87 results about "Nasal intubation" patented technology

The present invention is a headgear for noninvasive ventilation interface made up of a nasal cannula including cannula tubing having a given outside diameter, and a headgear yoke with ends including tubing retainers. The yoke is adapted to extend transversely over a wearer's head. The tubing retainers are C-shaped projections having a given length and an inside diameter substantially equal to the tubing outside diameter. The present invention further includes a retainer mating element for each of the C-shaped tubing retainers to prevent the tubing from kinking near the C-shaped tubing retainers. The retainer mating element has an elbow section with an open side and a clip section connected to the elbow section by a rigid beam having a length substantially equal to the C-shaped tubing retainer given length, wherein both of the sections have an inside diameter substantially equal to the tubing given outside diameter.

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 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 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. The invention also relates to a respiratory therapy system incorporating the nasal cannula, a method of treating a patient with sleep disorder by using the nasal cannula, a diagnostic tool for measuring nasal cavity pressure of a patient, and a method of using the diagnostic tool for measuring nasal cavity pressure of a patient.

A system controls and manages administration of a therapeutic gas, such as NO, O2, or the like, to a spontaneously breathing, non-ventilated patient such that concentrated NO is as low as reasonably possible while delivering the desired amount of NO to the distal portions of the lungs. The system includes an entrainment cell that provides remote, turbulent mixing with low temporal latency and can be used with a nasal cannula or a mask. The entrainment cell uses room air to dilute the therapeutic gas; however, supplementary gases can also be used. A baffle can be included to promote mixing and a flow sensor can also be used if desired. Multiple ports can be included in the entrainment cell. An equalizing valve is also disclosed.

A system for sensing respiratory pressure includes a portable pressure transducer configured to be carried by or proximate to a respiratory conduit, such as a breathing circuit or a nasal canula. The portable pressure transducer may removably couple with a pneumotach, in the form of an airway adapter, disposed along the respiratory conduit. The pneumotach may include two pressure ports positioned at opposite sides of an obstruction, which partially blocks flow through a primary conduit of the pneumotach. Corresponding sample conduits of the portable pressure transducer removably couple with the pressure ports. The pressure ports may have sealing elements which are configured to seal against piercing members of the sample conduits upon introduction of the piercing members therethrough. Upon removal of the piercing members, the sealing elements substantially reseal. Methods for using the system are also disclosed.

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.

A patient interface device includes a mask having a shell defining a chamber. A component, such as a nasal cannula coupled to a sensor, is structured to be selectively positioned within the chamber. A manipulation mechanism for selectively manipulating the position of the component within the chamber from an exterior of the mask when the mask is placed against the patient's face. The manipulation mechanism may include an attachment element, such as a magnet, attached to the component and structured to be selectively positioned on the interior surface of the shell, and a manipulation element, such as a magnet, structured to be selectively positioned on the exterior surface of the shell and coupled to the attachment element through the shell, wherein movement of the manipulation element causes movement of the attachment element and the component.

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 resilient nasal intubation tube supporter is provided having an adhesive coated base and a nasal intubation tube groove having an adhesive layer separated by a resilient foam body for anchoring a sinusoidal shaped nasal intubation tube in place for surgical procedures. The invention includes provision for length and height adjustment of the novel intubation tube holder. The novel intubation tube holder provides a cushioned pliantly resilient support for nasal intubation tubes and provides support for conduits and hoses that need to be attached during surgical procedures.

A nasal cannula diffuses a gas stream to distribute the volume of the gas stream as it is delivered into a user's nostril. The nasal cannula can direct flow of gas, such as oxygen, away from the more sensitive nasal tissues. The nasal cannula can diffuse the gas flow out of a plurality of orifices formed in the nostril prongs of the nasal cannula device, rather than sending the entire volume of gas out of a single orifice, as is the case with conventional nasal cannula devices.

The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

The invention concerns a breathing assistance apparatus having a source of Nitric Oxide in fluid communication with a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

The invention concerns a combination control for use in nasal cannula therapy, and includes a high flow, nasal cannula respiratory assistance ducted system, and a pressure relief valve having indicator structure, which typically includes a tubular body, a carrier slidable in the body, a plunger-indicator carried by the carrier, and a spring resisting carrier movement toward a cap on the body that defines an indicator window.

Nasal cannula assemblies for providing respiratory therapy to patients are provided. A nasal cannula assembly can include a cannula, an optional manifold which may be removable, a gas supply tube, and a securement mechanism. Securement mechanisms can include headgear straps, cheek pads, or an adhesive nose strip. A nasal cannula assembly can also include a lanyard, lanyard clip, and / or lanyard connector to help support the weight of a main gas delivery conduit.

The disclosure relates to a nasal cannula comprising a port configured for delivery of a medicament into a flow of a fluid being delivered by the nasal cannula to a user and / or configured for interfacing with a medicament delivery device or an instrument. The disclosure also relates to a nasal cannula comprising an asymmetric profile to reduce an amount of occlusion of one nare of a user to provide access for an instrument to the nare with the nasal cannula in use.

Apparatus to permit a delivery of a flow of breathable gas to a patient's airways. In one version, a coupler extension may include a seat portion to permit use of a mask with a nasal cannula. In some versions, the coupler extension is configured to conduct the flow of gas to prongs of a nasal cannula. The seat portion can receive and seal with a cushion of a respiratory mask and may have a sealing bevel to promote sealing between the cushion of the respiratory mask and a facial contact surface of a user. In some versions, a conduit adapted to communicate a flow of gas may comprise a slit valve formed by a portion of the wall material of the conduit. In some versions, a nasal interface may include naris pillows to seal with and conduct a flow of breathable gas into a nares of a user. Each naris pillow may include a nasal projection to conduct a further flow of gas. The nasal projection may extend within the naris beyond the seal of the naris pillow.

The invention concerns a breathing assistance apparatus having a source of Nitric Oxide in fluid communication with a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

An oxygen vending machine receives payment from a user. The payment is validated for appropriateness and sufficiency. If a valid payment is made, then concentrated oxygen is provided to a nipple or coupling located in an accessible place. In addition, a packaged breathing device, such as a nasal cannula, is dispensed. The user retrieves the packaged nasal device and uses it to direct the concentrated oxygen from the nipple into the user's nose or mouth. The user may select the particular breathing device which is to be dispensed. The flow of concentrated oxygen to the nipple is ceased after a predetermined period of time has passed.

The invention discloses an automatic high-frequency ultrasonic atomization medicine leading-in device for the whole respiratory tract. The automatic high-frequency ultrasonic atomization medicine leading-in device comprises a base, wherein the base is provided with an automatic controller, an adjusting bracket, an automatic alarm and a display screen, the automatic controller is provided with a signal base station and a control button, a lifting guide apparatus is arranged on the adjusting bracket, the adjusting bracket is connected with a medicine leading-in apparatus, a patient interface device, a medicine atomizing device, a connector and a pressure regulator are arranged on the medicine leading-in apparatus, the patient interface device is connected with the respiratory system of a patient, the patient interface device is provided with a nasal intubation tube and a face mask, and the medicine atomizing device is composed of a storage cavity, a medicine box and a vibration type microporous atomizer. The leading-in device provided by the invention is convenient to use and high in medicine leading-in efficiency, thus having very good popularization and use values.

The invention concerns a combination control for use in nasal cannula therapy, and includes a high flow, nasal cannula respiratory assistance ducted system.

The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

The present invention is a nasal oxygen supply cannula and head support structure, having a tube with a proximal end connected to an oxygen supply and a distal end connected to a nosepiece having a one or more intra-nasal oxygen delivery output ports, a head support on the head of a patient, and a mechanism for securing the cannula to the cap.

An acoustic sensor platform based method and apparatus provides for improved pain mitigation, apnea detection, aspiration detection and patient communication in anesthesia patients. The platform includes an acoustic sensor configured to be coupled to one of a nasal cannula or face mask of the anesthesia patient; a processer coupled to the acoustic sensor and configured to i) Detect patient speech and isolate and amplify the patient speech, and ii) Detect at least one of a breathing rate of the patient or aspiration of the patient; and an audio visual display coupled to the processor and providing an audio and / or visual display of the isolated and amplified speech of the patient, and displaying results for at least one of a breathing rate of the patient or aspiration of the patient.

The invention discloses an intermittent peroral and transnasal intubation tube feeding fixator. The intermittent peroral and transnasal intubation tube feeding fixator comprises a stomach tube fixingplate and an elastic band, wherein a stomach tube inserting opening with the inner diameter larger than the outer diameter of a stomach tube is formed in the middle of the stomach tube fixing plate, and a stomach tube clamping piece A right opposite to the stomach tube inserting opening is upwards arranged on the lower middle portion of the front end face of the stomach tube fixing plate; and a stomach tube clamping piece B over against the stomach tube clamping piece A is arranged at the middle upper part of the front end surface of the stomach tube fixing plate. The intermittent peroral andtransnasal intubation tube feeding fixator has the effects that the intermittent peroral and transnasal intubation tube feeding fixator is not prone to shaking, rotating or falling off after being fixed to the head of a patient, the outer end of the stomach tube for tube feeding diet extending into the mouth of the patient can be clamped through the stomach tube clamping piece A, the outer end ofthe stomach tube for tube feeding diet extending into the nose of the patient can be clamped through the stomach tube clamping piece B, the outer ends of the stomach tubes for tube feeding diet are good in fixity and not prone to displacement, and the situation that outward moving is prone to generating to cause tube falling off is avoided; and the elastic band replaces a traditional string, the facial skin of the patient cannot be tightened, the patient is not prone to discomfort, the use comfort is good, and then the device is high in practicability and good in use effect.