Abstract: In some examples, a dressing suitable for treating a tissue site may include a fluid management assembly including a fluid restraint configured to reduce a fluid capacity of the fluid management assembly proximate to the fluid restraint. Other features may be associated with the dressing including, by way of example and without limitation, abase layer, an adhesive, one or more wicking layers, and an absorbent layer. Other dressings, apparatus, systems, and methods are disclosed.

Abstract: An apparatus for applying negative pressure to a tissue site proximate a patient's foot may include a tissue interface, a sole, a toe box, a cover, and an interface. The tissue interface may be configured to be circumferentially disposed around the tissue site. The sole may be configured to support the tissue interface. The toe box may be coupled to the sole. The cover may be configured to be coupled to the leg and to the sole to cover the tissue interface. The cover and the sole may form a chamber containing the tissue interface and may seal the tissue interface within the chamber. The interface may be configured to fluidly couple the tissue interface to a source of negative pressure, which can be delivered to the tissue interface for distribution to the tissue site.

Abstract: A negative pressure therapy dressing includes a drape layer, an adhesive border configured to provide a seal between the drape layer and skin, and a manifold layer coupled to the drape layer. The manifold layer includes a body portion extending in a first direction, a first wing positioned at a first side of the body portion, and a second wing positioned at a second side of the body portion opposite the first side. The first wing extends away from the first side and partially in the first direction such that a first gap is provided between a first tip of the first wing and the first side of the body portion. The second wing extends away from the second side and partially in the first direction such that a second gap is provided between a second tip of the second wing and the second side of the body portion.

Abstract: A cover for sealing a tissue site may include a shell having a first side, a second side, and an edge between the first side and the second side; an adhesive disposed on the first side; and a release liner adjacent to the adhesive. The release liner may comprise a flap folded over at least a portion of the edge of the shell. The flap may be configured to prevent the adhesive from migrating past the portion of the edge of the shell. In some examples, the shell, the adhesive, and the release liner can be folded, and the flap can be at least partially disposed between a first portion and a second portion of the second side of the shell. The cover may additionally comprise a sealing layer with apertures disposed between the adhesive and the release liner in some embodiments.

Abstract: A treatment system includes an dressing having a decompression layer and an occlusive layer that secures the dressing about a treatment site, and defines a treatment chamber within which the decompression layer is positioned. Operation of an air displacement device fluidly coupled to the chamber causes the decompression layer to compress away from the tissue site, resulting in a pulling force being imparted onto the treatment site. This decompression of the tissue site increases the perfusion of blood and other fluids, and advantageously may reduce swelling at the treatment site. To increase the degree of lifting of the treatment site, the decompression layer is advantageously constructed to exhibit a parallel plate effect during use of the treatment system. For example, the decompression layer is constructed having a center of stiffness located closer to an outwardly-facing surface of the decompression layer than a tissue-facing surface of the decompression layer.

Abstract: A dressing for managing an incision and surrounding tissue where edema and swelling may be present post-operation. The dressing may maximize coverage of area in articulating joints, such as a knee or elbow, while allowing for substantial range of motion. In some embodiments, the dressing may comprise an adhesive border configured to be adhered to skin around an articulating joint, a skin-interfacing fabric for minimizing skin irritation, a foam body for manifolding negative pressure and absorbing exudate and other body fluids, and a thin polymer film cap for sealing the assembly so negative pressure can be maintained throughout the dressing.

Abstract: An apparatus for applying negative pressure to a tissue site of a patient may include a tissue interface, a cover, an aperture in the cover, and a sealing member. The tissue interface may have an anatomical shape configured to cover the tissue site. The cover may be configured to cover the tissue interface. The aperture in the cover may be fluidly coupled to the tissue interface. The sealing member may be configured to seal the cover to the patient, wherein the cover and the sealing member are configured to cooperate to form a sealed chamber containing the tissue interface. The tissue interface may be coupled to a source of negative pressure, which can be delivered to the tissue interface for distribution to the tissue site. The source of negative pressure may be coupled to the cover of the apparatus.

Abstract: An apparatus for applying negative pressure to a tissue site proximate a patient's foot may include a tissue interface, a sole, a toe box, a cover, and an interface. The tissue interface may be configured to be circumferentially disposed around the tissue site. The sole may be configured to support the tissue interface. The toe box may be coupled to the sole. The cover may be configured to be coupled to the leg and to the sole to cover the tissue interface. The cover and the sole may form a chamber containing the tissue interface and may seal the tissue interface within the chamber. The interface may be configured to fluidly couple the tissue interface to a source of negative pressure, which can be delivered to the tissue interface for distribution to the tissue site.

Abstract: A negative pressure wound treatment (NPWT) dressing system for treating shoulder incisions. The NPWT dressing system includes a wound dressing, an immobilization device configured to immobilize a shoulder of a patient, and a negative pressure source coupled to the immobilization device. The wound dressing includes a drape layer, a manifold layer, and a reduced-pressure interface integrated with the drape layer and the negative pressure source. The drape layer has a first surface and a second, wound-facing, surface. The drape layer is substantially impermeable to liquid and substantially permeable to vapor. The manifold layer has a first surface and a second, wound-facing surface. The manifold layer has a first lobe, a second lobe substantially aligned with the first lobe, and a third lobe extending substantially perpendicular to the first lobe and the second lobe.

Abstract: A system for treating a linear wound on a patient that has a closing dressing bolster for placing on the patient's epidermis over the linear wound, a sealing subsystem for providing a seal over the closing dressing bolster and the patient, and a reduced-pressure subsystem for delivering reduced pressure to the sealing subsystem. The sealing subsystem and reduced pressure subsystem are operable to deliver reduced pressure to the closing dressing bolster. The closing dressing bolster is operable under reduced pressure to develop a inward closing. The closing dressing bolster may include one or more closing members on each side of a center wound area to create the inward closing when under reduced pressure. A compressive force may also be developed. Other systems and methods are presented.

Abstract: An apparatus for promoting circulation through a subcutaneous lymph vascular network may comprise a first manifold layer, a second manifold layer coupled to the first manifold layer, and a cover layer coupled to the second manifold layer. The first manifold may have a first stiffness, and the second manifold may have a second stiffness greater than the first stiffness. In some embodiments, the apparatus may additionally have a fluid interface configured to fluidly couple at least one of the first manifold layer and the second manifold layer to a fluid conductor through the cover layer. The fluid conductor may be coupled to or configured to be coupled to a source of negative pressure.

Abstract: A negative pressure wound dressing for use with breast incisions. The wound dressing includes a drape layer, a manifold layer, a base layer, and a reduced pressure interface. The drape layer has a first surface and a second, wound-facing, surface. The drape layer is substantially impermeable to liquid and substantially permeable to vapor. The manifold layer has a first surface and a second, wound-facing surface. The manifold layer has a perimeter defined by a first convex curved side surface defining a first lobe, a second convex curved side surface defining a second lobe, and a connecting portion between the first lobe and the second lobe. The base layer is configured to: (i) couple the drape layer to the manifold layer, and (ii) the dressing to a patient's tissue. The reduced pressure interface is integrated with the drape layer.