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Copyright ©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Virol. Jun 25, 2025; 14(2): 102674
Published online Jun 25, 2025. doi: 10.5501/wjv.v14.i2.102674
COVID-19 management in patients with comorbid conditions
Adekunle Sanyaolu, Chuku Okorie, Aleksandra Marinkovic, Stephanie Prakash, Vyshnavy Balendra, Amine Lehachi, Abu Fahad Abbasi, Nafees Haider, Amos Abioye, Verner N Orish, Afolabi Antonio, Olanrewaju Badaru, Rajashree Pandit, Ricardo Izurieta
Adekunle Sanyaolu, Chuku Okorie, Rajashree Pandit, Department of Biomedical Science, D’Youville University, Buffalo, NY 14201, United States
Aleksandra Marinkovic, Stephanie Prakash, Vyshnavy Balendra, Amine Lehachi, Department of Basic Medical Science, Saint James School of Medicine, The Quarter 2640, Anguilla
Abu Fahad Abbasi, Department of Internal Medicine, Loyola University Medical Center, Maywood, IL 60153, United States
Nafees Haider, Department of Basic Science, All Saints University School of Medicine, Roseau 00152, Dominica
Amos Abioye, College of Pharmacy and Health Sciences, Belmont University, Nashville, TN 37212, United States
Verner N Orish, Department of Microbiology and Immunology, School of Medicine, University of Health and Allied Sciences, Ho PMB31, Ghana
Afolabi Antonio, Department of Medicine, Lloydminster Regional Hospital, Lloydminster S9V 1Y5, Saskatchewan, Canada
Olanrewaju Badaru, Department of Public Health, Federal Ministry of Health, Abuja 083, Federal Capital Territory, Nigeria
Ricardo Izurieta, School of Public Health and Health Sciences, California State University, Los Angeles, CA 90747, United States
Author contributions: Sanyaolu A contributed to conceptualization and design, approved the final version, and responsible for the accuracy and integrity of all the aspects of the research; Marinkovic A, Prakash S, Balendra V, Lehachi A, Abbasi AF, and Haider N contributed to drafting of the article; Marinkovic A contributed to project administration; Okorie C, Abioye A, Orish VN, Antonio A, Badaru O, Pandit R, and Izurieta R contributed to review and revise the article for intellectual content and editing.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Adekunle Sanyaolu, PhD, Professor, Department of Biomedical Science, D’Youville University, 320 Porter Avenue, Buffalo, NY 14201, United States. sanyakunle@hotmail.com
Received: October 27, 2024
Revised: March 16, 2025
Accepted: April 28, 2025
Published online: June 25, 2025
Processing time: 241 Days and 5.8 Hours
Abstract

The novel coronavirus disease 2019 (COVID-19) causes serious respiratory illness and related disorders. Vulnerable populations, including those with chronic obstructive pulmonary disease, heart disease, diabetes, chronic kidney disease, obesity, and the elderly, face an increased risk of severe complications. As the pandemic evolves, various diagnostic techniques are available to detect severe acute respiratory distress syndrome (SARS-CoV-2), including clinical presentation, rapid antigen/antibody testing, molecular testing, supplemental laboratory analysis, and imaging. Based on peer-reviewed data, treatment options include convalescent plasma transfusion, corticosteroids, antivirals, and immunomodulatory medications. Convalescent plasma therapy, historically used in outbreaks like Middle East respiratory syndrome, Ebola, and SARS, is suggested by the World Health Organization for critically ill COVID-19 patients when vaccines or antiviral drugs are unavailable. Neutralizing antibodies in convalescent plasma help control viral load and improve patient outcomes, especially when administered early, though effectiveness varies. The United States Food and Drug Administration has authorized its emergency use for severe COVID-19 cases, but potential risks such as transfusion reactions and transfusion-related acute lung injury require further investigation to establish definitive efficacy. Antiviral agents like Remdesivir, an adenosine nucleotide analog, inhibit viral RNA polymerase and have shown efficacy in reducing COVID-19 severity, leading to its emergency use authorization for hospitalized patients. Other antivirals like ritonavir, lopinavir, and umifenovir disrupt viral replication and entry, but their effectiveness against SARS-CoV-2 remains under investigation. Dexamethasone, a corticosteroid, has been used in critically ill COVID-19 patients to reduce inflammation and prevent respiratory failure, as shown in the RECOVERY trial. Other immunosuppressants like ruxolitinib, baricitinib, and colchicine help modulate the immune response, reducing cytokine storms and inflammation-related complications. However, corticosteroids carry risks such as hyperglycemia, immunosuppression, and delayed viral clearance, requiring careful administration. Systematic reviews of clinical studies revealed that hydroxychloroquine with or without azithromycin did not decrease viral load nor reduce the severity of symptoms, but increased mortality among acutely hospitalized patients. There was no improvement in patients’ clinical conditions after 15 days compared to standard treatment. The United States Food and Drug Administration has revoked the authorization for the use of hydroxychloroquine in COVID-19 patients due to the null benefit-risk balance. Monoclonal antibodies like itolizumab, gimsilumab, sarilumab, and tocilizumab are being studied for their ability to reduce the severe inflammatory response in COVID-19 patients, particularly cytokine release syndrome and acute respiratory distress syndrome. These antibodies target specific immune pathways to decrease pro-inflammatory cytokines, with some showing promising results in clinical trials, though their use remains under investigation. The Clustered Regularly Interspaced Short Palindromic Repeats/Cas13 family of enzymes, sequenced from many COVID-19-positive patients, can potentially inhibit SARS-CoV-2 replication, cleave the RNA genome, and aid in the amplification of the genome assay. Cas13 can also target emerging pathogens via an adeno-associated virus vector when delivered to the infected lungs. In addition to pharmacological agents, vaccines effectively prevent symptomatic infection, reduce hospitalizations, minimize mortality rates, and ultimately reduce the severity of the disease. This paper aims to explore the management of patients with underlying conditions who present with COVID-19 to lessen the burden on healthcare systems.

Keywords: COVID-19; Comorbidity; Diabetes; Heart disease; Chemotherapy; Vaccine; Therapeutic management

Core Tip: Effective management of coronavirus disease 2019 in patients with comorbid conditions is vital to reduce severe complications, limit hospitalizations and ease the pressure on healthcare systems. This requires employing thorough diagnostic methods, tailoring pharmacological treatments to individual patient profiles, and encouraging widespread vaccination to boost immunity efforts. An integrated approach ensures better patient outcomes and supports public health resilience during ongoing and future infectious disease challenges.