Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission.

Plast Reconstr Surg Glob Open

Department of Surgery, University of Arizona, Tucson, Ariz.; Department of Biomedical Engineering, University of Arizona, Tucson, Ariz.; and Research and Development, Musculoskeletal Transplant Foundation (MTF), Edison, N.J.

Published: October 2017

Background: Repetitive stress on the neuropathic plantar foot is the primary cause of diabetic foot ulcers. After healing, recurrence is common. Modulating plantar pressure has been associated with extension of ulcer free days. Therefore, the goal of this study was to determine the effects of an injectable allograft adipose matrix in providing a protective padding and reducing the pressure in the plantar foot.

Methods: After healing his recurrent ulcer using total contact casting, a 71-year-old man with a 9-year history of recurrent diabetic foot ulcers was treated with injection of allograft adipose matrix, procured from donated human tissue. This was delivered under postulcerative callus on the weight-bearing surface of the distal end of the first ray resection. As is standard in our clinic for tissue augmentation procedures, our patient underwent serial plantar pressure mapping using an in-shoe pressure monitoring system.

Results: There was a 76.8% decrease in the mean peak pressure due to the fat matrix injected into the second metatarsal region and a 70.1% decrease in mean peak pressure for the first ray resection at the site of the postulcerative callus. By 2 months postoperatively, there was no evidence of residual callus. This extended out to the end of clinical follow-up at 4 months.

Conclusion: The results from this preliminary experience suggest that allograft adipose matrix delivered to the high risk diabetic foot may have promise in reducing tissue stress over pre- and postulcerative lesions. This may ultimately assist the clinician in extending ulcer-free days for patients in diabetic foot remission.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682189PMC
http://dx.doi.org/10.1097/GOX.0000000000001555DOI Listing

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