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Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies

OBJECTIVE: To examine differences in somatosensory phenotypes of patients with positive and negative neurodynamic tests and compare these with healthy participants. DESIGN: Case-control study. SETTING: University department. PARTICIPANTS: Patients with electrodiagnostically confirmed carpal tunnel s...

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Autores principales: Baselgia, Larissa T., Bennett, David L., Silbiger, Robert M., Schmid, Annina B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: W.B. Saunders 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324720/
https://www.ncbi.nlm.nih.gov/pubmed/27449322
http://dx.doi.org/10.1016/j.apmr.2016.06.019
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author Baselgia, Larissa T.
Bennett, David L.
Silbiger, Robert M.
Schmid, Annina B.
author_facet Baselgia, Larissa T.
Bennett, David L.
Silbiger, Robert M.
Schmid, Annina B.
author_sort Baselgia, Larissa T.
collection PubMed
description OBJECTIVE: To examine differences in somatosensory phenotypes of patients with positive and negative neurodynamic tests and compare these with healthy participants. DESIGN: Case-control study. SETTING: University department. PARTICIPANTS: Patients with electrodiagnostically confirmed carpal tunnel syndrome (CTS) (n=53) and people without CTS (n=26) participated in this study (N=79). Patients with CTS were subgrouped according to the results of the upper limb neurodynamic tests biasing the median nerve into patients with positive or negative neurodynamic tests. INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURE: All participants underwent quantitative sensory testing in the median innervated territory of their hand. RESULTS: Only 46% of patients with CTS had positive neurodynamic tests. No differences were identified between groups for pain thresholds (P>.247). However, patients with CTS had increased mechanical (P<.0001) and thermal detection thresholds (P<.0001) compared with people without CTS. Patients with negative neurodynamic tests had a more pronounced vibration detection deficit (mean, 7.43±0.59) than people without CTS (mean, 7.89±0.22; P=.001). Interestingly, warm detection was the only domain differentiating positive (mean, 4.03°C±2.18°C) and negative neurodynamic test groups (6.09°C±3.70°C, P=.032), with patients with negative neurodynamic tests demonstrating increased loss of function. CONCLUSIONS: Patients with negative neurodynamic tests seem to have a more severe dysfunction of the unmyelinated fiber population. Our findings suggest that neurodynamic tests should not be used in isolation to judge neural involvement. Rather, they should be interpreted in the context of loss of function tests of the small fiber domain.
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spelling pubmed-53247202017-03-08 Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies Baselgia, Larissa T. Bennett, David L. Silbiger, Robert M. Schmid, Annina B. Arch Phys Med Rehabil Original Research OBJECTIVE: To examine differences in somatosensory phenotypes of patients with positive and negative neurodynamic tests and compare these with healthy participants. DESIGN: Case-control study. SETTING: University department. PARTICIPANTS: Patients with electrodiagnostically confirmed carpal tunnel syndrome (CTS) (n=53) and people without CTS (n=26) participated in this study (N=79). Patients with CTS were subgrouped according to the results of the upper limb neurodynamic tests biasing the median nerve into patients with positive or negative neurodynamic tests. INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURE: All participants underwent quantitative sensory testing in the median innervated territory of their hand. RESULTS: Only 46% of patients with CTS had positive neurodynamic tests. No differences were identified between groups for pain thresholds (P>.247). However, patients with CTS had increased mechanical (P<.0001) and thermal detection thresholds (P<.0001) compared with people without CTS. Patients with negative neurodynamic tests had a more pronounced vibration detection deficit (mean, 7.43±0.59) than people without CTS (mean, 7.89±0.22; P=.001). Interestingly, warm detection was the only domain differentiating positive (mean, 4.03°C±2.18°C) and negative neurodynamic test groups (6.09°C±3.70°C, P=.032), with patients with negative neurodynamic tests demonstrating increased loss of function. CONCLUSIONS: Patients with negative neurodynamic tests seem to have a more severe dysfunction of the unmyelinated fiber population. Our findings suggest that neurodynamic tests should not be used in isolation to judge neural involvement. Rather, they should be interpreted in the context of loss of function tests of the small fiber domain. W.B. Saunders 2017-03 /pmc/articles/PMC5324720/ /pubmed/27449322 http://dx.doi.org/10.1016/j.apmr.2016.06.019 Text en © 2016 by the American Congress of Rahabilitation Medicine. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research
Baselgia, Larissa T.
Bennett, David L.
Silbiger, Robert M.
Schmid, Annina B.
Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies
title Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies
title_full Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies
title_fullStr Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies
title_full_unstemmed Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies
title_short Negative Neurodynamic Tests Do Not Exclude Neural Dysfunction in Patients With Entrapment Neuropathies
title_sort negative neurodynamic tests do not exclude neural dysfunction in patients with entrapment neuropathies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324720/
https://www.ncbi.nlm.nih.gov/pubmed/27449322
http://dx.doi.org/10.1016/j.apmr.2016.06.019
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