1. Systematic Review and Subgroup Meta-analysis of Randomized Trials to Determine Tocilizumab’s Place in COVID-19 Pneumonia
- Author
-
Jean-Charles Balblanc, Pierre-Yves Royer, Souheil Zayet, Marc Puyraveau, Thierry Conrozier, Vincent Gendrin, Aurélie Gerazime, Cerise Guillochon, Julio Badie, Alix Pierron, Anne Lohse, Timothée Klopfenstein, Lynda Toko, Chaouki Mezher, and N.’dri Juliette Kadiane-Oussou
- Subjects
Microbiology (medical) ,medicine.medical_specialty ,medicine.medical_treatment ,Population ,Subgroup analysis ,Review ,law.invention ,chemistry.chemical_compound ,Tocilizumab ,Randomized controlled trial ,law ,Internal medicine ,medicine ,Cumulative incidence ,education ,Mechanical ventilation ,education.field_of_study ,Coronavirus disease 2019 ,business.industry ,Mortality rate ,Incidence (epidemiology) ,Meta-analysis ,Infectious Diseases ,chemistry ,Randomized clinical trial ,business - Abstract
Introduction Tocilizumab randomized clinical trial results are heterogeneous because of the heterogenous population included in them. Methods We conducted a meta-analysis with subgroup meta-analysis (PRISMA guidelines) between severe and non-severe COVID-19. Results We included nine trials. Overall, the mortality rate was 24.5% (821/3357) in the tocilizumab group and 29.1% (908/3125) in the control group at day 28–30 (pooled OR, 0.85; 95% CI 0.76–0.96; p = 0.006). Considering the subgroup analysis, this benefit on mortality was confirmed and amplified in the severe COVID-19 group (pooled OR, 0.82; 95% CI 0.73–0.93; p = 0.001) but not in the non-severe COVID-19 group (pooled OR, 1.46; 95% CI 0.91–2.34; p = 0.12). For patients who were not mechanically ventilated at baseline (5523/6482), the pooled OR (0.74; 95% CI 0.64–0.85; p
- Published
- 2021