Your browser doesn't support javascript.
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters

Database
Language
Document Type
Year range
1.
Critical Care Medicine ; 51(1 Supplement):216, 2023.
Article in English | EMBASE | ID: covidwho-2190551

ABSTRACT

INTRODUCTION: Markedly elevated pro-inflammatory cytokines, including interleukin-6 (IL-6), are associated with severe COVID-19. Blocking inflammation may prevent disease progression. Tocilizumab is a monoclonal antibody that reduces inflammation by blocking the IL-6 receptor, potentially having an impact on improving outcomes in patients with COVID-19. The objective of this study was to evaluate the use of tocilizumab in critically ill patients with COVID-19. METHOD(S): This multicenter, retrospective study included adults admitted to an intensive care unit (ICU) with severe COVID-19 from June 2020 to November 2021. Patients were placed into two groups: those who received one dose of tocilizumab in addition to dexamethasone, and those who received dexamethasone alone. Patients were matched on age, sex, C-reactive protein (CRP) level, and time from symptom onset to hospitalization. The primary endpoint was hospital length of stay (LOS). Secondary endpoints were ICU LOS, in-hospital all-cause mortality, number of mechanically ventilated days, and incidence of secondary infections. RESULT(S): 120 patients were included (60 patients per group). The mean age was 57 years old, 60% were male, and the median time from symptom onset to hospitalization was 7 days. The median CRP level in the tocilizumab + dexamethasone group vs the dexamethasone group was 140.6 and 143 mg/L, respectively. The median hospital LOS was 11 days (IQR 8-17) in the tocilizumab + dexamethasone group vs 13 days (IQR 8 - 22.8) in the dexamethasone group. In-hospital all-cause mortality occurred in 17 patients (28%) in the tocilizumab + dexamethasone group vs 16 patients (26%) in the dexamethasone group. Of the 26 patients in the tocilizumab + dexamethasone group and 24 patients in the dexamethasone group that were mechanically ventilated, the median number of mechanically ventilated days was 10 (IQR 5 - 18.3) vs 10.5 (5 - 18.8), respectively. Secondary infections were similar in both groups. CONCLUSION(S): In this retrospective study evaluating tocilizumab in addition to dexamethasone for severe COVID-19 treated in the ICU, tocilizumab did not show a benefit in clinical outcomes. Given the size of the study and its limitations, these findings should be interpreted with caution and require confirmation by larger studies.

SELECTION OF CITATIONS
SEARCH DETAIL