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

• Type of Material: Article
• Authors: Ahmed Mady, King Saud Hospital Riyadh; Waleed Aletreby, King Saud Hospital Riyadh; Basheer Abdulrahman, King Saud Hospital Riyadh; Mohammed Lhmdi, King Saud Hospital Riyadh; Alfateh M. Noor, King Saud Hospital Riyadh; Saleh A. Alqahtani, Johns Hopkins University; Ibrahim Soliman, King Saud Hospital Riyadh; Abdulrahman Alharthy, King Saud Hospital Riyadh; Dimitrios Karakitsos, King Saud Hospital Riyadh; Ziad Memish, Emory University
• Language: English
• Date: 2020-12-01
• Publisher: Annals of Medicine and Surgery
• Publication Version: Final Published Version
• Copyright Statement: © 2020 The Authors
• License: Creative Commons Attribution 4.0 International
• Final Published Version (URL): http://dx.doi.org/10.1016/j.amsu.2020.10.061
• Title of Journal or Parent Work: Annals of Medicine and Surgery
• Volume: 60
• Start Page: 417
• End Page: 424
• Grant/Funding Information: No funding was received for this study.
• Keywords: Acute respiratory failure; COVID-19 pneumonia; Mechanical ventilation; Tocilizumab
• Research Categories: Health Sciences, Public Health; Biology, Virology

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.