Tocilizumab in the treatment of rapidly evolving COVID-19 pneumonia and multifaceted critical illness: A retrospective case series

Ahmed Mady; Waleed Aletreby; Basheer Abdulrahman; Mohammed Lhmdi; Alfateh M Noor; Saleh A Alqahtani; Ibrahim Soliman; Abdulrahman Alharthy; Dimitrios Karakitsos; Ziad A Memish

doi:10.1016/j.amsu.2020.10.061

Tocilizumab in the treatment of rapidly evolving COVID-19 pneumonia and multifaceted critical illness: A retrospective case series

Ann Med Surg (Lond). 2020 Dec:60:417-424. doi: 10.1016/j.amsu.2020.10.061. Epub 2020 Nov 5.

Authors

Ahmed Mady^{1

2}, Waleed Aletreby¹, Basheer Abdulrahman¹, Mohammed Lhmdi¹, Alfateh M Noor¹, Saleh A Alqahtani^{3

4}, Ibrahim Soliman¹, Abdulrahman Alharthy¹, Dimitrios Karakitsos^{1

5

6}, Ziad A Memish^{7

8

9}

Affiliations

¹ Critical Care Department, King Saud Medical City, Riyadh, Saudi Arabia.
² Department of Anesthesiology and Critical Care, Tanta University Hospitals, Tanta, Egypt.
³ Department of Medicine, Johns Hopkins University, Baltimore, USA.
⁴ Department of Medicine, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
⁵ Department of Medicine, South Carolina University School of Medicine, Columbia, SC, USA.
⁶ Critical Care Department, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
⁷ Research & Innovation Centre, King Saud Medical City, Riyadh, Saudi Arabia.
⁸ Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
⁹ College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

Abstract

Background: COVID-19 associated critical illness characterized by rapidly evolving acute respiratory failure (ARF) can develop, especially on the grounds of hyperinflammation.

Aim and methods: A case-series of 61 patients admitted to our intensive care unit (ICU) between August 12 and September 12, 2020 with confirmed COVID-19 pneumonia and rapidly evolving ARF requiring oxygen support therapy and/or mechanical ventilation was retrospectively analyzed. We examined whether intravenous administration of tocilizumab, a monoclonal interleukin-6 receptor antibody, was associated with improved outcome. All patients received empiric antivirals, dexamethasone 6 mg/day for 7 days, antibiotics, and prophylactic anticoagulation. Tocilizumab was administered at a dosage of 8 mg/kg [two consecutive intravenous infusions 12 h apart]. Outcome measures such as mortality on day-14, ICU length of stay, and rate of nosocomial acquired bacterial infections were also analyzed. Results: Patients were males (88.2%) aged 51 [interquartile range (IQR): 42.5-58.75)], with admission Acute Physiology and Chronic Health Evaluation (APACHE) 4 score of 53 (IQR: 37.75-72.5), and had more than one comorbidity (62.3%). On admission, twenty nine patients (47.5%) were mechanically ventilated, and thirty two patients (52.5%) were receiving oxygen therapy. No serious adverse effects due to tocilizumab therapy were recorded. However, twelve patients (19.6%) developed nosocomial acquired infections. ICU length of stay was 13 (IQR: 9-17) days, and mortality on day-14 was 24.6%. Six patients were shifted to other hospitals but were followed-up. The overall mortality on day-30 was 31.1%. Non-mechanically ventilated patients had higher survival rates compared to mechanically ventilated patients although results were not significant [hazards ratio = 2.6 (95% confidence intervals: 0.9-7.7), p = 0.08]. Tocilizumab did not affect the mortality of critically ill COVID-19 patients.

Conclusion: Tocilizumab could be an adjunct safe therapy in rapidly evolving COVID-19 pneumonia and associated critical illness.

Keywords: Acute respiratory failure; COVID-19 pneumonia; Mechanical ventilation; Tocilizumab.