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 closed suction system module is provided. In one embodiment, the closed suction system module includes a coupling member configured to couple to a suction port of a multi-port manifold or endotracheal tube adapter (e.g., dual-port or tri-port adapter). In one embodiment, the closed suction system module includes a suction catheter configured to clean the interior surfaces of body-inserted tubes or artificial airways (alone or in addition to suctioning natural airways or portions of the respiratory tract or other body lumens). The suction catheter may include a cleaning portion at a distal portion of the suction catheter (e.g., near the distal end or tip of the suction catheter). In some embodiments, the cleaning portion includes at least one expandable cleaning member (e.g., balloon, sleeve, wiper).

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus.

The invention is an endotracheal intubation for preventing injury to throat, vocal cords and trachea. The endotracheal intubation comprises a hollow intubation body with a variable outer diameter. The hollow intubation body comprises a front end and a tail end, an inner intubation wall and an outer intubation wall, and having a retracted state with a smaller outer diameter and an expanded state with a larger outer diameter. When the endotracheal intubation inserted into a patient’s trachea needs to be replaced, as long as the hollow intubation body of the new endotracheal intubation is in the retracted state, it can be inserted into the hollow intubation body to be replaced, and when reaching the position, the hollow intubation body to be replaced is withdrawn, and finally the new hollow intubation body is changed into the expanded state, i.e. the replacement operation of the endotracheal intubation is completed.

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 add-on device and method for an Endo-Tracheal Tube (ETT), the add-on device including a lengthy body having a major arc-shaped cross section sized and shaped to tightly fit over an ETT, at least one longitudinal cavity passing along the lengthy body, including a distal suction cavity ending with a suction inlet at a distal end of the lengthy body; and a distal suction outlet channel extending from a proximal end of the lengthy body, the channel is a continuous extension of the distal suction cavity and configured to provide suction to the distal suction cavity. The add-on device senses moisture at a distal end of the add-on device, and in case of detection of excessive wetness, provides suction to the distal end of the device through a cavity passing along the device, the suction is provided via a suction outlet channel extending from a proximal end of the device.

An endopharyngeal airway positive pressure ventilation device and method of use for ventilating a patient through a nasopharyngeal airway in surgical settings that is incapable of normal ventilation with current anesthetic techniques due to a risk for airway obstruction in surgical procedures requiring conscious sedation monitored anesthesia care (MAC). The invention includes a single-lumen endopharyngeal nasal tube with an eye shaped opening at its distal end and a cylindrical proximal end used as an adaptor for anesthetic applications such as positive airway pressure via JACKSON-REES modified ambu-bag or other various anesthesiology applications. Contiguous to the distal end of the nasal tube is an end-tidal CO2 monitoring port (ETCO2). On the distal end of the flexible nasal ventilation tube is an eye opening allowing air flow to the posterior pharynx. The device further includes a modified JACKSON-REES ambu bag which allows for controlled airflow to the patient during a REESE procedure.

An incision and dilation apparatus performs an incision in and dilates select tissue of a mammal. The apparatus includes a blade member, a dilator, and a frame. The blade member includes a blade having a cutting edge. The dilator is configured to dilate the select tissue. The frame includes a blade guide, and is adapted to position the blade guide over the select tissue. The blade guide retains the blade member in first and second perpendicular directions and allows substantially linear movement of the blade member in a third direction. The frame also supports the dilator and allows movement of the dilator in the third direction. The dilator includes a second blade guide that retains the blade member in first and second perpendicular directions and allow substantially linear movement of the blade member relative to the dilator in a third direction.

A non-ventilator ET tube cap used to oxygenate a patient during an intubation procedure. The ET tube cap generally comprises an oxygen source connector configured to connect to an oxygen source via an oxygen tube. This provides oxygen to a patient via an ET tube while being intubated. The ET tube cap further includes an ET tube receiving aperture that is specifically arranged to engage an ET tube in a removable relationship prior to the ET tube connected to a ventilator while the ET tube is deployed in a patient. Optionally, the ET tube cap can comprise a pressure relief valve that opens when pressure inside of the ET tube cap exceeds a predetermined pressure threshold to prevent harm to the patient that is being intubated.

An airway device facilitates the insertion of an ETT into a patient, the delivery of oxygenated air into a patient, an exchange of the pre-inserted ETT in an intubated patient, and an evaluation of the larynx and trachea in an intubated patient, The device comprises an overtube having a mask section attached to a distal portion of the overtube. An inflatable bladder affixed to the mask section includes a shape and surface configured to seamlessly contact the circumference of the elliptical construction of the laryngeal opening. Once the inflatable bladder is positioned adjacent the laryngeal opening enhanced sealing properties are created so that the axis of the airflow entering the device matches the axis of the trachea, allowing for the improved delivery of oxygenated air into the patient's lungs. The specific utilization of the bladder allows for the device to be constructed smaller than a typical airway device, which may more easily facilitate the insertion process. Additionally, the device may provide a seamless transition into endotracheal intubation when necessary.