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The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country
BACKGROUND: Remdesivir is a monophosphoramidate prodrug of an adenosine analog, and it has a broad-spectrum antiviral activity against paramyxoviruses, flaviviruses, and coronaviruses. Remdesivir is associated with decreased hospital stay and improved outcomes in coronavirus- disease 2019 (COVID-19)...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8823973/ https://www.ncbi.nlm.nih.gov/pubmed/35156078 http://dx.doi.org/10.1016/j.rcsop.2022.100107 |
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author | Malik, Muhammad Irfan Zafar, Sardar Al Fareed Malik, Muna Qayyum, Fabiha Akram, Iqra Arshad, Ammarah Waheed, Khalid Saleem, Jodat Jabbar, Abdul Tahir, Muhammad Junaid Yousaf, Zohaib |
author_facet | Malik, Muhammad Irfan Zafar, Sardar Al Fareed Malik, Muna Qayyum, Fabiha Akram, Iqra Arshad, Ammarah Waheed, Khalid Saleem, Jodat Jabbar, Abdul Tahir, Muhammad Junaid Yousaf, Zohaib |
author_sort | Malik, Muhammad Irfan |
collection | PubMed |
description | BACKGROUND: Remdesivir is a monophosphoramidate prodrug of an adenosine analog, and it has a broad-spectrum antiviral activity against paramyxoviruses, flaviviruses, and coronaviruses. Remdesivir is associated with decreased hospital stay and improved outcomes in coronavirus- disease 2019 (COVID-19). METHODOLOGY: Of 846 suspected COVID-19 patients admitted to the hospital, 612 SARS-CoV-2 nasopharyngeal RT-PCR positive patients were evaluated for enrollment in this prospective cohort study. 159 RT-PCR positive patients were given remdesivir. Their clinical, biochemical parameters, hospital stay, and outcomes related to morbidity and mortality were followed. RESULTS: Out of the 159 patients, 141 recovered after remdesivir use. The Chi-square test for independence examined the relation between the day of the first dose, dose of remdesivir, and clinical outcome. The standardized case fatality ratio (CFR) in the 453 hospitalized patients who did not receive remdesivir was 32.89% (N = 149) as compared to 11.32% (N = 18) in the patients who received remdesivir. These findings are in keeping with the therapeutic value of remdesivir in symptomatic SARS-CoV-2 infection of varying severity. CONCLUSION: The use of remdesivir is associated with a decrease in the severity of the SARS-CoV-2 infection. Its use is also associated with a decreased length of hospital stay and lower mortality than the patients who did not receive remdesivir. |
format | Online Article Text |
id | pubmed-8823973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-88239732022-02-09 The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country Malik, Muhammad Irfan Zafar, Sardar Al Fareed Malik, Muna Qayyum, Fabiha Akram, Iqra Arshad, Ammarah Waheed, Khalid Saleem, Jodat Jabbar, Abdul Tahir, Muhammad Junaid Yousaf, Zohaib Explor Res Clin Soc Pharm Article BACKGROUND: Remdesivir is a monophosphoramidate prodrug of an adenosine analog, and it has a broad-spectrum antiviral activity against paramyxoviruses, flaviviruses, and coronaviruses. Remdesivir is associated with decreased hospital stay and improved outcomes in coronavirus- disease 2019 (COVID-19). METHODOLOGY: Of 846 suspected COVID-19 patients admitted to the hospital, 612 SARS-CoV-2 nasopharyngeal RT-PCR positive patients were evaluated for enrollment in this prospective cohort study. 159 RT-PCR positive patients were given remdesivir. Their clinical, biochemical parameters, hospital stay, and outcomes related to morbidity and mortality were followed. RESULTS: Out of the 159 patients, 141 recovered after remdesivir use. The Chi-square test for independence examined the relation between the day of the first dose, dose of remdesivir, and clinical outcome. The standardized case fatality ratio (CFR) in the 453 hospitalized patients who did not receive remdesivir was 32.89% (N = 149) as compared to 11.32% (N = 18) in the patients who received remdesivir. These findings are in keeping with the therapeutic value of remdesivir in symptomatic SARS-CoV-2 infection of varying severity. CONCLUSION: The use of remdesivir is associated with a decrease in the severity of the SARS-CoV-2 infection. Its use is also associated with a decreased length of hospital stay and lower mortality than the patients who did not receive remdesivir. Elsevier 2022-02-08 /pmc/articles/PMC8823973/ /pubmed/35156078 http://dx.doi.org/10.1016/j.rcsop.2022.100107 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Malik, Muhammad Irfan Zafar, Sardar Al Fareed Malik, Muna Qayyum, Fabiha Akram, Iqra Arshad, Ammarah Waheed, Khalid Saleem, Jodat Jabbar, Abdul Tahir, Muhammad Junaid Yousaf, Zohaib The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country |
title | The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country |
title_full | The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country |
title_fullStr | The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country |
title_full_unstemmed | The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country |
title_short | The utility of remdesivir in SARS-CoV-2: A single tertiary care center experience from a developing country |
title_sort | utility of remdesivir in sars-cov-2: a single tertiary care center experience from a developing country |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8823973/ https://www.ncbi.nlm.nih.gov/pubmed/35156078 http://dx.doi.org/10.1016/j.rcsop.2022.100107 |
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