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COVID-19 presentation and outcomes in patients with inflammatory rheumatic and musculoskeletal diseases receiving IL6-receptor antagonists prior to SARS-CoV-2 infection.
Comarmond, Cloé; Drumez, Elodie; Labreuche, Julien; Hachulla, Eric; Thomas, Thierry; Flipo, René-Marc; Seror, Raphaëlle; Avouac, Jérôme; Balandraud, Nathalie; Desbarbieux, Renaud; Felten, Renaud; Gilson, Mélanie; Guyot, Marie-Hélène; Hittinger-Roux, Ambre; Pham, Thao; Renard, Myriam; Roux, Nicolas; Sobanski, Vincent; Tournadre, Anne; Richez, Christophe; Cacoub, Patrice.
Afiliación
  • Comarmond C; Department of Internal Medicine and Clinical Immunology, Lariboisière Hospital, Université de Paris, 75010, Paris, France.
  • Drumez E; ULR 2694 METRICS: Évaluation des Technologies de Santé et des Pratiques Médicales, Université de Lille, CHU Lille, Lille, France.
  • Labreuche J; ULR 2694 METRICS: Évaluation des Technologies de Santé et des Pratiques Médicales, Université de Lille, CHU Lille, Lille, France.
  • Hachulla E; Université de Lille, INSERM, CHU Lille, Service de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Autoimmunes Systémiques Rares Du Nord et Nord-Ouest de France, U1286-INFINITE: Institute for Translational Research in Inflammation, France.
  • Thomas T; Rheumatology, CHU de Saint-Etienne - Hôpital Nord, France.
  • Flipo RM; Rheumatology, CHRU de Lille, France.
  • Seror R; Rheumatology, APHP - Hôpital Bicêtre, Kremlin-Bicêtre, France.
  • Avouac J; Rheumatology, APHP - Hôpital Cochin, Université de, Paris, France.
  • Balandraud N; Rheumatology, APHM - Hôpital Sainte-Marguerite, Marseille, France.
  • Desbarbieux R; Rheumatology, CH de Boulogne-sur-Mer, France.
  • Felten R; Rheumatology, CHRU de Strasbourg - Hôpital de Hautepierre, France.
  • Gilson M; Rheumatology, CHU de Grenoble - Hôpital Sud, France.
  • Guyot MH; Rheumatology, CH de Roubaix, France.
  • Hittinger-Roux A; Rheumatology, CHU de Reims, France.
  • Pham T; Rheumatology, APHM - Hôpital Sainte-Marguerite, Marseille, France.
  • Renard M; Rheumatology, CH Métropole-Savoie - Hôpital Reine Hortense, France.
  • Roux N; Rheumatology, Hôpitaux Privés de Metz - Hôpital Belle-Isle, France.
  • Sobanski V; Université de Lille, INSERM, CHU Lille, Service de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Autoimmunes Systémiques Rares Du Nord et Nord-Ouest de France, U1286-INFINITE: Institute for Translational Research in Inflammation, France.
  • Tournadre A; Rheumatology, CHU de Clermont-Ferrand - Hôpital Gabriel Montpied, France.
  • Richez C; Rheumatology, GH Pellegrin - CHU Bordeaux, France.
  • Cacoub P; Department of Internal Medicine and Clinical Immunology, Pitié-Salpêtrière Hospital, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Sorbonne Université, UMR 959, 75013, Paris, France.
J Transl Autoimmun ; 6: 100190, 2023.
Article en En | MEDLINE | ID: mdl-36684808
Objective: COVID-19 outcome may be less favourable in patients with inflammatory rheumatic and musculoskeletal diseases (RMD) receiving immunosuppressive therapy. We aimed to investigate whether RMD patients on anti-IL6 therapy prior to SARS-CoV-2 infection have less severe disease and better outcomes of COVID-19. Methods: We conducted a retrospective national, multicentre cohort study using data from the French RMD COVID-19 cohort. We compared the severity and outcome of highly suspected or confirmed COVID-19 infection in RMD patients previously treated with tocilizumab or sarilumab (anti-IL6 group) with patients who did not receive anti-IL6 therapy (no anti-IL6 group). Results: Data were collected for 1883 patients with mean age of 55.2 years [SD 16.7] and 1256 (66.7%) female. Two hundred ten (11.1%) developed severe COVID-19 and 115 (6.4%) died. After adjusting for potential confounding factors, severe COVID-19 was less frequent in the anti-IL6 group compared with the no anti-IL6 group (aOR for moderate vs. mild severity, 0.23 [95% CI, 0.10 to 0.54], p ≤ 0.01 and aOR for severe vs. mild, 0.29 [95% CI, 0.10 to 0.81], p ≤ 0.01). No significant differences were found for the evolution of COVID-19 between the anti-IL6 group and the no anti-IL6 group (aOR for recovery with sequelae vs recovery without sequelae, 0.78 [95% CI, 0.41 to 1.48] and aOR for death vs recovery without sequelae, 0.29 [95% CI, 0.07 to 1.30]). Conclusion: RMD patients receiving anti-IL6 therapy prior to SARS-CoV-2 infection have less severe forms of COVID-19. No difference was observed in COVID-19 evolution, i.e., sequelae or death, between the groups.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: J Transl Autoimmun Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: J Transl Autoimmun Año: 2023 Tipo del documento: Article