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Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis

The purpose of this report is to recommend evidence-based strategies for polyneuropathy (PNP) electrodiagnosis based on a large cohort of patients examined prospectively. Nerve conduction studies (NCS) of bilateral tibial, peroneal and sural nerves, the latter with both near-nerve-technique (NNT) an...

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Autores principales: Tankisi, H., Pugdahl, K., Beniczky, S., Andersen, H., Fuglsang-Frederiksen, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921232/
https://www.ncbi.nlm.nih.gov/pubmed/31886447
http://dx.doi.org/10.1016/j.cnp.2019.10.005
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author Tankisi, H.
Pugdahl, K.
Beniczky, S.
Andersen, H.
Fuglsang-Frederiksen, A.
author_facet Tankisi, H.
Pugdahl, K.
Beniczky, S.
Andersen, H.
Fuglsang-Frederiksen, A.
author_sort Tankisi, H.
collection PubMed
description The purpose of this report is to recommend evidence-based strategies for polyneuropathy (PNP) electrodiagnosis based on a large cohort of patients examined prospectively. Nerve conduction studies (NCS) of bilateral tibial, peroneal and sural nerves, the latter with both near-nerve-technique (NNT) and surface recordings, were done in 313 patients with clinically suspected PNP. Bilateral dorsal sural and medial plantar nerves, and unilateral median and ulnar nerves were further examined in a subgroup of patients. The final clinical diagnosis retrieved from the patientś medical records 1–6 years after the neurophysiological investigation served as diagnostic reference standard. The clinical follow-up diagnosis confirmed PNP in 219 patients. The tibial nerve was the most sensitive nerve (75%), with prolonged tibial F-wave as the most sensitive parameter (72%). Sural NNT recordings were more sensitive (66%) than surface recordings (49%) (p < 0.05), however, dorsal sural (68%) and medial planter (70%) nerves had similar sensitivities as NNT. There was no side difference in the incidence of abnormality for any nerve. Based on these results, we recommend a strategy starting with tibial and sural NCS on one side for electrophysiological screening for distal symmetric PNP. If one of these is abnormal, we recommend examining the other lower and upper extremity nerves, including distal sensory nerves, particularly if NNT is not applicable. While one abnormal parameter is sufficient to interpret a nerve as abnormal, we recommend at least two abnormal nerves for PNP diagnosis, preferentially one being the sural nerve. We believe that the strategies recommended in this study may improve PNP electrodiagnosis.
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spelling pubmed-69212322019-12-27 Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis Tankisi, H. Pugdahl, K. Beniczky, S. Andersen, H. Fuglsang-Frederiksen, A. Clin Neurophysiol Pract Reviews, Expert Opinions and Guideline The purpose of this report is to recommend evidence-based strategies for polyneuropathy (PNP) electrodiagnosis based on a large cohort of patients examined prospectively. Nerve conduction studies (NCS) of bilateral tibial, peroneal and sural nerves, the latter with both near-nerve-technique (NNT) and surface recordings, were done in 313 patients with clinically suspected PNP. Bilateral dorsal sural and medial plantar nerves, and unilateral median and ulnar nerves were further examined in a subgroup of patients. The final clinical diagnosis retrieved from the patientś medical records 1–6 years after the neurophysiological investigation served as diagnostic reference standard. The clinical follow-up diagnosis confirmed PNP in 219 patients. The tibial nerve was the most sensitive nerve (75%), with prolonged tibial F-wave as the most sensitive parameter (72%). Sural NNT recordings were more sensitive (66%) than surface recordings (49%) (p < 0.05), however, dorsal sural (68%) and medial planter (70%) nerves had similar sensitivities as NNT. There was no side difference in the incidence of abnormality for any nerve. Based on these results, we recommend a strategy starting with tibial and sural NCS on one side for electrophysiological screening for distal symmetric PNP. If one of these is abnormal, we recommend examining the other lower and upper extremity nerves, including distal sensory nerves, particularly if NNT is not applicable. While one abnormal parameter is sufficient to interpret a nerve as abnormal, we recommend at least two abnormal nerves for PNP diagnosis, preferentially one being the sural nerve. We believe that the strategies recommended in this study may improve PNP electrodiagnosis. Elsevier 2019-11-18 /pmc/articles/PMC6921232/ /pubmed/31886447 http://dx.doi.org/10.1016/j.cnp.2019.10.005 Text en © 2019 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. http://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 Reviews, Expert Opinions and Guideline
Tankisi, H.
Pugdahl, K.
Beniczky, S.
Andersen, H.
Fuglsang-Frederiksen, A.
Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
title Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
title_full Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
title_fullStr Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
title_full_unstemmed Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
title_short Evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
title_sort evidence-based recommendations for examination and diagnostic strategies of polyneuropathy electrodiagnosis
topic Reviews, Expert Opinions and Guideline
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921232/
https://www.ncbi.nlm.nih.gov/pubmed/31886447
http://dx.doi.org/10.1016/j.cnp.2019.10.005
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