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Tocilizumab for the treatment of severe COVID-19 pneumonia with hyperinflammatory syndrome and acute respiratory failure: A single center study of 100 patients in Brescia, Italy

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  • Additional Information
    • Contributors:
      Toniati P.; Piva S.; Cattalini M.; Garrafa E.; Regola F.; Castelli F.; Franceschini F.; Airò, P.; Bazzani C.; Beindorf E.; Berlendis M.; Bezzi M.; Bossini N.; Castellano M.; Cattaneo S.; Cavazzana I.; Contessi G.; Crippa M.; Delbarba A.; De Peri E.; Faletti A.; Filippini M.; Frassi M.; Gaggiotti M.; Gorla R.; Lanspa M.; Lorenzotti S.; Marino R.; Maroldi R.; Metra M.; Matteelli A.; Modina D.; Moioli G.; Montani G.; Muiesan M.; Odolini S.; Peli E.; Pesenti S.; Pezzoli M.; Pirola I.; Pozzi A.; Proto A.; Rasulo F.; Renisi G.; Ricci C.; Rizzoni D.; Romanelli G.; Rossi M.; Salvetti M.; Scolari F.; Signorini L.; Taglietti M.; Tomasoni G.; Tomasoni L.; Turla F. Valsecchi A.; Zani D.; Zuccalà, F.; Zunica F.; Focà, E.; Andreoli L.; Latronico N.
    • Publication Date:
      2020
    • Collection:
      Università degli Studi di Brescia: OPENBS - Open Archive UniBS
    • Abstract:
      A hyperinflammatory syndrome (HIS) may cause a life-threatening acute respiratory distress syndrome (ARDS) in patients with COVID-19 pneumonia. A prospective series of 100 consecutive patients admitted to the Spedali Civili University Hospital in Brescia (Italy) between March 9th and March 20th with confirmed COVID-19 pneumonia and ARDS requiring ventilatory support was analyzed to determine whether intravenous administration of tocilizumab (TCZ), a monoclonal antibody that targets the interleukin 6 receptor, was associated with improved outcome. Tocilizumab was administered at a dosage of 8 mg/kg by two consecutive intravenous infusions 12 h apart. A third infusion was optional based on clinical response. The outcome measure was an improvement in ARDS assessed by means of the Brescia COVID Respiratory Severity Score (BCRSS 0 to 8, with higher scores indicating higher severity) at 24-72 h and 10 days after tocilizumab administration. Out of 100 treated patients (88 M, 12 F; median age: 62 years), 43 received TCZ in the intensive care unit (ICU), while 57 in the general ward as no ICU beds were available. Of these 57 patients, 37 (65%) improved and suspended noninvasive ventilation (NIV) (median BCRSS: 1 [IQR 0-2]), 7 (12%) patients remained stable in NIV, and 13 (23%) patients worsened (10 died, 3 were admitted to ICU). Of the 43 patients treated in ICU, 32 (74%) improved (17 of them were taken off the ventilator and were discharged to the ward), 1 (2%) remained stable (BCRSS: 5) and 10 (24%) died (all of them had BCRSS≥7 before TCZ). Overall at 10 days, the respiratory condition was improved or stabilized in 77 (77%) patients, of whom 61 showed a significant clearing of diffuse bilateral opacities on chest x-ray and 15 were discharged from the hospital. Respiratory condition worsened in 23 (23%) patients, of whom 20 (20%) died. All the patients presented with lymphopenia and high levels of C-reactive protein (CRP), fibrinogen, ferritin and interleukin 6 (IL-6) indicating a HIS. During the 10-day follow-up, ...
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/32376398; info:eu-repo/semantics/altIdentifier/wos/WOS:000538137300015; volume:19; issue:7; firstpage:102568; journal:AUTOIMMUNITY REVIEWS; https://hdl.handle.net/11379/530098
    • Accession Number:
      10.1016/j.autrev.2020.102568
    • Online Access:
      https://hdl.handle.net/11379/530098
      https://doi.org/10.1016/j.autrev.2020.102568
    • Rights:
      info:eu-repo/semantics/openAccess
    • Accession Number:
      edsbas.A8B4D839