Comparison of clinical characteristics and outcomes of hospitalized patients with seasonal coronavirus infection and COVID-19: a retrospective cohort study
| dc.contributor.author | Rodriguez Nava, Guillermo | |
| dc.contributor.author | Goar, Egoryan | |
| dc.contributor.author | Dong, Tianyu | |
| dc.contributor.author | Zhang, Qishuo | |
| dc.contributor.author | Hyser, Elise | |
| dc.contributor.author | Poudel, Bidhya | |
| dc.contributor.author | Yanez Bello, Maria Adriana | |
| dc.contributor.author | Trelles Garcia, Daniela Patricia | |
| dc.contributor.author | Chung, Chul won | |
| dc.contributor.author | Pyakuryal, Bimatshu | |
| dc.contributor.author | Imani Ramos, Taraz | |
| dc.contributor.author | Trelles Garcia, Valeria Patricia | |
| dc.contributor.author | Bustamante Soliz, Daniel Sebastian | |
| dc.contributor.author | Stake, Jonathan J. | |
| dc.date.accessioned | 2023-01-23T20:44:43Z | |
| dc.date.available | 2023-01-23T20:44:43Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | Background: Unlike SARS-CoV and MERS-C0V, SARS-CoV-2 has the potential to become a recurrent seasonal infection; hence, it is essential to compare the clinical spectrum of COVID-19 to the existent endemic coronaviruses. We conducted a retrospective cohort study of hospitalized patients with seasonal coronavirus (sCoV) infection and COVID-19 to compare their clinical characteristics and outcomes. Methods: A total of 190 patients hospitalized with any documented respiratory tract infection and a positive respiratory viral panel for sCoV from January 1, 2011, to March 31, 2020, were included. Those patients were compared with 190 hospitalized adult patients with molecularly confirmed symptomatic COVID-19 admitted from March 1, 2020, to May 25, 2020. Results: Among 190 patients with sCoV infection, the Human Coronavirus-OC93 was the most common coronavirus with 47.4% of the cases. When comparing demographics and baseline characteristics, both groups were of similar age (sCoV: 74 years vs. COVID-19: 69 years) and presented similar proportions of two or more comorbidities (sCoV: 85.8% vs. COVID-19: 81.6%). More patients with COVID-19 presented with severe disease (78.4% vs. 67.9%), sepsis (36.3% vs. 20.5%), and developed ARDS (15.8% vs. 2.6%) compared to patients with sCoV infection. Patients with COVID-19 had an almost fourfold increased risk of in-hospital death than patients with sCoV infection (OR 3.86, CI 1.99–7.49; p <.001). Conclusion: Hospitalized patients with COVID-19 had similar demographics and baseline characteristics to hospitalized patients with sCoV infection; however, patients with COVID-19 presented with higher disease severity, had a higher case-fatality rate, and increased risk of death than patients with sCoV. Clinical findings alone may not help confirm or exclude the diagnosis of COVID-19 during high acute respiratory illness seasons. The respiratory multiplex panel by PCR that includes SARS-CoV-2 in conjunction with local epidemiological data may be a valuable tool to assist clinicians with management decisions. | |
| dc.identifier.doi | 10.1186/s12879-022-07555-4 | |
| dc.identifier.issn | 1471-2334 | |
| dc.identifier.uri | https://www.scopus.com/record/display.uri?eid=2-s2.0-85134224351&origin=resultslist&sort=plf-f&src=s&sid=90d26bb4684d6ffa68dc4bba9ca94628&sot=b&sdt=b&s=TITLE-ABS-KEY%28Comparison+of+clinical+characteristics+and+outcomes+of+hospitalized+patients+with+seasonal+coronavirus+infection+and+COVID-19%3A+a+retrospective+cohort+study%29&sl=170&sessionSearchId=90d26bb4684d6ffa68dc4bba9ca94628 | |
| dc.language.iso | es_ES | |
| dc.source | BMC Infectious Diseases | |
| dc.subject | COVID-19 | |
| dc.subject | Human coronavirus | |
| dc.subject | MERS | |
| dc.subject | SARS | |
| dc.subject | Seasonal coronavirus | |
| dc.title | Comparison of clinical characteristics and outcomes of hospitalized patients with seasonal coronavirus infection and COVID-19: a retrospective cohort study | |
| dc.type | ARTÍCULO | |
| dc.ucuenca.afiliacion | Rodriguez, G., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Goar, E., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Dong, T., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Zhang, Q., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Hyser, E., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Poudel, B., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Yanez, M., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Trelles, D., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Chung, C., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Pyakuryal, B., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.afiliacion | Imani, T., AMITA Health Saint Joseph Hospital, Chicago, Estados unidos | |
| dc.ucuenca.afiliacion | Trelles, V., John H Stroger Jr Hospital of Cook County, Chicago, Estados unidos | |
| dc.ucuenca.afiliacion | Bustamante, D., Universidad de Cuenca, Facultad de Ciencias Médicas, Cuenca, Ecuador | |
| dc.ucuenca.afiliacion | Stake, J., AMITA Health Saint Francis Hospital, Evanston, Estados unidos | |
| dc.ucuenca.areaconocimientofrascatiamplio | 3. Ciencias Médicas y de la Salud | |
| dc.ucuenca.areaconocimientofrascatidetallado | 3.3.10 Epidemiología | |
| dc.ucuenca.areaconocimientofrascatiespecifico | 3.3 Ciencias de la Salud | |
| dc.ucuenca.areaconocimientounescoamplio | 09 - Salud y Bienestar | |
| dc.ucuenca.areaconocimientounescodetallado | 0912 - Medicina | |
| dc.ucuenca.areaconocimientounescoespecifico | 091 - Salud | |
| dc.ucuenca.correspondencia | Rodriguez Nava, Guillermo, Guillermo.RodriguezNava@amitahealth.org | |
| dc.ucuenca.cuartil | Q2 | |
| dc.ucuenca.factorimpacto | 1.042 | |
| dc.ucuenca.idautor | 0000-0001-9826-7050 | |
| dc.ucuenca.idautor | 0000-0001-5203-8156 | |
| dc.ucuenca.idautor | 57365234900 | |
| dc.ucuenca.idautor | 0000-0002-7006-9391 | |
| dc.ucuenca.idautor | 57203209717 | |
| dc.ucuenca.idautor | 0000-0003-0164-5858 | |
| dc.ucuenca.idautor | 0000-0002-8703-1832 | |
| dc.ucuenca.idautor | 0000-0001-6333-4540 | |
| dc.ucuenca.idautor | 0000-0001-5544-1514 | |
| dc.ucuenca.idautor | 0000-0002-7133-3924 | |
| dc.ucuenca.idautor | 0000-0003-2563-0909 | |
| dc.ucuenca.idautor | 0000-0003-4387-3365 | |
| dc.ucuenca.idautor | 0105381032 | |
| dc.ucuenca.idautor | 57221384417 | |
| dc.ucuenca.indicebibliografico | SCOPUS | |
| dc.ucuenca.numerocitaciones | 0 | |
| dc.ucuenca.urifuente | https://bmcinfectdis.biomedcentral.com/ | |
| dc.ucuenca.version | Versión publicada | |
| dc.ucuenca.volumen | Volumen 22, número 1 |
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