Aspects of the cutaneous stimulation devices include a cutaneous stimulation module and a cutaneous association element configured to stably associate the module with a skin location. The cutaneous stimulation module may be an active or passive module. Also provided are methods of using the devices, e.g., in rehabilitation and/or pain mitigation applications.

Aspects of the cutaneous stimulation devices include a cutaneous stimulation module and a cutaneous association element configured to stably associate the module with a skin location. The cutaneous stimulation module may be an active or passive module. Also provided are methods of using the devices, e.g., in rehabilitation and/or pain mitigation applications.

A medical dressing is provided. The dressing has a central portion and a border portion, and comprises a backing layer, an adhesive body contact layer and a pad arranged in the central portion between the backing layer and the adhesive body contact layer. The pad is symmetric about a longitudinal center line and the dressing comprises a lobed portion on each side of the center line. The medical dressing comprises a gripping tab which is coplanar with the border portion and which projects outwardly from the border portion. The medical dressing may be used for pressure ulcer prevention, such as at the sacrum region of a human body.

A medical dressing is provided. The dressing has a central portion and a border portion, and comprises a backing layer, an adhesive body contact layer and a pad arranged in the central portion between the backing layer and the adhesive body contact layer. The pad is symmetric about a longitudinal center line and the dressing comprises a lobed portion on each side of the center line. The medical dressing comprises a gripping tab which is coplanar with the border portion and which projects outwardly from the border portion. The medical dressing may be used for pressure ulcer prevention, such as at the sacrum region of a human body.

A system and method for donning and labeling a body cast provides a protective body cast that is labeled. The system and method provides a protective body cast that forms padded protection around the body of a bedridden patient; and especially around the hip, buttock, and lower extremity pressure points. The body cast is composed of a nanomaterial and serves as an envelope for an inner lining of a softer material such as a composite foam rubber. The body cast is sectioned into a multi-layered enclosing cloth support wrap that is fabricated from a nanomaterial, an inner surface having padding, and at least one auxiliary padding that detachably attaches to the body cast for additional padding. Labels detachably attach to the lower portion of the support wrap for indicating information pertinent to the patient. A caregiver accesses the label to read and mark directly on a bedridden patient.

A system and method for donning and labeling a body cast provides a protective body cast that is labeled. The system and method provides a protective body cast that forms padded protection around the body of a bedridden patient; and especially around the hip, buttock, and lower extremity pressure points. The body cast is composed of a nanomaterial and serves as an envelope for an inner lining of a softer material such as a composite foam rubber. The body cast is sectioned into a multi-layered enclosing cloth support wrap that is fabricated from a nanomaterial, an inner surface having padding, and at least one auxiliary padding that detachably attaches to the body cast for additional padding. Labels detachably attach to the lower portion of the support wrap for indicating information pertinent to the patient. A caregiver accesses the label to read and mark directly on a bedridden patient.

A use of an umbilical splint for shaping an umbilicus after an abdominal operation is described. The umbilical splint may comprise an insertion portion extending in a longitudinal direction and terminating at an insertion end for insertion into the umbilicus. Furthermore, the insertion portion may comprise a bulbous section near the insertion end. The bulbous section may be operable to apply pressure to a tissue of the umbilicus after the abdominal operation. The insertion portion may have different cross-sectional shapes including circular and oval. Finally, the insertion portion may be configured to engage the umbilicus such that the umbilical splint is retained within the umbilicus.

A back-bracing apparatus and associated methods of use and/or manufacture are provided. The apparatus includes support and belt portions. The support portion includes a plurality of posterior ribs configured to abut and extend along a low back of a user and a bracing web component having a plurality of crossing structures coupling adjacent ribs. At least one rib includes first and second upper slots disposed at opposite sides of an upper portion of the rib and first and second lower slots disposed at opposite sides of a lower portion of the rib. The belt portion includes an inner strap coupled to the support portion and configured to wrap around a torso and a low back of the user, and upper and lower outer straps configured to pass through the first and second upper slots and the first and second lower slots, respectively, and wrap around the inner strap.

A back-bracing apparatus and associated methods of use and/or manufacture are provided. The apparatus includes support and belt portions. The support portion includes a plurality of posterior ribs configured to abut and extend along a low back of a user and a bracing web component having a plurality of crossing structures coupling adjacent ribs. At least one rib includes first and second upper slots disposed at opposite sides of an upper portion of the rib and first and second lower slots disposed at opposite sides of a lower portion of the rib. The belt portion includes an inner strap coupled to the support portion and configured to wrap around a torso and a low back of the user, and upper and lower outer straps configured to pass through the first and second upper slots and the first and second lower slots, respectively, and wrap around the inner strap.

A protective dressing includes an outer dressing and an adhesive layer. The outer dressing includes an opening and a cavity sized to receive a phase-change material (PCM) insert inserted through the opening. The adhesive layer is configured to adhere to a patient's skin surrounding an anatomic site. When adhered to the patient's skin, the PCM insert modifies the patient's skin at the anatomic site. The PCM insert may be removed and replaced with another PCM insert. For example, a warm PCM insert may be replaced with a refrigerated PCM insert. The opening of the outer dressing may be self-sealing. The opening of the outer dressing may be sealed with an upper layer dressing coupled to the PCM cooling insert.