Abstract: A nasal cannula having a face piece including first and second nares which each communicate with a respective nostril of a patient. A septum divides the face piece into first and second flow paths such that the first flow path communicates with the first nare and the second flow path communicates with the second nare. A leading end of the first nare is configured to form a fluid barrier within a first nostril and facilitate only supplying an insufflation gas, via the first flow path, to the patient and prevent exhausting any exhaust gas, of the patient, through the first nostril. A leading end of the second nare is configured to facilitate collecting some of the exhaust gas, from the patient, via the second flow path as well as exhausting a remainder of the exhaust gas out through a second nostril of the patient.

Abstract: A divided cannula comprising a cannula body which is divided by a partitioning wall into first and second flow chambers. The first flow chamber has first and second spaced apart nare passages while the second flow chamber has first and second spaced apart nare passages. The cannula body supports spaced apart first and second nares and each of the first and the second nares defines a common nare passage. The first nare passage of the first internal flow chamber and the first nare passage of the second internal flow chamber both communicate with the common nare passage of the first nare and the second nare passage of the first internal flow chamber and the second nare passage of the second internal flow chamber both communicate with the common nare passage of the second nare. A pressure sensing line and a gas supply line interconnected to the divided cannula with a gas supply system.

Abstract: 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.

Abstract: A nasal cannula for supplying a respiratory gas to a patient and a method of treating a patient with sleep disorder. The nasal cannula comprises a pair of spaced apart supply lines which each have a head at one end thereof with a discharge opening located therein. The opposite end of each supply line is connectable to a high flow respiratory gas source. Each head is sized to be snugly received and retained within one of the nasal cavities of the patient while forming a sufficient leakage passage, between a portion of inwardly facing nasal cavity skin of a patient and a portion of an exterior surface of the head, to facilitate exhausting of any excess respiratory gas supplied to the patient through the leakage passage and also facilitate inhalation of any room air required in excess of the respiratory gas to be supplied to the patient.

Abstract: A nasal cannula, for supplying a respiratory gas to a patient, comprising: a pair of spaced apart supply lines which each have a head at one end thereof with a discharge opening therein. The opposite end of each supply line is connectable to a respiratory gas source. Each head is sized to be snugly received and retained within one of the nasal cavities of the patient while forming a sufficient leakage passage, between a portion of inwardly facing nasal cavity skin of a patient and a portion of an exterior surface of the head, to facilitate exhausting of any excess respiratory gas supplied to the patient through the leakage passage and also facilitate inhalation of any room air required in excess of the respiratory gas to be supplied to the patient.

Abstract: A method of forming a cannula from a cannula mandrel assembly comprising a pair of mouthpiece/nasal mandrels and a mating facepiece mandrel. The facepiece mandrel has a pair of conical holes, in an intermediate section thereof, for receiving a leading end of one mouthpiece/nasal mandrel. The conical holes allow the facepiece mandrel to slide along the mouthpiece/nasal mandrels until the conical holes abut with respective mating tapering conical sections and prevent further sliding movement along the mouthpiece/nasal mandrels. Following assembly, the assembly is heated, at least one coating of a polymeric material is applied thereto and heat from the assembly at least partially cures the polymeric material on the assembly. Following curing, the facepiece mandrel and formed cannula are slide along the mouthpiece/nasal mandrels until the facepiece mandrel and formed cannula are removed therefrom. Lastly, the facepiece mandrel is removed from the formed cannula.

Abstract: A nasal cannula comprising a hollow main body having opposed first and second openings formed therein and the main body defining an internal chamber. A partition divides the internal chamber into first and second flow compartments. A flow passageway of a first nasal prong communicates with the first compartment and a flow passageway of the first mouth piece communicates with the first compartment to define a first flow passageway which communicates with both a first nostril and a mouth of the patient. A flow passageway of a second nasal prong communicates with the second compartment and a flow passageway of the second mouth piece communicates with the first compartment to define a second flow passageway which communicates with both a second nostril and the mouth of the patient.

Abstract: A cannula having at least three separate flow passages and comprising separate nasal and mouth main bodies. The nasal body has first and second nares and first and second main flow chambers respectively communicating with first and second ports, and the first and second flow chambers are separated from one another by a septum. The mouth main body is adjacent the nasal main body and has at least one mouthpiece and at least a third main flow chamber therein communicating with a third port. The cannula has at least first, second and third flow paths which can be connected with a desired supply, monitoring or detection device. The invention also relates to the method of manufacturing the cannula.

Abstract: A method of monitoring breathing of a patient with a nasal cannula. The method comprising the steps of forming the nasal cannula with at least one nare, and at least one nare having a primary inlet/outlet opening formed in a remote end thereof. Coupling the nasal cannula to a detection device for monitoring breathing characteristics of the patient while the patient is sleeping. Detecting breathing characteristics of the patient, while the patient is sleeping, via at least the primary inlet/outlet opening of the nare and sending the detected breathing characteristics of the patient to detection device for evaluation.

Abstract: A method of forming a cannula from a cannula mandrel assembly comprising a pair of mouthpiece/nasal mandrels and a mating facepiece mandrel. The facepiece mandrel has a pair of conical holes, in an intermediate section thereof, for receiving a leading end of one mouthpiece/nasal mandrel. The conical holes allow the facepiece mandrel to slide along the mouthpiece/nasal mandrels until the conical holes abut with respective mating tapering conical sections and prevent further sliding movement along the mouthpiece/nasal mandrels. Following assembly, the assembly is heated, at least one coating of a polymeric material is applied thereto and heat from the assembly at least partially cures the polymeric material on the assembly. Following curing, the facepiece mandrel and formed cannula are slide along the mouthpiece/nasal mandrels until the facepiece mandrel and formed cannula are removed therefrom. Lastly, the facepiece mandrel is removed from the formed cannula.

Abstract: A pressure sensing device for coupling to a cannula and receiving respiratory breathing information from a patient to be monitored. The pressure sensing device comprising an exterior housing accommodating a snore detection circuit which processes information and outputs a signal indicative; an airflow detection circuit which processes information and outputs a signal indicative thereof; and an internal test circuit for testing an integrity of the airflow and snore detection circuits prior to use of the pressure sensing device to ensure that both circuits are operational. An input port for pressure sensing device extends from the housing of the pressure sensing device so as to space a connector, for the cannula, a sufficient distance away from the bottom surface whereby the bottom surface will always remain flush with and in constant and continuous intimate contact with a support surface for the pressure sensing device.

Abstract: A cannula and method of forming a cannula by forming a cannula mandrel assembly having a nare mandrel, a main body mandrel and mouthpiece mandrel; heating the cannula mandrel assembly, applying a polymeric material to the cannula mandrel assembly to provide a desired material thickness on the mandrel assembly to form the cannula, curing the polymeric material of the formed cannula and extracting the mandrel assembly from the cannula by disassembly and removal of the mandrel assembly parts.

Abstract: A cannula comprising a main body which defines an internal chamber therein. A first and second nasal prongs, respectively, communicate with the internal chamber to define first and second nasal prong passages. A mouthpiece has a gas passageway and a retainer passageway and a first end of the gas passageway communicates with the internal chamber while a second free end of the mouthpiece has a gas opening therein. A shape retaining member is received within the retainer passageway to facilitate retaining an adjusted position of an opening of the gas passageway with respect to a remainder of the cannula. A method of forming the cannula is also disclosed.

Abstract: A spacer assembly for a ventilator or other respiratory equipment for dispensing aerosol drugs from metered dose inhaler (MDI) canisters or nebulized drugs from a nebulizer into a respiratory gas stream delivered from a ventilator or other respiratory equipment connected to a patient. The improvements involve optimizing the shape of the spacer assembly body member and providing an efficient MDI nozzle assembly to allow maximal evaporation of the propellant before the propellant droplets impact the walls of the body member while providing a compact volume for directing the output of an MDI canister or a nebulizer into the gas stream.

Abstract: This invention is a device (10) for inspiration of a mist from a nebulizer, having an inlet connector (12, 32) adapted to engage an outlet port of a nebulizer, a hollow mouthpiece element (126 34) for insertion into a patient's mouth; a conduit (14) forming a fluid connection between the inlet connector, and the hollow mouthpiece element. An exhaust valve (26) is provided for removing expiratory gases which are exhaled into the mouthpiece element to the ambient atmosphere via an exhaust/positive expiratory pressure (PEP) valve (26, 50). The PEP valve is positioned on the conduit between the inlet connector, and the mouthpiece element; and a filter housing (44) containing a filter (60) for filtering the exhaled gases passing from the exhaust/PEP valve.

Abstract: A method of forming a cannula by forming a cannula mandrel assembly having a nare mandrel, a main body mandrel and mouthpiece mandrel; heating the cannula mandrel assembly, applying a polymeric material to the cannula mandrel assembly to provide a desired material thickness on the mandrel assembly to form the cannula, curing the polymeric material of the formed cannula and extracting the mandrel assembly from the cannula by disassembly and removal of the mandrel assembly parts.

Abstract: A bubble humidifier for adding humidity to supplied oxygen. The bubble humidifier has a humidifier base, for containing a quantity of liquid, and a cover for the humidifier base. The bubble humidifier has an oxygen inlet for supplying oxygen to the bubble humidifier and an moisturized oxygen outlet for connection to a moisturized oxygen supply conduit for supplying humidified oxygen to a patient, and the oxygen inlet being connected to a diffuser for diffusing the supplying oxygen within the bubble humidifier. The bubble humidifier has a pressure relief device for relieving excess pressure generated within the bubble humidifier during operation thereof. The bubble humidifier defining a longitudinal axis and the diffuser is arranged to discharge the oxygen from the diffuser substantially at an angle normal to the longitudinal axis of the bubble humidifier to minimize flow of liquid, contained within the humidifier base, from entering the moisturized oxygen outlet during operation of the bubble humidifier.

Abstract: A nasal cannula for insufflating a patient with oxygen through one nare of the cannula and separately analyzing the exhaled gases from the patient by drawing the sampling of the exhaled gas from the other nare of the cannula into a conventional carbon dioxide analyzer. A further addition of holes or vents in the nares of the cannula are provided on both the interior and posterior of one or both nares in order to substantially reduce or eliminate the incidence of occlusion of the tip of the carbon dioxide sampling nare.

Abstract: A laryngoscope device for use in the performance of direct laryngoscopy, the device including a laryngoscope blade portion connectable to a laryngoscope handle through a connector, the laryngoscope blade comprising an ultraviolet light, a white light and an imaging or viewing device at the same distance relative to the distal end of the laryngoscope blade.