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10.1016/j.ejim.2020.05.011

http://scihub22266oqcxt.onion/10.1016/j.ejim.2020.05.011
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32448770!7241995!32448770
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suck abstract from ncbi


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pmid32448770      Eur+J+Intern+Med 2020 ; 76 (ä): 36-42
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  • Off-label use of tocilizumab for the treatment of SARS-CoV-2 pneumonia in Milan, Italy #MMPMID32448770
  • Morena V; Milazzo L; Oreni L; Bestetti G; Fossali T; Bassoli C; Torre A; Cossu MV; Minari C; Ballone E; Perotti A; Mileto D; Niero F; Merli S; Foschi A; Vimercati S; Rizzardini G; Sollima S; Bradanini L; Galimberti L; Colombo R; Micheli V; Negri C; Ridolfo AL; Meroni L; Galli M; Antinori S; Corbellino M
  • Eur J Intern Med 2020[Jun]; 76 (ä): 36-42 PMID32448770show ga
  • BACKGROUND: Tocilizumab, a humanized monoclonal antibody, targets IL-6 receptors blocking downstream pro-inflammatory effects of IL-6. In preliminary reports it was suggested to be beneficial in patients with severe COVID-19. METHODS: In this open-label prospective study we describe clinical characteristics and outcome of 51 patients hospitalized with confirmed and severe COVID-19 pneumonia treated with tocilizumab intravenously. All patients had elevated IL-6 plasma level (>40 pg/mL) and oxygen saturation <93% in ambient air. Clinical outcomes, oxygen support, laboratory data and adverse events were collected over a follow-up of 30 days. RESULTS: Forty-five patients (88%) were on high-flow oxygen supplementation, six of whom with invasive ventilation. From baseline to day 7 after tocilizumab we observed a dramatic drop of body temperature and CRP value with a significant increase in lymphocyte count (p<0.001). Over a median follow-up time of 34 days from tocilizumab, 34 patients (67%) showed an improvement in their clinical severity class; 31 were discharged; 17 (33%) showed a worsening of their clinical status, of these 14 died (27%). The mortality rate was significantly associated with mechanical ventilation at baseline (83.3% vs 20% of patients on non-invasive oxygen support; p=0.0001). The most frequent side effects were an increase of hepatic enzymes (29%), thrombocytopenia (14%), and serious bacterial and fungal infections (27%). CONCLUSION: Tocilizumab exerts a rapidly beneficial effect on fever and inflammatory markers, although no significant impact on the clinical outcome can be inferred by our results. Critically ill patients seem to have a high risk of serious infections with this drug.
  • |*Antibodies, Monoclonal, Humanized/administration & dosage/adverse effects[MESH]
  • |*Coronavirus Infections/blood/epidemiology/physiopathology/therapy[MESH]
  • |*Pandemics[MESH]
  • |*Pneumonia, Viral/blood/diagnosis/drug therapy/epidemiology/etiology/physiopathology/therapy[MESH]
  • |*Respiratory Insufficiency/etiology/therapy[MESH]
  • |Antiviral Agents/adverse effects[MESH]
  • |Betacoronavirus/drug effects/isolation & purification[MESH]
  • |COVID-19[MESH]
  • |Female[MESH]
  • |Fever/diagnosis/drug therapy[MESH]
  • |Humans[MESH]
  • |Italy/epidemiology[MESH]
  • |Lymphocyte Count/methods[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Outcome and Process Assessment, Health Care[MESH]
  • |Receptors, Interleukin-6/*antagonists & inhibitors[MESH]
  • |Respiration, Artificial/*methods[MESH]
  • |Retrospective Studies[MESH]


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