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SARS-CoV-2 infection among patients with systemic autoimmune diseases

OBJECTIVES: This study aimed to evaluate the prevalence of clinically overt SARS-CoV-2 infection (COVID-19) among patients with systemic autoimmune diseases residing in Tuscany, and to compare it with that observed in the general Tuscan population. METHODS: In this cross-sectional study, Tuscan outp...

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Autores principales: Emmi, Giacomo, Bettiol, Alessandra, Mattioli, Irene, Silvestri, Elena, Di Scala, Gerardo, Urban, Maria Letizia, Vaglio, Augusto, Prisco, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200134/
https://www.ncbi.nlm.nih.gov/pubmed/32376395
http://dx.doi.org/10.1016/j.autrev.2020.102575
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author Emmi, Giacomo
Bettiol, Alessandra
Mattioli, Irene
Silvestri, Elena
Di Scala, Gerardo
Urban, Maria Letizia
Vaglio, Augusto
Prisco, Domenico
author_facet Emmi, Giacomo
Bettiol, Alessandra
Mattioli, Irene
Silvestri, Elena
Di Scala, Gerardo
Urban, Maria Letizia
Vaglio, Augusto
Prisco, Domenico
author_sort Emmi, Giacomo
collection PubMed
description OBJECTIVES: This study aimed to evaluate the prevalence of clinically overt SARS-CoV-2 infection (COVID-19) among patients with systemic autoimmune diseases residing in Tuscany, and to compare it with that observed in the general Tuscan population. METHODS: In this cross-sectional study, Tuscan outpatients with systemic autoimmune diseases followed at a tertiary referral centre were telephonically interviewed between April 1st-14th 2020 to collect demographic and clinical data, information on ongoing immunomodulating/immunosuppressive treatments, and on the presence of symptoms suspected of SARS-CoV-2 or of a confirmed infection. RESULTS: 458 patients were interviewed [74% female, median age 56 years (IQR 43–68)]; 56% of them were receiving corticosteroids, 44% traditional disease-modifying anti-rheumatic drugs (DMARDs), of whom 23% hydroxychloroquine, 5% colchicine, while 41% were on biologic DMARDs (of whom 9% on tocilizumab). Thirteen patients reported symptoms suggesting SARS-CoV-2 infection. Of them, 7 had undergone nasopharyngeal swab and only one was positive and developed severe SARS-CoV-2 complications. Within our cohort, the prevalence of SARS-CoV-2 infection was therefore 0.22% (0.01–1.21%), comparable to that observed in the general population of Tuscany [0.20% (0.20–0.21%), p = .597]. CONCLUSIONS: Patients with systemic autoimmune diseases do not seem to carry an increased risk of SARS- CoV-2 infection as compared to the general population.
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spelling pubmed-72001342020-05-06 SARS-CoV-2 infection among patients with systemic autoimmune diseases Emmi, Giacomo Bettiol, Alessandra Mattioli, Irene Silvestri, Elena Di Scala, Gerardo Urban, Maria Letizia Vaglio, Augusto Prisco, Domenico Autoimmun Rev Article OBJECTIVES: This study aimed to evaluate the prevalence of clinically overt SARS-CoV-2 infection (COVID-19) among patients with systemic autoimmune diseases residing in Tuscany, and to compare it with that observed in the general Tuscan population. METHODS: In this cross-sectional study, Tuscan outpatients with systemic autoimmune diseases followed at a tertiary referral centre were telephonically interviewed between April 1st-14th 2020 to collect demographic and clinical data, information on ongoing immunomodulating/immunosuppressive treatments, and on the presence of symptoms suspected of SARS-CoV-2 or of a confirmed infection. RESULTS: 458 patients were interviewed [74% female, median age 56 years (IQR 43–68)]; 56% of them were receiving corticosteroids, 44% traditional disease-modifying anti-rheumatic drugs (DMARDs), of whom 23% hydroxychloroquine, 5% colchicine, while 41% were on biologic DMARDs (of whom 9% on tocilizumab). Thirteen patients reported symptoms suggesting SARS-CoV-2 infection. Of them, 7 had undergone nasopharyngeal swab and only one was positive and developed severe SARS-CoV-2 complications. Within our cohort, the prevalence of SARS-CoV-2 infection was therefore 0.22% (0.01–1.21%), comparable to that observed in the general population of Tuscany [0.20% (0.20–0.21%), p = .597]. CONCLUSIONS: Patients with systemic autoimmune diseases do not seem to carry an increased risk of SARS- CoV-2 infection as compared to the general population. Elsevier B.V. 2020-07 2020-05-05 /pmc/articles/PMC7200134/ /pubmed/32376395 http://dx.doi.org/10.1016/j.autrev.2020.102575 Text en © 2020 Elsevier B.V. All rights reserved. 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
Emmi, Giacomo
Bettiol, Alessandra
Mattioli, Irene
Silvestri, Elena
Di Scala, Gerardo
Urban, Maria Letizia
Vaglio, Augusto
Prisco, Domenico
SARS-CoV-2 infection among patients with systemic autoimmune diseases
title SARS-CoV-2 infection among patients with systemic autoimmune diseases
title_full SARS-CoV-2 infection among patients with systemic autoimmune diseases
title_fullStr SARS-CoV-2 infection among patients with systemic autoimmune diseases
title_full_unstemmed SARS-CoV-2 infection among patients with systemic autoimmune diseases
title_short SARS-CoV-2 infection among patients with systemic autoimmune diseases
title_sort sars-cov-2 infection among patients with systemic autoimmune diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200134/
https://www.ncbi.nlm.nih.gov/pubmed/32376395
http://dx.doi.org/10.1016/j.autrev.2020.102575
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