Abstract: An item of clothing is adapted to be worn against the skin, and having at least one panel adapted to provide targeted compression of at least 20% of the total length of a specific surface vein in the body, or adapted to provide targeted compression of at least 20% of a specific plexus of veins, a specific lymphatic plexus, drainage plexus or a collection of lymphatic vessels. The clothing is useful in a method of reducing recovery time in a human or other mammal, after a period of activity and in a method of enhancing performance, in particular sports performance, in a human or other mammal. It may also improve the conditioning of the skin and aid lymphatic drainage, and can be used in the treatment of certain medical conditions.

Abstract: A band (1) comprising, on its inner surface, an irregular array of tacky areas or protrusions (6) that dissipate foci of stress in the skin (of the abdominal wall or other body areas). Wearing such a band around the abdomen is intended to help prevent the occurrence of stretch marks.

Abstract: An item of clothing is adapted to be worn against the skin, and comprises at least one panel adapted to provide targeted compression of at least 20% of the total length of a specific surface vein in the body, or adapted to provide targeted compression of at least 20% of a specific plexus of veins, a specific lymphatic plexus, drainage plexus or a collection of lymphatic vessels. The clothing is useful in a method of reducing recovery time in a human or other mammal, after a period of activity and in a method of enhancing performance, in particular sports performance, in a human or other mammal. It may also improve the conditioning of the skin and aid lymphatic drainage, and can be used in the treatment of certain medical conditions.

Abstract: An item of clothing is adapted to be worn against the skin, and comprises at least one panel adapted to provide targeted compression of at least 20% of the total length of a specific surface vein in the body, or adapted to provide targeted compression of at least 20% of a specific plexus of veins, a specific lymphatic plexus, drainage plexus or a collection of lymphatic vessels. The clothing is useful in a method of reducing recovery time in a human or other mammal, after a period of activity and in a method of enhancing performance, in particular sports performance, in a human or other mammal. It may also improve the conditioning of the skin and aid lymphatic drainage, and can be used in the treatment of certain medical conditions.

Abstract: An item of clothing is adapted to be worn against the skin, and comprises at least one panel adapted to provide targeted compression of at least 20% of the total length of a specific surface vein in the body, or adapted to provide targeted compression of at least 20% of a specific plexus of veins, a specific lymphatic plexus, drainage plexus or a collection of lymphatic vessels. The clothing is useful in a method of reducing recovery time in a human or other mammal, after a period of activity and in a method of enhancing performance, in particular sports performance, in a human or other mammal. It may also improve the conditioning of the skin and aid lymphatic drainage, and can be used in the treatment of certain medical conditions.

Abstract: A sensor suitable for measuring the pressure applied by a bandage, the sensor being in the form of an elongate strip having a plurality of pads arranged along its length, wherein the sensor includes a connection to each pad, whereby the pressure applied to each pad can be determined independently, wherein each pad is inflatable to form an expanded pad protruding above the surface of the strip, and deflatable so that it does not impede removal of the sensor from the bandage. Such a sensor is primarily intended for single use, i.e. is disposable.

Abstract: A sensor suitable for measuring the pressure applied by a bandage, the sensor being in the form of an elongate strip having a plurality of pads arranged along its length, wherein the sensor includes a connection to each pad, whereby the pressure applied to each pad can be determined independently, wherein each pad is inflatable to form an expanded pad protruding above the surface of the strip, and deflatable so that it does not impede removal of the sensor from the bandage. Such a sensor is primarily intended for single use, i.e. is disposable.

Abstract: An item of graduated compression hosiery additionally comprises a compression panel adapted to provide targeted compression of one or more of the sites for perforating vein communication between the superficial and deeper vein systems in the lower leg.

Abstract: A band (1) comprising, on its inner surface, an irregular array of tacky areas or protrusions (6) that dissipate foci of stress in the skin (of the abdominal wall or other body areas). Wearing such a band around the abdomen is intended to help prevent the occurrence of stretch marks.

Abstract: A method of profiling skin comprises comparing the rugosity and/or the length of rete ridges beneath the skin relative to a length of skin and optionally also the relative thicknesses (or volumes) of the dermis and the epidermis. The method allows for determination of the ability of a cosmetic formulation to hydrate or “plump” skin.

Abstract: A device which comprises an enclosure of a plastics material, having an opening at an end thereof with fastening means to enable the opening to be closed around a limb or stump with an affected part contained within the enclosure, and including a fluid-absorbent material within the enclosure. The device is particularly suitable for use in the treatment of leg ulcers.

Abstract: Vascular endothelial growth factor (VEGF) has utility in the treatment of intimal hyperplasia, hypertension and atherosclerosis, and of conditions susceptible to treatment with agents that produce nitric oxide or prostacyclin. Instead of VEGF, an equivalent agent such as an agonist of VEGF receptors may be given, as may nucleic acid encoding such an agonist. The agent may successfully be administered via the adventitial surface of a blood vessel, e.g. using a device which defines a reservoir between the body wall and the vessel's adventitial surface, the reservoir being at least part-filled by a pharmaceutical formulation containing the agent to be delivered.

Abstract: A surgical clip (5) is provided for clipping a tubular structure (9) in vivo to ligate the tubular structure. The clip comprises first and second clip portions (6, 7). A hinge portion (8) is provided connecting the clip portions together and to enable the clip portions to be hinged together from an open clip condition to a closed clip condition thereby to ligate a tubular structure placed between the clip portions. A lock is provided for locking the clip portions together in the closed clip condition. In the closed clip condition the clip has a substantially smooth external profile, for example including blunt ends (21), so as to reduce the possibility of the clip (in use) eroding surrounding tissue structures.

Abstract: An illuminated medical instrument comprises an insertion portion (1) for insertion into a body opening and defining an elongate passageway (2), the passageway extending along a longitudinal axis (3) and having a proximal end (4) and a distal end (5). An obturator (19) is fitted into the passageway (2). A light emitting structure (7) has a distal end arranged to direct light from the insertion portion (1) into the body opening. The obturator (19) is movable in the passageway (2) between a first position within the passageway and a second position proximal of the first position and is constructed and arranged so that when in its first position it substantially covers in the direction of the longitudinal axis the distal end of the light emitting structure (7).

Abstract: An implantable prosthesis intended, primarily for the repair of muscle wall defects such as occur in inguinal hernias is fabricated from a surgically compatible mesh material having a prismatic external mesh wall (1). The prismatic shape includes three lobes (2), providing a generally triangular cross-sectional shape. The shape is maintained by internal reinforcing ribs (3), which here extend the length of the prism. The ribs are formed through the connection of three individual mesh strips (4), with each rib comprising two strip parts forming a lamination extending the length of the prism. With this construction closure of elongate legions is readily achieved and a wide range of elongate shapes and dimensions of hernias can be treated.

Abstract: A device which comprises an enclosure of a plastics material, having an opening at an end thereof with fastening means to enable the opening to be closed around a limb or stump with an affected part contained within the enclosure, and including a fluid-absorbent material within the enclosure. The device is particularly suitable for use in the treatment of leg ulcers.

Abstract: An endoluminal prosthesis is provided for use in the treatment of a dilation in a body vessel. This dilation might be an abdominal aortic aneurysm or a dilation in a blood vessel wall following a balloon angioplasty procedure. The prosthesis comprises a radially expandable tubular member and a covering provided on the outer surface of the tubular member. The covering comprises first and second layers of material. The first layer comprises an agent that promotes swelling of the covering on exposure of the covering to contact with body fluid, such as blood. The second layer comprises space-filling material. When the prosthesis is delivered into the body vessel the tubular member can automatically expand or be expanded radially. The covering will also swell on the tubular member. This expansion and swelling forces the exterior of the swollen covering into intimate sealing contact with the surrounding inner wall of the vessel.

Abstract: An illuminated medical instrument comprises an insertion portion (1) for insertion into a body opening and defining an elongate passageway (2), the passageway extending along a longitudinal axis (3) and having a proximal end (4) and a distal end (5). An obturator (19) is fitted into the passageway (2). A light emitting structure (7) has a distal end arranged to direct light from the insertion portion (1) into the body opening. The obturator (19) is movable in the passageway (2) between a first position within the passageway and a second position proximal of the first position and is constructed and arranged so that when in its first position it substantially covers in the direction of the longitudinal axis the distal end of the light emitting structure (7).

Abstract: A device (10) is provided for use in reinforcing a boundary wall of a patient's abdominal cavity at a site at which a portion of the patient's alimentary tract passes through that boundary wall. The device comprises a collar portion (11) for extending, in use, around the alimentary tract (17) at the approach of the alimentary tract to the interior of the boundary wall at said site. The device also comprises a plurality of petal-like elements (12) extending from the collar portion (11), said elements being arranged so as to extend, in use, outwardly with respect to the longitudinal axis of the portion of the alimentary tract passing through the collar portion and to be attached, in use, to the interior of the boundary wall around said side. The device is preferably, but not exclusively, for use in the prevention or treatment of parastomal herniation in patients having a colostomy or ileostomy or the like.

Abstract: Vascular endothelial growth factor (VEGF) has utility in the treatment of intimal hyperplasia, hypertension and atherosclerosis, and of conditions susceptible to treatment with agents that produce nitric oxide or prostacyclin. Instead of VEGF, an equivalent agent such as an agonist of VEGF receptors may be given, as may nucleic acid encoding such an agonist. The agent may successfully be administered via the adventitial surface of a blood vessel, e.g. using a device which defines a reservoir between the body wall and the vessel's adventitial surface, the reservoir being at least part-filled by a pharmaceutical formulation containing the agent to be delivered.