81 results about "Compression therapy" patented technology

A disposable sleeve for compression therapy, with at least one inflatable air cell defined between a first airtight wall adjacent a patient's body to be treated and a second airtight wall. Each of the first and second walls comprises an external porous layer and an internal layer comprising air-tight polyethylene (PE). The walls are bonded by molten portions of the PE internal layer penetrating and set in their corresponding external porous layers and welded to each other, the bonding enduring at least 250 inflation-deflation cycles associated with the therapy.

A connector apparatus includes first and second mating connectors that can be joined to make a fluid connection. The connectors are constructed to discriminate improper connectors so that no fluid tight connection can be formed with improper connectors. The connector apparatus can be used with a system for compression therapy to prevent deep vein thrombosis.

The present invention is directed to a device that provides thermal energy therapy, compression therapy and negative pressure therapy simultaneously and / or in conjunction with each therapy. The outcome of the present invention is that a patient's bodily fluids can be maintained, controlled, and / or adjusted with decreased medication dependence. Using these three therapies individually does not obtain these desired results of controlling, maintaining or adjusting the patient's bodily fluid. This combination of therapies is beneficial to the patient.

A compression treatment system is provided that detects the number of and type of garments connected thereto. The system includes a plurality of ports, valves connected thereto and a number of garments having one or more bladders. The bladders are in fluid communication with a fluid source in a pneumatic circuit, to provide compression therapy once a user confirms the number of and type of garments connected to the system for use by a patient. A single pressure sensor communicates with a plurality of detected bladders located in the one or more garments.

The present invention relates to a replaceable module for use with a thermal contrast therapy systems. The replaceable module may be an automated thermal contrast therapy module which includes a casing, a manual mixing valve, an automated mixing valve, an automated mixing valve actuator, a temperature sensor, and an interface. A cold and a hot fluid are mixed to generate a therapy fluid. The therapy fluid may be output to a therapy bladder. The second replaceable module is a compression therapy module which includes a casing, an air pump, a pneumatic solenoid, and a pressure monitor. The casing may include a pressurized air pathway including an air outlet. The pump may pressurize the air within the pathway, and the solenoid may regulate the air pressure using feedback from the pressure sensor. Additionally, a pressure relief valve may release pressure if it gets above a safety threshold. The compression therapy module may also include a fluid pathway.

A connector assembly includes first and second mating connectors that can be joined to make a fluid connection. The connectors are constructed to discriminate improper connectors so that no fluid tight connection can be formed with improper connectors. The connector assembly can be used with a system for compression therapy to prevent deep vein thrombosis.

Systems, devices and methods for providing active and / or passive compression therapy to a body part can include a compression device worn over a compression stocking. The compression device can have a pulley based drive train that is driven by a motor to tighten and loosen compression elements, such as compression straps, in a precise, rapid, and balanced manner. Sensors can be used in the compression device and / or compression stockings to provide feedback to modulate the compression treatment parameters.

Methods and apparatus for providing rapid compression to at least one appendage positioned within an inflatable sleeve are disclosed. Rapid compression is provided by filling the inflatable sleeve containing the appendage with a gas. A portion of the gas is then repeatedly withdrawn and inserted back into the inflatable sleeve to apply a compression therapy to the at least one appendage.

A disposable sleeve for compression therapy, with at least one inflatable air cell defined between a first airtight wall adjacent a patient's body to be treated and a second airtight wall. Each of the first and second walls comprises an external porous layer and an internal layer comprising air-tight polyethylene (PE). The walls are bonded by molten portions of the PE internal layer penetrating and set in their corresponding external porous layers and welded to each other, the bonding enduring at least 250 inflation-deflation cycles associated with the therapy.

A connector apparatus includes first and second mating connectors that can be joined to make a fluid connection. The connectors are constructed to discriminate improper connectors so that no fluid tight connection can be formed with improper connectors. The connector apparatus can be used with a system for compression therapy to prevent deep vein thrombosis.

A combined heating, cooling, and compression therapy system is provided. The system is configured for automated use with a controller. The system can have a core with separate channels for providing cold and heat and compression therapy; a cover for receiving the core; and a skin sensitive temperature node attached to the core cover.

A method for providing a combined DVT and compression therapy to a patient is provided. The method includes providing a control unit configured to condition heat transfer fluid and to selectively provide a compressed gas, providing a thermal compression device that is mountable to a select portion of the patient, and programming the control unit to supply heat transfer fluid to the thermal compression device and to supply compressed gas to the thermal compression device.

Systems, devices and methods for providing active and / or passive compression therapy to a body part can include a compression device worn over a compression stocking. The compression device can have a pulley based drive train that is driven by a motor to tighten and loosen compression elements, such as compression straps, in a precise, rapid, and balanced manner. Sensors can be used in the compression device and / or compression stockings to provide feedback to modulate the compression treatment parameters.

An apparatus and method for treatment of patients suffering from lymphedema. The apparatus includes a multiple chamber sleeve positioned in a wrap around fashion on a body extremity to be treated. The chambers are sequentially inflated and maintained so until all chambers are inflated and then all the chambers are simultaneously deflated except the proximal end chamber to move edema fluids out of the afflicted area. The apparatus includes the capability of applying interferential therapy either alone or in combination with compression therapy. Advantageously, the sleeve chambers capture pressurized air when applied thereto, at designated locations, so as to form air pockets that can selectively apply isolated points of pressure, and in combination with the application of electrical current to a patient's affected area, provide effective lymphedema therapy without disrupting normal vascular and lymphatic functioning.

The present invention relates to a replaceable module for use with a thermal contrast therapy systems. The replaceable module may be an automated thermal contrast therapy module which includes a casing, a manual mixing valve, an automated mixing valve, an automated mixing valve actuator, a temperature sensor, and an interface. A cold and a hot fluid are mixed to generate a therapy fluid. The therapy fluid may be output to a therapy bladder. The second replaceable module is a compression therapy module which includes a casing, an air pump, a pneumatic solenoid, and a pressure monitor. The casing may include a pressurized air pathway including an air outlet. The pump may pressurize the air within the pathway, and the solenoid may regulate the air pressure using feedback from the pressure sensor. Additionally, a pressure relief valve may release pressure if it gets above a safety threshold. The compression therapy module may also include a fluid pathway.

A knitted garment (10) for the support and / or compression of parts of the body and / or for compression therapy is knitted in the shape of a tube (11, 12, 13, 14, 15, 16) using at least one elastic knitting thread and at least one elastic weft thread, at least in sections, on a flat bed knitting machine.

The present invention is directed to a device that provides thermal energy therapy, compression therapy and negative pressure therapy simultaneously and / or in conjunction with each therapy. The outcome of the present invention is that a patient's bodily fluids can be maintained, controlled, and / or adjusted with decreased medication dependence. Using these three therapies individually does not obtain these desired results of controlling, maintaining or adjusting the patient's bodily fluid. This combination of therapies is beneficial to the patient.

A device which combines pneumatic compression therapy and ultrasound based therapy for the prevention and treatment of thrombosis. Ultrasound transducers (11) are placed in specially designed pockets (12) in stockings (23) or leggings (25). This allows for convenient use of ultrasound therapy. Pneumatic compression is also carried out by air bladders (14) which are placed in leggings. The overall result is an easy to use device which should produce significantly better results in the prevention and treatment of thrombosis, ultimately reducing patient morbidity and mortality.

Disclosed is a monitoring system for determining the efficacy of at least one compression device for use in compression therapy. The monitoring system comprises at least one pressure sensor for measuring a pressure exerted onto a body part of a user by the compression device and at least one evaluation unit which is connectable to the pressure sensor. The evaluation unit is adapted to acquire at least one resting pressure prest with the user being in a resting position. The evaluation unit is further adapted to determine at least one extended standing pressure pstanding, extended with the user being in a standing position, by using the following procedure: the evaluation unit acquires a measurement curve of pressure values after a position change of the user into the standing position and a slope of the measurement curve is automatically compared to at least one endpoint threshold value and, depending on a result of the comparison, an endpoint of a change in the measurement curve induced by the position change is automatically detected, and a pressure value acquired at or after the endpoint is assigned to the extended standing pressure pstanding, extended.

A disposable sleeve for compression therapy, with at least one inflatable air cell defined between a first airtight wall adjacent a patient's body to be treated and a second airtight wall. Each of the first and second walls includes an external porous layer and an internal layer including air-tight polyethylene (PE). The walls are bonded by molten portions of the PE internal layer penetrating and set in their corresponding external porous layers and welded to each other, the bonding enduring at least 250 inflation-deflation cycles associated with the therapy.

A limb wound treatment device is described having a first end, a second end and an interior therebetween for accommodating a treatment gas. The device can include a flexible housing that can be inflated. The first end can include an inflatable cuff seal for hermetically sealing against the limb being treated. The second end can include a closed end or an access port that is releasably sealed with a clamping mechanism. Further, the device can include a controller that can inflate that housing, inflate the cuff seal and provide treatment gas to the interior, in response to pressures within the cuff seal and the housing. Further, the device can accommodate different types of wound treatments, such as hyperbaric therapy, compression therapy or negative pressure therapy.

A device for providing thermal treatment to a patient's hand is provided. The device includes a therapy component for applying thermal therapy, compression therapy, or both; a sleeve for receiving the therapy device and sized and shaped to cover the patient's hand; and a hand support for supporting the patient's hand in a relaxed state.

The subject of the present invention is a system for measuring contact surface pressure applied on the skin, especially for use in compression therapy, comprising a support member carrying a sensor comprising at least two sensors arranged separately on said support member. pressure sensors capable of measuring pressure applied at two predetermined locations; and an electronic system connected to said sensors and capable of obtaining values ​​simultaneously measured by these sensors, and each pressure sensor comprises preferably approximately a flat transforming element having a surface in contact with the skin at the site of use, the transforming element being in direct contact with the skin or via an intermediate layer of material covering this surface of the transforming element, the transforming element or The compressive elastic modulus of the intermediate layer measured when the surface is in contact with the skin is 30-500 kPa, preferably 80-400 kPa, more preferably 200-400 kPa. Uses: Compression therapy.

The present invention is directed to a specialized method of treating a severe diabetic ulcer that penetrates the subcutaneous fat layer of a patient. The method comprises the steps of: administering a treatment session to a diabetic patient having a severe diabetic ulcer, the treatment session comprising at least three pulsed electromagnetic fields (PEMF) applications, PEMF applications 1, 2, and 3, and at least two intermittent compression therapy (ICT) applications. The PEMF application and ICT therapy settings address specific factors that are necessary to induce healing of the diabetic ulcer and prevent amputation. In a preferred embodiment, the treatment session further comprises the step of applying a dressing having a silver and / or honey anti-infection composition thereon to the ulcer area to impede microbial growth in the ulcer area. In another embodiment, the method includes the step of applying ultrasound to the ulcer area for a time sufficient to inhibit microbial growth.

The present invention is directed to a specialized method of treating a severe diabetic ulcer that penetrates the subcutaneous fat layer of a patient. The method comprises the steps of: administering a treatment session to a diabetic patient having a severe diabetic ulcer, the treatment session comprising at least three pulsed electromagnetic fields (PEMF) applications, PEMF applications 1, 2, and 3, and at least two intermittent compression therapy (ICT) applications. The PEMF application and ICT therapy settings address specific factors that are necessary to induce healing of the diabetic ulcer and prevent amputation. In a preferred embodiment, the treatment session further comprises the step of applying a dressing having a silver and / or honey anti-infection composition thereon to the ulcer area to impede microbial growth in the ulcer area. In another embodiment, the method includes the step of applying ultrasound to the ulcer area for a time sufficient to inhibit microbial growth.

The invention relates to fitting of compression garment. Optimizing fit of a compression garment for use with a patient receiving compression therapy. Sensors formed on the garment detect characteristics of the fit of the garment in the vicinity of each sensor. The fit sensors may be capacitive disks imprinted on the garment. A controller computes overall fit of the garment on the patient based on signals from the sensors.

A method of operating a circulation facilitating assembly having a thermal treatment assembly having the steps of: providing pump assembly; placing a bladder of a first leg assembly in fluid communication with the pump assembly; placing a bladder of a second leg assembly in fluid communication with the pump assembly; placing a bladder of a thermal treatment assembly in fluid communication with the pump assembly, the thermal treatment assembly further comprising a thermal pad which is one of heated or cooled so that it is at a temperature other than ambient temperature; sequentially cycling at least one or both of the first leg assembly and second leg assembly, and, the thermal treatment assembly to complete a single cycle, comprising the steps of by: inflating the respective bladder to a predetermined pressure, holding the predetermined pressure for a predetermined period of time; and deflating the respective bladder.

A compression device (100) configured to provide compression therapy is provided. The compression device includes a wrap (101) having an outer face (105) defining a proximal edge (106), a distal edge (107), a first side edge (108), and a second side edge (109). The second side edge may include a plurality of attachment tabs (110,111,112). An index line (113) can be disposed on at least one of the plurality of attachment tabs. A measurement scale (114) can be disposed along the outer face. The measurement scale can include longitudinal boundaries (115,116) identifying a range within which the index line should position for the compression device to provide an appropriate fit for compression therapy when the compression device is wrapped about a patient's limb.