Correlation of Neutrophil-Lymphocyte Ratio and Critical Illness in Adults on Vancomycin: A Cross-Sectional Study
- PMID: 40766859
- PMCID: PMC12323880
- DOI: 10.2147/IJGM.S537039
Correlation of Neutrophil-Lymphocyte Ratio and Critical Illness in Adults on Vancomycin: A Cross-Sectional Study
Abstract
Background: Early risk-stratification in patients receiving vancomycin (VAN) is crucial but reliable markers are scarce. Herein, the correlates and determinants of neutrophil-lymphocyte ratio (NLR), an emerging inflammatory marker, with ICU admission in VAN-treated adults were investigated.
Methods: Demographic and clinical data for 295 adults treated with VAN at King Khalid University Hospital from January 2024 to February 2025 were retrospectively analyzed using Mann-Whitney U and Chi-square tests, Spearman rank correlation, regression analysis, effect size measures, and calculation of areas under the receiver operating characteristic curve (AUC).
Results: NLR was significantly elevated in ICU compared to non-ICU patients (p <0.0001) and the proportion of ICU patients with elevated NLR was significantly higher than those with normal NLR (X 2 = 33.69, p <0.0001) irrespective of age or gender. In particular, ICU requirement was 2.49 and 2.54 times more prevalent in males and females with elevated NLR, respectively (p = 0.0002). Also, ICU admission was 4.25 and 4.40 times more likely when NLR was elevated in males and females, respectively (p = 0.0001). Notably, ICU admission was independently associated with a 9.65-unit increase in NLR (p = 0.0005) of which age, body mass index, and conjugated bilirubin were identified as independent predictors. Moreover, NLR showed good diagnostic ability for ICU requirement with AUC ranging from 0.71 to 0.78 (p <0.0001).
Conclusion: NLR is easily accessible, cost-effective, and demonstrates promising potential to complement existing markers for identifying high-risk patients and optimizing early intervention in critically ill adults receiving VAN therapy.
Keywords: ICU; NLR; inflammation; sepsis; vancomycin.
© 2025 Alfhili et al.
Conflict of interest statement
The authors declare no conflicts of interest.
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