Abstract: A controller or processor for a respiratory pressure treatment device determines an estimate of patient respiratory flow based on a measure of pressure associated with flow generated by a flow generator and a measure of frequency of the flow generator, such as a rotational velocity of a servo-controlled blower motor. The estimate can be made without data from a flow sensor. The measure of frequency may be converted to an expected pressure based on characteristics of the flow generator and subtracted from the measured pressure to determine the flow estimate. The flow estimate can be implemented in the provision of respiratory pressure treatment with the flow generator. For example, the flow estimate may be utilized to trigger expiratory pressure relief during a patient's expiration as detected with the estimated flow signal.

Abstract: The present invention is a method and system for adaptively detecting a patient trigger threshold. The system and method uses fuzzy-logic control algorithm to detect an appropriate trigger threshold by monitoring the number of patient triggers within a predetermined time frame. The system and method also detects an appropriated trigger threshold by monitoring the complete absence of false triggers over a predetermined time frame, increases in average flow, increases in pressure differential, and pressure drop, in order to lower the trigger threshold. The method and system of the present invention is selectable to the user, and adaptively changes the inspiratory trigger threshold.

Abstract: The method and the apparatus are used for monitoring a patient's breathing. A respiratory movement of the patient is detected by means of a thoracic expansion sensor that is placed near the rib cage and by means of an abdominal expansion sensor that is placed near the abdomen. Moreover, a phase difference is detected between a thoracic measuring signal delivered by the thoracic expansion sensor and an abdominal measuring signal delivered by the abdominal expansion sensor. The phase difference thus detected is monitored to determine whether it exceeds at least a phase threshold or whether it increases over time, and the presence of a disorder in the respiratory tract of the monitored patient is recognized on the basis of an increasing phase difference.

Abstract: An anesthetic evaporator with a pressure control circuit has a differential pressure pick-up (18) can be calibrated in a simple manner. A switchover device (20) is provided according to the present invention at a bypass gap (3), which is designed to connect the gas inlet (4) directly with the gas outlet (5) via a first bypass line (23) and to bridge over the bypass gap (3) via a second bypass line (26) connected to a ventilation duct (27) in a first switching position. The gas flow from the gas inlet (4) to the gas outlet (5) is established via the bypass line (2) in a second switching position. The calibration of the differential pressure pick-up (18) with the pneumatic connections (16, 17) is performed in the first switching position of the switchover means (20) via the ventilation duct (27), which is open toward the ambient atmosphere.

Abstract: A monitor includes a measurement line segment adapted to be coupled between a patient interface and a positive airway pressure device. The measurement line segment defines a gas flow path. A sensor includes two ports in communication with the gas flow path through the measurement line segment, and a recording device is adapted to record data collected by the sensor.

Abstract: A sensor main unit 1 is axially split into three sub-segments. A light-emitting element 2 is attached to one end portion, and a light-receiving element 3 is attached to the other end portion. A respiratory flow path 4 is formed so as to penetrate through the center portion. The sensor main unit 1 is attached to a position on the face below the nostrils, and respiratory gas from the nostrils is guided into the respiratory flow path 4 and is caused to cross over the optical axis connected the light-emitting element 2 and the light-receiving element 3, thereby measuring a carbon dioxide gas in the respiratory gas.

Abstract: A ventilator (10) for use by a clinician in supporting a patient presenting pulmonary distress. A controller module (20) with a touch-screen display (26) operates a positive or negative pressure gas source (40) that communicates with the intubated or negative pressure configured patient through valved (46) supply and exhaust ports (42, 44). A variety of peripheral, central, and or supply/exhaust port positioned sensors (54) may be included to measure pressure, volumetric flow rate, gas concentration, transducer, and chest wall breathing work.

Abstract: A respiratory component measurement system that includes an airway adapter adapted to be placed in fluid communication with an airway of a patient and a sensor element in physical communication with the airway adapter. The sensor element is adapted to detect an orientation related characteristic of the airway adapter, a motion related characteristic of the airway adapter, or both. A respiratory component sensor is also adapted to be disposed on the airway adapter so as to measure a characteristic associated with a flow of gas through the airway adapter.

Abstract: The present invention concerns a method for detecting the start of a dive for implementation in a portable electronic device (1) of the diving computer type. More specifically, the method is for implementation in a device of this type having at least a first operating mode and a second operating mode, called the dive mode. This device includes a pressure sensor (5) for measuring the ambient pressure value (P) and electronic circuits (2) for processing the pressure measurement results including a time base (4) and at least one memory zone (7, 8). The detection method according to the present invention more particularly proposes making correction to certain measured pressure values before storing them as reference pressure values (Pref). Thus, the start of a dive can be detected with a high level of reliability solely on the basis of ambient pressure measurements.

Abstract: An information processing device for a diver used for diving by using a plurality of mixed gases in which the mixture ratios of a plurality of diving gases are the same or different determines the switch timing of the mixed gas on the basis of a preset scheduled dive pattern and an actual dive pattern up to present. A notification is issued regarding the switch timing and information for specifying the mixed gas to which a switch is to be made based on this switch timing. When the diver selects one of the cylinders as the cylinder to which the switch is to be made and in which the mixture ratio of the diving gas is different, processing is carried out that prohibits switching to the selected cylinder when it is determined that the selected cylinder may create a danger of oxygen deficiency or oxygen poisoning.

Abstract: The concentration of xenon, in a medical gas mixture of xenon as an active component with a known composition of oxygen and, optionally, nitrogen and/or helium recirculating through a medical device (103) in which carbon dioxide is introduced into the mixture, is monitored by removal (135, 133) of carbon dioxide downstream of the medical device (103) and subsequently passing the carbon dioxide-free gas through an ultrasonic gas analyser (143) upstream of the medical device. The gas analyzer determines the xenon concentration by measuring the time delay between transmission of an ultrahigh frequency ultrasonic pulse of at least 100 kHz axially through the sample chamber from a location at one end thereof and reflection of said pulse axially from the other end of the sample chamber back to said location. An analyser of novel construction is disclosed.

Abstract: A monitoring system for cardiac operations with cardiopulmonary bypass comprising: a processor operatively connected to a heart-lung machine; a pump flow detecting device connected to a pump of the heart-lung machine to continuously measure the pump flow value and send it to the processor; a hematocrit reading device inserted inside the arterial or venous line of the heart-lung machine to continuously measure the blood hematocrit value and to send it to the processor; a data input device to allow the operator to manually input data regarding the arterial oxygen saturation and the arterial oxygen tension; computing means integrated in the processor to compute the oxygen delivery value on the basis of the measured pump flow, the measured hematocrit value, the preset value of arterial oxygen saturation, and the preset value of arterial oxygen tension; and a display connected to the processor to display in real-time the computed oxygen delivery value.

Abstract: An oxygen enrichment apparatus includes a main body including an oxygen enriching unit and a pump unit for supplying oxygen-enriched air obtained by the oxygen enriching unit to a predetermined place; a ventilating unit for suctioning exterior air into the main body and discharging the exterior air out of the main body after supplying the exterior air into the oxygen enriching unit; and a control unit for controlling the pump unit and the ventilating unit. The ventilating unit and the control unit are installed in the main body. The main body further includes therein a secondary battery serving as a power supply for supplying a power to the pump unit, the ventilating unit and the control unit.

Abstract: Anaesthesia machine arrangement and a method in connection with an anaesthesia machine arrangement comprising a gas dispenser of an anaesthesia machine connected to a patient circuit that comprises a monitor device, a control device and an interface unit. The gas dispenser is configured to deliver a desired concentration of fresh gas to the patient circuit, the desired concentration being set by using the interface unit. The monitor device is configured by using a sample line to monitor gas concentration in the patient circuit and the control device is configured to control the gas dispenser from the basis of the data received from the monitor device to keep the desired fresh gas concentration.

Abstract: A system for mechanical ventilation treatment is described. In one embodiment the system provides advice on treatment and/or weaning of patients from mechanical ventilation based on the patient's conditions. In another embodiment the system includes apparatus to monitor and analyze the patient's data and data from the mechanical ventilator and controls the ventilator automatically.

Abstract: A method of setting inspiratory time, expiratory time, and a subject's breath size in controlled mechanical ventilation comprises: a) setting a subject's expiratory time; b) setting the subject's inspiratory time; and c) setting the subject's breath size, all based on various criteria.

Abstract: Inhalation anaesthesia delivery system and a leak detecting method, whereby the system comprises a fresh gas feeding arrangement connected to a breathing circuit, a monitor device, The monitor device is configured to monitor gas concentrations in the breathing circuit by using a sampling line. The monitor device is configured to measure at least two gas components' concentrations and identify changes, which are simultaneous towards the known ambient air concentration values of the two gas components' concentrations measured.

Abstract: A method of setting a subject's breath size in controlled mechanical ventilation, comprising varying a subject's tidal volumes and/or inspiratory pressures for a predetermined inspiratory time and predetermined expiratory time; determining end tidal gas concentrations associated with said tidal volumes and/or inspiratory pressures; and curve-fitting a relationship between said tidal volumes and/or inspiratory pressures and said end tidal gas concentrations.

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: An oxygen enrichment apparatus includes an oxygen enriching unit for generating oxygen-enriched air and a discharge unit for discharging the oxygen-enriched air transferred from the suction unit. The oxygen-enriched air generated by the oxygen enriching unit has an oxygen concentration ranging from about 25% to 35%. The apparatus also includes a suction unit for suctioning the oxygen-enriched air from the oxygen enriching unit and a control unit for controlling the operation of the suction unit. The main body is provided with a display unit for indicating a state that the oxygen-enriched air is being discharged out by the discharge unit. The oxygen enriching unit has at least one oxygen enriching membrane for generating the oxygen-enriched air and a condensed water treating unit is installed at an air passage for guiding the oxygen-enriched air from the oxygen enriching unit to the discharge unit via the suction unit.

Abstract: A pair of solenoid air/oxygen mixing systems used by an adaptive controller for delivering fractional inspired oxygen to a patient is described. The solenoid control system comprises either a bi-modal solenoid or a proportional solenoid air/oxygen mixing system to derive a fraction of inspired oxygen delivered to a patient. In the bi modal solenoid air/oxygen mixing system, a derived fraction of insipid oxygen is delivered to a patient. The bi-modal mixer uses a three-way valve solenoid. The solenoid has two input gas ports and one output gas port. Toggling between the two input port gases generates an output gas oxygen concentration. In contrast with the bi-modal solenoid, variation or proportionality between the two input port gases generates an output gas oxygen concentration. Both solenoid systems use a mini-computer and digital controller with software to control the fraction of inspired oxygen delivered to a patient. Finally, several therapeutic applications are described.

Abstract: A gas delivery system, having a gas identification, by which a gas supplied to the gas delivery system is identified, a blender, blending oxygen and the gas to provide a gas mixture with an oxygen flow rate set up by an operator, and at least one flow sensor, to measure a flow rate of the gas mixture. The blender is driven by an actuator motor to various blender positions with the blender positions being calibrated based on the specific heat ratio and the gas constant of the gas. The flow sensor can be installed at the inspiratory circuit, the proximal circuit and the expiratory circuit of the gas delivery system. The flow sensor output is corrected based on the actual conditions, including the temperature, pressure and humidity, and characteristics of the gas mixture.

Abstract: A mainstream gas monitoring system and method that includes a using a mainstream airway adapter, and a gas sensing assembly associated with the mainstream airway adapter to measure an analyte of a gas flow through the adapter. A gas sensing portion outputs a signal indicative of the analyte in a gas flow in the mainstream airway adapter. A processing portion receives the signal from the gas sensing portion and determines an amount of the analyte in the gas flow based on the signal from the gas sensing portion. The processing portion also compensates for volumetric differences between the gas flow during inspiration and the gas flow during expiration to maximize the accuracy in the measurements made using such a system and method.

Abstract: An inhalation system is disclosed that, in an exemplary embodiment, includes an ejector that ejects medicated droplets during an activation event, a conduit fluidically coupled to the ejector and configured to transport the droplets to a patient during an in-breath, and a particle detection system configured to determine whether the droplets have properly passed through the conduit and to the patient during an activation event. Also disclosed are methods for detecting particles in an inhaler system, with an exemplary method including generating a dose of medicament particles from an inhaler system; detecting particles emitted in the inhaler system; and determining if a desired particle flux has been achieved for inhalation by a patient.

Abstract: A gas-mixing device for respirators can be used both in stationary operation and in mobile operation. The gas-mixing device has a storage tank (5), into which compressed air and oxygen can be introduced by dispensing valves (3, 8). In addition, a blower (10), which draws in gas from the environment (11), is connected to the storage tank (5). To dispense gas from the pressurized gas sources (4, 6) by means of the dispensing valves (3, 8), a first operating pressure level is set in the storage tank (5). When changing over to the blower operation, the operating pressure level is lowered to a pressure level adapted to the maximum respiration pressure.

Abstract: A ventilator includes a sensor to monitor a characteristic associated with the delivery of gas to the patient, such as pressure. A sensor power supply (100, 130) is feeding a sensor in the form of a Wheatstone bridge. A first end (104) of the bridge is coupled to a first positive voltage source (112, 142) and a second end (116) is coupled to a second positive voltage source (118, 156, 180). A capacitor (120) is coupled to the second end of the bridge.

Abstract: The invention relates to an apparatus for the acquisition and interpretation of expirograms comprising: a gas measuring probe that is designed to determine the gas concentration ƒmess of a gas in exhaled respiratory air; a reading device that is connected to the gas measuring probe via signal and is designed to read for a plurality of values x1, . . . , xN of an exhaled volume of the exhaled respiratory air the respective determined gas concentrations ƒmess(x1), . . . , ƒmess(xN) from the gas measuring probe; a storage device that is designed to store the values x1, . . . , xN assigned to the gas concentrations ƒmess(x1), . . . , ƒmess(xN); a function fitting unit that is connected to the storage device via signal and that is designed to determine a non-linear fit function ƒ(x)=g(x)·h(x)+OffsetGas for the stored gas concentrations ƒmess(x1), . . .

Abstract: An esophageal intubation system includes a main tube with a tapered body, proximal and distal ends and a bore extending between and open at the ends. The main tube is inserted into the oropharynx and its distal end extends into the upper esophagus in order to provide a conduit for esophagoscopes, gastroscopes and related diagnostic and treatment equipment. A first auxiliary tube assembly delivers O2 close to the larynx. A second ancillary tube assembly samples CO2 from the larynx region. An esophageal intubation method includes the steps of moderately sedating a patient, placing a main esophageal tube in the oropharynx and partway into the upper esophagus, passing an esophagoscope or a gastroscope through the main tube and into the esophagus or stomach while minimizing the gag reflex, delivering O2 and sampling CO2 from the pharynx region.

Abstract: The present invention comprises systems and methods for handling large amounts of data prone to ambiguity and artifact in real-time in order to ensure patient safety while performing a procedure involving a sedation and analgesia system. The invention utilizes neural networks to weight data which may be more accurate or more indicative of true patient condition such that the patient condition reported to the controller and the user of a sedation and analgesia system will have increased accuracy and the incidence of false positive alarms will be reduced.

Abstract: The present invention relates to a method of compensating the pressure drop in an ordinary ventilator tube. The method comprises the measurement of a first air flow at a first pressure on the apparatus' side of the ventilator tube and with the respiratory mask taken off. Moreover, a parameter is calculated in a function which provides the pressure drop in the ventilator tube in dependence on the air flow. The parameter for the air flow and pressure is calculated. Later, the air flow is calculated with the respiratory mask being put on. By means of the function a correction pressure is calculated from the air flow. Finally, a target pressure is set which results as a sum of the selected mask pressure and the correction pressure. The invention moreover relates to ventilator for performing the aforementioned method and to a memory medium for storing a corresponding program.

Abstract: An electronic controller having at least one microprocessor controls the solenoid operated valve adding oxygen to the breathing loop of a closed circuit mixed gas rebreather with carbon dioxide scrubbing in maintenance of an oxygen set point in the rage of 0.13-0.50 without any need for monitoring or interpretation of signal data by the operator. The controller receives signals from at least one oxygen sensor located in the breathing loop and sends signals to an indicator: visual, aural, or tactile; during operation providing only intuitively understood normal functioning, limited time remaining, and bail out indications. Automatic diagnosis including oxygen sensor calibration, indication of actions required such as scrubber replacement, and confirmation of an action taken with signals from an action sensor are provided.

Abstract: A Heliox delivery system with positive pressure support is disclosed. The positive pressure support Heliox delivery system comprises at least two inlet ports, one of which is coupled to a source of Heliox gas and another coupled to a source of oxygen gas. The system further includes a gas blender, one or more control valves, a gas analyzer, an outlet port, a breathing circuit and a control unit. The control unit is adapted to operatively control both the gas blender to adjust the blending of oxygen and Heliox and the control valve to adjust the flow rate or pressure of the blended gas mixture in response to user inputs as well as the measured parameters from the gas analyzer, flow meters and associated sensors.

Abstract: A respiratory breathing circuit prevents heat loss and condensation in a flow of humidified air through a conduit from a humidification system to a patient interface, such as a nasal cannula. The circuit directly impedes heat loss or insulates the flow of a humidified gas therein, and provides a heating source inside the circuit along the length of the circuit to prevent net heat loss from the circuit tubing by providing thermal energy and/or insulation to impede convective, conductive, or radiative heat loss by the gas as it flows through the system. A temperature, humidity, or other flow quality measuring probe is disposed at the distal end of the circuit near the patient interface to actively measure a corresponding quality of the humidified gas flow to provide feedback to the system. A pressure relief valve is provided on the circuit to prevent a pressure build-up and/or structural failure.

Abstract: A device with a respirator (1) and with a humidifier (11) for breathing gas. Breathing gas humidification is adapted to the different operating states of the respirator (1). A connection (13) is provided for bidirectional data transmission between the control and operating unit (8) of the respirator (1) and the control and operating unit (9) of the humidifier (11).

Abstract: A safety system and method of an air distribution system of a tunnel structure is disclosed. In one embodiment, the air distribution includes a supply unit installed on a particular wall of the first set of walls to facilitate delivery of breathable air from a source of compressed air to an emergency support system of the tunnel structure, a fill site interior to the tunnel structure to provide the breathable air to a breathable air apparatus at multiple locations of the tunnel structure, a secure chamber of the fill site as a safety shield that confines a possible rupture of an over-pressurized breathable air apparatus within the secure chamber, a distribution structure that is compatible with use with compressed air that facilitates dissemination of the breathable air of the source of compressed air to multiple locations of the tunnel structure.

Abstract: A portable oxygen concentrator includes a pair of sieve beds having first and second ends, a compressor for delivering air to the first ends of the sieve beds, a reservoir communicating with the second ends of the sieve beds, and an air manifold attached to the first ends of the sieve beds. The air manifold includes passages therein communicating with the compressor and the first ends of the sieve beds. A set of valves is coupled to the air manifold, and a controller is coupled to the valves for selectively opening and closing the valves to alternately charge and purge the sieve beds to deliver concentrated oxygen into the reservoir. An oxygen delivery manifold communicates with the second ends of the sieve beds for delivering oxygen from the reservoir to a user. Pressure sensors may be provided in the reservoir and/or delivery line for controlling operation of the controller.

Abstract: An apparatus and method to characterize NO gas exchange dynamics in human lungs, including performing a plurality of breathing maneuvers of substantially constant flow rates within a predetermined range, measuring data relating to at least one of an NO concentration and an NO elimination rate as a function of exhaled volume or exhalation flow rate, applying a lung model to the measured data, and obtaining at least one parameter indicative of disease states of the lung based on the lung model and the measured data, wherein the lung model, when applied in the predetermined range, predicts a substantially linear relationship between the NO elimination rate and the exhalation flow rate.

Abstract: Ventilator systems include: (a) a mass flow controller; (b) a gas delivery valve in communication with the mass flow controller and configured to selectively dispense a plurality of different gases to a subject; (c) a first gas source in fluid communication with the gas delivery valve; (d) a second gas source in fluid communication with the gas delivery valve; (e) a first pressure sensor located upstream of the gas delivery valve; (f) a second pressure sensor located downstream of the gas delivery valve; and (g) a controller operatively associated with the first and second pressure sensors and the mass flow controller, the controller comprising computer program code that monitors the pressures measured by the first and second pressure sensors and automatically dynamically adjusts the flow rate of the mass flow controller.

Abstract: A meter for visual determination of proper oxygen or gas flow to a facemask or cannula from a pressurized gas supply. The device features a body with a central cavity extending axially therein adapted for translation of a piston biased toward an incoming gas stream from the pressurized supply. A cup-shaped endwall of the piston increases the area on which the incoming air stream acts. The incoming air stream is focused to impact a center portion of the endwall at a higher rate of speed using a narrowing incoming conduit resulting in increased force and translation of the piston even under the low pressures in which cannulas operate. The piston translates to a point where it may be viewed alone or adjacent to indica to ascertain proper oxygen flow to the user, by a caretaker from a distance.

Abstract: A flow probe for use in a humidification system is positioned in a humidified gases flow such as that which is provided to a patient in a hospital environment. The flow probe is designed to provide both temperature and flow rate sensing of the gases flow by incorporating two sensors into the gases flow. The flow probes are shaved and aligned within the gases flow to enable accurate gas flow readings to be taken whilst reducing the occurrence of condensation on the sensors. The flow probe can also be included in a humidification control systems to provide a patient with a desired humidity level or simplify the amount of user input required to set humidity levels. Furthermore, the flow probe can provide a controller with flow information which may then be used to determine certain conditions that could prove to be dangerous to a patient.

Abstract: A breathing gas supply system for supplying breathable gas in an aircraft includes an oxygen enriching apparatus which is operable in at least two modes to provide product gas with varying oxygen concentrations. A first feed line feeds more highly enriched product gas to one or more breathing gas outlets, and a second feed line feeds less highly enriched product gas e.g. to an aircraft cabin for breathing during normal high altitude flight. A control means controls oxygen enrichment apparatus to provide highly enriched product gas to the breathing gas outlet or outlets in the first mode of operation or less highly enriched product gas e.g. to the cabin for normal breathing, and controls a diverter valve. Which directs the product gas to the respective feed line.

Abstract: The invention provides an improved ventilation method and method for controlling a ventilator apparatus in accordance with same. More specifically, the present invention relates to a method of controlling a ventilator apparatus comprising the steps of placing a ventilator in a mode capable of adjusting airway pressure (P) and time (T), monitoring expiratory gas flow, analyzing the expiratory gas flow over time (T) to establish an expiratory gas flow pattern, and setting and/or adjusting a low time (T2) based on the expiratory gas flow pattern. Alternatively, the present invention relates to a method of controlling a ventilator apparatus comprising the steps of placing a ventilator in a mode capable of adjusting airway pressure (P) and time (T), and setting a low airway pressure (P2) of substantially zero cmH2O.

Abstract: An oxygen concentrator is utilized in combination with a compressor, preferably a radial compressor, to provide a highly enriched and compressed oxygen gas in a mobile container such as a gas cylinder. The combination and method of production provides for the facile preparation of an enriched source of oxygen for use by an ambulatory or wheelchair-confined patient. The oxygen concentrator utilizes two or more molecular sieves to provide a breathable gas of at least about 85% or 90% oxygen from atmospheric air. The oxygen-enriched gas can be stored in a buffer tank and prioritized so as to supply a patient with a proper amount and concentration of oxygen and secondarily to supply an amount of the enriched oxygen to a compressor. The radial compressor utilizes multiple stages to produce the highly compressed oxygen-enriched gas and has radially arranged pistons. The radial compressor is compact and lightweight.

Abstract: A detector that monitors the presence of halogenated agents and the presence of N2O includes a base to which a filter cannister is removably coupled. The cannister has an input for accepting exhalent from a patient or an anesthesia machine and an outlet for outputting the filtered exhalent as gases to the base. The filtered gases are routed a gas measurement or monitor cell housed in the base. The cell has a halogenated agents sensing system and a N2O sensing system. When the filter material in the filter cannister could no longer filter out the halogenated agents, the agents are passed from the filter to the measuring cell, which would detect the presence of the halogenated agents. An audible alarm sounds when halogenated agents are detected. This tells the user that it is time to replace the filter cannister.

Abstract: A pressure support system and method of treating disordered breathing that optimizes the pressure delivered to the patient to treat the disordered breathing while minimizing the delivered pressure for patient comfort. The controller in the pressure support system operates as a set of prioritized control layers, wherein each control layer competes for control of the pressure generating system to implement a unique pressure control process. The pressure support system also controls the pressure provided to the patient based on the variability of the monitored data and a trend analysis of this data, including an indication of the skewness of the patient's inspiratory waveform.

Abstract: A device for measuring the volume flow or other substance properties of a gas, whose direction of flow can reverse. The arrangement contains a specially designed Y-piece, which is used for branching into direction-dependent flow paths and can be used at the same time for the measurement. Such devices can be preferably used in the area of mechanical respiration.

Abstract: Disclosed is an apparatus and method for the delivery of inspired gas, e.g., supplemental O2, to a person combined with gas sampling, including for the purpose of monitoring of the ventilation of the person. In the invention, the delivery of inspired gas and gas sampling are accomplished without the use of a sealed face mask. The apparatus of one embodiment of the present invention comprises an oxygen delivery device, nasal airway pressure sampling devices, optionally an oral airway pressure sampling device and at least one pressure analyzer connected to the sampling devices which determine the phase of the person's respiration cycle and the person's primary airway. The oxygen delivery device is connected to a controller such that it delivers a higher flow of oxygen to the person during the inhalation phase of the person s respiratory cycle. The invention thus increases end tidal oxygen concentrations.

Abstract: A system for filling a portable cylinder with therapeutic gas, and providing therapeutic gas to a patient. Therapeutic gas delivery to a patient may be through a conserver, or may be in a continuous mode. Some embodiments of the invention may test the contents of the portable cylinder prior to filling. The specification also discloses a silent mode of operation where therapeutic gas is provided from the system by means of internal and/or external cylinders.

Abstract: The present invention relates to an evaporator for respirators, including a storage tank for a liquid, a gas intake flange and a gas outlet flange as well as an apparatus for heating the liquid, which is formed such that it can heat a small portion of the liquid and inject the formed vapor into the gas to be humidified, with the gas to be enriched with the liquid being passed through the upper part of the storage tank over the surface of the liquid, which may be located in the lower part of the storage tank, so as to provide a simple evaporator for respirators having a low consumption of energy. Moreover, the present invention relates to a method of evaporating liquids.

Abstract: This invention provides a medical diagnosis and therapy system particularly adapted for the combined uses of emergency cardiac defibrillation and pulmonary oxygen administration, including automated patient cardiopulmonary assessment and voice prompted therapy and resuscitation: electrocardio diagnosis/monitoring/defibrillation and electropulmonary blood oximetry/oxygen administration. The system has a case having access opening(s) and clear cover(s) to view the apparatus and contents, to dispel all doubt as to know how to open the case and to make it easy for a user to quickly find and use the various components.