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POS0054 THE IMPACT AND OUTCOME OF COVID-19 ON SYSTEMIC SCLEROSIS PATIENTS FROM THE EUROPEAN SCLERODERMA TRIAL AND RESEARCH GROUP (EUSTAR)
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  1. A. M. Hoffmann-Vold1,
  2. C. Brunborg2,
  3. F. Tirelli3,
  4. P. Carreira4,
  5. N. Del Papa5,
  6. A. Mekinian6,
  7. M. Vonk7,
  8. A. Giollo8,
  9. G. De Luca9,
  10. M. De Santis10,
  11. C. Campochiaro9,
  12. C. Mihai3,
  13. P. Airò11,
  14. M. G. Lazzaroni11,
  15. E. Zanatta12,
  16. R. Foti13,
  17. Y. Allanore14,
  18. D. Furst15,
  19. M. Matucci-Cerinic16,
  20. A. Gabrielli17,
  21. O. Distler3
  1. 1Oslo University Hospital, Rheumatology, Oslo, Norway
  2. 2Oslo University Hospital, Centre for Biostatistics and Epidemiology, Research Support Services, Oslo, Norway
  3. 3University Hospital Zurich, University of Zurich, Rheumatology, Zurich, Switzerland
  4. 412 de Octubre University Hospital, Rheumatology, Madrid, Spain
  5. 5ASST G. Pini-CTO, University of Milan, Rheumatology, Milan, Italy
  6. 6Hôpital Saint Antoine, Internal Medicine, Paris, France
  7. 7Radboud University Medical Center, Rheumatology, Nijmegen, Netherlands
  8. 8University of Verona, Rheumatology, Verona, Italy
  9. 9IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Immunology, Rheumatology, Allergy and Rare Diseases, Milan, Italy
  10. 10IRCCS Humanitas Research Hospital, Rheumatology and Clinical Immunology, Milan, Italy
  11. 11ASST Spedali Civili of Brescia, Rheumatology and Clinical Immunology, Brescia, Italy
  12. 12University of Padova, Rheumatology, Padova, Italy
  13. 13A.O.U. Policlinico S. Marco, Rheumatology, Catania, Italy
  14. 14Cochin Hospital, Université de Paris, Rheumatology, Paris, France
  15. 15University of California in Los Angeles, Rheumatology, Los Angeles, United States of America
  16. 16University of Florence, Rheumatology, Florence, Italy
  17. 17Università Politecnica delle Marche, Scienze Cliniche e Molecolari, Ancona, Italy

Abstract

Background: Coronavirus disease-19 (COVID-19) has been a major clinical challenge worldwide. Sex, age and comorbidities have been associated with worse outcome in the general population. Systemic sclerosis (SSc) is a severe, autoimmune disease with frequent multi-organ involvement.

Objectives: To assess the impact of COVID-19 and to determine factors associated with worse outcome in SSc patients from the European Scleroderma Trial and Research (EUSTAR) database.

Methods: SSc patients from the EUSTAR database with COVID-19 were prospectively collected between 15.03.-31.12.2020. Two outcomes were chosen: (1) hospitalization; and (2) severe outcome defined as either non-invasive ventilation, mechanical ventilation/extracorporeal membrane oxygenation (ECMO) or death. General risk factors assessed were sex, age and number of comorbidities. SSc related risk factors were SSc subtype, autoantibodies, disease duration, SSc associated organ manifestations including interstitial lung disease (ILD), pulmonary arterial hypertension (PAH), cardiac, gastrointestinal (GI), and musculoskeletal involvement; digital ulcers (DU), CRP at last visit, renal disease (scleroderma renal crisis and SSc associated renal insufficiency), modified Rodnan skin score (mRSS) and immunosuppressive treatment. Descriptive statistics and logistic regression models were applied.

Results: In total, 178 European SSc patients with COVID-19 were registered with a median observation time of 5.5 weeks (Table 1). 95 patients (53%) could recall SAR-Cov-2 contact, while 47 (26%) had no contact. 156 (88%) were symptomatic at COVID-19 onset with fever, cough, malaise and dyspnea being most prevalent. Over the disease course, 63 (36%) developed pneumonia. In total, 67/176 (38%) were hospitalized which were in 84% due to COVID-19. 41/170 (24%) had a severe outcome including 21 (12%) deaths. 128 (72%) recovered completely, while 14 (8%) complained of sequela, with 7 (50%) stating respiratory complications. Age, non-SSc comorbidities, presence of ILD, PAH and SSc associated renal or cardiac disease were numerically associated with hospitalization and severe outcome (Table 1). Univariable logistic analyses for hospitalization and severe outcome are shown in Figure 1. In multivariable logistic regression, age (OR 1.03, 95%CI 1.01-1.07, p=0.019), presence of non-SSc comorbidities (OR 2.52, 95%CI 1.16-5.47, p=0.019) and SSc-related renal disease (predicting success perfectly) were associated with hospitalization and for severe outcome age (OR 1.05, 95%CI 1.01-1.08).

Conclusion: SSc patients at older age, with non-SSc comorbidities, SSc related renal disease or ILD are at risk of a more severe outcome and should follow precautions to avoid COVID-19 infections and need careful monitoring in case of COVID-19.

Table 1.

SSc disease characteristics of COVID-19 patients

Figure 1.

Univariable logistic analyses for hospitalization and severe outcome

Disclosure of Interests: Anna-Maria Hoffmann-Vold Speakers bureau: Actelion, Boehringer Ingelheim, Roche, Merck Sharp & Dohme, ARXX, Lilly and Medscape, Consultant of: Actelion, Boehringer Ingelheim, Bayer, ARXX, and Medscape

, Grant/research support from: Boehringer Ingelheim, Cathrine Brunborg: None declared, Francesca Tirelli: None declared, Patricia Carreira: None declared, Nicoletta Del Papa: None declared, Arsene Mekinian: None declared, Madelon Vonk: None declared, Alessandro Giollo: None declared, Giacomo De Luca: None declared, Maria De Santis: None declared, Corrado Campochiaro: None declared, Carina Mihai: None declared, Paolo Airò Speakers bureau: Bristol Myers Squibb, Bohringer Ingelheim, Consultant of: Bristol Myers Squibb, Bohringer Ingelheim, non-financial support from CSL Behring, SOBI, Janssen, Roche, Sanofi, Pfizer, Maria Grazia Lazzaroni: None declared, Elisabetta Zanatta: None declared, Rosario Foti: None declared, Yannick Allanore: None declared, Daniel Furst: None declared, Marco Matucci-Cerinic: None declared, Armando Gabrielli: None declared, Oliver Distler Speakers bureau: Actelion, Kymera Therapeutics, Mitsubishi Tanabe Pharma, Abbvie, Acceleron, Alexion, Amgen, AnaMar, Arxx Therapeutics, Baecon, Discovery, Blade Therapeutics, Corbus Pharmaceuticals, Drug Development International, Ltd, CSL Behring, Galapagos NV, Glenmark Pharmaceuticals, GSK, Horizon (Curzion) Pharmaceuticals, Inventiva, iQvia, Kymera Therapeutics, Lilly, Novartis, Pfizer, Topadur and UCB, Consultant of: Actelion, Kymera Therapeutics, Mitsubishi Tanabe Pharma, Abbvie, Acceleron, Alexion, Amgen, AnaMar, Arxx Therapeutics, Baecon, Discovery, Blade Therapeutics, Corbus Pharmaceuticals, Drug Development International, Ltd, CSL Behring, Galapagos NV, Glenmark Pharmaceuticals, GSK, Horizon (Curzion) Pharmaceuticals, Inventiva, iQvia, Kymera Therapeutics, Lilly, Novartis, Pfizer, Topadur and UCB, Grant/research support from: Boehringer Ingelheim.

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