Abstract

Background and objectivesRecent randomized controlled trials (RCTs) have indicated potential therapeutic benefits with high-dose dexamethasone (HDD) or tocilizumab (TCZ) plus standard care in moderate to severe coronavirus disease 2019 (COVID-19) with acute respiratory distress syndrome (ARDS). No study has compared these two against each other. We aimed to compare the efficacy and safety of HDD against TCZ in moderate to severe COVID-ARDS.MethodsPatients admitted with moderate to severe COVID-19 ARDS with clinical worsening within 48 hours of standard care were randomly assigned to receive either HDD or TCZ plus standard care. The primary outcome was ventilator-free days (VFDs) at 28 days. The main secondary outcomes were 28-day all-cause mortality and the incidence of adverse events. Our initial plan was to perform an interim analysis of the first 42 patients.ResultsVFDs were significantly lower in the HDD arm (median difference: 28 days; 95% confidence interval (CI): 19.35-36.65; Cohen’s d = 1.14;p < 0.001). We stopped the trial at the first interim analysis due to high 28-day mortality in the HDD arm (relative risk (RR) of death: 6.5; p = 0.007; NNT (harm) = 1.91). The incidence of secondary infections was also significantly high in the HDD arm (RR: 5.5; p = 0.015; NNT (harm) = 2.33).ConclusionsIn our study population, HDD was associated with a very high rate of mortality and adverse events. We would not recommend HDD to mitigate the cytokine storm in moderate to severe COVID-19 ARDS. TCZ appears to be a much better and safer alternative.

Highlights

  • Coronavirus disease 2019 (COVID-19) has been associated with high mortality in moderate and severe acute respiratory distress syndrome (ARDS)

  • ventilator-free days (VFDs) were significantly lower in the high-dose dexamethasone (HDD) arm (median difference: 28 days; 95% confidence interval (CI): 19.35-36.65; Cohen’s d = 1.14; p < 0.001)

  • We stopped the trial at the first interim analysis due to high 28-day mortality in the HDD arm (relative risk (RR) of death: 6.5; p = 0.007; NNT = 1.91)

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Summary

Introduction

Coronavirus disease 2019 (COVID-19) has been associated with high mortality in moderate and severe acute respiratory distress syndrome (ARDS). Intervening timely with immunomodulatory therapies might mitigate the severity Based on this assumption, researchers have been focusing on several interventions, including IL-6 inhibitors and corticosteroids [3,4,5,6,7,8,9,10]. The results of two recent randomized controlled trials (RCTs) have shown potential therapeutic benefits with dexamethasone, the practice remains variable [12,13]. Recent randomized controlled trials (RCTs) have indicated potential therapeutic benefits with high-dose dexamethasone (HDD) or tocilizumab (TCZ) plus standard care in moderate to severe coronavirus disease 2019 (COVID-19) with acute respiratory distress syndrome (ARDS). We aimed to compare the efficacy and safety of HDD against TCZ in moderate to severe COVID-ARDS

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