Abstract: The invention relates to a laryngeal mask airway device (1) for insertion into a patient to provide an airway passage to the patient's glottic opening, the device (1) comprising an airway tube (2) a mask (3) attached to the airway tube (2), the mask (3) comprising a body (4) having a distal end (5) and a proximal end (6), a peripheral inflatable cuff (7), and defining an outlet (8) for gas, the mask (3) being attached to the airway tube (2) for gaseous communication between the tube (2) and the outlet (8), the device (1) further comprising an oesophageal drain (10), the drain (10) comprising a conduit extending from an inlet (12) at the distal end (5) to an outlet (13) disposed to the outside of the patient when the device (1) is in place, the conduit including a mask section (11) and an airway tube section (41), wherein the conduit mask section (11) is formed integrally in the material of the body (4).

Abstract: The invention relates to a laryngeal mask airway device (1) for insertion into a patient to provide an airway passage to the patient's glottic opening, the device (1) comprising an airway tube (2) a mask (3) attached to the airway tube (2), the mask (3) comprising a body (4) having a distal end (5) and a proximal end (6), a peripheral inflatable cuff (7), and defining an outlet (8) for gas, the mask (3) being attached to the airway tube (2) for gaseous communication between the tube (2) and the outlet (8), the device (1) further comprising an oesophageal drain (10), the drain (10) comprising a conduit extending from an inlet (12) at the distal end (5) to an outlet (13) disposed to the outside of the patient when the device (1) is in place, the conduit including a mask section (11) and an airway tube section (41), wherein the conduit mask section (11) is formed integrally in the material of the body (4).

Abstract: The invention relates to a laryngeal mask airway device (1) for insertion into patient to provide an airway passage to the patient's glottic opening, the device (1) comprising an airway tube (2), a mask (3) attached to the airway tube (2), the mask (3) comprising a body (4) having a distal end (5) and a proximal end (6), a peripheral inflatable cuff (7), and an outlet (8), the mask (3) being attached to the airway tube (2) for gaseous communication between the tube (2) and the outlet (8), the device (1) further comprising means to prevent occlusion of the outlet (8) by the patient's anatomy, the means comprising a support (11), and a conduit (28a) to allow gas to flow out of the outlet (8), past the support.

Abstract: 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.

Abstract: 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.

Abstract: 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.

Abstract: The invention relates to a laryngeal mask airway device (1) for insertion into a patient to provide an airway passage to the patient's glottic opening, the device (1) comprising an airway tube (2), a mask (3) attached to the airway tube (2), the mask (3) comprising a body (4) having a distal end (5) and a proximal end (6), a peripheral inflatable cuff (7), and defining an outlet (8) for gas, the mask (3) being connected to the airway tube (2) for gaseous communication between the tube (2) and the mask, the distal end of the mask being ventrally displaced, relative to the proximal end.

Abstract: The invention relates to a laryngeal mask airway device (1) for insertion into a patient to provide an airway passage to the patient's glottic opening, the device comprising an airway tube(2), a mask (3) attached to the airway tube, the mask comprising a body (4) including a peripheral inflatable cuff (5), an outlet (6) and an inlet (7), the mask being attached to the airway tube via the inlet for gaseous communication between the tube and the outlet, there being at least one fibre-optic cable (23, 24) terminating adjacent the outlet for receiving, in use, an image of the patient's glottic opening, and means (50) for viewing the image, the viewing means being disposed such that the viewing means remains in the user's field of view during manipulation of the device by the user to view the glottic opening.

Abstract: The disclosed endotracheal tube includes a silicone tubular member that has a proximal end, a distal end, and a lumen extending through the member to supply air from the proximal end to the distal end. The tubular member defines a first zone and a second zone. At least a portion of the first zone has a first outer diameter. The second zone has a second outer diameter. The first outer diameter is less than the second outer diameter. The first and second zones are adjacent to one another and are configured for insertion into the trachea of a human patient. A silicone cuff is attached to the tubular member such that the cuff extends over at least a portion of the first zone. The silicone cuff is mounted such that when the cuff is inflated in a trachea, the cuff reaches its plateau pressure prior to circumferentially contacting the inner wall of the trachea so that an accurate pressure reading may be taken of the pressure the cuff exerts on an inner wall of the trachea.

Abstract: The disclosed method of monitoring the cuff pressure of an LMA provides an estimation of a patient's anesthetic state. Cuff pressure tends to rise and fall during IPPV and spontaneous breathing. One of the disclosed methods activates an alarm if an instantaneous value of the cuff pressure exceeds selected levels. This method may also automatically adjust the selected levels. One of the disclosed methods activates an alarm if activity of the cuff pressure as observed over a period of time exceeds a selected level.

Abstract: A reversibly operable motor is mechanically connected to automatically position the piston of an air syringe that is pneumatically connected to the inflatable/deflatable seal ring or cuff of a laryngeal mask airway device (LMA) that is installed in a patient, who is being ventilated and/or anaesthetized via the airway of the LMA device. Air pressure in the cuff corrected as necessary to conform to a predetermined pressure level. The system continuously monitors for abnormal patterns of response, with audibly and visually reported warnings to the anaesthetist; these warnings include system detection of a patient's incipient sign of premature awareness while still under surgery, system detection and warning of a system or LMA malfunction, and continual microprocessor survey and integration of historical data to determine decremental recovery from administered anaesthesia.

Abstract: 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.

Abstract: 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.

Abstract: The disclosed laryngeal mask airway device includes an inflatable cuff, an airway tube, and a tab. The cuff defines a central opening at least when inflated. The cuff 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 at the inserted location. The airway tube extends from a proximal end to a distal end. The airway tube defines an internal passage. 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 at the inserted location. The tab is fixed to the airway tube near the proximal end of the airway tube. The tab is disposed outside of the mouth of the patient when the cuff is at the inserted location. The tab extends outwardly from the airway tube in a first direction when the cuff is at the inserted location.

Abstract: 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.

Abstract: 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.

Abstract: An artificial airway device for use in unconscious patients comprises a laryngo-pharyngeal mask including an expandable masking ring. The expandable mask sealingly surrounds the laryngeal inlet when expanded to obstruct communication between the laryngeal inlet and oesophagus. One or more airway tubes connected to the mask provide for fluid flow to a portion of the mask facing the laryngeal inlet when said mask sealingly surrounds the laryngeal inlet. A gastro-tube connected to the mask provides a fluid flow-path to the mask when the mask sealingly surrounds the laryngeal inlet. The distal end of the gastro tube passes through the masking ring at its narrower distal region where, when installed in a patient, it abuts against the oesophagus; and the distal portion of the gastro-tube flattens when the mask is deflated to facilitate smooth passage behind the larynx during insertion through the mouth and throat of the patient.

Abstract: 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.

Abstract: The disclosed laryngeal mask airway device includes an inflatable cuff and an airway tube. The inflatable cuff defines a central opening at least when inflated. The cuff 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 the cuff is inflated and at the inserted location. The airway tube extends from a proximal end to a distal end. The airway tube defines an internal passage, an anterior portion, a posterior portion, a left portion, and a right portion. An airway passage extends from the proximal end of the tube through the internal passage to the glottic opening when the cuff is inflated and at the inserted location. The anterior portion is characterized by a thinner wall thickness than the left and right portions. The posterior portion is characterized by a thinner wall thickness than the left and right portions.

Abstract: The disclosed laryngeal mask airway device includes an inflatable cuff and an airway tube. The inflatable cuff defines a central opening at least when inflated. The cuff 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 the cuff is inflated and at the inserted location. The airway tube extends from a proximal end to a distal end. The airway tube defines an internal passage, an anterior portion, a posterior portion, a left portion, and a right portion. An airway passage extends from the proximal end of the tube through the internal passage to the glottic opening when the cuff is inflated and at the inserted location. The anterior portion is characterized by a thinner wall thickness than the left and right portions. The posterior portion is characterized by a thinner wall thickness than the left and right portions.