Characteristics associated with poor COVID-19 outcomes in individuals with systemic lupus erythematosus: data from the COVID-19 Global Rheumatology Alliance

被引:65
|
作者
Ugarte-Gil, Manuel Francisco [1 ,2 ]
Alarcon, Graciela S. [3 ,4 ]
Izadi, Zara [5 ,6 ]
Duarte-Garcia, Ali [7 ,8 ]
Reategui-Sokolova, Cristina [2 ,9 ]
Clarke, Ann Elaine [10 ]
Wise, Leanna [11 ]
Pons-Estel, Guillermo J. [12 ,13 ]
Santos, Maria Jose [14 ,15 ]
Bernatsky, Sasha [16 ]
Euzebio Ribeiro, Sandra Lucia [17 ]
Al Emadi, Samar [18 ]
Sparks, Jeffrey A. [19 ]
Hsu, Tiffany Y-T [19 ]
Patel, Naomi J. [20 ]
Gilbert, Emily L. [21 ]
Valenzuela-Almada, Maria O. [7 ]
Jonsen, Andreas [22 ]
Landolfi, Gianpiero [23 ]
Fredi, Micaela [24 ,25 ]
Goulenok, Tiphaine [26 ,27 ]
Devaux, Mathilde [28 ]
Mariette, Xavier [29 ]
Queyrel, Viviane [30 ]
Romao, Vasco C. [15 ,31 ]
Sequeira, Graca [32 ]
Hasseli, Rebecca [33 ]
Hoyer, Bimba [34 ]
Voll, Reinhard E. [35 ]
Specker, Christof [36 ]
Baez, Roberto [37 ]
Castro-Coello, Vanessa [38 ]
Ficco, Hernan Maldonado [39 ]
Reis Neto, Edgard Torres [40 ]
Aparecida Ferreira, Gilda Aparecida [41 ,42 ]
Andre Monticielo, Odirlei Andre [43 ,44 ]
Sirotich, Emily [45 ,46 ]
Liew, Jean [47 ]
Hausmann, Jonathan [48 ,49 ]
Sufka, Paul [50 ]
Grainger, Rebecca [51 ]
Bhana, Suleman [52 ]
Costello, Wendy [53 ]
Wallace, Zachary S. [20 ]
Jacobsohn, Lindsay [6 ]
Taylor, Tiffany [6 ]
Ja, Clairissa [6 ]
Strangfeld, Anja [54 ]
Mateus, Elsa F. [55 ,56 ]
Hyrich, Kimme L. [57 ,58 ]
机构
[1] Univ Cient Sur, Grp Peruano Estudio Enfermedades Autoinmunes Sist, Lima, Peru
[2] Hosp Nacl Guillermo Almenara Irigoyen, Rheumatol Dept, EsSalud, Lima, Peru
[3] Univ Alabama Birmingham, Heersink Sch Med, Birmingham, AL USA
[4] Univ Peruana Cayetano Heredia, Sch Med, Lima, Peru
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
[6] Univ Calif San Francisco, Dept Med, Div Rheumatol, San Francisco, CA 94143 USA
[7] Mayo Clin, Div Rheumatol, Rochester, MN USA
[8] Mayo Clin, Robert D & Patricia E Kern Ctr Sci Hlth Care Deli, Rochester, MN USA
[9] Univ San Ignacio de Loyola, Unidad Invest Generac & Sintesis Evidencias Salud, Lima, Peru
[10] Univ Calgary, Div Rheumatol, Dept Med Cumming, Sch Med, Calgary, AB, Canada
[11] Univ Southern Calif, Dept Internal Med, Div Rheumatol, Los Angeles, CA 90007 USA
[12] Ctr Reg Enfermedades Autoinmunes & Reumat GO CREA, Rosario, Argentina
[13] Argentine Soc Rheumatol, Res Unit, Buenos Aires, DF, Argentina
[14] Hosp Garcia de Orta, Rheumatol, Almada, Portugal
[15] Univ Lisbon, Fac Med, Rheumatol Res Unit, Inst Med Mol Joao Lobo Antunes, Lisbon, Portugal
[16] McGill Univ, Div Rheumatol, Hlth Ctr, Montreal, PQ, Canada
[17] Univ Fed Amazonas, Fac Med, UFAM, Manaos, Amazonas, Brazil
[18] Hamad Med Corp, Rheumatol Dept, Doha, Qatar
[19] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, 75 Francis St, Boston, MA 02115 USA
[20] Harvard Med Sch, Div Rheumatol Allergy & Immunol, Massachusetts Gen Hosp, Boston, MA 02115 USA
[21] Mayo Clin, Div Rheumatol, Jacksonville, FL 32224 USA
[22] Lund Univ, Lund, Sweden
[23] Italian Soc Rheumatol, Epidemiol Res Unit, Milan, Italy
[24] ASST Spedali Civili, Rheumatol & Clin Immunol, Brescia, Italy
[25] Univ Brescia, Dept Clin & Expt Sci, Brescia, Italy
[26] Bichat Claude Bernard Hosp, AP HP, Internal Med Dept, Paris, France
[27] Univ Paris, Paris, France
[28] Poissy St Germain En Laye Hosp, Internal Med Dept, Poissy, France
[29] Univ Paris Saclay, AP HP, Dept Rheumatol, Le Kremlin Bicetre, France
[30] Univ Nice Sophia Antipolis, Dept Rheumatol, Pasteur 2 Hosp, Nice, France
[31] Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Rheumatol Dept, Lisbon, Portugal
[32] Ctr Hosp Univ Algarve, Unidade Faro, Faro, Portugal
[33] Justus Liebig Univ Giessen, Dept Rheumatol & Clin Immunol, Campus Kerckhoff, Bad Nauheim, Germany
[34] Univ Hosp Schleswig Holstein, Dept Rheumatol & Clin Immunol, Clin Internal Med 1, Kiel, Germany
[35] Albert Ludwigs Univ Freiburg, Univ Med Ctr Freiburg, Fac Med, Dept Rheumatol & Clin Immunol, Freiburg, Germany
[36] Kliniken Essen Mitte, Dept Rheumatol & Clin Immunol, Essen, Germany
[37] Hosp Francisco Lopez Lima, Gen Roca, Argentina
[38] Sanatorio Guemes Hosp Privado, Buenos Aires, DF, Argentina
[39] Hosp San Antonio de Padua, Rio Cuarto, Argentina
[40] Univ Fed Sao Paulo, Hosp Sao Paulo, Sao Paulo, Brazil
[41] Hosp Clin, Belo Horizonte, MG, Brazil
[42] Univ Fed Minas Gerais, Belo Horizonte, MG, Brazil
[43] Hosp Clin Porto Alegre, Porto Alegre, RS, Brazil
[44] Univ Fed Rio Grande do Sul, Porto Alegre, RS, Brazil
[45] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
[46] Canadian Arthrit Patient Alliance, Toronto, ON, Canada
[47] Boston Univ, Sch Med, Dept Med, Sect Rheumatol, Boston, MA 02118 USA
[48] Boston Childrens Hosp, Rheumatol, Boston, MA USA
[49] Harvard Med Sch, Div Rheumatol & Clin Immunol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[50] Healthpartners, St Paul, MN USA
关键词
lupus erythematosus; systemic; COVID-19; epidemiology;
D O I
10.1136/annrheumdis-2021-221636
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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收藏
页码:970 / 978
页数:9
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