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How closely is COVID-19 related to HCoV, SARS, and MERS? : Clinical comparison of coronavirus infections and identification of risk factors influencing the COVID-19 severity using common data model (CDM)
Yeon Hee Kim; Ye-Hee Ko; Sooyoung Kim; Kwangsoo Kim.
Afiliação
  • Yeon Hee Kim; Biomedical Research Institute, Seoul National University Hospital
  • Ye-Hee Ko; Biomedical Research Institute, Seoul National University Hospital
  • Sooyoung Kim; Biomedical Research Institute, Seoul National University Hospital
  • Kwangsoo Kim; Transdisciplinary Department of Medicine & Advanced Technology, Seoul National University Hospital
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20237487
ABSTRACT
BackgroundSouth Korea was one of the epicenters for both the 2015 Middle East Respiratory Syndrome and 2019 COVID-19 outbreaks. However, there has been a lack of published literature, especially using the Electronic Medical Records (EMR), that provides a comparative summary of the prognostic factors present in the coronavirus-derived diseases. Therefore, in this study, we aimed to evaluate the distinct clinical traits between the infected patients of different coronaviruses to observe the extent of resemblance within the clinical features and to identify unique factors by disease severity that may influence the prognosis of COVID-19 patients. MethodsWe utilized the common data model (CDM), which is the database that houses the standardized EMR. We set COVID-19 as a reference group in comparative analyses. For statistical methods, we used Levenes test, one-way Anova test, Scheffe post-hoc test, Games-howell post-hoc test, and Students t-test for continuous variables, and chi-squared test and Fishers exact test for categorical variables. With the variables that reflected similarity in more than two comparisons between the disease groups yet significantly different between the COVID-19 severity groups, we performed univariate logistic regression to identify which common manifestations in coronaviruses are risk factors for severe COVID-19 outcomes. FindingsWe collected the records of 2840 COVID-19 patients, 67 MERS patients (several suspected cases included), 43 SARS suspected patients, and 87 HCoV patients. We found that a significantly higher number of COVID-19 patients had been diagnosed with comorbidities compared to the MERS and HCoV groups (48.5% vs. 10.4 %, p < 0.001 and 48.5% vs. 35.6%, p < 0.05) and also that the non-mild COVID-19 patients reported more comorbidities than the mild group (55.7% vs. 47.8%, p < 0.05). There were overall increases in the levels of fibrinogen in both sets of disease and severity groups. The univariate logistic regression showed that the male sex (OR 1.66; CI 1.29-2.13, p < 0.001), blood type A (OR 1.80; CI 1.40-2.31, p < 0.001), renal disease (OR 3.27; CI 2.34-4.55, p < 0.001), decreased creatinine level (OR 2.05; CI 1.45-2.88, p < 0.001), and elevated fibrinogen level (OR 1.59, CI 1.21-2.09, p < 0.001) are associated with the severe COVID-19 prognosis, whereas the patients reporting gastrointestinal symptoms (OR 0.42; CI 0.23-0.72, p < 0.01) and increased alkaline phosphatase (OR 0.73; CI 0.56-0.94, p < 0.05) are more less likely to experience complications and other severe outcomes from the SARS-CoV-2 infection. InterpretationThe present study observed the highest resemblance between the COVID-19 and SARS groups as clinical manifestations that were present in SARS group were linked to the severity of COVID-19. In particular, male individuals with blood type A and previous diagnosis of kidney failure were shown to be more susceptible to developing the poorer outcomes during COVID-19 infection, with a presentation of elevated level of fibrinogen.
Licença
cc_by_nc_nd
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint
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