219 results about "Respiratory air" patented technology

A nasal mask assembly is configured to provide a direct flow of a fluid, e.g., breathable air, oxygen or anesthesia, directly into the patient's nasal cavity by combining the nasal prongs of a nasal cannula with a nasal cup. The nasal cup is made of clear plastic and has a general shape of a human nose such that it easily and comfortably fits over a patient's nose. An input port extends through the nasal cup into the internal cavity of the nasal cup and a fluid source is connected to the input port via a source tube system. The nasal cup can be molded to approximate the surface of a patient's face surrounding the patient's nose. The nasal prongs are extended in length. The source tube is rotatably connected to the external end of the input port of the nasal cup.

A nasal air filtration device includes a pair of either planar or concave-convex filters, a support structure incorporating a pair of generally annular bases or sleeves for supporting the filters, and a bridge that couples the bases or sleeves to maintain them in a desired spaced-apart relation and to determine a desired angular relationship. The support structure is insertable into the nasal cavities to position the filters within corresponding nasal cavities. Flexible rims maintain the support structure and the filters in spaced-apart relation to the surrounding nasal wall. The rims conform to surrounding nasal tissue to form seals. The rims can be selectively inclined to facilitate insertion and resist accidental removal. In certain embodiments the device is combined with a filter that covers the mouth to provide an air filtration system.

A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient, including a breathable air outlet, an outside air inlet, and an pneumatic block module, wherein the pneumatic block module includes: a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage; the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; a casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly, wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet.

The present invention relates to a ventilation system for a protective suit for use in hazardous environments. In a further aspect it concerns the protective suit itself. An air purifying respirator draws air from outside the protective suit through a filter, supplies filtered breathing air via a breathing hose to a space within the face piece, and supplies filtered ventilating air via a ventilating hose to the interior of the protective suit. A ventilation valve in the ventilating hose automatically closes only during periods of high breathing demand to counter a pressure drop inside the face piece.

This invention relates to a method, process and apparatus for disinfecting and sterilizing all types of surfaces contaminated with microorganisms and toxic substances to render both inactive. Furthermore, this invention relates to both a method and apparatus for disinfecting and / or sterilizing breathable air and then using this air to protect a confined space from external contamination. The apparatus consists of a new ultra-violet (NUV) source that is more effective than mercury based 254 nm light for destroying DNA of virus, bacteria, spores and cists. It is most effective in breaking chemical bonds in toxic gases and Biotoxins that are useful to terrorists. It is combined with other apparatus that remove particulates and byproducts sometimes produced by the NUV source and maintains positive pressure of the confined space so as to prevent the influx of air from outside the protected zone.

A storage system for an apparatus that delivers a supply of pressurized breathable air to a patient includes a container including a first portion and a second portion. The first portion provides a storage compartment adapted to receive a flow generator of the apparatus. The second portion is movably mounted to the first portion for movement between (1) an open position in which the second portion uncovers the storage compartment to allow access to the storage compartment and (2) a closed position in which the second portion closes the storage compartment to inhibit access to the storage compartment. At least one of the first and second portions provides at least one opening therethrough that allows access to at least one of the control panel, the power inlet, and the outlet of the flow generator supported by the container when the container is in the closed position.

An apparatus for protecting a user in a hazardous or contaminated environment caused by chemical, fire, biological, and / or nuclear contamination includes a self-contained breathing apparatus (SCBA) for providing tank stored breathable air, a powered air purifying respirator (PAPR) for purifying ambient air and a valve system that can be used to control the source of air from either the SCBA or the PAPR. The source of breathable air can be selectively controlled via manual or automatic controls while a protective body suit can be operably coupled with the SCBA and the PAPR to protect a user within the contaminated environment.

A nasal air filtration device includes a pair of either planar or concave-convex filters, a support structure incorporating a pair of generally annular bases or sleeves for supporting the filters, and a bridge that couples the bases or sleeves to maintain them in a desired spaced-apart relation and to determine a desired angular relationship. The support structure is insertable into the nasal cavities to position the filters within corresponding nasal cavities. Flexible rims maintain the support structure and the filters in spaced-apart relation to the surrounding nasal wall. The filters may be placed within the bases at an angle with respect to the walls of the bases. Also, the filtration device may be flesh tone in color, thereby blending with the skin tone of the user. In some embodiments, a post structure is supplied for supplying a scent or aroma to the wearer.

An apparatus for protecting a user in a hazardous or contaminated environment caused by chemical, fire, biological, and / or nuclear contamination includes a selfcontained breathing apparatus (SCBA) for providing tank stored breathable air, a powered air purifying respirator (PAPR) for purifying ambient air and a valve system that can be used to control the source of air from either the SCBA or the PAPR. The source of breathable air can be selectively controlled via manual or automatic controls while a protective body suit can be operably coupled with the SCBA and the PAPR to protect a user within the contaminated environment.

The invention features methods and apparatus for the treatment of asthma patients. A controlled supply of breathable air delivered to a patient interface or mask (4) is controlled for patient comfort to maintain a steady pressure level in a range 2 to 4 cm H2O to accommodate patient respiration. The breathable air is cleaned by a high efficiency particulate arresting filter (10) to remove allergens from the air supply. The apparatus may be programmed to automatically detect asthma-related symptoms such as an asthma attack by analyzing the respiratory flow of the patient. In response to the detection of such an attack, the apparatus may provide an audible warning or if configured with a treatment delivery module (14A, 14B), the device may administer a therapeutically effective dose of a drug or substance, for example, a broncho-dilator, to alleviate the patient's breathing difficulty. Preferred mask designs allow for proper CO2 washout to accommodate the low pressures supplied to the mask and prevent asphyxia.

A system and method for sleep monitoring, diagnosing and sensing temperature and pressure for a breathing cycle of a patient including a sensing device suitable for both nasal and oral breath monitoring for measuring respiratory air wave and airflow information during a sleep apnea diagnostic session and processing the acquired air wave and airflow breathing information for input to conventional polysomnography equipment.

Methods and apparatus for determining the occurrence of an apnea, patency and / or partial obstruction of the airway are disclosed. Respiratory air flow from a patient is measured to give an air flow signal. The determination of an apnea is performed by calculating the variance of the air flow signal over a moving time window and comparing the variance with a threshold value. One determination of partial obstruction of the airway is performed by detecting the inspiratory part of the air flow signal, scaling it to unity duration and area and calculating an index value of the amplitude of the scaled signal over a mid-portion. Alternatively, the index value is a measure of the flatness of the air flow signal over the mid-portion. One determination of patency of the airway is performed by applying an oscillatory pressure waveform of known frequency to a patient's airway, calculating the magnitude of the component of said air flow signal at the known frequency induced by the oscillatory pressure waveform and comparing the calculated magnitude with a threshold value. Alternatively, the air flow signal is analysed to detect the presence of a component due to cardiogenic activity.

Methods, systems and devices are presented that provide improved medical diagnostic and intervention procedures such as magnetic resonance imaging, cardiac imaging, cardiac nuclear scintigraphy, computed tomography, echocardiography, imaging to direct laser ablation, imaging to direct radio frequency radiation ablation, imaging to direct gamma knife radiation therapy, and imaging to direct radiation therapy by respiratory gating. In a preferred embodiment, one or more balloon pressure probes within a catheter are placed into the esophagus and detect pressure within the esophagus to infer respiratory air-flow. Other probes such as those based on fiber optics and other useful materials are described. Many of these devices interact poorly or not at all with magnetic and electromagnetic fields, and are particularly useful for use in respiratory gating of MRI.

A device is provided for increasing humidity for respirating patients, especially for a respiration humidifier or an anesthesia reflector. The device includes a gas channel for passing through breathing air, a control and / or regulating device, a temperature sensor and a dew sensor for measuring the humidity present in the breathing air by electromagnetic radiation with a generating device and with a detection device for electromagnetic radiation. The humidity of the breathing air is determined at a low cost and in a reliable manner and condensation is avoided in the respiration system without any additional effort for sterilization. Humidity in the breathing air is determined by the a dew sensor by the change in the reflection of the electromagnetic radiation as a function of dew formation at a condensation-fogged and condensation-free boundary surface between breathing air and a medium having an optical density higher than that of breathing air.

The present invention relates to a method for controlling the pressure supplied by a CPAP device. The method comprises repeated measurement of a respiratory air flow during operation of the device and determining at least one respiratory event from the measured time-dependent behavior of the respiratory flow, the respiratory event representing an indication that the pressure supplied by the CPAP device is too low. Furthermore, the method comprises a slow, quasi ramp-like lowering of the pressure supplied by the CPAP device as long as no respiratory event is detected. Furthermore, the invention relates to a CPAP device for carrying out such a method and to a storage medium with a corresponding program.

An integrated tele-health system / device for monitoring and reporting medical information for the evidence-based management of patients with chronic respiratory disease. The device includes a central unit which measures and collects information related to the state of health of the patient, and is provided with elements for wireless or cable transmission of the collected data using a microprocessor based system with a touch screen display, USB communication port and Bluetooth. The device further includes: a removable sensor for the measurement of respiratory air flow and volume, a removable pulse oximetry sensor and a motion sensor. Stored data can be then delivered through landline, broadband, wireless and cell-phone technology to be received by a web server and can then be accessed by medical staff. Being completely portable, the device is provided with a battery of known type, which can be substituted by the user or can be rechargeable.

A vehicle evacuation system for aiding the escape of a person trapped in a motor vehicle having a vehicle seat, a vehicle seat belt and vehicle windows, which has entered a body of water, includes a cutting tool for cutting through a vehicle seat belt; a glass breaking tool for breaking a glass vehicle window for escape; a combined compressed breathable air tank and mouthpiece; an inflatable buoy bag and compressed gas cartridge for lifting the person to the water surface; a distress and position indicating signal generating mechanism for sending an alarm signal to a receiving station, the alarm signal being trackable by a tracking device; and an element unification structure for holding elements of the system together in a readily accessible configuration prior to and during use.

Use of compressed air for indoor ambient temperature conditioning is disclosed. Thermal energy is imparted to or extracted from a quantity of compressed air, and the compressed air is then directed to be released inside a structure enclosing a space, whose ambient temperature needs to be controlled. Thus, the compressed air may be used as a direct heat conduction / extraction medium. A flow of external air is created over a heat exchanger mass (a “heating mass” or a “cooling mass”), so that thermal energy of the compressed air flowing inside the heat exchanger mass is transferred to the external flow of air flowing outside the heat exchanger mass. Thus, in addition to being a direct heat conduction / extraction medium, the compressed air is being used as a heat transfer medium, that ultimately gets mixed with the flow of external air. A fresh supply of external air may be used rather than using re-circulated air, in order to maintain a high quality of breathable air. A local feedback loop may be used to route back a portion of temperature-conditioned air produced by a system according to the present invention, to regulate a flow of external air over a heat exchanger mass. Other types of environmentally benign compressible fluids may be used as a heat transport / transfer fluid instead of compressed air.

A system and method for monitoring resuscitation and respiratory mechanics of a patient is provided. A pressure sensor detects air pressure within an air-flow path of a resuscitator and generates a first detection signal in response thereto. A flow-rate sensor detects the flow-rate within the air-flow path and generates a second detection signal In response thereto. A processor receives and processes the first and second detection signals using an algorithm to identify a ventilation rate, a lung pressure, and an air volume corresponding to the respiratory air. A report is generated of real-time feedback about respiration of the patient that includes the ventilation rate, lung pressure, and air volume.

A system and method for sleep monitoring, diagnosing and sensing temperature and pressure for a breathing cycle of a patient including a sensing device suitable for both nasal and oral breath monitoring for measuring respiratory air wave and airflow information during a sleep apnea diagnostic session and processing the acquired air wave and airflow breathing information for input to conventional polysomnography equipment.

A nasal air filtration device includes a pair of either planar or concave-convex filters, a support structure incorporating a pair of generally annular bases or sleeves for supporting the filters, and a bridge that couples the bases or sleeves to maintain them in a desired spaced-apart relation and to determine a desired angular relationship. The support structure is insertable into the nasal cavities to position the filters within corresponding nasal cavities. Flexible rims maintain the support structure and the filters in spaced-apart relation to the surrounding nasal wall. The rims conform to surrounding nasal tissue to form seals. The rims can be selectively inclined to facilitate insertion and resist accidental removal. In certain embodiments the device is combined with a filter that covers the mouth to provide an air filtration system.

The present invention relates to a device for conditioning breathing air comprising a housing (1) provided with an inlet (5) for non treated breathing air and an outlet (6) for the treated breathing air, wherein said housing (1) comprises passive humidifying means (7) and active humidifying means wherein said active humidifying means comprises a water supply inlet (13), a heating device for the supplied water, a membrane (12) having substantial water impermeable and water vapor permeable characteristics, and a heat exchange element (14), characterized by the fact that said membrane (12) is divided into a hydrophilic membrane (12a) and a water vapor permeable and water impermeable membrane (12b), and that said heat exchange element is selected from the group comprising perforated metal plate (14) and / or a heating resistance. The invention further relates to a method for the conditioning of breathing air, comprising the steps of supplying through the inlet opening non treated breathing air, passively humidifying said supplied air through the passive humidifying means, and actively humidifying said breathing air, through the active humidifying means of a device.

A combined air-supplying / air-purifying breathing system that includes a self-contained breathing apparatus, a facepiece for delivering breathable air from the self-contained breathing apparatus to a user, and a powered air-purifying respirator having at least one filter and a blower and having an output connected by a hose assembly to the facepiece. A control interface operationally connects the self-contained breathing apparatus to the powered air-purifying respirator. The self-contained breathing apparatus includes a pressure vessel, a cylinder valve assembly and a pressure reducer, all carried by a back frame, and the powered air-purifying respirator is adapted to be mounted on, and carried by, the back frame, by coupling the back frame and the respirator together at respective attachment points.

A device for capturing and concentrating volatile organic compounds (VOCs) in a sample of breath air. The device includes an intake for accepting an air sample; a disposable mouth piece; a sensor array for measuring physical parameters of the air sample; an exhaled air sampler for capturing a pre-determined volume of air; a concentrator for concentrating VOCs in the air sample; and an ionic liquid collector, the latter of which may be removed from the device. The ionic liquid collector, which may have one compartment or multiple compartments, includes at least one ionic liquid. Analysis of VOCs in the ionic liquid or liquids may identify biomarkers that can provide a medical diagnosis for a human patient based on a sample of breath air.

A device for removing airborne contaminants and inhaled biopathogens, particularly particulate or aerosol contaminants, from respired air that can be either stationary or incorporated into a garment or accessory worn upon the body. In a preferred embodiment, a negative electrode is connected to voltage multiplier and modulation circuit and then to a discharge electrode having an electron emissive surface disposed near the wearer's airway. The positive (counter) electrode is similarly disposed away from the airway such as, for example, near the forehead. Electrons, ejected from the electron emissive surface, transfer a negative charge to airborne particulate contaminants which are accelerated toward, and collected by, the counter electrode.

A device is provided for increasing humidity for respirating patients, especially for a respiration humidifier or an anesthesia reflector. The device includes a gas channel for passing through breathing air, a control and / or regulating device, a temperature sensor and a dew sensor for measuring the humidity present in the breathing air by electromagnetic radiation with a generating device and with a detection device for electromagnetic radiation. The humidity of the breathing air is determined at a low cost and in a reliable manner and condensation is avoided in the respiration system without any additional effort for sterilization. Humidity in the breathing air is determined by the a dew sensor by the change in the reflection of the electromagnetic radiation as a function of dew formation at a condensation-fogged and condensation-free boundary surface between breathing air and a medium having an optical density higher than that of breathing air.