RESUMEN
Background: Tocilizumab, an interleukin-6 (IL-6) antagonist, is being evaluated for the management of covid-19 pneumonia. The objective of this study was to assess the effectiveness of Tocilizumab in severe covid-19 pneumonia. Method(s): This was a retrospective, observational, single centre study performed in 121 patients diagnosed with severe covid-19 pneumonia. 83 patients received standard of care treatment whereas 38 patients received tocilizumab along with standard of care. Tocilizumab was administered intravenously at 8mg/kg (upto a maximum of 800mg). The second dose of Tocilizumab was given 12 to 24 hours apart. The primary outcome measure was ICU related and hospital related mortality. The secondary outcome measures were change in clinical status of patients measured by WHO (World Health Organisation) 7 category ordinary scale, changes in interleukin-6 (IL-6) levels, secondary infections and duration of ICU stay. Result(s): Tocilizumab was administered between 3-27 days after the patient reported symptoms ( a median of 10.9 days ) and between the 1st to 3rd day of ICU admission (median of 2.1 days) . In Tocilizumab group, 16(42.1%) of 38 patients died in ICU whereas in standard of care group, 27(32.53%) of 83 patients died. The difference in clinical status assessed using WHO (World Health Organisation) 7 category ordinary scale at 28 days between Tocilizumab group and standard of care group was not statistically significant (odds ratio 1.35, 95% confidence interval 0.61 to 2.97, p = 0.44). Conclusion(s): Tocilizumab plus standard care was not superior to standard care alone in reducing mortality and improving clinical outcomes at day 28.Copyright © RJPT All right reserved.
RESUMEN
Background:Bevacizumab, an antiangiogenic drug, is being evaluated for the management of novel coronavirus disease (COVID-19) pneumonia among critically ill patients. The objective of this study was to assess the effectiveness of bevacizumab in severe COVID-19 pneumonia. Methods:This was a retrospective, observational study performed in 111 patients diagnosed with COVID-19 pneumonia. Bevacizumab was administered intravenously at 7.5 mg/kg along with standard care in a non-randomly selected subset of patients (n = 29) with evidence of acute respiratory distress syndrome (ARDS) within 72 hours of worsening of oxygenation. The primary outcome measure was intensive care unit (ICU)-related mortality. Results:Bevacizumab was administered for a median of 9.4 (4-24) days from the onset of symptoms and 2.2 (1-3) days from the day of ICU admission. Bevacizumab-treated patients showed a statistically significant improvement in PF ratio and reduction in radiological severity score. In the bevacizumab group, 13 (44.8%) of 29 patients died in ICU, and in the standard-of-care group, 37 (45.1%) of 82 patients died. The difference in clinical status assessed using the World Health Organization 7-category Ordinary Scale at 28 days between the bevacizumab group and the standard-of-care group was not statistically significant (odds ratio 1.02, 95% confidence interval 0.44-2.4, P = .94). Conclusion:Bevacizumab plus standard care was not superior to standard care alone in reducing mortality and improving clinical outcomes at day 28.