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Predictive Value of Systemic Immune-inflammation Index in Determining Mortality in COVID-19 Patients
Tahsin Karaaslan1, Esra Karaaslan2
1Medeniyet University Göztepe Training and Research Hospital, Istanbul, Turkey.
Insights
The systemic immune-inflammation index (SII) can predict COVID-19 mortality. A higher SII value (>618.8) was associated with a 4.68-fold increased risk of death in patients with COVID-19.
Area of Science:
- Infectious Diseases
- Immunology
- Critical Care Medicine
Background:
- The COVID-19 pandemic caused by SARS-CoV-2 has led to significant global mortality.
- Identifying reliable biomarkers for predicting COVID-19 outcomes is crucial for patient management.
Purpose of the Study:
- To evaluate the predictive value of the systemic immune-inflammation index (SII) for mortality in patients diagnosed with COVID-19.
Main Methods:
- A retrospective study involving 191 COVID-19 patients diagnosed via nucleic acid testing.
- The SII was calculated using neutrophil, platelet, and lymphocyte counts.
- The correlation between SII, inflammatory markers, and mortality was analyzed.
Main Results:
- The mortality rate among the studied patients was 18.3%.
- The SII showed a strong positive correlation with other inflammatory markers like PNL, NLR, and PLR, and a moderate correlation with CRP.
- A significant correlation was found between SII and mortality, with a cut-off value of 618.8 predicting mortality with 80.0% sensitivity and 61.5% specificity.
Conclusions:
- The SII serves as a valuable marker of systemic inflammation.
- The SII can be effectively utilized as an independent predictor of mortality in COVID-19 patients, similar to NLR and PLR.
Aim:
The aim of this study was to evaluate whether systemic immune-inflammation index (SII) could predict mortality in patients with novel coronavirus 2019 (COVID-19) disease.
Methods:
This two-center, retrospective study included a total of 191 patients with confirmed diagnosis of COVID-19 via nucleic acid test (NAT). The SII was calculated based on the complete blood parameters (neutrophil × platelet/lymphocyte) during hospitalization. The relationship between the SII and other inflammatory markers and mortality was investigated.
Results:
The mortality rate was 18.3%. The mean age was 54.32±17.95 years. The most common symptoms were fever (70.7%) and dry cough (61.3%), while 8 patients (4.2%) were asymptomatic. The most common comorbidities were hypertension (37.7%), diabetes (23.0%), chronic renal failure (14.7%), and heart failure (7.9%) which all significantly increased the mortality rate (p<0.001). There was a highly positive correlation between the SII and polymorphonuclear leukocyte (PNL), neutrophil-to-lymphocyte ratio (NLR), and platelet-to-lymphocyte ratio (PLR) (r=0.754, p<0.001; r=0.812, p<0.001; r=0.841, p<0.001, respectively), while a moderate, positive correlation was found between the SII and C-reactive protein (CRP) (r=0.439, p<0.001). There was a significant correlation between the SII and mortality (U=1,357, p<0.001). The cut-off value of SII was 618.8 (area under the curve=0.751, p<0.001) with 80.0% sensitivity and 61.5% specificity. A cut-off value of >618.8 was associated with a 4.68-fold higher mortality.
Conclusion:
Similar to NLR and PLR, the SII is a proinflammatory marker of systemic inflammation and can be effectively used in independent predicting COVID-19 mortality.
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