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Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain

Although extensive research shows an association between distal radius fractures and the development of median nerve related pathologies such as carpal tunnel syndrome, none directly track how the resulting angular deformity relates to likelihood of development of median nerve pathology. METHODS: Me...

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Autores principales: Obiofuma, Chukwuka, Dy, Christopher, Iannucci, Leanne E., Lake, Spencer P., Brogan, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947617/
https://www.ncbi.nlm.nih.gov/pubmed/35350145
http://dx.doi.org/10.1097/GOX.0000000000004177
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author Obiofuma, Chukwuka
Dy, Christopher
Iannucci, Leanne E.
Lake, Spencer P.
Brogan, David
author_facet Obiofuma, Chukwuka
Dy, Christopher
Iannucci, Leanne E.
Lake, Spencer P.
Brogan, David
author_sort Obiofuma, Chukwuka
collection PubMed
description Although extensive research shows an association between distal radius fractures and the development of median nerve related pathologies such as carpal tunnel syndrome, none directly track how the resulting angular deformity relates to likelihood of development of median nerve pathology. METHODS: Median nerve strain was measured with a custom-built system using a camera, optical markers, and a proprietary segmentation algorithm. After initial validation of the system in a cadaver model, our system was used to assess strain in 10 cadaver arms with a simulated distal radius fracture and increasing dorsal angulation. The measured strain at each angle was then analyzed using a linear regression model. RESULTS: The linear regression model in the validation experiment demonstrated a regression coefficient of 1.00067 (P < 0.0001) with r(2) = 0.899, thus validating the use of the optical tracking system. The average strain at maximum dorsal angulation (50 degrees) across all specimens was −0.2%. Linear regression analysis of the effect of increasing dorsal angulation on strain in the osteotomy model yielded a regression coefficient of −0.000048 (P = 0.714), r(2) = 0.00129, suggesting no significant correlation between increasing dorsal tilt and median nerve strain. CONCLUSIONS: Increases in median nerve strain at the wrist are negligible with increasing dorsal tilt in a distal radius fracture model. It is therefore likely that other factors, such as increased pressure within the carpal tunnel, are the primary cause of median neuropathy in distal radius malunions. Therefore, correction of dorsal tilt may not be required to improve neurologic symptoms.
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spelling pubmed-89476172022-03-28 Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain Obiofuma, Chukwuka Dy, Christopher Iannucci, Leanne E. Lake, Spencer P. Brogan, David Plast Reconstr Surg Glob Open Hand Although extensive research shows an association between distal radius fractures and the development of median nerve related pathologies such as carpal tunnel syndrome, none directly track how the resulting angular deformity relates to likelihood of development of median nerve pathology. METHODS: Median nerve strain was measured with a custom-built system using a camera, optical markers, and a proprietary segmentation algorithm. After initial validation of the system in a cadaver model, our system was used to assess strain in 10 cadaver arms with a simulated distal radius fracture and increasing dorsal angulation. The measured strain at each angle was then analyzed using a linear regression model. RESULTS: The linear regression model in the validation experiment demonstrated a regression coefficient of 1.00067 (P < 0.0001) with r(2) = 0.899, thus validating the use of the optical tracking system. The average strain at maximum dorsal angulation (50 degrees) across all specimens was −0.2%. Linear regression analysis of the effect of increasing dorsal angulation on strain in the osteotomy model yielded a regression coefficient of −0.000048 (P = 0.714), r(2) = 0.00129, suggesting no significant correlation between increasing dorsal tilt and median nerve strain. CONCLUSIONS: Increases in median nerve strain at the wrist are negligible with increasing dorsal tilt in a distal radius fracture model. It is therefore likely that other factors, such as increased pressure within the carpal tunnel, are the primary cause of median neuropathy in distal radius malunions. Therefore, correction of dorsal tilt may not be required to improve neurologic symptoms. Lippincott Williams & Wilkins 2022-03-24 /pmc/articles/PMC8947617/ /pubmed/35350145 http://dx.doi.org/10.1097/GOX.0000000000004177 Text en Copyright © 2022 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. https://creativecommons.org/licenses/by-nc-nd/4.0/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) (https://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 Hand
Obiofuma, Chukwuka
Dy, Christopher
Iannucci, Leanne E.
Lake, Spencer P.
Brogan, David
Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain
title Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain
title_full Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain
title_fullStr Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain
title_full_unstemmed Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain
title_short Increasing Dorsal Tilt in Distal Radius Fractures Does Not Increase Median Nerve Strain
title_sort increasing dorsal tilt in distal radius fractures does not increase median nerve strain
topic Hand
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947617/
https://www.ncbi.nlm.nih.gov/pubmed/35350145
http://dx.doi.org/10.1097/GOX.0000000000004177
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