A device (100) for facilitating the positioning of a catheter for the administration of a liquid medicament to a spontaneously breathing patient. The method and system according to preferred embodiments of the present invention allows optimizing the dispensing said medicaments. In particular the system according to a preferred embodiment of the present invention allows the administration of an exogenous pulmonary surfactant to preterm patients.

A tracheostomy collar is described herein having a number of features providing ease of use in caring for a tracheostomy and securing a tracheostomy tube inserted therein.

A medical appliance for the treatment of one or more sleep disorders such as obstructive sleep apnea in a patient, the appliance comprising: a biasing member for inserting behind and exerting a force upon the patient's soft palate or tongue, wherein the biasing member is inserted in a reduced or minimized form and then expanded or firms once in place to exert the force. The appliance may be nasally inserted or be placed through the mouth. In a particular configuration, both the soft palate and tongue are biased to prevent obstruction of the flow of air in the nasopharyngeal airway.

Systems, devices, and methods for coupling a tracheostomy tube to a source of humidified breathing gas are disclosed. An adaptor includes a housing, a tracheostomy tube connection device, and a baffle. The housing has an interior surface, an exterior surface, and a breathing gas port. The tracheostomy tube connection device is positioned within the housing and includes an input port for receiving a flow of humidified breathing gas from the breathing gas port and an output port for coupling with the tracheostomy tube. The tracheostomy tube connection device has an internal surface defining a breathing gas passage and an external surface spaced from the interior surface of the housing to create a condensation passage. The baffle may be positioned between the breathing gas port and the input port to cause controlled condensation from the flow of humidified breathing gas by disrupting the flow of humidified breathing gas.

A sanitary device for securing a breathing tube to a patient during anesthesia administration, which also prevents leaking anesthetic gases from entering the operating room environment. The novel design allows rapid application by the user and prevents potential transmission of infectious agents to the patient while securing the breathing tube. A unique, integrated suction system efficiently evacuates leaking anesthetic gases. The device may be manufactured inexpensively and is provided in sanitary packaging. It is intended for single use.

An adjustable tracheostoma valve is disclosed. The adjustable tracheostoma valve includes a passageway for connecting the trachea with the surroundings. A valve disk is provided in the passageway. The disk is moveable to allow for inhalation and exhalation through the passageway and is configured to close in response to pressure to direct air to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx.

An airway stabilization system including an airway device and a securing mechanism or faceplate therefor is provided which includes active stabilizing components on both the airway device and the faceplate which prevent clinically significant movement of the airway device with respect to the patients vocal cords in response to the application of significant forces in any direction to the device, be they longitudinal, torsional/rotational or bending. The system includes an airway device and an attached retention collar which interacts with a securing device/patient to ensure proper airway insertion depth and provide unparalleled strength and stability against movement. The airway stabilization system includes a unique stabilizer readily adapted for use in field situations to releasably engage or release a retention structure on the airway device to facilitate ease of application in all conditions, a twist-off 15 mm connector which allows a secure connection of the 15 mm connector to the airway device while facilitating easy disconnection thereof, and a universal bite block which cooperates with the securing system to prevent oral and/or dental damage and discomfort to the patient when the system is installed.

Oral gas catheters and methods of inducing gas in a patient orally. The oral gas catheter includes one or more delivery cannulas configured to be inserted into the patient's mouth with a distal end of the delivery cannula disposed adjacent the patient's laryngeal inlet, and a clip disposed on the delivery cannula. The clip is configured to secure the delivery cannula to a tooth of the patient. The oral gas catheter may have two such delivery cannulas and clips with the delivery cannulas coupled together by a coupler. The delivery cannulas are placed in an operative position in a patient's mouth and secured in the operative position by releasably securing the clips to the patient's teeth. The oral gas catheter makes it possible to bypass the nasal cavity and deliver oxygen or other gas directly adjacent the laryngeal entrance and into an anatomical dead space of the airway.

Endotracheal tube holders having bottom surface including protrusions that contact the endotracheal tube, and a strap that wraps around the bottom surface and the tube to secure the endotracheal tube to the tube holder.

A retrieval probe for insertion of a bridle into a nasal passageway of a patient is provided. The retrieval probe includes a proximal end and a distal end, a catheter between the proximal end and the distal end, an inner core within a lumen of the catheter, and a magnetic tip disposed at the proximal end. The catheter includes a hollow section disposed between the magnetic portion and a distal end of the stiff inner core. The hollow section may be flexible and can be configured to bend at an angle of about 180 degrees. The system for securing a nasal tube can include a bridle having a magnetic connection portion; and a retrieval probe as described above. The magnetic connection portion of the bridle and the magnetic tip of the retrieval probe can be configured to magnetically couple during a procedure for inserting the bridle in a nasal passageway of a patient.