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

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 inj...

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Autores principales: Shahin, Tala B., Vaishnav, Kairavi V., Watchman, Marcy, Subbian, Vignesh, Larson, Ethan, Chnari, Evangelia, Armstrong, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682189/
https://www.ncbi.nlm.nih.gov/pubmed/29184753
http://dx.doi.org/10.1097/GOX.0000000000001555
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author Shahin, Tala B.
Vaishnav, Kairavi V.
Watchman, Marcy
Subbian, Vignesh
Larson, Ethan
Chnari, Evangelia
Armstrong, David G.
author_facet Shahin, Tala B.
Vaishnav, Kairavi V.
Watchman, Marcy
Subbian, Vignesh
Larson, Ethan
Chnari, Evangelia
Armstrong, David G.
author_sort Shahin, Tala B.
collection PubMed
description 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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spelling pubmed-56821892017-11-28 Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission Shahin, Tala B. Vaishnav, Kairavi V. Watchman, Marcy Subbian, Vignesh Larson, Ethan Chnari, Evangelia Armstrong, David G. Plast Reconstr Surg Glob Open Case Report 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. Wolters Kluwer Health 2017-10-23 /pmc/articles/PMC5682189/ /pubmed/29184753 http://dx.doi.org/10.1097/GOX.0000000000001555 Text en Copyright © 2017 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Report
Shahin, Tala B.
Vaishnav, Kairavi V.
Watchman, Marcy
Subbian, Vignesh
Larson, Ethan
Chnari, Evangelia
Armstrong, David G.
Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission
title Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission
title_full Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission
title_fullStr Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission
title_full_unstemmed Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission
title_short Tissue Augmentation with Allograft Adipose Matrix For the Diabetic Foot in Remission
title_sort tissue augmentation with allograft adipose matrix for the diabetic foot in remission
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682189/
https://www.ncbi.nlm.nih.gov/pubmed/29184753
http://dx.doi.org/10.1097/GOX.0000000000001555
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