According to one aspect, a medical device may be configured to couple to a body. The medical device may comprise a material layer; a plurality of adhesive layers coupled to the material layer and configured to couple to a user's skin, wherein each adhesive layer of the plurality of adhesive layers includes a plurality of micro passages; a channel extending between two adjacent adhesive layers of the plurality of adhesive layers; and a superhydrophobic coating covering at least a portion of each of the two adjacent adhesive layers and the material layer forming the channel.

A system for detecting potential for infection includes a wound dressing and an electronics component. The wound dressing includes a temperature sensing layer and a cover layer comprising a substrate and a backing layer. The electronics component includes a power source, an electronic control unit (ECU), and a communications interface positioned within a housing and removably coupled to the temperature sensing layer of the wound dressing. The electronics component is configured to receive a plurality of temperature readings from the temperature sensing layer, and provide an indication of potential infection of the wound based the plurality of temperature readings. In various embodiments, each of the plurality of temperature readings corresponds to a temperature of an area around a wound. Methods for preventing infections using the system are also described.

A bandage includes a top film, an absorbent layer and a perforated adhesive lower layer positioned under the absorbent layer for adhering the bandage to a user's skin. The absorbent layer includes at least one incision that improves the flexibility of the bandage.

A dressing for a wound includes a drape, an absorbent core, and a wicking member. The drape can be configured to sealingly couple with a patient's skin surrounding the wound. The drape may enclose an inner volume of the dressing. The absorbent core layer may be positioned within the inner volume of the dressing. The wicking member is positioned within the inner volume, wherein the wicking member extends from an underside of the absorbent core layer to the drape. The indicator may be configured to fluidly couple with the wicking member through the drape and receive fluid from the wicking member. The indicator may be configured to provide a visual wound status indication in response to receiving fluid from the wound through the wicking member.

Embodiments disclosed herein are directed to negative pressure treatment systems and wound dressing systems, apparatuses, and methods that may be used for the treatment of wounds. In particular, some embodiments are directed to improved wound dressings comprising an obscuring layer that may hide fluid contained therein. Some embodiments may further comprise one or more viewing windows disposed therethrough so as to enable monitoring or examination of fluids contained therein.

A wound dressing is disclosed, the wound dressing comprising a first adhesive layer with a proximal surface configured for attachment of the wound dressing to the skin surface of a user; an absorbent core layer; an electrode assembly comprising a plurality of electrodes arranged on a distal side of the absorbent core layer, the electrode assembly comprising a plurality of sensor points distributed along a distal surface of the absorbent core layer; and a top layer on a distal side of the electrode assembly.

An absorbent component for a wound dressing comprises a stitch bonded nonwoven substrate wherein the nonwoven substrate is stitch bonded with an elastomeric yarn and wherein the nonwoven substrate comprises a superabsorbent material and/or a gelling material. Also disclosed is a method of manufacturing the absorbent component, a wound dressing or a negative pressure apparatus comprising the absorbent component and a method of treating a wound using said wound dressing or negative pressure apparatus comprising the absorbent component.

A dressing for the treatment of incisional wounds includes an upper cover, a patient interface layer, and an absorbent material. The upper cover is configured to substantially cover the incisional wound. The upper cover includes a drape and a plurality of spines coupled to the drape. The drape includes a first side and a second, wound-facing side. The patient interface layer is coupled to the second side of the drape and includes a plurality of openings that are configured to receive fluid from the incisional wound. The absorbent material is disposed between the second side of the drape and the patient interface layer.

Disclosed embodiments relate to apparatuses and methods for wound treatment. In certain embodiments, a negative pressure wound therapy apparatus can include a wound dressing with a spacer layer separated from the absorbent layer by intermediate layers or drapes. The wound dressing can include a first portion comprising a wound contact or tissue contact layer, a first spacer layer, and a first backing layer comprising a first aperture. The spacer layer can be positioned between the contact layer and the first backing layer. The dressing can have a second portion comprising an intermediate drape with a second aperture, an absorbent layer, and a second backing layer. The absorbent layer is positioned between the intermediate drape and the second backing layer. The first aperture and the second aperture are configured to be sealed and allow fluid communication between the first portion and the second portion of the wound dressing.

Disclosed embodiments relate to apparatuses and methods for wound treatment. In certain embodiments, a negative pressure wound therapy apparatus can include a wound dressing with a spacer layer separated from the absorbent layer by intermediate layers or drapes. The wound dressing can include a first portion comprising a wound contact or tissue contact layer, a first spacer layer, and a first backing layer comprising a first aperture. The spacer layer can be positioned between the contact layer and the first backing layer. The dressing can have a second portion comprising an intermediate drape with a second aperture, an absorbent layer, and a second backing layer. The absorbent layer is positioned between the intermediate drape and the second backing layer. The first aperture and the second aperture are configured to be sealed and allow fluid communication between the first portion and the second portion of the wound dressing.