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dc.contributor.authorYıldırım F.
dc.contributor.authorGulhan P.Y.
dc.contributor.authorDiken Ö.E.
dc.contributor.authorCapraz A.
dc.contributor.authorSimsek M.
dc.contributor.authorYildirim B.B.
dc.contributor.authorTaysi M.R.
dc.date.accessioned2024-03-12T19:35:54Z
dc.date.available2024-03-12T19:35:54Z
dc.date.issued2021
dc.identifier.issn2220315X
dc.identifier.urihttps://doi.org/10.5493/WJEM.V11.I4.44
dc.identifier.urihttps://hdl.handle.net/20.500.12450/3016
dc.description.abstractBACKGROUND Although the detection of viral particles by reverse transcription polymerase chain reaction (RT-PCR) is the gold standard diagnostic test for coronavirus disease 2019 (COVID-19), the false-negative results constitute a big challenge. AIM To examine a group of patients diagnosed and treated as possible COVID-19 pneumonia whose multiple nasopharyngeal swab samples were negative for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by RT-PCR but then serological immunoglobulin M/immunoglobulin G (IgM/IgG) antibody against SARS-CoV-2 were detected by rapid antibody test. METHODS Eighty possible COVID-19 patients who had at least two negative consecutive COVID-19 RT-PCR test and were subjected to serological rapid antibody test were evaluated in this study. RESULTS The specific serological total IgM/IgG antibody against SARS-CoV-2 was detected in twenty-two patients. The mean age of this patient group was 63.2± 13.1-years-old with a male/female ratio of 11/11. Cough was the most common symptom (90.9%). The most common presenting chest computed tomography findings were bilateral ground glass opacities (77.2%) and alveolar consolidations (50.1%). The mean duration of time from appearance of first symptoms to hospital admission, to hospital admission, to treatment duration and to serological positivity were 8.6 d, 11.2 d, 7.9 d, and 24 d, respectively. Compared with reference laboratory values, serologically positive patients have shown increased levels of acute phase reactants, such as C-reactive protein, ferritin, and procalcitonin and higher inflammatory markers, such as erythrocyte sedimentation rate, lactate dehydrogenase enzyme, and fibrin end-products, such as D-dimer. A left shift on white blood cell differential was observed with increased neutrophil counts and decreased lymphocytes. CONCLUSION Our study demonstrated the feasibility of a COVID-19 diagnosis based on rapid antibody test in the cases of patients whose RT-PCR samples were negative. Detection of antibodies against SARS-CoV-2 with rapid antibody test should be included in the diagnostic algorithm in patients with possible COVID-19 pneumonia. © The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherBaishideng Publishing Group Coen_US
dc.relation.ispartofWorld Journal of Experimental Medicineen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCOVID-19en_US
dc.subjectHigh resolution computed tomographyen_US
dc.subjectPneumoniaen_US
dc.subjectRapid antibody testen_US
dc.subjectReverse transcription polymerase chain reactionen_US
dc.subjectSerologyen_US
dc.titleRole of serological rapid antibody test in the management of possible COVID-19 casesen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.identifier.volume11en_US
dc.identifier.issue4en_US
dc.identifier.startpage44en_US
dc.identifier.endpage54en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85116515535en_US
dc.identifier.doi10.5493/WJEM.V11.I4.44
dc.department-tempYıldırım, F., Department of Pulmonary and Critical Care Medicine, University of Health Sciences, Diskapi Yildirim Beyazit Research and Education Hospital, Ankara, 06110, Turkey; Gulhan, P.Y., Department of Pulmonary Medicine, Düzce University, Faculty of Medicine, Düzce, 81100, Turkey; Diken, Ö.E., Department of Chest Diseases, Adana Research and Education Hospital, University of Health Sciences, Adana, 01230, Turkey; Capraz, A., Department of Pulmonary Medicine, Amasya University Sabuncuoglu Serefeddin Research and Education Hospital, Amasya, 05200, Turkey; Simsek, M., Medical Intensive Care Unit, University of Health Sciences, Diskapi Yildirim Beyazit Research and Education Hospital, Ankara, 06110, Turkey; Yildirim, B.B., Department of Pulmonology, Research and Education Hospital of Baskent University, Konya, 42030, Turkey; Taysi, M.R., Department of Infectious and Clinical Microbiology, University of Health Sciences, Diskapi Yildirim Beyazit Research and Education Hospital, Ankara, 06110, Turkey; Ozturk, S.Y., Department of Pulmonary Medicine, Vezirkopru State Hospital, Samsun, 55090, Turkey; Demirtas, N., Department of Pulmonary Medicine, Kumluca State Hospital, Antalya, 07070, Turkey; Ergil, J., Department of Anaesthesiology and Reanimation, Diskapi Yildirim Beyazit Research and Education Hospital, University of Health Scieen_US
dc.authorscopusid56924955200
dc.authorscopusid57199508851
dc.authorscopusid56002962900
dc.authorscopusid57221552997
dc.authorscopusid56257725800
dc.authorscopusid57189211402
dc.authorscopusid57221597030


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