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POS1247 (2021)
CLINICAL FEATURES AND OUTCOMES OF COVID-19 IN PATIENTS WITH IGG4-RELATED DISEASE. A COLLABORATIVE EUROPEAN MULTI-CENTRE STUDY
G. A. Ramirez1,2, M. Lanzillotta1,2, M. Ebbo3,4, A. Fernandez-Codina5,6,7,8, G. Mancuso1,2, F. Martínez-Valle9,10, O. Orozco-Galvez9,10, N. Schleinitz3,4, L. Dagna1,2, E. L. Culver11,12, E. Della Torre1,2
1IRCCS Ospedale San Raffaele, Unit of Immunology, Rheumatology, Allergy and Rare Diseases, Milan, Italy
2Università Vita-Salute San Raffaele, Immunology, Milan, Italy
3CHU de Marseille - Hôpital de la Timone, Département de Médecine Interne, Marseille, France
4Aix-Marseille University, Internal Medicine, Marseille, France
5Windsor Regional Hospital, General Internal Medicine, Windsor, Canada
6Saint Joseph’s Health Care London, Rheumatology, London, Canada
7University of Western Ontario, Rheumatology, London, Canada
8Hospital Clinic i Provincial, Emergency Department, Barcelona, Spain
9Universitat Autònoma de Barcelona, Autoimmune Diseases Research Lab., Barcelona, Spain
10Vall d’Hebrón Hospital, Systemic Diseases Unit, Internal Medicine Service, Barcelona, Spain
11Oxford University Hospitals NHS Foundation Trust, Hepatology, Oxford, United Kingdom
12University of Oxford, Translational Gastroenterology Unit, Oxford, United Kingdom

Background: Coronavirus disease 2019 (COVID-19) is a pandemic-spread systemic infectious disease with prominent respiratory manifestations and significant associated morbidity and mortality. Elderly people are most significantly affected with mortality ranging from 2.4% (age 60-69) to 19.6% (age>80) in European Countries. The prevalence of COVID-19 and of its complications in patients with immune-mediated disorders, remains unclear. The frequency and impact of COVID-19 on patients with IgG4-related diease (IgG4-RD), many of whom are on concurrent immunosuppression has not been addressed.


Objectives: To assess the epidemiological and clinical relevance of COVID-19 in patients with IgG4-RD.


Methods: This is a multi-centre retrospective observational study of IgG4-RD patients from France, Italy, Spain and the United Kingdom. Demographics, comorbidities, IgG4-RD features, current and past treatment along with COVID-19-suggestive symptoms and COVID-19 diagnoses from February 2020 to January 2021 were recorded by means of direct or phone interviews. Patients with reverse-transcriptase polymerase chain reaction-confirmed (cCOVID) or presumed COVID-19 based on clinical, serological or imaging features (pCOVID) were pooled for analysis (totCOVID) and compared to patients who were not diagnosed with COVID-19. Inter-group comparison of categorical and quantitative variables were performed by using the chi-square test with Fisher’s correction and the Mann-Whitney’s test respectively. Data are expressed as median (interquartile range) unless otherwise specified.


Results: A total of 305 patients [71% males, median age 64 (54-74) years] were studied. Pancreato-biliary disease was the most frequently observed IgG4-RD phenotype (39%). Fifty-one percent of patients were taking corticosteroids at time of interview and 30% were on biological or conventional immunosuppressants. Thirty-two totCOVID cases (23 cCOVID, nine pCOVID) were identified: 11/32 were hospitalised, two needed intensive care and four (13%; 3/4 aged >80 years) died. Having one or more infected family members was a risk factor for COVID-19 in patients with IgG4-RD (OR=19.9; p<0.001). No other demographic, clinical or treatment features associated with COVID-19. In particular there was no association between adverse outcomes with COVID-19 and higher doses of steroids (>20mg) or rituximab administration.


Conclusion: The prevalence and course of COVID-19 in IgG4-RD patients are similar to those of the general population of the same age, with no evident impact of disease- or treatment-related factors to the basal infectious risk. Effective public health countermeasures might be beneficial for patients with IgG4RD.


REFERENCES:

[1]European Centre for Disease Prevention and Control (ECDC): https://covid19-surveillance-report.ecdc.europa.eu/

[2]Yang H, Ann Rheum Dis, 2021


Disclosure of Interests: Giuseppe Alvise Ramirez: None declared, Marco Lanzillotta: None declared, Mikael Ebbo: None declared, Andreu Fernandez-Codina Consultant of: consulting fees from Atheneum Consulting, Gaia Mancuso: None declared, Fernando Martínez-Valle: None declared, Olimpia Orozco-Galvez: None declared, Nicolas Schleinitz: None declared, Lorenzo Dagna Consultant of: Abbvie, Amgen, Biogen, BristolMyers Squibb, Celltrion, Galapagos, GlaxoSmithKline, Novartis, Pfizer, Roche, Sanofi-Genzyme, and SOBI, Grant/research support from: The Unit of Immunology, Rheumatology, Allergy and Rare Diseases (UnIRAR) received unresctricted research/educational grants from Abbvie, Bristol-Myers Squibb, Celgene, GlaxoSmithKline,Janssen, Merk Sharp & Dohme, Mundipharma Pharmaceuticals, Novartis, Pfizer, Roche, Sanofi Genzyme, and SOBI, Emma L. Culver: None declared, Emanuel Della Torre: None declared


Citation: Ann Rheum Dis, volume 80, supplement 1, year 2021, page 907
Session: COVID-19 (POSTERS only)