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Cover of Dressings and Care of Skin Graft Sites: A Review of Clinical Evidence and Guidelines

Dressings and Care of Skin Graft Sites: A Review of Clinical Evidence and Guidelines

Rapid Response Report: Summary with Critical Appraisal

A skin graft is sheet of skin harvested from a donor site; it may include the epidermis and part of the dermis (split thickness skin graft) or both the epidermis and dermis (full thickness graft) to cover skin lost due to surgery or trauma. Dressings are used to cover the donor site or the grafted skin; this is done to enhance healing, improve patients’ comfort and reduce the pain. Skin dressings can be broadly classified into medicated and non-medicated dressings. Medicated dressings include hydrocolloid dressings, hydrogel dressings. alginate dressings, fibrous absorbent dressings, dressings that contribute to odour management, antimicrobial dressings, and Manuka Honey dressings. The non-medicated dressings include vapour permeable dressings, foam dressings, low adherent dressings, non-adherent wound contact layers, atraumatic absorbent dressings, post-operative dressings, and hydrocapillary dressings. Dressing change may be a traumatic experience for patients and can tax healthcare resources. Pain and discomfort of patients while the dressing is in place and during dressing change may be related to the characteristics of the wound dressing used. Furthermore, dressing type may affect the incidence of wound infection which would affect the frequency of dressing change and the overall success of the skin graft procedure.

The purpose of this review is to evaluate the evidence regarding the optimal dressing type, protocol of dressing change, and clinical practice guidelines for the use of dressings at skin graft sites.

Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic reviews. The intent is to provide a list of sources of the best evidence on the topic that CADTH could identify using all reasonable efforts within the time allowed. Rapid responses should be considered along with other types of information and health care considerations. The information included in this response is not intended to replace professional medical advice, nor should it be construed as a recommendation for or against the use of a particular health technology. Readers are also cautioned that a lack of good quality evidence does not necessarily mean a lack of effectiveness particularly in the case of new and emerging health technologies, for which little information can be found, but which may in future prove to be effective. While CADTH has taken care in the preparation of the report to ensure that its contents are accurate, complete and up to date, CADTH does not make any guarantee to that effect. CADTH is not liable for any loss or damages resulting from use of the information in the report.

Copyright © 2013 Canadian Agency for Drugs and Technologies in Health.

Copyright: This report contains CADTH copyright material and may contain material in which a third party owns copyright. This report may be used for the purposes of research or private study only. It may not be copied, posted on a web site, redistributed by email or stored on an electronic system without the prior written permission of CADTH or applicable copyright owner.

Links: This report may contain links to other information available on the websites of third parties on the Internet. CADTH does not have control over the content of such sites. Use of third party sites is governed by the owners’ own terms and conditions.

Except where otherwise noted, this work is distributed under the terms of a Creative Commons Attribution-NonCommercial- NoDerivatives 4.0 International licence (CC BY-NC-ND), a copy of which is available at http://creativecommons.org/licenses/by-nc-nd/4.0/

Bookshelf ID: NBK195739PMID: 24741725

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