Fib-4 score is able to predict intra-hospital mortality in 4 different SARS-COV2 waves

Luca Miele1,2, Marianxhela Dajko3, Maria Chiara Savino4

  • 1Dipartimento di Scienze Mediche e Chirurgiche (DiSMeC), Fondazione Policlinico Gemelli IRCCS, Università Cattolica del S. Cuore, 8, Largo Gemelli, 00168, Rome, Italy. luca.miele@policlinicogemelli.it.

PubMed

Insights

The FIB-4 index can predict mortality risk in hospitalized COVID-19 patients. Higher FIB-4 scores (over 2.53) are linked to a significantly increased risk of death, aiding in early patient risk stratification.

Area of Science:

  • Internal Medicine
  • Infectious Diseases
  • Biostatistics

Background:

  • Elevated FIB-4 index values correlate with adverse clinical outcomes in COVID-19 patients.
  • Accurate risk stratification is crucial for managing hospitalized COVID-19 patients.

Purpose of the Study:

  • To develop and validate predictive mortality models for hospitalized COVID-19 patients.
  • To assess the association between the FIB-4 index and mortality risk during different pandemic waves.

Main Methods:

  • A single-center cohort study included 4936 hospitalized COVID-19 patients across four waves (March 2020-January 2022).
  • Artificial intelligence and big data processing were utilized for data retrieval from the Gemelli Generator Real World Data (G2 RWD).
  • A multivariable logistic regression model was developed and validated using a 75%:25% training-test split, with performance assessed by ROC curves.

Main Results:

  • The study identified hypertension, cancer, and diabetes as common comorbidities.
  • A FIB-4 score greater than 2.53 was significantly associated with increased COVID-19 mortality risk (OR = 4.53, p ≤ 0.001).
  • The developed model demonstrated predictive capability for patient mortality.

Conclusions:

  • The FIB-4 index serves as a valuable tool for early risk stratification of hospitalized COVID-19 patients.
  • These findings can assist clinicians in identifying high-risk individuals upon admission.
  • Further validation in diverse cohorts is recommended to confirm generalizability.

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