Journal of Clinical Medicine (Mar 2022)

A Simple Prognostic Score for Critical COVID-19 Derived from Patients without Comorbidities Performs Well in Unselected Patients

  • Vasiliki E. Georgakopoulou,
  • Nikolaos I. Vlachogiannis,
  • Dimitrios Basoulis,
  • Irene Eliadi,
  • Georgios Georgiopoulos,
  • Georgios Karamanakos,
  • Sotiria Makrodimitri,
  • Stamatia Samara,
  • Maria Triantafyllou,
  • Pantazis M. Voutsinas,
  • Fotinie Ntziora,
  • Mina Psichogiou,
  • Michael Samarkos,
  • Petros P. Sfikakis,
  • Nikolaos V. Sipsas

DOI
https://doi.org/10.3390/jcm11071810
Journal volume & issue
Vol. 11, no. 7
p. 1810

Abstract

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We aimed to search for laboratory predictors of critical COVID-19 in consecutive adults admitted in an academic center between 16 September 2020–20 December 2021. Patients were uniformly treated with low-molecular-weight heparin, and dexamethasone plus remdesivir when SpO2 n = 241, 49 year-old median, 71% males), 22 (9.1%) developed critical disease and 2 died (0.8%). White-blood-cell counts, neutrophils, neutrophil-to-lymphocyte ratio, CRP, fibrinogen, ferritin, LDH and γ-GT at admission were each univariably associated with critical disease. ROC-defined cutoffs revealed that CRP > 61.8 mg/L, fibrinogen > 616.5 mg/dL and LDH > 380.5 U/L were each associated with critical disease development, independently of age, sex and days from symptom-onset. A score combining higher-than-cutoff CRP (0/2), LDH (0/1) and fibrinogen (0/1) predicted critical disease (AUC: 0.873, 95% CI: 0.820–0.926). This score performed well in an unselected patient cohort (n = 1228, 100% unvaccinated) predominantly infected by the alpha variant (AUC: 0.718, 95% CI: 0.683–0.753), as well as in a mixed cohort (n = 527, 65% unvaccinated) predominantly infected by the delta variant (AUC: 0.708, 95% CI: 0.656–0.760). Therefore, we propose that a combination of standard biomarkers of acute inflammatory response, cell death and hypercoagulability reflects the severity of COVID-19 per se independently of comorbidities, age and sex, being of value for risk stratification in unselected patients.

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