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dc.contributor.authorPablos, José L.
dc.contributor.authorAbasolo, Lydia
dc.contributor.authorÁlvaro-Gracia, José M.
dc.contributor.authorBlanco García, Francisco J
dc.contributor.authorBlanco, Ricardo
dc.contributor.authorCastrejón, Isabel
dc.contributor.authorFernández-Fernández, David
dc.contributor.authorFernández-Gutiérrez, Benjamín
dc.contributor.authorGalindo-Izquierdo, María
dc.contributor.authorGonzález-Gay, Miguel Á.
dc.contributor.authorManrique-Arija, Sara
dc.contributor.authorMena Vázquez, Natalia
dc.contributor.authorMera Varela, Antonio
dc.contributor.authorRetuerto, Miriam
dc.contributor.authorSeijas-López, Álvaro
dc.date.accessioned2020-08-06T11:26:16Z
dc.date.available2020-08-06T11:26:16Z
dc.date.issued2020-06-12
dc.identifier.citationPablos JL, Abasolo L, Alvaro-Gracia JM, Blanco FJ, Blanco R, Castrejón I, et al. Prevalence of hospital PCR-confirmed COVID-19 cases in patients with chronic inflammatory and autoimmune rheumatic diseases. Ann Rheum Dis. 2020. Epub 2020 Jun 12es_ES
dc.identifier.issn0003-4967
dc.identifier.urihttp://hdl.handle.net/2183/26115
dc.description.abstract[Abstract] Background: The susceptibility of patients with rheumatic diseases and the risks or benefits of immunosuppressive therapies for COVID-19 are unknown. Methods: We performed a retrospective study with patients under follow-up in rheumatology departments from seven hospitals in Spain. We matched updated databases of rheumatology patients with severe acute respiratory syndrome coronavirus 2-positive PCR tests performed in the hospital to the same reference populations. Rates of PCR+ confirmed COVID-19 were compared among groups. Results: Patients with chronic inflammatory diseases had 1.32-fold higher prevalence of hospital PCR+ COVID-19 than the reference population (0.76% vs 0.58%). Patients with systemic autoimmune or immune-mediated disease (AI/IMID) showed a significant increase, whereas patients with inflammatory arthritis (IA) or systemic lupus erythematosus did not. COVID-19 cases in some but not all diagnostic groups had older ages than cases in the reference population. Patients with IA on targeted-synthetic or biological disease-modifying antirheumatic drugs (DMARDs), but not those on conventional-synthetic DMARDs, had a greater prevalence despite a similar age distribution. Conclusion: Patients with AI/IMID show a variable risk of hospital-diagnosed COVID-19. Interplay of ageing, therapies and disease-specific factors seem to contribute. These data provide a basis to improve preventive recommendations to rheumatic patients and to analyse the specific factors involved in COVID-19 susceptibility.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III; RD16/0012 RETICS Programes_ES
dc.language.isoenges_ES
dc.publisherBMJes_ES
dc.relation.urihttp://dx.doi.org/10.1136/annrheumdis-2020-217763es_ES
dc.rightsThis article is made freely available for use in accordance with BMJ's website terms and conditions for the duration of the covid-19 pandemic or until otherwise determined by BMJ. You may use, download and print the article for any lawful, non-commercial purpose (including text and data mining) provided that all copyright notices and trade marks are retained.es_ES
dc.subjectArthritises_ES
dc.subjectAutoimmune diseaseses_ES
dc.subjectBiological therapyes_ES
dc.subjectEpidemiologyes_ES
dc.titlePrevalence of hospital PCR-confirmed COVID-19 cases in patients with chronic inflammatory and autoimmune rheumatic diseaseses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleAnnals of the Rheumatic Diseaseses_ES


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