Abstract: Methods and systems are disclosed for determining patient compliance for using a compression therapy device. The systems may include a compression therapy sleeve and a controller having a non-transitory memory device. During a therapy session, the controller may record in the memory device operational therapy data obtained from sensors associated with the controller and/or sleeve. The controller may calculate a compliance metric based in part on the therapy data. The controller may then communicate the data or metric to one or more recipients. The methods may include allowing the patient to transfer a removable memory device from the controller to a personal computer, and uploading the therapy data or metric stored on it to a recipient website. Alternative methods may include the patient receiving the metric from the controller at the end of the therapy session, and then providing the metric to a recipient by phone.

Abstract: Methods are disclosed for measuring the size of body parts treated by a compression therapy device. Either the volume or circumference of the body part may be measured. The methods may include evacuating an inflatable compression sleeve to a known pressure, inserting the body part into the compression sleeve, inflating the sleeve to a pre-set condition, and then measuring one or more inflation related parameters. The pre-set conditions may include a pre-determined pressure, volume, or size of the inflatable cells comprising the sleeve. The inflation related parameters may include the time to fill the cell to a pre-set pressure, the pressure attained after a pre-set time of inflation, or the measured volume of a cell after a pre-set amount of air is introduced into it. The methods may also include deflating the cells from the known inflation state to a second inflation state and measuring similar parameters.

Abstract: Systems for auto-calibrating a pneumatic compression system may include one or more manifolds from an inflation fluid source and one or more individually inflatable cells. One or more pressure sensors may be associated with the one or more manifolds and/or each of the individually inflatable cells. Each of the pressure sensors may provide either dynamic or static pressure data to a controller. A method for auto-calibrating the compression system may include introducing a portion of inflation fluid into a cell while measuring a dynamic cell pressure, stopping the introduction of fluid, measuring a static cell pressure, and comparing, by the computing device, the dynamic cell pressure and the static cell pressure. sure. The comparison between dynamic and static cell pressures may be used to calculate a dynamic target cell pressure equivalent to a desired static target cell pressure.

Abstract: Pneumatic compression devices and methods for using the same are disclosed. A pneumatic compression device may include a compression pump, a fill/exhaust valve, a transducer, a plurality of cell valves, and a controller. The compression pump may output a pressurized fluid via an output. The fill/exhaust valve may connect one or more cell valves to the compression pump when in an open state and to the atmosphere when in a closed state. The transducer may sense a pressure level. Each cell valve may correspond to a cell and may connect the fill/exhaust valve to the corresponding cell when in an open state. The controller may determine a state (either open or closed) for each of the fill/exhaust valve and the plurality of cell valves based on at least the pressure level sensed by the transducer.

Abstract: Systems for auto-calibrating a pneumatic compression system may include one or more manifolds from an inflation fluid source and one or more individually inflatable cells. One or more pressure sensors may be associated with the one or more manifolds and/or each of the individually inflatable cells. Each of the pressure sensors may provide either dynamic or static pressure data to a controller. A method for auto-calibrating the compression system may include introducing a portion of inflation fluid into a cell while measuring a dynamic cell pressure, stopping the introduction of fluid, measuring a static cell pressure, and comparing, by the computing device, the dynamic cell pressure and the static cell pressure. The comparison between dynamic and static cell pressures may be used to calculate a dynamic target cell pressure equivalent to a desired static target cell pressure.

Abstract: Methods are disclosed for measuring the size of body parts treated by a compression therapy device. Either the volume or circumference of the body part may be measured. The methods may include evacuating an inflatable compression sleeve to a known pressure, inserting the body part into the compression sleeve, inflating the sleeve to a pre-set condition, and then measuring one or more inflation related parameters. The pre-set conditions may include a pre-determined pressure, volume, or size of the inflatable cells comprising the sleeve. The inflation related parameters may include the time to fill the cell to a pre-set pressure, the pressure attained after a pre-set time of inflation, or the measured volume of a cell after a pre-set amount of air is introduced into it. The methods may also include deflating the cells from the known inflation state to a second inflation state and measuring similar parameters.

Abstract: Pneumatic and therapeutic compression systems are disclosed including treatment protocols that may be used with such systems. A pneumatic compression system may include a source and sink of a pressurizing fluid. The pressurizing fluid may be sourced to a number of valves, each valve controllable by a control device including a computing device. The computing device may control each valve separately to allow any one or more of the valves to connect to the fluid source or the fluid sink. The computing device may include one or more therapeutic protocols that may direct one, two, or more valves to switch between fluid sourcing and fluid sinking, substantially simultaneously or in a sequence. A therapeutic compression system may include the pneumatic system in fluid communication with an inflation sleeve composed of multiple cells. Each cell may be inflated or deflated by a valve according to the therapeutic protocol.

Abstract: Pneumatic compression devices and methods for using the same are disclosed. A pneumatic compression device may include a compression pump, a fill/exhaust valve, a transducer, a plurality of cell valves, and a controller. The compression pump may output a pressurized fluid via an output. The fill/exhaust valve may connect one or more cell valves to the compression pump when in an open state and to the atmosphere when in a closed state. The transducer may sense a pressure level. Each cell valve may correspond to a cell and may connect the fill/exhaust valve to the corresponding cell when in an open state. The controller may determine a state (either open or closed) for each of the fill/exhaust valve and the plurality of cell valves based on at least the pressure level sensed by the transducer.

Abstract: A method of measuring pressure for a cell in a pneumatic compression device may include performing an inflate/exhaust cycle including, for one or more cells of a plurality of cells in a pneumatic compression device, inflating a cell to a target pressure, wherein the target pressure is based on at least a desired pressure, measuring a pressure of the cell, determining an overpressure value associated with the cell based on at least the measured pressure, determining a subsequent target pressure associated with the cell based on at least the measured pressure and the overpressure value, deflating the cell, and inflating the cell until the subsequent target pressure is achieved.

Abstract: Pneumatic compression devices and methods for using the same are disclosed. A pneumatic compression device may include a compression pump, a fill/exhaust valve, a transducer, a plurality of cell valves, and a controller. The compression pump may output a pressurized fluid via an output. The fill/exhaust valve may connect one or more cell valves to the compression pump when in an open state and to the atmosphere when in a closed state. The transducer may sense a pressure level. Each cell valve may correspond to a cell and may connect the fill/exhaust valve to the corresponding cell when in an open state. The controller may determine a state (either open or closed) for each of the fill/exhaust valve and the plurality of cell valves based on at least the pressure level sensed by the transducer.

Abstract: This invention is a method of treating a patient's injured tissue by applying platelet-rich plasma and laser energy to the injured tissue. The applied energy is low-level, and the patient feels no sensation of the low-level laser energy being applied. The laser energy can be applied before, after, or during the platelet-rich plasma application, or any combination thereof. Additional laser therapy may be applied over the entire extremity containing the injury, any non-injured adjacent tissue, as well as to the patient's entire body for stimulation of other body systems. Additionally, laser energy can be applied to the platelet-rich plasma before the platelet-rich plasma is applied to the patient.

Abstract: The present invention is a treatment for reducing serum cholesterol levels. The method involves analyzing a patient's lipid levels to determine a therapeutically sufficient amount of laser energy to apply to reduce a patient's LDL level while preserving his or her HDL level. The therapeutically sufficient amount of laser energy is determined by conducting a standard blood draw from the patient, conducting a lipid panel, and analyzing the results. In the preferred embodiment, a laser having a wavelength of about 635 nm is used to apply a therapeutic amount of laser energy of approximately 6.6 J/cm2, provided over six treatments, each laser treatment two days apart.

Abstract: The present invention is a method and device for reducing exposure to undesirable electromagnetic radiation. The dissipation device uses a varying angle antenna design to capture radiation from an active emission source, such as a cellular telephone when it is transmitting. The device converts the captured radiation into an electric current and dissipates the collected current by spending it to operate a thermal, mechanical, or electrical device. The varying angle antenna is a printed circuit board trace antenna comprising a microstrip having several serially connected meandering segments. One or more meandering segments include 90-degree bends in the microstrip, and one or more meandering segments include bends of more and less than 90 degrees. Portions of the microstrip that are horizontally oriented are all parallel, while portions of the microstrip that are vertically oriented can be parallel or angled, depending on the bend angle.

Abstract: A device and method for increasing the number and type of ions in a hydrotherapy treatment to assist in removing unwanted chemicals from the body. A battery-powered array is submerged into a liquid foot bath to generate ions through electrolysis. The array has at least two electrodes, one containing copper and/or zinc, the other steel. The device can be run in two modes, thereby creating different types of ions and enabling the removal of different types of chemicals. The device uses a current and voltage regulator to deliver a regulated amount of current into the array regardless of the conductivity of the liquid, and electrical circuitry is used to control the duration and mode of the treatment. Excessive heat is dissipated with a heat sink.

Abstract: Therapy apparatus for the exercise of the patient's trunk, back, spine, abdomen and shoulders consisting of a platform having a periphery and upper and lower sides. A pedestal or column extending vertically above the platform upper side supports a seat receiving the patient, and the platform lower side includes a central supporting projection extending below the platform periphery wherein the platform will engage a flat supporting surface, such as the floor, at the support projection and the platform periphery in a tilted manner and a patient located upon the seat may shift their weight to change the angle of platform tilting for exercising the patient's trunk, back, spine, shoulders and torso muscles and ligaments. Support projections of various vertical dimension may be employed to vary the extent of tilting from the vertical, and the apparatus may be utilized with computerized equipment to obtain accurate determination of the extent of exercise and body flexibility.

Abstract: An improved cervical traction apparatus comprises a cradle including a bowl-shaped cranial cavity for supporting the head of a user and an occipital shelf support comprising a concave wall extending across the cradle. The cradle is secured on a base assembly which provides for movement of the cradle relative thereto to provide for both independent horizontal and vertical plane movements.

Abstract: An improved seat shower for facilitating the care and treatment of patients in a clean shower environment, including a framework of such a height as to permit 360.degree. access to the seated patient, and a plurality of adjustable shower nozzles positioned about the seating area. Clean, disposable plastic liners are draped over the framework and base to maintain aseptic conditions.