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The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion

Terminal hip flexion contributes to increased strain in peripheral nerves at the level of the hip joint. The effects of hip abduction and femoral version on sciatic nerve biomechanics are not well understood. A decrease in sciatic nerve strain will be observed during terminal hip flexion and hip abd...

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Autores principales: Martin, Hal David, Khoury, Anthony N., Schroder, Ricardo, Gomez-Hoyos, Juan, Yeramaneni, Samrat, Reddy, Manoj, James Palmer, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467418/
https://www.ncbi.nlm.nih.gov/pubmed/28630740
http://dx.doi.org/10.1093/jhps/hnx008
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author Martin, Hal David
Khoury, Anthony N.
Schroder, Ricardo
Gomez-Hoyos, Juan
Yeramaneni, Samrat
Reddy, Manoj
James Palmer, Ian
author_facet Martin, Hal David
Khoury, Anthony N.
Schroder, Ricardo
Gomez-Hoyos, Juan
Yeramaneni, Samrat
Reddy, Manoj
James Palmer, Ian
author_sort Martin, Hal David
collection PubMed
description Terminal hip flexion contributes to increased strain in peripheral nerves at the level of the hip joint. The effects of hip abduction and femoral version on sciatic nerve biomechanics are not well understood. A decrease in sciatic nerve strain will be observed during terminal hip flexion and hip abduction, independent of femoral version. Six un-embalmed human cadavers were utilized. Three Differential Variable Reluctance Transducers (DVRTs) sensors were placed on the sciatic nerve while the leg was flexed to 70° with a combination of − 10°, 0°, 20° and 40° adduction/abduction. DVRT placement included: (i) under piriformis, (ii) immediately distal to the gemelli/obturator, (iii) four centimeters distal to sensor two. A de-rotational osteotomy to decrease femoral version 10° was performed, and sciatic nerve strain was measured by the same procedure. Data were analyzed with three-way analysis of variance and Bonferroni post-hoc analysis to identify differences in the mean values of sciatic nerve strain between native and decreased version state, hip abduction angle and DVRT sensor location. Significant main effects were observed for femoral version (P = 0.04) and DVRT sensor location (P = 0.01). Sciatic nerve strain decreased during terminal hip flexion and abduction in the decreased version state. An 84.23% decrease in sciatic nerve strain was observed during hip abduction from neutral to 40° in the presence of decreased version at terminal hip flexion. The results obtained from this study confirm the role of decreased femoral version and hip abduction at terminal hip flexion to decrease the strain in the sciatic nerve.
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spelling pubmed-54674182017-06-19 The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion Martin, Hal David Khoury, Anthony N. Schroder, Ricardo Gomez-Hoyos, Juan Yeramaneni, Samrat Reddy, Manoj James Palmer, Ian J Hip Preserv Surg Research Articles Terminal hip flexion contributes to increased strain in peripheral nerves at the level of the hip joint. The effects of hip abduction and femoral version on sciatic nerve biomechanics are not well understood. A decrease in sciatic nerve strain will be observed during terminal hip flexion and hip abduction, independent of femoral version. Six un-embalmed human cadavers were utilized. Three Differential Variable Reluctance Transducers (DVRTs) sensors were placed on the sciatic nerve while the leg was flexed to 70° with a combination of − 10°, 0°, 20° and 40° adduction/abduction. DVRT placement included: (i) under piriformis, (ii) immediately distal to the gemelli/obturator, (iii) four centimeters distal to sensor two. A de-rotational osteotomy to decrease femoral version 10° was performed, and sciatic nerve strain was measured by the same procedure. Data were analyzed with three-way analysis of variance and Bonferroni post-hoc analysis to identify differences in the mean values of sciatic nerve strain between native and decreased version state, hip abduction angle and DVRT sensor location. Significant main effects were observed for femoral version (P = 0.04) and DVRT sensor location (P = 0.01). Sciatic nerve strain decreased during terminal hip flexion and abduction in the decreased version state. An 84.23% decrease in sciatic nerve strain was observed during hip abduction from neutral to 40° in the presence of decreased version at terminal hip flexion. The results obtained from this study confirm the role of decreased femoral version and hip abduction at terminal hip flexion to decrease the strain in the sciatic nerve. Oxford University Press 2017-04-11 /pmc/articles/PMC5467418/ /pubmed/28630740 http://dx.doi.org/10.1093/jhps/hnx008 Text en © The Author 2017. Published by Oxford University Press http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Articles
Martin, Hal David
Khoury, Anthony N.
Schroder, Ricardo
Gomez-Hoyos, Juan
Yeramaneni, Samrat
Reddy, Manoj
James Palmer, Ian
The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
title The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
title_full The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
title_fullStr The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
title_full_unstemmed The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
title_short The effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
title_sort effects of hip abduction on sciatic nerve biomechanics during terminal hip flexion
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467418/
https://www.ncbi.nlm.nih.gov/pubmed/28630740
http://dx.doi.org/10.1093/jhps/hnx008
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