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Published on: March 22, 2022
Identifying Key Hematological and Biochemical Indicators of Disease Severity in COVID-19 and Non-COVID-19 Patients
Soo-Kyung Kim1, Daewoo Pak2, Jong-Han Lee3
1Department of Laboratory Medicine, Ewha Womans University College of Medicine, Seoul 07985, Republic of Korea.
Insights
Hematological and biochemical markers, including cell population data, can predict COVID-19 severity. Elevated neutrophil side fluorescence light and platelet-to-lymphocyte ratio indicate higher risk, aiding disease monitoring.
Area of Science:
- Hematology
- Biochemistry
- Infectious Diseases
- Critical Care Medicine
Background:
- Investigated hematological and biochemical parameters, including cell population data (CPD), for association with disease severity in COVID-19 and non-COVID-19 patients.
- Aims to identify parameters for improved disease monitoring and clinical decision-making.
Purpose of the Study:
- To identify hematological and biochemical biomarkers associated with severe COVID-19 outcomes.
- To assess the utility of these biomarkers in disease monitoring and clinical management.
Main Methods:
- Retrospective analysis of 8401 patients (603 COVID-19, 7546 non-COVID-19).
- Analysis of complete blood count (CBC) and chemistry results near PCR testing.
- Matched cohort analysis to control for age and sex.
Main Results:
- Elevated neutrophil side fluorescence light (NE-SFL), platelet-to-lymphocyte ratio (PLR), glucose, and AST, with decreased plateletcrit, correlated with severe COVID-19 outcomes.
- Decreased hemoglobin, lymphocyte side scatter (LY-SSC), albumin, and increased monocyte side scatter (MO-SSC) associated with severity, irrespective of COVID-19 status.
Conclusions:
- Identified specific hematologic and chemical assay biomarkers correlating with severe COVID-19.
- Findings support biomarker integration into clinical decision support systems for personalized treatment and severity stratification.
Abstract:
Background: This study investigated hematological and biochemical parameters, including cell population data (CPD), to evaluate their association with severity in COVID-19 and non-COVID-19 patients. Identifying these parameters could aid in disease monitoring and clinical decision-making. Methods: A retrospective analysis of 8401 patients, including 603 COVID-19 cases and 7546 non-COVID-19 cases, were conducted. Complete blood count (CBC) and routine chemistry results obtained near the time of real-time polymerase chain reaction testing were analyzed to assess their associations with disease severity. A matched cohort analysis was performed to adjust for potential confounding factors, such as age and sex. Results: COVID-19 patients with elevated neutrophil side fluorescence light (NE-SFL), platelet-to-lymphocyte ratio (PLR), glucose, and aspartate aminotransferase (AST), along with decreased plateletcrit, were more likely to experience severe outcomes, such as hospitalization or death. In addition, decreased hemoglobin, lymphocyte side scatter (LY-SSC), and albumin, as well as increased leukocyte and monocyte side scatter (MO-SSC), were associated with a greater severity, regardless of COVID-19 status. Conclusions: We identified hematologic and chemical assay biomarkers that correlate with severe COVID-19. These findings may provide important information regarding the disease progression and clinical management. Incorporating these biomarkers into clinical decision support systems could facilitate personalized treatment strategies, optimize resource allocation, and enable real-time severity stratification.
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