Cargando…

Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction

Autologous tissue transfer, in addition to replacing tissue that was lost during injury or surgery, offers women an excellent option to improve cosmetic appearance and self-confidence following mastectomy due to breast cancer. However, flap necrosis is a complication in obese patients undergoing thi...

Descripción completa

Detalles Bibliográficos
Autores principales: Womac, Daniel John, Palanisamy, Arun Prathap, Eslick, Rene, Schimpf, Dennis Kenneth, Chavin, Kenneth David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538734/
https://www.ncbi.nlm.nih.gov/pubmed/23308122
http://dx.doi.org/10.1371/journal.pone.0052829
_version_ 1782255004885712896
author Womac, Daniel John
Palanisamy, Arun Prathap
Eslick, Rene
Schimpf, Dennis Kenneth
Chavin, Kenneth David
author_facet Womac, Daniel John
Palanisamy, Arun Prathap
Eslick, Rene
Schimpf, Dennis Kenneth
Chavin, Kenneth David
author_sort Womac, Daniel John
collection PubMed
description Autologous tissue transfer, in addition to replacing tissue that was lost during injury or surgery, offers women an excellent option to improve cosmetic appearance and self-confidence following mastectomy due to breast cancer. However, flap necrosis is a complication in obese patients undergoing this procedure. We created a mouse model to study the flap-related complications that leads to decreased flap survival in autologous breast reconstruction. METHODS: Left superficial inferior epigastric (SIE) pedicle abdominal-cutaneous flaps were elevated in 8 week-old, obese ob/ob male mice and their lean littermates. Flaps were followed by serial photography. Area of flap necrosis was measured at 7 days. Statistical analysis was performed. RESULTS: Necrosis was observed at the distal margin of the flaps, in both lean and obese groups. Lean left SIE flaps (n = 8) had a total area flap necrosis of 9.1% at 7 days whereas obese left SIE flaps (n = 8) had a total area flap necrosis of 45.5% at 7 days. Obese flaps had a statistically significant increase in necrosis compared to the lean flaps, p = 0.001. CONCLUSIONS: There was a significant difference between flap survival in lean and obese SIE pedicle flaps in our mouse model. We have developed the first flap model of obesity utilizing the superficial epigastric pedicle in the mouse. This model is optimal for future studies to dissect out mechanisms that lead to the complications related to flap survival for breast reconstruction, especially in obese subjects.
format Online
Article
Text
id pubmed-3538734
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35387342013-01-10 Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction Womac, Daniel John Palanisamy, Arun Prathap Eslick, Rene Schimpf, Dennis Kenneth Chavin, Kenneth David PLoS One Research Article Autologous tissue transfer, in addition to replacing tissue that was lost during injury or surgery, offers women an excellent option to improve cosmetic appearance and self-confidence following mastectomy due to breast cancer. However, flap necrosis is a complication in obese patients undergoing this procedure. We created a mouse model to study the flap-related complications that leads to decreased flap survival in autologous breast reconstruction. METHODS: Left superficial inferior epigastric (SIE) pedicle abdominal-cutaneous flaps were elevated in 8 week-old, obese ob/ob male mice and their lean littermates. Flaps were followed by serial photography. Area of flap necrosis was measured at 7 days. Statistical analysis was performed. RESULTS: Necrosis was observed at the distal margin of the flaps, in both lean and obese groups. Lean left SIE flaps (n = 8) had a total area flap necrosis of 9.1% at 7 days whereas obese left SIE flaps (n = 8) had a total area flap necrosis of 45.5% at 7 days. Obese flaps had a statistically significant increase in necrosis compared to the lean flaps, p = 0.001. CONCLUSIONS: There was a significant difference between flap survival in lean and obese SIE pedicle flaps in our mouse model. We have developed the first flap model of obesity utilizing the superficial epigastric pedicle in the mouse. This model is optimal for future studies to dissect out mechanisms that lead to the complications related to flap survival for breast reconstruction, especially in obese subjects. Public Library of Science 2013-01-07 /pmc/articles/PMC3538734/ /pubmed/23308122 http://dx.doi.org/10.1371/journal.pone.0052829 Text en © 2013 Womac et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Womac, Daniel John
Palanisamy, Arun Prathap
Eslick, Rene
Schimpf, Dennis Kenneth
Chavin, Kenneth David
Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction
title Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction
title_full Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction
title_fullStr Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction
title_full_unstemmed Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction
title_short Development of a Mouse Model of Abdominal Cutaneous Flaps for Breast Reconstruction
title_sort development of a mouse model of abdominal cutaneous flaps for breast reconstruction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538734/
https://www.ncbi.nlm.nih.gov/pubmed/23308122
http://dx.doi.org/10.1371/journal.pone.0052829
work_keys_str_mv AT womacdanieljohn developmentofamousemodelofabdominalcutaneousflapsforbreastreconstruction
AT palanisamyarunprathap developmentofamousemodelofabdominalcutaneousflapsforbreastreconstruction
AT eslickrene developmentofamousemodelofabdominalcutaneousflapsforbreastreconstruction
AT schimpfdenniskenneth developmentofamousemodelofabdominalcutaneousflapsforbreastreconstruction
AT chavinkennethdavid developmentofamousemodelofabdominalcutaneousflapsforbreastreconstruction