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10.1136/annrheumdis-2020-217763

http://scihub22266oqcxt.onion/10.1136/annrheumdis-2020-217763
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suck abstract from ncbi


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pmid32532753      Ann+Rheum+Dis 2020 ; 79 (9): 1170-1173
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  • Prevalence of hospital PCR-confirmed COVID-19 cases in patients with chronic inflammatory and autoimmune rheumatic diseases #MMPMID32532753
  • Pablos JL; Abasolo L; Alvaro-Gracia JM; Blanco FJ; Blanco R; Castrejon I; Fernandez-Fernandez D; Fernandez-Gutierrez B; Galindo-Izquierdo M; Gonzalez-Gay MA; Manrique-Arija S; Mena Vazquez N; Mera Varela A; Retuerto M; Seijas-Lopez A
  • Ann Rheum Dis 2020[Sep]; 79 (9): 1170-1173 PMID32532753show ga
  • BACKGROUND: The susceptibility of patients with rheumatic diseases and the risks or benefits of immunosuppressive therapies for COVID-19 are unknown. METHODS: We performed a retrospective study with patients under follow-up in rheumatology departments from seven hospitals in Spain. We matched updated databases of rheumatology patients with severe acute respiratory syndrome coronavirus 2-positive PCR tests performed in the hospital to the same reference populations. Rates of PCR+ confirmed COVID-19 were compared among groups. RESULTS: Patients with chronic inflammatory diseases had 1.32-fold higher prevalence of hospital PCR+ COVID-19 than the reference population (0.76% vs 0.58%). Patients with systemic autoimmune or immune-mediated disease (AI/IMID) showed a significant increase, whereas patients with inflammatory arthritis (IA) or systemic lupus erythematosus did not. COVID-19 cases in some but not all diagnostic groups had older ages than cases in the reference population. Patients with IA on targeted-synthetic or biological disease-modifying antirheumatic drugs (DMARDs), but not those on conventional-synthetic DMARDs, had a greater prevalence despite a similar age distribution. CONCLUSION: Patients with AI/IMID show a variable risk of hospital-diagnosed COVID-19. Interplay of ageing, therapies and disease-specific factors seem to contribute. These data provide a basis to improve preventive recommendations to rheumatic patients and to analyse the specific factors involved in COVID-19 susceptibility.
  • |*Betacoronavirus[MESH]
  • |Adult[MESH]
  • |Age Distribution[MESH]
  • |Aged[MESH]
  • |Antirheumatic Agents/adverse effects[MESH]
  • |Arthritis, Rheumatoid/drug therapy/epidemiology/virology[MESH]
  • |Autoimmune Diseases/drug therapy/*epidemiology/virology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/diagnosis/*epidemiology/virology[MESH]
  • |Female[MESH]
  • |Hospitalization/*statistics & numerical data[MESH]
  • |Humans[MESH]
  • |Lupus Erythematosus, Systemic/drug therapy/epidemiology/virology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/diagnosis/*epidemiology/virology[MESH]
  • |Polymerase Chain Reaction[MESH]
  • |Prevalence[MESH]
  • |Retrospective Studies[MESH]
  • |Rheumatic Diseases/drug therapy/*epidemiology/virology[MESH]
  • |SARS-CoV-2[MESH]


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