An emergency head trauma bandage cap with a detachable strap system and method of use, which, when applied to the head, delivers minimal pressure to control bleeding, doesn't compromise cervical spine immobilization, allows for fast and effective application of cooling gel to control intracranial/internal swelling or hot packs to prevent hypothermia in non-trauma situations, doesn't come apart during treatment and transport, and doesn't require a caregiver to re-wrap the dressing.

A wound dressing, including: a first outer layer, a second outer layer, and a middle layer disposed between the first outer layer and the second outer layer. The volume density of the first outer layer and a volume density of the second outer layer are greater than that of the middle layer; the first outer layer, the second outer layer, and the middle layer are bonded together.

A reduced pressure tissue treatment system includes an applicator having an aperture, a first pad section, and a second pad section substantially covering the aperture and positioned substantially adjacent the first pad section. A fabric layer is located at least partially between the second pad section and the drape, and the fabric layer includes a woven or non-woven fabric made from a fiber material. A drape substantially covers the first pad section, the second pad section, the fabric layer, and the applicator. A reduced pressure source is in fluid communication with at least one of the first pad section and the fabric layer for providing reduced pressure to the aperture.

Described generally herein are tissue therapy devices, which may comprise a sealant layer and a suction apparatus. The sealant layer functions so as to create a sealed enclosure between it and the surface of a patient by forming, preferably, an airtight seal around an area of tissue that requires negative pressure therapy. The tissue therapy device may comprise a suction apparatus. The suction apparatus is typically in fluid communication with the sealant layer and functions so as to reduce the amount of pressure present underneath the sealant layer. The reduced pressure is self-created by the suction apparatus. Together the sealant layer and the suction apparatus preferably create a closed reduced pressure therapy system. Preferably, the pressure under the sealant layer is reduced by expanding the volume of the enclosure space and thereby decreasing the density of the air molecules under the sealant layer.

The invention relates to an absorbent article for application to human or animal skin surfaces in the region of wounds, consisting of an outer covering (2) which is permeable for liquid substances, and of an inner layer (1) which is surrounded by the covering (2) and which consists essentially of a mixture of an amount of strongly osmotically active substances with an amount of osmotically comparatively weak or osmotically inactive substances, such as cellulose. The inner layer (1) is filled with osmotically active substances in such a way that it is possible to exert on a wound, with the wound fluids contained therein, an osmotic pressure via which the wound fluid can be removed from the organism to be treated, and thus it is possible to assist both in the surfaced wound region and in the depth of the tissue a normal interstitial hydration of tissue by directing endogenous fluids in their direction of flow to the patient's skin surface into the absorbent article, and keeping them there.

Provided are orthopedic, dual density pressure pads designed to transfer pressure onto a focused anatomical structure; typically through the assistance of a device that applies a perpendicular or downward force. The pad includes an outer layer including a relatively soft material and an interior support including a rigid material, with the interior support typically having a substantially greater hardness than the outer layer.

The present invention pertains to a bandage for improved monitoring, healing and pain-reduction of a wound. The bandage also increases compliance for patients and for caring personal. The bandage is useful with most any wound being exposed to pressure, trauma and/or irritation. The bandage is especially useful with incisions upon surgery, preferably incisions upon abdominal and hip surgery as well as incisions upon dorsal surgery. The above features are accomplished by the wound being visible through the bandage, external pressure on the wound being redirected to areas around the wound not being compromised by surgery and possible exudate from the wound being absorbed within the bandage, as well as pressure from the bandage being exerted inwards against the wound edges thereby improving the cosmetic result.

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.

Systems, methods, and apparatuses for treating a tissue site are described. In some embodiments, the system may include a pouch having an upstream layer, a downstream layer, and an absorbent member enclosed between the upstream layer and the downstream layer. The upstream layer and the downstream layer may each include a hydrophobic side and a hydrophilic side. The hydrophilic side of both the upstream layer and the downstream layer may be positioned facing the absorbent member. The hydrophobic side of both the upstream layer and the downstream layer may form a portion of an exterior surface of the pouch such that fluid incident on the pouch is distributed laterally along the exterior surface of the pouch before being absorbed by the absorbent member.

A wound bolster includes an inner non-adherent face, a compressible and expandable body, and an outer elastic face where the inner non-adherent face is configured for contact with a wound on a subject and the outer elastic face is configured, upon securing of the wound bolster to a periphery of the wound, to generate a compressive force within the compressible and expandable body in response to applied deformation, which is transmitted as a normal compressive force to the subject. A method of affixing a wound bolster to a subject includes: recording a circumference associated with an outer region of a wound area on a subject, altering a size of the wound bolster based on the recorded circumference to form an altered wound bolster, positioning the altered wound bolster on the wound area, and affixing an outer edge of the altered wound bolster to the periphery of the wound area.