Issue |
J Extra Corpor Technol
Volume 38, Number 3, September 2006
|
|
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Page(s) | 260 - 264 | |
DOI | https://doi.org/10.1051/ject/200638260 | |
Published online | 15 September 2006 |
Abstract
Platelet-Rich Plasma Combined With Skin Substitute for Chronic Wound Healing: A Case Report
Address correspondence to: Rebecca L. Knox, Trinity Medical Center, WOR 2701 17th Street Rock Island, IL 61201. E-mail: rebeccaahlgren@hotmail.com
Contemporary management of chronic wounds focuses on improving natural healing and individualization of treatment. Incorporating multiple therapies has become increasingly common. Of interest are autologous growth factors, which are especially important in chronic wound healing and may contribute to tissue formation and epithelialization. Autologous platelet concentrate or platelet-rich plasma (PRP) is a concentration of at least five autologous growth factors and has been shown to accelerate wound healing and may have infection-fighting properties. Chronic wound healing is complicated by both decreased growth factor availability and infection, making PRP use valuable in these types of wounds. In this report, the use of PRP therapy alone and in combination with a bioengineered skin substitute as a platelet-rich tissue graft in a chronic, non-healing wound is detailed. Over 27 weeks, the patient received multiple therapies in attempts to heal a severe decubitus ulcer of the sacrum. The introduction of PRP therapy at Week 14 led to a 26% reduction in wound depth over 4 weeks. At Week 19, PRP therapy was combined with a powdered skin substitute to create a platelet-rich tissue graft. The combination brought dramatic results, eliminating wound tunneling and reducing the wound dimensions from 6.2 cm long × 6.7 cm wide × 2.7 cm deep to 5.0 cm long × 6.0 cm wide × 1.4 cm deep. The promising observations from this case report indicate that further study on the combining of PRP therapy and skin substitutes is necessary.
Key words: platelet-rich plasma / chronic wounds / growth factors / skin substitutes / infection
© 2006 AMSECT
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