Abstract: A method and apparatus to improve swing velocity, hand speed, and time to impact when swinging weighted, club-like equipment such as sporting equipment and tools. The method and apparatus include an enlarged flange positioned on the handle of the equipment. The flange includes a greater size than the handle to contact against the user's hand. The apparatus may be manufactured on new equipment, or added to existing equipment. The device and methods also improve safety by preventing hand injury during a swing, and prevent accidental release of the equipment during a swing.

Abstract: A method and apparatus to improve swing velocity, hand speed, and time to impact when swinging weighted, club-dike equipment such as sporting equipment and tools. The method and apparatus include an enlarged flange positioned on the handle of the equipment. The flange includes a greater size than the handle to contact against the user's hand. The apparatus may be manufactured on new equipment, or added to existing equipment. The device and methods also improve safety by preventing hand injury during a swing, and prevent accidental release of the equipment during a swing.

Abstract: Methods and devices for treating patients using high partial pressures of dissolved gas in a liquid. Greater than hyperbaric partial pressures of gas may be dissolved and maintained in the liquid when mixing occurs at ambient pressure. Additional increases in dissolved gas partial pressure may be achieved when the temperature of the liquid is further decreased. The method further includes administering the liquid intravenously via a conventional catheter. Gas exchange occurs due to diffusion upon mixing of the liquid and blood within the vasculature of the patient.

Abstract: Methods and devices for creating a supersaturated liquid solution having dissolved gas with hyperbaric partial pressures and aerosolizing the supersaturated solution via a nebulizer. High partial pressures of the dissolved gas may be maintained before, during, and after the aerosolization process. Thus, the hyperbaric partial pressures may be retained in the aerosol particles even after the particles are exposed to ambient barometric pressure. The aerosolized particles may be inhaled to improve oxygenation and blood flow to the lung or alternatively, the aerosolized particles can be topically applied to accelerate wound healing. Nebulizers may produce aerosol particles in some embodiments have mass median aerodynamic diameters of between about 0.25 and about 5 microns, thereby allowing sufficient deposition in the lung parenchyma, proximal to alveoli.

Abstract: Methods and devices for treating patients using high partial pressures of dissolved gas in a liquid. Greater than hyperbaric partial pressures of gas may be dissolved and maintained in the liquid when mixing occurs at ambient pressure. Additional increases in dissolved gas partial pressure may be achieved when the temperature of the liquid is further decreased. The method further includes administering the liquid intravenously via a conventional catheter. Gas exchange occurs due to diffusion upon mixing of the liquid and blood within the vasculature of the patient.

Abstract: Methods and devices for creating a supersaturated liquid solution having dissolved gas with hyperbaric partial pressures and aerosolizing the supersaturated solution via a nebulizer. High partial pressures of the dissolved gas may be maintained before, during, and after the aerosolization process. Thus, the hyperbaric partial pressures may be retained in the aerosol particles even after the particles are exposed to ambient barometric pressure. The aerosolized particles may be inhaled to improve oxygenation and blood flow to the lung or alternatively, the aerosolized particles can be topically applied to accelerate wound healing. Nebulizers may produce aerosol particles in some embodiments have mass median aerodynamic diameters of between about 0.25 and about 5 microns, thereby allowing sufficient deposition in the lung parenchyma, proximal to alveoli.

Abstract: A CPAP enclosure used in the treatment of breathing disorder comprises a base connected to a bed, a canopy connected to the base, and a sealing member that connects the canopy to the base. The sealing member forms a substantially airtight seal such that the canopy and the base form a substantially airtight enclosure around at least a portion of the bed. A Continuous Positive Airway Pressure (CPAP) compressor connects to the enclosure via flexible tubing, and generates a continuous positive airway pressure within the enclosure to treat a patient. A blender blends one or more compressed gasses with the compressed air from the CPAP compressor for delivery to the enclosure.

Abstract: This invention is a method of preparing and utilizing oxygenated liquids for medical and therapeutic purposes. Non-blood liquid solutions are oxygenated using a gas liquid contact apparatus. Conditions of increased ambient pressure and decreased temperature are created to maximally dissolve gaseous oxygen into liquids. In addition, an electromagnetic stirring is used to homogeneously mix the gaseous oxygen and liquid. Following the oxygenation of the liquid is anaerobically procured from the gas liquid contact apparatus in order to maintain high dissolved oxygen partial pressures in the liquid. The oxygenated liquid may be intravenously injected to titrate blood oxygen levels, or the oxygenated liquid may be systemically administered for absorption into tissues and the bloodstream.

Abstract: The present invention is a stethoscope which provides the user with continuous access to physiologic sounds. The stethoscope consists of multiple, lightweight, disposable sound receiving sensors and shutoff valves which allow selective auscultation of specific sites without patient disturbance. In addition, depending upon the positions of the shutoff valves, the stethoscope may enhance sound conduction by producing constructive interference of sound waves. A means of attaching the sound receiving sensors to the skin is also described. Because the sound receiving sensors are disposable, the risk of infection due to cross-examination is minimized. Therefore, this invention is safer than known stethoscopes.