2005
DOI: 10.1016/s0140-6736(05)67192-9
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Skin construct or biological bandage?

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Cited by 7 publications
(6 citation statements)
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“…Phillips et al (2002) reported that the patients treated with a bilayered skin substitute (Apligraf) showed no persistence of allogeneic DNA at 2 months after initial grafting. Our results may explain why the ordinary skin substitutes do not appear to survive permanently after grafting (Scott and Tredget, 2005). These results demonstrate that it might be necessary to increase the ratio of epidermal stem cells in epidermis and the expression of markers in order to create closer resemblance normal skin.…”
Section: Discussionmentioning
confidence: 68%
“…Phillips et al (2002) reported that the patients treated with a bilayered skin substitute (Apligraf) showed no persistence of allogeneic DNA at 2 months after initial grafting. Our results may explain why the ordinary skin substitutes do not appear to survive permanently after grafting (Scott and Tredget, 2005). These results demonstrate that it might be necessary to increase the ratio of epidermal stem cells in epidermis and the expression of markers in order to create closer resemblance normal skin.…”
Section: Discussionmentioning
confidence: 68%
“…In the areas where dermis is lost, the newly formed epidermal layer lacks support as it can easily break down under pressure. As a consequence, cells and matrices were integrated in a number of different strategies to introduce bioengineered skin, tissue-engineered skin constructs, bio-synthetic skin substitutes, bio-constructs and other terms [ 21 , 4 ]. These solutions aim to restore the intact barrier that protects the wound from infections, provides pain relief, enables temperature control and prevents fluid loss from the wound surface.…”
Section: Reviewmentioning
confidence: 99%
“…The survival rate became even higher in children, with up to 50% enhanced survivability with 95% burns of TBSA [ 3 ]. The enhanced survival was associated with the emergence of novel solutions for wound coverage that tackle later complications, limit fluid loss, control pain and reduce the risk of hypertrophic scarring [ 4 ].…”
Section: Introductionmentioning
confidence: 99%
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“…There are two explanations for the results of this study: migration of fetal dermal cells into the wound bed, or that these cells only provided growth factors, chemokines and cytokines by paracrine signaling (Chen et al 2008 ; Gnecchi et al 2008 ; Hocking and Gibran 2010 ). Furthermore, the burn wounds of the children treated with the fetal dermal constructs seemed relatively small, and were possibly not completely full-thickness wounds (Scott and Tredget 2005 ). Therefore, the beneficial effects of dermal substitutes containing fetal dermal cells for the application in full-thickness (burn) wounds remain to be elucidated.…”
Section: Introductionmentioning
confidence: 99%