A method of an apparatus control pressure in the patient interface. A vent valve may be used with a respiratory device, where the vent valve may selectively block fluid communication between components, such as the flow generator, the patient interface, and/or the vent. An expiratory flow model may be used to determine an expiratory characteristic such as an expiratory flow rate or pressure in the patient interface where an indicative measure may not be available. The expiratory flow model may receive inputs based on a measure of the patient's respiration, such as the tidal volume, peak inspiratory flow rate or length of inspiration. The expiratory characteristic may be used by a controller to control a pressure in the patient interface to provide respiratory therapy to a patient at or close to a target pressure.

A patient interface for sealed delivery of a flow of air at a continuously positive pressure with respect to ambient air pressure to an entrance to the patient's airways including at least entrance of a patient's nares to ameliorate sleep disordered breathing may include a seal-forming structure comprising a foam undercushion and a textile membrane for contact with the patient's face; a positioning and stabilising structure to maintain the seal-forming structure in sealing contact with an area surrounding an entrance to the patient's airways while maintaining a therapeutic pressure at the entrance to the patient's airways; and a plenum chamber pressurised at a pressure above ambient pressure in use.

A sleep apnea treatment/anti-snoring device optionally having controlled positive air-flow using a micro-blower to maintain an individual's upper airway unobstructed (pharynx area). Optionally the device includes a lower jaw mandibular advancement component. The device has built-in sensors, microprocessor and other items required for data acquisition and transfer.

Respiration system for non-invasive positive-pressure respiration, with a pressure source providing respiratory gas, with a control and evaluation unit connected to sensors detecting a leakage volume, spontaneous respiration frequency, tidal volume and the inspiration time. The control and evaluation unit I) checks the leakage volume and reduces the inspiratory pressure assistance proceeding to ii) or triggers an alarm and returns to I), ii) checks the frequency and triggers an alarm and returns to I) or reduces or increases the inspiratory pressure and returns to I) or proceeds to step iii), iii) checks the volume and reduces or increases the inspiratory pressure and returns to I) or leaves the pressure assistance unchanged proceeding to step iv), iv) adjusts the time period of the pressure assistance, depending on the inspiration time, the time period being left unchanged if the inspiration time lies in the predefined inspiration time interval, and returns to I).

Provided is a respiratory monitoring device that measures and outputs the substantial use time of an oxygen supply device. A respiratory monitoring device (4) used in combination with an oxygen supply device (1) delivering highly concentrated oxygen gas includes a detection unit (6) that detects a change in breathing-related information representing at least one of a pressure, a flow rate, and a gas temperature, based on exhalation and inhalation, a calculation unit (725) that calculates a respiratory rate, based on the change in breathing-related information, a determination unit (726) that determines whether breathing is present, and whether a user of the oxygen supply device is present, based on the respiratory rate, a measurement unit (727) that measures a duration in which a user of an oxygen supply device has been determined to be present, based on a determination result obtained by the determination unit, and an output unit (728) that outputs a cumulative measurement result for the duration.

A ventilator (100) ventilates a patient (102) by a high-flow oxygen therapy via a tube system (104). The ventilator has at least one sensor element (110), at least one actuatable inhalation valve or exhalation valve (120) and a control unit (130). The sensor element is arranged and configured to determine and to output a measured variable (112) within the tube system. The measured variable indicates a gas flow within the tube system. The actuatable inhalation valve or exhalation valve is arranged and configured to make possible a flow of a breathing gas from a ventilation circuit (107) of the ventilator. The control unit regulates a ventilation pressure provided by the ventilator via the at least one sensor element and the at least one inhalation valve or exhalation valve such that a predefined maximum pressure is not exceeded in a predefined area (140) of the tube system.

Various methods and systems for delivery of an ETT for intubation are provided. In one example, an ETT delivery system includes a rail system for guiding insertion of an ETT and at least partially defining the motion of the ETT. The ETT delivery system further may include a video laryngoscope blade coupled to the rail system and a delivery mechanism. In some examples, the ETT delivery system further includes a positioner configured to adjust the motion of the ETT. As a further example, the ETT delivery system may include a swing arm and a guide rail to at least partially define the motion of the swing arm. Further, a drive-down mechanism may effect motion of the swing arm. As another embodiment, a rail system, a disposable blade and a positioner may be provided. Further, a delivery mechanism may be operatively linked with the integrated rail system.

A method of controlled delivery of breathing gases is described the method comprising: applying breathing gas pressure within the first naris of a patient during inhalation; applying breathing gas pressure within the second naris of the patient during inhalation; applying breathing gas pressure within the first naris of the patient during exhalation; and applying breathing gas pressure within the second naris of the patient during exhalation, wherein the breathing gas pressure applied to the first naris during inhalation is higher than the gas pressure applied to the second naris during inhalation and the breathing gas inflow to the patient is substantially through the first naris during inhalation and wherein the breathing gas pressure applied to the first naris during exhalation is lower than the gas pressure applied to the second naris during exhalation and the gas outflow from the patient is substantially through the first naris during exhalation. An apparatus and system implementing the method is also described.

A respiratory care system includes a user interface. A flow indicator is movable in response to inhalation and/or exhalation, or both, by a user through the user interface. An electronic indicator is operable in response to an electronic signal transmitted in response to the movement of the floe indicator. Methods of use and assembly are also provided.

Systems and methods for detecting extubation of an endotracheal tube (ETT) are described. Extubation of the ETT can be identified by comparing to a threshold, a difference between a determined first volume of breathing gas during a first inspiratory period to a determined second volume of breathing gas during a second inspiratory period. If the difference exceeds the threshold, an alarm can be activated indicating extubation. Extubation detection may also be based on a difference between inspiratory pressures during separate inspiratory periods. Partial extubation and full extubation may also be discerned. Further, extubation of an ETT may be detected without the use of an exhalation flow sensor.