654 results about "Exhaled air" patented technology

Methods involving extraction of information from the inherent variability of physiometrics, including data on cardiovascular and pulmonary functions such as heart rate variability, characteristics of ECG traces, pulse, oxygenation of subcutaneous blood, respiration rate, temperature or CO2 content of exhaled air, heart sounds, and body resonance, can be used to identify individual subjects, particularly humans. Biometric data for use in the methods can be obtained either from contact sensors or at a distance. The methods can be performed alone or can be fused with previous identification algorithms.

An electronic cigarette particularly adaptable to vaporize liquid material also having exhale filter function is disclosed herein. The exhale function is useful to prevent second hand smoke in an enclosed environment, for example. An innovative diverter valve assembly comprises a unique duckbill valve configuration diverting air through a cooker chamber and into a mouthpiece in an inhale function and diverting exhaled air around the cooker chamber in the exhale function and through a filter assembly. A preferred embodiment further introduces a unique shape to the smoking instrument being elliptical in the cross-section and tapering to proximal and distal ends.

An air filtering device is presented with a face mask of nonporous material, the face mask held onto the user's head by standard elastic straps. The face mask has a flexible gasket about its perimeter to provide an airtight seal between the mask and the user's face. The face mask has an exhaust filter that lets exhaled air out of the mask, but does not let unfiltered air into the mask. A flexible tube enters the face mask at one end and enters an air filtering assembly on the opposite end. The air filtering assembly is enclosed in a housing with the housing having an air intake opening. The air filtering assembly has an air moving device such as a fan or pump, a carbon filter cartridge, a particulate matter filter, a battery power supply, and an on-off switch.

In an air sterilization system that includes a UV kill chamber for sterilizing air that is to be supplied to users, the effectiveness of killing or neutralizing pathogens is increased by including not only a UV light source of a certain intensity but also including a particle filter and providing short duration high intensity UV radiation. In the case of a user specific system that includes a face mask to supply air to a specific user, exhaled air from the face mask may be sterilized as well, either by using the same kill chamber or by using a separate kill chamber.

The ventilation interface for sleep apnea therapy interfaces a ventilation device to the patient's airways. The ventilation interface includes a pair of nasal inserts made from flexible, resilient silicone which are oval shaped in cross-section and slightly tapered from a base proximal the ventilation supply to the distal tip end. A bead flange is disposed about the exterior of each insert at the distal end of the insert. A bleed port for release of exhaled air is defined through a conical vent projecting normally to the path of the incoming air flow, and continues through a nipple extending to the exterior of the air conduit. In one embodiment, a pair of nasal inserts are integral with a nasal cannula body, with bleed ports axially aligned with each insert. In another embodiment, each insert is independently connected to a separate, thin-walled, flexible supply line.

A respiratory treatment device comprising at least one chamber, a chamber inlet configured to receive exhaled air into the at least one chamber, at least one chamber outlet configured to permit exhaled air to exit the at least one chamber, and an exhalation flow path defined between the chamber inlet and the at least one chamber outlet. A restrictor member positioned in the exhalation flow path is moveable between a closed position, where a flow of exhaled air along the exhalation flow path is restricted, and an open position, where the flow of exhaled air along the exhalation flow path is less restricted. A vane in fluid communication with the exhalation flow path is operatively connected to the restrictor member and is configured to reciprocate between a first position and a second position in response to the flow of exhaled air along the exhalation flow path.

In an air sterilization system that includes a UV kill chamber for sterilizing air that is to be supplied to users, the effectiveness of killing or neutralizing pathogens is increased by including not only a UV light source of a certain intensity but also including a particle filter and providing short duration high intensity UV radiation. In the case of a user specific system that includes a face mask to supply air to a specific user, exhaled air from the face mask may be sterilized as well, either by using the same kill chamber or by using a separate kill chamber.

A multipurpose aerosol medication delivery apparatus that includes a collapsible / expandable, or a fixed volume, or a combination of partially fixed volume and partially collapsible / expandable holding chamber for use with a metered dosed inhaler (MDI) and / or any standard small volume nebulizer. The holding chamber is designed to deliver-aerosol medication particles generated by an MDI; aerosol medication particles generated by a nebulizer; a single gas or a mixture of gases; a single gas or a mixture of gases that can yield a gas density that will enhance aerosol delivery of medication with both MDI and nebulizer; a single gas or a mixture of gases that will yield and deliver an oxygen concentration to a patient ranging from room air concentration to 100%. The device includes a reservoir that stores nebulized aerosol generated during exhalation to be inhaled during the next breath. The device also included a one way valve to prevent carbon dioxide generated during exhalation from rebreathing by not allowing the exhaled air from entering the holding chamber. The device includes an exit port with a second one way valve that allows the exhaled air to exit the device but closes during inhalation to prevent any entrainment of room air gas. The exit port may instead have a filter with one-way valve to trap the exhaled aerosol particles while allowing the exhaled gases to escape. The filter valve will similarly close during inhalation to prevent entrainment of room air gas. The holding chamber will allow a uniform mixture of aerosol medication and gases to flow together during inhalation to the patient via a mouthpiece or a facemask. The holding chamber is connected to a nebulizer chamber with a single or multiple connecting tubes that allow gas mixtures with varying density, viscosity, humidity and concentration of oxygen to flow into the holding chamber from the nebulizer chamber. The pattern of flow of the gas(es) does not disturb the flow of the nebulized medication from the nebulizer chamber to the holding chamber or interfere with the plume generated by an MDI. The device also serves as a facemask for delivering precise concentrations of oxygen or as a 100% non-rebreather mask. The device also serves to deliver precise concentrations of different density gases i.e. nitrogen, helium, oxygen, etc. This will allow varying fractions of inspired oxygen to deliver aerosol medication via MDI or a nebulizer. Thus, the device has the ability to deliver aerosol medication with an MDI or a nebulizer while retaining the ability to simultaneously deliver different density gas mixtures and varying fraction of inspired oxygen without interrupting one for the other.

A respiratory therapy device including a housing and an interrupter valve assembly. The housing includes a patient inlet, an exhaust outlet, a chamber, and a supply inlet. The interrupter valve assembly is associated with the housing and includes a control port fluidly connecting the patient inlet and the first chamber, and a valve body adapted to selectively obstruct fluid flow through the control port. In a passive mode, positive fluid flow to the supply inlet does not occur, and the interrupter valve assembly interacts with exhaled air create an oscillatory PEP effect. In an active mode, fluid flow to the supply inlet occurs and the interrupter valve assembly operates to create a CHFO effect. The respiratory device can serve as a passive oscillatory PEP device, and when connected to a positive pressure source, as an active device.

A device for determining the level of nitric oxide in an exhaled airstream belonging to a living organism selected to have its lung function evaluated, where an initial device is arranged to determine the current portion of nitric oxide and / or the distribution of nitric oxide over time during an exhalation phase. During the commencing period of the exhalation phase, the exhaled air is arranged to pass with no or with only a very small resistance or back-pressure to a free space, and during the remaining period, the exhaled air is arranged to pass through the initial device against the action of a suitable resistance or back-pressure. The level of nitric oxide is measured during this remaining period.

In accordance with non-limiting examples, a nebulizer includes a main body comprising an air channel section and further comprising a mixing chamber and a venturi positioned to be placed within the patient's oral cavity and configured to receive medicine and air and mix the medicine and air within the mixing chamber and receive the air flow through the venturi and cause the medicine entering the mixing chamber to be atomized by the action of air flowing through the venturi. An air flow sensor is associated with the main body and configured to measure the air flow created by the patient's one of at least inhaling and exhaling air.

An oscillating positive expiratory pressure device comprising a housing enclosing at least one chamber, a chamber inlet configured to receive exhaled air into the at least one chamber, and a chamber outlet configured to permit exhaled air to exit the at least one chamber. A channel is positioned in an exhalation flow path between the chamber inlet and the chamber outlet, with the channel being moveably connected to a chamber of the at least one chamber. An air flow regulator is moveable with respect to the channel between a first position, where the flow of air through the channel is restricted and a second position, where the flow of air through the channel is less restricted, the air flow regulator being configured to repeatedly move between the first position and the second position in response to a flow of exhaled air.

A nasal delivery device for delivering substance to a nasal cavity of a subject, the delivery device comprising: a substance supply unit for supplying a dose of substance to be delivered to the nasal cavity of the subject, the substance supply unit including an inlet and an outlet; a nosepiece unit including a nosepiece for fitting to a nasal cavity of the subject and being in fluid communication with the outlet of the substance supply unit; and a mouthpiece unit including a mouthpiece in fluid communication with the inlet of the substance supply unit and through which the subject in use exhales such as to entrain substance from the container chamber and deliver the same through the nosepiece, and at least one temperature modifier for reducing a temperature of the exhaled air flow such as to reduce the absolute humidity thereof.

The present invention relates to noninvasive methods for obtaining exhaled breath condensate (EBC) samples from the airways and lungs of a subject for use in diagnosing various conditions and diseases associated with biomarkers present in EBC, including diagnosis of lung cancer. The methods of the subject invention include generating and / or applying an oscillating airflow to a subject during inhalation and / or exhalation to induce increased concentration of biomarkers in EBC; collecting EBC from exhaled breath; and analyzing the collected EBC for biomarkers associated with disorders and / or diseases.

A respiratory therapy device including a housing and an interrupter valve assembly. The housing is sized for handling by a patient and defines a patient breathing passage extending from a patient end and through which a patient inhales and exhales air. The interrupter valve assembly is carried by the housing and includes a control port, a valve body, and a drive mechanism. Expiratory airflow is released from the patient breathing passage through the control port. The valve body is sized to at least partially obstruct fluid flow through the control port. The drive mechanism moves the valve body relative to the control port in response to the expiratory airflow such that the valve body repeatedly transitions between a position of maximum obstruction and a position of minimum obstruction relative to the control port to create an oscillatory positive expiratory pressure effect.

A filtering face mask that includes a mask body and an exhalation valve. The mask body is adapted to fit at least over the nose and mouth of a wearer to create an interior gas space when worn, and the exhalation valve is in fluid communication with the interior gas space. The exhalation valve comprises a valve seat that has a seal surface and an orifice through which an exhale flow stream may pass to leave the interior gas space. A flexible flap is mounted to the valve seat such that the flap makes contact with the seal surface when the valve is in its closed position and such that the flap can flex away from the seal surface during an exhalation to allow exhaled air to pass through the orifice to ultimately enter an exterior gas space. The flexible flap has at least first and second juxtaposed layers where at least one of the layers is stiffer or has a different elastic modulus than the other layer.

A respiratory therapy device including a housing and an interrupter valve assembly. The housing includes a patient inlet, an exhaust outlet, a chamber, and a supply inlet. The interrupter valve assembly is associated with the housing and includes a control port fluidly connecting the patient inlet and the first chamber, and a valve body adapted to selectively obstruct fluid flow through the control port. In a passive mode, positive fluid flow to the supply inlet does not occur, and the interrupter valve assembly interacts with exhaled air create an oscillatory PEP effect. In an active mode, fluid flow to the supply inlet occurs and the interrupter valve assembly operates to create a CHFO effect. The respiratory device can serve as a passive oscillatory PEP device, and when connected to a positive pressure source, as an active device.

A disposable mask and suction catheter includes a mask having a front side and a back side, the back side being disposed in contact with a user's face during use. The disposable mask and suction catheter also includes a catheter tube having a first and a second end, the first end being removably attachable to a suction source for removing exhaled air and the second end being attached to the back side of the mask. The disposable mask and suction catheter helps to prevent fogging of glasses or other eyewear due to moist, exhaled air that escapes from behind the mask, and improves user comfort by constantly removing the warm, moist air behind and around the mask and drawing cool dry air into the mask.

A filtering face mask that includes a mask body that is adapted to fit at least over the nose and mouth of a wearer to create an interior gas space when worn; and an exhalation valve that is in fluid communication with the interior gas space. The exhalation valve includes a valve seat with a seal surface and an orifice through which exhaled air may pass to leave the interior gas space; and a flexible flap that is mounted to the valve seat such that the flap makes contact with the seal surface when the valve is in its closed position and such that the flap can flex away from the seal surface during an exhalation to allow exhaled air to pass through the orifice. The flap is unbiased when in its closed position and exhibits a cantilever bend ratio of 0.0050 or less.

The invention concerns noninvasive apparatus and methods for determining the internal temperature of the lungs in real time in connection with treatments that involve heating or cooling the lungs. The method involves using a specified apparatus preferably comprising a breathing tube, temperature sensor and other elements to measure the temperature of exhaled air, and optionally combining said measurement with other measurements and parameters, in order to calculate the internal lung temperature.

A cannula assembly and a medical system. The cannula assembly includes a cannula, a capnometer, a reservoir, a pathway, and a barrier. The cannula is positionable on the face of a patient. The capnometer measures carbon dioxide gas concentration and is operably connected to the cannula. The reservoir is adapted for containing a known concentration of carbon dioxide gas. The pathway connects carbon dioxide gas in the reservoir with the capnometer. The barrier has a first state preventing gas flow along the pathway and has a second state allowing gas flow along the pathway. The medical system includes the cannula assembly and includes a drug delivery assembly. The drug delivery assembly is adapted for administering a drug to the patient according to a drug delivery schedule based at least in part on the carbon dioxide gas concentration of the exhaled air of the patient as measured by the capnometer.

A diving mask comprises a mask and a breathing tube. The mask is provided with a viewing compartment, a breathing compartment, a first airway and a second airway. The breathing tube is provided with a single breathing airway. The first airway connects the breathing airway and the viewing compartment. The second airway connects the breathing compartment and the breathing airway. The viewing compartment and the breathing compartment are connected through a first check valve. The breathing compartment and the second airway are connected through a second check valve. When the above-mentioned diving mask is in use, outside air can enter the breathing compartment through the breathing airway, the first airway, the viewing compartment and the first check valve. The exhaled air in the breathing compartment can be expelled out of the mask through the second check valve, the second airway, and the breathing airway.

A personal air filtration device has a cylindrical exhalation tube, with a one-way valve thereon. Concentric around the periphery of the exhalation tube and integrally connected to the exhalation tube rearward (proximate the user's mouth) of the one-way valve is a filter media housing. Filter media is contained between the housing and the tube. A plurality of perforations in the exhalation tube, rearward of the one way valve but forward from the housing connection ring, provide inhaled air ingress to the exhalation tube. Inhaled air forces the one-way valve closed, so that air is directed through the filter media, passes through the perforations and into the exhalation tube where the user can take in the cleansed air. The pressure of the exhaled air through the exhalation tube causes the one-way valve to open, so that exertion by the user is minimized.

An accessory for an inhaler unit may be retrofit into a conventional nebulizer system having a manifold or an inlet air tube. The accessory includes a one-way air valve that closes except when air is being inhaled. The one-way valve closes to prevent exhaled air / gas from flowing through the manifold and inlet air tube and out to the surrounding atmosphere. Thus, exhaled air / gas does not flow out of the system and does not carry medicine with it, greatly reducing medicine waste. Because the preferred inhaler system does not include any exhale / exhaust valve or any other outlet for exhaled air / gas, the user may loosen his lips, for example, to exhale. The accessory may be provided simply as a single one-way valve retrofit into an existing air tube of a conventional nebulizer system, as an air tube-valve combination that may be attached to a nebulizer system manifold, or as original equipment manufacture (OEM) for a nebulizer system.

A nasal delivery device for delivering substance to a nasal cavity of a subject, the delivery device comprising: a substance supply unit for supplying a dose of substance to be delivered to the nasal cavity of the subject, the substance supply unit including an inlet and an outlet; a nosepiece unit including a nosepiece for fitting to a nasal cavity of the subject and being in fluid communication with the outlet of the substance supply unit; and a mouthpiece unit including a mouthpiece in fluid communication with the inlet of the substance supply unit and through which the subject in use exhales such as to entrain substance from the container chamber and deliver the same through the nosepiece, and at least one temperature modifier for reducing a temperature of the exhaled air flow such as to reduce the absolute humidity thereof.

A nasal ventilation interface comprising a hollow body having at least one and preferably two nasal apertures, and at least one and preferably two inhale apertures, and at least one and preferably two nasal insert tubes each associated with one of the nasal apertures and having an annular sleeve that forms a seal with a nostril of the patient. The hollow body has at least one and preferably two exhale apertures and at least one valve assembly associated with the exhale apertures that are capable of preventing air from passing through the exhale aperture upon the patient inhaling and allowing air to pass through the exhale aperture upon exhaling. The hollow body may also have at least one and preferably two filters for retaining heat and moisture from the exhale air and transferring the retained heat and moisture into the inhale air.

A filter mask includes an oronasal cup, an inhalation directional cover, and an exhalation diverter body. The oronasal cup encloses a nose and mouth of a user. The oronasal cup is fluidly coupled with a filter. The inhalation directional cover is configured to be joined to the filter. The inhalation directional cover includes an elongated wing portion that is oriented in an inhalation direction that is angled with respect to the center axis of the filter. The exhalation diverter body is fluidly coupled with the oronasal cup. The exhalation diverter body defines an exhalation duct that directs exhaled air out of the oronasal cup along an exhalation direction. The inhalation direction and the exhalation direction are oriented away from a plane of interaction between the user and another person.

An underwater breathing device, such as a snorkel, may include an exhalation valve. The exhalation valve is configured to produce positive end-expiratory pressure in the airway of a user of the underwater breathing device in order to reduce the overall work of underwater breathing. The exhalation valve includes a plate defining an exhalation port. The exhalation valve also includes a flexible membrane that is sealable against a surface of the plate and is sized and positioned to be capable of sealing the exhalation port. The flexible membrane is configured to have a sealed position in which the flexible membrane seals the exhalation port such that substantially no exhaled air escapes the snorkel. The flexible membrane is also configured to have an unsealed position in which exhaled air escapes the snorkel.