Abstract: A method of supplying oxygen to an oxygen mask for an aircraft includes detecting, with at least one sensor and during a first time period, a first blood-oxygen saturation level at a first altitude. The method may also include detecting, with the at least one sensor and during a second time period, a second blood-oxygen saturation level at a second altitude that is different from the first altitude. The method may include determining a minimum flow rate of a gas that includes oxygen for the second altitude such that the second blood-oxygen saturation level at least matches the first blood-oxygen saturation level at the same altitude.

Abstract: Disclosed are an apparatus and a method for monitoring the disconnection of a patient interface system during the ventilation, in which values which are indicative for the time curve of the respiratory gas flow are established and subjected to data evaluation, and wherein an alarm is triggered on the basis of the data evaluation if at least one value which is indicative for the time curve of the respiratory gas flow deviates from a specific limit value for a specific period of time.

Abstract: Described herein is a method and apparatus for storing a sample of human breath, which includes a metering device having an inlet port and a delivery port; a dispenser device in fluid communication with the delivery port of the metering device; a supply unit configured for delivering a flow of fluid through a delivery port of its own; an acquisition port configured for intake of a sample of human breath; and a selection valve. The selection valve includes a first operating condition, in which a fluid communication is obtained between the acquisition port and the inlet port of the metering device, and a second operating condition, in which a fluid communication is obtained between the delivery port of the supply unit and said metering device.

Abstract: Described is a system including a sensor and a processing arrangement. The sensor measures data corresponding to a patient's breathing patterns. The processing arrangement analyzes the breathing patterns to determine whether the breathing patterns are indicative of a REM sleep state. In another embodiment, the processing arrangement analyzes the breathing patterns to determine whether the breathing patterns are indicative of one of the following states: (i) a wake state and (ii) a sleep state. In another embodiment, a neural network analyzes the data to determine whether the breathing patterns are indicative of one of the following states: (i) a REM sleep state, (ii) a wake state and (iii) a sleep state. In another embodiment, the processing arrangement analyzes the data to determine whether the breathing pattern is indicative of an arousal.

Abstract: A blower filter device (3) is connectable to a voltage supply unit (2) and includes a blower unit (5), a filter mount (14), an internal energy storage unit (7), an energy interface (9), a current limitation device (13), a sensor array (16, 17, 18) and a control device (6). The current limitation device is activated upon disconnecting the energy interface from the voltage supply unit. The activated current limitation device limits the intensity of a current from the energy interface to the internal energy storage device. Upon the voltage supply unit being connected to the energy storage device and a predefined deactivating event is detected, the control device deactivates the current limitation device. The deactivating event is based on a charging voltage of the internal energy storage unit and/or on a time period that has elapsed since the connection. A process is provided for operating such a blower filter device.

Abstract: Embodiments relate generally to respirator face masks, and specifically to powered face masks which may be custom-controllable to better provide for the specific air needs of the individual user wearing the mask. For example, the face mask embodiments typically include a filter and a motorized fan, both generally located on the face mask itself, along with a processor. The processor then may use inputs, for example specific to the user and/or the environment, to control the fan speed. Thus, the fan speed of the face mask may be custom controlled to provide the appropriate amount of filtered air as the specific user needs it.

Abstract: A vent system for use during respiratory therapy with a flow of pressurized gas may provide a continuous vent flow of gas. The vent system may include a vent housing having an outer wall; an inner wall, the inner wall defining an inlet for the flow of gas; and a base positioned between the outer wall and the inner wall, the base having at least one first orifice and at least one second orifice. The vent system may include a membrane, the membrane being shaped and dimensioned such that the membrane does not cover the at least one first orifice to allow the vent flow through the at least one first orifice, and the membrane being shaped and dimensioned such that in a first position the membrane is positioned over the at least one second orifice to allow the vent flow through the at least one second orifice.

Abstract: This disclosure describes systems and methods for providing drive pressure ventilation of a patient. The disclosure describes a novel breath type that provides a spontaneous breath type that allows for the calculation of drive pressure that does not require invasive monitoring.

Abstract: Devices, systems and methods provide forms of asymptomatic diaphragmatic stimulation (ADS) therapy that affect pressures within the intrathoracic cavity, including: 1) dual-pulse ADS therapy, during which a first ADS pulse is delivered during a diastolic phase of a cardiac cycle and a second ADS pulse is delivered during a systolic phase, 2) paired-pulse ADS therapy, during which a first ADS pulse is delivered, closely followed by a second ADS pulse, with the second ADS pulse functioning to extend or enhance a phase of a transient, partial contraction of the diaphragm, and 3) multiple-pulse ADS therapy, during which a stream of ADS pulses is delivered, wherein the time between pulses is based on heart rate. Devices, systems and methods also monitor electromyography (EMG) activity of the diaphragm relative to baseline activity to assess the health of a diaphragm subject to ADS therapy and to adjust ADS therapy parameters or sensing parameters.

Abstract: An integrated oxygen supply device that is configured to generate oxygen continuously and release the oxygen non-continuously is provided. In some embodiments, the oxygen generated by the integrated oxygen supply device is stored in a porous material with the integrated oxygen supply device. The delivery of the oxygen produced by integrated oxygen supply device to a patient, in those embodiments, is controlled. In some embodiments, the control of the delivering oxygen is according one or more breathing patterns. The breathing pattern(s) may or may not be a current breathing pattern of the patient. For example, in one embodiment, the breathing pattern is a predetermined breathing pattern with a specified inspiration period followed by a specified expiration period.

Abstract: This disclosure describes systems and methods for providing adaptive base flow scheduling during ventilation of a patient to optimize patient-machine synchrony and accuracy of estimated exhaled as well as inhaled tidal volumes. Further, this disclosure describes systems and methods for providing adaptive inspiratory trigger threshold scheduling during the adaptive base flow scheduling. Further still, this disclosure describes systems and methods for determining an estimated leak flow and adjusting the adaptive base flow scheduling and the adaptive inspiratory trigger threshold scheduling based on the estimated leak flow. Moreover, this disclosure describes systems and methods for determining a change in the estimated leak flow and adjusting the adaptive base flow scheduling and the adaptive inspiratory trigger threshold scheduling based on the change in the estimated leak flow.

Abstract: The present invention is a wearable device for comprehensive bio-monitoring of physiologic metrics to determine metabolic, pulmonary and cardiac function and oxygen saturation measurements from breathing mask apparatuses. The device non-invasively monitors the physiologic profile of the subject, and is capable of detecting physiologic changes, predicting onset of symptoms, and alerting the wearer or another person or system. In some embodiments, the device comprises both a wearable sensor suite and a portable gas composition and flow analysis system. In preferred embodiments, it comprises a miniaturized non-invasive sensor suite for detecting physiologic changes to detect dangerous breathing or other health conditions. The system utilizes advanced fast-response sensors with improved efficiency and lifespan, and provides rapid analysis for substantially real-time monitoring of the subject's present condition to predict, mitigate and/or prevent the onset of dangerous conditions.

Abstract: Gas mixture used for ventilation of passengers and crew in emergency situations. Depending on the density altitude, it has 7±5% CO2 at 15,000 ft flying altitude increasing to 17±5% CO2 at 30,000 ft flying altitude. The carbon dioxide improves the bioavailability of oxygen in the body. The gas mixture is produced by additive dosage of CO2 to either pure O2 or to a gas mixture having a fraction of N2 and a fraction of O2. The method for ensuring good ventilation in case of loss of cabin pressure, or generally in case of hyperventilation, involves making the gas mixture above available via respiration masks. The use of such a gas mixture also for ensuring good ventilation of people with limited mobility, if such ventilation is required. The prescribed amount of onboard oxygen for aircraft can thus be reduced and flight routes leading directly over high-altitude terrain may be taken.

Abstract: The present invention relates to a plurality of ventilation devices, to ventilation devices having visualization apparatuses, and to methods for operating the ventilation devices. The intent is to minimize the energy input into the at least one airway of a patient as a result of the ventilation.

Abstract: A nasal interface is provided that can allow for delivery of flow of a gas to a patient for respiratory support while preventing injury or irritation to the patient. The nasal interface can include a nasal pillow set having a nasal pillow, which can engage against a nose, and relief port, which can permit a gas to be released from the nasal interface. A nasal cannula can include a cannula body to direct a gas through the nasal interface, and can have an opening to direct a gas out of the cannula body. The gas can be directed from the cannula body, through the opening, toward a nasal pillow and a patient's nare. The nasal interface can be coupled with a head harness, which can be worn on the patient's head, and can include a guide that extends toward the nasal interface.

Abstract: A system for obtaining and providing enhanced PAP metrics of a patient's sleep period includes: a pressure support device for use in providing a flow of breathing gas to the patient; a processing unit; and a number of auxiliary devices in wireless communication with the processing unit. Each auxiliary device of the number of auxiliary devices is structured to detect and collect sleep-related data of the patient. The processing unit is programmed to: receive data obtained by a number of sensors of the pressure support device during operation of the pressure support device in providing the flow of breathing gas to the patient; receive supplemental data obtained by the number of auxiliary devices while the pressure support device is not providing the flow of breathing gas to the patient; and determine the enhanced PAP metrics of the sleep period of the patient utilizing the data and the supplemental data.

Abstract: The present invention relates to an integrated sleep diagnosis and treatment device, and more particularly to an integrated apnea diagnosis and treatment device. The present invention additionally relates to method of sleep diagnosis and treatment.

Abstract: Embodiments of negative pressure wound therapy systems and methods for operating the systems are disclosed. In some embodiments, a system includes a negative pressure source, a sensor, and a controller. The negative pressure source can provide negative pressure via a fluid flow path to the wound dressing. The sensor can monitor pressure in the fluid flow path. The controller can determine whether the wound dressing is coupled to a wound from a change in magnitude of pressure in the fluid flow path over time being more indicative of a steady state condition than a chaotic condition while the negative pressure source maintains negative pressure in the fluid flow path within a pressure range. In addition, the controller can output a first indication denoting that the wound dressing is coupled to the wound and a second indication denoting that the wound dressing is not coupled to the wound.

Abstract: Provided is a configuration capable of executing a detection test for a comfort level including the quality of sleep, which is measurable at home without requiring the measurement of brain waves or electrocardiogram. The respiratory waveform of a subject during sleep is continuously measured and recorded from the respiratory gas flow, etc., and is window-Fourier transformed at each measurement time to generate a frequency spectrum, and a bandwidth including a respiratory frequency is extracted. The index indicating the regularity of the respiratory period of the subject is also calculated at each time point during the sleep, and the time-dependency of this index during the sleep is represented as a graph. A medical device includes a sleep evaluation system equipped with a control means for performing control so that a sleep cycle repeated at a cycle of about 90 minutes is clearly observed if the comfort level including the quality of sleep of the subject is favorable.

Abstract: A diving mask includes a transparent visor, a frame, a gasket to guarantee the watertight seal and appropriate belts for fitting the mask, a breathing tube associated with the facial part is fitted onto the upper part of the mask and which enables the flow of air to enter into the compartment between the frame and the visor. The path of air in the inhalation phase and in the exhalation phase both in the mask and tube are different from each other. The tube is made with separate ducts for inhalation and exhalation and the inside of the mask is made with two compartments, one upper front and one lower oronasal separated by a wall. The path provides that inhalation air is introduced by the tube into the frontal compartment and then into the oronasal one and air exhaled from the oronasal compartment travels up to the tube.

Abstract: A system that enables remote adjustment of oxygen flow from an oxygen source includes a gas source device fluidly coupled to a gas source, a remote delivery device with an outlet for providing gas to a user and an inlet fluidly coupled to an outlet of the gas source device, wherein the gas source device has a control system. The control system determines a current control setting of the remote delivery device based on pneumatic feedback from the remote delivery device and modifies a pressure of gas flowing from the gas source device to the remote delivery device based on the current control setting of the remote delivery device, so that a target flow volume of supply gas associated with the current control setting is delivered to the inlet.

Abstract: A respiratory flow therapy apparatus including a sensor module can measure a flow rate of gases or gases concentration provided to a patient. The sensor module can be located after a blower and/or mixer. The sensor module can include at least an ultrasonic transmitter, a receiver, a temperature sensor, a pressure sensor, a humidity sensor and/or a flow rate sensor. The receivers can be immersed in the gases flow path. The receivers can cancel delays in the transmitters and improve accuracy of measurements of characteristics of the gases flow. The receivers can allow for detection of a fault condition in a blower motor of the apparatus.

Abstract: Embodiments relate generally to respirator face masks, and specifically to powered face masks which may be custom-controllable to better provide for the specific air needs of the individual user wearing the mask. For example, the face mask embodiments typically include a filter and a motorized fan, both generally located on the face mask itself, along with a processor. The processor then may use inputs, for example specific to the user and/or the environment, to control the fan speed. Thus, the fan speed of the face mask may be custom controlled to provide the appropriate amount of filtered air as the specific user needs it.

Abstract: A kit includes at least one facemask configured to cover a respective user's mouth and nose. The facemask contains at least one layer impregnated with a first chemical. When the facemask covers the respective user's mouth and nose, airborne particles of the first chemical are released from the at least one layer through the user's breathing. A sensor is configured to measure airborne concentration of the first chemical. A processing circuitry is configured to receive outputs of the sensor, to calculate a change in airborne concentration of the first chemical, and to issue a notification when the airborne concentration of the first chemical increases at above a predetermined rate.

Abstract: Oxygen-delivery systems are described. The systems may supply emergency respiratory gas on demand to aircraft passengers. To reduce risk of blockage of tubes delivering anti-blocking gas to the face masks worn by the passengers, the systems may be designed to provide a continuous trickle flow of respiratory gas, or one or more anti-blocking pulses of gas, into a delivery tube.

Abstract: The present invention relates to a plurality of ventilation devices, to ventilation devices having visualization apparatuses, and to methods for operating the ventilation devices. The intent is to minimize the energy input into the at least one airway of a patient as a result of the ventilation.

Abstract: A valve assembly attached to a capacitor such that pressurizing the capacitor to a first positive pressure threshold induces the valve assembly to open, the pressurized air is released to the patient, and then as the pressure in the capacitor drops to a second pressure threshold the valve closes and the capacitor begins to build pressure until the first positive pressure threshold is achieved and the process repeats. Relative to the valve assembly and integrated therein, is an incrementally adjustable index knob to vary the rate of a biasing force performing work against the actionable valve face of the diaphragm functional surface to set the performance of the valve assembly, thereby increasing the potential for correct operation across a range of oscillating rates supporting a broad spectrum of patient therapies and types.

Abstract: Various methods and systems are provided for performing nasal high flow therapy. In one example, a method for respiratory support includes: delivering an air and oxygen mixture for nasal high flow therapy to a patient at a flow setting, the flow setting determined based on a peak inspiratory flow obtained during a previous, spontaneous breathing mode during mechanical ventilation of the patient. The flow setting may be a flow rate of a heated and humidified mixture of air and oxygen delivered via a high flow nasal cannula.

Abstract: A face mask for filtering air includes a face seal for providing an airtight flexible seal around the nose and mouth of a user, a support sealably attached to the face seal, wherein the support has an open area that allows for passage of incoming air and outlet valves for expelling exhaled air, a front shell for removably attaching to the support, wherein the front shell has inlet holes for allowing the incoming air to pass through the open area of the support, and a filter for filtering particulate elements from air. The filter is configured to be housed between the front shell and the support. The face seal provides a direct connection between the filter and the user.

Abstract: A respiratory protection device that includes a valve assembly operable between an open configuration and a closed configuration. In some exemplary embodiments, the respiratory protection device includes an elastomeric seal, and a valve assembly and a breathing air source component that are in sealing engagement with the elastomeric seal when the valve assembly is in a closed configuration.

Abstract: Automated methods provide leak detection that may be implemented in a respiratory treatment apparatus. In some embodiments, the detection apparatus may automatically determine and score different types of leak events during a treatment session, including, for example, continuous mouth leak events and valve-like mouth leak events. The detection methodologies may be implemented as a data analysis of a specific purpose computer or a detection device that measures a respiratory airflow or a respiratory treatment apparatus that provides a respiratory treatment regime based on the detected leak. In some embodiments, the leak detector may determine and report a leak severity index. Such an index may combine data that quantifies different types of leak events.

Abstract: A pressure swing adsorption (PSA) system and methods for controlling each PSA cycle performed by the PSA system to produce oxygen enriched gas during productive portions of a user breathing cycle, and to cease production of oxygen enriched gas during non-productive portions of the user breathing cycle, is provided. The PSA system synchronizes PSA cycle phases including adsorption and desorption phases with a user's individual inhalation and exhalation phases, on a breath by breath basis, such that each PSA cycle can be dynamically varied from a succeeding PSA cycle, in real time in response to variations in the user's breathing cycle. An oxygen delivery device including a breathing cycle sensor provides breathing cycle inputs to a controller for use with at least one algorithm to detect breathing flow phases during each user breath, and to synchronize each PSA cycle to the user's breathing flow phases, on a breath-by-breath basis.

Abstract: A breathing bag (20) has a tray section (21) and a bag section (22). The tray section (21) and the bag section enclose an inner volume (24) of variable size, the bag section dipping at least partially into the tray section to reduce the size of the inner volume. A system (10) includes the breathing bag, for a closed-circuit respirator (100), with a dispensing valve unit (40) having a dispensing valve (41) providing a quantity of gas in a breathing circuit. An actuating unit (42) is functionally connected mechanically to the dispensing valve for actuating the dispensing valve. A lever component (50) is functionally connected mechanically to the actuating unit for activating the actuating unit. A closed-circuit respirator has the system including the breathing bag and the dispensing valve unit. A process is provided for mounting the system, including breathing bag and dispensing valve unit, in the closed-circuit respirator.

Abstract: A breathing apparatus includes a flow outlet airline in fluid communication with the tubing and breath detection software. The flow outlet airline includes an airline outlet, and the flow outlet airline is configured to supply an output gas to a user via the airline outlet. The breathing apparatus further includes a breath detection airline including an airline inlet. The breath detection airline is configured to receive breathing gas from the user during exhalation by the user via the airline inlet. The breathing apparatus further includes a pressure sensor in direct fluid communication with the breath detection airline. The pressure sensor is configured to measure breathing pressure from the user and to generate sensor pressure data indicative of breathing by the user. The controller is programmed to predict the breathing by the user based on the sensor breathing data received from the pressure sensor.

Abstract: A respirator mask for automatically activating an air-saver switch within a regulator by rotation of the regular as the regulator is mounted and dismounted from a facepiece of the mask. The mask includes a facepiece including a regulator engagement region having an aperture and a protrusion proximate the aperture, and a regulator including a regulator body having a facepiece engagement region matably engageable with the regulator engagement region, a fluid flow path within the regulator body, and a latch within the regulator body, the latch causing obstruction of the fluid flow path when actuated. The latch is engageable with the protrusion, the regulator being rotatable within the facepiece aperture between a first rotational position and a second rotational position, rotation of the regulator within the facepiece aperture from the second to the first rotational position engaging and actuating the latch to obstruct the fluid flow path.

Abstract: A pneumatic system for delivering oxygen to a subject, including an oxygen supply channel having an inlet, a patient delivery outlet and an exhaust; and a flow control element configured to control the flow from the oxygen inlet to the patient delivery outlet, or to the exhaust; wherein inhalation by the patient causes the flow control element to assume a first position, allowing oxygen to flow from the oxygen inlet to the patient delivery outlet; and wherein exhalation by the patient causes the flow control element to assume a second position, directing oxygen flow from the oxygen inlet to the exhaust.

Abstract: A pressure swing adsorption (PSA) system and methods for controlling each PSA cycle performed by the PSA system to produce oxygen enriched gas during productive portions of a user breathing cycle, and to cease production of oxygen enriched gas during non-productive portions of the user breathing cycle, is provided. The PSA system synchronizes PSA cycle phases including adsorption and desorption phases with a user's individual inhalation and exhalation phases, on a breath by breath basis, such that each PSA cycle can be dynamically varied from a succeeding PSA cycle, in real time in response to variations in the user's breathing cycle. An oxygen delivery device including a breathing cycle sensor provides breathing cycle inputs to a controller for use with at least one algorithm to detect breathing flow phases during each user breath, and to synchronize each PSA cycle to the user's breathing flow phases, on a breath-by-breath basis.

Abstract: An oxygen system supplies either 100% oxygen to a demand valve in a mask or pulses of oxygen to the mask. Switching is automatic during a parachute descent. The system includes a valve manifold that is responsive to ambient pressure such that at low pressures it is configured to deliver gas from either an oxygen cylinder or an aircraft supply line to the mask demand valve and at higher pressures it is configured to deliver gas from the cylinder to a pulse gas delivery system. The mask also includes an inhalation valve that is closed if oxygen is supplied to the demand valve. Otherwise, the inhalation valve opens to allow ambient air to be drawn in and the pulse gas delivery system delivers a pulse of oxygen in response to the onset of inhalation.

Abstract: Disclosed is a respirator mask management system. The respirator mask management system comprises a database storage, a data processing unit operatively coupled to the database storage, a user mobile device communicatively coupled with the data processing unit over a communication network, and a respirator mask including a filter configured to prevent inhalation of pollutants by a user, an exhalation valve, a sensor configured to determine a state of the exhalation valve, and a microprocessor operatively coupled with the sensor and having a wireless connectivity to the user mobile device for transmitting the sensed states of the exhalation valve to a respirator mask manager of the user mobile device.

Abstract: A pressure swing adsorption (PSA) system and methods for controlling each PSA cycle performed by the PSA system to produce oxygen enriched gas during productive portions of a user breathing cycle, and to cease production of oxygen enriched gas during non-productive portions of the user breathing cycle, is provided. The PSA system synchronizes PSA cycle phases including adsorption and desorption phases with a user's individual inhalation and exhalation phases, on a breath by breath basis, such that each PSA cycle can be dynamically varied from a succeeding PSA cycle, in real time in response to variations in the user's breathing cycle. An oxygen delivery device including a breathing cycle sensor provides breathing cycle inputs to a controller for use with at least one algorithm to detect breathing flow phases during each user breath, and to synchronize each PSA cycle to the user's breathing flow phases, on a breath-by-breath basis.

Abstract: The present invention is a wearable device for comprehensive bio-monitoring of physiologic metrics to determine metabolic, pulmonary and cardiac function and oxygen saturation measurements from breathing mask apparatuses. The device non-invasively monitors the physiologic profile of the subject, and is capable of detecting physiologic changes, predicting onset of symptoms, and alerting the wearer or another person or system. In some embodiments, the device comprises both a wearable sensor suite and a portable gas composition and flow analysis system. In preferred embodiments, it comprises a miniaturized non-invasive sensor suite for detecting physiologic changes to detect dangerous breathing or other health conditions. The system utilizes advanced fast-response sensors with improved efficiency and lifespan, and provides rapid analysis for substantially real-time monitoring of the subject's present condition to predict, mitigate and/or prevent the onset of dangerous conditions.

Abstract: A gas demand device cycles through five successive operation phases: gas is prevented from flowing through the timing gas and demand gas flow paths; gas is allowed to flow through the timing gas flow path and gas is prevented from flowing through the demand gas flow path; gas is allowed to flow through the timing gas and demand gas flow paths; gas is prevented from flowing through the timing gas flow path and gas is allowed to flow through the demand gas flow path; and gas is prevented from flowing through the timing gas and demand gas flow paths.

Abstract: A nasal breathing apparatus with multifunction has two nasal inserts and one tubular chamber. In one embodiment, the first nasal insert forms an airtight barrier inside one nostril for delivering gases. The second nasal insert does not block the other nostril and is for sampling gases. The tubular chamber is in fluid communication with the first nasal insert but not the second nasal insert and has an outlet for discharging and delivering gases and for providing continuous positive airway pressure and ventilation. In another embodiment, both nasal inserts form an airtight barrier in the corresponding nostrils. The first nasal insert is dedicated for delivering gases and the second nasal insert for sampling gases. The tubular chamber is in fluid communication with both nasal inserts and has an outlet for discharging and delivering gases and for providing continuous positive airway pressure and ventilation.

Abstract: A nasal cannula including a base portion defining a gas passageway and one or more nozzles defining a second gas passageway in gaseous communication with the first gas passageway for directing a therapeutic flow of gas to a user's nares, that may further include one or more sensors for measuring the properties of gas within a user's nares. The one or more nozzles may be a nasal insert that includes recesses or grooves that prevent sealing of the nozzle with the nare. The nozzle may be shaped to avoid insertion into the user's nares, thus preventing sealing with the nares. A stop may be positioned between two nozzles to engage a user's columella and prevent the nozzles from inserting into the user's nares. Elongate extensions are provided for inserting into the user's nares and supporting sensors for measuring gas properties therein.

Abstract: A powered air purifying respirator (PAPR) for delivering a forced flow of filtered air to a wearer is disclosed.

Abstract: A nasal cannula assembly includes a breathing gas supply lumen assembly splitting into a first inspiratory gas lumen and a second inspiratory gas lumen. An inspiratory gas nasal end portion is in fluid communication with the first inspiratory gas lumen and a second inspiratory gas lumen. The inspiratory gas nasal end portion has a pair of nasal prongs extending outwardly therefrom. An expiratory gas assembly splits into a first expiratory gas lumen and a second expiratory gas lumen. An expiratory gas nasal end portion is in fluid communication with the first expiratory gas lumen and a second expiratory gas lumen. A passage is disposed across the inspiratory nasal end portion from the pair of nasal prongs. The passage provides fluid communication between the inspiratory nasal end portion and the expiratory nasal end portion.

Abstract: A vent arrangement for a respiratory pressure therapy device may include one or a plurality of vents configured with a variable aperture for communicating a flow of breathable gas. The vent arrangement may be configured with a cross section profile exposed to the flow of breathable gas communicating through the vent that does not change as the aperture size changes. A vent arrangement may include a plurality of the vents and the aperture size of each vent may be controlled independently or together, and may be controlled according to one or more input signals from one or more sensors. Examples of suitable input signals include flow, pressure, noise, accelerometer outputs, orientation of a patient or presence of any obstructions. A patient interface or an air circuit may include the vent arrangement, or the vent arrangement may be configured to connect with a patient interface or an air circuit.

Abstract: Regulator assemblies for breathing masks of aircraft crewmembers are described, with such an assembly including a mode selection knob mounted on a support. The knob is movable between at least two positions, allowing an associated regulator to operate in at least two modes of supplying breathing gas to a crewmember. One or more protrusions of the knob, when contacted by fingers of the crewmember, may bias the knob toward a particular one of the at least two positions.

Abstract: The present invention pertains to a system, method, and device for treating sleep disorders. The present invention is particularly useful in the delivery of carbon dioxide (CO2) to a subject and in the treatment of sleep apnea. Furthermore, integration of components with various sensors and apparatuses associated therewith and attached thereto preferably complete a rebreathing circuit in the present invention. In various embodiments of the present invention where the above components are integrated as a rebreathing circuit, a subject is both the source and recipient of a controlled concentration of carbon dioxide. In such embodiments, treatment of sleep disorders becomes much more efficient and effective.

Abstract: A demand regulator (1) for aircraft breathing device (100) comprising: —a respiratory chamber (9) supplied with respiratory gas comprising breathable gas and dilution gas, —a breathable gas supply line (12, 13), —a dilution gas supply line (14, 15), —a first adjusting device (50, 60) of non-electrical type adjusting the pressure in the respiratory chamber (9), and —a second adjusting device (22, 24, 40, 41-49) adjusting the rate of dilution gas in the respiratory gas supplied to the respiratory chamber (9), the second adjusting device comprising a dilution valve (24) disposed in the dilution gas supply line (14, 15), a sensor (41-49) and an electrical control unit (40) adjusting the rate of dilution gas in the respiratory gas by controlling the dilution valve (24).