Abstract: Described are methods and devices for therapeutic or medical gas delivery that utilize at least one proportional control valve and at least one binary control valve. The proportional control valve may be in series with the binary control valve to provide a valve combination capable of pulsing therapeutic gas at different flow rates, depending on the setting of the proportional control valve. Alternatively, the proportional control valve and binary control valve may be in parallel flow paths.

Abstract: A header for a medical implant device is configured to provide an electrical connection to a circuit within the housing of the medical implant device. The header includes at least one circuit board; a header housing enclosing the circuit board and configured to be connected to the housing of the medical implant device; and a sensor system on the circuit board.

Abstract: Provided are a method for controlling an oxygen provider and a portable device. The method includes: acquiring measurement data at a patient side; determining an oxygen demand volume and an output pattern of an oxygen provider based on the acquired measurement data and a desired oxygen fraction ratio; and controlling the oxygen provider with the oxygen demand volume and the output pattern. With the method or device for controlling an oxygen provider, oxygen with an amount that actually needed by a patient is provided to produce the blended gas to be delivered to the patient, and the blended gas delivered to the patient are regulated according to the output pattern to guarantee the blended gas is delivered in synchronization with the inspiration of the patient, so that a therapeutic effect is achieved with a lower oxygen consumption amount.

Abstract: A novel clinical decision support system (CDS) helps the clinician setup, maintain, and interpret esophageal pressure measurement. The esophageal pressure CDS (Pes CDS) would remind the clinician to do an occlusion test whenever the balloon is first inserted or changes dramatically. It could monitor the occlusion test and provide feedback on the performance and success of the occlusion test. Changes in the patient or monitored data can be tracked by looking for changes in the balloon baseline pressure, changes in the amplitude of the pressure waveform, or changes in the pattern of the Pes waveform. Having information from the ventilator will further increase the ability of the system to determine when Pes is changing unexpectedly.

Abstract: A medical device of the type used for assisting a user in manually delivering repetitive therapy to a patient (e.g., chest compressions or ventilations in cardiac resuscitation), the device comprising a feedback device configured to generate feedback cues to assist the user in timing the delivery of the repetitive therapy, at least one sensor or circuit element configured to detect actual delivery times, at which the user actually delivers the repetitive therapy, and a processor, memory, and associated circuitry configured to compare the actual delivery times to information representative of desired delivery times to determine cue times at which the feedback cues are generated by the feedback device.

Abstract: Methods and apparatus for treating a respiratory disorder, in one aspect, include an apparatus that delivers backup breaths at a sustained timed backup rate that is a function of the patient's spontaneous respiratory rate. Other aspects include apparatus that delivers backup breaths at a rate that gradually increases from a spontaneous backup rate to a sustained timed backup rate or, alternatively, apparatus that oscillates a treatment pressure in antiphase with the patient's spontaneous respiratory efforts when a measure indicative of ventilation is greater than a threshold. Other aspects include apparatus configured to treat Cheyne-Stokes respiration by computing the treatment pressure so as to bring a measure indicative of ventilation of the patient towards a target ventilation that is dependent on the measure indicative of ventilation or, alternatively, by periodically elevating the treatment pressure to a high level for a short time.

Abstract: A controller or processor(s) implements detection of respiratory related conditions, such as asynchrony, associated with use of a respiratory treatment apparatus or ventilator. Based on data derived from sensor signals associated with the respiratory treatment, the detector may evaluate a feature set of detection values to determine whether or not an asynchrony occurs in a breath of the patient's respiratory cycle such as by comparing the values against a set of thresholds. Different events may also be identified based on the particular feature set and threshold(s) involved in the detection processing. Automated determination of feature sets may also be implemented to design different asynchrony event classifiers. The methodologies may be implemented by computers or by respiratory treatment apparatus.

Abstract: A system for adjusting extrinsic positive end expiratory pressure during an expiratory phase of a ventilator is provided. The system includes a computer system that comprises one or more physical processors programmed with computer program instructions which, when executed cause the computer system to: determine a respiratory reactance from airway flow information of the patient and airway pressure information of the patient, the airway flow information and airway pressure information of the patient being obtained from one or more sensors, and adjust the extrinsic positive end expiratory pressure during the expiratory phase of the ventilator such that the determined respiratory reactance falls within a defined respiratory reactance range.

Abstract: A test device for testing of an oxygen sensor uses a compressor to draw air from an external environment and deliver compressed air into a gas separation unit. A gas separation membrane is located in a passage of the gas separation unit such that compressed air from the compressor travels through the passage and passes through the gas separation membrane. The gas separation membrane separates at least one of nitrogen and oxygen from the compressed air to produce a calibration gas having a calibrated amount of oxygen that is different from an amount of oxygen in the air. The calibration gas coupling is configured to be fluidly connected to the oxygen sensor such that the calibration gas is deliverable from the calibration gas coupling to the oxygen sensor.

Abstract: A device provides a first data signal that indicates an activity of at least one muscle of a patient that is relevant for an inspiratory breathing effort and a second data signal that indicates an activity of at least one muscle of the patient that is relevant for an expiratory breathing effort. The data signals are generated from electromyography (EMG) signals detected by surface electromyography sensors. A computer is configured to determine breathing phase information on the basis of a breathing signal and to check at least one of the electromyography signals or at least one of the separated signals for detectability of a heart signal component and further to assign the signals to an inspiratory breathing activity as well as to an expiratory breathing activity of the patient as a function of the breathing phase information.

Abstract: A system is for alarm management in connection with a lung recruitment manoeuvre performed by a breathing apparatus on a mechanically ventilated patient. The system is configured to obtain information on at least one optimized ventilation setting for the patient, determined during the lung recruitment manoeuvre, and to automatically initiate at least one alarm setting for a period of ventilation following the recruitment manoeuvre, based on the optimized ventilation setting.

Abstract: Some embodiments of the present disclosure comprise improved systems and methods for monitoring physiological parameters such as intracranial pressure (“ICP”), intracranial temperature, and subject head position. For example, in some embodiments, an implantable apparatus for measuring ICP can be implanted into a subject skull. The apparatus can comprise an implant body having a hermetically sealed chamber housing a gas at a reference pressure, and a pressure conduction catheter having a proximal end and a distal end, wherein the distal end is configured to extend into the brain through a burr hole in the skull and includes a plurality of ports. A barrier can cover the ports of the distal end of the pressure conduction catheter, wherein the barrier and pressure conduction catheter are filled with a number of gas molecules so that the barrier is not in tension in a predefined range of ICPs.

Abstract: A system monitors fatigue of a user. The system (100) may include one or more data sources, such as a non-obtrusive sleep sensor, configured to generate objective sleep measures of the user. The system may also include a fatigue monitoring module, which may be configured to generate an assessment, such as in one or more processors, of the fatigue state of the user based on the data from the one or more data sources.

Abstract: A combined exhaled air and environmental gas sensor apparatus for mobile respiratory equipment includes a housing, wherein the housing includes a port aperture, a connector configured to attach the port aperture to a respiratory exhaust port, and at least an ambient aperture connecting to an exterior environment, a sensor positioned within the housing, the sensor configured to detect a carbon dioxide level and generate sensor outputs indicating detected carbon dioxide level, a processor communicatively connected to the sensor, the processor including a memory, a breath analysis mode and an environmental analysis mode, wherein the processor is configured to receive a plurality of sensor outputs from the sensor, match the plurality of sensor outputs to mode parameter profile, and switch between the breath analysis mode and the environmental analysis mode as a function of the mode parameter profile.

Abstract: The embodiments disclose a method including using a monitor system for monitoring and detecting chemical compositions and biological pathogens, providing the monitor system configured to communicate with a cell phone, using at least one monitor/detector component, providing a plurality of biological sensors for detecting certain biological pathogens, and providing a plurality of chemical sensors for detecting certain chemical compositions.

Abstract: Mouth-breathing can be detected in early phase expiration during respiratory treatments involving a pressure support device. In accordance with some embodiments, an output signal is received from a sensor that conveys information relating to one or more parameters of the pressurized flow of breathable gas as it is delivered to an air-way of a subject. Transitions are estimated between inspiratory phases and expiratory phases of respiration by the subject based on the one or more determined parameters. A local extreme is identified in a level of a first parameter during a given expiratory phase of respiration by the subject. The level of the first parameter is analyzed as a function of time within a sampling window to determine whether the subject is breathing by mouth during the given expiratory phase. The sampling window begins at or proximate to the identified local extreme in the level of the first parameter.

Abstract: In certain example embodiments, a system and/or method of guiding transitions between therapy modes in connection with the treatment and/or diagnosis of a patient for a respiratory disorder is/are provided. Respiratory disorder treatment according to a first therapy mode is provided. Input indicating a second therapy mode to be transitioned to following provision of the first therapy mode is received, with the second therapy mode being different from the first therapy mode. At least one default treatment parameter suitable for the second therapy mode is assigned or calculated. Each default treatment parameter of the second therapy mode is presented, with each default treatment parameter being adjustable by an operator during the presenting. Transitioning from the first therapy mode to the second therapy mode is performed by providing respiratory disorder treatment in accordance with the second therapy mode and each default treatment parameter and any adjustments made thereto prior to the transitioning.

Abstract: The invention relates to a system for breath test of a person. It includes a sensor unit configured to sense the presence/concentration of a volatile substance, e.g. alcohol, present in air flowing through a predefined inlet area and generating a signal corresponding to the concentration of said substance. An analyzer determines the concentration of said substance in the breath of said person. It comprises means for the temporary interruption of said air flow at a point in time coinciding with the detection of a breath. It also relates to a method comprising interrupting the flow through said predefined area for a predetermined period of time, and detecting the concentration of said substance during said interruption.

Abstract: In some examples, a system includes a medical device comprising an elongate body configured to advance through layers of tissue of a patient, a lumen extending through the elongate body, a fluid line configured to supply fluid to the lumen, and a pressure sensor positioned within the lumen or the fluid line. The system may further include processing circuitry configured to receive, from the pressure sensor, a signal corresponding to the pressure of the fluid at each of a plurality of time points, determine, for each time point: a corresponding amplitude value of the signal, a difference between two amplitude values of the signal, an amplitude oscillation status of the signal, a position of the elongate body based on the difference and the amplitude oscillation status; and provide an indication of the position of the elongate body relative to the layers of tissue.

Abstract: An apparatus includes a processor and an output device. The processor is configured to receive positions, within a heart of a patient, of one or more electrodes that apply Radio Frequency (RF) energy to ablate tissue in the heart, in a coordinate system having a vertical axis. The processor is further configured to receive positions, within a heart of a patient, of one or more electrodes that apply Radio Frequency (RF) energy to ablate tissue in the heart, in a coordinate system having a vertical axis, and to calculate, based on the received positions, a subset of one or more smallest heights among respective heights of the electrodes above an esophagus of the patient along the vertical axis, and to generate a graphical user interface that visualizes the electrodes and the respective heights above the esophagus. The output device is configured to present the graphical user interface to a user.

Abstract: Apparatus to permit a delivery of a flow of breathable gas to a patient's airways. In one version, a coupler extension may include a seat portion to permit use of a mask with a nasal cannula. In some versions, the coupler extension is configured to conduct the flow of gas to prongs of a nasal cannula. The seat portion can receive and seal with a cushion of a respiratory mask and may have a sealing bevel to promote sealing between the cushion of the respiratory mask and a facial contact surface of a user. In some versions, a conduit adapted to communicate a flow of gas may comprise a slit valve formed by a portion of the wall material of the conduit. In some versions, a nasal interface may include naris pillows to seal with and conduct a flow of breathable gas into a nares of a user. Each naris pillow may include a nasal projection to conduct a further flow of gas. The nasal projection may extend within the naris beyond the seal of the naris pillow.

Abstract: A device for detecting physiological parameters is used to detect a degree of user hypoxemia in response to flight conditions; degree of hypoxemia may be used automatically to modify actions by a training device such as a reduced oxygen breathing device or centrifuge and generate feedback or modifications to training profiles for future use. Machine learning processes may be combined with sensor activity to discover relationships between maneuvers, environmental conditions, physiological parameters, and degrees of impairment to develop optimal flight or training plans.

Abstract: A non-invasive, optical-based physiological monitoring system is disclosed. In an embodiment, the non-invasive, optical-based physiological monitoring system comprises an emitter configured to emit light into a tissue site of a living patient; a detector configured to detect the emitted light after attenuation by the tissue site and output a sensor signal responsive to the detected light; and a processor configured to determine, based on the sensor signal, a first physiological parameter indicative of a level of pain of the patient.

Abstract: Methods and/or apparatus automate setting of a pressure ramp to permit pressure to gradually arrive at a treatment pressure such as in the initial or pre-sleep stages of use of a respiratory therapy pressure device for treatment of a respiratory disorder during sleep (e.g., sleep disordered breathing). In an example, apparatus for treating a respiratory disorder may include a breathable gas pressure generating device. The apparatus may include a controller, including a processor(s). The controller may be configured to collect historic sleep onset parameter(s) concerning timing of a patient falling asleep. The apparatus may determine, based on the historic sleep onset parameter(s), a pre-sleep limit. The apparatus may determine a pre-sleep profile of pressure versus time having a duration spanning the pre-sleep limit and having a plurality of ramping sub-therapeutic pressures. The apparatus may control, upon initiation of treatment, setting of the pressure generating device according to the pre-sleep profile.

Abstract: A positive airway pressure apparatus is automatically adjusting. Pressure increases in response to apnea events when the apparatus is in one or more responsive states. Pressure does not increase in response to apnea events when the apparatus is in a non-responsive state. The apparatus switches between responsive and nonresponsive states depending upon any of a number of different criteria that help differentiate between open airway apnea events and closed airway apnea events.

Abstract: A therapeutic vaporizer is disclosed having two or more housing portions configured to form an inner cavity. The housing portions are movable between an open and closed position, such that at least a portion of the inner cavity is enclosed when the housing portions are in the closed position. The vaporizer includes at least one accessory-receiving element configured to receive at least one accessory within the inner cavity when the housing portions are in the closed position.

Abstract: A method of avoiding a contaminant which would skew an analyte result in a breath analysis method and of calibrating subject of the breath analysis includes, immediately before the breath analysis method or the collection of breath for the breath analysis method, administering to the subject a predetermined gas composition. A system for analyzing an analyte in breath of a subject while avoiding a local contaminant which would skew an analyte result and calibrating the subject of so that the result of the analyte analysis will be the same regardless of where the test is performed geographically, includes a source of a predetermined gas composition immediately before the breath analysis method or the collection of gas for the breath analysis method, administering to the subject a predetermined gas mixture.

Abstract: Systems and methods for estimating a leak flow in a breathing assistance system including a ventilation device connected to a patient are provided. Data of a flow waveform indicating the flow of gas between the ventilation device and the patient is accessed. A specific portion of the flow waveform is identified, and a linear regression of the identified portion of the flow waveform is performed to determine an estimated leak flow in the breathing assistance system.

Abstract: A system for dispensing fluid in response to a sensed property such as an ambient sound comprises a sensor for detecting one or more properties, a processing stage for determining if the one or more sensed properties is/are within a predetermined range and/or above and/or below a predetermined level and dispenser for dispensing a fluid into an area surrounding the system if the one or more sensed properties is/are determined by the processing stage to be within a predetermined range and/or above and/or below a predetermined level and/or value.

Abstract: A method for estimating patient airway flow in a non-invasive ventilator system. The method includes the steps of (i) determining an estimated gas flow at the proximal end of the tubing; (ii) determining a proximal pressure error value by subtracting the measured pressure at the proximal end of the tubing from the estimated pressure at the proximal end of the tubing; (iii) compensating for the determined proximal pressure estimate error value; (iv) compensating for an error in the estimated gas flow at the proximal end of the tubing by feeding the estimate back into a sum of accumulated flows; (v) determining an estimated gas flow leak; (vi) monitoring for a leak in the non-invasive ventilator system; (vii) determining a gas flow leak factor; (viii) adjusting the estimated gas flow leak; and (ix) compensating for bias in the patient airway flow.

Abstract: Disclosed is a method of controlling a respiratory assistance apparatus delivering a flow of gas, particularly a flow of air, having the steps of measuring at least one parameter indicative of the flow of gas; converting at least one parameter indicative of the flow of gas into at least one signal indicative of the flow of gas; processing at least one signal indicative of the flow of gas in order therefrom to deduce at least one item of information relating to cardiac massage being performed on a patient in cardiac arrest; on the basis of at least one deduced item of information, automatically selecting a given ventilation mode from among a number of stored ventilation modes, and controlling the respiratory assistance apparatus by applying the selected ventilation mode. Respiratory assistance apparatus capable of implementing this control method.

Abstract: A method and a device for detecting OSAHS provided that the method comprises: acquiring a vibration signal of a subject during sleep, and determining a breathing signal of the subject (S1), wherein the breathing signal comprises an inspiration signal generated upon inspiration and an expiration signal generated upon expiration; acquiring strength of a first vibration signal within a specified frequency range and superimposed on the inspiration signal, and strength of a second vibration signal within a specified frequency range and superimposed on the expiration signal adjacent to the inspiration signal (S2); and comparing, according to a preset method, the strength of the first vibration signal with the strength of the second vibration signal, and determining, according to a comparison result, whether the subject is snoring (S3).

Abstract: Systems and methods for determining lung recruitment/derecruitment dynamics of an individual are disclosed. The disclosed embodiments advantageously use variable ventilation of the individual to determine lung dynamics without necessitating additional, potentially harmful ventilation maneuvers.

Abstract: A cable guide is configured to be detachably attached to a detection device having a cable lead-out portion from which a cable extends in a predetermined direction. The cable guide includes a guide portion configured to change a lead-out direction of the cable with respect to the cable lead-out portion, and an attachment portion configured to attach the guide portion to the detection device.

Abstract: A tool is provided for use in conjunction with a pressure support system that is structured to provide therapy to a patient to treat a condition of the patient by delivering a flow of breathing gas to the patient. The tool may be implemented on a portable electronic device or a PC and is configured to, among other things, provide customized/personalized education and feedback to the patient based, at least in part, on data that is measured by the pressure support system during the provision of therapy to the patient. The tool utilizes certain patient/therapy metrics, where each patient/therapy metric includes raw data that was measured by the pressure support system and that has been processed (e.g., summarized and/or otherwise manipulated) to form the patient/therapy metric.

Abstract: The present disclosure describes a system that automatically detects patient-ventilator asynchrony and trends in patient-ventilator asynchrony. The present disclosure describes a framework that uses pressure, flow, and volume waveforms to detect patient-ventilator asynchrony and the presence of secretions in the ventilator circuit.

Abstract: The embodied invention is a new inspiration/expiration ventilator flow design, with a constant inspiration flow and intermittent-concurrent expiratory flow based on lung pressure setpoints. This mode is possible by using a new dual lumen tube inserted into a patient Trachea. Additionally, the control provides support for patient initiated breathing which is initiated by a lung pressure drop. This control provides continuous and gentle recruitment of lung alveoli.

Abstract: A device and method for controlling a level of ventilatory assist applied to a patient by a mechanical ventilator measures, during patient's assisted breath, an inspiratory volume Vassist produced by both the patient and the mechanical ventilator, an inspiratory volume Vvent contributed by the mechanical ventilator, and an inspiratory assist pressure Pvent produced by the mechanical ventilator. A first relation between pressure Pvent and volume Vassist and a second relation between pressure Pvent and volume Vvent are calculated. Using the first and second relations, a ratio is determined between pressure Pvent at volume Vvent and pressure Pvent at volume Vassist, with volume Vvent equal to volume Vassist, for a plurality of volumes Vvent and Vassist. Values of Pvent are multiplied by the corresponding calculated ratios to calculate a third relation between a predicted inspiratory pressure Ppred and volume Vassist.

Abstract: Methods and systems for delivering a pharmaceutical gas to a patient. The methods and systems provide a known desired quantity of the pharmaceutical gas to the patient independent of the respiratory pattern of the patient over a plurality of breaths every nth breath, where n is greater than or equal to 1. The pharmaceutical gases include CO and NO, both of which are provided as a concentration in a carrier gas. The gas control system determines the delivery of the pharmaceutical gas to the patient to result in the known desired quantity (e.g. in molecules, milligrams or other quantified units) of the pharmaceutical gas being delivered. Upon completion of that known desired quantity of pharmaceutical gas over a plurality of breaths, the system can either terminate, continue, activate and alarm, etc.

Abstract: A method for the management of secretions in an intubated patient by means of an endotracheal tube to which an inflatable cuff is externally associated, includes the steps of inflating the inflatable cuff for isolating the broncho-pulmonary zone of the patient from the external environment, generating a succession of overpressures inside the endotracheal tube in order to induce breathing in the patient, and a step of deflating the inflatable cuff during the generation of one of the overpressures in order to permit a drainage of the secretions generated by the patient along the trachea towards the outside.

Abstract: Positive airway pressure (“PAP”) systems and methods are provided which supply a patient with a range of pressures for treatment when the patient is determined to be asleep, and an awake pressure for use when the patient is determined to be awake, the awake pressure configured for the comfort of the patient. The awake pressure is configured to be lower than the lower bound of the pressure range and can be a therapeutic or sub-therapeutic pressure. The PAP systems and methods disclosed herein advantageously allow for the pressure range to be tailored for effective treatment of sleep disordered breathing while allowing the awake pressure to be set for the comfort of the patient. This can advantageously increase both the efficacy of the treatment of SDB and patient compliance with the treatment.

Abstract: A system and method for providing a therapy to a subject may include a lumen configured to be coupled to a portion of a respiration passage of the subject to receive air respired by the subject. A sensor is configured to monitor the lumen and generate a signal based on the air respired by the subject. A pressure pulse delivery system is configured to deliver a pressure pulse along the lumen to the subject and a reservoir of therapeutic agent is coupled to the lumen. A processor is configured to receive the signal from the sensor, determine, from at least the signal, an exhalation period of the subject, and based on the exhalation period, cause the pressure pulse delivery system to deliver a pressure pulse to the subject. Following the pressure pulse, the processor can cause the therapeutic agent to be delivered from the reservoir.

Abstract: An anesthesia delivery and monitoring system for use during outpatient surgery performed under sedation level anesthesia that includes a ventilatory system, a system for supplying sedation anesthesia, a respiratory sensor adapted to detect a respiration parameter of such a patient, and a system for supplying a timed back-up breath to such a patient through the ventilatory system. The timed back-up breaths are supplied in response to the respiration parameter falling outside a preset threshold and at a positive pressure exceeding a base operating pressure of the respiratory system. The system for supplying sedation anesthesia is an intravenous supply system for anesthesia, a ventilatory system coupled to the patient, a needle and syringe, or any combination thereof. The respiratory system includes a PC-based physiologic monitor with user modified feedback control signal.

Abstract: Systems (100) and methods (300) for controlling coughing by subjects (106) control the opening and closing of a valve (12) (as well as partially opening and/or partially closing) to establish and disestablish a fluid communication between the airway of the subject and atmospheric pressure. The valve is opened and closed more than once during individual exhalations by the subject. Control of the valve is adjusted based on a pressure level in or near the airway of the subject.

Abstract: There is provided an airway tube for breath sampling, comprising a breath sampling port comprising two or more inlets adapted to sample breath from the airway tube. The inlets are connected to each other through a junction located outside of the air passageway of the airway tube.

Abstract: Devices and systems for monitoring weaning of a subject from a respiratory ventilator including a processing logic configured to characterize distinct patterns in a series of CO2 waveforms, the distinct patterns indicative of the effectiveness of a weaning process; and to provide an indication relating to the effectiveness of the weaning process.

Abstract: A gas measurement adapter includes a flow tube portion configured to allow gas to pass through the flow tube portion, and a window portion configured to allow measurement light for measuring a component of the gas passing through the flow tube portion to pass through the window portion. The window portion is thinner than the flow tube portion and is molded integrally with the flow tube portion. The window portion comprises an effective portion configured to allow the measurement light to pass through the effective portion and an outer peripheral portion provided on an outer periphery of the effective portion. An inner surface of the window portion is configured such that an outer perimeter of the effective portion is contiguously coplanar with the outer peripheral portion.

Abstract: A mechanical ventilator (10) provides pressure support ventilation (PSV) to a patient (12). A power of breathing (PoB) or work of breathing (WoB) estimator (30) generates a PoB or WoB signal (34) for the patient. An error calculator (36) computes an error signal as a difference between the PoB or WoB signal and a set point PoB or WoB value (22). A controller (20) inputs a PSV control signal (24) equal to the product of the controller transfer function and the error signal to the mechanical ventilator. A patient adaptation component (52, 54, 56, 60) fits parameters of a model of a controlled mechanical ventilation system comprising the mechanical ventilator and the patient to data comprising the PoB or WoB signal and the PSV control signal generated by the operating closed loop controller, and adjusts parameters of the controller transfer function to maintain stability of the operating closed loop controller.

Abstract: A respiratory event determination system can have a controller that determines the presence of a respiratory event. The respiratory event can be a mouth puff event. The controller determines the presence as a function of a sub-window of an expiratory window of the breath. The expiratory window extends between a first time ti and a second time t2. The sub-window is limited to a portion of the expiratory window. The sub-window can extend between a third time t3 and a fourth time I4. The fourth time U can be before the second time t2.

Abstract: The present artificial respiration ventilator (10) comprises, inter alia, a flow sensor arrangement (44, 48) for quantitatively detecting a gas flow in a breathing line arrangement (30), comprising a distal flow sensor (48) located farther from the patient end of the ventilation line arrangement (30). and a proximal flow sensor (44) located closer to the patient end of the ventilation line arrangement (30), and has a control device (18) at least for processing measurement signals of the flow sensor arrangement (44, 48), wherein the control device (18) is designed for error detection based on the measurement signals of the distal (48) and/or the proximal sensor (44).