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Clinical Trial
. 2003 Apr;50(4):367-72.
doi: 10.1097/01.SAP.0000041484.22953.6D.

Hemostatic effect of Vivostat patient-derived fibrin sealant on split-thickness skin graft donor sites

Affiliations
Clinical Trial

Hemostatic effect of Vivostat patient-derived fibrin sealant on split-thickness skin graft donor sites

David B Drake et al. Ann Plast Surg. 2003 Apr.

Abstract

Topical hemostatic agents are used frequently to control bleeding of skin graft donor sites. In this study, the hemostatic properties of Vivostat (Vivolution A/S, Birkerød, Denmark) patient-derived fibrin sealant were compared with a control group of spray thrombin solution, which is considered an industry standard for topical hemostasis. Treatments were applied simultaneously to two randomly chosen halves of a single split-thickness single donor site in patients in five United States surgical centers. The time to achieve satisfactory hemostasis (< or =10 min) was estimated on each half of the wound as the time at which active bleeding had stopped and the wound was suitable for application of a surgical dressing. The time to hemostasis of wounds treated with Vivostat (Vivolution A/S) patient-derived sealant was significantly shorter in comparison with wounds treated with thrombin solution (medians: Vivostat, 31 seconds; thrombin, 58 seconds; p=0.0012). No abnormalities in wound healing were reported for either treatment site 1 week after the operation. Vivostat (Vivolution A/S) sealant is a more rapidly effective topical hemostatic agent than thrombin on split-thickness skin graft donor sites.

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