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COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases

OBJECTIVES: COVID-19 outcomes in population with systemic autoimmune diseases (SAD) remain poorly understood. The aim was to examine demographic and clinical factors associated with COVID-19 infection in people with rheumatic disease. METHODS: Two phases cross-sectional survey of individuals with rh...

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Autores principales: Gracia, Borja Del Carmelo, Sáez, Luis, Pallarés, Lucio, Velilla, Jose, Marín, Adela, Martinez-Lostao, Luis, Simeón, Carmen Pilar, Fanlo, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828974/
https://www.ncbi.nlm.nih.gov/pubmed/35155485
http://dx.doi.org/10.3389/fmed.2021.808608
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author Gracia, Borja Del Carmelo
Sáez, Luis
Pallarés, Lucio
Velilla, Jose
Marín, Adela
Martinez-Lostao, Luis
Simeón, Carmen Pilar
Fanlo, Patricia
author_facet Gracia, Borja Del Carmelo
Sáez, Luis
Pallarés, Lucio
Velilla, Jose
Marín, Adela
Martinez-Lostao, Luis
Simeón, Carmen Pilar
Fanlo, Patricia
author_sort Gracia, Borja Del Carmelo
collection PubMed
description OBJECTIVES: COVID-19 outcomes in population with systemic autoimmune diseases (SAD) remain poorly understood. The aim was to examine demographic and clinical factors associated with COVID-19 infection in people with rheumatic disease. METHODS: Two phases cross-sectional survey of individuals with rheumatic disease in April 2020 and October 2020. COVID infection, severity of disease, age, sex, smoking status, underlying rheumatic disease diagnosis, comorbidities and rheumatic disease medications taken immediately prior to infection were analyzed. RESULTS: A total of 1,529 individuals with autoimmunity disease diagnosis were included. Out of 50 positive patients, 21 required telephone medical assistance, 16 received assessment by primary care physician, 9 were evaluated in Emergency Department and 4 patient required hospitalization. Multivariate analysis was performed without obtaining differences in any of the systemic autoimmune diseases. Regarding the treatments, significant differences were found (p 0.011) in the treatment with anti-TNF-alpha agents with OR 3.422 (1.322–8.858) and a trend to significance (p 0.094) was observed in patients receiving mycophenolate treatment [OR 2.016 (0.996–4-081)]. CONCLUSIONS: Anti-TNF-alpha treatment was associated with more than 3-fold risk of suffering from SARS-CoV-2 infection, although in all cases infection was mild. Cumulative incidence in patients with SAD was up to 5 times higher than general population but with great differences between autoimmune diseases.
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spelling pubmed-88289742022-02-11 COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases Gracia, Borja Del Carmelo Sáez, Luis Pallarés, Lucio Velilla, Jose Marín, Adela Martinez-Lostao, Luis Simeón, Carmen Pilar Fanlo, Patricia Front Med (Lausanne) Medicine OBJECTIVES: COVID-19 outcomes in population with systemic autoimmune diseases (SAD) remain poorly understood. The aim was to examine demographic and clinical factors associated with COVID-19 infection in people with rheumatic disease. METHODS: Two phases cross-sectional survey of individuals with rheumatic disease in April 2020 and October 2020. COVID infection, severity of disease, age, sex, smoking status, underlying rheumatic disease diagnosis, comorbidities and rheumatic disease medications taken immediately prior to infection were analyzed. RESULTS: A total of 1,529 individuals with autoimmunity disease diagnosis were included. Out of 50 positive patients, 21 required telephone medical assistance, 16 received assessment by primary care physician, 9 were evaluated in Emergency Department and 4 patient required hospitalization. Multivariate analysis was performed without obtaining differences in any of the systemic autoimmune diseases. Regarding the treatments, significant differences were found (p 0.011) in the treatment with anti-TNF-alpha agents with OR 3.422 (1.322–8.858) and a trend to significance (p 0.094) was observed in patients receiving mycophenolate treatment [OR 2.016 (0.996–4-081)]. CONCLUSIONS: Anti-TNF-alpha treatment was associated with more than 3-fold risk of suffering from SARS-CoV-2 infection, although in all cases infection was mild. Cumulative incidence in patients with SAD was up to 5 times higher than general population but with great differences between autoimmune diseases. Frontiers Media S.A. 2022-01-27 /pmc/articles/PMC8828974/ /pubmed/35155485 http://dx.doi.org/10.3389/fmed.2021.808608 Text en Copyright © 2022 Gracia, Sáez, Pallarés, Velilla, Marín, Martinez-Lostao, Simeón and Fanlo. 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 Medicine
Gracia, Borja Del Carmelo
Sáez, Luis
Pallarés, Lucio
Velilla, Jose
Marín, Adela
Martinez-Lostao, Luis
Simeón, Carmen Pilar
Fanlo, Patricia
COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases
title COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases
title_full COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases
title_fullStr COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases
title_full_unstemmed COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases
title_short COVID GEAS: COVID-19 National Survey in Patients With Systemic Autoimmune Diseases
title_sort covid geas: covid-19 national survey in patients with systemic autoimmune diseases
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828974/
https://www.ncbi.nlm.nih.gov/pubmed/35155485
http://dx.doi.org/10.3389/fmed.2021.808608
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