377 results about "Laryngeal Masks" patented technology

The disclosed laryngeal mask airway device includes a rigid airway tube, a mask portion, and one or more optical fibers. The airway tube extends from a proximal end to a distal end. The airway tube defines an internal passage and a first notch. The first notch extends along a length of the tube from a location on the tube towards the distal end of the tube. The mask portion is coupled to the distal end of the airway tube. The mask portion includes an inflatable cuff. The cuff defines a central opening at least when inflated. The mask portion is insertable through a mouth of a patient to an inserted location within the patient. The cuff surrounds a glottic opening of the patient when inflated and when the mask portion is at the inserted location. A sealed airway passage extends from the proximal end of the tube through the internal passage to the glottic opening when the cuff is inflated and when the mask portion is at the inserted location. The mask portion includes an epiglottis elevator bar that extends from a proximal end to a distal end. The distal end of the bar defines an aperture. The bar is positionable in a resting position and an open position. The optical fibers extend from a proximal end to a distal end. A lens is connected to the distal end of the fibers. The fibers extend through the first notch. The lens is disposed near the aperture defined by the bar when the bar is in the resting position. The fibers and lens provide a view of a region that extends from the lens through the aperture defined by the bar.

A laryngeal mask airway device is provided that incorporates a video sensor, such as a CCD, CMOS or NMOS imaging chip, arranged to provide an image of the laryngeal inlet or other airway structures. The video sensor is electrically coupled to a reusable processing unit that receives the signals generated by the video sensor and generates a digital image of the interior of the patient's airway, thereby enabling the clinician to have immediate optical confirmation of the position of the mask aperture relative to the laryngeal inlet from the moment of insertion of the device.

The disclosed method for fabricating low cost laryngeal mask devices includes providing a mold, the mold including interior walls that define a hollow interior volume. The interior volume includes a first portion and a second portion. A liquid plastic material is introduced into the mold, and then the mold is moved so as to coat the mold's interior walls. The liquid plastic material and then allowed to cure. The cured plastic material is then removed from the mold and the cured plastic material includes a generally elliptically shaped plate and a cuff. The cuff is formed from plastic material that coated the portion of the interior walls that defined the first portion. The plate defines a laryngeal side, a pharyngeal side, and a central aperture. An interior perimeter of the cuff is attached to the laryngeal side of the plate proximal to a perimeter of the central aperture. An outer perimeter of the cuff is attached to the laryngeal side of the plate proximal to an outer perimeter of the plate.

A gastro-laryngeal mask features softly compliant construction of the distal half of the mask, wherein the mask is of generally elliptical configuration, with an inflatable peripheral cuff to seal and support the mask around the laryngeal inlet. A back cushion is inflatable to engage the back wall of the pharynx and thus to forwardly load the peripheral-cuff seal to the laryngeal inlet. An evacuation tube for external removal of a possible gastric discharge completes an evacuation or discharge passage contained within the mask and opening through the distal end of the peripheral cuff. Special provision is made for assuring integrity of the discharge passage within the flexible distal half of the mask, i.e., assuring against collapse of the distal-end half of the softly compliant evacuation tube in the distal region of the mask, such that inflation of the mask does not compromise viability of the evacuation tube by compressing softly compliant material of the evacuation tube during periods of mask inflation. The special provision also favors such collapse of the mask when deflated as to provide a leading flexible edge for piloting a safe and correct advancing insertional advance of the deflated mask in the patient's throat, in avoidance of epiglottis interference and to the point of locating engagement in the upper sphincter of the oesophagus.

An intubating LMA construction features a rigid airway tube wherein curvature in a single plane establishes essentially an arcuate path of angular extent in the preferred range of 130°, plus or minus 5°, which I have found to be in substantial anatomical conformance with the adult human's airway path, between a proximal end of the arc at substantial register with the longitudinal midpoint of the hard palate, and a distal end that faces and is at short offset from the glottic aperture, it being understood that my findings apply to suitably quantified allowance for variations in patient-head anatomy, as is for example customary for different sizes of LMA devices, each of which is adapted to serve one of five selected patient-size ranges. The proximal end of the rigid tube is suitably a short straight portion which is tangentially and integrally related to the proximal end of the arc. And the distal end of the arc is fitted with flexible mask structure of preferably elastomeric material such as silicone rubber, wherein an internal ramp formation within the mask structure assures a limited but important measure of further and stabilized guidance of an ET which has emerged from the distal end of the rigid tube, such that unguided displacement of the ET (i.e., beyond the ramp) is oriented to target safe entry of the ET into the glottic opening.

The disclosed laryngeal mask airway device includes a mask portion and an airway tube. The mask portion includes an inflatable cuff, which defines a central opening when the cuff is inflated. The airway tube defines an internal passage extending from a proximal end of the tube to a distal end of the tube. The airway tube further defines two or more tabs disposed near the distal end of the tube. The mask portion is coupled to the airway tube near the distal end of the airway tube, and the tabs extend from the airway tube into the central opening defined by the cuff when the cuff is inflated.

A laryngeal-mask airway device including provision for drainage of the oesophagus comprises an inflatable main-cuff and a backplate having a laryngeal-side and a pharyngeal-side. The backplate also has an external tube-joint adjacent to the proximal region of the main-cuff. The backplate is hermetically bonded to the periphery of the main-cuff establishing separation between a laryngeal-chamber region and a pharyngeal region. An distally open evacuation tube includes a distal portion which longitudinally traverses the interior of the distal region of the main-cuff in sealed relation therewith for operative engagement and communication with the inlet of the oesophagus. The evacuation tube traverses the laryngeal-chamber region generally adjacent to the laryngeal-side of the backplate and passages through a proximally located tube-joint to the pharyngeal region. An airway tube also extends into the tube-joint for communication with an airway port to provide a flowpath between the airway tube and laryngeal-chamber region.

A modified laryngeal mask airway device (LMA-device) is provided with means to improve ease of insertion, reliability of function and higher seal pressure (i.e., cuff pressure ratio). The LMA-device includes an indented section of the airway tube to offer locating means and purchase for the inserting finger, and extended mask aperture bars to increase the effective ventilating area of the mask and reduce the possibility of epiglottis displacement occasioned by mask insertion. The LMA-device further includes a modification of the airway tube angle of attachment to the mask, and provision of a posterior or back-cushion covering the entire posterior surface of the mask.

A method of making a laryngeal airway of the type that includes a respiratory tube and an inflatable positioning shield having a base and an inflatable, hollow peripheral portion is described herein. The method includes introducing at least one molding material into a mold, wherein the mold has a cavity defined by internal walls, wherein the internal walls conform to external walls of the laryngeal mask, and wherein the mold has a core within its cavity that is adapted to form the hollow portions of the laryngeal airway.

A device (10) for maintaining an airway in a patient comprises a mask (12), the mask having a resilient conformable peripheral portion (20, 22) shaped such that the mask (12) forms a seal with the larynx when the mask is positioned in the laryngo pharynx to thereby prevent ingress of extraneous fluids into the larynx, the peripheral portion (20, 22) of the mask defining at least one cavity (32, 34) for providing fluid communication to the oesophagus when the mask is inserted into the laryngo pharynx, and an airway tube (14) connected to or formed with the mask for passing gas to the larynx when the mask is properly inserted into the laryngo pharynx. The airway tube (14) preferably is curved as it leaves the mask.

Devices and methods for preventing tracheal aspiration as described where a cuff assembly having an inflatable member with an inflation tube fluidly coupled may be placed over a proximal end of an endotracheal tube or laryngeal mask and inserted into the patient trachea with the endotracheal tube or separately after the endotracheal tube has already been positioned. In either case, the inflatable member may be positioned distal (or inferior) to the vocal cords and proximal to the endotracheal balloon via a delivery instrument which automatically positions the balloon in proximity to the vocal cords.

The invention relates to a laryngeal mask for being introduced level with a patient's larynx and including at least one tubular structure designed to open out level with the patient's vocal chords to enable a mandrel and/or an intubation probe to be introduced, and including means for releasing the mandrel or the intubation probe, these release means being such that the tubular structure is open over at least a fraction of its length so as to allow the mandrel or the intubation probe to be released after it has been introduced therein.

An oropharyngeal device, for example, an endotracheal tube or a laryngeal mask airway, intended for insertion into a patient includes a tube portion defining a lumen which permits flow of a ventilating gas to the patient who may be under anesthesia for performance of surgery. The device includes a reinforcement member in a bite-resistant zone, which keeps the lumen open during patient biting to prevent occlusion of the lumen and/or interruption of the flow of ventilating gas. The reinforcement member can have a number of adjacent or closely-spaced wire turns or another suitable structure, and can cooperate with the tube portion to provide good bite-resistance. The tube portion optionally can be yieldable in the bite-resistant zone and provide cushioning during biting to inhibit dental or other damage.

It is intended to provide a laryngeal mask comprising: an inflation cuff having an inflatable hollow tubular part, a back plate which is air-tightly bonded to the hollow tubular part so as to cover one end of the inside diameter side space, and a cuff inside space which is surrounded by the inside diameter curved face and the inside face of the back plate and has an opening in the side opposite to the back plate; an airway tube which has one end opening toward the cuff inside space and the other end opening toward the space outside the oral cavity; and a gastric tube insertion guide wherein a guide face, which aims at inserting a gastric tube from the mouth until its front edge reaches the stomach or esophagus region in the state of inserting the inflation cuff into the pharyngeal region, is continuously or intermittently provided from the inflation cuff to the outside of the oral cavity.

A laryngeal mask airway has a main tubular shaft (1) with a mask portion (5) attached at its patient end (3). The mask portion (5) comprises a mount (50) and a sealing cuff (60) attached to the mount. The interior of the mount (50) defines a large volume atrium (54) communicating with the bore of the shaft (1) at one end and with an opening (61) through the cuff (60) at its other end. The join between the shaft (1) and the mount (50) is located above the rear part (63) of the cuff (60). The height of the atrium (54) is between 2.5 and 3.5 the internal diameter of the shaft. The volume of the atrium (54) is such that the ratio of the internal diameter of the shaft cubed to the internal volume of the atrium is between 50 and 68.

A method for constructing a supraglottic airway of the type used to facilitate lung ventilation and the insertion of endo-tracheal tubes or related medical instruments through a patient's laryngeal opening where the shield is constructed of a generally single-use generally blow-molded structure.

An endo-tracheal tube retainer used to facilitate the removal of a laryngeal mask of the type used to facilitate lung ventilation and the insertion of endo-tracheal tubes or related medical instruments through a patient's laryngeal opening is provided. The endo-tracheal tube retainer includes a semi-rigid stylet having proximate and distal ends and a soft curved stylet cap secured to the proximal end. The endo-tracheal tube also includes a connection adapter that is tapered from front to rear for secure insertion within a range of endo-tracheal tubes, removably secured to the distal end.