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dc.contributor.author | Ugarte Gil, Manuel Francisco | |
dc.contributor.author | Alarcón, Graciela S. | |
dc.contributor.author | Izadi, Zara | |
dc.contributor.author | Duarte-Garcia, Ali | |
dc.contributor.author | Reategui-Sokolova, Cristina | |
dc.contributor.author | Clarke, Ann Elaine | |
dc.contributor.author | Wise, Leanna | |
dc.contributor.author | Pons-Estel, Guillermo J. | |
dc.contributor.author | Santos, Maria Jose | |
dc.contributor.author | Bernatsky, Sasha | |
dc.contributor.author | Euzebio Ribeiro, Sandra Lucia | |
dc.contributor.author | Al Emadi, Samar | |
dc.contributor.author | Sparks, Jeffrey A. | |
dc.contributor.author | Hsu, Tiffany Y-T | |
dc.contributor.author | Patel, Naomi J. | |
dc.contributor.author | Gilbert, Emily L. | |
dc.contributor.author | Valenzuela-Almada, Maria O. | |
dc.contributor.author | Jonsen, Andreas | |
dc.contributor.author | Landolfi, Gianpiero | |
dc.contributor.author | Fredi, Micaela | |
dc.contributor.author | Goulenok, Tiphaine | |
dc.contributor.author | Devaux, Mathilde | |
dc.contributor.author | Mariette, Xavier | |
dc.contributor.author | Queyrel, Viviane | |
dc.contributor.author | Romao, Vasco C. | |
dc.contributor.author | Sequeira, Graca | |
dc.contributor.author | Hasseli, Rebecca | |
dc.contributor.author | Hoyer, Bimba | |
dc.contributor.author | Voll, Reinhard E. | |
dc.contributor.author | Specker, Christof | |
dc.contributor.author | Baez, Roberto | |
dc.contributor.author | Castro-Coello, Vanessa | |
dc.contributor.author | Ficco, Hernan Maldonado | |
dc.contributor.author | Reis Neto, Edgard Torres | |
dc.contributor.author | Aparecida Ferreira, Gilda Aparecida | |
dc.contributor.author | Andre Monticielo, Odirlei Andre | |
dc.contributor.author | Sirotich, Emily | |
dc.contributor.author | Liew, Jean | |
dc.contributor.author | Hausmann, Jonathan | |
dc.contributor.author | Sufka, Paul | |
dc.contributor.author | Grainger, Rebecca | |
dc.contributor.author | Bhana, Suleman | |
dc.contributor.author | Costello, Wendy | |
dc.contributor.author | Wallace, Zachary S. | |
dc.contributor.author | Jacobsohn, Lindsay | |
dc.contributor.author | Taylor, Tiffany | |
dc.contributor.author | Ja, Clairissa | |
dc.contributor.author | Strangfeld, Anja | |
dc.contributor.author | Mateus, Elsa F. | |
dc.contributor.author | Hyrich, Kimme L. | |
dc.contributor.author | Carmona, Loreto | |
dc.contributor.author | Lawson-Tovey, Saskia | |
dc.contributor.author | Kearsley-Fleet, Lianne | |
dc.contributor.author | Schaefer, Martin | |
dc.contributor.author | Machado, Pedro M. | |
dc.contributor.author | Robinson, Philip C. | |
dc.contributor.author | Gianfrancesco, Milena | |
dc.contributor.author | Yazdany, Jinoos | |
dc.date.accessioned | 2022-03-23T16:54:20Z | |
dc.date.available | 2022-03-23T16:54:20Z | |
dc.date.issued | 2022 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/11466 | |
dc.description.abstract | Aim: To determine characteristics associated with more severe outcomes in a global registry of people with systemic lupus erythematosus (SLE) and COVID-19. Methods: People with SLE and COVID-19 reported in the COVID-19 Global Rheumatology Alliance registry from March 2020 to June 2021 were included. The ordinal outcome was defined as: (1) not hospitalised, (2) hospitalised with no oxygenation, (3) hospitalised with any ventilation or oxygenation and (4) death. A multivariable ordinal logistic regression model was constructed to assess the relationship between COVID-19 severity and demographic characteristics, comorbidities, medications and disease activity. Results: A total of 1606 people with SLE were included. In the multivariable model, older age (OR 1.03, 95% CI 1.02 to 1.04), male sex (1.50, 1.01 to 2.23), prednisone dose (1–5 mg/day 1.86, 1.20 to 2.66, 6–9 mg/day 2.47, 1.24 to 4.86 and ≥10 mg/day 1.95, 1.27 to 2.99), no current treatment (1.80, 1.17 to 2.75), comorbidities (eg, kidney disease 3.51, 2.42 to 5.09, cardiovascular disease/hypertension 1.69, 1.25 to 2.29) and moderate or high SLE disease activity (vs remission; 1.61, 1.02 to 2.54 and 3.94, 2.11 to 7.34, respectively) were associated with more severe outcomes. In age-adjusted and sex-adjusted models, mycophenolate, rituximab and cyclophosphamide were associated with worse outcomes compared with hydroxychloroquine; outcomes were more favourable with methotrexate and belimumab. Conclusions: More severe COVID-19 outcomes in individuals with SLE are largely driven by demographic factors, comorbidities and untreated or active SLE. Patients using glucocorticoids also experienced more severe outcomes. | en_US |
dc.language.iso | eng | |
dc.publisher | BMJ Publishing Group | |
dc.relation.ispartofseries | Annals of the Rheumatic Diseases | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | COVID-19 | en_US |
dc.subject | systemic lupus erythematosus | en_US |
dc.subject | COVID-19 Global Rheumatology Alliance | en_US |
dc.title | Characteristics associated with poor COVID-19 outcomes in individuals with systemic lupus erythematosus: data from the COVID-19 Global Rheumatology Alliance | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1136/annrheumdis-2021-221636 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.02.17 | |
dc.relation.issn | 1468-2060 |
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