dc.contributor.author |
Ugarte Gil, Manuel Francisco |
|
dc.contributor.author |
Alarcón, Graciela S. |
|
dc.contributor.author |
Izadi, Zara |
|
dc.contributor.author |
Duarte-Garcia, Ali |
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dc.contributor.author |
Reategui-Sokolova, Cristina |
|
dc.contributor.author |
Clarke, Ann Elaine |
|
dc.contributor.author |
Wise, Leanna |
|
dc.contributor.author |
Pons-Estel, Guillermo J. |
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dc.contributor.author |
Santos, Maria Jose |
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dc.contributor.author |
Bernatsky, Sasha |
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dc.contributor.author |
Euzebio Ribeiro, Sandra Lucia |
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dc.contributor.author |
Al Emadi, Samar |
|
dc.contributor.author |
Sparks, Jeffrey A. |
|
dc.contributor.author |
Hsu, Tiffany Y-T |
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dc.contributor.author |
Patel, Naomi J. |
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dc.contributor.author |
Gilbert, Emily L. |
|
dc.contributor.author |
Valenzuela-Almada, Maria O. |
|
dc.contributor.author |
Jonsen, Andreas |
|
dc.contributor.author |
Landolfi, Gianpiero |
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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 |
|