Abstract: A wound dressing includes a hydrophilic foam layer, a plurality of wicking strips, and a drape layer. The hydrophilic foam layer is configured to engage a wound bed and has a first side and a second side, the second side configured to face the wound bed. The plurality of wicking strips also have a first side and a second side, the second side configured to face the first side of the hydrophilic foam layer. The drape layer also has a first side and a second side, the second side configured to face the first side of the plurality of wicking strips. One or more of the plurality of wicking strips also have a removable tab, wherein the tab extends beyond a periphery of the wound dressing.

Abstract: A dressing includes a first felted foam layer, a superabsorbent material printed on the first felted foam layer, and a second felted foam layer coupled to the first felted foam layer. The superabsorbent material is confined between the first felted foam layer and the second felted foam layer.

Abstract: A system for providing reduced-pressure treatment to a moveable tissue site, such as a joint, includes a flexible dressing bolster. The flexible dressing bolster has a first side and a second, inward-facing side, and a plurality of flexion joints formed on the flexible dressing bolster. The system further includes a sealing subsystem for providing a fluid seal over the flexible dressing bolster and the patient's epidermis and a reduced-pressure subsystem for delivering a reduced pressure to the sealing subsystem. The sealing subsystem and reduced-pressure subsystem are operable to deliver a reduced pressure to the moveable tissue site. The flexible dressing bolster is operable to allow articulation or movement of the moveable tissue site. The sealing subsystem may include a drape with folds. Other systems, apparatuses, and methods are presented.

Abstract: A dressing assembly for use with a reduced pressure treatment system, the dressing assembly develops a directed force under reduced pressure. The directed force may be a radial force or a closing force. The dressing assembly includes a shaped dressing bolster having a shaped extremity that is operable to evenly deliver the radial force and to distribute reduced pressure. Numerous shapes may be used for the shaped extremity. The dressing assembly may further include an over-drape to assist in creating a seal over the shaped dressing bolster and against a portion of a patient's epidermis.

Abstract: Systems, apparatuses, and methods for providing negative pressure and/or instillation fluids to a tissue site and sensing properties of fluids at a tissue site are disclosed. Systems, apparatuses, and methods for wirelessly activating and pairing a sensing device with a wireless communication device and/or therapy device to transfer sensor data from the tissue site is also disclosed.

Abstract: A reduced-pressure system for treating tissue, such as damaged subcutaneous tissue, includes a shaped dressing bolster for placing on the patient's epidermis and substantially sized to overlay the damaged subcutaneous tissue. The system further includes a sealing subsystem for providing a fluid seal over the shaped dressing bolster and a portion of the patient's epidermis, and a reduced-pressure subsystem for delivering a reduced pressure to the sealing subsystem. The reduced-pressure system may develop a force, which may include a vertical force that is realized at tissue site deeper than the epidermis or a closing force directed towards the incision. The shaped dressing bolster is shaped to evenly distribute the force. Other methods and systems are included.

Abstract: Tissue dressing materials and associated methods of forming such dressing materials are disclosed. In one example embodiment, a dressing material may include a foam and a film formed on a first side of the foam. The film may be integrally-formed on the side of the foam. The film may include a plurality of apertures. A method of making the dressing material may include placing a pre-polymer mixture and water into a mold to create the dressing material comprising a foam and an integral film on at least one surface of the foam. The method may further include forming a plurality of openings in at least the integral film, with the openings being formed within the mold or subsequent to removal of the dressing material from the mold.

Abstract: A system or apparatus including a dressing, a dressing interface, and a humidity sensor may be suitable for use with systems and methods for treating a tissue site. Embodiments of the apparatus are provided for treating a tissue site with reduced pressure provided by a source of reduced pressure. The dressing may include abase layer, a sealing member disposed proximate the base layer to define an enclosure providing a sealed space over the tissue site, and an absorbent member disposed within the enclosure. The dressing interface may comprise a reduced-pressure port configured to be coupled to the source of reduced pressure and a therapy port covered by a hydrophobic filter defining a reduced-pressure pathway between the hydrophobic filter and the source of reduced pressure.

Abstract: 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.

Abstract: The illustrative embodiments described herein are directed to systems, methods, and apparatuses for applying a reduced pressure to a subcutaneous tissue site. In one instance, a manifold for applying reduced pressure to a subcutaneous tissue site includes a plurality of first conduits, each of the plurality of first conduits having a wall with at least one first aperture and at least one second aperture. At least one of the plurality of first conduits is operable to deliver reduced pressure to the subcutaneous tissue site. The plurality of first conduits is coupled in a spaced arrangement that forms an interior space. The manifold further includes a second conduit comprising the interior space and formed by a portion of each wall of the plurality of first conduits. The second conduit is in fluid communication with the plurality of first conduits via the at least one second aperture.

Abstract: A system for negative-pressure therapy is described. The system includes a dressing configured to be positioned adjacent a tissue site and a piezoelectric pump having at least one inlet and at least one outlet. An adapter is coupled to the piezoelectric pump and configured to be fluidly coupled to the dressing. The adapter is configured to aggregate fluid flow into the at least one inlet. The adapter can have a block. A first recess depends into the block, and a second recess depends into the block from the first recess, the second recess having an area less than the area of the first recess. A bore depends through the block from the second recess to the first side, and a conduit is coupled to the first side and fluidly coupled to the bore.

Abstract: A system for applying negative-pressure therapy to an abdominal cavity. The system comprises: a tissue interface comprising a first contact layer and a second contact layer, each of the first contact layer and the second contact layer having perforations formed therein. The system also comprises a spacer layer disposed between the first contact layer and the second contact layer, the spacer layer configured to extend to different zones within the abdominal cavity. The system also includes a first sensor associated with the spacer layer and configured to acquire data associated with fluid at a first zone within the abdominal cavity and a first wireless transceiver associated with the first sensor and configured to transmit the data to an external therapy control device.

Abstract: A dressing for treating a tissue site, particularly a peritoneal or abdominal site, is disclosed. The dressing may comprise: a substrate; an adherent layer coupled to a surface of the substrate; and a fibrous layer comprising fibers coupled to a surface of the adherent layer opposite the substrate. Typically, the fibrous layer satisfies one or more of the following: at least 75% of the fibers are coupled approximately perpendicular to the surface of the substrate; at least 95% of the fibers in the fibrous layer have a length to diameter aspect ratio from about 10 to about 1000; and no more than 10% of the fibers are coupled approximately tangential to the surface of the substrate. Optionally, the fibrous layer may be formed by a flocking process. Methods of treating various tissue sites using the dressings and negative-pressure therapy are also disclosed.

Abstract: Systems, apparatuses, and methods for providing negative pressure and/or instillation fluids to a tissue site are disclosed. Some embodiments are illustrative of an apparatus or system for delivering negative-pressure and/or therapeutic solution of fluids to a tissue site, which can be used in conjunction with sensing properties of fluids extracted from a tissue site and/or instilled at a tissue site. For example, an apparatus may comprise a dressing interface or connector that includes a pH sensor, a humidity sensor, a temperature sensor and/or a pressure sensor embodied on a single pad within the connector and proximate the tissue site to provide data indicative of acidity, humidity, temperature and pressure. Such apparatus may further comprise an ambient port for providing the pressure sensor and the humidity sensor with access to the ambient environment providing readings relative to the atmospheric pressure and humidity.

Abstract: A surgical retractor assembly for providing surgical exposure. The surgical retractor assembly consists of multiple ring segments connected by adjustable ratchet mechanisms to form a complete ring. The ratchet mechanisms are attached to tissue retractor blades which provide exposure of the wound when expanded, without the requirement of a direct connection/attachment to an operating table. The tissue retractor blades are attached in a manner which is adjustable and facilitates the ability of the overall surgical retractor assembly (ring segments and connectors) to be raised or lowered with respect to the patient. The ring segments also allow attachments of additional retractor blades or other surgical retractor accessories for additional surgical exposure.

Abstract: This disclosure includes wound dressings and systems for effluent management of topical wound therapy and related methods. Some devices, which are configured to dilute therapeutic gas effluent flowing from a dressing, comprise a therapeutic gas source configured to provide therapeutic gas to the dressing; a container comprising a sidewall that defines a chamber configured to receive therapeutic gas effluent from the dressing; a negative pressure source configured to be coupled to the container such that the negative pressure source can be activated to draw fluid from the dressing through the chamber of the container; and a diluent gas source configured to deliver a diluent gas to dilute therapeutic gas effluent before the therapeutic gas effluent enters the negative pressure source.

Abstract: An evaporative bridge dressing that may be used with negative-pressure treatment of tissue. The evaporative bridge dressing may have one or more fluid transfer layers comprised of high-density wicking material enclosed between layers of film having high moisture-vapor transfer rates to manage liquid storage and pressure drop. The evaporative bridge may have an absorbent in some embodiments. An evaporation channel may be disposed adjacent to or combined with the evaporative bridge. A means for measuring pressure across the evaporative bridge may include a feedback path. A support means may reduce or prevent collapse of one or more of the evaporative bridge, the evaporation channel, the feedback path.

Abstract: A surgical retractor assembly for providing surgical exposure. The surgical retractor assembly consists of two frame segments connected by adjustable ratchet mechanisms to form a retractor frame. The ratchet mechanisms can be attached to tissue retractor blades that provide exposure of the wound when expanded, without the requirement of a direct connection/attachment to an operating table or bed frame. The tissue retractor blades are attached in a manner that is adjustable and facilitates the ability of the overall surgical retractor assembly to be raised or lowered with respect to the patient. The retractor frame also allows attachments of additional retractor blades or other surgical retractor accessories for additional surgical exposure.

Abstract: Wound dressings and wound inserts comprising substantially dry reactive agents, methods of forming wound inserts comprising dry reactive agents, and wound-treatment methods.

Abstract: This disclosure includes wound dressings and systems for effluent management of topical wound therapy and related methods. Some devices, which are configured to dilute therapeutic gas effluent flowing from a dressing, comprise a therapeutic gas source configured to provide therapeutic gas to the dressing; a container comprising a sidewall that defines a chamber configured to receive therapeutic gas effluent from the dressing; a negative pressure source configured to be coupled to the container such that the negative pressure source can be activated to draw fluid from the dressing through the chamber of the container; and a diluent gas source configured to deliver a diluent gas to dilute therapeutic gas effluent before the therapeutic gas effluent enters the negative pressure source.