Abstract: High flow therapy is used to treat Cheyne-Stokes respiration and other types of periodic respiration disorders by periodic application of high flow therapy, adjustment of high flow therapy flow rates and/or periodic additions of CO2 or O2 into the air flow provided to the patient.

Abstract: A humidifier heater base assembly has a heater plate with a thermally conductive portion and a perimeter portion around a perimeter of the heater plate. A resilient member has an inner part attached to the perimeter portion and an outer part adapted to provide a resilient perimeter flange around at least part and preferably the whole of the perimeter portion. The resilient member fixes the heater base to the humidifier by the resilient perimeter flange such that the heater plate and the inner part can move relative to the humidifier in a direction substantially transverse to the general plane of the heater plate. At least a portion of the resilient perimeter flange remains stationary relative to the humidifier.

Abstract: An air quality monitoring device and an associated method of manufacturing. An example air quality monitoring device may include a housing having a chamber and an inlet port. The inlet port may be structured to receive an air flow from outside the housing and provide the air flow to the chamber. The air quality monitoring device may include a plurality of sensors disposed within the chamber and configured to measure air quality data associated with the air flow. The air quality monitoring device may include an adapter configured to be connected to the inlet port and a continuous positive airway pressure machine. The inlet port may be configured to receive the air flow from the continuous positive airway pressure machine via the adapter. The air quality monitoring device may include a controller connected with the plurality of sensors and configured to transmit the air quality data to a computing device.

Abstract: Apparatus, methods, and systems for delivery and administration of pharmaceutical, therapeutic and cosmetic substances to users. The method includes providing a removable capsule having an atomizer, inserting the removable capsule in a channel of a base unit of a device. The channel is in fluid communication with a mixing chamber of the base unit, and the base unit defines openings on the base unit configured to receive a portion of a conduit and a removable air mover unit. Further, the method includes dispensing, using the atomizer, the at least one medication from the removable capsule to the mixing chamber of the base unit, and using the removable air mover unit, causing air and the at least one medication within the mixing chamber to be conveyed from the mixing chamber to the conduit such that air and the at least one medication dispensed from the removable capsule exits the conduit.

Abstract: A flow generator is configured to pressurize a flow of breathable gas to within a range of about 2-30 cm H2O for delivery to a patient's airways. The flow generator includes a blower with at least one impeller and a motor configured to drive the at least one impeller. The flow generator also includes a substantially planar blower mount configured to support the blower. The blower mount includes a flexible blower receptacle portion configured to receive and support the blower. The blower receptacle portion includes an outlet opening that is axially aligned with an air outlet of the blower. The flow generator also includes housing that encloses the blower and the blower mount. The housing has an inner surface that engages a perimeter of the blower mount.

Abstract: Provided are a mask device and a method for controlling the same. The mask device includes a mask body configured to cover a nose and mouth of a user, a first air cleaner connected to one side of the mask body, and a second air cleaner connected to the other side of the mask body. Also, the mask device includes a first suction fan module installed in the first air cleaner, a second suction fan module installed in the second air cleaner, and an exhaust fan module disposed in the mask body.

Abstract: The oxygen supply device supplying a user with an oxygen gas for inhalation comprises: a first sensor unit acquiring information on percutaneous arterial oxygen saturation (SpO2) of the user, a second sensor unit acquiring information on respiratory frequency per minute (BPM), and a control unit. Under the condition where the SpO2 level acquired by the first sensor unit is equal to or larger than the predetermined first threshold and the BPM value acquired by second sensor unit is equal to or larger than the predetermined second threshold, the control unit regards the condition as a possible sign of CO2 narcosis that exhibits an increase in PaCO2 level, and thus judges the condition as an abnormal sign. Then the control unit executes controls such as stopping supply of the oxygen gas to the user, and the like.

Abstract: A ventilator includes electronic control circuitry configured to control a supply of breathing gas for a plurality of respiratory cycles, measure a volume received by the patient in each of the plurality of respiratory cycles, and determine, for each cycle of the plurality of respiratory cycles, a cycle score corresponding to a deviation between the volume of the cycle and a predetermined target volume. The determined cycle score can be selected from a predetermined number of cycle scores that span positive and negative numbers based on the deviation. A pressure step value can be determined based on a plurality of cycle scores corresponding to the plurality of respiratory cycles, and a current pressure of the breathing gas is adjusted by an amount corresponding to the determined pressure step value. The pressure step value may be generated by dividing a sum of the plurality of cycle scores by a sample size.

Abstract: A gases flow rate sensing system may be configured to operate in at least two different target temperature modes, based upon a measured temperature of the gases flow. In some embodiments, the gases flow sensing system may have a voltage divider containing a thermistor. The gases flow rate may be determined based upon a voltage output indicating an amount of power needed to maintain the thermistor at a target temperature as specified by the target temperature mode, and a measured temperature of the gases flow.

Abstract: The invention relates to a container (1) for pressurized fluid, in particular a gas cylinder, having a given internal volume (2), having a fluid distribution valve (3) having a member for selecting the flow rate (12) able to adopt a plurality of distinct positions each corresponding to a given fluid flow rate, and an electronic device (7) having means for measuring pressure, microprocessor (15)-based data processing means (5) for processing the pressure measurements, and display means (6) for displaying the remaining fluid calculated by the data processing means (5).

Abstract: A method for changing the effective ventilation of a mechanically ventilated subject to enable or carry out non-invasive determination of hemodynamic parameters is disclosed. The method includes a step of ventilating the subject using a ventilation pattern comprising at least one phase of increased ventilation and at least one phase of decreased ventilation, wherein the phase of decreased ventilation comprises at least one prolonged breath including a respiratory pause (IRP). The respiratory pause is initiated when the lung pressure (Palv) of the subject is between a minimum lung pressure and a maximum lung pressure of the subject during the prolonged breath.

Abstract: This document generally describes a system and method configured to generate vapor samples from one or more smoking articles used for testing purposes. The system can be configured in a manner that generates a predetermined flow profile by driving a fluid pump in a scheme that accounts for fluid inertia.

Abstract: This specification generally discloses a system and method configured to generate vapor samples from one or more smoking articles used for testing purposes. The system may be configured in a manner that reduces the likelihood of exposing particular mechanical components to the smoking article vapor, which may in turn reduce effects of fouling or corroding such components of the system over a period time.

Abstract: An ostomy appliance system includes an ostomy appliance having a stoma opening and a first electrical interface, and at least one thermal sensor configured to detect at least one thermal property, such as temperature, at the ostomy appliance, the at least one temperature sensor connected to the first electrical interface with electrical circuitry. A wearable device may be removably connected to the ostomy appliance and operably connected to the at least one thermal sensor. The wearable device includes a housing, a second electrical interface configured for electrical connection to the first electrical interface, a power supply and a controller operably connected to the power supply. The controller is configured to determine a condition of the ostomy appliance based on the at least one thermal property detected at the at least one thermal sensor. The wearable device may also include a wireless transceiver configured to communicate with a personal communication device.

Abstract: A respiratory assistance system including a humidification apparatus used for delivery of heated and humidified gases to a patient includes a humidification chamber with an associated heater and sensor, an inspiratory conduit with an associated heater and sensor, and an unheated patient interface, such as a face mask. A controller of the humidification apparatus is configured to determine a gas source and change the set point accordingly to maintain patient comfort regardless of the humidity level of the gas source.

Abstract: The invention comprises a method of operating a breathing apparatus comprising measuring a baseline breath flow parameter being respiratory rate and/or tidal volume or a parameter derived therefrom, varying the flow rate provided by the breathing apparatus, measuring a current breath flow parameter being respiratory rate and/or tidal volume or a parameter derived therefrom, comparing the baseline and current breath flow parameters, and altering operation of the breathing apparatus based on the comparison. The invention also comprises a breathing apparatus that implements the above method.

Abstract: A control system of a respiratory device for the at least supportive-partial artificial respiration of patients, in particular human patients, comprising a respiratory gas conduit arrangement, a pressure changing arrangement for changing the pressure of respiratory gas in the respiratory gas conduit arrangement during the respiratory operation of the respiratory device, and the control system for controlling the respiratory operation of the respiratory device. The control system has a data input for transmitting operational or/and patient data to the control system. The control system is configured to determine a respiratory operating parameter for the operation of the respiratory device selectively by means of a predetermined first data relationship or by means of a predetermined second data relationship that is different from the first data relationship.

Abstract: A semi-closed circuit gas recycling scuba diving breathing apparatus having a breathing loop. The breathing loop has a breathing bag to be supplied by at least one gas tank and a recycling chamber. The gas tank is connected to an inlet of the breathing bag by a first duct and a second duct having respectively a demand regulator and a fixed nozzle configured to deliver respectively a first gas input and a second gas input to the breathing bag. Advantageously, the apparatus has a third duct having a gas flow regulator configured to deliver at a variable mass flow, a third gas input to the breathing bag, and a diving condition sensor, configured to measure a physiological parameter of the diver or the depth. The apparatus is advantageously configured to make the variable mass flow vary according to data of the sensor to optimise the consumption of gas.

Abstract: Breath sensor calibration methods and apparatus are described herein where a breath sensor device may generally comprise a sampling unit having a housing configured to receive a sample breath from a user and a sensor positioned within the housing. A processor in electrical communication with the sensor may be configured to determine a dissipation time when the sensor is exposed to a near-constant concentration level of CO detected from the breath sample down to an ambient level of CO detected. The processor may also be configured to calculate a time constant based on the dissipation time and a reduction from the near-constant concentration level to the ambient level. Furthermore, the processor may also be configured to apply the time constant to a transient response of the sensor to account for drift in calibrating the sensor.

Abstract: A respiratory treatment apparatus and method in which a leak is determined by using an averaging window. The window starts at the present time and extends back in time to a point determined according to a current one of progressively detected phase measures of a first respiratory cycle and a corresponding phase measure attributable to a preceding second respiratory cycle. In another aspect, a jamming index indicates whether the leak is rapidly changing. To the extent that jamming is high, the leak estimate used progressively changes from that using sliding breath-window averaging to a more robust and faster responding low-pass filter method, and adjustment of ventilatory support based on measures employing estimated respiratory flow is slowed down or stopped.

Abstract: Systems and methods can determine respiratory rates of a patient using a respiratory device by performing one or more frequency analyses of a signal from the gases flow. The signal from the gases flow can be one that varies with the patients breathing. The system can include a non-sealed patient interface, such as a nasal cannula in a nasal high flow therapy, or any other patient interfaces. The respiratory system can also detect whether the patient has taken off the patient interface and/or whether the patient connected to the patient interface is talking or eating. Data of the patients use of the respiratory system and the patients respiratory rates can provide therapy compliance and long-term trend of use information and/or progress in the patients respiratory functions and/or other physiological functions.

Abstract: A device and a method for respiratory therapy. The device is configured with at least two operating modes, which include a first operating mode for providing HFNC support for a patient and a second operating mode for providing NIV support or INV support for the patient; the device includes a memory stored with instructions and a processor, the processor is configured to call and run the instructions stored in the memory to execute operations of: obtaining an ROX index based on first parameters; and triggering mode switching of the device according to the ROX index and a preset triggering strategy for switching the operating mode of the device.

Abstract: A method is disclosed for administering medication to conscious or unconscious patients using a device with a tubular chamber. The method involves the use of a device with a tubular chamber, wherein a liquid medication is contained within a capsule. The medication is atomized by activating an atomizer, thereby generating an atomized medication consisting of particles with a maximum diameter of four microns. The atomized medication is then dispensed into the tubular chamber. Using the device, the atomized medication is administered to the patient. In cases of unconsciousness, a resilient air bladder connected to the chamber is partially deflated, allowing air transfer into the chamber. This facilitates the administration of the atomized medication. This method enables effective medication delivery in various emergency scenarios, ensuring appropriate treatment even for unresponsive patients by providing a method of using a device with modular components.

Abstract: A method of detecting hypoxia. Detecting hypoxia includes detecting, in exhaled breath, at least one indicator for hypoxia. The at least one indicator is selected from the group consisting of pentanal, 2-pentanone, 2-hexanone, 2-heptanone, 2-cyclopenten-1-one, and 4-butyrolactone.

Abstract: A respiratory assistance system can provide high flow therapy to patients. The respiratory assistance system can include a patient interface that can deliver a gas flow to a patient and a gas source that can drive the gas flow towards the patient interface at an operating flow rate. The system can include a controller for controlling the operating flow rate of the gas. The controller can apply multiple test flow rate values in a range as the operating flow rate. For each of the test flow rate values, the controller can measure a patient parameter. The controller can determine a new flow rate value based on the measured patient parameters. Patient parameters can include respiration rate, work of breathing, or any other parameters related to the respiratory circuit.

Abstract: A ventilator system, comprising: an inhalation pathway comprising an ambient air inlet, a bi-directional emergency valve, and a dynamic blower; and an exhalation pathway comprising a bi-directional exhalation valve and an exhalation port; wherein when a blockage occurs in the inhalation pathway, ambient air can be drawn from the exhalation port and through the bi-directional exhalation valve, and during exhalation exhalant exits the ventilator through the bi-directional exhalation valve and the exhalation port; wherein when a blockage occurs in the exhalation pathway, inhalant is delivered by the dynamic blower, and during exhalation the dynamic blower lowers its speed or stops and the exhalant exits the ventilator through the bi-directional emergency valve, the dynamic blower, and the ambient air inlet.

Abstract: A process (10), with a computer program, a device (30) and a ventilation system (40) detect a leak in a patient gas module, which suctions and analyzes a continuous sample gas stream from a ventilated patient (20), in a ventilation system for ventilating a patient (20). The process includes a determination (12) of a first time curve of a carbon dioxide concentration in a breathing gas mixture of the patient (20) and the determination (14) of a second time curve of a concentration of another gas in the breathing gas mixture, which gas is different from carbon dioxide. The process (10) further includes a determination (16) of a statistical similarity indicator between the first time curve and the second time curve and the detection (18) of the leak based on the similarity indicator.

Abstract: In certain example embodiments, an air delivery system includes a controllable flow generator operable to generate a supply of pressurized breathable gas to be provided to a patient for treatment and a pulse oximeter. In certain example embodiments, the pulse oximeter is configured to determine, for example, a measure of patient effort during a treatment period and provide a patient effort signal for input to control operation of the flow generator. Oximeter plethysmogram data may be used, for example, to determine estimated breath phase; sleep structure information; autonomic improvement in response to therapy; information relating to relative breathing effort, breathing frequency, and/or breathing phase; vasoconstrictive response, etc. Such data may be useful in diagnostic systems.

Abstract: The present invention provides a method and apparatus for reducing condensation in a respiratory circuit during a delivery of humidifying agent into the respiratory circuit. A first amount of humidification agent to a first volume of gas is delivered to a patient respiratory circuit during a patient inhalation cycle or immediately after a patient exhalation cycle, and the humidification agent or the first volume of gas is heated. Condensation is removed from the respiratory circuit at least in part by providing, during a patient exhalation cycle or immediately after a patient inhalation cycle, a second amount of the humidification agent to a second volume of gas being delivered from the gas source to the patient respiratory circuit, the second amount of the humidification agent being significantly less than the first amount of the humidification agent.

Abstract: A rebreather apparatus includes at least one pressurized container of oxygen, at least one pressurized container of a diluting gas, and at least one valve to supply the oxygen and diluting gas to a rebreathing loop. The valve is controlled by a signal from at least one oxygen sensor, wherein the oxygen and diluting gas combine to form a breathing gas that is circulated by the rebreathing loop. At least one container of calibrating gas stores the calibrating gas at ambient pressure and temperature. At least one valve is connected to the at least one oxygen sensor presenting the calibrating gas to the oxygen sensor during calibration of the oxygen sensor and presenting the breathing gas to the oxygen sensor at all other times.

Abstract: The breathing assistance apparatus of the present invention includes a manifold that is provided with or retrofittable to gases supply and humidifying devices. The manifold allows gases from an oxygen concentrator to be combined with the flow through a gases supply and humidifying device, most usually air. The combined output of oxygen and other breathing gases (air) is then humidified. The breathing assistance apparatus and manifold of the present invention provides a safe method to add oxygen to the input air stream of a gases supply and humidifying device and reduces the amount of accumulation of oxygen within the gases supply device, reducing fire risk should sparking occur within the device.

Abstract: Described herein are methods which involve minimizing or eliminating the occurrence of delayed negative effects that may arise from exposure to reduced oxygen partial pressure. An amount of supplemental oxygen, which substantially mimics a target oxygen partial pressure, is administered to an individual that is exposed to a reduced oxygen partial pressure environment, to compensate for the reduced oxygen partial pressure. The target partial pressure may be selected such that the individual experiences substantially no change in the oxygen partial pressure. Individuals receiving the supplemental oxygen may be healthy, have special sensitivities, or have a pre-existing neurological condition.

Abstract: The present disclosure pertains to a system configured to enhance deep sleep in a subject during positive airway pressure therapy. A pressure generator is configured to generate a pressurized flow of breathable gas for delivery to an airway of the subject. Sensors are configured to generate output signals conveying information related to breathing of the subject. One or more hardware processors are configured to cause the pressure generator to generate the pressurized flow of breathable gas in accordance with a positive airway pressure therapy regime based on the information in the output signals; determine sleep stages of the subject based on the information in the output signals; and responsive to the sleep stages indicating the subject is in deep sleep, cause the pressure generator to adjust the pressurized flow of breathable gas to deliver a stimulus to the subject, the stimulus configured to enhance deep sleep in the subject.

Abstract: A nitric oxide delivery system, which includes a gas bottle having nitrogen dioxide in air, converts nitrogen dioxide to nitric oxide and employs a surface-active material, such as silica gel, coated with an aqueous solution of antioxidant, such as ascorbic acid. A nitric oxide delivery system may be used to generate therapeutic gas including nitric oxide for use in delivering the therapeutic gas to a mammal.

Abstract: A monitoring device (1) for a system for generating medical compressed air includes a measured air line (3) removing compressed air from a compressed air supply line downstream of a compressed air conditioning unit. A sensor (2) generates a measured signal as a function of a property of the compressed air fed through the measured air line. A humidifier (8) humidifies the compressed air upstream of the sensor. An output unit (12) outputs information about the property of the compressed air to a user on the basis of the measured signal. A tap (4) removes compressed air and an actuator (5) changes a volume flow and/or mass flow of the compressed air, which volume flow and/or mass flow prevails in the measured air line. The actuator is inserted into the tap in a measuring mode and is removed from the tap in a compressed air removal mode.

Abstract: Methods and systems for monitoring multiple sensors over a distributed sensor network to enhance various monitoring operations. In some implementations, an identification of a sensor located in a property and a token that enables the mobile device to obtain data from the sensor are each received by a mobile device from a server. The mobile device is then determined to be within a communication range with the server that is indicated by the identification from the server. In response, data is obtained from the sensor by the mobile device using the token received from the server.

Abstract: According to one embodiment, a CPAP device includes a housing, a fan, and a sound absorbing material. The housing has a first air inlet and a first air outlet, and a flow channel guiding air sucked through the first air inlet to the first air outlet. The fan has a second air inlet and a second air outlet, the second air inlet is disposed in the direction intersecting the flow channel, and the second air outlet is disposed in the direction along the flow channel. The sound absorbing material is provided with a recess constituting a part of the flow channel and facing the second air inlet of the fan, the recess having a diameter which is greater than a diameter of the second air inlet of the fan and which is equal to or smaller than the width of the flow channel.

Abstract: A method of ventilator control that includes receiving machine data from a mechanical ventilator and detecting one or more clinical events in the received machine data. The method further includes evaluating the machine data within the detected one or more clinical events for compliance with lung protective ventilation (LPV) recommendations. The method further includes at least one of producing a visual indication or a graphical display of the evaluated compliance with the LPV recommendations and controlling the mechanical ventilator based on the evaluated compliance with the LPV recommendations.

Abstract: Disclosed are methods, apparatus and systems for treating a respiratory disorder in a patient. The apparatus comprises a pressure generator configured to generate a flow of air so as to provide ventilatory support to the patient; a transducer configured to generate a flow signal representing a property of the flow of air; and a controller configured to analyse the flow signal to estimate the inspiratory volume and the expiratory volume of a breath of the patient and servo-control the degree of ventilatory support to adjust an estimated tidal volume toward a target tidal volume. A gain of the servo-control is dependent on a difference between the estimated inspiratory volume and the estimated expiratory volume. The method comprises operating an apparatus or system in a similar manner.

Abstract: A gas flow indicator device has a housing defining a chamber. An annular indicator extends over the chamber enabling gas to enter along a bore and is spaced from an inner surface, defining an annular space. A moveable concealment member has an annular skirt receivable into the annular space so one end provides a seal against an annular surface at an end wall while a transverse wall at the other end defines an opening providing resistance to gas flow. The skirt can be held in sealing engagement at the annular surface to conceal the indicator through a window. Increasing gas flow rate overcomes the bias of a biasing member and moves the concealment member to expose the indicator and provide a visual indication of gas flow. A fitting member has an engagement portion operable to constrain the biasing member to preclude vibrations and/or prevent its full compression.

Abstract: The invention relates to a pressurized gas container, having an internal volume for storing gas under pressure comprising a valve for distributing fluid, a pressure sensor for measuring the pressure of the gas and delivering at least one measurement signal, a microprocessor for processing the measurement signal delivered by the pressure sensor and a digital display. The microprocessor converts the measurement signal delivered by the pressure sensor into a measured pressure value, and compares the measured pressure value with at least one preset threshold-pressure value. The digital display displays at least one predefined term reflecting the amount of gas in the container, which is dependent on the comparison performed by the microprocessor.

Abstract: A respiratory gas analyzer device (10), such as a capnograph device, is disclosed. A gas measurement component (28), such as a carbon dioxide measurement component in the case of a capnograph, is configured to measure at least one respired gas component (e.g. carbon dioxide). A pump (20) is connected to draw respired gas through the gas measurement component. A pressure gauge (30) is connected to measure pressure in an airflow pathway including the gas measurement component and the pump. An electronic pump controller (40) is programmed to start the pump in response to pressure measured by the pressure gauge satisfying a pump turn on criterion.

Abstract: A respiratory system is configured to pressurize and deliver a flow of respiratory gas to a patient's airways. The respiratory system includes a cushion configured to sealingly engage the patient's face and a blower mounted to the cushion and configured to pressurize a flow of respiratory gas. An interface structure is attached to an outlet of the blower and an aperture in the cushion. The interface structure forms a gas flow path between the cushion and the blower. The gas flow path is configured to deliver the pressurized respiratory gas from the blower through the aperture in the cushion. The gas flow path is also configured to vent exhaled gas from the aperture in the cushion to atmosphere. The respiratory system also includes headgear configured to support the cushion and the blower on the patient's face.

Abstract: Apparatuses and methods are disclosed for improving the Weight/Duration ratio of Self Contained Breathing Apparatuses (SCBAs) by decreasing the amount of fresh breathing gas required from the system by saving exhaled air that is low in carbon dioxide in a reservoir and reusing it at the subsequent inhalation. Electronic control units (“ECUs”) including conventional oxygen sensors and special types of carbon dioxide sensors are used to monitor and predictably regulate the consumption of breathing gas, further contributing to a significantly lower overall system weight for any given duration of the SCBA.

Abstract: An anesthesia ventilator, for the automated ventilation of a patient, includes an expiratory port and an inspiratory port for connecting a ventilation tube facing the patient for a breathing gas, a breathing gas delivery unit, at least one breathing gas sensor for detecting an anesthetic gas concentration, at least one pressure sensor for detecting a pressure of the breathing gas, as well as at least one computer. The computer is configured to actuate the breathing gas delivery unit as a function of the detected pressure of a preset desired pressure value. The computer is further configured to perform an adaptation of the desired pressure value as a function of the detected anesthetic gas concentration.

Abstract: A method for controlling the delivery of a breathing gas to a patient. The method comprises: delivering a flow of breathing gas to a patient, the breathing gas having a breathing gas flowrate and a fraction of inspired oxygen; measuring an oxygen saturation level of the patient; determining a respiratory rate of the patient; automatically adjusting the fraction of inspired oxygen of the breathing gas based on the measured oxygen saturation level of the patient and a breathing gas flowrate set-point; and automatically adjusting the breathing gas flowrate set-point based on the determined respiratory rate of the patient.

Abstract: There is disclosed a method and system for determining the partial pressure of at least one gas in a mixture of gasses contained in a pressure vessel, in particular a pressure vessel in the form of a life support pressure chamber/decompression chamber, or a diving gas storage cylinder. The method comprises the steps of: coupling a gas analysis sensor (14) to a pressure vessel (10); directing a portion of the mixture of gasses in the pressure vessel to the sensor for analysis; reducing the pressure of the portion of the mixture which is to be analysed by the sensor to a level which is below the pressure in the vessel but above local atmospheric pressure; operating the sensor to measure the partial pressure of the at least one gas at the reduced pressure level; and using the partial pressure of the at least one gas, measured at the reduced pressure level, to determine the actual partial pressure of said gas in the mixture contained in the vessel.

Abstract: In one embodiment of an aircraft emergency oxygen delivery system, power can be generated by the flow of gas over a transducer disposed inside an oxygen delivery tube. A pressure differential gives rise to a temperature difference across the transducer, and the temperature difference can be converted to a voltage. The voltage can be quadratically dependent upon the Mach number M (e.g. flow velocities from 1 to 140 m/s) and proportional to a Seebeck coefficient of the transducer. The power thus generated may be used to operate LED indicators visible from the exterior of the tube, a variety of sensors, and wireless communication with a central control system. Oxygen flow to a mask may be adjusted based on ambient oxygen content and data collected from a passenger wearing the mask, including a blood oxygen saturation level, pulse or respiration rate.

Abstract: A respiratory assistance system including a humidification apparatus used for delivery of heated and humidified gases to a patient includes a humidification chamber with an associated heater and sensor, an inspiratory conduit with an associated heater and sensor, and an unheated patient interface, such as a face mask. A controller of the humidification apparatus is configured to determine a gas source and change the set point accordingly to maintain patient comfort regardless of the humidity level of the gas source.

Abstract: A method for measuring a patient's expired CO2 level in a non-invasive ventilator system while maintaining a positive inspiratory pressure. The method includes the steps of: receiving, by the non-invasive ventilator system, a signal comprising an instruction to obtain a CO2 measurement from a patient; lowering, by the non-invasive ventilator system in response to the signal, the expiratory positive airway pressure from a first, higher level to a second, lower level for a first time period comprising one or more breaths; obtaining, by a CO2 sensor, a CO2 measurement during the first time period; and returning, after the first time period, the expiratory positive airway pressure to the first, higher level.