Wound dressings including a skin contact layer and a cover layer removably adhered to the top surface of the skin contact layer are described. The skin contact layer includes a lower substrate extending around a central aperture and a lower adhesive. The lower substrate includes a top surface and a bottom surface opposite the top surface. The lower adhesive is disposed on the bottom surface of the lower substrate. The cover layer substantially covers the central aperture of the lower substrate, and includes an upper substrate and a backing layer. An upper adhesive is positioned between the top surface of the lower substrate and a bottom surface of the backing layer. In embodiments, the cover layer can be removed and changed while the skin contact layer remains adhered to the skin around a wound.

A suction-based medical dressing assembly and method of dermal irrigation provides a flexible tube that is fluidly coupled to at least two bifurcated tube portions defined by a plurality of apertures. The tube has a proximal end opening for discharging ambient fluid. The length of the bifurcated tube portions is surrounded by an absorbent gauze material covered substantially with an occlusive sheet material, and having an adhesive strip thereon. A vacuum assembly creates a negative pressure in the tubes. The ambient fluid is absorbed by the absorbent material, and the negative pressure sucks the fluid through the apertures in the bifurcated tube portions for discharge through the opening in the tube. In operation, a patient applies the adhesive side of the occlusive device to the skin where liquid removal is desired and activates the vacuum-inducing source, thereby causing fluid runoff from the patient to be effectively removed for disposal.

A device for protecting an umbilical stump-catheter interface, includes: a shield having a wall that defines a cavity for accommodating an umbilical stump, wherein the shield further includes a base for attachment to a patient; and an opening at the shield for allowing an umbilical catheter to extend therethrough. A method for protecting an umbilical stump-catheter interface, includes: providing a device having a shield with a wall that defines a cavity for accommodating an umbilical stump, wherein the shield further includes a base for attachment to a patient, and wherein the device further includes an opening at the shield; shielding the umbilical stump from an environment using the shield; and accommodating an umbilical catheter using the opening at the shield.

A barrier system is provided for use in reducing infections associated with post-operative surgical incision and/or a percutaneous medical device, such as a catheter, that is disposed within the surgical incision. Such a barrier system may include: a barrier device having a skin-contacting surface and a catheter-receiving surface; and an adhesive composition configured for adhering to skin, the barrier device, and/or the catheter so as to form a barrier at or adjacent to an incision in the skin where the catheter is percutaneously inserted through the skin. A tensioning anchor and associated system of two or more tensioning anchors is provided for post-operative wound closure. A method for applying and removing the barrier device and tensioning anchors is also provided.

A system for providing a force to a desired area on a curved body part of a person includes a dressing assembly shaped and configured to be placed on the desired area of the person, a releaseable circumferential member surrounding the curved body part that holds the dressing assembly against the desired area, a sealing subsystem for providing a fluid seal over the dressing assembly and the person's skin, and a reduced-pressure subsystem for providing a reduced pressure to the dressing assembly. When reduced pressure is supplied, the system generates the force against the desired area on the curved body part.

Systems and methods can promote wound healing, including a wound dressing having a wound-facing surface and a second surface. The wound-facing surface can be configured to contact a wound of a patient. There can also be at least one conduit having an interior lumen operably connectable to the second surface of the wound dressing, a central window configured to allow air flow from the interior lumen of the conduit to the wound-facing surface of the wound dressing, and a flexible wrap operably connectable to the conduit.

The invention relates to a flexible application aid for the treatment of wounds. The application aid can be used in particular for the debridement and/or cleansing of wounds, including the skin surrounding the wound. The application aid according to the invention including a flexible or elastically deformable application wand, facilitates debridement of superficial to deep wounds without the risk of injury to the wound.

A barrier system is provided for use in reducing infections associated with post-operative surgical incision and/or a percutaneous medical device, such as a catheter, that is disposed within the surgical incision. Such a barrier system may include: a barrier device having a skin-contacting surface and a catheter-receiving surface; and an adhesive composition configured for adhering to skin, the barrier device, and/or the catheter so as to form a barrier at or adjacent to an incision in the skin where the catheter is percutaneously inserted through the skin. A tensioning anchor and associated system of two or more tensioning anchors is provided for post-operative wound closure. A method for applying and removing the barrier device and tensioning anchors is also provided.

Skin compression devices are disclosed that are formed of a shape memory material and that have multiple tensioning members. Disposal of one or more skin compression devices on the skin of a subject increases the temperature of the shape memory material and causes the tensioning members to bend inward, thereby compressing the area of skin disposed between the tensioning members; this compression shields the compressed skin from tensile loading. Methods of production and use of the skin compression devices are also disclosed.

An appendage cover assembly includes cover 101 having a body that forms a cavity. The cover body is seamless and waterproof and has an upper portion adjacent an open end, a tip portion adjacent a distal end, and a central portion between the upper portion and the tip portion. The upper portion of the cover body is configured to selectively expand and contract in size larger and smaller than the size as compared to the other portions. The upper portion is configured to secure the cover to the appendage and/or bandage. The upper portion compresses onto the bandage away from the wound. The central portion avoids compression on the wound.