1452results about "Feet bandages" patented technology

A modified vacuum assisted wound closure system adapted for concurrent applications of phototherapy having a foam pad for insertion substantially into the wound site and a wound drape for sealing enclosure of the foam pad at the wound site. The foam pad includes an optical pigtail, whereby desired wavelength of light may be directed into and about the wound site. The foam pad is placed in fluid communication with a vacuum source for promotion of fluid drainage. The foam pad is made of a highly reticulated, open-cell polyurethane or polyether foam for good permeability of wound fluids while under suction and is also embedded with an optical pigtail. The optical pigtail comprises an optical fiber that has been formed to fan into a plurality of sections. The fibers of the most distal fanned sections, which are implanted in the foam pad at its base, are provided with tiny optical slots, oriented away from the foam pad and toward the wound site. Each optical slot is made by stripping the cladding from the optical fiber in the desired areas of the fanned sections to form slot radiators. Because it is necessary to trim the foam pad in preparation for therapy, the optical fibers comprise plastics, such as acrylic or styrene. Upon placement of the pad, having the optical pigtail embedded therein, the wound drape is firmly adhered about the VAC therapy suction hose as well as the extending optical fiber to prevent vacuum leakage.

An instrument access device (500) comprises a distal O-ring (11) for insertion into a wound interior, a proximal member for location externally of a wound opening and a sleeve (12) extending in two layers between the distal O-ring (11) and the proximal member. The proximal member comprises an inner proximal ring member (25) and an outer proximal ring member (24) between which the sleeve (12) is led. A seal housing (300) is mounted to the inner proximal ring member (25). A gelatinous elastomeric seal (302) with a pinhole opening (303) therethrough is received in the housing (300). An instrument may be extended through the seal (302) to access the wound interior through the retracted wound opening in a sealed manner.

A device is provided for compression of objects such as parts of the body. The device has the form of a band that can be shaped like a sleeve, wrap or garment that is sized to encircle the body part or other compressible object and having a component or components made of an elastic material. Indicia such as tick marks or scales are printed on the device. The stretch of the elastic material as the device is tensioned around the body part causes increased separation of the indicia or movement of a free end of the band with respect to the indicia. A system measures the separation of the indicia and converts it to compression as a function of the circumference of the body part. The system may be a card having edges with measurement scales or the scales may be printed on the device and the displacement of a free end of a band or sub-band of the device with respect to the scales indicates the compression for particular circumferences of the body part. The device may have additional scales printed on it for measuring the circumference of the body part.

A method, and apparatus (10) for the controlled acceleration, and / or retardation of the body's inflammatory response generally comprises a foam pad (11) for insertion substantially into a wound site, a heating, a cooling pad (13) for application over the wound site (12), a wound drape (14) or sealing enclosure of the foam pad (11), the heating, and cooling pad (13) at wound site (12). The foam pad (11) is placed in fluid communication with a vacuum source for promotion of the controlled acceleration or retardation of the body's inflammatory response. The heating, and cooling provision controls the local metabolic function as part of the inflammatory response.

An apparatus includes a pressure housing configured to be coupled to a vacuum source and a diaphragm sealingly coupled to the pressure housing. The diaphragm is configured to move in response to the vacuum source. A magnet is coupled to the diaphragm. A magnetic switch is disposed opposite the magnet and is configured to be actuated by the magnet when the magnet is a predetermined distance from the magnetic switch. The magnetic switch is configured to selectively actuate the vacuum source.

A method and apparatus for the introduction to a wound under negative pressure therapy of a wound healing agent, generally comprises a foam pad (11) for insertion substantially into a wound site (12), and a wound drape (13) for sealing enclosure of the foam pad at the wound site. The foam pad is placed in fluid communication with a vacuum source for promotion of fluid drainage. Additionally, the foam pad is predisposed, through grafting or other techniques known to those of ordinary skill in the art, with basic fibroblast growth factor (bFGF), anti-microbial or other factors, also known to those of ordinary skill in the art, for the promotion of increased wound healing.

Provided is a smart garment for measuring a physiological signal which can improve comfort and convenience of wear and correctly measure a physiological signal. The smart garment for measuring physiological signals includes an electrode which is made of an electro-conductive fabric and detects a physiological signal, a physiological signal transmission line through which the detected physiological signal is transmitted, a physiological signal measuring unit which is connected to the transmission line, receives the physiological signal, and measures information regarding body conditions related to the physiological signal, and a pocket where the physiological signal measuring unit in inserted.

A wound treatment dressing for applying negative pressure wound therapy to a wound of an extremity, such as on the heel of a foot. The dressing comprises a fluid manifold 14 positioned within a fenestrated drape 16 to form a contoured occlusive wrapping 10 for placement over a wound on an extremity. A contoured porous pad 26 is placed adjacent or within the wound, such that the contoured pad 26 is enveloped by the occlusive wrapping 10. Flexible tubing 42 is attached to or through a fluid communication port 18, which forms an opening to the outer layer 16b of the occlusive wrapping 10, so as to allow for fluid communication of negative pressure to the contoured pad 26 from a source of negative pressure 44 connected to an opposite end of the flexible tubing 42. The negative gauge pressure is communicated from the source 44, through the tube 42, through the fenestrations 19 of the occlusive wrapping 10, such that negative gauge pressure is applied to the wound on the extremity. The fluid manifold 14 serves to direct the negative pressure from a position away from the wound site to the contoured pad 26 at the wound site.

The device comprises a rigid former reproducing the volume of a portion of the body and suitable for receiving the compressive orthosis. The former (10) incorporates a plurality of sensors (22) distributed over various points of the former and configured in such a manner as to avoid significantly modifying the surface profile of the former, the sensors essentially measuring the pressure applied locally on the former by the orthosis at the location of the sensor and perpendicularly to the surface of the former. Advantageously, at the location of the measurement point, each sensor comprises a thin wall capable of being subjected to microdeformation under the effect of the pressure applied by the orthosis, and means such as a strain gauge bridge, for example. The thin wall can constitute a portion of a support pellet which is fitted to the former in such a manner that its outside surface, which includes the thin wall, is flush with the outside surface of the former.

A therapeutic compression garment made of flexible, foldable, light weight Velcro-type loop fabric having a central region for wrapping partially around a body part and a plurality of bands integrally connected to the central region and extending outwardly in opposite directions from both sides of the central region to cross each other and encompass the body part.

The present invention provides a method of treating a leg ulcer comprising contacting the leg ulcer with a collagen biofabric. The leg ulcer may be a venous, arterial, diabetic or decubitus (pressure) ulcer. The invention further provides kits comprising one or more pieces of collagen biofabric for the treatment of a leg ulcer.

The invention relates to a wound dressing, a method of manufacturing a wound dressing, and in particular to a material for use as and in a wound dressing. A wound dressing can comprise a material movable between an initial conformation and an expanded conformation resulting from applying an extensive force to the material, such that removal of the extensive force can cause a contraction of the material toward a center of a wound. In addition, the wound dressing can comprise a retaining mechanism removably coupled to the material and configured to retain the material in the expanded conformation.

A therapeutic compression garment made of flexible, foldable, light weight Velcro-type loop fabric having a central region for wrapping partially around a body part and a plurality of bands integrally connected to the central region and extending outwardly in opposite directions from both sides of the central region to cross each other and encompass the body part.

A suspension walker having a hard, outer boot shell with upright brace members attached on either side and a soft boot receivable thereon. The soft boot has a main pad in it with a removable, fitting pad or pads on top of the main pad. A cuff member is also provided that is securable to the patient's calf and to the upright brace members. In use, the fitting pad is removed during the initial fitting and subsequent uses to suspend the patient's foot in the walker. The cuff member is also infinitely adjustable along the brace members to vary the fit as desired.

A compression garment for selective application for treatment of lymphedema and prevention of local ischemia of tissues at various locations of the body. The garment includes a pair or series of layers of hermetically sealed material, that can capture pressurized air, when applied therein, and is formed through the patterned sealing of the layers of the garment together, at select locations, to form air pockets that can selectively apply isolated points of pressure to the patient's affected area, without disrupting normal vascular and lymphatic functioning. The garment is design cut, for application to various segments of the body, and applies encompassing pressure over the entire affected area, and includes valves that can allow for the injection of measurable air, to the desired pressure points, or its deflation, after treatment. The compression device of this invention may also be formed as a segmented pad or mat, into which pneumatic pressurized air may be applied, at various segments, so as to regulate the amount of pressure applied to the surface of the body that is in contact with the pad or mat of this invention.

A thermal treatment garment of the present invention includes an outer structure layer formed of a pliable material, an interior lining formed of a gel material which directly contacts the wearer skin and a thermal treatment layer to thermally treat and control temperature of the interior lining. The thermal treatment layer heats and / or cools the gel material to a desired temperature and is typically disposed between the structure and gel layers. The thermal treatment layer is controlled by a controller that receives a user-specified or desired temperature. An intervening layer can be disposed between the thermal treatment and structure layers. The intervening layer secures the structure, thermal treatment and / or gel layers to each other and can be an elastomeric material to which the gel and / or thermal treatment layers readily adhere. The garment may be adjustable in size to snugly fit body parts of users in a range of body sizes.

A compression garment includes a backing member with a proximal end portion and opposed distal end portion. The backing member is configured to be disposed about at least a portion of a lower leg between calf and heel and has an inner surface to be disposed facing the lower leg, and an opposite outer surface. The garment further includes at least one compression bladder disposed within the backing member configured to compress at least a portion of the lower leg to augment venous return flow in the lower leg, an elevation member operatively coupled to the backing member and configured to elevate the heel from an underlying support surface and at least one support member disposed along a portion of the elevation member and along a portion of the backing member to retain the elevation member in a desired position with respect to the backing member to elevate the heel.

A cast or support assembly includes inner double knit padding material in which the outer layer is woven or knit to have substantial size openings, while the inner layer of the double knit material to be located against the skin of the patient is more closely woven or knit. Additional casting fabric is also provided, with this casting fabric being impregnated with water hardenable material. The outer casting fabric may include openings extending through it, so that the entire cast assembly has ventilation openings allowing air circulation to accomplish rapid drying following wetting of the assembly by sweat, rain, or by swimming, for example.

A health monitoring and management device, system, and / or method can include a sensor adapted to detect changes in one or more health indicators and transmit data related to the health indicators. The system can further include an interventional element adapted to receive a health intervention command and provide a health intervention related to the health indicators. The system can further include a microprocessor adapted to receive and analyze the health indicator data transmitted by the sensor, formulate the health intervention command related to the health indicator data according to pre-determined parameters, and transmit the health intervention command to the interventional element. The health intervention command can be transmitted to the interventional element within a clinically relevant time period.

A close-fitting, compression garment is described for providing adjustable compressive force over a surgical site in the dorsocervical region of the human body below the neck, above and between the shoulder blades of the upper back. The vest body portion of the invented garment has graduated or increasing elasticity encircling the upper torso and shoulder region of the body. Wide adjustable elastic pressure bands pressure anchored at the dorsocervical apex at the back of the vest stretch over the shoulders of the patient and adjustably anchored to anchor strips secured to the front chest surface of the vest for establishing compression over a surgical site in the dorsocervical region during recovery as needed both for rehabilitation and comfort.

A compression garment for selective application for treatment of lymphedema and related illnesses manifested at various locations of the body. The garment includes a pair or series of layers of hermetically sealed material, that can capture pressurized air, when applied therein, and is formed through the patterned sealing of the layers of the garment together, at select locations, to form air pockets that can selectively apply isolated points of pressure to the patient's affected area, without disrupting normal vascular and lymphatic functioning. The garment is design cut, for application to various segments of the body, and applies encompassing pressure over the entire affected area, and includes valves that can allow for the injection of measurable air, to the desired pressure points, or its deflation, after treatment.