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HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study

Introduction: The coronavirus SARS CoV-2 (COVID-19) could cause damage to neural tissue. This injury is responsible for neuromuscular disturbance after the onset of respiratory symptoms in these patients. Objective: is to analyze the characteristics of all patients diagnosed with critical illness po...

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Autores principales: Wix Ramos, R.W., Rocio Martín, E.R.O.C.I., Luque Cárdenas, C.L., Lopez Viña, L.L.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843061/
http://dx.doi.org/10.1016/j.clinph.2021.11.035
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author Wix Ramos, R.W.
Rocio Martín, E.R.O.C.I.
Luque Cárdenas, C.L.
Lopez Viña, L.L.V.
author_facet Wix Ramos, R.W.
Rocio Martín, E.R.O.C.I.
Luque Cárdenas, C.L.
Lopez Viña, L.L.V.
author_sort Wix Ramos, R.W.
collection PubMed
description Introduction: The coronavirus SARS CoV-2 (COVID-19) could cause damage to neural tissue. This injury is responsible for neuromuscular disturbance after the onset of respiratory symptoms in these patients. Objective: is to analyze the characteristics of all patients diagnosed with critical illness polyneuropathy (CIP) reported from March 2020 to March 2021 in the Clinical Neurophysiology Department from La Princesa University Hospital. Methods: Patients were classified into two groups 17 patients admitted to the hospital with confirmed COVID-19 (Cases Group, CaG) and 12 patients without COVID-19 infection (Control Group, CoG). We performed both electroneurography and electromyography. Results: The distribution of the subtypes of the CIP was as follows: axonal motor polyneuropathy (24% in CaG vs 25% in CoG), axonal sensorimotor polyneuropathy (35% in CaG vs 58% in CoG), and mixed sensorimotor polyneuropathy (41% in CaG vs 16% in CoG). Needle EMG showed spontaneous activity in 100% in CaG vs 75% in CoG. The days of hospitalisation were 64.8 ± 7.9 in the CaG and 54.5 ± 9.9 in the CoG. Favourable evolution was observed in the 35% in CaG vs 42% in CoG, and unfavourable evolution was observed in the 41% in CaG vs 33% in CoG. Conclusion: We highlighted the nerves damaged in patients infected by COVID-19 and admitted to the Intensive Care Unit. Viral neuropathy is thought to be primarily axonal; however, we observe a high prevalence of demyelinating injuries in patients affected with this infection. Considering these results, we focus on the importance of early neurorehabilitation to improve nerve function.
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spelling pubmed-88430612022-02-15 HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study Wix Ramos, R.W. Rocio Martín, E.R.O.C.I. Luque Cárdenas, C.L. Lopez Viña, L.L.V. Clin Neurophysiol Article Introduction: The coronavirus SARS CoV-2 (COVID-19) could cause damage to neural tissue. This injury is responsible for neuromuscular disturbance after the onset of respiratory symptoms in these patients. Objective: is to analyze the characteristics of all patients diagnosed with critical illness polyneuropathy (CIP) reported from March 2020 to March 2021 in the Clinical Neurophysiology Department from La Princesa University Hospital. Methods: Patients were classified into two groups 17 patients admitted to the hospital with confirmed COVID-19 (Cases Group, CaG) and 12 patients without COVID-19 infection (Control Group, CoG). We performed both electroneurography and electromyography. Results: The distribution of the subtypes of the CIP was as follows: axonal motor polyneuropathy (24% in CaG vs 25% in CoG), axonal sensorimotor polyneuropathy (35% in CaG vs 58% in CoG), and mixed sensorimotor polyneuropathy (41% in CaG vs 16% in CoG). Needle EMG showed spontaneous activity in 100% in CaG vs 75% in CoG. The days of hospitalisation were 64.8 ± 7.9 in the CaG and 54.5 ± 9.9 in the CoG. Favourable evolution was observed in the 35% in CaG vs 42% in CoG, and unfavourable evolution was observed in the 41% in CaG vs 33% in CoG. Conclusion: We highlighted the nerves damaged in patients infected by COVID-19 and admitted to the Intensive Care Unit. Viral neuropathy is thought to be primarily axonal; however, we observe a high prevalence of demyelinating injuries in patients affected with this infection. Considering these results, we focus on the importance of early neurorehabilitation to improve nerve function. Published by Elsevier B.V. 2022-03 2022-02-14 /pmc/articles/PMC8843061/ http://dx.doi.org/10.1016/j.clinph.2021.11.035 Text en Copyright © 2021 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wix Ramos, R.W.
Rocio Martín, E.R.O.C.I.
Luque Cárdenas, C.L.
Lopez Viña, L.L.V.
HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study
title HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study
title_full HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study
title_fullStr HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study
title_full_unstemmed HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study
title_short HP37: Critical illness polyneuropathy in COVID-19 patients: A case-control study
title_sort hp37: critical illness polyneuropathy in covid-19 patients: a case-control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843061/
http://dx.doi.org/10.1016/j.clinph.2021.11.035
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