Abstract:
A method and apparatus for treating a stricture in a body lumen. The method comprises (a) sensing pressure being exerted by a treatment device on the stricture, (b) determining if enough force is being exerted on the stricture, (c) if enough force is being exerted on the stricture, timing the application of enough force, (d) determining if too much force is being exerted by the treatment device on the stricture, (e) if too much force is being applied to the stricture, decrementing the force being applied to the stricture, (f) determining if not enough force is being applied to the stricture, (g) if not enough force is being applied to the stricture incrementing the force being applied to the stricture, and (h) repeating (a)-(g) until (i) a desired pressure has been maintained on the tissue for a desired time. The apparatus comprises a device for exerting pressure on the stricture, a controller for controlling the amount of pressure the device exerts on the stricture, and a pressure sensor for sensing the pressure being exerted on the stricture by the device.
Abstract:
A tracheostoma valve to be applied to a tracheostomized person's neck comprises an air passage to be connected with the tracheostoma for connecting the trachea with the surroundings. A valve member is provided in the air passage, wherein the valve member is normally open and allows for inhalation and exhalation through the air passage. The valve further comprises a manually activated member for establishing an uninterrupted seal to block patient exhalation, thereby to direct it to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx.
Abstract:
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.
Abstract:
A tracheostoma valve to be applied to a tracheostomized person's neck comprises an air passage to be connected with the tracheostoma for connecting the trachea with the surroundings. A valve member is provided in the air passage, wherein the valve member is normally open and allows for inhalation and exhalation through the air passage. The valve further comprises a manually activated member for establishing an uninterrupted seal to block patient exhalation, thereby to direct it to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx
Abstract:
A tracheostoma valve to be applied to a tracheostomized person's neck comprises an air passage to be connected with the tracheostoma for connecting the trachea with the surroundings. A valve member is provided in the air passage, wherein the valve member is normally open and allows for inhalation and exhalation through the air passage. The valve further comprises a manually activated member for establishing an uninterrupted seal to block patient exhalation, thereby to direct it to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx.
Abstract:
This invention is an improved padding used by athletes and others to prevent or greatly reduce the instances of injury due to blows to the body. This is accomplished through the utilization of a radial expanding and contracting structure encapsulated in a foam type material.
Abstract:
This invention is an improved padding used by athletes and others to prevent or greatly reduce the instances of injury due to blows to the body. This is accomplished through the utilization of a radial expanding and contracting structure encapsulated in a foam type material.
Abstract:
This invention is an improved padding used by athletes and others to prevent or greatly reduce the instances of injury due to blows to the body. This is accomplished through the utilization of a radial expanding and contracting structure encapsulated in a foam type material.
Abstract:
An electrolarynx includes a motor having a locating diaphragm, a bobbin, and a magnetic assembly. The bobbin includes a striker and coil wires wound about a coil cylinder of an electromagnet. The locating diaphragm maintains the position of the bobbin along the longitudinal axis of the housing. The magnetic assembly includes a magnet and a non-magnetic guide disc that sandwiches the magnet to the housing. The magnet and the coil wires drive the striker and, in turn, a contact diaphragm in the cap of the electrolarynx that makes contact with a patient's throat to produce vibrations similar to those produced by the larynx. To avoid “gravitational wear” of the coil wires against a magnetic cup used to center the coil wires, the walls of the cup are made thinner and the magnetic cup may be replaced with a non-magnetic cup or the magnetic cup is removed altogether.
Abstract:
An electrolarynx includes a motor having a locating diaphragm, a bobbin, and a magnetic assembly. The bobbin includes a striker and coil wires wound about a coil cylinder of an electromagnet. The locating diaphragm maintains the position of the bobbin along the longitudinal axis of the housing. The magnetic assembly includes a magnet and a non-magnetic guide disc that sandwiches the magnet to the housing. The magnet and the coil wires drive the striker and, in turn, a contact diaphragm in the cap of the electrolarynx that makes contact with a patient's throat to produce vibrations similar to those produced by the larynx. To avoid “gravitational wear” of the coil wires against a magnetic cup used to center the coil wires, the walls of the cup are made thinner and the magnetic cup may be replaced with a non-magnetic cup or the magnetic cup is removed altogether.