Clinical and radiological diagnosis of non–SARS‐CoV‐2 viruses in the era of COVID‐19 pandemic
Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the clinical, laboratory, radiological distinctive features of viral pneumonia caused by viruses other than severe acute respiratory syndrome cor...
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Published in: | Journal of medical virology Vol. 93; no. 2; pp. 1119 - 1125 |
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Abstract | Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the clinical, laboratory, radiological distinctive features of viral pneumonia caused by viruses other than severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). A cross‐sectional study was conducted between 18 and 31 March 2020. COVID‐19 suspected cases admitted to pandemic policlinic, who had nasopharyngeal swab specimens tested for both SARS‐CoV‐2 and other respiratory viral pathogens, were included. Among 112 patients, SARS‐CoV‐2 was detected in 34 patients (30%). Among the non–SARS‐CoV‐2 viruses (n = 25, 22%), metapneumovirus (n = 10) was the most frequent agent. There were two coinfections with SARS‐CoV‐2. Sputum was less in the SARS‐CoV‐2 group (P = .003). The leukocyte, lymphocyte, and thrombocyte count and C‐reactive protein levels were the lowest in the SARS‐CoV‐2 group (P < .001, P = .04, P < .001, P = .007, respectively). Peripheral involvement (80% vs 20%; P ≤ .001), pure ground‐glass opacity (65% vs 33%; P = .04), apicobasal gradient (60% vs 40%; P = .08), involvement of greater than or equal to three lobes (80% vs 40%; odds ratio: 6.0; 95% confidence interval: 1.33‐27.05; P = .02), and consolidation with accompanying ground‐glass opacity (4% vs 33%; P = .031) were more common in SARS‐CoV‐2 group. Some clinical, laboratory, and radiological findings may help in the differential diagnosis of non–SARS‐CoV‐2 viruses from COVID‐19. However, coinfections may occur, and a non–SARS‐CoV‐2 pathogen positivity does not exclude accompanying COVID‐19.
Highlights
Non SARS‐CoV‐2 viruses have some clinical, laboratory and radiological distinctive parameters from SARS CoV‐2. However, it should always be considered that co‐infections may develop in the clinical course of COVID‐19. |
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AbstractList | Following the announcement of the first coronavirus disease 2019 (COVID-19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the clinical, laboratory, radiological distinctive features of viral pneumonia caused by viruses other than severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A cross-sectional study was conducted between 18 and 31 March 2020. COVID-19 suspected cases admitted to pandemic policlinic, who had nasopharyngeal swab specimens tested for both SARS-CoV-2 and other respiratory viral pathogens, were included. Among 112 patients, SARS-CoV-2 was detected in 34 patients (30%). Among the non-SARS-CoV-2 viruses (n = 25, 22%), metapneumovirus (n = 10) was the most frequent agent. There were two coinfections with SARS-CoV-2. Sputum was less in the SARS-CoV-2 group (P = .003). The leukocyte, lymphocyte, and thrombocyte count and C-reactive protein levels were the lowest in the SARS-CoV-2 group (P < .001, P = .04, P < .001, P = .007, respectively). Peripheral involvement (80% vs 20%; P ≤ .001), pure ground-glass opacity (65% vs 33%; P = .04), apicobasal gradient (60% vs 40%; P = .08), involvement of greater than or equal to three lobes (80% vs 40%; odds ratio: 6.0; 95% confidence interval: 1.33-27.05; P = .02), and consolidation with accompanying ground-glass opacity (4% vs 33%; P = .031) were more common in SARS-CoV-2 group. Some clinical, laboratory, and radiological findings may help in the differential diagnosis of non-SARS-CoV-2 viruses from COVID-19. However, coinfections may occur, and a non-SARS-CoV-2 pathogen positivity does not exclude accompanying COVID-19. Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the clinical, laboratory, radiological distinctive features of viral pneumonia caused by viruses other than severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). A cross‐sectional study was conducted between 18 and 31 March 2020. COVID‐19 suspected cases admitted to pandemic policlinic, who had nasopharyngeal swab specimens tested for both SARS‐CoV‐2 and other respiratory viral pathogens, were included. Among 112 patients, SARS‐CoV‐2 was detected in 34 patients (30%). Among the non–SARS‐CoV‐2 viruses ( n = 25, 22%), metapneumovirus ( n = 10) was the most frequent agent. There were two coinfections with SARS‐CoV‐2. Sputum was less in the SARS‐CoV‐2 group ( P = .003). The leukocyte, lymphocyte, and thrombocyte count and C‐reactive protein levels were the lowest in the SARS‐CoV‐2 group ( P < .001, P = .04, P < .001, P = .007, respectively). Peripheral involvement (80% vs 20%; P ≤ .001), pure ground‐glass opacity (65% vs 33%; P = .04), apicobasal gradient (60% vs 40%; P = .08), involvement of greater than or equal to three lobes (80% vs 40%; odds ratio: 6.0; 95% confidence interval: 1.33‐27.05; P = .02), and consolidation with accompanying ground‐glass opacity (4% vs 33%; P = .031) were more common in SARS‐CoV‐2 group. Some clinical, laboratory, and radiological findings may help in the differential diagnosis of non–SARS‐CoV‐2 viruses from COVID‐19. However, coinfections may occur, and a non–SARS‐CoV‐2 pathogen positivity does not exclude accompanying COVID‐19. Non SARS‐CoV‐2 viruses have some clinical, laboratory and radiological distinctive parameters from SARS CoV‐2. However, it should always be considered that co‐infections may develop in the clinical course of COVID‐19. Abstract Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the clinical, laboratory, radiological distinctive features of viral pneumonia caused by viruses other than severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). A cross‐sectional study was conducted between 18 and 31 March 2020. COVID‐19 suspected cases admitted to pandemic policlinic, who had nasopharyngeal swab specimens tested for both SARS‐CoV‐2 and other respiratory viral pathogens, were included. Among 112 patients, SARS‐CoV‐2 was detected in 34 patients (30%). Among the non–SARS‐CoV‐2 viruses ( n = 25, 22%), metapneumovirus ( n = 10) was the most frequent agent. There were two coinfections with SARS‐CoV‐2. Sputum was less in the SARS‐CoV‐2 group ( P = .003). The leukocyte, lymphocyte, and thrombocyte count and C‐reactive protein levels were the lowest in the SARS‐CoV‐2 group ( P < .001, P = .04, P < .001, P = .007, respectively). Peripheral involvement (80% vs 20%; P ≤ .001), pure ground‐glass opacity (65% vs 33%; P = .04), apicobasal gradient (60% vs 40%; P = .08), involvement of greater than or equal to three lobes (80% vs 40%; odds ratio: 6.0; 95% confidence interval: 1.33‐27.05; P = .02), and consolidation with accompanying ground‐glass opacity (4% vs 33%; P = .031) were more common in SARS‐CoV‐2 group. Some clinical, laboratory, and radiological findings may help in the differential diagnosis of non–SARS‐CoV‐2 viruses from COVID‐19. However, coinfections may occur, and a non–SARS‐CoV‐2 pathogen positivity does not exclude accompanying COVID‐19. Highlights Non SARS‐CoV‐2 viruses have some clinical, laboratory and radiological distinctive parameters from SARS CoV‐2. However, it should always be considered that co‐infections may develop in the clinical course of COVID‐19. Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the clinical, laboratory, radiological distinctive features of viral pneumonia caused by viruses other than severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). A cross‐sectional study was conducted between 18 and 31 March 2020. COVID‐19 suspected cases admitted to pandemic policlinic, who had nasopharyngeal swab specimens tested for both SARS‐CoV‐2 and other respiratory viral pathogens, were included. Among 112 patients, SARS‐CoV‐2 was detected in 34 patients (30%). Among the non–SARS‐CoV‐2 viruses (n = 25, 22%), metapneumovirus (n = 10) was the most frequent agent. There were two coinfections with SARS‐CoV‐2. Sputum was less in the SARS‐CoV‐2 group (P = .003). The leukocyte, lymphocyte, and thrombocyte count and C‐reactive protein levels were the lowest in the SARS‐CoV‐2 group (P < .001, P = .04, P < .001, P = .007, respectively). Peripheral involvement (80% vs 20%; P ≤ .001), pure ground‐glass opacity (65% vs 33%; P = .04), apicobasal gradient (60% vs 40%; P = .08), involvement of greater than or equal to three lobes (80% vs 40%; odds ratio: 6.0; 95% confidence interval: 1.33‐27.05; P = .02), and consolidation with accompanying ground‐glass opacity (4% vs 33%; P = .031) were more common in SARS‐CoV‐2 group. Some clinical, laboratory, and radiological findings may help in the differential diagnosis of non–SARS‐CoV‐2 viruses from COVID‐19. However, coinfections may occur, and a non–SARS‐CoV‐2 pathogen positivity does not exclude accompanying COVID‐19. Highlights Non SARS‐CoV‐2 viruses have some clinical, laboratory and radiological distinctive parameters from SARS CoV‐2. However, it should always be considered that co‐infections may develop in the clinical course of COVID‐19. |
Author | Simsek, Gokçen O. Soyturk, Mujde Gezer, Naciye S. Kutsoylu, Oya O. E. Oguz, Vildan A. Tertemiz, Kemal C. Guzel, Irmak Alpaydin, Aylin O. Zeka, Arzu N. Sayiner, Ayca A. |
AuthorAffiliation | 2 Department of Radiology, Faculty of Medicine Dokuz Eylul University Izmir Turkey 4 Department of Medical Microbiology, Division of Medical Virology, Faculty of Medicine Dokuz Eylul University Izmir Turkey 3 Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine Dokuz Eylul University Izmir Turkey 5 Department of Internal Medicine, Faculty of Medicine Dokuz Eylul University Izmir Turkey 1 Department of Pulmonary Diseases, Faculty of Medicine Dokuz Eylul University Izmir Turkey |
AuthorAffiliation_xml | – name: 1 Department of Pulmonary Diseases, Faculty of Medicine Dokuz Eylul University Izmir Turkey – name: 4 Department of Medical Microbiology, Division of Medical Virology, Faculty of Medicine Dokuz Eylul University Izmir Turkey – name: 2 Department of Radiology, Faculty of Medicine Dokuz Eylul University Izmir Turkey – name: 3 Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine Dokuz Eylul University Izmir Turkey – name: 5 Department of Internal Medicine, Faculty of Medicine Dokuz Eylul University Izmir Turkey |
Author_xml | – sequence: 1 givenname: Aylin O. surname: Alpaydin fullname: Alpaydin, Aylin O. email: aylin.alpaydin@deu.edu.tr organization: Dokuz Eylul University – sequence: 2 givenname: Naciye S. surname: Gezer fullname: Gezer, Naciye S. organization: Dokuz Eylul University – sequence: 3 givenname: Gokçen O. surname: Simsek fullname: Simsek, Gokçen O. organization: Dokuz Eylul University – sequence: 4 givenname: Kemal C. surname: Tertemiz fullname: Tertemiz, Kemal C. organization: Dokuz Eylul University – sequence: 5 givenname: Oya O. E. surname: Kutsoylu fullname: Kutsoylu, Oya O. E. organization: Dokuz Eylul University – sequence: 6 givenname: Arzu N. surname: Zeka fullname: Zeka, Arzu N. organization: Dokuz Eylul University – sequence: 7 givenname: Irmak surname: Guzel fullname: Guzel, Irmak organization: Dokuz Eylul University – sequence: 8 givenname: Mujde surname: Soyturk fullname: Soyturk, Mujde organization: Dokuz Eylul University – sequence: 9 givenname: Ayca A. orcidid: 0000-0001-6750-2353 surname: Sayiner fullname: Sayiner, Ayca A. organization: Dokuz Eylul University – sequence: 10 givenname: Vildan A. surname: Oguz fullname: Oguz, Vildan A. organization: Dokuz Eylul University |
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Cites_doi | 10.1586/14737159.2016.1156536 10.1164/rccm.2020C1 10.5152/dir.2020.20260 10.1056/NEJMcp2009249 10.1164/rccm.201908-1581ST 10.1016/S0140-6736(20)30211-7 10.1056/NEJMoa2002032 10.1001/jama.2020.6266 10.1038/s41586-020-2012-7 10.2807/1560-7917.ES.2020.25.8.2000170 10.1038/s41579-018-0118-9 10.1148/radiol.2020201365 10.1097/RTI.0000000000000524 10.1148/rg.2018170048 10.1001/jama.2020.2648 10.5152/dir.2020.20351 10.1148/radiol.2020200274 10.2807/1560-7917.ES.2020.25.3.2000045 |
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Snippet | Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the... Following the announcement of the first coronavirus disease 2019 (COVID-19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates, and the... Abstract Following the announcement of the first coronavirus disease 2019 (COVID‐19) case on 11 March 2020 in Turkey, we aimed to report the coinfection rates,... |
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SubjectTerms | Adult Aged Coinfection - diagnosis Coinfection - virology Confidence intervals Coronaviridae Coronaviruses COVID-19 COVID-19 - epidemiology Cross-Sectional Studies Diagnosis Diagnosis, Differential Differential diagnosis Hospitalization Humans Laboratories Leukocytes Lymphocytes Middle Aged Nasopharynx - virology non–SARS‐CoV‐2 viruses Opacity Pandemics Pathogens Pneumonia, Viral - diagnosis Pneumonia, Viral - epidemiology Respiratory diseases SARS‐CoV‐2 Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Sputum Sputum - virology Thrombocytes Tomography, X-Ray Computed Turkey - epidemiology Viral diseases viral pneumonia Virology Virus Diseases - diagnosis Virus Diseases - epidemiology Viruses Viruses - classification Viruses - genetics Viruses - isolation & purification |
Title | Clinical and radiological diagnosis of non–SARS‐CoV‐2 viruses in the era of COVID‐19 pandemic |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmv.26410 https://www.ncbi.nlm.nih.gov/pubmed/32770738 https://www.proquest.com/docview/2473801271 https://search.proquest.com/docview/2431807057 https://pubmed.ncbi.nlm.nih.gov/PMC7436306 |
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