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.

Abstract: Some embodiments of a manifold pad may be configured to distribute reduced pressure relative to a tissue site and to provide instillation to the tissue site. In some embodiments, the manifold pad may comprise open-cell foam and at least one skinned channel extending through the open-cell foam. The at least one skinned channel may be configured so that the skin is substantially impermeable to liquid, preventing liquid within the channel from seeping into the open-cell foam. In some embodiments, this may allow for two isolated pathways for fluid movement through the manifold pad. Some dressing embodiments may utilize such a manifold pad in conjunction with a treatment device. Other apparatus, dressings, systems, and methods are disclosed.

Abstract: A system for monitoring and tracking swelling of a patient's limb includes a dressing, an imaging device, and processing circuitry. The dressing is positioned on a patient's limb over a wound and includes a pattern indicator. The imaging device is configured to obtain an image of the dressing and the pattern indicator. The processing circuitry is configured to obtain an initial image of the pattern indicator, obtain one or more subsequent images of the pattern indicator at later times, and determine a swelling change of the patient's limb using the initial image and the one or more subsequent images.

Abstract: A kit (1500) for negative pressure and immobilization therapy includes a negative pressure dressing (100) configured to define a sealed volume between a patient's skin and the negative pressure dressing when applied to the patient, a pump (200) configured to be placed in pneumatic communication with the negative pressure dressing and operable to displace air from the sealed volume, and a heat-moldable splint (900). The heat-moldable splint includes a plurality of flexible tubes formed of a first material and coupled together to form a web and a second material positioned in the flexible tubes and having a lower softening or melting point than the first material.

Abstract: Disclosed embodiments may relate to dressings, covers, and/or drapes configured to provide negative-pressure therapy to a tissue site, such as an incision. In some embodiments, the drape or cover may have an external support layer configured to render the cover or drape self-supporting. In some embodiments, the support layer may comprise a skeleton support structure having a plurality of coupled supports. In some embodiments, the skeleton support structure may be non-planar, for example having abase portion configured to support the cover and a projection portion configured to extend over the manifold of the dressing at a height above the base portion. In some embodiments, the skeleton support structure may be removably coupled to an outer surface of the cover or drape, allowing removal after the dressing has been applied to the tissue site.

Abstract: Disclosed embodiments may relate to dressings configured to provide negative-pressure wound therapy to a tissue site, while simultaneously shielding a portion of the tissue site from the negative pressure. For example, dressing assembly embodiments may comprise an outer dressing configured for applying negative-pressure wound therapy to a tissue site, and an underlying isolation patch configured for use under the outer dressing. The isolation patch may be configured to seal the portion of the tissue site so that it does not experience the negative pressure. Additionally disclosed are other apparatus, dressings, systems, and methods.

Abstract: Disclosed embodiments may relate to dressings configured to provide negative-pressure wound therapy to a tissue site, while simultaneously shielding a portion of the tissue site from the negative pressure. For example, dressing assembly embodiments may comprise an outer dressing configured for applying negative-pressure wound therapy to a tissue site, and an underlying isolation patch configured for use under the outer dressing. The isolation patch may be configured to seal the portion of the tissue site so that it does not experience the negative pressure. Additionally disclosed are other apparatus, dressings, systems, and methods.

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.

Abstract: A decompression wrap includes an occlusive layer formed as a first strip having a longitudinal axis, a manifold layer coupled to the occlusive layer and formed as a second strip extending parallel to the longitudinal axis. The occlusive layer extends beyond the manifold layer in a first lateral direction perpendicular to the longitudinal axis. The decompression wrap also includes an adhesive provided on the occlusive layer and configured to seal a first longitudinal section of the occlusive layer to a second longitudinal section of the occlusive layer when the decompression wrap is wrapped around a tissue site.

Abstract: Disclosed embodiments may relate to dressings configured to provide negative-pressure wound therapy to a tissue site, while simultaneously shielding a portion of the tissue site from the negative pressure. For example, dressing assembly embodiments may comprise an outer dressing configured for applying negative-pressure wound therapy to a tissue site, and an underlying isolation patch configured for use under the outer dressing. The isolation patch may be configured to seal the portion of the tissue site so that it does not experience the negative pressure. Additionally disclosed are other apparatus, dressings, systems, and methods.

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: In some examples, an auxiliary port assembly may be configured to be coupled to a cover for providing a sealed space at a tissue site. The auxiliary port assembly may include an access portal and an adhesive. The access portal may include an exterior side and a mounting side opposite the exterior side. The mounting side may be configured to face the cover. The access portal may be configurable between an open state and a closed state, and may provide a passage through the cover in the open state. The adhesive may be configured to couple the mounting side of the access portal to the cover. Other systems, dressings, apparatuses, and methods are disclosed.

Abstract: In some examples, a dressing assembly suitable for treating a tissue site may include a dressing bolster, a sealing skin, and a gasket member. The sealing skin may cover at least a portion of a first side of the dressing bolster while an opposing second side of the dressing bolster may be configured to be positioned in fluid communication with the tissue site. The gasket member may be configured to create a sealed space between the sealing skin and the tissue site. In some examples, the sealing skin may be liquid impermeable and integrally formed with the dressing bolster. Further, in some examples, the dressing bolster may have a contoured shape including a tissue housing. Other systems, dressings, apparatuses, and methods are disclosed.

Abstract: A method for calculating range of motion of a patient's jointed limb includes providing one or more locators at an upper limb of the jointed limb, and one or more of the locators at a lower limb of the jointed limb. A first image of the patient's joint in a fully extended position a second image of the patient's joint in a fully flexed position are captured with an imaging device. The method includes identifying positions of the locators of both the first image and the second image, and determining an extended angle of the patient's joint based on the identified positions of the locators of the first image. The method includes determining a flexed angle of the patient's joint based on the identified positions of the locators of the second image. The method includes determining a range of motion angle based on the extended angle and the flexed angle.

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 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: In some examples, a dressing suitable for treating a tissue site may include a fluid management assembly configured to offload fluid extracted from the tissue site away from an articulation area at the tissue site. Other features may be associated with the dressing including, without limitation, a base layer, an adhesive, one or more wicking layers, and an absorbent layer. Other dressings, apparatus, systems, and methods are disclosed.

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.