CLINICAL OUTCOMES AND SAFETY IN COVID -19 PATIENTS TREATED WITH REMDESIVIR IN VINMEC INTERNATIONAL HOSPITAL

Dương Thanh Hải1, Khổng Trọng Thắng2, Trương Ngọc Hải2, Ngô Thị Thu Thủy2, Nguyễn Hoàng Phương Khanh2, Nguyễn Đỗ Quang Trung2, Lương Thị Hải Vân3, Nguyễn Lê Thùy Dung2, Lý Anh Thư2, Bùi Hồng Ngọc2, Lê Quốc Sử2, Phan Quỳnh Lan1,
1 Vinmec Times City International Hospital
2 Vinmec Central Park
3 Vinmec Nha Trang

Main Article Content

Abstract

Remdesivir is an antiviral drug that has been approved for the treatment of hospitalized COVID-19 patients in many countries, including Vietnam. However, clinical data of remdesivir is lacking in Vietnam. This study was carried out to investigate clinical outcome and safety of remdesivir in the treatment of COVID-19 in Vietnam. A retrospective observational study was performed in all hospitalized COVID-19 patients 12 years of age and older treated with at least one dose of remdesivir from 10 August 2021 to 10 September 2021 at Vinmec Central Park Hospital. The clinical outcome was measured by the WHO 6-point scale, mechanical ventilation at day 14, and 28-day mortality. The safety of remdesivir was evaluated based on the 2017 AIDS scale. Results: 152 patients were enrolled in this study with more than 50% had at least one comorbidity, mainly cardiovascular diseases or diabetes. Patients was treated with remdesivir at median 6 days after onset. 55.7% patients had significant clinical improvement at day 11. In this study, 14.6% of patients received invasive mechanical ventilation on day 14. The 28-day mortality was 12.5%. The most commonly reported adverse events included elevation of liver enzymes (29.6%), hypokalemia (26.3%), decreased glomerular filtration rate (17.8%), bradycardia (11.2%) and prolongation of prothrombin time (15.1%). Risk factor for poor outcome were advanced age, having at least one comorbidity, low ROX score, requirement of HFNC, non-invasive ventilation or invasive mechanical ventilation; elevated PCT, D-Dimer, ferritin; decreased lymphocyte count at baseline.

Article Details

References

1. WHO Solidarity Trial Consortium, Pan H, Peto R, et al. Repurposed Antiviral Drugs for Covid-19 - Interim WHO Solidarity Trial Results. N Engl J Med. 2021;384(6):497-511. doi:10.1056/NEJMoa2023184
2. Bansal V, Mahapure KS, Bhurwal A, et al. Mortality Benefit of Remdesivir in COVID-19: A Systematic Review and Meta-Analysis. Front Med. 2021;7:606429. doi:10.3389/fmed.2020.606429
3. Ader F, Bouscambert-Duchamp M, Hites M, et al. Remdesivir plus standard of care versus standard of care alone for the treatment of patients admitted to hospital with COVID-19 (DisCoVeRy): a phase 3, randomised, controlled, open-label trial. Lancet Infect Dis. Published online September 14, 2021. doi:10.1016/S1473-3099(21)00485-0
4. Beigel JH, Tomashek KM, Dodd LE, et al. Remdesivir for the Treatment of Covid-19 - Final Report. N Engl J Med. 2020;383(19):1813-1826. doi:10.1056/NEJMoa2007764
5. Spinner CD, Gottlieb RL, Criner GJ, et al. Effect of Remdesivir vs Standard Care on Clinical Status at 11 Days in Patients With Moderate COVID-19: A Randomized Clinical Trial. JAMA. 2020;324(11):1048-1057. doi:10.1001/jama.2020.16349
6. Singh A, Kamath A. Assessment of adverse events associated with remdesivir use for coronavirus disease 2019 using real-world data. Expert Opin Drug Saf. Published online August 5, 2021:1-6. doi:10.1080/14740338.2021.1962846
7. RECOVERY Collaborative Group et al. “Dexamethasone in Hospitalized Patients with Covid-19.” The New England journal of medicine vol. 384,8 (2021): 693-704.
8. U.S. Department of Health and Human Services, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Division of AIDS. Division of AIDS (DAIDS) Table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1. (2017).