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

Identifieur interne : 000C64 ( Main/Exploration ); précédent : 000C63; suivant : 000C65

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

Auteurs : Giacomo Emmi [Italie] ; Alessandra Bettiol [Italie] ; Irene Mattioli [Italie] ; Elena Silvestri [Italie] ; Gerardo Di Scala [Italie] ; Maria Letizia Urban [Italie] ; Augusto Vaglio [Italie] ; Domenico Prisco [Italie]

Source :

RBID : pubmed:32376395

Descripteurs français

English descriptors

Abstract

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.


DOI: 10.1016/j.autrev.2020.102575
PubMed: 32376395
PubMed Central: PMC7200134


Affiliations:


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Le document en format XML

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<b>OBJECTIVES</b>
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<p>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.</p>
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<b>METHODS</b>
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<p>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.</p>
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<b>RESULTS</b>
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<p>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].</p>
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<b>CONCLUSIONS</b>
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<p>Patients with systemic autoimmune diseases do not seem to carry an increased risk of SARS- CoV-2 infection as compared to the general population.</p>
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<CoiStatement>Declaration of Competing Interest None declared.</CoiStatement>
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<Citation>Nat Rev Rheumatol. 2020 Jun;16(6):293-294</Citation>
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<Citation>Ann Rheum Dis. 2020 Jun;79(6):839-840</Citation>
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<Citation>J Biol Regul Homeost Agents. 2020 Apr 07;34(2):</Citation>
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<Citation>Autoimmun Rev. 2020 May;19(5):102523</Citation>
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<Citation>Ann Rheum Dis. 2020 May;79(5):667-668</Citation>
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<ArticleId IdType="pubmed">32283152</ArticleId>
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<Reference>
<Citation>Lancet Rheumatol. 2020 Apr 16;:</Citation>
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<ArticleId IdType="pubmed">32309814</ArticleId>
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</Reference>
<Reference>
<Citation>Lancet. 2020 Mar 28;395(10229):1033-1034</Citation>
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<ArticleId IdType="pubmed">32192578</ArticleId>
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<Reference>
<Citation>Clin Rheumatol. 2020 Apr 10;:</Citation>
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<ArticleId IdType="pubmed">32277367</ArticleId>
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<Reference>
<Citation>Clin Exp Rheumatol. 2018 Mar-Apr;36(2):317-328</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">29303710</ArticleId>
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<Reference>
<Citation>Lancet. 2020 Apr 4;395(10230):1110-1111</Citation>
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