Abstract: Method and apparatus for an aerosol chamber having an input opening and an output opening with back pressure created in the chamber by an apertured barrier, such as a disk having a plurality of concentric and circumferentially disposed sets of openings to reduce the size of particles applied at the input opening before leaving the output opening, which is of lesser diameter than the input opening and extends to the input opening by an arcuate surface of revolution that serves to redirect interiorally of the chamber aerosol particles that have entered the chamber and reached the surface of revolution.

Abstract: This invention relates to a device for placement of an endotracheal tube, comprising a commonly used flexible fiberoptic Laryngoscope/Bronchoscope (FFLB), an anesthesia mask with a pluggable port, along with two hollow intubating stylettes, one short and one long, and a hook for retrieval of silk thread used in the intubating process with the shorter stylette. The anesthesia mask possesses a sealable port, with a distensible perforated membrane. The port is located over the mouth region of the mask, inferior to the gas circuit connecting inlet. The introducer/stylettes comprise a semi-rigid platic tubes. The shorter stylette/introducer has special thread holes, allowing the stylette to be secured with thread. The introducer allows an endotracheal tube to be slipped over it and into the patient's airway. The hook allows the rapid threading and advancing of the endotracheal tube over the shorter introducer/stylette.

Abstract: A system for dispensing a clinically effective dose of an inhalable, pharmaceutically active compound, which system includes a dry powder inhaler device containing a powder containing the pharmaceutically active compound, wherein (a) of the powder particles dispensed by the inhaler device (the “metered DPI dose”), at least 40% are less than about 10 microns in diameter at the point the particles exit the inhaler, (b) the metered DPI dose is sufficient to produce a clinically effective result in a patient; and (c) the amount of the compound in the metered DPI dose is not more than 70% of the minimal amount of the compound which, when dispensed in a pressurized metered dose inhaler, produces an equivalent clinically effective result in the same patient.

Abstract: A respiratory device is disclosed that optimizes delivery of oxygen and detection of carbon dioxide to a user through the use of a flexible lever arm and mouthpiece which may be adjusted to deliver the oxygen toward the user's oral and nasal cavities, and detect carbon dioxide, exhaled by the user, from a separate orifice of the mouthpiece. The lever is supported by a rotatable adapter attached to a head mounted brace. The adapter can rotate through 180° for placement of the lever on either side of the user's head. The adapter is hinged to eliminate occluding and kinking during rotation. A hose having tubular members therein delivers the gases to and from the user. The hose traverses through the lever arm and adapter, terminating at the lever arm into the mouthpiece. The mouthpiece has a plurality of ports for fluid flow. The hose terminates at the other end in gas detection and delivery equipment. The hose may be segmented or one continuous piece.

Abstract: An emergency breathing device including a hood having use and storage configurations, which when compactly wrapped proximate to an oxygen control device for storage is recoverable for use. In use configuration, the hood is capable of being worn upon a user's head, which substantially surrounds the user's head. Hood surface beneath the user's head includes an opening lined with elastic material, which forms a seal about the user's neck at the opening when the hood is donned. An oxygen control device connected to a hood includes a valve body, an actuator, and an oxygen bottle. The valve body provides airflow communication with the interior of the hood, and the oxygen control device is connected to a plumbed breathable oxygen supply through a plumbed source disconnect means removably connected to the valve body. When connected, the oxygen control device permits airflow from the plumbed breathable oxygen supply and valve body to the interior of the hood.

Abstract: A product dispensing system comprises a calibrated nebulizer having a nebulizer jet, mouthpiece, means for sourcing compressed air, a manifold for distributing the source of compressed air in at least one direction, a nebulizer accommodation means which is accessed by port, and a valve means for controlling the manifold and thereby the flow of compressed air to the port. The manifold and the port are linked by a length of tube, wherein the internal volume of the tube from the manifold outlet to the nebulizer jet is less than 0.7 ml.

Abstract: 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.

Abstract: Apparatus and methods for the estimation of flow and the detection of breathing (respiration) in continuous positive airway pressure (CPAP) treatment are disclosed. CPAP apparatus typically includes a flow generator for supplying air to a mask via a gas delivery tube. With changing air flow, the flow generator's speed and/or driving electrical current will alter in a manner defined by the controlling circuitry. Signals can be derived from measurements of motor speed and current, and these signals vary cyclically with patient respiration. By filtering to reject non-respiratory components, the resultant signal can be utilized to determine the instants in time at which the patient starts to inhale and exhale. The filtered signal also can be linearized using a predetermined knowledge of the pressure/flow/speed characteristics of the flow generator, and thus to derive a volumetric measure of airflow.

Abstract: An inhaler for use by an individual to inhale a particulate medicament from a reservoir comprises a chamber having a first end connectable to the reservoir to be in air flow communication therewith, a second end for delivering the medicament to the individual upon inhalation and a conduit defining an air flow path extending between the first end and the second end; and, an orifice in the chamber between the first end and the second end, the orifice utilizing the Coanda Effect when the reservoir is in air flow communication with the chamber and upon inhalation by the individual to draw medicament from the reservoir into the air flow path.

Abstract: An improved respiratory suction apparatus catheter includes a manifold for attachment to the distal hub of an endotracheal tube to form a ventilation circuit, a catheter tube which is displaceable through the manifold and into the endotracheal tube to suction secretions from the tube and lungs, and a valve mechanism disposed adjacent the ventilation circuit to minimize the draw of air from the ventilation circuit of a patient while the catheter is being cleaned. In a preferred embodiment of the invention, the catheter is cleaned more thoroughly than in the prior art while simultaneously drawing little or no air from the patient's ventilation circuit.

Abstract: The present invention relates to a wearable aerosol delivery apparatus for releasing an aerosol with an active ingredient into an oral or nasal passage of a user. The apparatus comprises a housing comprising a first and a second surface, the first surface being adapted to be disposed against a wrist of the user, the housing defining a reservoir for containing the aerosol under pressure, an aerosol release mechanism connected with the reservoir for releasing a dose of the aerosol from the reservoir when actuated, and a fastener member attached to the housing to fasten the housing onto the user's wrist, whereby the apparatus is worn by the user and effective for delivering the active ingredient into the user's passage on demand.

Abstract: A nebulizer and method for forming a finely atomized aerosol are provided. A first aerosol is formed by passing a gas jet across the mouth of a liquid channel that communicates with a liquid reservoir. The first aerosol then strikes a stop surface and is converted into a second, more finely atomized aerosol. The second aerosol impacts a buffer plate. The larger liquid particles in the second aerosol strike the plate and are either broken up or returned to the liquid reservoir. The smaller particles follow a labyrinthine path through at least one slit-shaped passage in the buffer plate, in the process forming a third, final aerosol. Selection of the passage size allows control of the particle size distribution of the third, final aerosol.

Abstract: An improved compressor system (10) designed for use with a patient assist medical ventilator is provided which includes a compressor (12) and a pressurized gas delivery conduit (14); a hollow fiber membrane dryer (16) is interposed within the conduit (14) for final dehumidification of the pressurized gas and suppression of the dew point thereof In preferred forms, the membrane dryer output air may be recycled via a conduit (50) to the compressor (12) during phases of the system operation, so that such dried, pressurized air may be mixed with ambient air and fed to the compressor (12).

Abstract: A method and system for rapid control of set inspired gas concentration is disclosed for operating a medical anesthesia delivery system and for controlling the flow and concentration of gases and anesthesia vapor delivered to a patient. Control of the inspired gas and agent concentration is accomplished by operating in different control priority modes. In a flow priority control mode, the user may set, either directly or indirectly, the total fresh gas flow rate. The total fresh gas flow rate can then be slowly be varied by the control algorithm, while the vaporizer concentration is actively controlled to achieve the user set inspired gas concentration. The invention includes a process for switching from the flow priority control mode into a concentration priority mode for low flow rates. By throttling the flow, the patient will receive nearly an instantaneous change in the amount of agent and fresh gas without having the transport delay associated with a change in the agent concentration.

Abstract: A detector for determining the volume and volumetric changes of respiratory gases in a closed circuit anaesthesia circuit having a bellows ventilator. The device includes a first sensor positioned with respect to the bellows for detecting and indicating when the bellows assumes a given expanded position in a bellows housing indicative of the given volume of respiratory gas in the circuit. A second sensor detects and indicates when the bellows assumes an expanded position indicative of the greater amount of expansion than that corresponding to the given expanded position. During respiratory cycles of the patient, indications from the first sensor in the absence of indications from the second sensor indicates that the volume of gas in the closed circuit anaesthesia circuit is not changing, but is remaining at that corresponding to the given expanded position of the bellows.

Abstract: The present invention provides a small-size, small-weight, low-cost artificial respiration apparatus which can easily be used in an ordinary hospital. The artificial respiration apparatus 10 includes: a positive blower 12p for generating a positive air pressure Ap; a negative blower 12n for generating a negative air pressure An; a rotary valve mechanism 54 for alternately selecting the positive pressure Ap generated by the positive blower 12p and the negative pressure An generated by the negative blower 12n and converting them into an oscillating air pressure Apn; and a diaphragm block 56 urged by the oscillating air pressure Apn from the rotary valve mechanism 54 to operate to supply air to a patient P. Use of the positive blower 12p and the negative blower 12n significantly reduces the load, enabling to use ones available on market, i.e., small-size, small-weight, low-consumption blowers.

Abstract: A combination face mask and dental device for improved breathing during sleeping is provided in which a face mask (10) is connected through an air tube (14) to a gas supply system (16). The face mask (10) is connected through a connector (20) to a dental device (18).

Abstract: An inhalation-activated inhalator having a primary inhalation passage and a secondary inhalation passage disposed in communication with the primary inhalation passage and a source of medicament. The primary inhalation passage has airflow inhibiting mechanism connected to a blocking plate positioned to selectively block fluid flow in the secondary inhalation passage. As the user's inhalation reaches a defined rate, the flow inhibiting mechanism restricts flow through the primary inhalation passage and moves the blocking plate to enable airflow through the secondary passage. Thus, as the user achieves a desired inhalation rate, the medicament is provided through the secondary inhalation passage, thereby optimizing the delivery of medicament to the lungs.

Abstract: A hydrophobic electrostatic breathing filter is fabricated by applying a thin layer of adhesive to the pinch ring of a patient side filter housing portion. A hydrophobic membrane is positioned over the adhesively coated pinch ring to effect a hermetic seal between the pinch ring and membrane using the adhesive interface. Electrostatic filter media and scrim are positioned adjacent the pinch ring of a machine side filter housing portion, and the patient and machine side portions of the housing are then welded together to hold the electrostatic filter media/scrim in place adjacent the hermetically sealed hydrophobic membrane by a mechanical clamping force exerted by the pinch rings. The resultant filter includes a hydrophobic membrane which is hermetically sealed across the patient side of the filter housing, and an electrostatic filter media/scrim element which is independent of the hydrophobic membrane and which is mechanically held in place adjacent the hydrophobic membrane.

Abstract: The invention is a special modified scuba diving apparatus intended for use by an animal, and more specifically the famous diving dog “Shadow.” The invention includes a helmet, a harness for supporting the helmet and a source of breathable gas, a special regulator providing a supply of breathable gas to the interior of the helmet, an exhaust for withdrawing exhaled air and residue water from the helmet without depressurizing the helmet, and a system of weights to compensate for the buoyancy of the user, and to counteract a net moment created about the center of buoyancy. The breathing system includes a muffler. An intercom system for providing voice instructions to Shadow can also be included.