Abstract: A flow generator for a CPAP system configured to deliver a pressurized flow of respiratory gas to a patient's airways includes a housing and a motorized fan positioned within the housing. The motorized fan is configured to pressurize the flow of respiratory gas. In addition, an outlet port is provided in the housing. The outlet port is configured to connect to a humidifier or an air delivery tube and is in communication with an outlet of the motorized fan. The flow generator further includes a water collection receptacle in communication with the outlet port and the motorized fan outlet. The water collection receptacle is configured to collect water entering the flow generator through the outlet port before the water reaches the motorized fan outlet.

Abstract: The present disclosure pertains to an apparatus configured to facilitate monitoring of gas in a therapeutic gas delivery system with a catalytic sensor. The gas delivery system comprises a pressure generator having an inlet and an outlet, and a gas delivery flow path configured to communicate the gas between the pressure generator and a subject. The apparatus comprises a receiver body configured to receive the catalytic sensor such that the catalytic sensor removably couples with the receiver body, the receiver body located remotely from/outside the gas delivery flow path; a delivery port configured receive a portion of gas obtained from the gas delivery system that has passed through the pressure generator outlet and guide the received portion of gas toward the catalytic sensor; and a return port configured to exhaust the received portion of gas from the receiver body to the gas delivery system through the pressure generator inlet.

Abstract: A dressing for treating a tissue site may include a base layer, a sealing member, a first and a second wicking layer, and an absorbent layer. The base layer may have a plurality of apertures and may be adapted to cover the tissue site. The sealing member and the base layer may define an enclosure. The first and the second wicking layer may each be disposed in the enclosure with the absorbent layer positioned between the first and the second wicking layer. A conduit comprised of an absorbent material that is vapor permeable and liquid impermeable may be in fluid communication with the dressing for providing reduced pressure to the dressing. Other dressings, systems, and methods are disclosed.

Abstract: A dressing for treating a tissue site may include a base layer, a sealing member, a first and a second wicking layer, and an absorbent layer. The base layer may have a plurality of apertures and may be adapted to cover the tissue site. The sealing member and the base layer may define an enclosure. The first and the second wicking layer may each be disposed in the enclosure with the absorbent layer positioned between the first and the second wicking layer. A conduit comprised of an absorbent material that is vapor permeable and liquid impermeable may be in fluid communication with the dressing for providing reduced pressure to the dressing. Other dressings, systems, and methods are disclosed.

Abstract: A dressing for treating a tissue site may include a base layer, a sealing member, a first and a second wicking layer, and an absorbent layer. The base layer may have a plurality of apertures and may be adapted to cover the tissue site. The sealing member and the base layer may define an enclosure. The first and the second wicking layer may each be disposed in the enclosure with the absorbent layer positioned between the first and the second wicking layer. A conduit comprised of an absorbent material that is vapor permeable and liquid impermeable may be in fluid communication with the dressing for providing reduced pressure to the dressing. Other dressings, systems, and methods are disclosed.

Abstract: The invention relates to a respiratory circuit appliance with a respiratory line, a CO2 absorber (6) in the respiratory line, and a cooling device for cooling the respiratory gas after it exits the CO2 absorber. Provision is made that the cooling device cools a heating pump with a compressor (33) for compressing/condensing a cooling medium, a condenser (30), which receives the condensed cooling medium, and in so doing releases heat to the surroundings, and with a heat exchanger body (8) which receives the cooled cooling medium and is in heat-conducting contact with a section of the respiratory line.

Abstract: A dressing for treating a tissue site may include a base layer, a sealing member, a first and a second wicking layer, and an absorbent layer. The base layer may have a plurality of apertures and may be adapted to cover the tissue site. The sealing member and the base layer may define an enclosure. The first and the second wicking layer may each be disposed in the enclosure with the absorbent layer positioned between the first and the second wicking layer. A conduit comprised of an absorbent material that is vapor permeable and liquid impermeable may be in fluid communication with the dressing for providing reduced pressure to the dressing. Other dressings, systems, and methods are disclosed.

Abstract: A method and apparatus for humidifying breathable gas provided to a user includes providing a breathable gas, producing moisture or water derived from ambient environmental surroundings, e.g., via condensation and/or dehumidified air, and directing the breathable gas along an air flow path. The air flow path optionally includes access to at least a portion of the moisture or water for increased humidification of the breathable gas, for delivery to the user.

Abstract: A collection device for exhaled vapor is provided. The exhaled vapor collection device collects a wearer's exhalant to provide for later hydration. In at least one embodiment, the collection device for exhaled vapor includes a facial mask; a one-way intake valve disposed within the facial mask and configured to allow the one-way intake of air into the facial mask; an exit port disposed within the facial mask and configured to allow the one-way exit of air out from the facial mask; a proximal condensation tube fluidly coupled to the exit port of the facial mask, an interior surface upon which exhaled vapor collects; and a collection bag tube fluidly coupled to the condensation tube to collect a wearer's exhalant. The exhaled vapor collection device is configured to collect a wearer's exhalant in the collection bag to provide for later hydration.

Abstract: A portable air conditioning and ambient fresh air supply system that provides ambient fresh or conditioned air to a user wearing a respirator. The apparatus comprises a cabinet having an upper chamber and a lower chamber. The lower chamber holds a refrigerant air conditioning system and the upper chamber holds a blower that supplies cold air to the surroundings. The user is able to control the temperature of the conditioned air by means of a control panel and the air flow rate by a blower control switch. An air outlet manifold supplies fresh or conditioned air through an air supply line to a respirator mask.

Abstract: The present invention provides a practical method for treating atopic dermatitis. By subjecting patients suffering from atopic dermatitis to filtered temperature controlled laminar air flow disease symptoms have been significantly reduced and even removed. The velocity of the laminar air flow is balanced such that body convections are braked without the generation of draught.

Abstract: A medical breathing apparatus incorporating a regulator for supplying breathing gas to a patient from an air hose (11). The regulator supplies breathing gas on demand to the patient via a mouthpiece or similar attached to an output connector (55). The connector forms part of a removable output unit (4) incorporating a filter (53) and an exhale flap valve (57/58) on the patient side of the filter. When the patient exhales, exhaled gas entering the connector (55) exits to atmosphere via the exhale valve without passing through the filter into the interior of the regulator, thus reducing cross-contamination between patients. Also described is an improved valve seat (16)/valve member (18) assembly in which multiple spaced pivot points (22, 23) are defined to cause the mechanical advantage for operating the valve member to reduce as the valve opens, thus reducing the force needed to operate the valve at lower flow rates.

Abstract: Closed system breathable gas regeneration systems comprising temperature swing adsorption (“TSA”) using metabolic regeneration, such systems being useful for EVA in extraterrestrial environments having hostile atmospheres.

Abstract: Method for the removal of volatile anesthetic agents from breathing gas in an apparatus for respirating of patients provided with a closed line or conduit system in which breathing gas may be circulated, comprising leading the breathing gas or a part thereof through a filtering apparatus with activated carbon, wherein the breathing gas is cooled to a temperature below the boiling point of the anesthetic agent when it passes through the filtering apparatus, characterized in that the breathing gas, after anesthetic agent has condensed out of it, is warmed.

Abstract: This invention relates in general to methods and devices for displacing body convection and thereby reducing exposure to allergens and other airborne fine particles within a personal breathing zone during situations of or corresponding to sleep thereby reducing or removing symptoms of asthma and allergic rhinitis while improving quality of sleep and in particular to methods and devices that utilize Temperature controlled Laminar Airflow (abbreviated TLA from herein and onwards). Also, business methods involving such methods and devices are disclosed.

Abstract: An apparatus for providing pressure into which a patient must exhale is provided. The canister has a canister axis and is disposed to hold liquid. The canister also has indicia of pressure on the canister. The apparatus also includes a substantially rigid lid disposed to substantially cover a mouth of the canister and having a first inlet through the lid. The apparatus also includes an adapter in the first inlet. The apparatus also includes a conduit being retained by the adapter such that the conduit is substantially immovable relative to the canister axis.

Abstract: An adjustable airway pressure system is provided. The system may include a cap and a canister. The cap may include a substantially hollow conduit having indicia indicative of a plurality of airway pressure values and adapted to receive and output exhaled gas. The conduit may have screw threads on an exterior surface of the conduit. The cap may also include an adjust collar circumscribing the conduit and having an interior surface with a second plurality of screw threads. The second plurality of screw threads may couple and be complementary to the first plurality of screw threads such that a rotation of the adjust collar causes the conduit to move in a substantially vertical direction. The conduit may be adapted to be adjusted to heights along a continuum. The canister may contain liquid and receive the conduit such that the received exhaled gas is output from the conduit into the liquid.

Abstract: A condensate separator is provided for a coaxial tube system, which has an inner gas duct (3) and an outer gas duct (4). A first liquid duct (10) is arranged between the inner gas duct and a first collection volume (8) and a second liquid duct (11) is located between the outer gas duct (4) and a second collection volume (9). The collection volumes (8, 9) are located with a partition (7) in between in a liquid collecting container (6).

Abstract: A breath condensate sampler for use with a mechanical ventilator, the breath condensate sampler includes an airflow valve, a condensate formation tube, a condensate trap, and a condensate collection receptacle. The airflow valve directs air from the expiratory limb into the condensate formation tube wherein the condensate portion of exhaled gases are separated from the gaseous portion of the exhaled gases. A method of collecting a breath condensate sample is also herein disclosed.

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 single ended column design in which all flow paths and valves can be co-located on a single integrated manifold. The apparatus also can be used in conjunction with a satellite conserver and a mobility cart.

Abstract: A method and apparatus are disclosed for recovering and separating anesthetic gas components from waste anesthetic gases to be purged from a healthcare facility. Prior to a condensation step, a compressor is used to increase the waste anesthetic gas pressure in order to facilitate condensation of anesthetic gas components at higher temperatures and in greater amounts than through condensation at lower pressures. Condensing the anesthetic gas components from the compressed waste anesthetic gas stream is then achieved using conventional condensation systems, which remove anesthetic gases as either liquid condensates or solid frosts. A preferred embodiment of the invention may be used with existing high-flow scavenging or reclamation systems but is more preferably used with low-flow scavenging or reclamation systems, which employ intelligent waste anesthetic gas collection units to minimize the ingress of atmospheric gas when no waste anesthetic gas is to be purged from the healthcare facility.

Abstract: A method and apparatus are disclosed for recovering and separating anesthetic gas components from waste anesthetic gases to be purged from a healthcare facility. With minimal reliance on the utility infrastructure and supplies of a healthcare facility, the method and apparatus needs only electrical or mechanical power, a source of waste anesthetic gases, and an atmospheric vent in order to operate. A heat exchanger/condenser, which uses a dedicated heat transfer fluid as a refrigerant, is employed to condense anesthetic gas components from the waste anesthetic gases as either liquid condensates or solid frosts. The warmed heat transfer fluid is cooled in a separate refrigeration unit and recycled back to the heat exchanger/condenser. A preferred embodiment of the invention is a self-contained, packaged unit which can be easily accommodated in a physician's office, small animal clinic, dental office or other healthcare facility requiring effective waste anesthetic gas management.

Abstract: A method and system for removal of nitrous oxide and volatile halocarbon gas components from waste anesthetic gases using a low-flow scavenging or reclamation system preferably including an intelligent waste anesthetic gas collection unit fluidly coupled between each individual anesthetic machine and the waste gas evacuation manifold. Through a system including a collection chamber, a pressure detector, and a exhaust valve which is actuated based on the detected pressure in the collection chamber, the waste anesthetic gas collection unit allows flow to the waste suction manifold only in the presence of waste gas and interrupts all flow into the suction manifold when no waste gas is present.

Abstract: A method and system for the fractionation and removal of nitrous oxide and other volatile halocarbon gas components from waste anesthetic gases using liquid oxygen are disclosed. Liquid oxygen is warmed for use in a healthcare facility by cooling and condensing waste anesthetic gases. A cold trap/fractionator is provided wherein selective components of the waste anesthetic gas are collected as a frost on the coils of the cold trap/fractionator by desublimation/deposition and/or condensation/solidification. In a periodic batch process, the collected frost is first thawed and the melted liquids or gases are then collected at various increasing temperatures, thereby separating the nitrous oxide and other halocarbon gas components by their varying melting points. The thawed anesthetic components are collected in separate tanks based on their melting points. Warmed by the waste anesthetic gases in the cold trap/fractionator, the oxygen is supplied to the healthcare facility for its normal uses.

Abstract: Disclosed and claimed herein are devices and method for the recovery of one or more anesthetic agents after they have been exhaled from a patient undergoing surgery and before they have been vented to the atmosphere. Typical anesthetic agents include, but are not limited to, isoflurane, desflurane, sevoflurane, and the like. Recovery of the anesthetic agents should result in numerous benefits including, but not limited to, reduction of their production costs, protection of the environment, and the like.

Abstract: The invention relates to a device and a method for the generation of respirational air. The device according to the invention makes it possible to dehumidify air optimally. The dehumidification problem is achieved with a tapering passage, in particular with a nozzle. The nozzle is contained in a tube in which the mixture of air and water flows. A pressure which is higher on one side and which leads to a local increase in the flow rate in the nozzle and to a lower temperature prevails in the nozzle. These circumstances result in the water further condensing out of the air in the nozzle. The water which is condensed out is entrained by the air stream and can be separated off in a water separator connected directly after the nozzle, even before the gas or the air (after the nozzle) can become saturated again.

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 single ended column design in which all flow paths and valves can be co-located on a single integrated manifold. The apparatus also can be used in conjunction with a satellite conserver and a mobility cart.

Abstract: A cool air inhaler for use in treating croup, having a body having at least one side wall and a bottom wall forming an enclosed space open at an upper portion of the body wherein the upper portion of the body is adapted to generally conform to contours of a lower part of a patient face. An air chamber is formed in an upper part of the body and has an exhaust vent for exhausting the patient's exhaled air to an exterior space while an ice reservoir is formed in a lower part of the body to contain ice and meltwater from the ice and an air passage is connected from the exterior space and passing through the ice reservoir to conduct air to the air chamber.

Abstract: Methods and systems are provided for enhancing the air quality in buildings during a chemical and/or biological attack and/or when the air quality around a building drops to unacceptable levels. Preferably, relatively non-contaminated (clean) air is stored in one or more clean air reservoirs. Once stored, the clean air is selectively delivered to buildings when a chemical and/or biological attack is detected, and/or when the air quality around a building drops to unacceptable levels.

Abstract: A method of making thin-walled permeable tubing using air blown extrusion, and of using the tubing in a device which enables a substantial humidification or drying of patient breathing gases in the breathing lines for patient monitoring or anesthesia results in cost savings and increased efficiency.

Abstract: A system for removing halocarbon gas components from waste anesthetic gases using the resource of cold oxygen from liquid oxygen which is stored cryogenically at a healthcare facility. The oxygen is warmed while cooling of waste anesthetic gases from anesthetizing locations of a healthcare facility. Two heat exchangers/condensers are provided. In the first, the waste gas is cooled to about 0° C. thereby condensing any water vapor in the waste gas. In the second, the waste gas is further cooled to about −150° C. thereby condensing and liquefying the halocarbon gas components, which are removed to a tank for recycling and/or destruction. The remainder of the waste gases (e.g., nitrogen, oxygen and nitrous oxide) are vented to the atmosphere. The warmed oxygen is piped to the healthcare facility for its normal uses after it has been warmed by the waste anesthetic gases in the two heat exchangers/condensers.

Abstract: Embodiments of the present invention described and shown in the specification and drawings include a respiratory system for automatically and variably controlling the supply of a pressurized breathing gas to a patient via a breathing circuit that is in fluid communication with the lungs of the patient. The respiratory system has a demand valve in fluid communication with a source of pressurized gas. The demand valve is switchable between a open position, in which an inhalation conduit of the breathing circuit is in fluid communication with the source of pressurized gas, and a closed position, in which the inhalation conduit is not in fluid communication with the source of pressurized gas. The demand valve is proportionally moveable between the open and closed positions in response to a pressure within a reference chamber which is in fluid communication with the trachea of the patient.

Abstract: The present invention allows a low-flow anesthesia method to be executed while hindering temperature increases in a carbon dioxide absorbent, thereby reducing evaporation of water from the carbon dioxide absorbent and the amount of condensation formed in an anesthetic circuit, but without increasing the amount of decomposed compounds.

Abstract: A breathing circuit component includes an inlet, an outlet and an enclosing wall. The enclosing wall defines a gases passageway between the inlet and the outlet. At least a region of the enclosing wall is formed from a breathable material that allows the passage of water vapor without allowing the passage of liquid water or respiratory gases. The breathing circuit component may be the expiratory limb of a breathing circuit.

Abstract: A heat and moisture exchanger including a gas-permeable element, preferably a fibrous media, adapted to be warmed and to trap moisture from a patient's breath during exhalation and to be cooled and to release the trapped moisture for return to the patient during inspiration to effectively conserve the humidity and body heat of the patient's respiratory tract, wherein the media comprises a hydrophilic nylon polymer. The gas-permeable element can be formed entirely of monocomponent fibers of the hydrophilic nylon polymer or, preferably, fibers comprising at least a sheath of the hydrophilic nylon polymer can be bonded at their points of contact by a bonding agent, such as a polyester.