Abstract: The invention relates to a device for the regulation of PEEP and FiO2 of a ventilator for achieving an arterial oxygen partial pressure in the blood of a mechanically ventilated patient. At reading which is representative of the success of the oxygen supply, i.e. the oxygen saturation of the blood is measured with the device, and assigned to one of three regions, which are defined by two characteristic lines. A first control loop is designed to optimise PEEP and FiO2 on assigning a reading to a region which demands a change of the settings, or to retaining the settings with an assignment to the normal region between the characteristic lines. This first control loop carries out such an optimisation at predefined temporal intervals on account of the representative reading (SaO2REP) and a predefined necessary supply intensity. The ventilator is subsequently activated accordingly.

Abstract: A blower filter system (10) includes a blower filter device (20) with a blower (22), with a filter mount (24) and with a tube port (26) for connecting a respirator device (40) by a tube (42). The filter mount (24) is designed to receive a filter (30), on which a color coding (32) with a color specific to the pneumatic resistance of the filter (30) is arranged, and the blower filter device (20) has an optical sensor device (50) for recognizing different colors of the color coding (32).

Abstract: The present invention relates to a method of delivering gas during ventilation of a patient using a system for breath delivery. The method of gas delivery includes real-time compensation of gas compression losses, in the current breath delivery phase, and gas leakage losses. The present invention further relates to a system for breath delivery. Still further, the present invention relates to a computer implemented method adapted of delivering gas during ventilation of a patient using a system for breath delivery.

Abstract: A method or device for assaying physiological gas levels in a human, comprising: repeatedly measuring a gas in samples of breath or blood, or continuously measuring the gas through the skin or fingernail, while he or she holds his or her breath for a specified time interval (BHt) before each measurement, wherein these time intervals are selected from the group consisting of BHt=0, 4-6, 20-25 and 35-40 seconds, and recording the results to form a series of values including at least one measurement at BHt=35-40 which is treated as representing the average gas level in all the tissues of the body (T) at that time, to determine if the individual is net inhaling, net exhaling or in equilibrium with the gas.

Abstract: A yarn or multi-fiber formed of a plurality of micron diameter stainless steel monofilaments which have been rendered more conductive by one or more coatings of electrolytically-deposited metal or metal alloy materials. The metallized yarn provided by the invention has a very low electrical resistance, with consequent benefit in electrical performance, and is particularly useful as an RFI/EMI shielding material.

Abstract: The present disclosure pertains to a ventilation therapy system configured to control a pressure or flow generator to apply an intra-pulmonary percussive ventilation therapy regime to a pressurized flow of breathable gas during baseline ventilation therapy. The ventilation therapy system is configured to automatically control the pressurized flow of breathable gas. The system may automatically control an extent of hyperinflation during IPPV in a subject. The system is configured such that therapy set points, alarm settings, and/or other factors are automatically adjusted during the application of IPPV relative to the set points and alarm settings during baseline ventilation therapy. In some embodiments, the system comprises one or more of a pressure or flow generator, a subject interface, one or more sensors, one or more processors, a user interface, electronic storage, and/or other components.

Abstract: A method of controlling a flow rate includes selecting an operating condition defined by an operating flow rate and an operating pressure, comparing the operating flow rate to a threshold flow rate, and executing an adaptive calibration routing if the operating flow rate is greater than or equal to the threshold flow rate. The adaptive calibration routine includes measuring the operating pressure, measuring a first flow rate through a first meter, and modifying a pressure-flow table based on the operating pressure and the first flow rate.

Abstract: A gas analyzer system for analyzing and monitoring samples of compressed or ambient gas such as breathing air and informing the user as to the results of the sample's gas purity without the gas sample having to be physically transported to an accredited laboratory. The system comprises a gas analysis module situated at a user facility for receiving the contents of a gas sample and detecting gas impurity characteristics, and a server situated at a remote certification and monitoring center and electrically coupled to the gas analysis module via a bi-directional communications link such a computer network connection. The remote server receives and stores the gas purity characteristics in the form of gas impurity data obtained from the analysis module. The module includes a calibration canister containing a known gas. The module executes onboard calibration by analyzing the calibration gas and comparing it to known data stored on the module.

Abstract: The present invention provides a negative pressure generator comprising a vacuum pump having an intake end and an exhaust end, a soundproofing module having a compartment for accommodating the vacuum pump, the soundproofing module being configured to insulate noise and vibration generated when the vacuum pump is in operation, and a silencing tube module comprising a flexible intake tube having one open end communicating with the intake end of the vacuum pump and a flexible exhaust tube having one open end communicating with the exhaust end of the vacuum pump, the silencing tube module being configured to reduce noise generated at the intake end and/or the exhaust end of the vacuum pump when the vacuum pump is in operation. The negative pressure generator can provide a vacuum source to an oral interface device to favorably create a negative pressure environment in a user's oral cavity so that the patency of the user's upper airway is maintained.

Abstract: An apparatus for the collection of samples of exhaled air during normal respiration, comprising a flow generator, an orally insertable exhalation air receiver, and a device for isolating the nasal airways, wherein the apparatus further comprises: a sensor for detecting a change in a parameter representing the change from inhalation to exhalation and to transmit said change as a signal; a control unit adapted to receive said signal and to control said device for isolating the nasal airways; wherein the flow generator is connected to or integrated with the exhalation air receiver.

Abstract: An apparatus for the collection of samples of exhaled air during normal respiration, comprising a flow generator, an orally insertable exhalation air receiver, and a device for isolating the nasal airways, wherein the apparatus further comprises: a sensor for detecting a change in a parameter representing the change from inhalation to exhalation and to transmit said change as a signal; a control unit adapted to receive said signal and to control said device for isolating the nasal airways; wherein the flow generator is connected to or integrated with the exhalation air receiver.

Abstract: A device for drying a root canal includes a cannula configured to inject a gas stream into the root canal. The cannula is a conduit having a proximal end in fluidic communication with a distal end. A handpiece is configured to removably hold the proximal end of the cannula at a distal handpiece end. A gas stream source is connectable to a proximal end of a tube. A distal end of the tube is connectable to the proximal handpiece end. A cut-off valve is disposed within the handpiece in fluidic communication in series between the distal handpiece end and the proximal handpiece end. The cut-off valve is configured to cut off the gas stream flowing through the handpiece. A manually-controlled operating element is mechanically coupled to the cut-off valve, where the operating element is configured to be controlled by a dentist or technician holding the handpiece.

Abstract: A mask configured to be attached to the face of a subject includes a wall section that defines an internal space and covers at least a portion of a nose and a mouth of the subject, an expired gas introduction section that is disposed in the internal space and introduce the subject's expired gas, and a communication section defining a communication channel through which the subject's expired gas introduced from the expired gas introduction section is introduced into an expired gas concentration detection sensor. The position of the expired gas introduction section in the internal space is variable.

Abstract: The present invention provides for a method and device for monitoring an ambient humidity sensor in a combustion engine, where the monitoring of the ambient humidity sensor is made by comparing the ambient humidity measured by said humidity sensor and an ambient humidity determined from an oxygen measurement of at least another sensor in the engine system, such as a NOX, or Lambda and/or an oxygen sensor. Said comparison is made using an offset of the oxygen signal reading of said at least another sensor, in a fuel cut condition where the drift or offset of said another sensor is related to the variation of the ambient humidity.

Abstract: There is provided herein methods, apparatus and systems for evaluating carbon dioxide (CO2) concentration in a subject's breath, for example in subjects ventilated with High Frequency Ventilation (HFV), the method includes inserting to a trachea of a subject an endotrachial tube (ETT), sampling breath from an area in the trachea located in proximity to a distal end of the endotrachial tube (ETT) and evaluating one or more CO2 related parameters of the sampled breath.

Abstract: The present disclosure relates to methods and systems for resuscitation of an infant which maintains healthy blood oxygen saturation values in the infant by titration of supplemental oxygen concentrations.

Abstract: In accordance with the present invention, there is provided a mask for achieving positive pressure mechanical ventilation (inclusive of CPAP, ventilator support, critical care ventilation, emergency applications), and a method for a operating a ventilation system including such mask. The mask of the present invention includes a piloted exhalation valve that is used to achieve the target pressures/flows to the patient. The pilot for the valve may be pneumatic and driven from the gas supply tubing from the ventilator. The pilot may also be a preset pressure derived in the mask, a separate pneumatic line from the ventilator, or an electro-mechanical control. Additionally, the valve can be implemented with a diaphragm or with a flapper.

Abstract: A method and an apparatus for controlling a ventilator to automatically adjust ventilation assistance to an active or passive subject. The method includes determining volume and flow rate of gas to the patient during inspiration on an ongoing basis, and generating control signals in proportion to the volume and flow rate of gas to the patient wherein proportionality factors, and support levels for the elastic and resistive components of pressure are automatically adjusted by the ventilator. The ongoing pressure applied by the ventilator is a sum of elastic and resistive pressures that are automatically controlled by the system. When the patient breathes spontaneously, the support levels are automatically adjusted based on the patient's requirements. If the patient does not breathe spontaneously, the ventilator provides ventilation at an optimal level and rate. The method may be used in weaning or in a management phase of ventilation.

Abstract: The present invention related to an iron bus bar coated with copper and a method of manufacturing the same. The present invention provides an iron bus bar including an iron core and a copper layer applied on the iron core, and a method of manufacturing the same. According to the present invention, an iron bus bar having high strength and durability as well as excellent electrical conductivity can be manufactured at low cost.

Abstract: Sidestream sampling of gas to determine information related to the composition of gas at or near the airway of a subject is implemented. From such information one or more breathing parameters of subject 12 (e.g., respiratory rate, end-tidal CO2, etc.) are determined, respiratory events (e.g., obstructions, apneas, etc.) are identified, equipment malfunction and/or misuse is identified, and/or functions are performed. To improve the accuracy of one or more of these determinations, information related to pressure at or near the airway of subject is implemented. This information may include detection of pressure at or near a sidestream sampling cell.

Abstract: A reliable and secure activation of an access based on a detection of movement in a remote access system by providing a secure method for opening/closing of an access in hands-free access mode. The detection of movement relates to the displacement of a lower member of a user by a remote access system, this access system including at least two elements of detection which each emit a signal whose variations (31, 33, 35) are analyzed. The detection of a movement of a lower member is validated by the application of a double verification step according to parameters (dAsA, dAsB) of a criterion for identification (tA, tB; dAsA, dAsB) of a form of variation (F2; A, B) of each signal (31, 33, 35) with a model form of the movement, and according to a criterion for simultaneity of detection of the forms of variation (F2) identified on the two signals.

Abstract: A system for controlling machine-induced expiratory airflow of a subject, the subject having an airway, the system comprising: a pressure generator (140) configured to generate a pressurized flow of breathable gas for delivery to the airway of the subject; and one or more processors (110) configured to execute computer program modules, the computer program modules comprising: a control module (170) configured to control the pressure generator a metric determination module (154) configured to determine a value of a flow metric during expiration by the subject, a flow analysis module (156) configured to compare the determined value of the flow metric with a target level of the flow metric; and an adjustment module (160) configured to adjust one or more of exsufflation pressure.

Abstract: A flowmeter for liquids has a measuring housing, which encloses and rotatably mounts an impeller, said measuring housing comprising a one-piece supply pipe and discharge pipe, wherein the impeller is eccentrically arranged in the discharge pipe after a nozzle-forming constriction. A sensor encoder is associated with the impeller and a sensor which responds to the sensor encoder is provided on the measuring housing for determining the amount of liquid flowing through the measuring housing on the basis of the revolutions of the impeller. The outer diameter corresponding to the impeller is smaller than the nominal inner diameter of the discharge pipe, enabling it to be pushed into the one-piece pipe.

Abstract: An air delivery system includes a controllable flow generator operable to generate a supply of pressurized breathable gas to be provided to a patient for treatment and a pulse oximeter configured to determine a measure of patient effort during a treatment period and provide a patient effort signal for input to control operation of the flow generator.

Abstract: Systems and methods are configured to inexsufflate a subject and provide cough-by-cough feedback during treatment and/or therapy of the subject. Through sensors that are included in the systems, various gas and/or respiratory parameters maybe measured and/or determined in real-time, such as, for example, peak cough flow and/or inspiratory tidal volume.

Abstract: A carbon-dioxide sampling system for accurately monitoring carbon dioxide in exhaled breath. The system includes a ventilator. The ventilator is configured to ventilate a patient with respiratory gases. The ventilator includes a carbon-dioxide sampling control unit and a carbon-dioxide analyzer. The carbon-dioxide sampling control unit is configured to control the timing of sampling of carbon dioxide in the exhaled breath of a patient, and to control the timing of the analysis of exhaled gases by the carbon-dioxide analyzer.

Abstract: An oxygen supply device, preferably a pilot oxygen supply device, has an oxygen source and at least one oxygen mask. A breathing regulator is arranged between the oxygen source and the oxygen mask. An oxygen sensor is arranged downstream of this breathing regulator.

Abstract: Systems and methods to estimate, on a breath-by-breath basis, the fraction of inhaled oxygen during ventilation of a subject. The fraction of inhaled oxygen may be based on exhaled tidal volume, a volume of dead space within the subject interface, leaked exhalation volume, and subsequently inhaled tidal volume and leaked inhalation volume.

Abstract: The present invention relates to a solution for controlling the pressure/flow of breathing gas to a mechanical ventilator (4) by using an energy of breathing analysis and further to provide a pressure relief during exhalation and a trigger determination when to start the pressure relief using energy content of breathing in analysis for determining a pressure curve form during at least a portion of the expiration phase.

Abstract: The present invention is a breathing improvement monitor that continuously measures involuntary breathing. The monitor is a sensor apparatus that is attached to a patient's mask which is connected to the monitoring apparatus. The sensor may be reusable and attachable and detachable to a mask or it may be an integral part of a breathing mask. The sensor technology may be any type sufficient in the art, including but not limited to solid state sensors, transducers, electromagnetic microturbines and the like. Since the mask does not have to be removed and the sensor provides constant signal to the monitoring apparatus, a real time status of a patient's involuntary breathing capability may be determined for a doctor's consideration.

Abstract: An anesthesia system is disclosed herein. The anesthesia system includes a sensor configured to measure an anesthetic agent concentration, and a processor connected to the sensor. The processor is configured to generate an exponential agent model based on the measured anesthetic agent concentration. The exponential agent model represents a plurality of future anesthetic agent concentrations.

Abstract: An anesthetic breathing apparatus has a first gas analyzer arranged to provide gas measurement data related to a first sample point to a control unit that is arranged in a servo or feedback control system configured to adjust delivery of a vaporized anesthetic agent from an anesthetic vaporizer to a delivery point in an inspiratory branch of a breathing circuit of the anesthetic breathing apparatus, The first sampling point is arranged in the breathing circuit downstream and close to the delivery point. A second gas analyzer arranged to be operated in a first mode of operation to provide gas measurement data for patient monitoring, and arranged to be operated in a second mode of operation to provide gas measurement data to the control unit. A switch over unit is fluidly connected to the second gas analyzer, and arranged to switch fluid communication of said second gas analyzer between the first sample point for the second mode of operation and a second sample point for the first mode of operation.

Abstract: A ventilator for use by a clinician in supporting a patient presenting pulmonary distress. A controller with a touch-screen display operates a positive or negative pressure gas source that communicates with the intubated or negative pressure configured patient through valved supply and exhaust ports. A variety of peripheral, central, and/or supply/exhaust port positioned sensors may be included to measure pressure, volumetric flow rate, gas concentration, transducer, and chest wall breathing work. Innovative modules and routines are incorporated into the controller module enabling hybrid, self-adjusting ventilation protocols and models that are compatible with nearly every conceivable known, contemplated, and prospective technique, and which establish rigorous controls configured to rapidly adapt to even small patient responses with great precision so as to maximize ventilation and recruitment while minimizing risks of injury, atelectasis, and prolonged ventilator days.

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 breathing apparatus includes a source of compressed air and a lung demand valve that receives compressed air from the source. A pneumatic valve assembly is connected between the source and the lung demand valve. The pneumatic valve assembly is moveable between a first closed position that prevents a flow of compressed air to the lung demand valve and a second open position that provides a path for compressed air to flow to the lung demand valve. A mask receives the lung demand valve therein. The mask provides the compressed air to a user and having a first operational mode providing filtered ambient air to the user and a second operational mode providing compressed air to the user. A control device is coupled to the pneumatic valve assembly. The control device detects a condition in the air surrounding the apparatus and controlling the pneumatic valve assembly to move between the first closed and second open position and the mask to operate in a respective one of the first and second operational modes.

Abstract: Systems and methods for providing respiratory therapy to a subject respond and/or adapt to the detection of an occurrence of a respiratory event. For example, the pressure level of a pressurized flow of breathable gas may be increased responsive to the occurrence of one or more apneas. Based on usage information spanning more than one therapy session, such as the tracked pressure levels, a starting pressure level for a pressurized flow of breathable gas for a subsequent therapy session is determined. The starting level at the beginning of the subsequent therapy session(s) may be the 90% pressure level as determined during the preceding period during which usage information has been gathered.

Abstract: A flow sensor comprises a flow restriction disposed within a passage such that a fluid passing through the passage must pass through the flow restriction. The flow sensor also has an upstream pressure sensor coupled to the passage at a point upstream of the flow restriction and configured to measure and provide an upstream pressure of the fluid within the passage, a downstream pressure sensor coupled to the passage at a point downstream of the flow restriction and configured to measure and provide a downstream pressure of the fluid within the passage, and a temperature sensor coupled to the passage and configured to measure and provide a temperature of the fluid within the passage. The flow sensor also includes a flow sensor processor coupled to the upstream and downstream pressure sensors and the temperature sensor and configured to accept measurements therefrom and calculate a compensated flow rate based at least in part on the measured pressures and temperature.

Abstract: An oxygen generating apparatus that includes a container containing potassium super oxide, an inhale valve, and an inhale valve filter between the potassium super oxide and the inhale valve. The filter is configured to prevent particles having a diameter of 10 ?m from passing through the filter, and to neutralize KOH and KO2 particles having a diameter of less than 10 ?m that contact the filter into a food grade compound.

Abstract: A system and method are configured to utilize patient effort to increase cough flow of a subject by limiting airway collapse by causing a series of exsufflation events over an individual exhalation of the subject. A single exhalation of the subject is segmented into a series of exsufflation events by a processor configured to toggle a pressure regulator between a first airway closed mode and a second airway open mode. The processor is configured such that the transitions between the closed and open modes are initiated based on predetermined timing or based on output signals generated by sensors monitoring one or more gas parameters (for example, pressure) in the airway of the patient.

Abstract: A system and method for conserving oxygen in a breathing assistance device are disclosed. A method may include delivering breathable gas with a first average oxygen concentration during a first portion of an inhalation phase for a patient. The method may also include delivering breathable gas with a second average oxygen concentration during a second portion of an inhalation phase for a patient.

Abstract: An apparatus assesses a condition of a patient. The apparatus may contain a patient interface for communicating a treatment generated by a respiratory treatment apparatus to the respiratory system of a patient. The apparatus may also include a sensing module containing one or more electrochemical sensors to sense chemicals in exhaled breath in real time, or over an extended period of time. The apparatus may also include one or more collectors to accumulate a breath condensate over an extended period of time. The sample collectors may contain an absorbent material, and may also be adapted for replacement within a sensing module. The absorbent material may also include a preservative for preserving a chemical component of the breath, such as an analyte of the exhaled breath. The technology may provide treatment recommendations based on the detected condition of the breath condensate or the chemical components thereof.

Abstract: A carbon dioxide sensor for use in a respiratory therapy system. The carbon dioxide sensor determines whether a patient interface is fluidly coupled to a patient.

Abstract: Systems and methods are described for application of a transitory corrective modification to a hot-wire anemometer flow voltage and/or calculated flow rate to compensate for transient thermal response of the anemometer during a change in mixture of a mixed gas being measured. According to one embodiment a method of applying the transitory corrective modification is provided. An output signal of an exhalation flow sensor of a medical ventilator is received. The flow sensor includes a hot-wire anemometer. The output signal is indicative of a rate of flow of expired gas by a patient. Transient thermal response of the hot-wire anemometer is compensated for by applying a corrective modification to the output signal or a value based thereon. The corrective modification is based at least in part on a fraction of inspired oxygen (FiO2) being supplied by the medical ventilator to the patient.

Abstract: An oxygen concentrator system includes a portable unit and a base unit. The portable unit includes an air separation device. The base unit includes a vacuum pump. The portable unit is moveable with respect to the base unit between a connected position, in which the vacuum pump of the base unit is connected to the air separation device of the portable unit for applying vacuum pressure at the air separation device of the portable unit, and a disconnected position, in which the vacuum pump is not connected to the air separation device of the portable unit. The air separation device operates using a vacuum pressure swing adsorption (VPSA) cycle when the portable unit is in the connected position. The air separation device operates using a pressure swing adsorption (PSA) cycle when the portable unit is in the disconnected position.

Abstract: A disposable breathing assistance device with manometer for monitoring the pressure within the device is capable of providing CPAP and in some embodiments includes a deflection face to prevent injected jets of supplementary respirable gas from directly striking the patient's mucosa. The breathing assistance device further optionally includes a safety pressure relief valve as an additional safety against overpressure within the device. A specialized supplementary respirable gas inlet provides improved pressure characteristics.

Abstract: A trans-fill method and system comprising obtaining therapeutic gas from a therapeutic gas source, compressing the therapeutic gas from the therapeutic gas source in at least two stages to create an intermediate therapeutic gas stream and a high pressure therapeutic gas stream, supplying therapeutic gas to a patient from the intermediate therapeutic gas stream, and filling a cylinder with the therapeutic gas from the high pressure therapeutic gas stream substantially simultaneously with supplying therapeutic gas to the patient.

Abstract: The invention relates to an apparatus for the ventilatory anaesthesia of a patient by administration of a gas containing gaseous xenon that comprises a main gas circuit (CP) and a means for determining the xenon content (S6, M1) adapted for and capable of determining the gaseous xenon content in the main circuit (CP), and comprising at least one hot wire sensor (S6-E) including at least one electrically conducting wire (FC1) in direct contact with at least a portion of the xenon-containing gaseous flow.

Abstract: A processor obtains input of a logistically attainable end tidal partial pressure of gas X (PetX[i]T) for one or more respective breaths [i] and input of a prospective computation of an amount of gas X required to be inspired by the subject in an inspired gas to target the PetX[i]T for a respective breath [i] using inputs required to utilize a mass balance relationship, wherein one or more values required to control the amount of gas X in a volume of gas delivered to the subject is output from an expression of the mass balance relationship. The mass balance relationship is expressed in a form which takes into account (prospectively), for a respective breath [i], the amount of gas X in the capillaries surrounding the alveoli and the amount of gas X in the alveoli, optionally based on a model of the lung which accounts for those sub-volumes of gas in the lung which substantially affect the alveolar gas X concentration affecting mass transfer.

Abstract: Disclosed herein is a system including a patient support unit having an enclosed patient environment, a heating module, a skin temperature sensor module, an environmental sensor module and a control system. The control system is configured to selectively operate the system in a pre-programmed weaning mode configured to gradually wean the patient from the warmed patient environment according to a series of stepped air temperature decreases performed over a series of stepped time durations to achieve a goal air temperature while maintaining a goal skin temperature within a weaning abort deviation. Related apparatus, systems, methods and/or articles are described.

Abstract: Devices and systems provide methods of detecting a heart failure condition of a patient that may be based on one or more respiratory parameters of a patient. In an example embodiment, a monitoring device determines one or more heart failure condition indicators based on a measure of the patient respiratory airflow and/or a measure of treatment pressure. Respiratory parameters such as respiration rate, hypopneas, apneas, Cheyne-Stokes breathing patterns or apnea-hypopnea counts may be compared to thresholds that are selected to represent a change in the condition of a heart failure patient such as an onset of a decompensation event. Results of the comparisons may trigger a pressure treatment change and/or one or more warnings or messages to notify a patient or physician of a pending change to the patient's heart failure condition so that the patient may more immediately seek medical attention to treat the heart failure condition.