Clinical Features and Prognosis of Acute Kidney Injury in Hospital-Admitted Patients with COVID-19 in Egypt: A Single-Center Experience
et al., Mansoura Medical Journal, doi:10.58775/2735-3990.1433, Jan 2025
Retrospective 236 hospitalized COVID-19 patients showing favipiravir use associated with increased risk of acute kidney injury (AKI). AKI was associated with higher mortality.
Potential risks of favipiravir include kidney injury1-3, liver injury2-4, and mutagenicity, carcinogenicity, teratogenicity, embryotoxicity, and the creation of dangerous variants5-11.
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AKI, 148.7% higher, OR 2.49, p = 0.03, treatment 57, control 179, RR approximated with OR.
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| Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates |
1.
Abdulaziz et al., Clinical Features and Prognosis of Acute Kidney Injury in Hospital-Admitted Patients with COVID-19 in Egypt: A Single-Center Experience, Mansoura Medical Journal, doi:10.58775/2735-3990.1433.
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Ülger et al., Experimental evaluation of favipiravir (T-705)-induced liver and kidney toxicity in rats, Food and Chemical Toxicology, doi:10.1016/j.fct.2025.115472.
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El-Fetouh et al., Experimental Studies on Some Drugs Used in Covid-19 Treatment (Favipiravir and Dexamethasone) in Albino Rats, Journal of Advanced Veterinary Research, 13:10, www.advetresearch.com/index.php/AVR/article/view/1635.
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Almutairi et al., Liver Injury in Favipiravir-Treated COVID-19 Patients: Retrospective Single-Center Cohort Study, Tropical Medicine and Infectious Disease, doi:10.3390/tropicalmed8020129.
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Zhirnov et al., Favipiravir: the hidden threat of mutagenic action, Journal of microbiology, epidemiology and immunobiology, doi:10.36233/0372-9311-114.
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Waters et al., Human genetic risk of treatment with antiviral nucleoside analog drugs that induce lethal mutagenesis: the special case of molnupiravir, Environmental and Molecular Mutagenesis, doi:10.1002/em.22471.
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Hadj Hassine et al., Lethal Mutagenesis of RNA Viruses and Approved Drugs with Antiviral Mutagenic Activity, Viruses, doi:10.3390/v14040841.
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Shum, C., An investigational study into the drug-associated mutational signature in SARS-CoV-2 viruses, The University of Hong Kong, PhD Thesis, hub.hku.hk/handle/10722/344396.
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Shiraki et al., Convenient screening of the reproductive toxicity of favipiravir and antiviral drugs in Caenorhabditis elegans, Heliyon, doi:10.1016/j.heliyon.2024.e35331.
Abdulaziz et al., 1 Jan 2025, retrospective, Egypt, peer-reviewed, median age 68.5, 3 authors, study period September 2020 - February 2021.
Contact: hodamma@mans.edu.eg, hodamma@yahoo.com.
Clinical Features and Prognosis of Acute Kidney Injury in Hospital-Admitted Patients with COVID-19 in Egypt: A Single-Center Experience
Mansoura Medical Journal, doi:10.58775/2735-3990.1433
Background: While coronavirus disease 2019 primarily manifests clinically as a respiratory disease, it can also impact other organs, such as the kidneys. Acute kidney injury (AKI) is frequently seen in hospital-admitted patients with COVID-19 and is linked to poorer outcomes. This research sought to explore the rate, contributing elements, and consequences of AKI in individuals with COVID-19. Patients and methods: Data from 236 COVID-19-infected patients hospitalized in isolation wards and ICUs between September 2020 and February 2021 were analyzed. Comparisons between patients with and without AKI were done using statistical tests as appropriate. Binary logistic regression analyses were performed at the univariable and multivariable levels to identify the risk factors for AKI. Survival data based on AKI status was analyzed using the KaplaneMeier curve. Results: Overall, 81 (34.3 %) of the 236 participants developed AKI during hospitalization. Hospitalized COVID-19 individuals with age more than 64 years, those who received Favipiravir or vasopressors, and those with pH less than or equal to 7.4, HCO3 less than or equal to 19.2, and blood glucose more than 212 mg/dl have 2.4, 2.5, 2.4, 3.4, 3.2, and 2.9times higher odds to exhibit AKI. A significantly lower survival probability was found in individuals with AKI than in non-AKI [log-rank c 2 (2) ¼ 41.187, P < 0.001]. A shorter median survival time for patients with AKI compared with those without was also noticed [8 days (95 % confidence interval: 7.132e8.868) vs. 12 days (95 % confidence interval: 10.910e13.090)]. Conclusion: AKI is not uncommonly encountered in patients with COVID-19 in the course of their hospitalization and is linked to increased mortality.
Ethics information The Mansoura Faculty of Medicine Institutional Research Board (MFM-IRB) (code MS.22.08.2103)
Conflicts of interest There are no conflicts of interest.
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