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Critical illness neuropathy in severe COVID-19: a case series
INTRODUCTION: Neurological complications of SARS-CoV-2 disease have received growing attention, but only few studies have described to date clinical and neurophysiological findings in COVID patients during their stay in intensive care units (ICUs). Here, we neurophysiologically assessed the presence...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414960/ https://www.ncbi.nlm.nih.gov/pubmed/34477990 http://dx.doi.org/10.1007/s10072-021-05471-0 |
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author | Bocci, Tommaso Campiglio, Laura Zardoni, Manuela Botta, Stefano Coppola, Silvia Groppo, Elisabetta Chiumello, Davide Priori, Alberto |
author_facet | Bocci, Tommaso Campiglio, Laura Zardoni, Manuela Botta, Stefano Coppola, Silvia Groppo, Elisabetta Chiumello, Davide Priori, Alberto |
author_sort | Bocci, Tommaso |
collection | PubMed |
description | INTRODUCTION: Neurological complications of SARS-CoV-2 disease have received growing attention, but only few studies have described to date clinical and neurophysiological findings in COVID patients during their stay in intensive care units (ICUs). Here, we neurophysiologically assessed the presence of either critical illness neuropathy (CIP) or myopathy (CIM) in ICU patients. MATERIALS AND METHODS: Patients underwent a neurophysiological assessment, including bilateral examination of the median, ulnar, deep peroneal and tibial motor nerves and of the median, ulnar, radial and sural sensory nerves. Needle electromyography (EMG) was performed for both distal and proximal muscles of the lower and upper limbs. In order to differentiate CIP from CIM, Direct Muscle Stimulation (DMS) was applied either to the deltoid or tibialis anterior muscles. Peak to peak amplitudes and onset latencies of the responses evoked by DMS (DMS(amp), DMS(lat)) or by motor nerve stimulation (MNS(amp), MNS(lat)) were compared. The ratio MNS(amp) to DMS(amp) (NMR) and the MNS(lat) to DMS(lat) difference (NMD: MNS(lat) − DMS(lat)) were also evaluated. RESULTS: Nerve conduction studies showed a sensory-motor polyneuropathy with axonal neurogenic pattern, as confirmed by needle EMG. Both MNS(amp) and NMR were significantly reduced when compared to controls (p < 0.0001), whereas MNS(lat) and NMD were markedly increased (p = 0.0049). CONCLUSIONS: We have described COVID patients in the ICU with critical illness neuropathy (CIP). COVID-related CIP could have implications for the functional recovery and rehabilitation strategies. |
format | Online Article Text |
id | pubmed-8414960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84149602021-09-03 Critical illness neuropathy in severe COVID-19: a case series Bocci, Tommaso Campiglio, Laura Zardoni, Manuela Botta, Stefano Coppola, Silvia Groppo, Elisabetta Chiumello, Davide Priori, Alberto Neurol Sci Covid-19 INTRODUCTION: Neurological complications of SARS-CoV-2 disease have received growing attention, but only few studies have described to date clinical and neurophysiological findings in COVID patients during their stay in intensive care units (ICUs). Here, we neurophysiologically assessed the presence of either critical illness neuropathy (CIP) or myopathy (CIM) in ICU patients. MATERIALS AND METHODS: Patients underwent a neurophysiological assessment, including bilateral examination of the median, ulnar, deep peroneal and tibial motor nerves and of the median, ulnar, radial and sural sensory nerves. Needle electromyography (EMG) was performed for both distal and proximal muscles of the lower and upper limbs. In order to differentiate CIP from CIM, Direct Muscle Stimulation (DMS) was applied either to the deltoid or tibialis anterior muscles. Peak to peak amplitudes and onset latencies of the responses evoked by DMS (DMS(amp), DMS(lat)) or by motor nerve stimulation (MNS(amp), MNS(lat)) were compared. The ratio MNS(amp) to DMS(amp) (NMR) and the MNS(lat) to DMS(lat) difference (NMD: MNS(lat) − DMS(lat)) were also evaluated. RESULTS: Nerve conduction studies showed a sensory-motor polyneuropathy with axonal neurogenic pattern, as confirmed by needle EMG. Both MNS(amp) and NMR were significantly reduced when compared to controls (p < 0.0001), whereas MNS(lat) and NMD were markedly increased (p = 0.0049). CONCLUSIONS: We have described COVID patients in the ICU with critical illness neuropathy (CIP). COVID-related CIP could have implications for the functional recovery and rehabilitation strategies. Springer International Publishing 2021-09-03 2021 /pmc/articles/PMC8414960/ /pubmed/34477990 http://dx.doi.org/10.1007/s10072-021-05471-0 Text en © Fondazione Società Italiana di Neurologia 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Covid-19 Bocci, Tommaso Campiglio, Laura Zardoni, Manuela Botta, Stefano Coppola, Silvia Groppo, Elisabetta Chiumello, Davide Priori, Alberto Critical illness neuropathy in severe COVID-19: a case series |
title | Critical illness neuropathy in severe COVID-19: a case series |
title_full | Critical illness neuropathy in severe COVID-19: a case series |
title_fullStr | Critical illness neuropathy in severe COVID-19: a case series |
title_full_unstemmed | Critical illness neuropathy in severe COVID-19: a case series |
title_short | Critical illness neuropathy in severe COVID-19: a case series |
title_sort | critical illness neuropathy in severe covid-19: a case series |
topic | Covid-19 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414960/ https://www.ncbi.nlm.nih.gov/pubmed/34477990 http://dx.doi.org/10.1007/s10072-021-05471-0 |
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