Deferoxamine in the management of COVID-19 adult patients admitted to ICU: a prospective observational cohort study

Author:

Almutary Abdulaziz M.1ORCID,Althunayyan Saqer2,Bagalb Amal S.3,Mady Ahmed F.45ORCID,Alenazi Latifa6,Mumtaz Shahzad A.4,Al-Hammad Zahrah7,Abdulrahman Basheer43ORCID,Al-Odat Mohammed A.4,Mhawish Huda4,Aletreby Waleed Th.4,Altartouri Maymouna8,Memish Ziad A.91011ORCID

Affiliation:

1. Emergency

2. Department of Accident and Trauma, Prince Sultan Bin Abdulaziz College for Emergency Medical Services, King Saud University

3. Pharmaceutical Service Administration and Medication Safety Unit, King Saud Medical City

4. Critical Care

5. Anesthesia Department, Faculty of Medicine, Tanta University, Tanta, Egypt

6. Family Medicine

7. Section of Endocrinology, Internal Medicine Department, King Faisal Specialist Hospital and Research Center

8. Section of Medical Oncology, Oncology Center, King Faisal Specialist Hospital and Research Center

9. Research & Innovation Centre

10. College of Medicine, Alfaisal University, Riyadh, Saudi Arabia

11. Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA

Abstract

Background: COVID-19 infection is associated with high mortality, and despite extensive studying the scientific society is still working to find a definitive treatment. Some experts postulated a beneficial role of Deferoxamine. Aim: The aim of this study was to compare the outcomes of COVID-19 adult patients admitted to the ICU who received deferoxamine to those who received standard of care. Methods: Prospective observational cohort study, in the ICU of a tertiary referral hospital in Saudi Arabia to compare all-cause hospital mortality between COVID-19 patients who received deferoxamine and standard of care. Results: A total of 205 patients were enrolled, with an average age of 50.1±14.3, 150 patients received standard of care only, and 55 patients received deferoxamine additionally. Hospital mortality was lower in deferoxamine group (25.5 vs. 40.7%, 95% CI=1.3–29.2%; P=0.045). Clinical status score upon discharge was lower in deferoxamine group (3.6±4.3 vs. 6.2±4, 95% CI: 1.4–3.9; P<0.001), as was the difference between discharge score and admission score (indicating clinical improvement). More patients admitted with mechanical ventilation were successfully extubated in the deferoxamine group (61.5 vs. 14.3%, 95% CI: 15–73%; P=0.001), with a higher median ventilator-free days. There were no differences between groups in adverse events. Deferoxamine group was associated with hospital mortality [odds ratio=0.46 (95% CI: 0.22–0.95); P=0.04]. Conclusions: Deferoxamine may have mortality and clinical improvement benefits in COVID-19 adults admitted to ICU. Further powered and controlled studies are required.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference18 articles.

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