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dc.contributor.authorBabayigit, Cenk
dc.contributor.authorKokturk, Nurdan
dc.contributor.authorKul, Seval
dc.contributor.authorCetinkaya, Pelin Duru
dc.contributor.authorNayci, Sibel Atis
dc.contributor.authorBaris, Serap Argun
dc.contributor.authorKarcioglu, Oguz
dc.date.accessioned2023-11-16T18:30:22Z
dc.date.available2023-11-16T18:30:22Z
dc.date.issued2022
dc.identifier.issn2296-858X
dc.identifier.urihttps://doi.org/10.3389/fmed.2022.894126
dc.identifier.urihttps://hdl.handle.net/20.500.14065/5642
dc.description.abstractBackground and objectivesAlthough several repurposed antiviral drugs have been used for the treatment of COVID-19, only a few such as remdesivir and molnupiravir have shown promising effects. The objectives of our study were to investigate the association of repurposed antiviral drugs with COVID-19 morbidity. MethodsPatients admitted to 26 different hospitals located in 16 different provinces between March 11-July 18, 2020, were enrolled. Case definition was based on WHO criteria. Patients were managed according to the guidelines by Scientific Board of Ministry of Health of Turkey. Primary outcomes were length of hospitalization, intensive care unit (ICU) requirement, and intubation. ResultsWe retrospectively evaluated 1,472 COVID-19 adult patients; 57.1% were men (mean age = 51.9 +/- 17.7years). A total of 210 (14.3%) had severe pneumonia, 115 (7.8%) were admitted to ICUs, and 69 (4.7%) were intubated during hospitalization. The median (interquartile range) of duration of hospitalization, including ICU admission, was 7 (5-12) days. Favipiravir (n = 328), lopinavir/ritonavir (n = 55), and oseltamivir (n = 761) were administered as antiviral agents, and hydroxychloroquine (HCQ, n = 1,382) and azithromycin (n = 738) were used for their immunomodulatory activity. Lopinavir/ritonavir (beta [95% CI]: 4.71 [2.31-7.11]; p = 0.001), favipiravir (beta [95% CI]: 3.55 [2.56-4.55]; p = 0.001) and HCQ (beta [95% CI]: 0.84 [0.02-1.67]; p = 0.046) were associated with increased risk of lengthy hospital stays. Furthermore, favipiravir was associated with increased risks of ICU admission (OR [95% CI]: 3.02 [1.70-5.35]; p = 0.001) and invasive mechanical ventilation requirement (OR [95% CI]: 2.94 [1.28-6.75]; p = 0.011). ConclusionOur findings demonstrated that antiviral drugs including lopinavir, ritonavir, and favipiravir were associated with negative clinical outcomes such as increased risks for lengthy hospital stay, ICU admission, and invasive mechanical ventilation requirement. Therefore, repurposing such agents without proven clinical evidence might not be the best approach for COVID-19 treatment.en_US
dc.language.isoengen_US
dc.publisherFrontiers Media Saen_US
dc.relation.ispartofFrontiers in Medicineen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAntiviral Agentsen_US
dc.subjectCovid-19 Morbidityen_US
dc.subjectLength Of Hospitalizationen_US
dc.subjectIcu Requirementen_US
dc.subjectInvasive Mechanical Ventilationen_US
dc.subjectIcu Admission Ratesen_US
dc.subjectFavipiraviren_US
dc.subjectHydroxychloroquineen_US
dc.subjectRemdesiviren_US
dc.subjectCollegeen_US
dc.titleThe association of antiviral drugs with COVID-19 morbidity: The retrospective analysis of a nationwide COVID-19 cohorten_US
dc.typearticleen_US
dc.authoridTure, Zeynep/0000-0001-6895-0318
dc.authoridKetencioğlu, Burcu Baran/0000-0002-6757-3140
dc.authoridBayram, Hasan/0000-0002-5236-766X
dc.authoridDuru Çetinkaya, pelin/0000-0002-4428-8590
dc.departmentUfuk Üniversitesien_US
dc.identifier.doi10.3389/fmed.2022.894126
dc.identifier.volume9en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidTure, Zeynep/AGF-0133-2022
dc.authorwosidKetencioğlu, Burcu Baran/AAO-9889-2021
dc.authorwosidBayram, Hasan/ABE-5094-2021
dc.authorwosidDuru Çetinkaya, pelin/JKJ-4986-2023
dc.identifier.wosWOS:000877589000001en_US
dc.identifier.scopus2-s2.0-85138400187en_US
dc.identifier.pmid36117966en_US


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