Abstract: A system and method are disclosed for the provision of assisted breathing by the delivery of a controlled pressurized airflow to the pulmonary airway of a user with breathing disorders. The system comprises a source of compressed respiratory gas (112), a user interface unit (115) including at least one Venturi device (120) and a thin flexible tubing (116) connecting between the source of high pressure gas (112) and the Venturi device. The system and method provide a regulated and controlled flow of air to the user (105) in accordance with the user needs. The invention further discloses a novel small light-weight user interface for replacing prior art breathing masks.

Abstract: A vent assembly for use with a respiratory mask of the type used in CPAP treatment includes a porous disk portion that is attached to a biasing member such that the disk portion is maintained in a substantially sealed position against a main vent to minimize airflow through at least one side vent of the vent assembly. Debris build-up on the disk portion can cause the biasing member to deflect to provide an additional path for airflow through the at least one side vent. In another embodiment, the vent assembly can also include an anti-asphyxia feature to provide an airflow path from the environment to the user. An oxygen diverter valve may be disposed between the breathing apparatus flow generator and an oxygen injection port.

Abstract: The disclosure provides a method for delivering pressurized gas to an airway of a subject. The disclosure also provides a system for delivering pressurized gas to an airway of a subject. The disclosure further provides a computer-readable storage medium containing a set of instructions executable on a processor that include routines to monitor a respiratory flow rate from a subject, generate a filtered flow and a dynamic flow from the respiratory flow rate, and control a gas generator connected to a breathing device.

Abstract: A method and apparatus is described for supporting the respiration of a patient. The spontaneous respiration of a patient can be detected by sensors and during inhalation an additional amount of oxygen can be administered to the lungs via a jet gas current. If required, during exhalation a countercurrent can be administered to avoid collapse of the respiration paths. This therapy can be realized by an apparatus including a transtracheal catheter, an oxygen pump connected to an oxygen source, spontaneous respiration sensor(s) connected to a control unit for activating the oxygen pump and, if needed, a tracheal prosthesis. The tracheal prosthesis may include a connection for the catheter and the breath sensor(s). The tracheal prosthesis, if used, and the catheter can be dimensioned so the patient can freely breathe, cough, swallow and speak without restriction, and the system can be wearable to promote mobility.

Abstract: An apparatus and method for performing warming therapy is described. In one exemplary embodiment, the apparatus includes a patient support platform, a patient chamber, a heating source, and a rigid connection member for connecting hoses to the patient chamber. The rigid connection member provide an interface between hoses disposed inside the patient chamber, and hoses disposed outside. The connection member preferably includes one or more interconnection nozzles, removably attached thereto, for connecting the internal hoses to the external hoses. Each of the interconnection nozzles preferably includes an interior connection surface exposed to an interior of the patient chamber, and an external connection surface exposed to an external of the patient chamber.

Abstract: A combination of an SCBA system for providing bottled air to a user and a PAPR system for purifying ambient air for use by a user wherein the two systems are used alternatingly depending on the contaminated condition of the ambient air and the oxygen content of the ambient air.

Abstract: There is an apparatus including a mandible positioner for positioning the mandible of a patient with respect to the maxilla of the patient and a breathing assistance apparatus. The breathing assistance apparatus has a sensor arranged to detect at least one element representative of a breathing state of the patient. A source of breathing gas includes a patient interface and has at least a first operable position and a second operable position. The source of breathing gas provides a different ratio of carbon dioxide and oxygen to the patient when in the first operable position than in the second operable position. The source of breathing gas may be moved between the first operable position and the second operable position in response to signals from the sensor. For example, the source of breathing gas may provide rebreathed air to the patient in the first position and atmospheric air in the second position.

Abstract: A method and apparatus for delivering a medicine to a patient via the patient's respiratory system with control and efficiency. A nebulization catheter is positioned in the patient's respiratory system so that a distal end of the nebulization catheter is in the respiratory system and a proximal end is outside the body. In a first aspect, the nebulization catheter may be used in conjunction with an endotracheal tube and preferably is removable from the endotracheal tube. The nebulization catheter conveys medicine in liquid form to the distal end at which location the medicine is nebulized by a pressurized gas or other nebulizing mechanism. The nebulized medicine is conveyed to the patient's lungs by the patient's respiration which may be assisted by a ventilator. By producing the aerosol of the liquid medicine at a location inside the patient's respiratory system, the nebulizing catheter provides for increased efficiency and control of the dosage of medicine being delivered.

Abstract: A ventilation system providing inspiratory air to a patient and receiving expiratory air from the patient. The ventilation system comprises a ventilator operable between an inspiratory phase and an expiratory phase of a respiration cycle. The ventilator has an inspiratory outlet for providing inspiratory air to a patient during the inspiratory phase and an expiratory inlet for receiving expiratory air from the patient during the expiratory phase. A patient circuit is configured in fluid communication with the lungs of a patient. The patient circuit conveys inspiratory air from the inspiratory outlet to a patient's lungs during the inspiratory phase and conveys expiratory air from the patient's lungs to the expiratory inlet during the expiratory phase. A flow transducer is provided in fluid communication with the patient circuit. The flow transducer is configured to detect a minimum volume of expiratory air in the patient circuit during the expiratory phase of a respiratory cycle.

Abstract: A methodology and apparatus for determining a target ventilation setting for delivering ventilatory support based upon a function of measured PCO2. Patient ventilation is measured over time during a learning period in which ventilatory support is provided. A target ventilation is calculated as a function of the measured ventilation. Adjustments to the target ventilation are then made using a measure of partial pressure of CO2 for the patient. Preferably, the measure is compared to a threshold PCO2 and the target ventilation may be increased or decreased based upon the comparison. The target ventilation may then be increased or decreased based upon a fixed percentage of the absolute value of the difference between the measured PCO2 and the threshold PCO2.

Abstract: A pressure driver for a ventilation system comprises a gas source, an inspiration flow control valve and a patient pressure sensor to form a closed loop control system. The inspiration flow control valve may be mounted within a housing and is operative to open and close in response to patient pressure measurements in order to produce a desired pressure at the patient. The pressure driver may further include a mixture control for allowing selective adjustment of the oxygen concentration in pressurized gas delivered to the patient. An oxygen mixer is connected between the gas source and the mixture control and is operative to deliver the desired mixture of oxygen and air to the inspiration flow control valve for delivery to the patient. An oxygen sensor monitors the oxygen concentration in the gas provided by the oxygen mixer.

Abstract: Methods that may provide a positive pressure therapy to a user are described. The methods include detecting the user's breathing parameters and increasing the pressure delivered to the user from a sub-therapeutic pressure to a therapeutic pressure based upon the breathing parameters.

Abstract: An apparatus (1) to assist a patient's respiration by delivering air to a patient through a mask (20), including a ramp module (10) connected to a control unit (2) to provide the control unit with a pressure value PM at mask (20), so that when apparatus (1) starts functioning, the pressure progressively rises until it reaches a treatment pressure PTi, the apparatus further including a comparator connected to ramp module (10), at least one device for detecting the patient's breathing parameters and sending them to the comparator, so that the comparator can determine whether an event (E1, E2 or E3) occurs in patient's breathing and to send the corresponding data to ramp module (10) which provides control unit (2) with a pressure value PM that will speed up with respect of time, so that the pressure rise at patient's mask (20) is accelerated.

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: A method of operating a CPAP apparatus in which the interface pressure is controlled to rapidly drop at the start of expiration by an expiratory relief pressure (ERP) that is independent of instantaneous respiratory flow, following which the pressure rises to an inspiratory level at or shortly before the end of expiration, or at the onset of an expiratory pause, if any. The ERP is an increasing function of the inspiratory pressure. The expiratory pressure follows a template that is a function of the expected expiration time, the magnitude of the template being equal to the ERP. The current estimated proportion of expiration is determined by comparing the expiration time of the breath in progress to low-pass filtered expiratory durations measured for a number of the preceding breaths.

Abstract: The present invention relates to a breath controlled air inlet valve for controlling a flow of air supplied to a wearer of a facemask, the valve permitting the flow of air when a wearer breathes in and restricting the flow of air when the wearer breathes out. The valve includes an inlet, an outlet, one or more pivotable shutters, and a shutter articulating mechanism for articulating the one or more shutters between an open state and a closed state. The shutter articulation mechanism actuates in response to the respiration of the wearer. The valve also enables a positive pressure to be maintained within the facemask by permitting an amount of air to flow around the one or more shutters when the one or more shutters are in the closed state.

Abstract: In one aspect, a product gas concentrator is provided. In one embodiment, the apparatus may include: a first process separating adsorbable components from a source gaseous mixture, a second process providing concentrated product gas in a continuous output mode, a third process providing concentrated product gas in a pulsed output mode, and a fourth process selectively switching between the continuous and pulsed output modes. In another embodiment, the apparatus may include: a first process pressurizing a source gaseous mixture, a second process separating adsorbable components from the pressurized gaseous mixture, a product tank accumulating concentrated product gas for dispensing, an output path, a third process selecting a volume to be dispensed during a predetermined time, a pressure sensor monitoring pressure of the concentrated product gas, and a fourth process controlling flow of the concentrated product gas in response to the selected volume and the monitored pressure.

Abstract: Breathing-gas delivery systems and methods are described. In one such system there is a movable partition, a housing and a filter body. The housing is disposed about the movable partition, and thereby provides a respirator side on a first side of the partition, and a patient side on a second side of the partition. The housing also has (a) a patient inspiration orifice on the patient side, which is adaptable to supply breathing-gas to a patient, and (b) a gas exhaust orifice on the patient side.

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: An apparatus for providing a breathing gas to a user may include: a headgear unit and a control unit. The headgear unit may include: a breathing interface, an adjustable structure to fit the headgear unit to the user's head with the breathing interface disposed in relation to the user's facial area, a blower motor assembly attached to the adjustable structure, and a plenum coupled to the breathing interface and the blower motor assembly to form a breathing gas flow path. The control unit controlling operation of the blower motor assembly based on a desired pressure for the breathing gas. Operation of the blower motor assembly provides the breathing gas to a user airway at an adjustable positive pressure via the breathing gas flow path. Additional embodiments of the apparatus and various embodiments of a related method are also provided herein.

Abstract: The inventive breath training device comprises a respiratory tube, a low-frequency mechanical air oscillation generator provided with an oscillation chamber embodied therein and provided with an input channel which is embodied in the form of an upwardly extending saddle-shaped body of revolution, contains a spherical ball and is connected to the respiratory tube and to an output channel communicating with ambient air, wherein the respiratory tube is provided with a jacket in which the body of the low-frequency mechanical air oscillation generator rotatable about a horizontal axis is fixed and a bypass chamber provided with an inspiratory tube is formed, said inspiratory tube comprises an inspiratory valve provided with a tubular attachment and the output channel of the oscillation chamber of the low-frequency mechanical air oscillation generator is also provided with an expiratory valve.

Abstract: A pneumatic oxygen conserving device for supplying oxygen to a user via a single-tube cannula connected to an outlet (12). A main control valve (2) connected to an inlet (1) for gas is controlled by the pressure in a main control volume (14) to open to deliver a pulse of gas at the commencement of inhalation. Inhalation is sensed by negative pressure in an output line (11) which causes a sensing valve (21) to open, thus allowing the volume to vent to atmosphere via vent line (22). The fall in pressure in volume causes the main control valve to open to supply a pulse of gas to the user. This also pressurises the output line which in turn causes the sensing valve to close, thus preventing further venting. A sensing delay valve (35) is incorporated in the vent line from volume to prevent the volume from venting after the first pulse has been delivered, until after the user has finished inhaling. The valve is controlled from a sensing delay volume (32).

Abstract: A respiratory mask assembly includes a frame and a forehead support secured to the frame. The forehead support includes a joining member secured to an upper portion of the frame and a cushion frame movably mounted to the joining member. One of the joining member and cushion frame includes a pair of shafts and the other of the joining member and cushion frame includes a pair of openings. The pair of shafts are respectively received in the pair of openings to couple the cushion frame to the joining member and enable the cushion frame to move relative to the joining member. Each of the shafts has a non-circular cross section defining a major longitudinal axis that is angled forwardly of a vertical axis of one of the joining member and cushion frame so as to angle toward a front portion of one the joining member and cushion frame.

Abstract: A fastenable air delivery conduit includes a body portion having a supply end and a delivery end and a fastener that substantially extends from the supply end to the delivery end. The fastener, when engaged, forms the body portion into a fastened configuration, and when disengaged, forms the body portion into an unfastened configuration. The body portion defines a longitudinal axis when in the fastened configuration, and the fastener extends from the source end to the delivery end of the body portion at an angle that is non-parallel with the longitudinal axis of the conduit.

Abstract: A pneumatic single-lumen medical gas conserver combines the advantages of typical single-lumen and dual-lumen conservers. In particular, a pneumatic single-lumen conserver can provide a rapid response to patient inhalations without the need for a more expensive dual-lumen cannula hose. In addition, after delivering oxygen the conserver has a specific pneumatically-implemented delay period before being able to detect the next inhalation to inhibit “double pulse” deliveries. In addition to a conserving or pulse flow mode, the conserver can provide a user-selectable gas flow at a continuous or constant flow mode.

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: Modes, methods, systems and devices are described for providing assisted ventilation to a patient, including wearable ventilation systems with integral gas supplies, special gas supply features, ventilation catheters and access devices, and breath sensing techniques.

Abstract: An improvement to a combination of an SCBA system for providing bottled air to a user and a PAPR system for purifying ambient air for use by a user wherein a sensor is included to determine the oxygen content of the breathing gas and the presence of contaminations in the atmosphere to control operation of the two systems depending on the contaminated condition of the ambient air and the oxygen content of the ambient air.

Abstract: An oxygen delivery system includes first and second sieve beds configured to selectively receive a supply fluid and separate a substantially oxygen-rich fluid therefrom. A patient conduit having a patient outlet is in alternate selective fluid communication with the sieve beds. The system includes a breath-detection device in fluid communication with the patient conduit, configured to calculate a rate of breathing and to trigger, in response to a breath detection, an output of a predetermined volume of the substantially oxygen-rich fluid alternately from a respective one of the sieve beds. The system also includes a device configured to measure the output flow rate at predetermined intervals. The output, having a target flow rate and a flow rate, occurs during a respective dynamically adjusted patient oxygen delivery phase, which is dependent upon the target flow rate, the output flow rate, and/or the breathing rate.

Abstract: An electronic oxygen conserving device for controlling a flow of oxygen from an oxygen storage container to a user. When a conserve setting is selected, a flow of oxygen travels through an oxygen regulating valve that has an open state and a closed state. A temporary electrical charge or current is provided to the oxygen regulating valve during the initial inhalation of oxygen by an individual, opening the regulating valve opens to delivery oxygen to the user. The oxygen regulating valve remains open even after termination of the electric current. After a predetermined timed delivery dose or upon exhalation by the individual, a subsequent temporary electric charge or current is provided to oxygen regulating valve, closing the regulating valve closes to prevent delivery of oxygen to the user, thus conserving oxygen. The oxygen regulating valve remains closed even after termination of the subsequent electric current.

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: The invention is multi-port oxygen conserver design, particularly suited for general aviation applications. The novel conserver provides separate bolus control capability for multiple users from a common oxygen supply. Thus a mix of gas usage reduction modes can be employed depending on whether the user is a pilot or passenger, operating altitude, and availability of oxygen, while maintaining safe operation.

Abstract: A group for controlling a second-stage regulator for scuba divers. The regulator comprises a regulator body with an inlet conduit for connection to a first-stage regulator which supplies a breathable gaseous mixture at a constant pressure and an outlet conduit for connection to a mouthpiece of the user. The group comprises a first bushing defining an intermediate chamber with a bottom wall wherein a central hole is formed, a poppet loosely engaged within the hole, the end of the poppet being connected to lever means, a second bushing engaged in the first bushing and defining an inlet chamber and a third bushing engaged in the second bushing and defining a regulator seat at one of its ends. The head of the poppet engages tightly in the seat and an elastic member is provided coaxial to the poppet in the intermediate chamber for maintaining the head against the regulator seat.

Abstract: A regulating device for supplying breathable gas to a diver, comprising a housing (1) which incorporates a regulating valve mechanism (3) between an inlet port (21) for the supply gas and an outlet port (2) where the gas emerges to be breathed, the housing (1) additionally comprising an exhalation port provided with an exhalation valve (4) to allow the exhalation gases to be expelled to the outside, the device comprising a deflector (5) which guides the exhaled gas between a first end connected to the exhalation valve (4) and a second end (15) situated in a defined region outside the housing (1), the gas being conveyed to the inlet port (21) via a hose (6) which can be connected to a pressurized gas source, wherein the exhalation port provided with a valve (4) is situated substantially in the vicinity of a lower end of the housing (1), and wherein the deflector (5) has a generally tubular shape, the second end (15) of the deflector (5) being open and forming an outlet for the exhaled gas that is situated conc

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: The portable ventilator of the present invention provide a hands-free ventilatory support device in critical care, emergency and resource limited environments. The portable ventilator utilizes ambient air and includes a two dual head compressor system to provide a consistent air supply to the patient. The ventilator device is battery operated and is capable of providing up to 60 minutes of care. In a preferred embodiment, the portable ventilator of the present invention also includes a pneumatic subsystem, a control subsystem, a power subsystem and an alarm subsystem. The portable ventilator of the preferred embodiment includes a dual head and single head compressor system that operates alternatively, to provide a consistent and continuous inhalation and exhalation cycle.

Abstract: An oxygen concentrating apparatus including an output variable type compressor. Oxygen-concentrated gas may be supplied either continuously or synchronized with inhalation or timing of inhalations. In one aspect, when synchronous operation is selected, the compressor is operated at a lower output in comparison with continuous supply operation. In a second aspect, when synchronous operation is selected, the supply quantity of oxygen-concentration gas is set to zero during the exhalation period.

Abstract: A system including methods and apparatus for treatment of a medical disorder such as obstructive sleep apnea or congestive heart failure. The system involves applying a gain to flow rate of pressurized gas delivered to a patient during inspiratory and/or expiratory phases of a respiratory cycle to deliver the pressurized gas in proportion to the respective gains during inspiration and/or expiration. A base pressure may be applied in addition to the gain-modified pressures and an elevated pressure profile may be employed to assist or control inspiration. The system may be fully automated responsive to feedback provided by a flow sensor that determines the estimated patient flow rate. A leak computer can be included to instantaneously calculate gas leakage from the system. The system may be utilized in connection with conventional continuous positive airway pressure treatments, such as CPAP or bi-level positive airway pressure equipment to effect various beneficial treatment applications.

Abstract: A reducing valve, which includes a water trap, especially useful in diving.

Abstract: A ventilator device delivers ventilatory support to a patient in a back up timed mode when patient respiration is not detected or a spontaneous mode when patient respiration is detected. The timing threshold governing the back-up mode is chosen to deviate from normal expected respiration time for the patient to promote patient initiated ventilation in the spontaneous mode but permit back-up ventilation in the event of apnea. Automated adjustments to the timing threshold during the timed mode are made from the less vigilant timing threshold to a more vigilant threshold at or near a timing of normal expected breathing of the patient. Such adjustments may be made from a minimum to a maximum vigilance timing settings or incrementally there between as a function of time in the timed mode which is preferably the number of delivered machine breaths.

Abstract: Method and apparatus for detecting disordered breathing in a patient and, in particular, to a method and apparatus for detecting patient snoring and/or for dynamically determining a snore detection threshold, and to a pressure support system and method of providing pressure support that uses this unique snore detection and/or snore detection dynamic adjustment technique to control the pressure provided to at patient.

Abstract: A method, system and device are provided for the determination of leaks in a respirator. An inspiration pressure pinsp is recorded during an inspiration time Tinsp with a measuring device. The inspiration pressure pinsp is varied during consecutive breaths I. Leaks are determined as to leak volumes VLi from the product of pinspi and Tinspi in accordance with the equation VLi=A×pinspiB×Tinspi while the parameters A and B are determined in an analyzing unit by a regression model with pinsp as the regressor.

Abstract: A ventilator device and system comprising a rotating compressor, preferably a drag compressor, which, at the beginning of each inspiratory ventilation phase, is accelerated to a sufficient speed to deliver the desired inspiratory gas flow, and is subsequently stopped or decelerated to a basal flow level to permit the expiratory ventilation phase to occur. The ventilator device is small and light weight enough to be utilized in portable applications. The ventilator device is power efficient enough to operate for extended periods of time on internal or external batteries. Also provided is an oxygen blending apparatus which utilizes solenoid valves having specific orifice sizes for blending desired amounts of oxygen into the inspiratory gas flow. Also provided is an exhalation valve having an exhalation flow transducer which incorporates a radio frequency data base to provide an attendant controller with specific calibration information for the exhalation flow transducer.

Abstract: A controlled enhanced-oxygen (hyperoxic) breathing system involving an oxygen source, a control valve system and a breathing interface, is disclosed. The control valve system may include a demand flow valve and a venturi valve arranged to introduce ambient air into an oxygen stream to provide a desired level of oxygen in the resultant hyperoxic air stream. Alternatively, the control valve system may include a nitrogen-removal unit, such as nitrogen scrubber, to increase the oxygen content above that of ambient air. The control valve system may further include a one-way flow valve and may further be joined to a plenum for storing hyperoxic air. The hyperoxic breathing system is typically connected to a breathing mask for use by an individual undergoing exercise or physical training activities.

Abstract: An apparatus (1) for administering a gas to a person or an animal, is provided with a chamber (9) for receiving a quantity of gas to be administered. The chamber is provided with a gas line (3) for supplying gas from a source to the chamber (9) and elements for pressurizing the gas in the chamber. The chamber (9) is connected to a breathing tube (5) for supplying pressurized gas from the chamber (9) to the person or the animal, wherein the breathing tube (5) connects to a discharge channel (26), for discharging gas exhaled by the person or the animal, via a valve (11), which restricts the flow of exhaled gas from the breathing tube (5) to the discharge channel (26) in order to build up gas pressure in the breathing tube (5) during exhalation.

Abstract: A portable ventilator uses a ROOTS-type blower as a compressor to reduce both the size and power consumption of the ventilator. Various functional aspects of the ventilator are delegated to multiple subassemblies having dedicated controllers and software that interact with a ventilator processor to provide user interface functions, exhalation control and flow control servos, and monitoring of patient status. The ventilator overcomes noise problems through the use of noise reducing pressure compensating orifices on the ROOTS-type blower housing and multiple baffling chambers. The ventilator is configured with a highly portable form factor, and may be used as a stand-alone device or as a docked device having a docking cradle with enhanced interface and monitoring capabilities.

Abstract: A ball and socket-type swivel connector for use with second stage regulators used by scuba divers. The ball is made from a metal with good corrosion resistance. The ball is then held into a true position by two separate low friction bushings. The two bushings, “sandwich” the metal swivel ball with light assembly pressure. This is accomplished by machining or molding the same radius of the swivel ball into one side of each of the two low friction bushings. As system pressure increases, the ball is forced rearwards and the squeeze increases. No seawater can enter the swivel. No area exists for seawater to collect around the O-ring. The bushing occupies all of the available space except for the gap provided around the O-ring gland an area used to hold lubrication. The preferred embodiment uses a high grade stainless steel swivel ball, virgin Teflon bushing material and an internally lubricated low friction O-ring.

Abstract: An aerosolization device comprises a housing having a mouthpiece, and a flow path arrangement in fluid communication with the mouthpiece. The flow path arrangement has a flow regulating valve and a threshold valve, where the threshold valve is configured to open at a first vacuum level and to close at a second vacuum level that is less than the first vacuum level. The housing includes a region that is adapted to hold a powder in fluid communication with the flow path arrangement so that air drawn through the mouthpiece opens the threshold valve once the first vacuum level is exceeded and remains open until the vacuum falls below the second vacuum level. The flow rate of the air drawn through the mouthpiece is regulated by the flow regulating valve to remain within a certain range while the threshold valve remains open.

Abstract: Described are a positive airway pressure system and method for treatment of a sleeping disorder in a patient. The system includes a generator, a sensor and a processing arrangement. The generator supplies airflow and applies a pressure at to an airway of a patient. The sensor measures data corresponding to patient's breathing patterns. The processing arrangement analyzes the breathing patterns to determine whether the breathing patterns are indicative of at least one of the following patient's states: (i) a regular breathing state, (ii) a sleep disorder breathing state, (iii) a REM sleep state and (iv) a troubled wakefulness state. The processing arrangement adjusts the applied pressure as a function of the patient's state.

Abstract: Regulator for underwater breathing devices including a relatively hard material box-like body having a pipe for the connection with a mouthpiece, at least one air inlet duct and at least one opening on which-it is positioned one air exhaust valve. The regulator box-like body is externally covered by at least one layer of a suitably shaped relatively soft material.