A wound dressing, a method of manufacturing a wound dressing, and a method of treating a patient are disclosed. The wound dressing may include an absorbent layer for absorbing wound exudate; and an obscuring element for at least partially obscuring a view of wound exudate absorbed by the absorbent layer in use.

The wound treatment apparatus combines an internal negative pressure (vacuum) pump and an internal positive pressure (compressor) pump connectable to an external oxygen supply for providing both negative pressure wound therapy and hyperbaric oxygen wound therapy to a wound site. The apparatus also includes a user interface operatively connected to an electronic controller that monitors and actuates the vacuum and compressor pumps. The user interface and controller enables the apparatus to provide multiple modes of operation and the ability to selectively change between negative pressure therapy operational modes and hyperbaric oxygen operational modes.

Systems and methods are described for monitoring compression applied by a compression bandage to a body portion of an individual. A system embodiment includes, but is not limited to, a textile configured to conform to a body portion of an individual subject; one or more strain gauges integrated with the textile, the one or more strain gauges configured to generate one or more sense signals associated with a strain of the textile; circuitry operably coupled to the one or more strain gauges and configured to receive the one or more sense signals associated with the strain of the textile; and a reporter operably coupled to the circuitry and configured to generate one or more communication signals associated with the strain of the textile responsive to instruction by the circuitry when the strain of the textile is less than or greater than a threshold strain value.

Systems and methods are described for monitoring compression applied by a compression bandage to a body portion of an individual. A system embodiment includes, but is not limited to, a deformable substrate integrated with a textile configured to conform to a body portion; a sensor assembly coupled to the deformable substrate, the sensor assembly including one or more strain gauges configured to generate one or more sense signals associated with a strain of the textile; circuitry operably coupled to the sensor assembly and configured to receive the one or more sense signals associated with the strain of the textile; and a reporter operably coupled to the circuitry and configured to generate one or more communication signals responsive to instruction by the circuitry, the one or more communication signals associated with the strain of the textile.

The invention provides an adhesive support article for supporting a body part of a user. A single-sided stretchable adhesive tape blank is precut into a sheet having a central anchoring portion and a plurality of outwardly extending fingers. The sheet is marked with visual indicators to guide the user of the support article for applying the central anchoring portion onto a first exterior surface of the body part and for stretching the fingers before adhering them at a predetermined distance away from the central anchoring portion. The adhesive support article can also be provided in a support system with at least one corresponding body landmark article, providing further guidance for applying the support article to the desired body part.

A system is provided comprising a columnar sleeve of stretchable fabric, the sleeve produced in various skin tone colors and configured to slip upon an individual toe or finger and an absorbent padding configured for attachment to an inside surface of the sleeve, the padding configured to cover about one half of an interior circumference of the inside surface, the padding optionally infused with at least one of pain killers, antiseptics, and soothing gels. The system also comprises wax paper covering the padding prior to use of the sleeve, an applicator shaped to facilitate slipping the sleeve upon the individual toe or finger, and convex-shaped flex bands placed lengthwise into the sleeve. The flex bands exert downward pressure on one of a toe and a finger and are placed in a U-shape, thus promoting the downward pressure.

A suboccipital compression pad may include a pad member configured to contact a suboccipital region of a patient. A suboccipital compression pad may include a pair of securing straps extending respectively from opposing ends of the pad member, the pair of securing straps having proximal ends diverging into upper rear straps and lower rear straps to form an open space between the upper rear straps and the lower rear straps such that portions of the upper rear straps are located above ears of the patient and portions of the lower rear straps are located below ears of the patient without covering ears of the patient, wherein one of the upper rear straps and the lower rear straps of the pair of securing straps is configured to be selectively attachable to different locations of a back side of the pad member.

An orthosis chosen from a venous support orthosis and an elastic venous compression orthosis, the orthosis including a ribbed top and a leg part, the ribbed top including an intermediate part extending the leg part, the stitch being different on each side of the boundary separating the leg part and the intermediate part, a welt extending the intermediate part and of a height less than 1.5 cm.

Some embodiments are directed to a system 10 for the application of topical negative pressure therapy to a site 18 on the body of a mammal. Some embodiments of the system 10 comprise a piston 22 and cylinder 24 device 12 having a self-contained power source for the generation of a reduced pressure and for aspirating the site 18. Some embodiments of the system 10 comprise a dressing 14 sealably surrounding the site 18 that can be operably connected to the device 12 by a conduit means 16 to apply the reduced pressure to the site 18.

Systems, instruments, methods, and compositions are described involving removing a portion of the epidermis within a donor site on a subject, and harvesting dermal plugs within the donor site. An injectable filler is formed by mincing the dermal plugs. The injectable filler is configured for injecting into a recipient site on the subject.