent flow rate data to the first vent flow rate data, a difference in resistance to flow through the first vent than through the second vent indicating that the second vent is not the same vent as the first vent.

A system for supporting pulmonary gas exchange in patients and for coupling to a ventilating system or for use in the case of non-ventilated patients, which has a flexible hose introducible into the trachea of a patient, a pump unit, a reservoir unit and a controller such that via the flexible hose and by means of the pump unit it is possible to regulate aspiration, especially end-expiratory aspiration, and recirculation, especially end-inspiratory recirculation, of the aspirated gas. In order that the system can be operated independently of a ventilating system, the system has a sensor.

A system for providing continuous positive air pressure therapy is provided. The system includes a flow generator, a sensor, and a computing device. The computing device is configured to control operation of the flow generator based on sensor data. The computing device is further configured to display, on a display device, one or more questions relating to demographic and/or subjective feedback; responsive to displaying the one or more questions, receive one or more inputs indicating answers to the one or more questions; transmit the answers to a remote processing system; receive, from the remote processing system, settings determined based on the transmitted answers; and adjust control settings of the system based on the received settings.

Systems and techniques for monitoring, predicting and/or alerting for short-term oxygen support needs of patients are presented. A system can include a data collection component that receives multimodal patient data for a patient having a respiratory condition in association with monitoring and treating the respiratory condition in real-time, the multimodal patient data comprising at least physiological data regarding physiological parameters tracked for the patient over a period of time, and current oxygen support data regarding a current oxygen support mechanism of the patient. The system can further include an oxygen support forecasting component that processes the multimodal patient data using an oxygen support forecasting model to generate an output forecast that indicates whether a change to the current oxygen support mechanism is recommended for the patient within a defined upcoming timeframe

Systems and methods for calibrating oxygen sensors in ventilators are provided. An oxygen sensor is coupled in flow communication with a first oxygen gas source. A calibration circuit including a second oxygen gas source is coupled in flow communication with the oxygen sensor and a third oxygen gas source is coupled in flow communication with the oxygen sensor. A controller is configured to determine a calibration curve for the oxygen sensor via the calibration circuit by measuring the second oxygen gas source and the third oxygen gas source. Based on the calibration curve, an oxygen concentration value of the first oxygen gas source is measured and distributed.

Disclosed herein is a system and method for controlling oxygen supply equipments. The system is equipped with pressure sensors coupled to the oxygen supply equipments. Depending on the oxygen supply selected by a user for the patient, the pressure sensor monitors the current pressure of the preset oxygen supply during an inhalation phase corresponding to the patient. If the current pressure is less than a minima value or if a pressure drop rate is higher than or equal to a threshold rate or both, the system generates an alarm notifying the user to check the preset oxygen supply and in the meanwhile switches the preset oxygen supply from one oxygen supply equipment to another oxygen supply equipment or vice-versa.