Abstract: Wound pads and systems and kits comprising wound pads whose total thickness can be modified by a user without the use of tools, comprising a plurality of separable layers having layer thicknesses less than the thickness of the wound pad. The wound pads may be used as wound fillers in the context of negative pressure wound therapy (also known as “vacuum treatment”, “reduced pressure” treatment).

Abstract: The present invention refers to a composition, comprising hemoglobin or myoglobin, wherein in at least 40% of said hemoglobin or myoglobin the oxygen binding site is charged by a non-O2 ligand, and at least one further ingredient, a method for preparing said composition and the use of hemoglobin or myoglobin charged with a non-oxygen ligand for external treatment of wounds.

Abstract: A method for preparing a composition for external treatment of wounds includes charging at least 90% of the oxygen binding sites of hemoglobin with carbon monoxide during or after isolation from its natural environment. The method further includes adding at least one further ingredient selected from the group consisting of electrolyte(s), preservative(s), stabilizer(s), anti-flocculant(s), anticoagulant(s), pH buffering agent(s), solvent(s), antioxidant(s), film-forming agent(s) and crosslinking agent(s). The method can further include packaging the composition, such as in an aerosol can.

Abstract: The present invention relates to a system and method for support and off-loading. The system includes an inner bladder filled with a flowable composition. An outer bladder filled with a flowable composition is positioned adjacent to the inner bladder. The composition of the inner bladder has greater flow characteristics than the composition of the outer bladder. The inner bladder micro-contours to the received body part and the outer bladder macro-contours to the inner bladder after the inner bladder is micro-contoured to the received body part. Alternatively, the system provides a pair of ultra low pressure plenums and a positioner. The patient body size and size and corresponding surface area of the positioner control the amount of gas which is displaced evenly against the walls of the ultra low pressure plenums.

Abstract: A medical dressing for application at a treatment area of a human body is provided. The dressing comprises a border area surrounding a central inspection area which is intended to be placed over said treatment area. The dressing also comprises a pad which may be arranged in the central inspection area and may be at least partly removed from the central inspection area for enabling visual inspection of the treatment area. There is also provided a medical dressing system and a method for reducing the workload for nursing personnel.

Abstract: A method of producing a hydrophilic polyurethane foam structure containing inert activated carbon particles, includes the steps of: (a) providing a water phase containing a surfactant and dispersed inert particles; (b) providing a isocyanate-terminated polyether having functionality of more than 2; (c) mixing the water phase and the isocyanate-terminated polyether, immediately transferring the resulting mixture to a mold or a continuous web, whereby a foam structure is obtained; and (d) drying the foam structure until it has a moisture content of at most 10% (wt). A foam structure produced by the method and a wound dressing containing the foam structure are also disclosed.

Abstract: The present invention pertains to antimicrobial compositions comprising inter alia at least one alkenyl- and/or alkynyl-substituted polysiloxane, at least one polysiloxane comprising silicon-bonded hydrogen atoms, and at least one hydrosilylation catalyst, as well as antimicrobial silicone gels, wound dressings, and methods of preparing the above.

Abstract: A wound care product is provided. It comprises a sealed chamber in which a wound care article is arranged around a support member in such a manner that a curved portion of the wound care article is in contact with the support member. The curved portion interconnects two other portions on opposite sides of the support member.

Abstract: The present invention relates to a suction device. The suction device comprises an attachment portion adapted to be attached to a wound cover member. The suction device comprises a fluid inlet which is at least partially circumscribed by the attachment portion. The suction device also comprises a fluid outlet. The suction device further comprising a connection portion adapted to, at least during one operation condition of the suction device, provide a fluid communication between the fluid inlet and the fluid outlet. The connection portion comprises an inspection portion that is transparent to thereby facilitate the positioning of the suction device relative to the wound cover member.

Abstract: A medical dressing is provided. The dressing has a central portion and a border portion, and comprises a backing layer, an adhesive body contact layer and a pad arranged in the central portion between the backing layer and the adhesive body contact layer. The pad is symmetric about a longitudinal center line and the dressing comprises a lobed portion on each side of the center line. The medical dressing comprises a gripping tab which is coplanar with the border portion and which projects outwardly from the border portion. The medical dressing may be used for pressure ulcer prevention, such as at the sacrum region of a human body.

Abstract: This relates to a wound therapy device, including an outer part and an inner part facing surface provided with an inner part facing opening, and a first connection channel to establish fluid communication between the inner part facing opening and a connector opening adapted to be connected to an external device. The wound therapy device can also be a part of a wound therapy arrangement, which can further include, a wound filler, an external device, a wound cover film, and tubing connections. Methods of using the wound therapy arrangement are also disclosed.

Abstract: Disclosed herein is a method of attaching a medical device to a surface, the medical device having at least one adhesive area, wherein the method comprises the steps of: contacting the surface with a composition comprising a T silicone resin and/or a DT silicone resin and/or an MQ silicone resin and/or an MT silicone resin, thereby providing non-tacky coating on the surface; and attaching the adhesive area to the surface such that the composition is located between, and in contact with, the surface and the adhesive area, thereby attaching medical device to the surface; thereby achieving an improve adherence between the medical device and the surface.

Abstract: The present invention provides a polymer fiber comprising a thermoplastic polymer comprising the following building blocks A and B: —O—(CH2—CH2—O)n— (A) —O—[CH2]y—O— (B), wherein n is an integer of 10-400, and y is an integer in the range of 2 to 16, wherein A is present in an amount of 15-30 mole %, B is present in an amount of 20-40 mole % and wherein building blocks A and B are linked by the following linking group C: —[(C?O)—NH—CH2—CH2—CH2—CH2—CH2—CH2—NH—(C?O)]— (C) wherein C is present in an amount of 45-55 mole %. The present invention further relates to a method for preparing a polymer fiber, absorbent articles comprising a polymer fiber and the use of a fiber in a product for treating wounds and/or burns.