The present invention relates to a wound healing PVA sponge dressing using negative capillary pressure of the dressing material together with auxiliary negative pressure for wound treatment. The PVA sponge dressing is pretreated with gram positive and gram negative biocidal dyes for insertion into or over a wound. A negative pressure pump is mounted to the PVA sponge dressing to produce additional capillary pressure for withdrawing fluid or water vapor from the sponge dressing and a cover is mounted over the sponge material and negative pressure pump forming a unitary sealed package for placement over a wound.

The present invention relates to a sponge dressing for treating wounds comprised of a polymer sponge containing a plurality of antimicrobial dyes with at least one dye being gram positive and at least one other dye being gram negative and a silicon adhesive secured to a sponge surface. The sponge dressing can be exposed initially to gamma radiation and later sterilized by ethylene oxide or alternatively it can be sterilized by ethylene oxide and later irradiated by gamma radiation. The sponge dressing has a morphology characterized by an average pore throat diameter of 0.5-500 m and a porosity ranging from about 60% to about 99.5%. The sponge dressing can also contain at least one biofilm reducing agent, at least one chelating agent and an ionic and non-ionic surfactant.

(Object) To prevent a high compression portion from being defectively formed and also a top sheet from being torn. (Means of Achieving the Object) A sanitary napkin (1) in which a low compression portion (15) and a high compression portion (16, 17, 18) are formed on a bottom surface of a compressed groove (10) that is recessed from a skin contact surface side. The high compression portion includes regularly-arranged high compression portions (16) that are regularly arranged in a longitudinal direction of the compressed groove (10), a large-area high compression portion (17) that is irregularly arranged in the compressed groove (10) and has an area larger than an area of each of the regularly-arranged high compression portions (16), and an auxiliary high compression portion (18) that is arranged at one side, in a longitudinal direction of the napkin, of the large-area high compression portion (17) through the low compression portion (15) so as to surround the one side, in the longitudinal direction of the napkin, of the large-area high compression portion (17).

A system for treating a linear wound on a patient that has a closing dressing bolster for placing on the patient's epidermis over the linear wound, a sealing subsystem for providing a seal over the closing dressing bolster and the patient, and a reduced-pressure subsystem for delivering reduced pressure to the sealing subsystem. The sealing subsystem and reduced pressure subsystem are operable to deliver reduced pressure to the closing dressing bolster. The closing dressing bolster is operable under reduced pressure to develop a inward closing. The closing dressing bolster may include one or more closing members on each side of a center wound area to create the inward closing when under reduced pressure. A compressive force may also be developed. Other systems and methods are presented.

A wound dressing comprising a multi-ply knit fabric, where the fabric contains a first and a second knit ply. The first knit ply contains a plurality of first yarns and forms the upper surface of the fabric. The second knit ply contains a plurality of polytetrafluoroethylene (PTFE) yarns, where the PTFE yarns have a transmission in the IR region of 8-10 m at least about 40%, and a thermal conductivity of at least about 0.2 W/(m.Math.K) forms the lower surface of the fabric. The first ply and the second ply are integrated through combined portions formed by interlacing first yarns among the PTFE yarns of the second knit ply, interlacing PTFE yarns among the first yarns of the first knit ply, or interlacing a plurality of third yarns among the first yarns and the PTFE. The multi-ply knit fabric also contains a composition comprising at least one silver ion-containing compound.

A medical device comprising a device that covers at least a portion of a patient's skin and has an inner surface designed to be in contact with the patient's skin. It contains a multi-ply knit fabric that contains a first knit ply and a second knit ply. The first knit ply contains a plurality of first yarns and forms the upper surface of the fabric. The second knit ply contains a plurality of polytetrafluoroethylene (PTFE) yarns which forms the lower surface of the fabric. The first and second ply are integrated through combined portions formed by interlacing first yarns among the PTFE yarns, interlacing PTFE yarns among the first yarns, and interlacing a plurality of third yarns among the first and the PTFE yarns. The multi-ply knit fabric also contains a composition comprising at least one silver ion-containing compound on at least the upper surface of the multi-ply knit fabric.

Systems and methods for managing fluid absorption from a tissue site are described. A dressing having an absorbent is positioned proximate the tissue site to receive fluid from the tissue site. A reduced-pressure source is fluidly coupled to the dressing and supplies reduced pressure to the dressing. The reduced pressure is periodically decreased to distribute fluid in the absorbent and managed fluid absorption. The system includes a reduced-pressure source and a container having an upstream layer, a downstream layer, and an absorbent between the upstream layer and the downstream layer. The system also includes a sealing member for forming a therapeutic environment having the container and a controller configured to operate the reduced pressure source to intermittently supply reduced pressure to the therapeutic environment and periodically decrease the reduced pressure in the therapeutic environment.

A wound cleansing assembly, which includes or is a wound cleansing cloth (1), having at least one carrier layer (2) and threads (3) disposed on the carrier layer (2) and protruding from the carrier (2), preferably made exclusively of synthetic fibers, preferably plastic fibers.

A wound cover device can comprise a backing, a micro-structure device, and one or more of a wound dressing and a skin replacement layer. The backing can be stretchable The micro-structure device can comprise a plurality of fasteners, such as micro-staples, micro-pins, micro-barbs and the like, that can be used to attach the wound cover device to tissue such as skin. The micro-structure device can be stretchable to stretch with the backing. The micro-structure device can be configured such that the fasteners are positioned in a two-dimensional pattern or fill-in an interior portion of the wound dressing or skin replacement layer. The fasteners of the micro-structure device can extend through the wound dressing or skin replacement layer. The micro-structure device can additionally be placed around a perimeter or edge region of the backing.

The present invention relates to a fluid-permeable primary dressing in strip form, having pores, perforations or honeycomb lattices, which enable the passage of fluid, further having a coating of a material comprising silicone.