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Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes
Autologous breast reconstruction is widely regarded as the gold standard approach following mastectomy. However, the lack of sensation continues to present a reconstructive challenge. In this study, clinical outcomes following abdominal flap neurotization with processed human nerve allograft were in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859176/ https://www.ncbi.nlm.nih.gov/pubmed/33564572 http://dx.doi.org/10.1097/GOX.0000000000003328 |
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author | Momeni, Arash Meyer, Shannon Shefren, Kerry Januszyk, Michael |
author_facet | Momeni, Arash Meyer, Shannon Shefren, Kerry Januszyk, Michael |
author_sort | Momeni, Arash |
collection | PubMed |
description | Autologous breast reconstruction is widely regarded as the gold standard approach following mastectomy. However, the lack of sensation continues to present a reconstructive challenge. In this study, clinical outcomes following abdominal flap neurotization with processed human nerve allograft were investigated. METHODS: In this prospective analysis, patients who underwent microsurgical breast reconstruction with (Group 1) or without (Group 2) abdominal flap neurotization at a single institution were investigated. Processed human nerve allograft (Avance, AxoGen, Alachua, Fla.) was used in all cases of flap neurotization. Only patients with a follow-up of ≥12 months were included. Cutaneous pressure threshold was tested using Semmes-Weinstein monofilaments (SWMF) at 9 pre-defined locations. RESULTS: A total of 59 patients (96 breasts) were enrolled into the registry. Of these, 22 patients (Group 1: N = 15, 22 breasts; Group 2: N = 7, 14 breasts) had a complete data set with ≥12 months follow-up. Measuring cutaneous pressure thresholds, we observed a greater likelihood for return of protective sensation (SWMF ≤ 4.31) in neurotized breasts in 8 of the 9 examined zones. Additionally, flap neurotization was associated with a greater likelihood for return of protective sensation in the majority of the reconstructed breast—that is, ≥5 zones (55% versus 7%; P < 0.01). CONCLUSION: Flap neurotization using processed nerve allograft resulted in a greater degree of return of protective sensation to the reconstructed breast than reconstructions without neurotization at ≥12 months. |
format | Online Article Text |
id | pubmed-7859176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-78591762021-02-08 Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes Momeni, Arash Meyer, Shannon Shefren, Kerry Januszyk, Michael Plast Reconstr Surg Glob Open Breast Autologous breast reconstruction is widely regarded as the gold standard approach following mastectomy. However, the lack of sensation continues to present a reconstructive challenge. In this study, clinical outcomes following abdominal flap neurotization with processed human nerve allograft were investigated. METHODS: In this prospective analysis, patients who underwent microsurgical breast reconstruction with (Group 1) or without (Group 2) abdominal flap neurotization at a single institution were investigated. Processed human nerve allograft (Avance, AxoGen, Alachua, Fla.) was used in all cases of flap neurotization. Only patients with a follow-up of ≥12 months were included. Cutaneous pressure threshold was tested using Semmes-Weinstein monofilaments (SWMF) at 9 pre-defined locations. RESULTS: A total of 59 patients (96 breasts) were enrolled into the registry. Of these, 22 patients (Group 1: N = 15, 22 breasts; Group 2: N = 7, 14 breasts) had a complete data set with ≥12 months follow-up. Measuring cutaneous pressure thresholds, we observed a greater likelihood for return of protective sensation (SWMF ≤ 4.31) in neurotized breasts in 8 of the 9 examined zones. Additionally, flap neurotization was associated with a greater likelihood for return of protective sensation in the majority of the reconstructed breast—that is, ≥5 zones (55% versus 7%; P < 0.01). CONCLUSION: Flap neurotization using processed nerve allograft resulted in a greater degree of return of protective sensation to the reconstructed breast than reconstructions without neurotization at ≥12 months. Lippincott Williams & Wilkins 2021-01-12 /pmc/articles/PMC7859176/ /pubmed/33564572 http://dx.doi.org/10.1097/GOX.0000000000003328 Text en Copyright © 2021 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 | Breast Momeni, Arash Meyer, Shannon Shefren, Kerry Januszyk, Michael Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes |
title | Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes |
title_full | Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes |
title_fullStr | Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes |
title_full_unstemmed | Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes |
title_short | Flap Neurotization in Breast Reconstruction with Nerve Allografts: 1-year Clinical Outcomes |
title_sort | flap neurotization in breast reconstruction with nerve allografts: 1-year clinical outcomes |
topic | Breast |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859176/ https://www.ncbi.nlm.nih.gov/pubmed/33564572 http://dx.doi.org/10.1097/GOX.0000000000003328 |
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