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Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection
OBJECTIVE: Several cases of Guillain-Barre syndrome (GBS) associated with SARS-CoV-2 infection have been described. This study illustrated the demographic, clinical, and neurophysiological characteristics of patients with GBS and COVID-19, as well as associated factors with disability at discharge....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356584/ https://www.ncbi.nlm.nih.gov/pubmed/37483451 http://dx.doi.org/10.3389/fneur.2023.1191520 |
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author | Sanchez-Boluarte, Sofía S. Aguirre-Quispe, Wilfor Tacunan-Cuellar, Jhon Sanchez-Boluarte, Arantxa N. Segura-Chavez, Darwin |
author_facet | Sanchez-Boluarte, Sofía S. Aguirre-Quispe, Wilfor Tacunan-Cuellar, Jhon Sanchez-Boluarte, Arantxa N. Segura-Chavez, Darwin |
author_sort | Sanchez-Boluarte, Sofía S. |
collection | PubMed |
description | OBJECTIVE: Several cases of Guillain-Barre syndrome (GBS) associated with SARS-CoV-2 infection have been described. This study illustrated the demographic, clinical, and neurophysiological characteristics of patients with GBS and COVID-19, as well as associated factors with disability at discharge. MATERIALS AND METHODS: A retrospective analytical observational study was conducted. It included patients diagnosed with GBS admitted in a national reference center in Peru between 2019 and 2021. Epidemiological, clinical, neurophysiological, and cerebrospinal fluid data were analyzed. A multivariate analysis, using the generalized linear model, was performed, considering the presence of disability at discharge as the dependent variable. RESULTS: Eight-one subjects diagnosed with GBS were included. The mean age was 46.8 years (SD: 15.2), with a predominance of males (61.73%). The most frequent clinical presentation was the classic sensory-motor form in 74 cases (91.36%) with AIDP (82.35%) as the most frequent neurophysiological pattern in the group with COVID-19, while AMAN pattern predominated (59.26%) in those without COVID-19 (p = <0.000). The disability prevalence ratio at discharge between subjects with COVID-19 and those without COVID-19 was 1.89 (CI 1.06–3.34), p = 0.030, adjusted for age, sex, and neurophysiological subtype. CONCLUSION: The neurophysiologic subtype AIDP, and a higher disability were associated with the presence of COVID-19. |
format | Online Article Text |
id | pubmed-10356584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103565842023-07-21 Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection Sanchez-Boluarte, Sofía S. Aguirre-Quispe, Wilfor Tacunan-Cuellar, Jhon Sanchez-Boluarte, Arantxa N. Segura-Chavez, Darwin Front Neurol Neurology OBJECTIVE: Several cases of Guillain-Barre syndrome (GBS) associated with SARS-CoV-2 infection have been described. This study illustrated the demographic, clinical, and neurophysiological characteristics of patients with GBS and COVID-19, as well as associated factors with disability at discharge. MATERIALS AND METHODS: A retrospective analytical observational study was conducted. It included patients diagnosed with GBS admitted in a national reference center in Peru between 2019 and 2021. Epidemiological, clinical, neurophysiological, and cerebrospinal fluid data were analyzed. A multivariate analysis, using the generalized linear model, was performed, considering the presence of disability at discharge as the dependent variable. RESULTS: Eight-one subjects diagnosed with GBS were included. The mean age was 46.8 years (SD: 15.2), with a predominance of males (61.73%). The most frequent clinical presentation was the classic sensory-motor form in 74 cases (91.36%) with AIDP (82.35%) as the most frequent neurophysiological pattern in the group with COVID-19, while AMAN pattern predominated (59.26%) in those without COVID-19 (p = <0.000). The disability prevalence ratio at discharge between subjects with COVID-19 and those without COVID-19 was 1.89 (CI 1.06–3.34), p = 0.030, adjusted for age, sex, and neurophysiological subtype. CONCLUSION: The neurophysiologic subtype AIDP, and a higher disability were associated with the presence of COVID-19. Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10356584/ /pubmed/37483451 http://dx.doi.org/10.3389/fneur.2023.1191520 Text en Copyright © 2023 Sanchez-Boluarte, Aguirre-Quispe, Tacunan-Cuellar, Sanchez-Boluarte and Segura-Chavez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Sanchez-Boluarte, Sofía S. Aguirre-Quispe, Wilfor Tacunan-Cuellar, Jhon Sanchez-Boluarte, Arantxa N. Segura-Chavez, Darwin Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection |
title | Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection |
title_full | Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection |
title_fullStr | Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection |
title_full_unstemmed | Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection |
title_short | Disability evaluation in patients with Guillain-Barre syndrome and SARS-CoV-2 infection |
title_sort | disability evaluation in patients with guillain-barre syndrome and sars-cov-2 infection |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356584/ https://www.ncbi.nlm.nih.gov/pubmed/37483451 http://dx.doi.org/10.3389/fneur.2023.1191520 |
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