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Differentiating Extensor Plantar Response in Pathological and Normal Population
INTRODUCTION: Approximately 5%–11% of neurologically normal population has extensor plantar response (EPR). METHOD: This study is aimed to identify differentiating features of EPR between physiological and pathological population. RESULTS: A total of 43 patients with pyramidal lesions and 113 normal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073965/ https://www.ncbi.nlm.nih.gov/pubmed/30122841 http://dx.doi.org/10.4103/aian.AIAN_254_17 |
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author | Loo, Shweh Fern Justin, Nicole Kelsie Lee, Ri An Hew, Yin Cheng Lim, Kheng Seang Tan, Chong Tin |
author_facet | Loo, Shweh Fern Justin, Nicole Kelsie Lee, Ri An Hew, Yin Cheng Lim, Kheng Seang Tan, Chong Tin |
author_sort | Loo, Shweh Fern |
collection | PubMed |
description | INTRODUCTION: Approximately 5%–11% of neurologically normal population has extensor plantar response (EPR). METHOD: This study is aimed to identify differentiating features of EPR between physiological and pathological population. RESULTS: A total of 43 patients with pyramidal lesions and 113 normal controls were recruited for this study. The pathological EPRs were more reproducible, with 89.4% having at least two positive Babinski responses and 91.5% having two positive Chaddock responses (vs. 14.3% and 4.8% in controls, P < 0.001). The pathological EPR was more sensitive to stimulation, in which 89.1% were elicited when the stimulation reached mid-lateral sole (vs. 11.9% in controls, P < 0.001). Most (93.6%) pathological cases had sustained big toe extension throughout stimulation (vs. 73.8% in controls, P < 0.001). As compared to those with brain lesion, the plantar responses in those with spinal lesion are less likely to have ankle dorsiflexion (5.3% vs. 25%, P < 0.05) more likely to have sustained extensor response with Babinski (94.7% vs. 71.4%, P < 0.05), Chaddock (89.5% vs. 64.3%, P < 0.05), and Schaefer (26.3% vs. 3.6%, P < 0.05) methods. A scoring system was computed using four variables, i.e., two consecutive positive Babinski or Chaddock responses, extensor response at mid-lateral sole, and sustained extension throughout stimulation. A score ≥3 is predictive of pathological origin, with sensitivity and specificity of 78.7% and 95.2%, respectively. CONCLUSION: The pathological EPR is more reproducible, sensitive to stimulation, and sustainable compared to physiological extensor response. |
format | Online Article Text |
id | pubmed-6073965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60739652018-08-17 Differentiating Extensor Plantar Response in Pathological and Normal Population Loo, Shweh Fern Justin, Nicole Kelsie Lee, Ri An Hew, Yin Cheng Lim, Kheng Seang Tan, Chong Tin Ann Indian Acad Neurol Original Article INTRODUCTION: Approximately 5%–11% of neurologically normal population has extensor plantar response (EPR). METHOD: This study is aimed to identify differentiating features of EPR between physiological and pathological population. RESULTS: A total of 43 patients with pyramidal lesions and 113 normal controls were recruited for this study. The pathological EPRs were more reproducible, with 89.4% having at least two positive Babinski responses and 91.5% having two positive Chaddock responses (vs. 14.3% and 4.8% in controls, P < 0.001). The pathological EPR was more sensitive to stimulation, in which 89.1% were elicited when the stimulation reached mid-lateral sole (vs. 11.9% in controls, P < 0.001). Most (93.6%) pathological cases had sustained big toe extension throughout stimulation (vs. 73.8% in controls, P < 0.001). As compared to those with brain lesion, the plantar responses in those with spinal lesion are less likely to have ankle dorsiflexion (5.3% vs. 25%, P < 0.05) more likely to have sustained extensor response with Babinski (94.7% vs. 71.4%, P < 0.05), Chaddock (89.5% vs. 64.3%, P < 0.05), and Schaefer (26.3% vs. 3.6%, P < 0.05) methods. A scoring system was computed using four variables, i.e., two consecutive positive Babinski or Chaddock responses, extensor response at mid-lateral sole, and sustained extension throughout stimulation. A score ≥3 is predictive of pathological origin, with sensitivity and specificity of 78.7% and 95.2%, respectively. CONCLUSION: The pathological EPR is more reproducible, sensitive to stimulation, and sustainable compared to physiological extensor response. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6073965/ /pubmed/30122841 http://dx.doi.org/10.4103/aian.AIAN_254_17 Text en Copyright: © 2006 - 2018 Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Loo, Shweh Fern Justin, Nicole Kelsie Lee, Ri An Hew, Yin Cheng Lim, Kheng Seang Tan, Chong Tin Differentiating Extensor Plantar Response in Pathological and Normal Population |
title | Differentiating Extensor Plantar Response in Pathological and Normal Population |
title_full | Differentiating Extensor Plantar Response in Pathological and Normal Population |
title_fullStr | Differentiating Extensor Plantar Response in Pathological and Normal Population |
title_full_unstemmed | Differentiating Extensor Plantar Response in Pathological and Normal Population |
title_short | Differentiating Extensor Plantar Response in Pathological and Normal Population |
title_sort | differentiating extensor plantar response in pathological and normal population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073965/ https://www.ncbi.nlm.nih.gov/pubmed/30122841 http://dx.doi.org/10.4103/aian.AIAN_254_17 |
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