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The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy

OBJECTIVE: To explore potential differences in motor nerve excitability testing (NET) variables at group levels between patients with a clinical diagnosis of polyneuropathy (PNP), which did not fulfil diagnostic criteria of conventional nerve conduction studies (NCS) and patients without polyneuropa...

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Autores principales: Krøigård, Thomas, Sodemann, Ulrik, Gaist, Laura M., Sindrup, Søren H., Tankisi, Hatice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803553/
https://www.ncbi.nlm.nih.gov/pubmed/35128215
http://dx.doi.org/10.1016/j.cnp.2021.12.001
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author Krøigård, Thomas
Sodemann, Ulrik
Gaist, Laura M.
Sindrup, Søren H.
Tankisi, Hatice
author_facet Krøigård, Thomas
Sodemann, Ulrik
Gaist, Laura M.
Sindrup, Søren H.
Tankisi, Hatice
author_sort Krøigård, Thomas
collection PubMed
description OBJECTIVE: To explore potential differences in motor nerve excitability testing (NET) variables at group levels between patients with a clinical diagnosis of polyneuropathy (PNP), which did not fulfil diagnostic criteria of conventional nerve conduction studies (NCS) and patients without polyneuropathy. Such differences could support a role for NET in increasing the diagnostic sensitivity of NCS in chronic axonal PNP. METHODS: Motor NET was performed using the median nerve in patients with a clinical suspicion of PNP in addition to conventional NCS, skin biopsies, corneal confocal microscopy and structured clinical evaluation including scoring of neuropathy symptoms and signs. RESULTS: Of the 57 patients included, 32 had PNP, half of which had NCS, which fulfilled criteria for PNP (NCS+ PNP). There were no significant differences for any of the NET variables between PNP patients with non-diagnostic conventional NCS (NCS− PNP) and patients without PNP. Rheobase was increased, and Ted (undershoot) and subexcitability were decreased in NCS+ PNP. Sural amplitude, peroneal nerve F-wave latency and tibial nerve F-wave-latency were correlated with subexcitability, and tibial nerve motor amplitude was correlated with rheobase. CONCLUSIONS: NET was correlated with conventional NCS and no differences were found between NCS− PNP patients and patients without PNP. SIGNIFICANCE: NET does not seem to offer any additional diagnostic value in chronic mixed etiology neuropathy.
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spelling pubmed-88035532022-02-04 The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy Krøigård, Thomas Sodemann, Ulrik Gaist, Laura M. Sindrup, Søren H. Tankisi, Hatice Clin Neurophysiol Pract Research Paper OBJECTIVE: To explore potential differences in motor nerve excitability testing (NET) variables at group levels between patients with a clinical diagnosis of polyneuropathy (PNP), which did not fulfil diagnostic criteria of conventional nerve conduction studies (NCS) and patients without polyneuropathy. Such differences could support a role for NET in increasing the diagnostic sensitivity of NCS in chronic axonal PNP. METHODS: Motor NET was performed using the median nerve in patients with a clinical suspicion of PNP in addition to conventional NCS, skin biopsies, corneal confocal microscopy and structured clinical evaluation including scoring of neuropathy symptoms and signs. RESULTS: Of the 57 patients included, 32 had PNP, half of which had NCS, which fulfilled criteria for PNP (NCS+ PNP). There were no significant differences for any of the NET variables between PNP patients with non-diagnostic conventional NCS (NCS− PNP) and patients without PNP. Rheobase was increased, and Ted (undershoot) and subexcitability were decreased in NCS+ PNP. Sural amplitude, peroneal nerve F-wave latency and tibial nerve F-wave-latency were correlated with subexcitability, and tibial nerve motor amplitude was correlated with rheobase. CONCLUSIONS: NET was correlated with conventional NCS and no differences were found between NCS− PNP patients and patients without PNP. SIGNIFICANCE: NET does not seem to offer any additional diagnostic value in chronic mixed etiology neuropathy. Elsevier 2022-01-07 /pmc/articles/PMC8803553/ /pubmed/35128215 http://dx.doi.org/10.1016/j.cnp.2021.12.001 Text en © 2022 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Krøigård, Thomas
Sodemann, Ulrik
Gaist, Laura M.
Sindrup, Søren H.
Tankisi, Hatice
The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
title The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
title_full The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
title_fullStr The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
title_full_unstemmed The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
title_short The additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
title_sort additional diagnostic value of motor nerve excitability testing in chronic axonal neuropathy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803553/
https://www.ncbi.nlm.nih.gov/pubmed/35128215
http://dx.doi.org/10.1016/j.cnp.2021.12.001
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