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Pearls for Practice: Managing Skin Grafts and Donor Sites
Skin grafts are frequently used over large and/or difficult-to-heal wounds such as burns, pressure ulcers, venous ulcers, diabetic ulcers, and traumatic wounds. They can be created and applied in various ways. The split-thickness skin graft (STSG), which involves removing the epidermis and part of the dermis from the donor site and applying it to a well vascularized wound bed, is the most common. When the patient does not have donor tissue available, various biological and synthetic options are available.
The coverage provided by the STSG is superficial while the tissue grows in to complete the graft process. In order for the skin graft to survive, the grafted area must be well vascularized and have a low bacterial burden because infection can cause graft failure. Mesh often is used to cover the graft and hold the graft in the correct position using sutures, staples, or glue. The area then may be immobilized with a firm dressing.
The donor site typically is dressed with petrolatum gauze and covered with sterile gauze, bandage roll, and a light compression wrap. The donor site dressing usually is changed within 3 days. Because dressing change can be painful, the patient usually needs to be medicated before wound care; the clinician also should ensure the dressing is moistened before removal in order to avoid traumatizing the area during the dressing change process.
The graft site initially is dressed with soft sterile gauze covered with ABD pads and then wrapped with soft bandage rolls in order to immobilize the area; after 7 days, the graft site dressing is changed. To avoid damage to the graft, the gauze dressing should be liberally moistened with saline solution before removal. The site then is redressed with petrolatum gauze, soft gauze, ABD pads, and soft bandage rolls. This dressing subsequently is changed two times per week. The graft site should be assessed for graft take/failure, infection, pain, and drainage at each dressing change.
Pearls for Practice is made possible through the support of Ferris Mfg. Corp, Burr Ridge, IL (www.polymem.com). The opinions and statements of the clinicians providing Pearls for Practice are specific to the respective authors and are not necessarily those of Ferris Mfg. Corp., OWM, or HMP Communications.
This article was not subject to the Ostomy Wound Management peer-review process.