Evaluation of a porcine origin acellular dermal matrix and small intestinal submucosa as dermal replacements in preventing secondary skin graft contraction

被引:75
作者
MacLeod, TM [1 ]
Sarathchandra, P
Williams, G
Sanders, R
Green, CJ
机构
[1] Mt Vernon Hosp, Restorat Appearance & Funct Trust, Northwood HA6 2RN, Middx, England
[2] Northwick Pk Hosp & Clin Res Ctr, Northwick Pk Inst Med Res, Harrow HA1 3UJ, Middx, England
关键词
dermis; porcine; small intestinal submucosa; skin graft contraction;
D O I
10.1016/j.burns.2004.01.018
中图分类号
R4 [临床医学];
学科分类号
1002 [临床医学]; 100602 [中西医结合临床];
摘要
The degree to which a split thickness skin graft (STSG) contracts after application to its recipient bed is related in part to the proportion of the dermis harvested from the donor site. Harvesting thicker skin grafts may produce better cosmetic results in the recipient bed but result in increased donor site morbidity. The combination of an autologous ultra thin split thickness graft with an underlying non-autologous dermal component may reduce secondary skin graft contraction without further increasing donor site morbidity. This study was aimed at assessing the suitability of two porcine derived biomaterials (Permacol(TM) and small intestinal submucosa, SIS) for use in combination with skin grafts in a Sprague-Dawley rat model. Full thickness wounds (1 cm(2)) were created in Sprague-Dawley rats and grafted with skin in combination with Permacol(TM) or SIS either as a one-stage operation or following a 2-week-period of vascularisation of these dermal matrices before a second stage operation to cover with skin. Skin graft viability and wound area were assessed at weekly intervals until 4 weeks after graft application. Both Perniacol(TM) and SIS were able to support an overlying skin graft but had no beneficial effect on skin graft contraction in this model compared to skin grafts alone. (C) 2004 Elsevier Ltd and ISBI. All rights reserved.
引用
收藏
页码:431 / 437
页数:7
相关论文
共 22 条
[1]
BELL E, 1983, J INVEST DERMATOL, V81, P2
[2]
SUCCESSFUL USE OF A PHYSIOLOGICALLY ACCEPTABLE ARTIFICIAL SKIN IN THE TREATMENT OF EXTENSIVE BURN INJURY [J].
BURKE, JF ;
YANNAS, IV ;
QUINBY, WC ;
BONDOC, CC ;
JUNG, WK .
ANNALS OF SURGERY, 1981, 194 (04) :413-428
[3]
USE OF CULTURED EPIDERMAL AUTOGRAFTS AND DERMAL ALLOGRAFTS AS SKIN REPLACEMENT AFTER BURN INJURY [J].
CUONO, C ;
LANGDON, R ;
MCGUIRE, J .
LANCET, 1986, 1 (8490) :1123-1124
[4]
de Vries H J, 1994, Wound Repair Regen, V2, P37, DOI 10.1046/j.1524-475X.1994.20107.x
[5]
FANG C-H, 1990, Journal of Burn Care and Rehabilitation, V11, P538, DOI 10.1097/00004630-199011000-00009
[6]
THE ACCEPTANCE AND EVOLUTION OF DERMAL HOMOGRAFTS FREED OF VIABLE CELLS [J].
GRILLO, HC ;
MCKHANN, CF .
TRANSPLANTATION, 1964, 2 (01) :48-59
[7]
RECONSTITUTION OF HUMAN-EPIDERMIS INVITRO IS ACCOMPANIED BY TRANSIENT ACTIVATION OF BASAL KERATINOCYTE SPREADING [J].
GRINNELL, F ;
TODA, K ;
LAMKESEYMOUR, C .
EXPERIMENTAL CELL RESEARCH, 1987, 172 (02) :439-449
[8]
BURN WOUND CLOSURE WITH CULTURED AUTOLOGOUS KERATINOCYTES AND FIBROBLASTS ATTACHED TO A COLLAGEN-GLYCOSAMINOGLYCAN SUBSTRATE [J].
HANSBROUGH, JF ;
BOYCE, ST ;
COOPER, ML ;
FOREMAN, TJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 262 (15) :2125-2130
[9]
Hansbrough John F., 1992, Journal of Burn Care and Rehabilitation, V13, P519, DOI 10.1097/00004630-199209000-00004
[10]
ARTIFICIAL DERMIS FOR MAJOR BURNS - A MULTI-CENTER RANDOMIZED CLINICAL-TRIAL [J].
HEIMBACH, D ;
LUTERMAN, A ;
BURKE, J ;
CRAM, A ;
HERNDON, D ;
HUNT, J ;
JORDAN, M ;
MCMANUS, W ;
SOLEM, L ;
WARDEN, G ;
ZAWACKI, B .
ANNALS OF SURGERY, 1988, 208 (03) :313-320