Provided are systems, dressings, and methods suitable for treating a tissue site, such as an incision or linear wound. The systems, dressings, and methods relate to a dressing assembly that may include a dressing bolster, sealing members that cover the tissue site and contain the dressing bolster, and a dressing attachment device. The dressing assembly also includes a base layer comprising a sealing member and a base attachment device for releasably coupling the base layer to the epidermis, wherein the dressing attachment device that may releasably coupled to the sealing member base layer. The dressing assembly may also include sealing ring that may be adapted to provide a fluid seal around the tissue site, and to absorb fluids from the tissue site. Other systems, apparatuses, and methods are disclosed.

An adhesive wound dressing is disclosed herein. The adhesive wound dressing comprises a first layer that is an outer layer. A second layer is a resilient layer and affixed to an inner surface of the first layer. A third layer is an inner gauze dressing and affixed to an inner surface of the second layer, wherein the first layer, the second layer, and the third layer define a generally tubular configuration having an open end and a closed end. An adhesive layer may be applied adjacent to the open end for configured securing the adhesive wound dressing to a wounded body part subsequent to the wounded body part being inserted within the open end.

The base of this bandaging system is attached to the skin around a wound by adhesive and supports the edges of the lid, which covers the wound and can easily be removed and replaced or re-used many times to facilitate examining or treating the wound while the base remains in place. The bandaging system has multiple embodiments to accommodate various situations. An embodiment with generally planar components is very simple but may cause vertical pressure on the skin near the wound when the lid is removed or attached. Such pressure is avoided by alternative embodiments in which the components have non-planar parts. Some embodiments have a hinge on an edge of the lid which allows the wound to be uncovered without detaching the lid. The components which latch lids to bases contribute to making the systems easy, quick, convenient, and comfortable to use.

A citric acid containing dressing for treating a tissue site with negative pressure may comprise a cover, a manifold, and a perforated polymer film and/or a sealing layer. The sealing layer can be a perforated silicone gel having a treatment aperture. The dressing can further contain an adhesive. The cover, the manifold, and the perforated polymer film and/or the sealing layer may be assembled in a stacked relationship with the cover and the sealing layer enclosing the manifold. Citric acid may be present on or incorporated in, for example, the perforated polymer film and/or the sealing layer.

A system of contactless adhesive bandages is taught that are customizable to extend and cover, but not touch, wounds that are long and/or curving. The system of contactless adhesive bandages comprises one or more sectional raised adhesive bandages sealed off at the ends of runs by end sectional raised adhesive bandages. The system of contactless adhesive bandages is preferably applied contiguously in an overlapping fashion to follow the contours of the wound.

A raised adhesive bandage is taught that covers but does not contact the wound. The raised adhesive bandage comprises a strip having an upper surface and a lower surface. An adhesive is at least partially disposed on the lower surface. A pad is disposed on the adhesive and/or lower surface. Raised edges are disposed on the pad creating a hollowed-out area. Raised edges are dimensioned such that they and the pad are not in contact with the wound.

A bandage and method of coupling the bandage to a skin of a patient. The method comprises placing an opening of a bandage over a wound. The bandage comprises a base substrate, a mechanical coupling system, and the opening. The base substrate includes an inner surface, an outer surface, a first side edge, and a second side edge. The mechanical coupling system includes a first mechanical coupling member disposed proximate to the first side edge of the base substrate and a second mechanical coupling member disposed proximate to the second side edge of the base substrate. The first and second mechanical coupling members each includes a plurality of gripping structures to hold a wound together. The opening is disposed through the base substrate, the opening being also disposed between the first and second mechanical coupling members.

A periocular dressing includes a base layer composed of a nonwoven material; a top layer having a composition bound to a polyurethane film, the composition including a hydrogel with a percentage by weight of bacitracin, the top layer to come into contact with a user's skin; and a removable membrane secured over the top layer and to be removed; the polyurethane film of the top layer is adhesively secured to the base layer; and the top layer promotes vasoconstriction and antibacterial properties.

A transparent dressing includes a portion without adhesive to allow placement over a catheter to reduce any effect of placing and positioning of a catheter at the time of removal of the dressing. The transparent dressing may include at least one tab for handling and removing the dressing, the at least one tab being positioned on at least one outer edge of the dressing.

A skin patch for the UV protection is contemplated as being formed from a vulcanized silicone substrate, an adhesive gel coating adhered to the internal surface of the silicone substrate, and a release liner removably attached to the adhesive gel coating, wherein following removal of the release liner from the adhesive gel coating, the coating is operative to enable adherence of the skin patch to skin. The skin patch is further contemplated as being operative to at least partially absorb solar ultraviolet radiation via the vulcanized silicone substate or the adhesive coating additionally comprising at least one UV-blocking compound having an absorption peak in the ultraviolet spectrum.

In some illustrative examples, a medical drape suitable for treating a tissue site may include an adherent surface including first adherent force profile oriented along a first axis and a second adherent force profile oriented along a second axis. The first adherent force profile may have an average force less than an average force of the second adherent force profile. Other apparatuses, systems, and methods are also provided.