2257 results about "Nasal cavity" patented technology

A mask system for use between a patient and a device to deliver a breathable gas to the patient includes a mouth cushion, a pair of nasal prongs, an elbow, and a headgear assembly. The mouth cushion is structured to sealingly engage around an exterior of a patient's mouth in use, and the pair of nasal prongs are structured to sealingly communicate with nasal passages of a patient's nose in use. The elbow delivers breathable gas to the patient. The headgear assembly maintains the mouth cushion and the nasal prongs in a desired position on the patient's face. The headgear assembly provides a substantially round crown strap that cups the parietal bone and occipital bone of the patient's head in use.

A nasal ventilation interface and method for providing nasal ventilation to a patient includes a hybrid face mask, covering only the mouth, coupled with removable nasal inserts extending from the upper surface of the mask. The nasal interface has modular, removable, and disposable nasal pillows connecting the upper surface of the mouth-portion of the mask to the user's nares. Each part of the hybrid mask is modular and can be formed in various shapes and sizes. The ventilation interface has differing gas line entry ports and can be shallow with a relatively deep soft facial interface or deep with a relatively shallow facial interface. In either case, the upper surface receives the nasal interface. The upper surface can have a removable ceiling in which is defined a nasal interface connector. The nasal interface can be integral with a removable ceiling. The entire hybrid mask can be made in one piece.

The present invention relates to pharmaceutical compositions for delivery of drugs intended to reside in the nose, compositions for nasal administration of drugs, e.g., antiviral agents, and particularly antiviral agents comprising the human major rhinovirus receptor, also known as intercellular adhesion molecule-1 (ICAM-1); to methods of making said nasal drug compositions, and to an improved process for the removal of residual solvent from pharmaceutical matrices.

A nasal assembly for delivering breathable gas to a patient includes a frame having an integrally formed first connector portion. A nozzle assembly includes a gusset or base portion and a pair of nozzles. At least one inlet conduit is structured to deliver breathable gas into the frame and nozzle assembly for breathing by the patient. A pair of second connector portions are removably and rotatably connected to respective first connector portions of the frame and are in communication with respective inlet conduits, e.g., directly or via angle connectors. A headgear assembly is removably connected to the pair of second connector portions and / or the angle connectors so as to maintain the frame and the nozzle assembly in a desired adjusted position on the patient's face.

A nasal assembly for delivering breathable gas to a patient includes a frame having an integrally formed first connector portion. A nozzle assembly includes a gusset or base portion and a pair of nozzles. At least one inlet conduit is structured to deliver breathable gas into the frame and nozzle assembly for breathing by the patient. A pair of second connector portions are removably and rotatably connected to respective first connector portions of the frame and are in communication with respective inlet conduits, e.g., directly or via angle connectors. A headgear assembly is removably connected to the pair of second connector portions and / or the angle connectors so as to maintain the frame and the nozzle assembly in a desired adjusted position on the patient's face.

A nasal ventilation interface including a pair of tubes configured to deliver a ventilation gas. The tubes are attachable at a first end to a ventilation gas supply hose and engageable at a second end with a person's nostril. A coupler is configured to align the pair of tubes with the person's nostrils, wherein each tube has an absence of pneumatic interconnection with the other tube.

The invention is directed to therapy devices for providing therapeutic light to a target region of tissue within a nasal cavity. The devices are adapted to include a light source communicating with a distal end of the first insertion member, wherein light from the light source illuminates a target region of tissue within a nasal cavity posterior to a limen nasi of the nasal cavity, and further wherein the insertion member is configured to prevent illumination of a region of tissue anterior to the limen nasi. The devices are further adapted to be positioned within the nasal cavity by a user without observing the location of the distal tip.

A patient interface for communicating fluids to and / or from a patient's nasal cavity and / or oral cavity is disclosed. In addition, a patient interface for fluid and physiological function monitoring proximate to the patient's nasal cavity and / or oral cavity is disclosed. An apnea monitor and a method for monitoring apnea are also disclosed.

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. In one embodiment, a valve is disposed between the nasal inserts and a source of positive airway pressure, the valve having a rim with a one-way diaphragm pivotally attached to the valve body with an inflatable bladder depending from the rim which seals against an exit port during inspiration and deflates to uncover the exit port on expiration. Another embodiment has nasal inserts without positive airway pressure but with a removable filter in the inserts for filtering inspired air.

A patient interface assembly that includes a patient interface device, a headgear, and coupling member joining the interface device to a headgear assembly. In one embodiment, a spring biases the patient interface device against the patient's face when in use. In a further embodiment, the patient interface device is a nasal cushion that includes a formable support mounted to the nasal cushion for providing support and adjustment of the nasal cushion to improve fit and comfort. The headgear assembly in one embodiment is a semi-rigid, minimal contact harness assembly and includes an adjustment assembly that allows for a simultaneous adjustment of multiple straps. An adjustment assembly on the headgear provide a gross adjustment of the position of the interface relative to the patient and a biasing force to urge the patient interface device against the patient's face. In a further embodiment, a pair of rigid connecting members coupling the patient interface device to the headgear.

Devices, systems and methods useable for dilating the ostia of paranasal sinuses and / or other passageways within the ear, nose or throat. A dilation catheter device and system is constructed in a manner that facilitates ease of use by the operator and, in at least some cases, allows the dilation procedure to be performed by a single operator. Additionally, the dilation catheter device and system may be useable in conjunction with an endoscope and / or a fluoroscope to provide for easy manipulation and positioning of the devices and real time visualization of the entire procedure or selected portions thereof. In some embodiments, an optional handle may be used to facilitate grasping or supporting a device of the present invention as well as another device (e.g., an endoscope) with a single hand.

A balloon catheter for treatment of a patient's lacrimal system is applied transnasally without the use of a guide wire or a curve retention member. The catheter uses a stainless steel hypotube of sufficient stiffness and column strength to be pushed from the patent's nasal cavity through an opening-formed through the lateral nasal wall and lacrimal fossa, into the lacrimal sac. The catheter has an inflatable member mounted about a rigid bent distal segment. The opening is first formed by pushing small holes through the medial sac, lacrimal fossa, and lateral nasal wall with an instrument and coalescing the holes. The catheter is then introduced into the nasal cavity and pushed laterally through the opening by manipulating its proximal end. Pressurized fluid is then applied to the catheter to inflate the inflatable member and dilate the opening.

Sinusitis, enlarged nasal turbinates, tumors, infections, hearing disorders, allergic conditions, facial fractures and other disorders of the ear, nose and throat are diagnosed and / or treated using minimally invasive approaches and, in many cases, flexible catheters as opposed to instruments having rigid shafts. Various diagnostic procedures and devices are used to perform imaging studies, mucus flow studies, air / gas flow studies, anatomic dimension studies, endoscopic studies and transillumination studies. Access and occluder devices may be used to establish fluid tight seals in the anterior or posterior nasal cavities / nasopharynx and to facilitate insertion of working devices (e.g., scopes, guidewires, catheters, tissue cutting or remodeling devices, electrosurgical devices, energy emitting devices, devices for injecting diagnostic or therapeutic agents, devices for implanting devices such as stents, substance eluting devices, substance delivery implants, etc.

A cannula (3) defined by a main body (1) having an internal passage (6). The internal passage (6) communicate with a nare (5, 7) and an oral prong or a mouthpiece (9) which is adjustable to provide a desirable signal from a patient's mouth and nose to indicate breathing by the patient.

A nasal ventilation interface including a pair of tubes configured to deliver a ventilation gas. The tubes are attachable at a first end to a ventilation gas supply hose and engageable at a second end with a person's nostril. A coupler is configured to align the pair of tubes with the person's nostrils, wherein each tube has an absence of pneumatic interconnection with the other tube.

An irrigation and aspiration system is disclosed. The system can be configured to aspirate and irrigate alone, sequentially or concurrently. The system can be configured to aspirate and irrigate the nasal cavity. The system can be manually controlled. The system can have removable and easily cleanable reservoirs for aspirant and irrigant.

A nasal dilator capable of introducing separating stresses in nasal outer wall tissues has a truss of a single body with a resilient member secured therein and a pair of spaced-apart end surfaces which, when forced toward one another from initial positions to substantially reduce direct spacing therebetween by a spacing reducing force external to said truss, results in restoring forces in the truss tending to return to the original direct spacing between the end surfaces. A resilient member, which is symmetrical with respect to a centerline of the truss that is perpendicular to the long axis of the truss, has a spring rate which continuously diminishes from the centerline to the end surfaces. An adhesive on the end surfaces adhesively engages exposed surfaces of nasal outer wall tissues sufficiently to keep the truss attached to the nasal wall surfaces while subjecting them to the restoring forces.

A face mask for ventilation of a patient. A face piece is disposed on the patient's face. An oral tube and a nasal tube are disposed through corresponding ports in the face piece. The oral tube extends through the mouth of the patient and the nasal tube extends through the nasal passage of the patient. The ends of the oral tube and the nasal tube are received in the posterior oropharynx of the patient. An adapter is connected to the ends of the oral tube and the nasal tube exteriorly of the face piece. Oxygen is introduced into an inlet port of the adapter wherein the oxygen enters the oral tube and the nasal tube concomitantly and ventilates the patient.

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.

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.

Irrigation and / or aspiration devices and methods may be configured to aspirate and irrigate alone, sequentially, or concurrently. The devices and methods may provide a base with a removable head, and adapted for partial or complete separation of the irrigation and aspiration functions. The devices and methods can be configured to aspirate and / or irrigate the nasal and sinus cavities. The devices and methods may be manually and / or automatically controlled. The devices and methods may include removable, and / or replaceable, and / or refillable, and easily cleanable reservoirs for aspirant and irrigant. The device head and / or aspirant reservoir may comprise a diagnostic device, i.e., test device and / or container after use of the devices and methods.

A nasal assembly for delivering breathable gas to a patient includes a frame having lateral connector, a cushion with a pair of nozzles, and a clip to secure the cushion to the frame. The frame includes a vent channel and a plurality of vent holes. The frame / cushion includes structure (lugs / cut outs) to prevent the assembly of an unvented frame with an unvented cushion, for safety purposes. The frame includes cored portions that interface with corner lugs provided on the cushion. A patient interface includes a frame, a cushion (nasal mask, nasal-oro mask, nozzles, etc.) and a vent assembly including a pattern of vent holes including at least two rows.

Described herein are nasal respiratory devices and methods for treating a variety of medical diseases including snoring and sleep apnea through the use of such devices. In general, these devices include an airflow resistor, such as a flap valve and a holdfast for securing the device in communication with the subject's nasal cavity. The devices may be configured to include leak paths to regulate the expiratory pressure when worn by a subject. Methods for using these devices may include securing a device over or at least partially within (or both of) a subject's nasal cavities.

A nasal ventilation interface and method for providing nasal ventilation to a patient includes a hybrid face mask, covering only the mouth, coupled with removable nasal inserts extending from the upper surface of the mask. The nasal interface has modular, removable, and disposable nasal pillows connecting the upper surface of the mouth-portion of the mask to the user's nares. Each part of the hybrid mask is modular and can be formed in various shapes and sizes. The ventilation interface has differing gas line entry ports and can be shallow with a relatively deep soft facial interface or deep with a relatively shallow facial interface. In either case, the upper surface receives the nasal interface. The upper surface can have a removable ceiling in which is defined a nasal interface connector. The nasal interface can be integral with a removable ceiling. The entire hybrid mask can be made in one piece.

Methods and devices for treating nasal airways are provided. Such devices and methods may improve airflow through an internal and / or external nasal valve, and comprise the use of mechanical re-shaping, energy application and other treatments to modify the shape, structure, and / or air flow characteristics of an internal nasal valve, an external nasal valve or other nasal airways.

The present invention comprises a nasal cannula (2), shaped to fit within a user's nares, where the nasal cannula includes at least one prong (24, 25) allowing high flow delivery of humidified gases and creates positive airway pressure in the patient's airway. The prongs have angled ends (31, 32), such that in use, gases flowing through the prongs are directed to the user's nasal passages. The nasal cannula body is partially swivelling and preferably has a ball joint connector (37, 39). In another embodiment the nasal cannula may have at least one flared end prong (31, 32) that preferably seals within a patient's nare.

An exhalation breath-actuated nasal delivery device for and a method of delivering a substance to a nasal cavity of a subject, the delivery device comprising: a nosepiece (40) for fitting to a nostril of a subject; a mouthpiece (42) through which the subject in use exhales; and delivery unit (64), as one of a mechanical delivery pump (66) or a nebulizer (115), for delivering a substance to the nosepiece (40); and an actuation mechanism (74) for actuating the delivery unit in response to oral exhalation through the mouthpiece, and preferably when at least one or both of the pressure at or the flow rate through the nosepiece exceeds a predetermined threshold.

Methods and devices for rhinoplasty and treating nasal valve stenosis are disclosed herein. The nasal valve acts as a flow-limiter and can contribute to airway obstruction if resistance within the nasal valve is excessive. In one embodiment, a system for treating nasal valve stenosis includes a first elongate implant and a second elongate implant configured to support the nasal valves when implanted. The implants can be coupled together by connecting elements, such as eyelets, tethers, complementary socket joints, and button-rivet supports.

A nasal prong for sealing with a nasal passage of a patient includes a head portion structured to seal and / or sealingly communicate with the patient's nasal passage and a column or stalk structured to interconnect the head portion with a base. The nasal prong is structured to redirect air flow direction, diffuse air flow or create turbulence, and / or orient a prong orifice in order to reduce and / or eliminate air jetting effects.