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The The UKM StimuGold (UKMSG) Wound Bed Preparation Method: A unique technique in combining Superabsorbent Polymer Polyacrylate Sodium with Collagen–Glycerine amorphous base dressing: A case series

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Keywords

chronic wound, recalcitrant wound, UKMSG method, Collagen-Glycerine base amorphous gel, Superabsorbent Polyacrylate Sodium, dressing, wound debridement.

How to Cite

sim, linkiat, & Farrah-Hani Imran. (2022). The The UKM StimuGold (UKMSG) Wound Bed Preparation Method: A unique technique in combining Superabsorbent Polymer Polyacrylate Sodium with Collagen–Glycerine amorphous base dressing: A case series. British Journal Of Surgical Science, 2(1). Retrieved from https://britishjournalofsurgicalscience.uk/index.php/bjoss/article/view/18

Abstract

Introduction: A wound is a disruption of the normal structure and function of the skin and its
architecture. An acute wound heals predictably, time frame, if any, with few complications but
the result is a well-healed wound. A chronic wound is defined as one that is physiologically
impaired due to the disruption of the wound healing cycle. Advanced dressings are designed to
maintain a moist environment at the site of application, allowing the fluids to remain close to the
wound and not spread to the unaffected, healthy skin areas. We developed a unique technique of
dressing combining Superabsorbent Polyacrylate Sodium (Gold Dust®) with Collagen-Glycerine
base amorphous gel (Stimulen®), A.K.A, UKMSG, in six patients with acute and chronic wounds
of various aetiology; referred for recalcitrant, non-healing wound.
Case Presentation & Methods: Six patients with acute and chronic wounds of various aetiology
were referred for recalcitrant, non-healing wounds. Patients’ data were obtained from medical
files and surgical databases. Depending on the size and condition of the wound, the average
duration of treatment varies from 1 - 6 weeks. The dressing was done mainly by wound nurses.
Dressings were changed from daily to once every three days, based on the type of wounds. It does
not need a lot of experience for the application of UKMSG. A short briefing and demonstration on
how to apply the dressing would suffice. We did not start adjuvant antibiotics for all our wounds.
Antibiotics were only started for infected wounds and based on cultures & sensitivity. There were
two females and four males. The youngest in the group was 2 years old and the oldest was 72
years old. We had two pressure ulcers, one gangrenous penis, one Surgical Site Infection wound
breakdown post total hysterectomy, one lower abdominal wall necrotizing fasciitis, and a 23%
infected burn wound. All patients’ wounds were initially managed by respective primary teams
(except the infected burn wound) with dressings and surgical debridement is done at least once
but a healthy wound bed was still not achieved.
Results: The UKMSG is part of our Wound Care Team approach to wound management across
a variety of wounds. Through the case series, we noted that UKMSG is ideal for the treatment
of recalcitrant, non-healing, moderate to highly exudative wounds. It produces a good result in
wound bed preparation. It is also easy to apply and removed, comfortable, has fewer peri-wound
complications, and does not need an expensive secondary dressing. In the future, we aim to
perform an RCT and comparison study to further evaluate the UKMSG method.      

References

Atiyeh BS, Ioannovich J, AlAmm CA, ElMusa KA. Management of acute and chronic open wounds: the importance of moist environment in optimal wound healing. Curr Pharm Biotechnol 2002; 3:179.

Schultz GS, Sibbald RG, Falanga V, et al. Wound bed preparation: a systematic approach to wound management. Wound Repair Regen 2003; 11 Suppl 1:S1.

Patel S, Marshall J, Fitzke 3rd FW. J Refract Surg 1995;11:100–5.

Peppas NA, Bures P, Leobandung W, Ichikawa H. Eur J Pharm Biopharm 2000;50:27–46.

A. E. Postlethwaite, J. M. Seyer and A. H. Kang, Pwe. Nati. Acad. Sei. USA 78, 871 (1978).

H. Ohara, S. Ichikawa, H. Matsumoto, M. Akiyama, N. Fujimoto, T. Kobayashi and S. Tajima,

J. Dermatol. 37, 330 (2010).

Beldon P. Wound Essentials 2010;5:140–4.

Trengove NJ, Stacey MC, Macauley S, Bennett N, Gibson J,Burslem F, Murphy G, Schultz G. Analysis of the acute and chronic wound environments: the role of proteases and their

inhibitors. Wound Rep Reg. 1999;7:442–52.

Barrick B, Campbell EJ, Owen CA. Leukocyte proteinases in wound healing: roles in physiologic and pathologic processes.Wound Rep Reg. 1999;7:410–22.

Rojkind M, Dominguez-Rosales J-A, Nieto N, Greenwel P. Role of hydrogen peroxide and oxidative stress in healing responses.Cell Mol Life Sci. 2002;59:1872–91.

Eming S, Smola H, Hartmann B, Malchau G, Wegner R, Krieg T,Smola-Hess S. The inhibition of matrix metalloproteinase activity in chronic wounds by a polyacrylate superabsorber. Biomaterials.2008;29:2932–40.

Wiegand C, Abel M, Ruth P, Hipler UC. Superabsorbent polymercontaining wound dressings have a beneficial effect on wound healing by reducing PMN elastase concentration and inhibiting microbial growth. J Mater Sci Mater Med. 2011;22:2583–90.

Park SN, Lee HJ, Lee KH, Suh H. Biological characterization of EDC-crosslinked collagen-hyaluronic acid matrix in dermal tissue restoration. Biomaterials 2003;24:1631-41.

Lazovic G, Colic M, Grubor M, Jovanovic M. The application of collagen sheet in open wound healing. Ann Burns Fire Disasters 2005;18:151-6.

Veves A, Sheehan P, Pham HT. A randomized, controlled trial of promogran (a collagen/oxidized regenerated cellulose dressing) vs standard treatment in the management of diabetic foot ulcers. Arch Surg 2002;137:822-7.

Schultz GS, Sibbald RG, Falanga V, et al. Wound bed preparation: a systematic approach to wound management. Wound Repair Regen 2003; 11 Suppl 1:S1.

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