Abstract: A medical ventilator includes a pressure generator for increasing a pressure of gas that produces heat during the operation thereof. A heat sink spaced from the pressure generator is provided for absorbing heat from the pressure generator. A bacteria filter requiring heating in excess of an ambient temperature for the effective operation thereof is coupled in thermal communication with the heat sink. A heat pipe is coupled in thermal communication with the heat sink and the pressure generator for conveying at least part of heat produced by the pressure generator to the bacteria filter via the heat sink.

Abstract: A heat and moisture exchanger for both conducting a stream of air produced by a ventilator to a moisturizing medium and internally bypassing the moisturizing medium if aerosolized medication is introduced into the stream includes a housing having a ventilator-side port coupled to an outlet of a ventilator and a source of aerosolized medication. The housing has a patient-side port for coupling to a patient to provide ventilation including either air or air carrying aerosolized medication. A first path conducts air from the ventilator-side port through the moisturizing medium and the patient-side port, and a second path conducts air carrying aerosolized medication from the ventilator-side port directly to the patient-side port. A two-way valve mechanism in the housing selectively couples the ventilator-side port into fluid communication with one or the other of the first and second paths.

Abstract: A portable gas fractionalization apparatus that provides oxygen rich air to patients is provided. The apparatus is compact, lightweight, and low-noise. The components are assembled in a housing that is divided into two compartments. One compartment is maintained at a lower temperature than the other compartment. The lower temperature compartment is configured for mounting components that can be damaged by heat. The higher temperature compartment is configured for mounting heat generating components. An air stream is directed to flow from an ambient air inlet to an air outlet constantly so that there is always a fresh source of cooling air. The apparatus utilizes a PSA unit to produce an oxygen enriched product. The PSA unit incorporates a novel compressor system which includes the use of free piston linear compressors so as to reduce power consumption, noise and vibration reduction.

Abstract: A PAP system for delivering breathable gas to a patient includes a flow generator to generate a supply of breathable gas to be delivered to the patient; a humidifier including a heating plate to vaporize water and deliver water vapor to humidify the supply of breathable gas; a heated tube configured to heat and deliver the humidified supply of breathable gas to the patient; a power supply configured to supply power to the heating plate and the heated tube; and a controller configured to control the power supply to prevent overheating of the heating plate and the heated tube.

Abstract: A disposable anesthesia conduit cover kit that includes a dispenser and pre-measured, or cut to length tubing segments with fasteners to secure each end of the tubing segment. The dispenser may be wall mounted or lay flat and alternative dispenser configurations are provided. The tubing segments protect the anesthesia conduit cover from blood or body fluids to protect patients and healthcare workers from infectious and pathogenic microorganisms and to assist with the compliance of both state and federal regulations.

Abstract: An oxygen concentrator comprises a plurality of adsorbent columns, each having an inlet, an outlet and abed of adsorbent material. The oxygen concentrator also includes a vacuum pump for removing separated nitrogen rich gas from the column inlets, a control valve for controlling flow of fluids in and out of the columns, and a breakthrough sensor for signaling the position of a mass transfer zone (MTZ), the breakthrough sensor controlling operation of the control valve as a function of the breakthrough sensor signal. An electric control module (ECM) receives the signal from the breakthrough sensor, and adjusts the control valve based on the signal.

Abstract: A medical breathing assistance apparatus (20) for supplying pressurised gases to a patient is disclosed. The breathing assistance apparatus (20) comprises a heating chamber (29) and a pressure chamber (27) both adapted to contain water, and at least one pressure adjusting means (24,25,26). The pressure chamber (27) is connected to the heating chamber (29) and the pressure adjusting means (24,25,26) is located between the heating chamber (29) and a gases supplying means (23) supplying gas to both the pressure chamber (27) and heating chamber (29). The pressure adjusting means (24,25,26) is adapted to convert pressurised gases from the gases supply means (23) to two different pressures, one to each of the heating chamber (29) and the pressure chamber (27), so that water flows from said pressure chamber (27) to the heating chamber (29).

Abstract: A breathing tube system has a heating element, wherein a resistance wire extends several times to and fro in the longitudinal direction of a tube with wire terminals at one end and is held in the tube in parallel by means of a plurality of spreading elements located at spaced locations from one another in the longitudinal direction of the tube. The resistance wire extends at least four times in the longitudinal direction of the tube. The spreading elements have guide elements for receiving the resistance wire at the inner tube wall of the tube. The spreading elements with the resistance wire are displaceable in the tube in the longitudinal direction.

Abstract: The present invention provides improvements in the feedback and control systems employed in the field of ventilation therapy. In particular, a system for delivering a supply of gases to a patient is described which incorporates a detachable cartridge or open tubular section (22) used to house a mechanism (11) which senses the humidity, temperature, flow and other attributes of the flowing gas. Information obtained from the sensor may be used to provide feedback to a controller (9) which controls the humidification mechanism in order to provide optimally humidified gases to a patient (1). It will be appreciated that the feedback and control system as described in the preferred embodiment of the present invention can be used in respiratory care generally or with a ventilator.

Abstract: A device for providing heated air for an individual to breathe. The device comprises a heating circuit with a heating element that is surrounded and supported by a pad. The pad is attachable to an article of clothing. The heating element and pad form a heating unit that is positionable proximate an individual's breathing region when the article of clothing is worn by the individual. The pad is configured to allow heat generated by the heating element to heat the air to be breathed in by the individual.

Abstract: The gases temperature supplied to a patient when the patient is undergoing treatment such as oxygen therapy or positive pressure treatment for conditions such as Obstructive Sleep Apnea (OSA) or Chronic Obstructive Pulmonary Disease (COPD) is often measured for safety and to enable controlling of the humidity delivered to the patient. The invention disclosed is related to measurement of properties, particularly temperature, of gases flowing through a heated tube, supplying gases to a patient, which utilises the heating wire within the tube.

Abstract: The invention relates to a nasal cannula for an anti-snoring apparatus, comprising a forked tube pneumatically connected to apertures, which are embodied and positioned in such a way that air can be administered into the nose of a user via these apertures. The nasal cannula further comprises a heating wire extending in the interior of forked tube in such a way that the heating wire can heat the air supplied through the forked tube. The invention moreover relates to a nosepiece and to a Y-shaped element for nasal cannula including internal radius steps at tube connection points. The invention further relates to a nosepiece and to a Y-shaped element having rounded off transition regions. The invention finally relates to a method for avoiding condensation in nasal cannulas. To this end, the gas is heated as it flows through the tubes of a nasal cannula.

Abstract: A heater unit includes power failure management to detect disruptions in the electrical power supply, such as the AC supply, for the unit. The heater unit emits an audible alarm in response to detection of such a disruption, and may shut down the heater(s) and visuals display(s). The heater unit advantageously includes a power storage device, such as a super-capacitor, to temporarily power the electronic circuitry of the heater unit. Operating parameters, such as of a processor of the electronic circuitry, may be stored in a non-volatile memory response to the disruption, and recalled if the disruption terminates before the level of power has gotten too low to sustain reliable operation of the processor.

Abstract: A method of humidifying a gas that includes supplying a gas to a surface of a humidification material that readily absorbs moisture and readily releases moisture when exposed to a dry environment and generating turbulence in the gas as it posses over the surface of the humidification material.

Abstract: A positive airway pressure (PAP) device for supplying a flow of breathable gas to a patient includes a first housing; a flow generator provided in the first housing, the flow generator configured to generate a flow of breathable gas; a second housing configured to be connected to the first housing, the second housing including a channel having an inlet configured to receive the flow of breathable gas and an outlet configured to discharge the flow of breathable gas, wherein the first housing is provided on top of the second housing such that a footprint of the PAP device is not substantially increased beyond a footprint of the second housing.

Abstract: This invention relates to methods for controlling a TNI-apparatus (1). One method can measure the actual gas temperature at the outlet of the humidifier (19). One method can determine a set gas temperature (34) of the gas at the outlet of a humidifier (19) of the TNI-apparatus (1) in dependence on an ambient temperature (25) of the TNI-apparatus (1), or a set gas temperature (34) of the gas at the outlet of a humidifier (19) of the TNI-apparatus (1) in dependence on a gas flow (28) in the TNI-apparatus. One method can determine a set gas temperature (34) of the gas at the outlet of a humidifier (19) of the TNI-apparatus (1) in dependence on a comfort value (30) predetermined by a user, or adjust the heating power of a heating wire (26) in a nasal cannula (27) of a TNI-apparatus (1) in such a way that a gas exiting the nasal cannula (27) has approximately the same temperature, which the gas had when it exited a humidifier (19) of the TNI-apparatus (1).

Abstract: A cuff for an air delivery conduit includes a first end portion provided to a tube and a second end portion adapted to engage a tubular connector. The second end portion includes an entry surface that is curved or chamfered along its length to provide a lead in for inserting the second end portion onto the tubular connector in use. The entry surface provides an internal diameter that is larger than an external diameter of the tubular connector.

Abstract: An improved, pumpless respirator (ventilator) humidifier is provided with a water refilling device (1, 2) and with an electrically heated evaporator (5). The evaporator (5) has a tubular housing, which is filled with a porous sintered material. A front side of the housing is in liquid connection with the automatic water refilling device (1, 2) and the other front side is in connection with an evaporator chamber (4), through which breathing gas flows. The evaporator (5) is provided with a porous sintered glass or ceramic with a pore size of 10 ?m to 40 ?m in a first, lower, unheated area (14), and the evaporator (5) is provided with a porous sintered metal with a mean pore size of 50 ?m to 200 ?m in a second, upper area (15) heated by means of a heater (6).

Abstract: A heating unit comprises a substrate having a first surface and a second surface. A chemical reactant material capable of undergoing an exothermic reaction is disposed on at least a portion of the first surface of the substrate. An igniter is in proximity with the chemical reactant material. A layer of adhesive material overlays at least a portion of at least one of the chemical reactant material and the first surface of the substrate. Other embodiments of the heating unit include a first and a second substrate, each having first and second surfaces positioned with the first surfaces opposing each other in a sandwich construction. A chemical reactant material is disposed on at least a portion of the first surface of at least one of the substrates. The first and the second substrates are sealed together to define a cavity containing the chemical reactant material and an igniter is provided in proximity with the chemical reactant material.

Abstract: A breathing tube system for connection to a respirator (2), which is provided with a tube heater, avoids a local increase in temperature during the heating of the tube (4, 7). Resistance wires (9, 10) are connected to one another on the breathing tubes (4, 7) in the form of a series connection and are contacted at the respirator (2) in the area of an inspiration port (3) and of an expiration port (6).

Abstract: A patient delivery tube for the delivery of a heated, humidified gas. The patient delivery tube includes an elongated tubing member molded from a flexible polymer, said elongated tubing member comprising a first end, a second end and an axially aligned passageway extending therethrough and an electric heater comprising a conductive material, said electric heater arranged along said axially aligned passageway for perimetrically heating said axially aligned passageway. A method of delivering a heated, humidified gas to a patient is also provided.

Abstract: A method of humidifying a gas that includes supplying a gas to a surface of a humidification material that readily absorbs moisture and readily releases moisture when exposed to a dry environment and generating turbulence in the gas as it passes over the surface of the humidification material.

Abstract: A vaporizer apparatus for vaporizing medical herbs and essences is described that uses an electrical power driven medium to vaporize the herbs and essences. The vaporizer apparatus has a heating element assembly mounted at an angle within an enclosure. The heating element assembly also includes an insulating shield which covers the heating element and which has a mating section for mating with a hand piece. The hand piece includes a vaporization chamber where herbs are packed, an inlet for connecting with the mating section of the shield, and an outlet for inhalation by a user. Methods for using the vaporizer apparatus is also discussed.

Abstract: An endoscopic mouthguard comprising a bite block comprising a generally annular body adapted to be inserted into the mouth of a patient so as to maintain the upper and lower teeth of the patient in a spaced apart relationship and define an endoscopic passage for introduction of an endoscope into the oral cavity of the patient. The bite block includes a gas delivery passage for delivery of a gas to the oral cavity of the patient, and a gas distribution manifold detachably engaged with the bite block. The gas distribution manifold comprises at least one inlet port for receiving gas from a gas supply, at least one nasal outlet port in fluid communication with the inlet port and adapted so as to direct gas to or toward the nasal passages of the patient; and an oral outlet port in fluid communication with the inlet port.

Abstract: The present apparatus includes a metered dose inhaler (MDI) portion housed with a heat and moisture exchanger (HME) portion. The MDI portion and the HME portion share an inlet. The MDI portion and the HME portion share an outlet. The MDI portion and the HME portion are in parallel to each other and are immediately lateral of one another. The present MDI/HME apparatus includes a valve to direct fluid flow to or away from the HME portion and to or away from the MDI portion. The present MDI/HME apparatus includes a valve arm to communicate to the caregiver whether fluid is passing through the MDI portion or the HME portion and to structurally close off an MDI port when the valve is open relative to the HME portion. The valve is structured such that fluid flow to the patient is never obstructed.

Abstract: An oxygen separator for separating oxygen from ambient air utilizing a vacuum swing adsorption process has a mass of less than 2.3 kg. A carrier is mountable on a person to support the oxygen separator for ambulatory use.

Abstract: A filter assembly for use in sidestream gas sampling assembly. The filter assembly of the present invention includes a hydrophilic member that is constructed from a porous material and is situated such that gas entering the filter assembly passes through at least a portion the hydrophilic member. In a further embodiment, the filter includes a hydrophobic member positioned downstream of the hydrophilic member. The hydrophobic member acts as a second line of defense against moisture reaching the sensing mechanism in the gas sampling assembly.

Abstract: A gases transportation pathway for use in supplying a humidified gases stream to a patient includes regulated conduit heating. The regulated conduit heating may include a section of positive temperature coefficient material wherein the localized electrical resistance of the material is positively related to the localized temperature. The regulated conduit heating may be a layer of positive temperature coefficient material within the wall of the gases transportation pathway with at least a pair of conductors running the length of the pathway and in electrically conductive contact with the positive temperature coefficient material.

Abstract: Aerosol drug delivery devices incorporating percussively activated heat packages are disclosed. The heat packages include a percussive igniter and a fuel capable of undergoing an exothermic oxidation-reduction reaction when ignited by the percussive igniter. The drug delivery devices disclosed can be activated by an actuation mechanism to vaporize a thin solid film comprising a drug disposed on the exterior of a hat package. Metal coordination complexes of volatile drugs, and in particular nicotine, from which the drug can be selectively vaporized when heated are also disclosed. The use of aerosol drug delivery devices comprising thin films of nicotine metal salt complexes for the treatment of nicotine craving and for effecting smoking cessation are also disclosed.

Abstract: A method of conveying humid breathing gases from a patient through a breathable breathing tube. The breathing tube includes a heater associated, at least in part, with a portion of hydrophilic material. The purpose of the heater is to evaporate any condensed liquid collecting in the conduit, which is first sucked tip by the hydrophilic material. The heated wick reduces the risk of collected water being passed to the patient and causing choking fits or discomfit. It is preferred that the heated wick lies freely in the conduit to settle at low points in the conduit where condensation may collect.

Abstract: A device for detecting the relative humidity in a respiratory circuit is provided which includes a housing closed towards the outside by a transparent element, and towards the inside by a membrane permeable to the humidified gas passing through the equipment to which the device is applied and wherein the housing includes a humidity indicator element.

Abstract: The present invention relates to a packaging system for airway devices that permits their rapid access. In particular, the packaging system is capable of maintaining the device in storage under sterile conditions, yet be capable of facilitating rapid unpackaging and use.

Abstract: A tracheal tube comprising a nematic polymer or nematic elastomer, wherein an outer diameter of the tracheal tube changes in size in response to exposure of the tracheal tube to light or heat.

Abstract: An anti-condensation arrangement (5) for catheters comprising a heated air generator (6), a sheath (9) covering a catheter (4) such as to create a cavity (I) with it, and a device (7,8) for the input of heated air produced by the generator (6) into the cavity (I). The sheath (9) has a venting opening (9b) to allow the exit of heated air from the cavity (I) and therefore continuous exchange of air.

Abstract: A heat and moisture exchanger (HME) adaptor for a closed suction catheter assembly having one end in communication with a closed suction catheter assembly and another end configured to rotationally engage and releasably hold the HME is disclosed herein. The adaptor may include a retainer having an aperture that engages projections on the HME to releasably secure the adaptor to the HME. The adaptor may include a retaining ring that may be deformed or rotated to engage or disengage projections on the HME. The adaptor may be used with extended use closed suction catheter assemblies.

Abstract: A nasal cannula assembly is disclosed having a face mount part, in use resting against a user's face, which includes at least one nasal prong capable of being fitted into a person's nares. The cannula assembly also includes a manifold part, in fluid communication with the face mount part, having a single horizontal side gases entry. In particular, this cannula assembly is for supplying heated, humidified gases to a patient suffering from COPD. A tie or lanyard is disclosed for use with a breathing assistance apparatus such as a nasal cannula, face or nasal mask or tracheostomy connector. The tie or lanyard transfers the weight of the conduits supplying gases to the breathing assistance apparatus from the breathing assistance apparatus and distributes it onto the neck of the patient.

Abstract: Devices and methods of entraining a substance within an airflow are disclosed. Condensation aerosol delivery devices and methods of consistently producing multiple doses of a substance, such as a drug, having high purity, high yield, characterized by a particle size distribution appropriate for pulmonary delivery, and which can be administered to a user in a single dose are also disclosed.

Abstract: A limb for a breathing circuit manufactured from very thin walled polymer materials has an elongate axial reinforcing spine lying freely inside the conduit and fixed to each end connector. The spine is laterally compliant but axially stiff. The spine provides resistance to tensile and compressive loads on the conduit, including that induced by prevailing internal pressures.

Abstract: A heated breathing circuit detection system verifies the proper set up and connection of a breathing circuit to a heater unit of a humidification system. The detection system automatically detects that the breathing circuit is connected to the heater unit, and the nature of the heating circuit(s) thereof. In one embodiment, the resistance of the heating circuit(s) is determined and compared to an expected resistance or range of acceptable resistances to determine if the heater circuit(s) is properly or actually attached and properly operating. The humidification system also has the ability to determine the delivery mode of the breathing circuit, i.e., whether a single inspiratory limb, or both inspiratory and expiratory limbs, is connected to the heater unit.

Abstract: A breathing circuit includes inspiratory and expiratory limbs, each having a respective electrically energizable heating circuit. The heating circuits are independently and selectively electrically energized through separate power circuits such as to control the temperature in each limb in a desired fashion so as to reduce rainout in the breathing circuit and particularly in the expiratory limb.

Abstract: Spontaneous respiration is detected by sensors. An additional amount of oxygen is administered to the lungs via a jet gas current at the end of an inhalation procedure. Breathing volume, absorption of oxygen during inhalation, and clearance of carbon dioxide during exhalation are improved. If required, the exhalation procedure of the patient can be arrested or slowed by a countercurrent to avoid a collapse of the respiration paths. An apparatus including an oxygen pump can be connected to an oxygen source and includes a tracheal prosthesis that can be connected via a catheter. The respiration detections sensors are connected to a control unit for activating the oxygen pump. The tracheal prosthesis includes a tubular support body with a connection for the catheter, and the sensors are associated with the support body. The tracheal prosthesis and jet catheter are dimensioned so the patient can freely breathe and speak without restriction.

Abstract: A heater system is provided for a respiratory system having a PID feedback control in which the coefficients are adjusted, such as in a warm-up process, to correspond to a likely flow rate of gas through a chamber of heated water based on the difference between heat input and heat output in relation to a temperature set point without the need to directly monitor flow rate or humidity level. A steady-state adjustment of the coefficients based on the behavior of the measured temperature in relation to the set point is also disclosed.

Abstract: A heat capacitor for a capillary aerosol generator comprises a phase change material that changes phases at a temperature approximately equal to a temperature sufficient to volatilize liquid material in a capillary passage of the capillary aerosol generator. The phase change material stores heat, which can be used to generate aerosol either continuously or intermittently over a given time. The use of stored heat in the phase change material to generate aerosol over time enables operation of the capillary aerosol generator remote from a large energy source.

Abstract: Apparatus and methods for delivering humidified breathing gas to a patient are provided. The apparatus includes a humidification system configured to deliver humidified breathing gas to a patient. The humidification system includes a vapor transfer unit and a base unit. The vapor transfer unit includes a liquid passage, a breathing gas passage, and a vapor transfer device positioned to transfer vapor to the breathing gas passage from the liquid passage. The base unit includes a base unit that releasably engages the vapor transfer unit to enable reuse of the base unit and selective disposal of the vapor transfer unit. The liquid passage is not coupled to the base unit for liquid flow therebetween when the vapor transfer unit is received by the base unit.

Abstract: A ventilator to replace or supplement a patient's breathing includes a control valve in the form of a proportional obstacle valve (POV) to provide improved air flow control and ventilator operation reliability. The POV includes an inlet, an outlet and a bypass. A stopcock controlled by a stepper motor directs the flow of air through the bypass and outlet permitting the turbine to operate a constant RPM yet allowing control of the airflow to a patient. The ventilator also includes inhalation and exhalation valve assemblies which improve air flow control and are easy to manufacture. The inhalation valve includes an orifice disk to allow pressure sensors to move accurately measure air flow. The exhalation valve assembly includes wings to reduce turbulence and enhance sensor accuracy. The exhalation valve assembly is arranged to have warm air from cooling the turbine blow over the assembly to reduce the possibility of condensation forming therein.

Abstract: A medical ventilator includes a pressure generator for increasing a pressure of gas that produces heat during the operation thereof. A heat sink spaced from the pressure generator is provided for absorbing heat from the pressure generator. A bacteria filter requiring heating in excess of an ambient temperature for the effective operation thereof is coupled in thermal communication with the heat sink. A heat pipe is coupled in thermal communication with the heat sink and the pressure generator for conveying at least part of heat produced by the pressure generator to the bacteria filter via the heat sink.

Abstract: A low flow heated/humidified respiratory gas delivery system, especially useful for low flow rates as preferred in the treatment of neonate and other such patients, wherein the respiratory gas is heated and humidified as desired for delivery to the patient and the temperature is monitored at the point of delivery to the patient.

Abstract: A low flow heated/humidified respiratory gas delivery system, especially useful for low flow rates as preferred in the treatment of neonate and other such patients, wherein the respiratory gas is heated and humidified as desired for delivery to the patient and the temperature is monitored at the point of delivery to the patient.

Abstract: A base unit for use in a breathing gas heating and humidification apparatus includes a gas source configured to generate an initial gas flow, the gas source having a gas source outlet and a flow divider in fluid communication with the gas source outlet. The flow divider is configured to divide the initial gas flow into a first flow of gas and a second flow of gas. The flow divider includes a first compartment including a first gas flow path for the first flow of gas and a second compartment including a second gas flow path for the second flow of gas. A heater is disposed in the second compartment. A method for use in generating breathing gas and insulating gas from a gas source is also disclosed.

Abstract: A flow probe for use in a humidification system is disclosed. The flow probe is adapted to be positioned in a humidified gases flow (for example oxygen or anaesthetic gases) such as that which is provided to a patient in a hospital environment. The flow probe is designed to provide both temperature and flow rate sensing of the gases flow by incorporating two sensors (preferably thermistors) and the shape and alignment of the probe enables accurate readings by reducing the occurrence of condensation on the sensors.