Abstract: A reduced-pressure treatment system for debriding a treatment area of a tissue site and applying reduced pressure is disclosed. The reduced-pressure treatment system includes a hydrogel having a blocked acid debriding agent. The hydrogel is adapted to cover the treatment area and enhance autolytic debridement at the treatment area. The reduced-pressure treatment system includes a manifold that is adapted to cover the hydrogel and distribute reduced pressure to the tissue site. The reduce-pressure treatment system also includes a sealing drape for forming a fluid seal over the tissue site and manifold. Other systems, methods, and dressings are presented.

Abstract: A manifold for use with a dressing for treating an area around an extremity of a patient may include a concave recess positioned at a first end of the manifold. A fold axis may bisect the concave recess and extend from the first end of the manifold to a second end of the manifold. A first portion of the manifold may extend orthogonal to the fold axis toward a first side of the manifold, and a second portion of the manifold may extend orthogonal to the fold axis toward a second side of the manifold opposite to the first side. The fold axis may be configured to extend lengthwise along the extremity. Additionally disclosed are other apparatus, dressings, systems, and methods.

Abstract: System and methods for stimulating cartilage formation at a first tissue site through a second tissue site is presented. The system includes a fluid source for supplying a therapeutic solution, a reduced pressure source for supplying reduced pressure, a fluid delivery manifold for deploying adjacent the first tissue site, and a vacuum manifold for deploying within the second tissue site. The fluid delivery manifold extends between a proximal end fluidly coupled to the fluid supply and a distal end having at least one aperture for delivering the therapeutic solution to the defect adjacent the articulating surface of the first tissue site. The vacuum manifold extends between a proximal end fluidly coupled to the reduced pressure source and a distal end having at least one aperture for delivering the reduced pressure to the first tissue site adjacent the opposing surface of the first tissue site.

Abstract: Systems, apparatuses, and methods for providing negative pressure with 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, a system may comprise a tissue interface adapted to be coupled to a source of instillation fluid and a dressing interface having a therapy cavity that includes a pH sensor, a humidity sensor, a temperature sensor, and a pressure sensor embodied on a single pad within the dressing interface to provide data indicative of acidity, humidity, temperature and pressure at the tissue site. Such apparatus may further comprise algorithms for processing such data for detecting leakage and blockage conditions as well as providing information relating to the progression of healing of wounds at the tissue site.

Abstract: A dressing for treating a tissue site, particularly an abdominal or peritoneal site, is disclosed. In some embodiments, the dressing may comprise a tissue interface formed from a first layer of a liquid-impermeable material and a plurality of manifolding bubbles formed as part of the first layer. In some embodiments, the tissue interface may further comprise a second layer of a permeable material, where the manifolding bubbles are formed as closed cells between the first layer and the second layer. The tissue interface may also include a third layer of liquid-impermeable material positioned adjacent to the second layer, where one or more fluid passageways may be formed between the second layer and third layer for delivering a therapeutic fluid to the tissue site.

Abstract: A wound therapy system includes a dressing sealable over a wound and defining a wound space between the dressing and the wound, tubing fluidly communicable with the wound space, and a canister fluidly communicable with the tubing. The canister, the tubing, and the dressing define a sealed space that includes the wound space. The wound therapy system also includes a therapy unit coupled to the canister. The therapy unit includes a sensor configured to measure a pressure in the sealed space, a valve positioned between the sealed space and a surrounding environment and controllable between an open position and a closed position, and a control circuit. The control circuit is configured to control the valve to alternate between the open position and the closed position to allow airflow through the valve, receive measurements from the sensor, and determine a volume of the wound space based on the measurements.

Abstract: A dressing for treating a tissue site with negative pressure includes a manifold having a first surface and a second surface opposite the first surface. The dressing also includes a first layer adjacent to the first surface and a second layer adjacent to the second surface. The first layer and the second layer each include a polymer film. The dressing also includes a plurality of fluid restrictions in the polymer film adjacent to at least the first surface, and a plurality of bonds between the first layer and the second layer. The plurality of bonds defines separable sections of the manifold.

Abstract: A volume of a wound is estimated using a dynamic pressure response measured during instillation of fluid to the wound using a negative pressure wound therapy system. A previously estimated wound volume may be used to detect and prevent overfill of fluid to the wound during future instillation events. For example, real-time pressure measurements may be compared to model data representative of expected pressure at a wound having a volume equal to the previously estimated wound volume, with instillation being stopped if the observed pressure varies from the expected pressure. A comparison of a total volume of fluid instilled to the wound may also be compared to the previously estimated wound volume to prevent overfill. The comparison of wound volume estimated based on an instillation event may also be compared to a wound volume estimated using other methods to provide a higher confidence wound volume estimate.

Abstract: Dressings for treating a tissue site with negative pressure are disclosed, which may include a dressing having at least three layers assembled in a stacked relationship. In one example embodiment, a first film may comprise a non-porous material and a plurality of fluid restrictions. A first manifold layer may be adjacent to the first film and may comprise a second film of a transparent material having blisters and a manifold area. The first manifold layer may further comprise apertures configured to allow fluid transfer through the second film. A second manifold layer may be adjacent to the first manifold layer and may comprise foam having a contact area that is less than the manifold area of the first manifold layer.

Abstract: A wound dressing includes a patient interface layer, a wicking layer, an absorbent layer, and a cover layer. The patient interface 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 wicking layer, absorbent layer, and cover layer all also have a first side and a second side. A perimeter of the first side of the wicking layer is adhered to the second side of the cover layer, forming an adhesive border surrounding the wicking layer and the absorbent layer, and the wicking layer is configured to peripherally wick perspiration from underneath the adhesive border towards the center of the wicking layer and upwards towards the absorbent layer.

Abstract: Dressings for closing an opening through a surface of a tissue site are described. The dressing includes a cover adapted to form a sealed space over the opening and a bolster. The bolster is adapted to be positioned adjacent the opening and includes a first plurality of holes. The holes have an average width to length ratio causing the plurality of holes to collapse in a direction substantially perpendicular to the opening. Systems, apparatuses, kits and methods including and/or using the dressing for closing the opening are also described.

Abstract: This disclosure describes devices, systems, and methods related to a connector for a dressing, such as a dressing of a hyperbaric oxygen therapy system. An example of a connector includes a connector body configured to define at least a portion of a first channel. The connector also includes a viewing member coupled to the connector body. The connector further includes a deformable member positioned within the first channel. The deformable member is configured to deform based on a pressure associated with the deformable member and to provide a visual indication, via the viewing member, of the pressure.

Abstract: A system for providing instillation fluid to a deep abdominal wound includes an instillation module and a connection structure. The instillation module defines a first surface and a second, abdominal contents-facing surface. The instillation module includes a distribution hub configured to receive instillation fluid from an instillation fluid source. The connection structure includes a first surface, a second, abdominal contents-facing surface; and a flow path extending between the first surface and the second surface. The flow path includes an inlet configured to receive an instillation fluid conduit engaged with the instillation fluid source and an outlet in fluid communication with the instillation module. The flow path defines an axis extending between the inlet and the outlet. The flow path is configured to compress in a direction defined by the axis.

Abstract: Disclosed herein is a device which is intended to deliver and maintain reduced pressure to body surfaces for application of reduced pressure wound therapy (RPWT) also known as negative pressure wound therapy (NPWT). During application of this type of therapy, a substantially airtight seal is formed around a section of tissue to be treated. This seal is formed by a dressing which provides fluid communication from a section of tissue to a reduced pressure source. Disclosed herein is a dressing system which is configured to enhance usability and functionality of this dressing. First, the system may be configured to allow full rotation of the fluid communication conduit to the reduced pressure source along the axis substantially normal to the dressing. Second, the system may be configured to include a one-way valve to prevent backflow of any drainage fluids. Third, the system may be configured with transparent windows covered by opaque flaps to allow inspection through the dressing.

Abstract: Dressings for treating a tissue site with negative pressure are disclosed, which may include a dressing having at least three layers assembled in a stacked relationship. In one example embodiment, a first film may comprise a non-porous material and a plurality of fluid restrictions. A first manifold layer may be adjacent to the first film and may comprise a second film of a transparent material having blisters and a manifold area. The first manifold layer may further comprise apertures configured to allow fluid transfer through the second film. A second manifold layer may be adjacent to the first manifold layer and may comprise foam having a contact area that is less than the manifold area of the first manifold layer.

Abstract: A therapy system for treating a tissue site with negative-pressure therapy and/or fluid instillation therapy in response to information received from a diagnostic module is disclosed. In some embodiments, the therapy system may include a dressing, a negative-pressure source, a container, and a diagnostic module. The dressing may be adapted to be placed on the tissue site, and the negative-pressure source may be adapted to be fluidly coupled to the dressing. The container may be adapted to be fluidly coupled to the dressing and to the negative-pressure source and to receive fluid from the tissue site. The diagnostic module may be adapted to be exposed to gas associated with the fluid from the tissue site. The diagnostic module may comprise a sensor configured to detect a condition of the tissue site and to generate an output based on the detected condition. The sensor may be configured to detect a volatile organic compound. In some embodiments, the diagnostic module may be positioned on the container.

Abstract: A wound treatment system comprises a wound-treatment apparatus and a wound dressing coupled to the apparatus. The wound dressing includes a foam structure wound insert having pores with a greater cross-sectional area when viewed from a first direction and a smaller cross-sectional area when viewed from an orthogonal direction. Methods for making such wound inserts may include compressing foam structure material having pores with a substantially uniform cross-sectional area. Methods for treating a wound using a wound insert.

Abstract: Disclosed embodiments may relate to devices, systems, and methods for providing negative-pressure therapy simultaneously to a plurality of tissue sites using a single negative-pressure source. For example, a fluid bridge may comprise a plurality of distal ends, each configured to interact fluidly with a tissue site. In some embodiments, each distal end may have an aperture. The bridge may also comprise a port for entry of negative pressure into the enclosed space of the bridge. In some embodiments, each distal end may comprise a one-way valve. The enclosed space of the fluid pathway between the distal ends and the port may be supported in some embodiments, to prevent collapse due to negative pressure and/or compression.

Abstract: Dressings for tissue treatment with negative pressure and methods of using the dressings for tissue treatment with negative pressure, which may comprise a dressing having at least three layers assembled in a stacked relationship. The first layer may comprise or consist essentially of a polymer film having a plurality of fluid restrictions that are normally unstrained or closed. The second layer may comprise a manifold, and the third layer may comprise or consist essentially of a polymer drape. A fourth layer, which may be coupled to the first layer opposite the second layer, may comprise or consist essentially of a silicone gel having a plurality of apertures. In some examples, the plurality of apertures in the fourth layer may be registered with the fluid restrictions of the first layer.

Abstract: A reduced-pressure, linear-wound closing bolster has a pivotable frame that moves from an extended position to a compressed position under the influence of reduced pressure. The closing bolster may have a first closing member, a second closing member, and an interior space. A manifold member is disposed within the interior space and may be coupled to the pivotable frame. When a reduced pressure is applied, the pivotable frame is urged from the extended position to the compressed position. A first gripping member for transmitting a closing force from the first closing member to a first edge of a linear wound may be attached. Likewise, a second gripping member for transmitting a closing force from the second closing member to a second edge of the linear wound may be attached. Systems and methods are also presented.