An irrigating intraluminal suction inner cannula system for a tracheostomy tube may be a suction-powered system that may be used for suction alone or a combination of rinse and intraluminal suction for tracheostomy tubes in place of conventional catheter-based intraluminal suction. An inner cannula includes chambers, or regions, and holes that facilitate intraluminal suction and cleaning at multiple locations within the tracheostomy tube. It may be applied/actuated by a patient, healthcare worker, caretaker, or via an electronic system either on-demand or on regular or triggered intervals, in either inpatient/hospital or outpatient/ambulatory care setting.

A cuff assembly for a tracheostomy tube includes an outer bladder and an inner cuff. The inner cuff is positioned adjacent to the tracheostomy tube, and the outer bladder is positioned adjacent to the inner cuff. The outer bladder is made with a less elastic material and operates at a higher relative pressure. The inner cuff is made with a more elastic or hyper-elastic material and operates at a lower relative pressure. A secondary airflow opening is formed on a lateral wall of the tracheostomy tube between the cuff assembly and a main distal opening of the tracheostomy tube.

An endotracheal tube airway patency system and method are provided. The system includes an endotracheal tube having a tube body having a proximal end, a distal end, an inner surface, a distal opening disposed at the distal end of the tube body, a proximal opening disposed at the proximal end of the tube body, and an airflow-effacing surface disposed within the tube body. The airflow-effacing surface includes a telescoping inner sleeve configured to be removed from the endotracheal tube body. The system further includes a tool for removal of the telescoping internal sleeve from the endotracheal tube body. The tool includes an elongated body having a proximal end and a distal end; a handle located at the proximal end of the elongated body; and at least one extension member disposed at the distal end of the elongated body. The at least one extension member is configured to couple to the telescoping internal sleeve for removal of the telescoping internal sleeve from the endotracheal tube body.

The present invention provides improved medical devices, including oral airway devices, equipped with a visualization device for intubation, extubation, ventilation, drug delivery, feeding and continuous remote monitoring of a patient. The present invention also provides methods for rapid and accurate placement of a medical device in a patient and continuous real time monitoring, including a remote monitoring, of the patient after the placement.

A tracheal tube assembly includes an outer cannula configured to be positioned in a patient airway and an inner cannula configured to be disposed inside the outer cannula. The tracheal tube assembly further includes a flange member secured about the outer cannula, and an outer cannula connector coupled to a proximal end of the outer cannula. The inner cannula includes a compressible proximal end region that is compressed while secured inside the outer cannula connector.

A method of using ultraviolet (UV) radiation to treat an infection in the respiratory system and far infrared radiation (FIR) to treat inflammation. The method uses a light probe inserted into the airway of a patient to apply UV radiation and FIR to a target site in the upper respiratory tract. The UV radiation applied may be broad-spectrum UV radiation or UVC radiation in the 222 nm range. FIR applied may be in the 3-10 μm range. The UV radiation kills any organisms, including COVID-19 and FIR reduces inflammation resulting from infection and subsequent UV treatment. The treatment may be applied to intubated or spontaneously breathing patients and via the oral or nasal passages.

A tracheostomy airway device is provided comprising an outer cannula (110) having open proximal and distal ends, an inner actuation member insertable into the proximal end of the outer cannula, and one or more retention members (130). The one or more retention members are movable relative to the outer cannula between a retracted configuration in which the tracheostomy device is insertable into, and removable from, the trachea of a patient, and an extended configuration in which the one or more retention members impede removal of the tracheostomy airway device from the trachea. The retention members are operably linked to the inner actuation member or the outer cannula, such that movement of the inner actuation member relative to the outer cannula actuates movement of the one or more retention members between the retracted configuration and the extended configuration.

A device to monitor movement of a tracheostomy tube is described. The device includes a faceplate that is releasably attached to a tracheostomy collar such that the faceplate may be used without the tracheostomy collar. The tracheostomy collar includes a sensor component and an actuator component each located proximate the faceplate. The actuator component actuates when the sensor component moves from a first position to a second position. The second position is further from the actuator component than the first position. The sensor component transmits a signal to an alarm assembly in response to the actuator component actuating. The alarm assembly produces an alert in response to receiving the signal from the sensor component.

A temporary tube placement system includes a tube having a proximal end and a distal end, a camera supported by the tube at the distal end, a plurality of fiber optic filaments through which light from a light source travels from the proximal end to the distal end, a screen for displaying images from the camera, and a power source electrically attached to the camera and the light source. The enteral tube includes a tube having a distal end portion for placement within a patient and a proximal end portion and a lumen increasing in cross section from the proximal end portion toward the distal end portion along at least a portion of the tube.

The embodied invention is a new inspiration/expiration ventilator flow design, with a constant inspiration flow and intermittent-concurrent expiratory flow based on lung pressure setpoints. This mode is possible by using a new dual lumen tube inserted into a patient Trachea. Additionally, the control provides support for patient initiated breathing which is initiated by a lung pressure drop. This control provides continuous and gentle recruitment of lung alveoli.