Your browser doesn't support javascript.
loading
A Tool to Early Predict Severe 2019-Novel Coronavirus Pneumonia (COVID-19) : A Multicenter Study using the Risk Nomogram in Wuhan and Guangdong, China
Jiao Gong; Jingyi Ou; Xueping Qiu; Yusheng Jie; Yaqiong Chen; Lianxiong Yuan; Jing Cao; Mingkai Tan; Wenxiong Xu; Fang Zheng; Yaling Shi; Bo Hu.
Afiliação
  • Jiao Gong; Third Affiliated Hospital of Sun Yat-sen University
  • Jingyi Ou; Guangzhou Eighth People's Hospital
  • Xueping Qiu; Zhongnan Hospital of Wuhan University
  • Yusheng Jie; Third Affiliated Hospital of Sun Yat-sen University
  • Yaqiong Chen; Third Affiliated Hospital of Sun Yat-sen University
  • Lianxiong Yuan; Third Affiliated Hospital of Sun Yat-sen University
  • Jing Cao; Third Affiliated Hospital of Sun Yat-sen University
  • Mingkai Tan; Guangzhou Eighth People's Hospital
  • Wenxiong Xu; Third Affiliated Hospital of Sun Yat-sen University
  • Fang Zheng; Zhongnan Hospital of Wuhan University
  • Yaling Shi; Clinical Laboratory of Guangzhou Eighth People's Hospital
  • Bo Hu; Third Affiliated Hospital of Sun Yat-sen University
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20037515
ABSTRACT
BackgroundDue to no reliable risk stratification tool for severe corona virus disease 2019 (COVID-19) patients at admission, we aimed to construct an effective model for early identifying cases at high risk of progression to severe COVID-19. MethodsIn this retrospective three-centers study, 372 non-severe COVID-19 patients during hospitalization were followed for more than 15 days after admission. Patients who deteriorated to severe or critical COVID-19 and patients who kept non-severe state were assigned to the severe and non-severe group, respectively. Based on baseline data of the two groups, we constructed a risk prediction nomogram for severe COVID-19 and evaluate its performance. ResultsThe train cohort consisted of 189 patients, while the two independent validation cohorts consisted of 165 and 18 patients. Among all cases, 72 (19.35%) patients developed severe COVID-19. We found that old age, and higher serum lactate dehydrogenase, C-reactive protein, the coefficient of variation of red blood cell distribution width, blood urea nitrogen, direct bilirubin, lower albumin, are associated with severe COVID-19. We generated the nomogram for early identifying severe COVID-19 in the train cohort (AUC 0.912 [95% CI 0.846-0.978], sensitivity 85.71%, specificity 87.58%); in validation cohort (0.853 [0.790-0.916], 77.5%, 78.4%). The calibration curve for probability of severe COVID-19 showed optimal agreement between prediction by nomogram and actual observation. Decision curve and clinical impact curve analysis indicated that nomogram conferred high clinical net benefit. ConclusionOur nomogram could help clinicians to early identify patients who will exacerbate to severe COVID-19, which will enable better centralized management and early treatment of severe patients. SummaryOlder age; higher LDH, CRP, RDW, DBIL, BUN; lower ALB on admission correlated with higher odds of severe COVID-19. An effective prognostic nomogram composed of 7 features could allow early identification of patients at risk of exacerbation to severe COVID-19.
Licença
cc_no
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Cohort_studies / Experimental_studies / Observational_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: Cohort_studies / Experimental_studies / Observational_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint