A cannula plugging device for rehabilitation after tracheotomy relates to the field of medical devices. The cannula plugging device includes a plugging device bracket. An outer wall of the plugging device bracket is fitted with a ring-shaped outer airbag. An inner wall of the plugging device bracket is fitted with a ring-shaped inner airbag. Two inflation tubes connecting the outer airbag and the inner airbag respectively are fitted on the plugging device bracket. The present invention makes the outer airbag and the inner wall of tracheotomy cannula pressed together by inflating the outer airbag. By gradually inflating the inner airbag and adjusting the size of the inner diameter of the lumen, the opening of the trachea gradually changes, so that the patient can gradually adapt to the process of plugging the cannula.

An intubation device utilizes a steerable endotracheal tube guide, a novel mechanism to automatically position an endotracheal tube at the laryngeal opening, and a novel system for soft tissue retraction to improve visualization of the laryngeal opening. An ETT is positioned within an overtube having proximal and distal ends and a flexible tip. The distal end houses a feeder mechanism for displacing the endotracheal tube through the overtube. A hood includes a stem, base, and expandable body, and may be affixed to the overtube's distal end. The ETT-containing overtube is precisely positioned at a laryngeal opening via positioning effects of body expansion, activation of a tip director, and/or flexible tip articulation. Unhindered visualization of the laryngeal opening is achieved by the expandable body, pushing the soft tissue outwardly and extensibly. An actuation module controls the feeder mechanism as well as the flexible tip to position flexible tip and endotracheal tube.

Nasal tracheal devices include a tube with visual indicia of insertion depth corresponding to patient height and an inflatable cuff. The tube comprises or provides a plurality of lumens that are in fluid isolation including an airpath lumen and a pressurized fluid source for inflating the cuff. The devices may also be configured to suction patient fluid from a location adjacent and/or above the cuff.

The present invention relates to a tracheal ventilation apparatus, in particular a tracheostomy cannula or an endotracheal tube, having a cannula tube, which from a point of view from a gas supply, has a proximal tube portion with a proximal opening and a distal tube portion with a distal opening. In order to provide an easy-to-handle tracheal ventilation apparatus that can easily be inserted and that impedes a swallowing process as little as possible, the proximal tube portion and the distal tube portion are connected to one another by way of an axially air-permeable joint that facilitates at least restricted mobility and, in particular, pivotability of a longitudinal axis of the distal tube portion with respect to a longitudinal axis of the proximal tube portion.

Embodiments of the invention relate to a ventilation device comprising: a. a ventilation tube having proximal and distal ends; and b. an inflatable cuff having a proximal bulge portion and a distal neck portion disposed distal to the bulge portion, the inflatable cuff being mounted around the ventilation tube to define proximal and distal cuff attachment locations which are both fixed on an outer surface of the ventilation tube.

An inflatable cuff for an endotracheal tube system has a sealing component that is one or a combination of (a) a proximal one-directional valve configured to deflect with underpressure during the intubation procedure and contact the tracheal wall of a patient to provide sealing, (b) a distal one-directional valve configured to deflect with overpressure during the intubation procedure and contact the tracheal wall to provide sealing; and (c) a cloud shape of the inflatable portion. The cloud shape is defined by at least one sealing section of the inflatable portion having a primary maximum inflated diameter and at least one non-sealing section of the inflatable portion having a maximum inflated diameter less than the primary maximum inflated diameter. The inflatable cuff may be inflatable by a ventilation tube. The system may include a cuff controller that senses airflow parameters and provides regulated flows of air during an intubation procedure.

An oropharyngeal glove for use with a rigid bronchoscope is provided for use during a rigid bronchoscopy procedure. When the oropharyngeal glove is in its installed state, it conforms to the patient's mouth and throat. The oropharyngeal glove includes upper and lower teeth guards that protect the patient's upper and lower front teeth, respectively, when the glove is in the installed state. A first opening is formed in the oropharyngeal glove in its proximal end that allows the rigid bronchoscope to enter glove. The oropharyngeal glove has a second opening formed in its distal end through which the rigid bronchoscope passes to enter the patient's trachea. The portions of the glove that conform to the patient's mouth and throat comprise a protective lining that protects the mouth, throat and vocal cords from being damaged by the rigid bronchoscope.

A pulmonary secretion clearing airway structure and related airway management system is disclosed that has a double lumen portion which each lumen of the double lumen portion operably secured to an airway management system so that inspiratory fluid (air/oxygen mixtures, with or without added water vapor) is delivered to the distal end of the ventilation catheter through one of the two lumens and expired inspiratory fluid, pulmonary secretions, and pulmonary fluids are removed from the patient through the other lumen. The expiratory fluid pathway preferably includes a secretion collection system for removing the pulmonary secretions and the like from the pathway, thereby improving operation and safety of the system. The airway structure can be a ventilation catheter or a supraglottic airway system such as laryngeal mask and the like.

A device for targeted delivery of a substance to an airway may include a conduit and at least two applicators. The conduit may include a proximal end and a bifurcated distal portion having two distal ends. Each applicator may be coupled with one of the distal ends of the conduit and may be configured to direct the substance out of the applicator toward one of two sides of an airway. A method for targeted delivery of a substance to an airway may involve advancing a substance delivery device into the airway, contacting two sides of the airway with at least two applicators of the substance delivery device, such that each applicator contacts the airway near a glossopharyngeal nerve and/or a superior laryngeal nerve on each of the two sides of the airway, and delivering the substance through the applicators to contact the airway along the two sides.

An expandable endotracheal tube includes a shaft that has an airway. The expandable endotracheal tube also includes an expandable segment mounted to a distal end of the shaft. The expandable segment includes an expandable membrane and a constant force spring positioned within the expandable membrane. The constant force spring has a compressed configuration to allow for placement of the expandable endotracheal tube within a patient and an expanded configuration in which the expandable membrane forms a seal with a trachea of the patient to enable positive pressure ventilation.