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Acute-phase reactants during tocilizumab therapy for severe COVID-19 pneumonia
Giulia Cassone1, Giovanni Dolci2, Giulia Besutti3
1University of Modena and Reggio Emilia, Modena; Clinical and Experimental Medicine PhD program, University of Modena and Reggio Emilia, Modena; and Rheumatology Unit, Azienda USL-IRCCS di Reggio Emilia, Italy.
Serial C-reactive protein (CRP) monitoring in the first week of tocilizumab (TCZ) therapy helps predict outcomes in severe COVID-19 patients. Higher baseline and early CRP levels indicate a greater risk of poor clinical improvement and intubation or death.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Immunology
Background:
- Severe COVID-19 pneumonia is associated with significant morbidity and mortality.
- Tocilizumab (TCZ), an interleukin-6 (IL-6) inhibitor, is used to treat severe COVID-19.
- Predictors of clinical response and adverse outcomes in TCZ-treated patients require identification.
Purpose of the Study:
- To identify predictors of clinical improvement and intubation/death in severe COVID-19 patients treated with tocilizumab.
- To evaluate the role of longitudinal monitoring of C-reactive protein (CRP) and IL-6 levels.
Main Methods:
- Prospective cohort study of 173 severe COVID-19 patients receiving tocilizumab.
- Clinical improvement and a composite outcome of intubation/death were assessed.
- CRP and IL-6 levels were measured at baseline (T0), day 3 (T3), and day 7 (T7).
Main Results:
- Elevated CRP levels at T0 and T3 were associated with poorer clinical improvement and increased risk of intubation/death.
- No significant association was found between IL-6 levels and clinical outcomes.
- Serial CRP measurements showed distinct trends differentiating patients based on outcome; a baseline CRP of 15.8 mg/dl best predicted intubation/death (AUC=0.711).
Conclusions:
- Longitudinal CRP measurements within the first week of tocilizumab therapy are valuable for predicting poor outcomes in severe COVID-19.
- CRP monitoring can aid in identifying patients at high risk for adverse events, potentially guiding treatment adjustments.
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