Background. The rapid onset of a systemic pro-inflammatory state followed by acute respiratory distress syndrome is the leading cause of mortality in patients with COVID-19. We performed a retrospective observational study to explore the capacity of different complete blood cell count (CBC)-derived inflammation indexes to predict in-hospital mortality in this group. Methods. The neutrophil to lymphocyte ratio (NLR), derived NLR (dNLR), platelet to lymphocyte ratio (PLR), mean platelet volume to platelet ratio (MPR), neutrophil to lymphocyte × platelet ratio (NLPR), monocyte to lymphocyte ratio (MLR), systemic inflammation response index (SIRI), systemic inflammation index (SII), and the aggregate index of systemic inflammation (AISI) were calculated on hospital admission in 119 patients with laboratory confirmed COVID-19. Results. Non-survivors had significantly higher AISI, dNLR, NLPR, NLR, SII, and SIRI values when compared to survivors. Similarly, Kaplan-Meier survival curves showed significantly lower survival in patients with higher AISI, dNLR, MLR, NLPR, NLR, SII, and SIRI. However, after adjusting for confounders, only the SII remained significantly associated with survival (HR = 1.0001; 95% CI, 1.0000-1.0001, p = 0.029) in multivariate Cox regression analysis. Conclusions. The SII on admission independently predicts in-hospital mortality in COVID-19 patients and may assist with early risk stratification in this group.

The systemic inflammation index on admission predicts in-hospital mortality in COVID-19 patients / A.G. Fois, P. Paliogiannis, V. Scano, S. Cau, S. Babudieri, R. Perra, G. Ruzzittu, E. Zinellu, P. Pirina, C. Carru, L.B. Arru, A. Fancellu, M. Mondoni, A.A. Mangoni, A. Zinellu. - In: MOLECULES. - ISSN 1420-3049. - 25:23(2020), pp. 5725.1-5725.13. [10.3390/molecules25235725]

The systemic inflammation index on admission predicts in-hospital mortality in COVID-19 patients

M. Mondoni;
2020

Abstract

Background. The rapid onset of a systemic pro-inflammatory state followed by acute respiratory distress syndrome is the leading cause of mortality in patients with COVID-19. We performed a retrospective observational study to explore the capacity of different complete blood cell count (CBC)-derived inflammation indexes to predict in-hospital mortality in this group. Methods. The neutrophil to lymphocyte ratio (NLR), derived NLR (dNLR), platelet to lymphocyte ratio (PLR), mean platelet volume to platelet ratio (MPR), neutrophil to lymphocyte × platelet ratio (NLPR), monocyte to lymphocyte ratio (MLR), systemic inflammation response index (SIRI), systemic inflammation index (SII), and the aggregate index of systemic inflammation (AISI) were calculated on hospital admission in 119 patients with laboratory confirmed COVID-19. Results. Non-survivors had significantly higher AISI, dNLR, NLPR, NLR, SII, and SIRI values when compared to survivors. Similarly, Kaplan-Meier survival curves showed significantly lower survival in patients with higher AISI, dNLR, MLR, NLPR, NLR, SII, and SIRI. However, after adjusting for confounders, only the SII remained significantly associated with survival (HR = 1.0001; 95% CI, 1.0000-1.0001, p = 0.029) in multivariate Cox regression analysis. Conclusions. The SII on admission independently predicts in-hospital mortality in COVID-19 patients and may assist with early risk stratification in this group.
CBC; Coronavirus; COVID-19; Inflammation; SII; Aged; Aged, 80 and over; Blood Cell Count; COVID-19; Comorbidity; Female; Humans; Inflammation; Lymphocyte Count; Male; Middle Aged; Neutrophils; ROC Curve; Retrospective Studies; Hospital Mortality
Settore MED/10 - Malattie dell'Apparato Respiratorio
2020
Article (author)
File in questo prodotto:
File Dimensione Formato  
molecules-25-05725 (1).pdf

accesso aperto

Descrizione: Article
Tipologia: Publisher's version/PDF
Dimensione 957.96 kB
Formato Adobe PDF
957.96 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/915453
Citazioni
  • ???jsp.display-item.citation.pmc??? 35
  • Scopus 232
  • ???jsp.display-item.citation.isi??? 227
  • OpenAlex ND
social impact